The Reactivity of Azidonitrobenzofuroxans towards 1,3-Dicarbonyl Compounds: Unexpected Formation of Amino Derivative via the Regitz Diazo Transfer and Tautomerism Study

Herein, we report on the reaction of nitro-substituted azidobenzofuroxans with 1,3-dicarbonyl compounds in basic media. The known reactions of benzofuroxans and azidofuroxans with 1,3-dicarbonyl compounds in the presence of bases are the 1,3-dipolar cycloaddition and the Beirut reaction. In contrast with this, azidonitrobenzofuroxan reacts with 1,3-carbonyl compounds through Regitz diazo transfer, which is the first example of this type of reaction for furoxan derivatives. This difference is seemingly due to the strong electron-withdrawing effect of the superelectrophilic azidonitrobenzofuroxan, which serves as the azido transfer agent rather than 1,3-dipole in this case.

Organic azides are valuable building blocks in synthetic organic chemistry due to the well-known ability of azides to undergo 1,3-dipolar cycloaddition reactions. We speculated that the presence of the azide moiety in the benzofuroxan molecule would allow for easy installation of various biologically relevant fragments via a "click" reaction. Surprisingly, the literature survey revealed that the chemistry of the azidobenzofuroxans is still unexplored. The only reaction of the furoxan-based azide with 1,3-dicarbonyl compounds resulting in the 3+2 cycloaddition in the basic media was reported by Fershtat and coworkers [27] (Scheme 1A). Notably, benzofuroxans are also known to undergo the Beirut reaction under the same conditions [28] (Scheme 1B). Thus, we decided to investigate the possible reaction modes of azidobenzofuroxans with 1,3-dicarbonyl compounds, and herein we report the results of our studies. In contrast with the known examples, superelectrophilic azidobenzofuroxans do not undergo 1,3-dipolar cycloaddition nor the Beirut reaction with 1,3-dicarbonyl compounds. Instead, the Regitz diazo transfer proceeds, which results in the appropriate diazo compound and aminobenzofuroxan (Scheme 1C). Additionally, we explored the obtained tautomerism using NMR and quantum chemistry calculations.
Organic azides are valuable building blocks in synthetic organic chemistry du well-known ability of azides to undergo 1,3-dipolar cycloaddition reactions. We lated that the presence of the azide moiety in the benzofuroxan molecule would a easy installation of various biologically relevant fragments via a "click" reaction. ingly, the literature survey revealed that the chemistry of the azidobenzofuroxan unexplored. The only reaction of the furoxan-based azide with 1,3-dicarbonyl com resulting in the 3+2 cycloaddition in the basic media was reported by Fershtat and c ers [27] (Scheme 1A). Notably, benzofuroxans are also known to undergo the Beir tion under the same conditions [28] (Scheme 1B). Thus, we decided to investigate sible reaction modes of azidobenzofuroxans with 1,3-dicarbonyl compounds, and we report the results of our studies. In contrast with the known examples, super philic azidobenzofuroxans do not undergo 1,3-dipolar cycloaddition nor the Beir tion with 1,3-dicarbonyl compounds. Instead, the Regitz diazo transfer proceeds results in the appropriate diazo compound and aminobenzofuroxan (Scheme 1C tionally, we explored the obtained tautomerism using NMR and quantum chemi culations. Scheme 1. Known reaction modes of the furoxan derivatives with 1,3-dicarbonyl compou 1,3-dipolar cycloaddition of azidofuroxan derivatives; (B) the Beirut reaction of the benzof (C) the Regitz diazo transfer of the azidobenzofuroxans (this work).

Results and Discussion
We initiated our studies through the synthesis of azidobenzofuroxan 2 via t reaction of chloro derivative 1 with sodium azide (Scheme 2). Next, we carried reaction of azide 2 with acetoacetic acid ester under the conditions described by and coworkers [27]. Surprisingly, the analysis of the mass spectra of the reaction indicated the complete absence of a cycloaddition product. The experiment was r in the NMR tube, and careful examination of the 1 H NMR spectrum revealed sign to three major products alongside some starting azide 2, starting ester, and trieth ( Figure 1). Scheme 1. Known reaction modes of the furoxan derivatives with 1,3-dicarbonyl compounds: (A) 1,3dipolar cycloaddition of azidofuroxan derivatives; (B) the Beirut reaction of the benzofuroxans; (C) the Regitz diazo transfer of the azidobenzofuroxans (this work).

Results and Discussion
We initiated our studies through the synthesis of azidobenzofuroxan 2 via the S N Ar reaction of chloro derivative 1 with sodium azide (Scheme 2). Next, we carried out the reaction of azide 2 with acetoacetic acid ester under the conditions described by Fershtat and coworkers [27]. Surprisingly, the analysis of the mass spectra of the reaction mixture indicated the complete absence of a cycloaddition product. The experiment was repeated in the NMR tube, and careful examination of the 1 H NMR spectrum revealed signals due to three major products alongside some starting azide 2, starting ester, and triethylamine ( Figure 1).
Extra evidence was sought to confirm the structure of 3A and 3B. So, aminbenzofuroxan 3 was independently synthesized by the reaction of 1 with excess ammonia in DMSO. The obtained NMR data of the compound appeared to be identical to the signals observed in the NMR of the reaction mixture ( Figure 1). Additionally, we were lucky enough to obtain crystals suitable for the X-ray analysis (Figure 3), which also proved the formation of amino derivatives 3A,B. The crystals of compound 3 consisted of two tautomers in a ratio of 1:1 ( Figure 3). The oxygen atom in one tautomer formed an intramolecular hydrogen bond with the amino group of the other tautomer, while in the second tautomer, the oxygen atom formedan intermolecular hydrogen bond with the amino group. The data on hydrogen One of these products was identified as ethyl 2-diazo-3-oxobutanoate 4a by the comparison of the spectrum with the published data [29]. The mass spectrometry data also indicated the presence of the hydrated molecular ion of 4a. This ion may be formed either from ionisation of the hydrated form of 4a or through rapid hydration of the ionised form of 4a during the mass spectrometric experiment. The obtained data do not allow fordistinguishing between these possibilities. In the EI mass spectrum peak of the molecular ion,   One of these products was identified as ethyl 2-diazo-3-oxobutanoate 4a by the comparison of the spectrum with the published data [29]. The mass spectrometry data also indicated the presence of the hydrated molecular ion of 4a. This ion may be formed either from ionisation of the hydrated form of 4a or through rapid hydration of the ionised form of 4a during the mass spectrometric experiment. The obtained data do not allow fordistinguishing between these possibilities. In the EI mass spectrum peak of the molecular ion, [ Figure 2).
indicated the presence of the hydrated molecular ion of 4a. This ion may be formed either from ionisation of the hydrated form of 4a or through rapid hydration of the ionised form of 4a during the mass spectrometric experiment. The obtained data do not allow fordistinguishing between these possibilities. In the EI mass spectrum peak of the molecular ion,  We speculate that the formation of the diazo compound 4a may be explained by the diazo transfer reaction described by Regitz [30] (Scheme 2). Based on this, we propose that the singlets in the 6.75-7.34 ppm range (see Figure 1) may be attributed to the tautomeric aminobenzofuroxans 3A and 3B, as well as the unreacted starting azidobenzofuroxan 2.
Similar results were obtained when acetylacetone and trifluoromethyl-3-oxobutanoic acid ester were employed instead of acetoacetic acid ester. Amino derivative 3 was We speculate that the formation of the diazo compound 4a may be explained by the diazo transfer reaction described by Regitz [30] (Scheme 2). Based on this, we propose that the singlets in the 6.75-7.34 ppm range (see Figure 1) may be attributed to the tautomeric aminobenzofuroxans 3A and 3B, as well as the unreacted starting azidobenzofuroxan 2.
Similar results were obtained when acetylacetone and trifluoromethyl-3-oxobutanoic acid ester were employed instead of acetoacetic acid ester. Amino derivative 3 was obtained in almost the same yield (ca 1-2% difference) alongside the appropriate diazo compound (see Supplementary Materials, Figures S1 and S2 for the spectra). Thus, the replacement of the electron-donating methyl group by the electron-withdrawing trifluoromethyl group, as well as the replacement of the ethoxy fragment by the methyl group, did not affect the reaction course. Taking this into account, we conclude that the reaction outcome was determined by azidofuroxan rather than by the nature of the 1,3-dicarbonyl compound.
This reaction pathway differs from both the 1,3-dipolar cycloaddition of azidofuroxans described by Fershtat and the Beirut reaction of benzofuroxans. Notably, the diazo transfer is the preferred reaction pathway in the case of tosylazide [29], which possesses an electronwithdrawing substituent next to the azide group. At the same time, the more electron-rich phenylazide undergoes cycloaddition with 1,3-dicarbonyl compounds under the same conditions [31,32]. Asnitro-substituted benzofuroxans are known for their superelectrophilic nature [7,21,[33][34][35][36], we attribute the difference between azidonitrobenzofuroxan 2 and azidofuroxan derivatives [27] to the strong electron-withdrawing effect of the former.
Extra evidence was sought to confirm the structure of 3A and 3B. So, aminbenzofuroxan 3 was independently synthesized by the reaction of 1 with excess ammonia in DMSO. The obtained NMR data of the compound appeared to be identical to the signals observed in the NMR of the reaction mixture ( Figure 1). Additionally, we were lucky enough to obtain crystals suitable for the X-ray analysis ( Figure 3), which also proved the formation of amino derivatives 3A,B.  Figures S1 and S2 for the spectra). Thus, the replacement of the electron-donating methyl group by the electron-withdrawing trifluoromethyl group, as well as the replacement of the ethoxy fragment by the methyl group, did not affect the reaction course. Taking this into account, we conclude that the reaction outcome was determined by azidofuroxan rather than by the nature of the 1,3-dicarbonyl compound. This reaction pathway differs from both the 1,3-dipolar cycloaddition of azidofuroxans described by Fershtat and the Beirut reaction of benzofuroxans. Notably, the diazo transfer is the preferred reaction pathway in the case of tosylazide [29], which possesses an electron-withdrawing substituent next to the azide group. At the same time, the more electron-rich phenylazide undergoes cycloaddition with 1,3-dicarbonyl compounds under the same conditions [31,32]. Asnitro-substituted benzofuroxans are known for their superelectrophilic nature [7,21,[33][34][35][36], we attribute the difference between azidonitrobenzofuroxan 2 and azidofuroxan derivatives [27] to the strong electron-withdrawing effect of the former.

Scheme 2. The Regitz diazo transfer of azidobenzofuroxan 2.
Extra evidence was sought to confirm the structure of 3A and 3B. So, aminbenzofuroxan 3 was independently synthesized by the reaction of 1 with excess ammonia in DMSO. The obtained NMR data of the compound appeared to be identical to the signals observed in the NMR of the reaction mixture ( Figure 1). Additionally, we were lucky enough to obtain crystals suitable for the X-ray analysis ( Figure 3), which also proved the formation of amino derivatives 3A,B. The crystals of compound 3 consisted of two tautomers in a ratio of 1:1 ( Figure 3). The oxygen atom in one tautomer formed an intramolecular hydrogen bond with the amino group of the other tautomer, while in the second tautomer, the oxygen atom formedan intermolecular hydrogen bond with the amino group. The data on hydrogen The crystals of compound 3 consisted of two tautomers in a ratio of 1:1 ( Figure 3). The oxygen atom in one tautomer formed an intramolecular hydrogen bond with the amino group of the other tautomer, while in the second tautomer, the oxygen atom formedan intermolecular hydrogen bond with the amino group. The data on hydrogen bonds are summarized in Table S1, Supplementary Materials. The plane of the nitro group leftthe plane of the benzene ring by 33.2 degrees; apparently this wasdue to the steric factor, asthe neighboring positions in the benzene ring wereoccupied. It should be noted that the tautomers formed planes parallel to 0bc consisting of one type of tautomer ( Figure S3, Supplementary Materials).

Study of the Tautomerism of Benzofuroxans
As mentioned previously, benzofuroxan and its derivatives can undergo tautomerisation, which is believed to proceed through the transient formation of 1,2-dinitrosoarenes (see Supplementary Materials, Figure S4 for the putative mechanism of the tautomerisation). Consequently, the determination of the tautomeric composition of the benzofuroxans is important for the correct determination of their structure. Taking this into account, the study of the tautomerism of compounds used was essential for our research.
First, we investigated the starting chlorobenzofuroxan 1 using various NMR techniques. As mentioned above, one of the main difficulties in studying thetitled compounds using NMR is a lack of a sufficient number of spin markers (protons) in these molecules (vide supra). This strongly complicates «direct» structure elucidation, i.e., using only experimental 2D correlation NMR data. To overcome such problems, anab initio analysis could be applied.
A variety of NMR correlation methods were used to establish the structure of the titled compound. The combination of 2D 1 H-13 C HSQC and 1 H-15 N/ 13 C HMBC correlations enabled directly establishing two heteroaromatic moieties.
The 1 H NMR spectrum of 1 at 303 K consisted of a broadened (ca 20 Hz) signal at 7.6 ppm with a weak broad shoulder on the lowfield side of the signal (Figure 4a). Thus, a chemical exchange wasobserved. DNMR showed that 313 K was a coalescence point, and a high resolution spectrum tookplace for T < 263 K ( Figures S5 and S6, Supplementary Materials). The components ratio was ca 91:9. Indeed, the theoretical analysis gave a 1.63 kCal/mol energy gap with a preference for the B form ( Figure 4). Moreover, a barrier of ca 18 kCal was estimated. bonds are summarized in Table S1, Supplementary Materials. The plane of the nitro group leftthe plane of the benzene ring by 33.2 degrees; apparently this wasdue to the steric factor, asthe neighboring positions in the benzene ring wereoccupied. It should be noted that the tautomers formed planes parallel to 0bc consisting of one type of tautomer ( Figure S3, Supplementary Materials).

Study of the Tautomerism of Benzofuroxans
As mentioned previously, benzofuroxan and its derivatives can undergo tautomerisation, which is believed to proceed through the transient formation of 1,2-dinitrosoarenes (see Supplementary Materials, Figure S4 for the putative mechanism of the tautomerisation). Consequently, the determination of the tautomeric composition of the benzofuroxans is important for the correct determination of their structure. Taking this into account, the study of the tautomerism of compounds used was essential for our research.
First, we investigated the starting chlorobenzofuroxan 1 using various NMR techniques. As mentioned above, one of the main difficulties in studying thetitled compounds using NMR is a lack of a sufficient number of spin markers (protons) in these molecules (vide supra). This strongly complicates «direct» structure elucidation, i.e., using only experimental 2D correlation NMR data. To overcome such problems, anab initio analysis could be applied.
A variety of NMR correlation methods were used to establish the structure of the titled compound. The combination of 2D 1 H-13 C HSQC and 1 H-15 N/ 13 C HMBC correlations enabled directly establishing two heteroaromatic moieties.
The 1 H NMR spectrum of 1 at 303K consisted of a broadened (ca20Hz) signal at 7.6 ppm with a weak broad shoulder on the lowfield side of the signal (Figure 4a). Thus, a chemical exchange wasobserved. DNMR showed that 313K wasa coalescence point, and a high resolution spectrum tookplace for T<263K ( Figures S5 and S6, Supplementary Materials). The components ratio was ca 91:9. Indeed, the theoretical analysis gave a 1.63 kCal/mol energy gap with a preference for the B form ( Figure 4). Moreover, a barrier of ca 18 kCal was estimated. NMR experiments allowed for establishing C-H connectivities for a part of the molecule. However, the earlier utilized level of theory was used again in order to accomplish NMR experiments allowed for establishing C-H connectivities for a part of the molecule. However, the earlier utilized level of theory was used again in order to accomplish the assignment (Table S2, Supplementary Materials). The experimentally identified 13 C CSs were used as reference points in order to choose an appropriate calculated set. C7a/C3a resonance CS, which was detected experimentally, strongly depends on the tautomer form (ca 110 ppm for A (C7a) and 150 ppm for B (C3a)) for a trustworthy assignment to bepossible.
The observed dependence of tautomers interconversion rates could probably be explained in terms of electrostatic repulsion. In the case of 1, the tautomer A became less favorable due to an additional chlorine atom on the side of N1, which shifted the equilibrium towards the B tautomer.
Additionally, the 1 H NMR spectra of both chlorobenzofuroxan 1 and aminobenzofuroxan 3, as well as its N-substituted analog 5, were recorded in various solvents ( Figures  S5-S23, Table S3, Supplementary Materials) and the ratio of the tautomers is given in the Table 1. As seen from the table, a strong preference for tautomer B existed in acetone and chloroform for the chloro derivative 1. In other solvents, signal broadening due to quick equilibrium was observed. In contrast with this, replacement of the chlorine atom by the amino group increased the amount of the second tautomer significantly and hindered tautomerization, so that signals of both tautomers were clearly distinguished in all solvents. This may be explained by the stabilization of tautomer A by the hydrogen bonding between the oxygen atom and amino group. Indeed, the quantum chemistry calculations indicated that in the case of compound 3, tautomer A was ca 1 kCal/mol lower in energy than tautomer B. The calculated tautomerization barrier was ca 23 kCal, which was considerably higher compared with chlorobenzofuroxan 1, and is in accordance with the experimental observations ( Figure S4, Supplementary Materials). Interestingly, in case of its N-butyl substituted analog, tautomer B again became lower in energy (ca 2.5 kCal/mol). This was presumably due to the steric hindrance caused by the n-Bu group, which overcame again in energy due to intramolecular hydrogen bonding. x FOR PEER REVIEW 6 of 11 the assignment (Table S2, Supplementary Materials). The experimentally identified 13 C CSs were used as reference points in order to choose an appropriate calculated set. C7a/C3a resonance CS, which was detected experimentally, strongly depends on the tautomer form (ca 110 ppm for A (C7a) and 150 ppm for B (C3a)) for a trustworthy assignment to bepossible. The observed dependence of tautomers interconversion rates could probably be explained in terms of electrostatic repulsion. In the case of 1, the tautomer A became less favorable due to an additional chlorine atom on the side of N1, which shifted the equilibrium towards the B tautomer.
Additionally, the 1 H NMR spectra of both chlorobenzofuroxan 1 and aminobenzofuroxan 3, as well as its N-substituted analog 5, were recorded in various solvents ( Figures  S5-S23, Table S3, Supplementary Materials) and the ratio of the tautomers is given in the Table 1. As seen from the table, a strong preference for tautomer B existed in acetone and chloroform for the chloro derivative 1. In other solvents, signal broadening due to quick equilibrium was observed. In contrast with this, replacement of the chlorine atom by the amino group increased the amount of the second tautomer significantly and hindered tautomerization, so that signals of both tautomers were clearly distinguished in all solvents. This may be explained by the stabilization of tautomer A by the hydrogen bonding between the oxygen atom and amino group. Indeed, the quantum chemistry calculations indicated that in the case of compound 3, tautomer A was ca 1 kCal/mol lower in energy than tautomer B. The calculated tautomerization barrier was ca 23 kCal, which was considerably higher compared with chlorobenzofuroxan 1, and is in accordance with the experimental observations ( Figure S4, Supplementary Materials). Interestingly, in case of its N-butyl substituted analog, tautomer B again became lower in energy (ca 2.5 kCal/mol). This was presumably due to the steric hindrance caused by the n-Bu group, which overcame again in energy due to intramolecular hydrogen bonding. a According to the 1 H NMR data, the spectra were recorded at 253K; b the spectra were recorded at 303K; n/o: tautomers not observed due to quick equilibrium.

Conclusions
In conclusion, we discovered that azidonitrobenzofuroxans react with 1,3-carbonyl compounds through the Regitz diazo transfer. This is in sharp contrast with both azidofuroxans and benzofuroxans, which undergo 1,3-dipolar cycloaddition or the Beirut reaction under the same conditions. This difference is presumably explained by the  (Table S2, Supplementary Materials). The experimentally identified 13 C CSs were used as reference points in order to choose an appropriate calculated set. C7a/C3a resonance CS, which was detected experimentally, strongly depends on the tautomer form (ca 110 ppm for A (C7a) and 150 ppm for B (C3a)) for a trustworthy assignment to bepossible. The observed dependence of tautomers interconversion rates could probably be explained in terms of electrostatic repulsion. In the case of 1, the tautomer A became less favorable due to an additional chlorine atom on the side of N1, which shifted the equilibrium towards the B tautomer.
Additionally, the 1 H NMR spectra of both chlorobenzofuroxan 1 and aminobenzofuroxan 3, as well as its N-substituted analog 5, were recorded in various solvents ( Figures  S5-S23, Table S3, Supplementary Materials) and the ratio of the tautomers is given in the Table 1. As seen from the table, a strong preference for tautomer B existed in acetone and chloroform for the chloro derivative 1. In other solvents, signal broadening due to quick equilibrium was observed. In contrast with this, replacement of the chlorine atom by the amino group increased the amount of the second tautomer significantly and hindered tautomerization, so that signals of both tautomers were clearly distinguished in all solvents. This may be explained by the stabilization of tautomer A by the hydrogen bonding between the oxygen atom and amino group. Indeed, the quantum chemistry calculations indicated that in the case of compound 3, tautomer A was ca 1 kCal/mol lower in energy than tautomer B. The calculated tautomerization barrier was ca 23 kCal, which was considerably higher compared with chlorobenzofuroxan 1, and is in accordance with the experimental observations ( Figure S4, Supplementary Materials). Interestingly, in case of its N-butyl substituted analog, tautomer B again became lower in energy (ca 2.5 kCal/mol). This was presumably due to the steric hindrance caused by the n-Bu group, which overcame again in energy due to intramolecular hydrogen bonding.

Conclusions
In conclusion, we discovered that azidonitrobenzofuroxans react with 1,3-carbonyl compounds through the Regitz diazo transfer. This is in sharp contrast with both azidofuroxans and benzofuroxans, which undergo 1,3-dipolar cycloaddition or the Beirut reaction under the same conditions. This difference is presumably explained by the x FOR PEER REVIEW 6 of 11 the assignment (Table S2, Supplementary Materials). The experimentally identified 13 C CSs were used as reference points in order to choose an appropriate calculated set. C7a/C3a resonance CS, which was detected experimentally, strongly depends on the tautomer form (ca 110 ppm for A (C7a) and 150 ppm for B (C3a)) for a trustworthy assignment to bepossible. The observed dependence of tautomers interconversion rates could probably be explained in terms of electrostatic repulsion. In the case of 1, the tautomer A became less favorable due to an additional chlorine atom on the side of N1, which shifted the equilibrium towards the B tautomer.
Additionally, the 1 H NMR spectra of both chlorobenzofuroxan 1 and aminobenzofuroxan 3, as well as its N-substituted analog 5, were recorded in various solvents ( Figures  S5-S23, Table S3, Supplementary Materials) and the ratio of the tautomers is given in the Table 1. As seen from the table, a strong preference for tautomer B existed in acetone and chloroform for the chloro derivative 1. In other solvents, signal broadening due to quick equilibrium was observed. In contrast with this, replacement of the chlorine atom by the amino group increased the amount of the second tautomer significantly and hindered tautomerization, so that signals of both tautomers were clearly distinguished in all solvents. This may be explained by the stabilization of tautomer A by the hydrogen bonding between the oxygen atom and amino group. Indeed, the quantum chemistry calculations indicated that in the case of compound 3, tautomer A was ca 1 kCal/mol lower in energy than tautomer B. The calculated tautomerization barrier was ca 23 kCal, which was considerably higher compared with chlorobenzofuroxan 1, and is in accordance with the experimental observations ( Figure S4, Supplementary Materials). Interestingly, in case of its N-butyl substituted analog, tautomer B again became lower in energy (ca 2.5 kCal/mol). This was presumably due to the steric hindrance caused by the n-Bu group, which overcame again in energy due to intramolecular hydrogen bonding. a According to the 1 H NMR data, the spectra were recorded at 253K; b the spectra were recorded at 303K; n/o: tautomers not observed due to quick equilibrium.

Conclusions
In conclusion, we discovered that azidonitrobenzofuroxans react with 1,3-carbonyl compounds through the Regitz diazo transfer. This is in sharp contrast with both azidofuroxans and benzofuroxans, which undergo 1,3-dipolar cycloaddition or the Beirut reaction under the same conditions. This difference is presumably explained by the a According to the 1 H NMR data, the spectra were recorded at 253 K; b the spectra were recorded at 303 K; n/o: tautomers not observed due to quick equilibrium.

Conclusions
In conclusion, we discovered that azidonitrobenzofuroxans react with 1,3-carbonyl compounds through the Regitz diazo transfer. This is in sharp contrast with both azidofuroxans and benzofuroxans, which undergo 1,3-dipolar cycloaddition or the Beirut reaction under the same conditions. This difference is presumably explained by the superelectrophilic nature of the azidonitrobenzofuroxan, which serves as an azido transfer agent rather than 1,3-dipole in this case.

Chemistry
The IR spectra were recorded as an emulsion in Vaseline oil (sample concentration 0.25%) on a Tensor 27 (Bruker GmbH, Germany) in the range 400-4000 cm −1 , which were the most intense absorption bands. Electron ionization (EI) mass spectra were obtained using gas chromatography−mass spectrometry with an Agilent 6890N-5973N (Agilent Technologies, Santa Clara, CA, USA) system at an electron ionization energy of 70 eV, and the temperature of the ion source was250 • C. Nuclear magnetic resonance (NMR) spectra were recorded on Bruker spectrometers AVANCEIII-500 (BrukerBioSpin, Rheinstetten, Germany) (500.1 MHz for 1 H, 125.8 MHz for 13 C) in different solvents at 303 K. Chemical shifts were measured in δ (ppm) with reference to the solvent (δ = 2.10 ppm and 30.5 ppm for (CD 3 ) 2 CO for 1 H and 13 C NMR, respectively). The pulse programs of the COSY, HSQC, and HMBC experiments were taken from the Bruker software library. Compound 3 obtained using Method 1 (see below) was used in all of the NMR experiments.
Elemental analysis was performed on a CHNS-O Elemental Analyser EuroEA3028-HT-OM (EuroVectorS.p.A., Milan, Italy) with an accuracy ±0.4% for C, H, and N. The melting points were determined in glass capillaries on a Stuart SMP 10 instrument (Keison Products, Chelmsford, UK). The progress of the reactions and the purity of the products were monitored usingTLC on Sorbfil UV-254 plates (Sorbpolimer, Krasnodar, Russia); the chromatograms were developed under UV light.

X-ray Crystallography Data
The data set for the single crystal 3A/3B obtained by Method 1 (see below) was collected on a Rigaku Synergy S instrument (Rigaku Oxford diffraction, Tokyo, Japan) with a HyPix detector and a PhotonJet microfocus X-ray tube using Cu Kα (1.54184 Å) radiation at a low temperature. Images were indexed and integrated using the CrysAlisPro data reduction package. Data were corrected for systematic errors and absorption using the ABSPACK module: numerical absorption correction based on Gaussian integration over a multifaceted crystal model and empirical absorption correction based on spherical harmonics according to the point group symmetry using equivalent reflections. The GRAL module was used for the analysis of the systematic absences and space group determination. The structure was solved withdirect methods using SHELXT [37], and was refined by the full-matrix least-squares on F2 using SHELXL [38]. Non-hydrogen atoms were refined anisotropically. The hydrogen atoms were inserted at the calculated positions and were refined as riding atoms. The figures were generated using the Mercury v4.1 [39] program. Crystals were obtained using the slow evaporation method.
CCDC number 2,099,880 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving. html, accessed on 28 July 2021 (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223-336-033; or deposit@ccdc.cam.uk).

Quantum-Chemical Computations
The GIAO DFT b3lyp/6-31+g(2d,p)//b3lyp/6-31+g(2d,p) basis set was used for geometry optimization and calculation of the NMR parameters, and b3lyp/6-31g(d)//b3lyp/ 6-31g(d) was used for the SCF energy calculation of thetransition states. Carbons with a chlorine substituent were excluded from the correlation analysis due to a known problem in the theoretical estimations of CS for nuclei of the 3d group of chemical elements [40]. All of the calculations were performed with the Gaussian 16 package [41]. All optimizations were followed by frequency calculations at the same level of theory in order to check that the optimized structures really corresponded to the true minima.