4,5,6-Trichloropyrimidine-2-carboxamide

: Reaction of 4,5,6-trichloropyrimidine-2-carbonitrile ( 1 ) with concentrated sulfuric acid at ca. 20 ◦ C gave 4,5,6-trichloropyrimidine-2-carboxamide ( 5 ) in 91% yield. The new compound was fully characterized by IR, MALDI-TOF, NMR and elemental analysis. Abstract: Reaction of 4,5,6-trichloropyrimidine-2-carbonitrile ( 1 ) with concentrated sulfuric acid at ca. 20 °C gave 4,5,6-trichloropyrimidine-2-carboxamide ( 5 ) in 91% yield. The new compound was fully characterized by IR, MALDI-TOF, NMR and elemental analysis.


Introduction
Pyrimidines are important aromatic N-heterocycles that exist in nature; for example, as components of pyrimidine nucleotides (cytosine, thymine and uracil) [1]. Pyrimidines are also frequently used in pharmaceuticals as they rank 10th in the most frequently used nitrogen heterocycles in U.S. FDA approved drugs [2]. Examples of pyrimidine drugs are the CNS depressant phenobarbital, the antibacterial trimethoprim, and the hyperthyroidism drug propylthiouracil (Figure 1). Additional pharmaceutical applications include uses as diuretics [3], anti-inflammatory [4], anti-malarial [5], and anti-tumor [6] agents. The chemistry of pyrimidines has been reviewed [7].

Introduction
Pyrimidines are important aromatic N-heterocycles that exist in nature; for example, as components of pyrimidine nucleotides (cytosine, thymine and uracil) [1]. Pyrimidines are also frequently used in pharmaceuticals as they rank 10th in the most frequently used nitrogen heterocycles in U.S. FDA approved drugs [2]. Examples of pyrimidine drugs are the CNS depressant phenobarbital, the antibacterial trimethoprim, and the hyperthyroidism drug propylthiouracil ( Figure 1). Additional pharmaceutical applications include uses as diuretics [3], anti-inflammatory [4], anti-malarial [5], and anti-tumor [6] agents. The chemistry of pyrimidines has been reviewed [7].

Scheme 1. Preparation of trichloropyrimidine 1 from TCNE and from tetrachlorothiadiazine 3.
We are interested in studying the use of trichloropyrimidine 1 as a synthetic scaffold as it offers multiple sites of reactivity towards heteroatom nucleophiles or organometallic reagents. To identify any potential side products from the chemistry of pyrimidine 1, we investigated its hydration to 4,5,6-trichloropyrimidine-2-carboxamide (5). Having frequently worked with cyano-substituted heterocycles, we often encountered the hydration products of the nitrile group [13]; therefore, we considered preparing, isolating, and characterizing this carboxamide worthwhile.
The reaction involved stirring a solution of trichloropyrimidine 1 in concentrated sulfuric acid for 6 h that, after workup, gave the desired compound with a 91% yield (Scheme 2). Product 5 was then isolated as colorless plates, melting point (mp) 162-164 °C (from chexane/DCE), while FTIR spectroscopy showed ν(N-H) stretches at 3402, 3291, 3219 and 3167 cm −1 , along with a C=O stretch at 1686 cm −1 , indicative of an amide (see Supplementary Material). Two diastereotopic protons in 1 H NMR (acetone-d6) were present as broad singlets, 8.04 and 7.32 ppm, assigned to the amide functionality, while 13 C NMR (acetone-d6) showed the presence of four quaternary carbon resonances at 161.9, 160.6, 155.8, and 131.1 ppm. Compared to the starting material 1, which had a C≡N resonance at 113.4 ppm, the new product 5 lacked this signal and displayed a new down-field signal at 160.6 ppm, which is typical for an amide C=O resonance supporting the hydration of the nitrile functionality. Finally, a correct elemental analysis (CHN) was obtained for the molecular formula C5H2Cl3N3O.
Pyrimidine 5 is potentially a useful synthetic scaffold and could be used instead of trichloropyrimidine 1 as it has one less leaving group that could lead to more regioselective substitution chemistry, while its higher melting point (162-164 °C vs. 62-63 °C for cyano 1 [10]) would make it more stable in storage.  We are interested in studying the use of trichloropyrimidine 1 as a synthetic scaffold as it offers multiple sites of reactivity towards heteroatom nucleophiles or organometallic reagents. To identify any potential side products from the chemistry of pyrimidine 1, we investigated its hydration to 4,5,6-trichloropyrimidine-2-carboxamide (5). Having frequently worked with cyano-substituted heterocycles, we often encountered the hydration products of the nitrile group [13]; therefore, we considered preparing, isolating, and characterizing this carboxamide worthwhile.
The reaction involved stirring a solution of trichloropyrimidine 1 in concentrated sulfuric acid for 6 h that, after workup, gave the desired compound with a 91% yield (Scheme 2). Product 5 was then isolated as colorless plates, melting point (mp) 162-164 • C (from c-hexane/DCE), while FTIR spectroscopy showed ν(N-H) stretches at 3402, 3291, 3219 and 3167 cm −1 , along with a C=O stretch at 1686 cm −1 , indicative of an amide (see Supplementary Material). Two diastereotopic protons in 1 H NMR (acetone-d 6 ) were present as broad singlets, 8.04 and 7.32 ppm, assigned to the amide functionality, while 13 C NMR (acetone-d 6 ) showed the presence of four quaternary carbon resonances at 161.9, 160.6, 155.8, and 131.1 ppm. Compared to the starting material 1, which had a C≡N resonance at 113.4 ppm, the new product 5 lacked this signal and displayed a new down-field signal at 160.6 ppm, which is typical for an amide C=O resonance supporting the hydration of the nitrile functionality. Finally, a correct elemental analysis (CHN) was obtained for the molecular formula C 5 H 2 Cl 3 N 3 O. We are interested in studying the use of trichloropyrimidine 1 as a synthetic scaffold as it offers multiple sites of reactivity towards heteroatom nucleophiles or organometallic reagents. To identify any potential side products from the chemistry of pyrimidine 1, we investigated its hydration to 4,5,6-trichloropyrimidine-2-carboxamide (5). Having frequently worked with cyano-substituted heterocycles, we often encountered the hydration products of the nitrile group [13]; therefore, we considered preparing, isolating, and characterizing this carboxamide worthwhile.
The reaction involved stirring a solution of trichloropyrimidine 1 in concentrated sulfuric acid for 6 h that, after workup, gave the desired compound with a 91% yield (Scheme 2). Product 5 was then isolated as colorless plates, melting point (mp) 162-164 °C (from chexane/DCE), while FTIR spectroscopy showed ν(N-H) stretches at 3402, 3291, 3219 and 3167 cm −1 , along with a C=O stretch at 1686 cm −1 , indicative of an amide (see Supplementary Material). Two diastereotopic protons in 1 H NMR (acetone-d6) were present as broad singlets, 8.04 and 7.32 ppm, assigned to the amide functionality, while 13 C NMR (acetone-d6) showed the presence of four quaternary carbon resonances at 161.9, 160.6, 155.8, and 131.1 ppm. Compared to the starting material 1, which had a C≡N resonance at 113.4 ppm, the new product 5 lacked this signal and displayed a new down-field signal at 160.6 ppm, which is typical for an amide C=O resonance supporting the hydration of the nitrile functionality. Finally, a correct elemental analysis (CHN) was obtained for the molecular formula C5H2Cl3N3O.
Pyrimidine 5 is potentially a useful synthetic scaffold and could be used instead of trichloropyrimidine 1 as it has one less leaving group that could lead to more regioselective substitution chemistry, while its higher melting point (162-164 °C vs. 62-63 °C for cyano 1 [10]) would make it more stable in storage. Pyrimidine 5 is potentially a useful synthetic scaffold and could be used instead of trichloropyrimidine 1 as it has one less leaving group that could lead to more regioselective substitution chemistry, while its higher melting point (162-164 • C vs. 62-63 • C for cyano 1 [10]) would make it more stable in storage.

Materials and Methods
The reaction mixture was monitored by thin layer chromatography (TLC) using commercial glass-backed TLC plates (Merck Kieselgel 60 F 254 ). The plates were observed under UV light at 254 and 365 nm. The melting point was determined using a PolyTherm-A, Wagner & Munz, Kofler hot-stage Microscope apparatus (Wagner & Munz, Munich, Germany). The solvent used for recrystallization is indicated after the melting point. The UV-vis spectrum was obtained using a Perkin-Elmer Lambda-25 UV/Vis spectrophotometer (Perkin-Elmer, Waltham, MA, USA); inflections are identified by the abbreviation "inf". The IR spectrum was recorded on a Shimadzu FTIR-NIR Prestige-21 spectrometer (Shimadzu, Kyoto, Japan) with a Pike Miracle Ge ATR accessory (Pike Miracle, Madison, WI, USA); strong, medium, and weak peaks are represented by s, m, and w, respectively. A Bruker Avance 500 machine (Bruker, Billerica, MA, USA) was used at 500 and 125 MHz to record the 1 H and 13 C NMR spectra, respectively. Deuterated solvents were used for the homonuclear lock; the signals are referenced to the deuterated solvent peaks. Attached proton test (APT) NMR studies were used for the assignment of the 13 C peaks as CH 3 , CH 2 , CH, and Cq (quaternary). The MALDI-TOF mass spectrum (+ve mode) was recorded on a Bruker Autoflex III Smartbeam instrument (Bruker). The elemental analysis was run by the London Metropolitan University Elemental Analysis Service. 4,5,6-Trichloropyrimidine-2carbonitrile (1) was prepared according to the literature procedure [9]. (5) To stirred concentrated sulfuric acid (2 mL) at ca. 20 • C was added 4,5,6-trichloropyrimidine-2-carbonitrile (1) (104 mg, 0.500 mmol), and the mixture was stirred at this temperature until complete consumption of the starting material (TLC, 6 h). The mixture was then poured into crushed ice and the mixture was then extracted with DCM (5 × 10 mL) and dried (Na 2 SO 4 ).