Synthesis, Reactions, and Agrochemical Studies of New 4,6-Diaryl-2-hydrazinylnicotinonitriles

Abstract

This work aimed to synthesize new derivatives of 2-hydrazinylpyridine-3-carbonitrile and to investigate their biological activity as safeners for the 2,4-D herbicide. The new 2-hydrazinylnicotinonitriles were obtained in high yields (up to quantitative) under mild conditions (25 °C, dioxane) by treating 4,6-diaryl-2-bromo-3-cyanopyridines with hydrazine hydrate. The latter were synthesized by brominating 2-(3-oxo-1,3-diarylpropyl)malononitriles, the Michael adducts, which are readily available from 1,3-diarylpropenones (chalcones) and malononitrile. An unusual side product of the bromination/carbocyclization was isolated and characterized; it consisted of co-crystals of 3-benzoyl-4-hydroxy-4-phenyl-2,6-di-(p-tolyl)cyclohexane-1,1-dicarbonitrile and 3-benzoyl-5-bromo-4-hydroxy-4-phenyl-2,6-di-(p-tolyl)cyclohexane-1,1-dicarbonitrile at a ~4:6 ratio. The new 2-hydrazinylnicotinonitriles react with halogen-containing aromatic aldehydes to form the corresponding hydrazones. The biological activity of the new nicotinonitriles was examined for their function as 2,4-D antidotes. It was found that, under laboratory conditions, eight of the synthesized compounds exhibited a notable antidote effect against 2,4-D on sunflower seedlings.

1. Introduction

2-Hydrazinylpyridines represent a promising class of compounds with diverse, though not yet fully realized, potential [1]. According to recent data, 2-hydrazinylpyridines 1 are of interest as antioxidants and antimicrobial agents [2]. Compounds 2 and 3 serve as intermediates in the synthesis of wheat growth regulators [3,4] (Figure 1). Hydrazones 4 exhibit antimicrobial action, with MIC values ranging from 12.5 to 25 μg/mL [5]. Nicotinonitrile 5 demonstrated significant activity against the breast cancer cell line MCF-7 in in vivo experiments [6]. The unsubstituted 2-hydrazinylpyridine 6 is used for inhibiting lysyl oxidase-2 (LOXL2) as an alternative to phenyl hydrazine [7,8], for preparing coordination compounds with various metals [9,10,11,12,13,14,15], and as an analytical reagent for derivatization in the determination of steroid hormones [16,17,18,19,20,21]. Recently, 2-hydrazinylpyridine 6 and 2-hydrazinyl-5-methylpyridine 7 were proposed as twin derivatization reagents for the rapid determination of α,β-unsaturated aldehydes in vegetable oils [22]. Hydrazines 6 and 7, in combination with nicotinonitrile 8, were recently proposed for identifying potential lung cancer carbonyl biomarkers in human plasma samples [23]. 6-Hydrazinylnicotinamide 9 is used to produce bifunctional coupling agents for ^99mTc labeling of small biomolecules [24,25]. In recent years, condensation products of 2-hydrazinylpyridine with carbonyl compounds have been proposed as chemosensors for detecting SO₄²⁻ and CO₃²⁻ [26], Cu²⁺ and Co²⁺ [27], Al³⁺ and OH⁻ [28], and Hg²⁺ and Au³⁺ [29,30,31], as viscosity-sensitive fluorescent probes [32], and as aggregation-induced emission dyes suitable for fluorescence imaging of cellular organelles [33]. Compound 10 showed 100% tumor inhibition, comparable to the standard drug Vincristine, and it also exhibited tremendous activity toward Leishmania major [34]. Cytotoxic activity has also been reported for 2-hydrazinylnicotinonitrile 11 [35], high fungicidal activity for compound 12 [36], and antimicrobial effects for nicotinonitrile 13 [37] and hydrazones 14 [38] (Figure 1). It is also worth mentioning that 2-hydrazinylpyridines and 2-hydrazinylnicotinonitriles are precursors to several practically important classes of heterocyclic compounds, such as 1,2,4-triazolo[4,3-a]pyridines [39,40,41,42,43,44], pyrazolo[3,4-b]pyridines [45,46,47,48,49,50,51,52,53,54,55], and pyrido-1,2,4-triazines [56].

Continuing our research in the chemistry of nicotinonitriles with agrochemical applications [57,58,59,60,61,62,63,64,65] on one hand, and the search for new derivatizing agents for UHPLC-HRMS determination of metabolites in biological fluids [66,67,68,69] on the other, we aimed to prepare new 4,6-diaryl-2-hydrazinylnicotinonitriles, study some of their reactions, and evaluate the biological activity of the products as antidotes for the herbicide 2,4-D.

Despite their potential, 4,6-diaryl-2-hydrazinylnicotinonitriles have not yet found application in analytical chemistry or agrochemistry. These compounds are expected to be more selective derivatizing agents for carbonyl compounds than the currently used 2-hydrazinylpyridine derivatives [16,17,18,19,20,21,22,23]. Support for their potential in agrochemistry comes from reports on analogous structures. Some related compounds 15 are known herbicide safeners and rice growth stimulants [70,71], others, like compounds 16, are growth regulators for winter wheat [72], and hydrazones 17 exhibit antifungal activity against Aspergillus flavus and A. niger [73] (Figure 2). Nevertheless, 4,6-diaryl-2-hydrazinylnicotinonitriles remain a scarcely studied group of compounds, and their practical application has not been reported in the literature to date.

The primary methods for the synthesis of 2-hydrazinylnicotinonitrile derivatives are based on the hydrazinolysis of 2-chloro-3-cyanopyridines [6,34,35,36,37,38,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92] or 2-alkoxy-3-cyanopyridines [73,92,93,94,95,96]. An alternative route involves the nucleophilic displacement of a sulfur-containing group in 2-mercaptonicotinonitrile derivatives [5,92,97,98,99,100] (Scheme 1). It is important to note certain limitations associated with these established synthetic pathways. A significant drawback is the multi-step nature of the synthesis for 2-hydrazinyl-3-cyanopyridines. The required starting 2-alkoxy-, 2-chloro-, or 2-alkylthio nicotinonitrile precursors are themselves predominantly obtained from starting materials that already contain the pre-formed nicotinonitrile core structure.

It should be noted that the chlorine atom or the RS group at the 2 position of a 3-cyanopyridine molecule is a relatively poor nucleofuge. Thus, it is known that in the case of 2,6-dichloronicotinonitriles, the halogen atom at the C-6 position is substituted first during hydrazinolysis [3,101,102,103,104] (Scheme 2). Furthermore, when hydrazinolysis is performed on esters of 3-cyanopyridine-2-(thio/oxy)acetic acid, the main product is often not the 2-hydrazinylnicotinonitrile but the corresponding carboxylic acid hydrazide (for example, [93,94,105]).

The hydrazinolysis reaction of 2-chloronicotinonitriles generally requires heating—for instance, refluxing in ethanol for 4–18 h [83,84,85,86,87,88,89,90,91,92], refluxing in DMF for 6 h [35], refluxing in dioxane for 3–12 h [74,75,76,77,78,79,80], or heating in 1-butanol at 110–112 °C [82]. In contrast, under relatively mild conditions (20–25 °C or with brief heating), the reaction between 2-chloropyridines and hydrazine occurs only if the pyridine ring contains two or more strong electron-withdrawing substituents [106,107,108,109,110] (Scheme 3).

However, the use of harsher reaction conditions promotes an intramolecular cyclization between the hydrazine fragment and the cyano group, yielding well-known 3-amino-1H-pyrazolo[3,4-b]pyridines [45,46,47,48,49,50,51,52,53,54,55]. This side reaction commonly accompanies or even competes with the formation of 2-hydrazinylnicotinonitriles. Moreover, in many cases, the isolation of 2-hydrazinyl-3-cyanopyridines is often impossible, and pyrazolo[3,4-b]pyridines are obtained as the sole products. Typical examples that demonstrate this pathway can be found in references [90,111,112,113,114,115,116,117,118] (Scheme 4).

Given the aforementioned drawbacks and limitations of existing methods, developing new and optimized approaches for synthesizing 2-hydrazinylnicotinonitriles is highly desirable. This work presents an efficient route to 4,6-diaryl-2-hydrazinyl-3-cyanopyridines based on the reaction of 4,6-diaryl-2-bromo-3-cyanopyridines with hydrazine hydrate under mild conditions. The starting 2-bromo-3-cyanopyridines are readily available in high yields from inexpensive, commercially available acyclic precursors in only two steps (Scheme 5). In general, literature reports on the use of 2-bromo-3-cyanopyridines for the synthesis of 2-hydrazinylnicotinonitriles are limited to isolated examples [78,119,120] (Scheme 5). Notably, the reaction with 2-bromopyridines proceeds more rapidly and in higher yields compared to their 2-chloropyridine analogs.

2. Results and Discussion

2.1. Synthesis

The starting 4,6-diaryl-2-bromo-3-cyanopyridines 15 were synthesized according to a modified procedure initially described by Shestopalov and Sharanin in papers [121,122]. Briefly, readily available α,β-unsaturated ketones (chalcones) were reacted with malononitrile in the presence of catalytic amounts of morpholine to yield the Michael adducts—δ-ketodinitriles 16a–j. These intermediates were then treated with a solution of bromine in AcOH under gentle heating to afford 2-bromopyridines 15a–j in 53–84% yields (Scheme 6). The reaction mechanism involves the initial formation of bromination products—2-bromo-2-(3-oxo-1,3-diarylpropyl)malononitriles A. Dehydrobromination of bromides A, followed by the addition of HBr to the cyano group of the unsaturated nitrile B, gives imidoyl bromides C. These intermediates subsequently undergo cyclization to form 2,3-dihydropyridine species D, which readily aromatize under the reaction conditions to give the 2-bromopyridines (Scheme 6). The structures of the bromides 15 were verified by FT-IR and NMR spectroscopy. Additionally, the structure of 2-bromo-4-(4-chlorophenyl)-6-phenylnicotinonitrile 15a was definitively confirmed through single-crystal X-ray diffraction analysis, as shown in Figure 3.

Interestingly, during an attempt to isolate additional crops of 4,6-diaryl-2-bromo-3-cyanopyridine 15 by slow evaporation of the acetic acid mother liquor, small amounts of crystalline products were obtained in several cases. However, the IR spectra of these products indicated the presence of a ketone C=O group and non-conjugated cyano groups (C_sp³–C≡N) in the region of ν 2250 cm⁻¹. At the same time, the absorption bands for the conjugated cyano group, characteristic of compounds 15 (ν 2222–2230 cm⁻¹), were absent from the spectra. X-ray structural analysis of the crystalline solid obtained by slow concentration from the mother liquor of compound 15c revealed a substitutional disorder and showed that the isolated product consisted of co-crystals of (2S*,3R*,4S*,6R*)-3-benzoyl-4-hydroxy-4-phenyl-2,6-di-p-tolylcyclohexane-1,1-dicarbonitrile 17 and (2S*,3R*,4S*,6R*)-3-benzoyl-5-bromo-4-hydroxy-4-phenyl-2,6-di-p-tolylcyclohexane-1,1-dicarbonitrile 17-Br at a ~4:6 ratio as a solvate with AcOH (Figure 4).

We propose the following pathway for the formation of this unusual product. During the reaction of chalcones with malononitrile, alongside the formation of the δ-ketodinitriles 16, by-products 18—the Michael adducts with a 2:1 stoichiometry—are also generated (Scheme 7). The formation of such bis-adducts under analogous conditions has been reported in the literature [123,124,125]. Bromination of bis-adducts 18 yields the only possible α-bromoketones 19. Subsequently, both the adducts 18 and their brominated derivatives 19 undergo an acid-catalyzed aldol-type addition, leading to the cyclohexanols 17 and 17-Br. Bromination likely precedes cyclization, as bromination of compounds like 17 would be expected to proceed with different regioselectivity.

The observed stereochemistry of the products appears to result from steric repulsion between the bulky aryl and benzoyl substituents and stabilization provided by the cis-orientation of the OH and C=O benzoyl groups, the latter being facilitated by hydrogen bonding during the cyclization.

It is important to note that compound 17-Br and related brominated analogs are not reported in the literature, in contrast to the well-documented compounds 17 [123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140]. Nevertheless, the reactions and properties of this class of compounds remain largely unexplored. While further research in this area is warranted, it lies beyond the scope of the current study and will be examined in detail in future works.

The prepared 4,6-diaryl-2-bromonicotinonitriles 15a–j react with hydrazine hydrate in 1,4-dioxane under mild conditions (25 °C) to form the expected 4,6-diaryl-2-hydrazinyl-3-cyanopyridines 20a–j. The reaction proceeds in high yields (80–97%) (Scheme 8), with no observed formation of further cyclization products—specifically, 3-amino-1H-pyrazolo[3,4-b]pyridines—in any of the cases. FT-IR, NMR, and HRMS spectral data were used to confirm the structures of the synthesized compounds 20.

Compounds 20 are yellow powders, typically sparingly soluble in water, Et₂O, or hydrocarbons and soluble in hot EtOH, dioxane, DMSO, or DMF.

The FT-IR spectra of 2-hydrazinylnicotinonitriles 20 exhibited absorption bands for the conjugated cyano group at ν 2206–2212 cm⁻¹. In addition, two strong bands corresponding to the NH–NH₂ fragment vibrations were observed at ν 3411–3302 cm⁻¹ and 3207–3326 cm⁻¹. In the ¹H NMR spectra of hydrazines 20a–j, the protons of the primary amino group appeared as a very broad singlet at δ 4.58–4.76 ppm. The signals of C(5)H and –NH– protons appeared as sharp singlets at δ 7.25–7.44 ppm and as broadened peaks at δ 8.27–8.55 ppm, respectively.

The ¹³C NMR spectra of 3-cyano-2-hydrazinylpyridines 20 showed characteristic signals for the following carbons: C-3 (δ 86.2–88.4 ppm), C-5 (δ 109.2–109.7 ppm), cyano group (δ 115.5–116.7 ppm), pyridine C-4 (δ 152.6–155.3 ppm), C-6 (δ 156.4–158.0 ppm), and C-2 (δ 160.2–161.0 ppm).

We investigated the properties of the synthesized compounds. Given the potential of hydrazinylnicotinonitriles and their derivatives in agrochemistry (see, e.g., [3,4,5,38,70,71,72,73,141]), we prepared a series of new hydrazones 21 by reacting compounds 20 with aromatic aldehydes (Scheme 9).

It is well-known that halogenated compounds play an important role in agrochemistry [142,143,144,145,146,147,148,149]. This can be explained by the physico-chemical effects (such as steric and electronic effects, C–Hal bond polarity, thermal and metabolic stability, etc.) that arise from the introduction of halogens or halogen-containing substituents into biologically active molecules, such as insecticides, acaricides, plant growth regulators, and herbicide safeners. Thus, in each area of crop protection (fungicides, insecticides, or herbicides), 12 halogen-containing products (~60%) are among the 20 best-selling agrochemicals [144]. As of 2020, out of 48 new agrochemicals provisionally approved by the International Organization for Standardization (ISO), 39 (~81%) contain halogen atoms as substituents [145]. The greater availability of chlorine compared to other halogens accounts for the prevalence of chlorinated agrochemicals [146,147,148,149].

On the other hand, pyridine is the most important heterocyclic scaffold in agrochemistry [150]. (Poly)halogenated pyridines exhibit pronounced activity and are widely represented on the market [150,151,152].

For this reason, we selected chlorinated aromatic aldehydes (4-chlorobenzaldehyde and 2,4-dichlorobenzaldehyde) to prepare a small library of new hydrazones 21. The synthesis, diversity, and yields of the resulting products 21 are presented in Scheme 9.

Hydrazones 21 are yellow powders that are moderately soluble in EtOH and 1,4-dioxane, and readily soluble in acetone, DMF, or DMSO. The FT-IR spectra of hydrazones 21 exhibit absorption bands assigned to N–H stretching vibrations in the region of ν 3178–3327 cm⁻¹. The bands corresponding to conjugated C≡N groups were observed at ν 2206–2218 cm⁻¹. In the ¹H NMR spectra of the hydrazones derived from 4-chlorobenzaldehyde, the proton signals of the –CH=N– group appear at δ 8.11–8.14 ppm, while the NH signals are observed at δ 11.73–11.97 ppm. In the derivatives of 2,4-dichlorobenzaldehyde, the corresponding signals are found at δ 8.48–8.56 ppm and δ 11.95–12.16 ppm, respectively.

2.2. Agrochemical Studies

The prepared compounds were evaluated as herbicide antidotes against herbicide 2,4-dichlorophenoxyacetic (2,4-D). Though this widely used herbicide is not considered significantly toxic to humans [153], its application can still have negative side effects, such as the inhibition of crop growth, potentially reducing yields by 15–60%. To mitigate these effects and improve crop yields, some agrochemicals known as herbicide safeners, or antidotes, are used. These antidotes (for reviews, see [154,155,156,157,158]) protect crops by neutralizing phytotoxins without reducing the herbicide’s effectiveness against weeds. Typically, herbicide safeners appear to be non-toxic to cultivated plants and can sometimes stimulate plant growth.

Following the reported procedures [159,160,161,162], we investigated the efficacy of the new nicotinonitriles as 2,4-D antidotes. The experiments were performed on sunflower seedlings of the Master cultivar. The antidote effect (A) was calculated as the ratio of the hypocotyl or root length of seedlings treated with both the herbicide and an antidote to the length of those treated with 2,4-D alone, as defined in Equation (1). Further details are provided in the Section 3.

A = (V_exp/V_ref) × 100%,

(1)

where V_exp is the organ length (in mm) of seedlings treated with both 2,4-D herbicide and an antidote and V_ref is the organ length of the reference seedlings treated with 2,4-D only.

We found that several of the novel 2-hydrazinylpyridines 20 and hydrazones 21 demonstrated a pronounced antidote effect in laboratory experiments (

Table 1. Protective effects of the most active compounds 20,21 against 2,4-D herbicide.

N	Pyridine	Plant Organ	Antidote Effect (A) at Different Concentrations, % 1
			10−2	10−3	10−4	10−5
1	20a	roots	141	134	178	186
		hypocotyls	135	134	146	130
2	20b	roots	132	113	116	136
		hypocotyls	140	97	93	96
3	20f	roots	130	93	140	134
		hypocotyls	111	73	102	98
4	20i	roots	170	130	180	138
		hypocotyls	104	117	92	88
5	21{1}	roots	154	154	150	184
		hypocotyls	123	112	101	132
6	21{2}	roots	163	173	167	152
		hypocotyls	156	119	119	122
7	21{17}	roots	186	171	168	161
		hypocotyls	148	152	138	145
8	21{18}	roots	188	197	180	159
		hypocotyls	146	152	127	137

¹ The differences are reliable at p = 0.95.

).

As shown in Table 1, 4-chlorophenyl derivative 20a is the most active compound among the 2-hydrazinyl pyridines 20. Compound 20a counteracts the negative effect of 2,4-D by 34–86% on sunflower seedling roots and by 30–46% on hypocotyls. Other notable compounds include hydrazines 20b,f,i, which demonstrate significant antidote activity on seedling roots (up to 80% effect), though their impact on hypocotyls is less consistent.

Among the hydrazones 21, compounds with 3-bromophenyl substituents unexpectedly showed the highest activity. Specifically, hydrazone 21{17} reduced the phytotoxic effects of the herbicide on hypocotyls by 38–52% and on sunflower roots by 61–86%. Hydrazone 21{18} reduced the negative effect on hypocotyls by 27–52% and on roots by 59–97%. Hydrazones 21{1,2} bearing 4-chlorophenyl substituents primarily influenced root growth (50–84% antidote effect) but exhibited only moderate activity on hypocotyls.

3. Materials and Methods

The ¹H, ¹³C, and ¹³C DEPTQ NMR spectra were recorded in DMSO-d₆ or acetone-d₆ solutions using a Bruker AVANCE-III HD spectrometer (Bruker, Göttingen, Germany) operating at 400.40 MHz for ¹H and 100.61 MHz for ¹³C nuclei or a JEOL JNM-ECA-400 spectrometer (JEOL, Tokyo, Japan) operating at 399.78 MHz for ¹H and 100.53 MHz for ¹³C nuclei. Residual solvent signals were used as internal standards, set at 2.49 ppm for ¹H and 39.50 ppm for ¹³C in DMSO-d₆. Elemental analyses were performed with a Carlo Erba 1106 Elemental Analyzer (Carlo Erba, Milan, Italy). FTIR spectra were acquired on a Bruker Vertex 70 spectrometer (Bruker, Ettlingen, Germany) using an ATR device or on an Infraspec FSM 2201 spectrometer (Infraspec, Saint-Petersburg, Russia) using KBr pellets or Nujol mulls. Single-crystal X-ray diffraction data were collected on an Agilent SuperNova, Dual, Cu at home/near, Atlas diffractometer (Agilent Technologies, Santa Clara, CA, USA). High-resolution mass spectra (HRMS) were obtained using a Bruker MaXis Impact spectrometer (Bruker, Bremen, Germany) with electrospray ionization and HCO₂Na–HCO₂H calibration. Samples were dissolved in acetonitrile at 37–38 °C under ultrasonication. NMR, FTIR, and HRMS spectral charts, along with X-ray analysis data, are provided in the Electronic Supplementary Materials (Figures S1–S104 and Tables S1–S15).

Reaction progress and compound purity were monitored by TLC on Sorbfil-A plates (Imid Ltd., Krasnodar, Russia) using solvent systems of Me₂CO–hexane (2:1), Me₂CO–PhMe (3:2), HCCl₃–PhMe (1:1), or AcOEt–light petroleum (1:1). Visualization was achieved under UV light and with iodine vapor. All reagents and solvents were purchased from BioInLabs (Rostov-on-Don, Russia) and used without further purification.

4,6-Diaryl-2-bromo-3-cyanopyridines (15a–j) (Scheme 6) were prepared as follows.

A. Synthesis of 2-(1,3-diaryl-3-oxopropyl)malononitriles (δ-ketodinitriles) 16.

The corresponding chalcone (0.01 mol) was dissolved or suspended in EtOH (20 mL) at 25 °C. With stirring, malononitrile (0.75 g, 0.0114 mol) was added, followed after 1–2 min by one drop of morpholine. The resulting mixture was vigorously stirred at 25 °C, and the reaction progress was monitored by TLC (eluent: acetone–toluene, 3:2). After 1–1.5 h, complete consumption of the chalcone and formation of the target Michael adduct 16 were observed. Depending on the structure of the starting chalcone, the product either crystallized directly from the reaction mixture or precipitated upon the addition of cold water (5–10 mL). The precipitated product was used in the next step without purification. If analytically pure samples were required, the Michael adducts 16 could be recrystallized from EtOH.

B. Bromination of the Michael adducts 16.

The corresponding δ-ketodinitrile 16 was dissolved in glacial AcOH (~100 mL per 5 g of ketodinitrile) with gentle heating (to about 60 °C). A solution of an equimolar amount of Br₂ in 10 mL of glac. AcOH was added dropwise to the resulting light-yellow transparent solution with vigorous stirring. The bromine solution must be added at a rate that prevents the reaction temperature from exceeding 75 °C. After approximately half of the bromine has been added, the solution decolorizes. Almost immediately after decolorization, intensive precipitation of the 2-bromopyridine 15 begins. If the reaction mixture solidifies and stirring becomes impossible, the mixture should be diluted with hot AcOH. After the complete addition of bromine, stirring was continued for another 1.5 h. The mixture was then cooled to 25 °C, and the solid of 2-bromopyridine was filtered off and washed sequentially with AcOH and aq. EtOH until the washings were neutral with petroleum ether. The resulting 2-bromonicotinonitriles 15 were obtained as fluffy light-yellow powders or fibrous crystals. The 2-bromonicotinonitriles 15 were used in the next step without purification. If analytically pure samples were required, the crude product was either recrystallized from AcOH or, in cases of insufficient solubility, the suspension was boiled in AcOH for 20–30 min.

2-Bromo-4-(4-chlorophenyl)-6-phenylnicotinonitrile 15a was isolated in 84% yield, m.p. 188–189 °C (Lit. [122]: m.p. 231–232 °C (from MeNO₂)). FTIR (KBr), ν_max, cm⁻¹: 2222 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 7.50–7.57 (m, 4H, H Ar), 7.66–7.69 (m, 3H, H Ar), 7.80–7.84 (m, 2H, H Ar), 8.22–8.28 (m, 2H, H Ar). ¹³C DEPTQ NMR (101 MHz, DMSO-d₆): 115.1 (C-3), 116.4 (C≡N), 119.8 * (C-5), 127.8 * (2 CH Ar), 129.0 * (2 CH Ar), 129.2 * (2 CH Ar), 130.5 * (CH Ph), 130.9 * (2 CH Ar), 134.1 (C Ar), 135.4 (C Ar), 135.1 (C Ar), 144.3 (C–Br), 155.0 (C-4), 159.4 (C-6). * Negatively phased signals. Elemental Analysis: found, %: C, 58.60; H, 2.91; N, 7.40. C₁₈H₁₀BrClN₂ (M 369.65). Calculated, %: C, 58.49; H, 2.73; N, 7.58.

2-Bromo-4-(2-chlorophenyl)-6-phenylnicotinonitrile 15b was isolated in 78% yield, m.p. 185–186 °C (Lit. [122]: m.p. 187–188 °C (from AcOH)). FTIR (KBr), ν_max, cm⁻¹: 2230 (C≡N). NMR spectral data were identical to those reported in [122].

2-Bromo-4-(4-methylphenyl)-6-phenylnicotinonitrile 15c was isolated in 59% yield, m.p. 191–191 °C. FTIR (nujol), ν_max, cm⁻¹: 2224 (C≡N). NMR spectral data were identical to those reported in [163].

2-Bromo-4-(3,4-dimethoxyphenyl)-6-phenylnicotinonitrile 15d was isolated in 71% yield, m.p. 194–195 °C. FTIR (KBr), ν_max, cm⁻¹: 2227 (C≡N).

2-Bromo-4-(4-chlorophenyl)-6-(4-methylphenyl)nicotinonitrile 15e was isolated in 54% yield, m.p. 187–188 °C (Lit. [122]: m.p. 282–283 °C (from dioxane)). FTIR (KBr), ν_max, cm⁻¹: 2222 (C≡N). NMR spectral data were identical to those reported in [122].

2-Bromo-4-(4-fluorophenyl)-6-phenylnicotinonitrile 15f was isolated in 53% yield, m.p. 181–183 °C (Lit. [164]: m.p. 184–187 °C). FTIR (KBr), ν_max, cm⁻¹: 2222 (C≡N). NMR spectral data were identical to those reported in [164].

2-Bromo-4-(2,4-dichlorophenyl)-6-phenylnicotinonitrile 15g was isolated in 67% yield, m.p. 180–181 °C (Lit. [122]: m.p. 160–161 °C (from MeNO₂)). Spectral data were identical to those reported in [122].

2-Bromo-4-(3-nitrophenyl)-6-phenylnicotinonitrile 15h was isolated in 69% yield, m.p. 186–188 °C. FTIR (KBr), ν_max, cm⁻¹: 2222 (C≡N).

2-Bromo-4-(3-bromophenyl)-6-phenylnicotinonitrile 15i was isolated in 63% yield, m.p. 191–192 °C. FTIR (KBr), ν_max, cm⁻¹: 2222 (C≡N).

2-Bromo-4-(4-methoxyphenyl)-6-phenylnicotinonitrile 15j was isolated in 83% yield, m.p. 192–195 °C (Lit. [122]: m.p. 218–218 °C (from MeNO₂)). Spectral data were identical to those reported in [122,164].

4,6-Diaryl-2-hydrazinyl-3-cyanopyridines (20a–j) (Scheme 8) were prepared as follows. The corresponding 2-bromonicotinonitrile 15a–j (5.5–6 mmol) was dissolved in 1,4-dioxane (~15 mL per 2 g of 2-bromopyridine 15). An excess of hydrazine hydrate (25–30 mmol) was added to the solution formed. The resulting emulsion was stirred vigorously at 25 °C. The reaction progress was monitored by TLC (eluent: chloroform–toluene, 1:1). Complete conversion was typically achieved within 5–6 h, though in some cases, stirring was continued for 24 h. Upon reaction completion, dioxane was removed under reduced pressure at ambient temperature. The residue was triturated with cold water to remove hydrazine and hydrazinium hydrobromide. The precipitate was filtered off and washed with water and then with petroleum ether, yielding hydrazines 20 as yellow powders. For purification, the compounds can be recrystallized from MeOH or dioxane.

4-(4-Chlorophenyl)-2-hydrazinyl-6-phenylnicotinonitrile 20a was isolated in 97% yield, m.p. 160–162 °C. FTIR (nujol), ν_max, cm⁻¹: 3304 br (N–H), 2206 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 4.67 (br s, 2H, NH₂), 7.32 (s, 1H, H-5), 7.47–7.51 (m, 3H, H Ph), 7.62 (d, ³J = 8.7 Hz, 2H, H-3, and H-5, 4-ClC₆H₄), 7.69 (d, ³J = 8.7 Hz, 2H, H-3, and H-5, 4-ClC₆H₄), 8.23–8.26 (m, 2H, H Ph), 8.41 (br s, 1H, NH). ¹³C DEPTQ NMR (101 MHz, DMSO-d₆): 86.3 (C-3), 109.2 * (C(5)H), 116.2 (C≡N), 127.5 * (2 CH Ar), 128.6 * (2 CH Ar), 128.8 * (2 CH Ar), 130.3 * (CH Ph), 130.4 * (2 CH Ar), 134.5 (C¹ Ar), 135.7 (C¹ Ar), 137.5 (C–Cl), 154.0 (C-4), 158.0 (C–6), 160.8 (C–NH). * Negatively phased signals. HRMS (ESI) m/z: calculated for C₁₈H₁₄ClN₄ [M + H]⁺: 321.090699, found 321.0891 (Δ 4.98 ppm). Elemental Analysis: found, %: C, 67.36; H, 4.21; N, 17.40. C₁₈H₁₃ClN₄ (M 320.78). Calculated, %: C, 67.40; H, 4.09; N, 17.47.

4-(2-Chlorophenyl)-2-hydrazinyl-6-phenylnicotinonitrile 20b was isolated in 96% yield, m.p. 158–160 °C. FTIR (nujol), ν_max, cm⁻¹: 3315, 3250 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 4.62 (br s, 2H, NH₂), 7.25 (s, 1H, H-5), 7.47–7.54 (m, 7H, H Ar), 7.64 (dd, ³J = 8.2 Hz, ⁴J = 1.4 Hz, 1H, H Ar), 8.21–8.24 (m, 2H, H Ph), 8.49 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 88.3 (C-3), 109.7 (C(5)H), 115.5 (C≡N), 127.4 (2 CH Ar), 127.5 (CH Ar), 128.7 (2 CH Ar), 129.7 (CH Ar), 130.3 (CH Ph), 130.6 (CH Ar), 130.9 (CH Ar), 131.3 (C Ar), 136.2 (C Ar), 137.3 (C Ar), 153.4 (C-4), 157.8 (C–6), 160.2 (C–NH). Elemental Analysis: found, %: C, 67.29; H, 4.24; N, 17.38. C₁₈H₁₃ClN₄ (M 320.78). Calculated, %: C, 67.40; H, 4.09; N, 17.47. HRMS (ESI) m/z: calculated for C₁₈H₁₄ClN₄ [M + H]⁺: 321.090699, found 321.0904 (Δ 0.93 ppm).

2-Hydrazinyl-4-(2-methylphenyl)-6-phenylnicotinonitrile 20c was isolated in 80% yield, m.p. 163–165 °C. FTIR (nujol), ν_max, cm⁻¹: 3315, 3267 br (N–H), 2206 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 2.38 (s, 3H, Me), 4.59 (br s, 2H, NH₂), 7.29 (s, 1H, H-5), 7.48–7.50 (m, 3H, H Ph), 7.56 (d, ³J = 7.8 Hz, 2H, H Ar), 8.23–8.25 (m, 2H, H Ph), 8.31 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 20.9 (Me), 88.4 (C-3), 109.3 (C(5)H), 116.4 (C≡N), 127.4 (2 CH Ar), 128.3 (CH Ar), 128.6 (2 CH Ar), 129.3 (CH Ar), 130.2 (CH Ph), 134.0 (C–Me), 137.6 (C¹ Ar), 139.4 (C¹ Ar), 155.2 (C-4), 157.7 (C–6), 160.9 (C–NH). Elemental Analysis: found, %: C, 75.90; H, 5.44; N, 18.66. C₁₉H₁₆N₄ (M 300.37). Calculated, %: C, 75.98; H, 5.37; N, 18.65.

2-Hydrazinyl-4-(3,4-dimethoxyphenyl)-6-phenylnicotinonitrile 20d was isolated as solvate with dioxane (2:1) in 93% yield, m.p. 152–155 °C. FTIR (nujol), ν_max, cm⁻¹: 3314, 3279 br (N–H), 2212 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.55 (br s, dioxane), 3.83 (s, 3H, MeO), 3.84 (s, 3H, MeO), 4.69 (br s, 2H, NH₂), 7.11 (d, ³J = 7.8 Hz, 1H, H Ar), 7.23–7.27 (m, 2H, H Ar), 7.34 (s, 1H, H-5), 7.48–7.50 (m, 3H, H Ph), 8.24–8.27 (m, 3H, H Ph, and NH overlapped). ¹³C NMR (101 MHz, DMSO-d₆): 55.6 (2 C, 2 MeO), 66.4 (CH₂O dioxane), 86.3 (C-3), 109.3 (C(5)H), 111.6 (CH Ar), 112.1 (CH Ar), 116.7 (C≡N), 121.2 (CH Ar), 127.5 (2 CH Ph), 128.6 (2 CH Ph), 129.0 (C¹ Ar), 130.1 (CH Ph), 137.7 (C¹ Ph), 148.6 (C–OMe), 150.1 (C–OMe), 155.0 (C-4), 157.6 (C–6), 161.0 (C–NH). HRMS (ESI) m/z: calculated for C₂₀H₁₉N₄O₂ [M + H]⁺: 347.150801, found 347.1503 (Δ 1.44 ppm).

4-(4-Chlorophenyl)-2-hydrazinyl-6-(4-methylphenyl)nicotinonitrile 20e was isolated in 96% yield, m.p. 160–162 °C. FTIR (nujol), ν_max, cm⁻¹: 3400, 3326 br (N–H), 2210 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 2.38 (s, 3H, Me), 4.60 (br s, 2H, NH₂), 7.31 (s, 1H, H-5), 7.35 (d, ³J = 7.8 Hz, 2H, H Ar), 7.53–7.57 (m, 4H, H Ar, two doublets overlapped), 8.29 (d, ³J = 8.2 Hz, 2H, H Ar), 8.34 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 20.9 (Me), 86.7 (C-3), 109.2 (C(5)H), 116.3 (C≡N), 128.4 (2 CH Ar), 128.6 (2 CH Ar), 129.25 (2 CH Ar), 129.27 (2 CH Ar), 133.8 (C–Me), 135.0 (C–Cl), 136.4 (C¹ Ar), 139.5 (C¹ Ar), 155.3 (C-4), 156.4 (C–6), 160.8 (C–NH). HRMS (ESI) m/z: calculated for C₁₉H₁₅ClN₄ [M + H]⁺: 335.106349, found 335.1061 (Δ 0.74 ppm).

4-(4-Fluorophenyl)-2-hydrazinyl-6-phenylnicotinonitrile 20f was isolated in 97% yield, m.p. 153–155 °C. FTIR (nujol), ν_max, cm⁻¹: 3302, 3246 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 4.59 (br s, 2H, NH₂), 7.31 (s, 1H, H-5), 7.37–7.41 (m, 2H, H Ar), 7.48–7.50 (m, 3H, H Ph), 7.71–7.74 (m, 2H, H Ar), 8.24–8.26 (m, 2H, H Ph), 8.39 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 86.5 (C-3), 109.4 (C(5)H), 115.7 (d, ²J_C–F = 21.1 Hz, 2 CH Ar), 116.3 (C≡N), 127.5 (2 CH Ph), 128.6 (2 CH Ph), 130.2 (C(4)H Ph), 130.9 (d, ³J_C–F = 8.6 Hz, 2 CH Ar), 133.3 (d, ⁴J_C–F = 2.9 Hz, C¹ Ar), 137.5 (C¹ Ph), 154.2 (C-4), 157.9 (C–6), 160.8 (C–NH), 161.7, 164.2 (d, ¹J_C–F = 247.3 Hz, C–F). HRMS (ESI) m/z: calculated for C₁₈H₁₄FN₄ [M + H]⁺: 305.120249, found 305.1205 (Δ −0.82 ppm).

4-(2,4-Dichlorophenyl)-2-hydrazinyl-6-phenylnicotinonitrile 20g was isolated in 95% yield, m.p. 142–143 °C. FTIR (nujol), ν_max, cm⁻¹: 3307, 3246 br (N–H), 2210 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 4.62 (br s, 2H, NH₂), 7.26 (s, 1H, H-5), 7.47–7.49 (m, 3H, H Ar), 7.53 (d, ³J = 8.2 Hz, 1H, H-6 Ar), 7.61 (dd, ³J = 8.2 Hz, ⁴J = 1.8 Hz, 1H, H-5 Ar), 7.85 (d, ⁴J = 1.8 Hz, 1H, H-3 Ar), 8.20–8.23 (m, 2H, H Ph), 8.55 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 88.0 (C-3), 109.6 (C(5)H), 115.5 (C≡N), 127.4 (2 CH Ar), 127.8 (CH Ar), 128.7 (2 CH Ar), 129.2 (CH Ar), 130.4 (CH Ph), 132.0 (CH Ar), 132.6 (C¹ Ar), 134.7 (C–Cl), 135.2 (C–Cl), 137.2 (C¹ Ph), 152.6 (C-4), 157.9 (C–6), 160.2 (C–NH). HRMS (ESI) m/z: calculated for C₁₈H₁₃Cl₂N₄ [M + H]⁺: 355.051727, found 355.0516 (Δ 0.36 ppm).

2-Hydrazinyl-4-(3-nitrophenyl)-6-phenylnicotinonitrile 20h was isolated as solvate with dioxane (2:1) in 93% yield, m.p. 157–159 °C. FTIR (nujol), ν_max, cm⁻¹: 3312, 3245 br (N–H), 2210 (C≡N), 1535 (NO_{2 asymm}), 1350 (NO_{2 symm}). ¹H NMR (400 MHz, DMSO-d₆): 3.55 (s, CH₂O, dioxane), 4.76 (br s, 2H, NH₂), 7.44 (s, 1H, H-5), 7.48–7.50 (m, 3H, H Ph), 7.62–7.63 (m, 1H, H Ar), 7.83–7.86 (m, 1H, H Ar), 8.12–8.20 (m, 2H, H Ar), 8.26–8.29 (m, 2H, H Ph), 8.53 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 66.4 (dioxane), 88.3 (C-3), 109.4 (C(5)H), 116.1 (C≡N), 123.4 (CH Ar), 124.3 (CH Ar), 127.6 (2 CH Ph), 128.6 (2 CH Ph), 128.8 (CH Ar), 130.2 (C(4)H Ph) 130.4 (CH Ar), 135.3 (C¹ Ar), 137.4 (C¹ Ph), 147.8 (C–NO₂), 155.6 (C-4), 158.2 (C–6), 160.8 (C–NH). HRMS (ESI) m/z: calculated for C₁₈H₁₄N₅O₂ [M + H]⁺: 332.114750, found 332.1143 (Δ 1.36 ppm).

4-(3-Bromophenyl)-2-hydrazinyl-6-phenylnicotinonitrile 20i was isolated as solvate with dioxane (1:1) in 97% yield, m.p. 165–166 °C. FTIR (nujol), ν_max, cm⁻¹: 3309, 3207 br (N–H), 2210 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.55 (s, CH₂O, dioxane), 4.66 (br s, 2H, NH₂), 7.36 (s, 1H, H-5), 7.48–7.54 (m, 4H, H Ar), 7.66–7.75 (m, 2H, H Ar), 7.86–7.87 (m, 1H, H Ar), 8.26–8.28 (m, 2H, H Ph), 8.43 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 66.4 (dioxane), 86.4 (C-3), 109.4 (C(5)H), 116.1 (C≡N), 121.9 (C–Br), 127.6 (2 CH Ph), 127.7 (CH Ar), 128.6 (2 CH Ph), 130.3 (C(4)H Ph) 130.8 (CH Ar), 131.1 (CH Ar), 132.4 (CH Ar), 137.5 (C¹ Ph), 139.1 (C¹ Ar), 153.6 (C-4), 158.0 (C–6), 160.7 (C–NH). HRMS (ESI) m/z: calculated for C₁₈H₁₄BrN₄ [M + H]⁺: 365.040182, found 365.0398 (Δ 1.05 ppm).

2-Hydrazinyl-4-(4-methoxyphenyl)-6-phenylnicotinonitrile 20j was isolated in 92% yield, m.p. 141–143 °C. FTIR (nujol), ν_max, cm⁻¹: 3390, 3321 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.83 (s, 3H, MeO), 4.58 (br s, 2H, NH₂), 7.10 (d, ³J = 8.7 Hz, 3H, H-3, and H-5, 4-MeOC₆H₄), 7.29 (s, 1H, H-5), 7.48–7.50 (m, 3H, H Ph), 7.64 (d, ³J = 8.7 Hz, 3H, H-2 and H-6, 4-MeOC₆H₄), 8.23–8.26 (m, 2H, H Ph), 8.28 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 55.4 (MeO), 86.2 (C-3), 109.2 (C(5)H), 114.2 (2 CH Ar), 116.6 (C≡N), 127.4 (2 CH Ph), 128.6 (2 CH Ph), 128.9 (C¹ Ar), 130.0 (2 CH Ar), 130.1 (CH Ph), 137.7 (C¹ Ph), 154.8 (C-4), 157.7 (C–6), 160.5 (C–OMe), 161.0 (C–NH). HRMS (ESI) m/z: calculated for C₁₉H₁₇N₄O [M + H]⁺: 317.140236, found 317.1399 (Δ 1.06 ppm).

Synthesis of 2-(2-arylidenehydrazinyl)-4,6-diarylnicotinonitriles 21{1–20}. General procedure. Into a 10 mL vial, 0.5 mmol of the corresponding hydrazine 20, an aromatic aldehyde (0.5 mmol), and 5 mL of EtOH were placed. The reaction mixture was heated under reflux with vigorous stirring for 1–1.5 h (conversion was monitored by TLC, eluent: chloroform/toluene, 1:1). The reaction mixture was cooled, and the product was precipitated by adding cold water. The resulting precipitate of hydrazone 21 was filtered off and purified by recrystallization from an appropriate solvent (MeOH, EtOH, or 1,4-dioxane). Hydrazones 21 are fine crystalline powders, ranging from light yellow to bright yellow in color, and are soluble in acetone, 1,4-dioxane, lower alcohols, and DMSO.

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(4-chlorophenyl)-6-phenylnicotinonitrile 21{1} was isolated in 83% yield. FTIR (nujol), ν_max, cm⁻¹: 3265 br (N–H), 2218 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 7.47 (d, ³J = 8.7 Hz, 2H, H-3, and H-5, 4-ClC₆H₄), 7.50–7.55 (m, 4H, H-5, and 3H Ph overlapped), 7.63 (d, ³J = 8.7 Hz, 2H, H-3, and H-5, 4-ClC₆H₄), 7.73 (d, ³J = 8.7 Hz, 2H, H-2, and H-6, 4-ClC₆H₄), 7.82 (d, ³J = 8.7 Hz, 2H, H-2, and H-6, 4-ClC₆H₄), 8.14 (br s, 1H, –CH=), 8.18–8.20 (m, 2H, H Ph), 11.86 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 89.6 (C-3), 115.8 (C(5)H), 117.4 (C≡N), 127.4 (2 CH Ar), 128.4 (2 CH Ar), 128.6 (2 CH Ar), 128.7 (2 CH Ar), 128.8 (2 CH Ar), 130.6 (CH Ph), 130.9 (2 CH Ar), 133.3, 133.6, 134.4, 136.3 (C¹ Ar), 136.8 (C¹ Ar), 155.8 (C-4), 158.1 (C–6), 159.9 (C–NH). Elemental Analysis: found, %: C, 67.66; H, 3.77; N, 12.60. C₂₅H₁₆Cl₂N₄ (M 443.33). Calculated, %: C, 67.73; H, 3.64; N, 12.64. HRMS (ESI) m/z: calculated for C₂₅H₁₇Cl₂N₄ [M + H]⁺: 443.083027, found 443.0808 (Δ 5.03 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(4-chlorophenyl)-6-phenylnicotinonitrile 21{2} was isolated in 80% yield. FTIR (nujol), ν_max, cm⁻¹: 3260 br (N–H), 2210 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 7.43–7.53 (m, 7H, H-5, and H Ar overlapped), 7.62–7.69 (m, 3H, H Ar), 8.18–8.23 (m, 3H, 2H Ph, H Ar), 8.50 (br s, 1H, –CH=), 12.06 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 89.6 (C-3), 115.3 (C(5)H), 117.5 (C≡N), 127.4 (2 CH Ar), 127.8 (CH Ar), 128.0 (CH Ar), 128.4 (2 CH Ar), 128.6 (2 CH Ar), 128.8 (2CH Ar), 129.3 (CH Ar), 130.6 (C(4)H Ph), 131.3, 132.9, 134.1, 135.8, 136.4, 136.6, 136.7, 156.2 (C-4), 158.0 (C–6), 160.3 (C–NH). HRMS (ESI) m/z: calculated for C₁₈H₁₄ClN₄ [M + H + H₂O–ArCHO]⁺: 321.090699, found 321.0891 (Δ 4.99 ppm). Elemental Analysis: found, %: C, 62.9; H, 3.30; N, 11.63. C₂₅H₁₅Cl₃N₄ (M 477.77). Calculated, %: C, 62.85; H, 3.16; N, 11.73.

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(2-chlorophenyl)-6-phenylnicotinonitrile 21{3} was isolated in 89% yield. FTIR (nujol), ν_max, cm⁻¹: 3314 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 7.44 (d, ³J = 8.7 Hz, 2H, H-3, and H-5, 4-ClC₆H₄), 7.48 (s, 1H, H-5), 7.51–7.57 (m, 6H, H Ar), 7.65–7.67 (m, 1H, H Ar), 7.79 (d, ³J = 8.7 Hz, 2H, H-2, and H-6, 4-ClC₆H₄), 8.14 (br s, 1H, –CH=), 8.16–8.19 (m, 2H, H Ph), 11.91 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 89.1 (C-3), 112.5 (C(5)H), 116.7 (C≡N), 127.3 (2 CH Ar), 127.4 (CH Ar), 128.4 (2 CH Ar), 128.7 (2 CH Ar), 128.8 (2 CH Ar), 129.5 (CH Ar), 130.6 (CH Ph), 130.7 (CH Ar), 130.8 (CH Ar), 131.4, 133.6, 133.9, 136.4 (C¹ Ar), 136.7 (C¹ Ar), 140.5, 155.5 (C-4), 156.1 (C–6), 158.0 (C–NH). HRMS (ESI) m/z: calculated for C₂₅H₁₇Cl₂N₄ [M + H]⁺: 443.083027, found 443.0803 (Δ 6.16 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(2-chlorophenyl)-6-phenylnicotinonitrile 21{4} was isolated in 80% yield. FTIR (nujol), ν_max, cm⁻¹: 3298 br (N–H), 2214 (C≡N). ¹H NMR (400 MHz, acetone-d₆): 7.35 (dd, ³J = 8.7 Hz, ⁴J = 1.8 Hz, 1H, H-5, 2,4-ClC₆H₃), 7.49 (s, 1H, H-5), 7.50–7.57 (m, 7H, H Ar), 7.62–7.64 (m, 1H, H Ar), 8.18–8.20 (m, 2H, H Ph), 8.36 (d, ³J = 8.7 Hz, 1H, H-6, 2,4-ClC₆H₃), 8.57 (br s, 1H, –CH=), 11.00 (br s, 1H, NH). ¹³C NMR (101 MHz, acetone-d₆): 91.3 (C-3), 114.0 (C(5)H), 117.2 (C≡N), 128.1 (2 CH Ar), 128.2 (2 CH Ar), 128.5 (CH Ar), 129.5 (CH Ar), 126.6 (2 CH Ar), 130.0 (CH Ar), 130.5 (CH Ph), 131.3 (CH Ar), 131.5 (2CH Ar), 132.4, 132.9, 134.2, 135.6, 137.7, 137.9, 156.7 (C-4), 156.9 (C–6), 159.3 (C–NH). HRMS (ESI) m/z: calculated for C₂₅H₁₆Cl₃N₄ [M + H]⁺: 477.044055, found 477.0415 (Δ 5.36 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(4-methylphenyl)-6-phenylnicotinonitrile 21{5} was isolated in 85% yield. FTIR (nujol), ν_max, cm⁻¹: 3273 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 2.41 (s, 3H, Me), 7.36 (d, ³J = 7.5 Hz, 2H, H Tol), 7.41–7.56 (m, 6H, H Ar, and H-5 overlapped), 7.60 (d, ³J = 7.5 Hz, 2H, H Tol), 7.82 (d, ³J = 7.8 Hz, 2H, H-2, and H-6, 4-ClC₆H₄), 8.14 (br s, 1H, –CH=), 8.17–8.21 (m, 2H, H Ph), 11.77 (br s, 1H, NH). HRMS (ESI) m/z: calculated for C₂₆H₂₀ClN₄ [M + H]⁺: 423.137649, found 423.1357 (Δ 4.6 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(4-methylphenyl)-6-phenylnicotinonitrile 21{6} was isolated in 78% yield. FTIR (nujol), ν_max, cm⁻¹: 3312, 3292 (N–H), 2218 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 2.40 (s, 3H, Me), 7.36 (d, ³J = 7.8 Hz, 2H, H Tol), 7.39–7.46 (m, 1H, H Ar), 7.50 (s, 1H, H-5), 7.51–7.56 (m, 3H, H Ph), 7.60 (d, ³J = 7.8 Hz, 2H, H Tol), 7.67–7.69 (m, 1H, H Ar), 8.17–8.21 (m, 2H, H Ph), 8.23 (d, ³J = 8.7 Hz, 1H, H Ar), 8.51 (br s, 1H, –CH=), 12.01 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 21.5 (Me), 86.6 (C-3), 111.5 (C(5)H), 116.3 (C≡N), 127.9 (2 CH Ar), 128.4 (CH Ar), 129.4 (2 CH Ar), 129.7 (2 CH Ar), 129.8 (CH Ar), 130.0 (2 CH Ar), 130.7 (CH Ph), 131.0 (CH Ar), 131.9, 133.4, 134.5, 134.6, 137.0, 137.4, 141.8, 153.0 (C-4), 157.1 (C–6), 158.4 (C–NH). Elemental Analysis: found, %: C, 68.33; H, 4.11; N, 12.19. C₂₆H₁₈Cl₂N₄ (M 457.36). Calculated, %: C, 68.28; H, 3.97; N, 12.25. HRMS (ESI) m/z: calculated for C₂₅H₁₇Cl₂N₄ [M + H–Me]⁺: 443.083027, found 443.0801 (Δ 6.6 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(3,4-dimethoxyphenyl)-6-phenylnicotinonitrile 21{7} was isolated in 72% yield. FTIR (nujol), ν_max, cm⁻¹: 3277 br (N–H), 2206 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.84 (s, 3H, MeO), 3.86 (s, 3H, MeO), 7.12 (d, ³J = 8.7 Hz, 1H, H Ar), 7.28 (d, ³J = 8.7 Hz, 1H, H Ar), 7.30 (s, 1H, H Ar), 7.46 (d, ³J = 8.3 Hz, 2H, H Ar), 7.50–7.53 (m, 4H, H-5, H Ar overlapped), 7.82 (d, ³J = 8.3 Hz, 1H, H Ar), 8.14 (br s, 1H, –CH=), 8.18–8.21 (m, 2H, H Ph), 11.73 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 55.6 (MeO), 55.7 (MeO), 87.5 (C-3), 111.5 (C(5)H), 112.4 (CH Ar), 112.6 (CH Ar), 117.8 (C≡N), 121.7 (C Ar), 127.3 (2 CH Ar), 128.3 (2 CH Ar), 128.7 (4 CH Ar), 129.3 (CH Ar), 130.3 (CH Ph), 133.5, 134.0, 137.1, 137.4, 140.2, 148.5 (C–OMe), 150.0 (C–OMe), 156.8 (C-4), 157.3 (C–6), 157.8 (C–NH). HRMS (ESI) m/z: calculated for C₂₇H₂₂ClN₄O₂ [M + H]⁺: 469.143129, found 469.1417 (Δ 3.05 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(3,4-dimethoxyphenyl)-6-phenylnicotinonitrile 21{8} was isolated in 73% yield. FTIR (nujol), ν_max, cm⁻¹: 3260 br (N–H), 2206 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.84 (s, 3H, MeO), 3.86 (s, 3H, MeO), 7.11 (d, ³J = 8.2 Hz, 1H, H Ar), 7.28 (dd, ³J = 8.2 Hz, ⁴J = 1.8 Hz, 1H, H Ar), 7.30 (d, ⁴J = 1.8 Hz, 1H, H Ar), 7.45 (dd, ³J = 8.2 Hz, ⁴J = 1.8 Hz, 1H, H Ar), 7.51–7.54 (m, 4H, H-5, H Ph overlapped), 7.65 (d, ⁴J = 1.8 Hz, 1H, H Ar), 8.17–8.20 (m, 2H, H Ph), 8.24 (d, ³J = 8.2 Hz, 1H, H Ar), 8.51 (br s, 1H, –CH=),), 11.95 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 55.6 (MeO), 55.7 (MeO), 87.7 (C-3), 111.5 (C(5)H), 112.6 (CH Ar), 112.8 (CH Ar), 117.8 (C≡N), 121.8 (C Ar), 127.3 (2 CH Ar), 127.8 (CH Ar), 128.0 (CH Ar), 127.6 (2 CH Ar), 129.2 (CH Ar), 130.4 (CH Ph), 131.4 (CH Ar), 132.8, 134.0, 136.4, 136.9, 148.5 (C–OMe), 150.0 (C–OMe), 156.6 (C-4), 157.2 (C–6), 157.8 (C–NH). HRMS (ESI) m/z: calculated for C₂₇H₂₂ClN₄O₂ [M + H–Cl]⁺: 469.14314, found 469.1408 (Δ 4.99 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(4-chlorophenyl)-6-(methylphenyl)nicotinonitrile 21{9} was isolated in 84% yield. FTIR (nujol), ν_max, cm⁻¹: 3269 br (N–H), 2218 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 2.39 (s, 3H, Me), 7.34 (d, ³J = 7.8 Hz, 2H, H Tol), 7.43–7.45 (m, 3H, H Ar, and H-5 overlapped), 7.55–7.58 (m, 4H, H Ar), 7.80 (d, ³J = 8.7 Hz, 2H, H Ar), 8.11 (br s, 1H, –CH=), 8.18 (d, ³J = 8.7 Hz, 2H, H Ar), 11.77 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 20.9 (Me), 87.8 (C-3), 112.3 (C(5)H), 117.5 (C≡N), 123.27 (2 CH Ar), 128.32 (2 CH Ar), 128.7 (2 CH Ar), 128.8 (2 CH Ar), 129.0 (2 CH Ar), 129.1 (2 CH Ar), 133.5, 134.0, 134.1, 135.2, 135.7, 139.2, 140.3, 156.5 (C-4), 156.7 (C–6), 157.5 (C–NH). Elemental Analysis: found, %: C, 68.36; H, 4.09; N, 12.22. C₂₆H₁₈Cl₂N₄ (M 457.36). Calculated, %: C, 68.28; H, 3.97; N, 12.25. HRMS (ESI) m/z: calculated for C₂₆H₁₉Cl₂N₄ [M + H]⁺: 457.098677, found 457.0967 (Δ 4.33 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(4-chlorophenyl)-6-(methylphenyl)nicotinonitrile 21{10} was isolated in 78% yield. FTIR (nujol), ν_max, cm⁻¹: 3306 br (N–H), 2210 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 2.39 (s, 3H, Me), 7.30 (s, CH Ar), 7.34 (d, ³J = 7.8 Hz, 2H, H Ar), 7.42 (br d, ³J = 8.7 Hz, 1H, H-5, 2,4-Cl₂C₆H₃), 7.49–7.54 (m, 4H, H Ar), 7.63 (d, ⁴J = 1.8 Hz, 1H, H-3, 2,4-Cl₂C₆H₃), 8.18 (d, ³J = 7.8 Hz, 2H, H Ar), 8.27 (d, ³J = 8.7 Hz, 1H, H Ar), 8.48 (br s, 1H, –CH=), 11.98 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 20.9 (Me), 86.7 (C-3), 112.7 (C(5)H), 117.5 (C≡N), 127.7 (CH Ar), 128.0 (CH Ar), 128.4 (2 CH Ar), 128.6 (2 CH Ar), 129.1 (2 CH Ar), 129.3 (2 CH Ar), 131.3 (CH Ar), 132.8, 134.0, 134.1, 135.3, 135.7, 136.5, 139.4, 156.5 (C-4), 156.4 (C-6), 159.1 (C–NH). Elemental Analysis: found, %: C, 63.38; H, 3.62; N, 11.33. C₂₆H₁₇Cl₃N₄ (M 491.80). Calculated, %: C, 63.50; H, 3.48; N, 11.39. HRMS (ESI) m/z: calculated for C₁₉H₁₆ClN₄ [M + H + H₂O–ArCHO]⁺: 335.106349, found 335.1046 (Δ 5.2 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(4-fluorophenyl)-6-phenylnicotinonitrile 21{11} was isolated in 85% yield as solvate with EtOH (1:1). FTIR (nujol), ν_max, cm⁻¹: 3479 br (OH of EtOH), 3323 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 1.04 (t, ³J = 7.1 Hz, 3H, CH₃CH₂OH), 3.40–3.46 (m, 2H, CH₃CH₂OH), 4.35 (t, ³J = 5.0 Hz, 3H, CH₃CH₂OH), 7.38–7.42 (m, 2H, H Ar), 7.46 (d, ³J = 8.5 Hz, 2H, H Ar), 7.50 (s, 1H, H-5), 7.51–7.53 (m, 3H, H Ph), 7.75–7.78 (m, 2H, H Ar), 7.82 (d, ³J = 8.5 Hz, 2H, H Ar), 8.14 (br s, 1H, –CH=), 8.17–8.20 (m, 2H, H Ph), 11.81 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 18.6 (CH₃CH₂OH), 56.0 (CH₃CH₂OH), 87.6 (C-3), 112.5 (C(5)H), 115.5 (d, ²J_C–F = 21.1 Hz, C(3)H C(5)H, 4-FC₆H₄), 117.5 (C≡N), 127.4 (2 CH Ph), 128.4 (2 CH Ph), 128.8 (4 CH, 4-ClC₆H₄), 130.5 (C(4)H Ph), 131.3 (d, ³J_C–F = 8.6 Hz, C(2)H C(6)H, 4-FC₆H₄), 133.5 (d, ⁴J_C–F = 3.8 Hz, C¹ 4-FC₆H₄), 133.6, 134.0, 136.9, 140.4, 156.5 (C-4), 156.7 (C–6), 158.0 (C–NH), 161.8, 164.2 (d, ¹J_C–F = 239 Hz, C–F). HRMS (ESI) m/z: calculated for C₂₅H₁₇ClFN₄ [M + H]⁺: 427.112577, found 427.1131 (Δ −1.23 ppm); calculated for C₁₈H₁₄FN₄ [M + H + H₂O–ArCHO]⁺: 305.120249, found 305.1203 (Δ −0.17 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(4-fluorophenyl)-6-phenylnicotinonitrile 21{12} was isolated in 81% yield as solvate with EtOH (1:1). FTIR (nujol), ν_max, cm⁻¹: 3458 br (OH of EtOH), 3327 br (N–H), 2206 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 1.04 (t, ³J = 7.1 Hz, 3H, CH₃CH₂OH), 3.40–3.46 (m, 2H, CH₃CH₂OH), 4.36 (t, ³J = 5.0 Hz, 3H, CH₃CH₂OH), 7.37–7.44 (m, 3H, H Ar), 7.51–7.52 (m, 4H, H Ph, and H-5 overlapped), 7.64 (br s, 1H, H-3, 2,4-Cl₂C₆H₃), 7.74–7.78 (m, 2H, H Ar), 8.17–8.19 (m, 2H, H Ph), 8.22 (d, ³J = 8.7 Hz, 1H, H-6, 2,4-Cl₂C₆H₃), 8.50 (br s, 1H, –CH=), 12.03 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 18.6 (CH₃CH₂OH), 56.0 (CH₃CH₂OH), 87.9 (C-3), 112.9 (C(5)H), 115.5 (d, ²J_C–F = 22.1 Hz, C(3)H C(5)H, 4-FC₆H₄), 117.6 (C≡N), 127.4 (2 CH Ph), 127.8 (CH Ar), 128.0 (CH Ar), 128.8 (2 CH Ph), 129.2 (CH Ar), 130.6 (C(4)H Ph), 131.3 (d, ³J_C–F = 8.6 Hz, C(2)H C(6)H, 4-FC₆H₄), 132.9 (C Ar), 133.4 (d, ⁴J_C–F = 2.9 Hz, C¹ 4-FC₆H₄), 134.1, 136.6, 136.8, 143.0, 156.4 (C-4), 156.5 (C–6), 158.0 (C–NH), 161.7, 164.2 (d, ¹J_C–F = 247.3 Hz, C–F). HRMS (ESI) m/z: calculated for C₁₈H₁₄FN₄ [M + H + H₂O–ArCHO]⁺: 305.120249, found 305.1185 (Δ 5.73 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(2,4-dichlorophenyl)-6-phenylnicotinonitrile 21{13} was isolated in 74% yield. FTIR (nujol), ν_max, cm⁻¹: 3304 (N–H), 2218 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 7.44 (d, ³J = 8.5 Hz, 2H, H Ar), 7.50–7.54 (m, 4H, H Ph, and H-5 overlapped), 7.58–7.64 (m, 2H, H Ar), 7.79 (d, ³J = 8.5 Hz, 2H, H Ar), 7.87 (d, ⁴J = 1.4 Hz, 1H, H Ar), 8.13 (s, 1H, –CH=), 8.15–8.18 (m, 2H, H Ph), 11.97 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 88.9 (C-3), 112.5 (C(5)H), 116.8 (C≡N), 127.3 (2 CH Ar), 127.7 (CH Ar), 128.4 (2 CH Ar), 128.8 (2 CH Ar), 128.9 (2 CH Ar), 129.1 (CH Ar), 130.7 (C(4)H Ph), 132.1 (CH Ar), 132.7 (CH Ar), 133.7, 133.9, 134.7, 135.4, 136.6, 140.7, 154.5 (C-4), 156.1 (C-6), 158.2 (C–NH). HRMS (ESI) m/z: calculated for C₂₅H₁₆Cl₃N₄ [M + H]⁺: 479.04111, found 477.0390 (Δ 4.4 ppm);

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(2,4-dichlorophenyl)-6-phenylnicotinonitrile 21{14} was isolated as solvate with 1,4-dioxane (1:1) in 81% yield. FTIR (nujol), ν_max, cm⁻¹: 3178 (N–H), 2216 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.55 (br s, 8H, dioxane), 7.42 (dd, ³J = 8.7 Hz, ⁴J = 1.8 Hz, 1H, H-5, 2,4-Cl₂C₆H₃), 7.52–7.54 (m, 3H, H Ph), 7.56 (br s, 1H, H-5), 7.60 (d, ³J = 8.2 Hz, 1H, H-6, 2,4-Cl₂C₆H₃), 7.63 (dd, ³J = 8.2 Hz, ⁴J = 1.8 Hz, 1H, H-5, 2,4-Cl₂C₆H₃), 7.67 (d, ⁴J = 1.8 Hz, 1H, H-3, 2,4-Cl₂C₆H₃), 7.87 (d, ⁴J = 1.8 Hz, 1H, H-3, 2,4-Cl₂C₆H₃), 8.16–8.18 (m, 3H, 2 H Ph, and H-6 2,4-Cl₂C₆H₃ overlapped), 8.52 (br s, 1H, –CH=), 12.16 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 66.3 (OCH₂ dioxane), 89.2 (C-3), 112.9 (C(5)H), 116.7 (C≡N), 127.3 (2 CH Ar), 127.69 (CH Ar), 127.74 (CH Ar), 127.9 (CH Ar), 128.9 (2 CH Ar), 129.1 (CH Ar), 129.2 (CH Ar), 130.7 (C(4)H Ph), 131.2 (CH Ar), 132.1 (CH), 132.7, 132.9, 134.2, 134.7, 135.3, 136.5, 136.9, 154.4 (C-4), 155.9 (C-6), 158.2 (C–NH). Elemental Analysis: found, %: C, 58.11; H, 3.64; N, 9.30. C₂₅H₁₄Cl₄N₄ × C₄H₈O₂ (M 600.32). Calculated, %: C, 58.02; H, 3.69; N, 9.33. HRMS (ESI) m/z: calculated for C₁₈H₁₃Cl₂N₄ [M + H + H₂O–ArCHO]⁺: 355.051727, found 355.0501 (Δ 4.58 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(3-nitrophenyl)-6-phenylnicotinonitrile 21{15} was isolated in 75% yield. FTIR (nujol), ν_max, cm⁻¹: 3308 br (N–H), 2208 (C≡N), 1531 (NO_{2 asymm}), 1356 (NO_{2 symm}). ¹H NMR (400 MHz, acetone-d₆): 7.43 (d, ³J = 8.2 Hz, 2H, H Ar), 7.49–7.54 (m, 3H, H Ar), 7.64 (s, 1H, H Ar), 7.87–7.92 (m, 3H, H Ar), 8.17–8.21 (m, 3H, 2 H Ph, and H Ar overlapped), 8.43 (dd, ³J = 8.1 Hz, ⁴J = 1.8 Hz, 1H, H Ar), 8.58–8.59 (m, 1H, H-2 3-NO₂C₆H₄), 8.66 (br s, 1H, –CH=), 10.79 (br s, 1H, NH). ¹³C NMR (101 MHz, acetone-d₆): 89.2 (C-3), 113.5 (C(5)H), 117.7 (C≡N), 124.7 (CH Ar), 124.9 (CH Ar), 128.3 (2 CH Ar), 129.5 (2 CH Ar), 129.6 (4 CH Ar), 129.9 (CH Ar), 130.8 (C(4)H Ph), 130.9 (CH Ar), 131.4 (CH Ar), 135.1, 135.2, 136.2, 138.0, 141.6, 149.1 (C–NO₂), 156.3 (C-4), 159.6 (C-6), 161.5 (C–NH). Elemental Analysis: found, %: C, 66.08; H, 3.64; N, 15.33. C₂₅H₁₆ClN₅O₂ (M 453.89). Calculated, %: C, 66.16; H, 3.55; N, 15.43. HRMS (ESI) m/z: calculated for C₁₈H₁₂N₃O₃ [M + H + H₂O–ArCH = N-NH₂]⁺: 318.087867, found 318.0856 (Δ 7.1 ppm); calculated for C₃₆H₂₃N₆O₆ [2M + H + 2H₂O–2ArCH = N-NH₂]⁺: 635.167909, found 635.1648 (Δ 4.9 ppm); calculated for C₃₆H₂₂N₆O₆Na [2M + Na + 2H₂O–2ArCH = N-NH₂]⁺: 657.149854, found 657.1463 (Δ 5.4 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(3-nitrophenyl)-6-phenylnicotinonitrile 21{16} was isolated in 76% yield. FTIR (nujol), ν_max, cm⁻¹: 3294 br (N–H), 2210 (C≡N), 1526 (NO_{2 asymm}), 1350 (NO_{2 symm}). ¹H NMR (400 MHz, DMSO-d₆): 7.44 (d, ³J = 8.7 Hz, 1H, H Ar), 7.50–7.56 (m, 4H, H Ar, and H-5 overlapped), 7.68 (br s, 1H, H Ar), 7.83–7.88 (m, 2H, H Ar), 8.17–8.21 (m, 3H, 2 H Ph, and H Ar overlapped), 8.41 (d, ³J = 8.2 Hz, 1H, H Ar), 8.53–8.55 (m, 2H, H-Ar, and –CH= overlapped), 12.13 (br s, 1H, NH). Elemental Analysis: found, %: C, 61.40; H, 3.24; N, 14.28. C₂₅H₁₅Cl₂N₅O₂ (M 488.33). Calculated, %: C, 61.49; H, 3.10; N, 14.34. HRMS (ESI) m/z: calculated for C₁₈H₁₂N₃O₃ [M + H + H₂O–ArCH = N-NH₂]⁺: 318.087867, found 318.0854 (Δ 7.75 ppm); calculated for C₃₆H₂₃N₆O₆ [2M + H + 2H₂O–2ArCH = N-NH₂]⁺: 635.167909, found 635.1647 (Δ 5.05 ppm).

4-(3-Bromophenyl)-2-[2-(4-chlorobenzylidene)hydrazinyl]-6-phenylnicotinonitrile 21{17} was isolated in 70% yield. FTIR (nujol), ν_max, cm⁻¹: 3300 br (N–H), 2214 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 7.38–7.42 (m, 1H, H Ar), 7.46 (d, ³J = 8.5 Hz, 2H, H Ar), 7.51–7.55 (m, 4H, H Ph, and H-5 overlapped), 7.69–7.76 (m, 2H, H Ar), 7.82 (d, ³J = 8.5 Hz, 2H, H Ar), 7.89–7.90 (m, 1H, H Ar), 8.14 (br s, 1H, –CH=), 8.19–8.21 (m, 2H, H Ph), 11.84 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 87.4 (C-3), 112.4 (C(5)H), 117.4 (C≡N), 121.7 (C–Br), 127.4 (2 CH Ar), 128.1 (2 CH Ar), 128.4 (2 CH Ar), 128.7 (2 CH Ar), 129.1 (CH Ar), 130.0 (CH Ar), 130.6 (C(4)H Ph), 131.4 (CH Ar), 132.2 (CH Ar), 133.6, 133.9, 136.8, 139.3, 140.4, 155.8 (C-4), 156.6 (C-6), 158.1 (C–NH). Elemental Analysis: found, %: C, 61.43; H, 3.44; N, 11.38. C₂₅H₁₆BrClN₄ (M 487.79). Calculated, %: C, 61.56; H, 3.31; N, 11.49. HRMS (ESI) m/z: calculated for C₁₈H₁₄BrN₄ [M + H + H₂O–ArCHO]⁺: 365.040182, found 365.0398 (Δ 7.07 ppm); calculated for C₂₅H₁₇BrClN₄ [M + H]⁺: 489.03047, found 489.0272 (Δ 6.69 ppm);

4-(3-Bromophenyl)-2-[2-(2,4-dichlorobenzylidene)hydrazinyl]-6-phenylnicotinonitrile 21{18} was isolated in 73% yield. FTIR (nujol), ν_max, cm⁻¹: 3234 br (N–H), 2218 (C≡N). 7.39–7.43 (m, 2H, H Ar), 7.51–7.55 (m, 4H, H Ph, and H-5 overlapped), 7.63 (d, ⁴J = 1.8 Hz, 1H, H Ar), 7.70–7.75 (m, 2H, H Ar), 7.88–7.90 (m, 1H, H Ar), 8.18–8.23 (m, 3H, H Ph, H Ar), 8.51 (br s, 1H, –CH=), 12.06 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 87.7 (C-3), 112.8 (C(5)H), 116.7 (C≡N), 121.7 (C–Br), 127.4 (2 CH Ph), 127.8 (CH Ar), 128.0 (CH Ar), 128.8 (2 CH Ph), 129.1 (CH Ar), 129.2 (CH Ar), 130.0 (CH Ar), 130.6 (C(4)H Ph), 131.7 (CH Ar), 132.3 (CH Ar), 128.1 (2 CH Ar), 128.4 (2 CH Ar), 128.7 (2 CH Ar), 129.1 (CH Ar), 130.0 (CH Ar), 130.6 (C(4)H Ph), 131.4 (CH Ar), 132.2 (CH Ar), 132.8, 133.9, 134.1, 136.7, 139.2, 143.6, 155.8 (C-4), 156.8 (C-6), 158.1 (C–NH). Elemental Analysis: found, %: C, 57.57; H, 3.06; N, 10.60. C₂₅H₁₅BrCl₂N₄ (M 522.23). Calculated, %: C, 57.50; H, 2.90; N, 10.73. HRMS (ESI) m/z: calculated for C₂₅H₁₇Cl₂N₄ [M + H–Br]⁺: 443.083027, found 443.0804 (Δ 5.9 ppm); calculated for C₁₈H₁₄BrN₄ [M + H + H₂O–ArCHO]⁺: 365.040182, found 365.0373 (Δ 7.9 ppm).

2-[2-(4-Chlorobenzylidene)hydrazinyl]-4-(4-methoxyphenyl)-6-phenylnicotinonitrile 21{19} was isolated in 75% yield. FTIR (nujol), ν_max, cm⁻¹: 3269 br (N–H), 2218 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.84 (s, 3H, MeO), 7.10 (d, ³J = 8.7 Hz, 2H, H-3 H-5 4-MeOC₆H₄), 7.44–7.47 (m, 3H, H Ar, and H-5 overlapped), 7.50–7.53 (m, 3H, H Ph), 7.67 (d, ³J = 8.7 Hz, 2H, H-Ar), 7.82 (d, ³J = 8.7 Hz, 2H, H-Ar), 8.13 (br s, 1H, –CH=), 8.16–8.18 (m, 2H, H Ph), 11.73 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 55.3 (MeO), 87.4 (C-3), 112.3 (C(5)H), 113.9 (2 CH Ar), 117.8 (C≡N), 127.3 (2 CH Ph), 128.3 (2 CH Ar), 128.8 (4 CH Ar), 129.2 (CH), 130.3 (C(4)H Ph), 130.4 (2 CH Ar), 133.5, 134.1, 137.0, 140.1, 156.9 (C-4), 157.1 (C–OMe), 157.8 (C-6), 160.4 (C–NH). Elemental Analysis: found, %: C, 71.08; H, 4.42; N, 12.75. C₂₆H₁₉ClN₄O (M 438.92). Calculated, %: C, 71.15; H, 4.36; N, 12.77. HRMS (ESI) m/z: calculated for C₂₆H₂₀ClN₄O [M + H]⁺: 439.132564, found 439.1297 (Δ 6.5 ppm).

2-[2-(2,4-Dichlorobenzylidene)hydrazinyl]-4-(4-methoxyphenyl)-6-phenylnicotinonitrile 21{20} was isolated in 73% yield. FTIR (nujol), ν_max, cm⁻¹: 3287 br (N–H), 2208 (C≡N). ¹H NMR (400 MHz, DMSO-d₆): 3.84 (s, 3H, MeO), 7.10 (d, ³J = 8.8 Hz, 2H, H-3 H-5 4-MeOC₆H₄), 7.42–7.44 (m, 1H, H Ar), 7.49–7.51 (m, 4H, 3 H Ph, and H-5 overlapped), 7.64–7.68 (m, 3H, H Ar), 8.15–8.17 (m, 2H, H Ph), 8.22–8.25 (m, 1H, H Ar), 8.49 (br s, 1H, –CH=), 11.97 (br s, 1H, NH). ¹³C NMR (101 MHz, DMSO-d₆): 55.4 (MeO), 87.7 (C-3), 112.7 (C(5)H), 114.0 (2 CH Ar), 117.9 (C≡N), 127.4 (2 CH Ph), 127.8 (CH Ar), 128.0 (CH Ar), 128.8 (2 CH Ph), 129.1 (CH), 129.2 (CH Ar), 130.4 (C(4)H Ph), 130.5 (2 CH Ar), 131.4, 132.8, 134.0, 136.3, 136.9, 156.7 (C-4), 157.0 (C–OMe), 157.8 (C-6), 160.4 (C–NH). Elemental Analysis: found, %: C, 65.94; H, 3.97; N, 11.77. C₂₆H₁₈Cl₂N₄O (M 473.36). Calculated, %: C, 65.97; H, 3.83; N, 11.84. HRMS (ESI) m/z: calculated for C₂₅H₁₇Cl₂N₄ [M + H–MeO]⁺: 443.083027, found 443.0809 (Δ 4.8 ppm).

X-ray studies of crystals of 2-bromo-4-(4-chlorophenyl)-6-phenylnicotinonitrile (15a).

Single crystals of 2-bromo-4-(4-chlorophenyl)-6-phenylnicotinonitrile (15a) were isolated from mother liquor (AcOH solution). A suitable crystal was selected and studied on a SuperNova, Dual, Cu at home/near, AtlasS2 diffractometer. The crystal was kept at 100.00 (11) K during data collection. Using Olex2 [165], the structure was solved using the SHELXT [166] structure solution program using Intrinsic Phasing and then refined with the SHELXL [167] refinement package using Least Squares minimization. The crystals of 15a (C₁₈H₁₀BrClN₂, M =369.64 g/mol) were monoclinic, space group P2₁/c (no. 14), a = 15.2876(4) Å, b = 7.21330(10) Å, c = 15.3758(4) Å, β = 118.885(3)°, V = 1484.61(7) ų, Z = 4, T = 100.00(11) K, μ(Cu Kα) = 5.392 mm⁻¹, and D_calc = 1.654 g/cm³, and 10,591 reflections were measured (6.604° ≤ 2Θ ≤ 152.484°), of which 3098 were unique (R_int = 0.0382, R_sigma = 0.0316), which were used in all calculations. The final R₁ was 0.0323 (I > 2σ(I)), and wR₂ was 0.0865 (all data). A full set of crystallographic data has been deposited in the Cambridge Crystallographic Data Center (CCDC Deposition Number 2499675).

X-ray studies of co-crystallized (2S*,3R*,4S*,6R*)-3-benzoyl-5-bromo-4- hydroxy-4-phenyl-2,6-di-p-tolylcyclohexane-1,1-dicarbonitrile 17-Br and (2S*,3R*,4S*,6R*)- 3-benzoyl-4-hydroxy-4-phenyl-2,6-di-p-tolylcyclohexane-1,1-dicarbonitrile 17, solvate with AcOH.

Single crystals of C₃₉H_37.39Br_0.61N₂O₆ (17 + 17-Br) were crystallized by slow evaporation of filtrate (glac. AcOH) that remained after the separation of 2-bromonicotinonitrile 15c. A suitable crystal was selected and studied on a SuperNova, Dual, Cu at home/near, AtlasS2 diffractometer. The crystal was kept at 293(2) K during data collection. Using Olex2 [165], the structure was solved with the SHELXT [166] structure solution program using Intrinsic Phasing and refined with the SHELXL [167] refinement package using Least Squares minimization. The co-crystals 17 + 17-Br (C₃₉H_37.39Br_0.61N₂O₆, M = 678.84 g/mol) were triclinic, space group P-1 (no. 2), a = 11.7101(2) Å, b = 12.1777(2) Å, c = 13.1548(3) Å, α = 105.5935(16)°, β = 95.2886(16)°, γ = 91.2975(15)°, V = 1796.97(6) ų, Z = 2, T = 293(2) K, μ(Cu Kα) = 1.436 mm⁻¹, and Dcalc = 1.255 g/cm³, and 26,097 reflections were measured (7.014° ≤ 2Θ ≤ 152.508°), of which 7469 were unique (R_int = 0.0156, R_sigma = 0.0143), which were used in all calculations. The final R₁ was 0.0527 (I > 2σ(I)), and wR₂ was 0.1366 (all data). A full set of crystallographic data has been deposited in the Cambridge Crystallographic Data Center (CCDC Deposition Number 2499676).

Herbicide-Safening Effect Studies

The evaluation of the antidote effect was performed on sunflower seedlings (cv. Master) according to the reported procedure [159,160,161,162] as follows. Sunflower seedlings having 2–4 mm long embryo roots were treated with a solution of 2,4-D (10⁻³% by weight) for 1 h to achieve 40–60% inhibition of hypocotyl growth. Following exposure to the herbicide, the germinated seeds were rinsed with distilled water and transferred to a solution containing either compound 20 or 21 (applied at weight concentrations of 10⁻², 10⁻³, 10⁻⁴, or 10⁻⁵% representing the “herbicide + antidote” test series). After one hour of immersion, the seedlings were again rinsed with distilled water and positioned on paper strips (10 × 75 cm), with 20 seeds per strip. The strips were subsequently rolled and placed into beakers containing 50 cm³ of distilled water. A reference group, designated for the “herbicide-only” series, was treated with a 2,4-D solution (10⁻³%) for one hour, followed by a one-hour immersion in water. Seeds for the “control” series were maintained in water for the entire two-hour period. All solutions were kept at a constant temperature of 28 °C. Subsequently, the samples were transferred to a thermostat for a 72 h incubation period at 28 °C. Each experimental variant was carried out in triplicate, with 20 seeds per replication. The obtained data are presented in Table 1.

4. Conclusions

In summary, we have developed a method for the synthesis of new 2-hydrazinylnicotinonitriles, prepared a series of hydrazones, and investigated their biological activity. A key advantage of this new synthetic approach is the use of 4,6-diaryl-2-bromo-3-cyanopyridines in the reaction with hydrazine, instead of the less reactive 2-chloro-, 2-alkoxy-, 2-mercapto-, or 2-(alkylthio)nicotinonitriles. This allows the reaction with N₂H₄ to proceed under milder conditions without heating to give products in nearly quantitative yields. Further benefits include the absence of the side reaction leading to 3-aminopyrazolo[3,4-b]pyridines. The starting 4,6-diaryl-2-bromo-3-cyanopyridines are readily available and can be prepared in high yield in two steps starting from cheap acyclic precursors. First, malononitrile and 1,3-diarylpropenones (chalcones) were reacted to afford intermediate Michael adducts. The latter were brominated with Br₂ in AcOH to give 2-bromonicotinonitriles. During an attempt to isolate additional crops of bromopyridine from the mother liquor, we isolated and characterized by X-ray diffraction a crystalline by-product resulting from a tandem bromination–carbocyclization of a Michael bis-adduct. This compound was identified as a previously unreported derivative of 2,6-diaryl-3-benzoyl-5-bromo-4-hydroxy-4-phenylcyclohexane-1,1-dicarbonitrile.

To explore the agrochemical potential, a small library of hydrazones was synthesized by reacting the new 2-hydrazinylnicotinonitriles with chlorine-substituted aromatic aldehydes. Laboratory experiments on sunflower seedlings revealed that four samples from the series of 2-hydrazinylnicotinonitriles and four samples of arylhydrazones exhibit a significant herbicide safening effect against 2,4-D.

The most active compounds were 4-(4-chlorophenyl)-2-hydrazinyl- 6-phenylnicotinonitrile 20a, which reduced the negative effect of the 2,4-D herbicide by 34–86% on roots and by 30–46% on hypocotyls and 4-(3-bromophenyl)-2-[2-(4-chlorobenzylidene)hydrazinyl]-6-phenylnicotinonitrile 21{17}, which reduced the negative effect on sunflower seedling hypocotyls by 38–52% and on roots by 61–86%.