Some scientific research about 1208170-17-5

At the same time, in my other blogs, there are other synthetic methods of this type of compound,1208170-17-5, 4-Chloro-6-methyl-2-(methylthio)pyrimidine-5-carbonitrile, and friends who are interested can also refer to it.

With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.1208170-17-5, name is 4-Chloro-6-methyl-2-(methylthio)pyrimidine-5-carbonitrile, molecular formula is C7H6ClN3S, molecular weight is 199.66, as common compound, the synthetic route is as follows.name: 4-Chloro-6-methyl-2-(methylthio)pyrimidine-5-carbonitrile

General procedure: A mixture of 3a,b (2.86 mmol), 4-methoxyaniline (0.36 g,2.88 mmol) and anhydrous K2CO3 (0.4 g, 5.76 mmol) inEtOH (15 ml) was heated under reflux for 5 h. It was thencooled, filtered and the filtrate was concentrated to half itsvolume. The obtained precipitate was filtered and crystallizedfrom EtOH-H2O (3:1 v/v).4-(4-Methoxyanilino)-6-methyl-2-(methylthio)-pyrimidine-5-carbonitrile (4a) Yield 71%; mp 158-160 C; IR v/cm-1:3300 (NH), 2214 (C?N), 1614 (C=N), 1604 (C=C-Ar),1293, 1134 (vas and vs C-O-C); 1H NMR (CDCl3, 60 MHz)delta/ppm: 7.49 (d, 2H, Ar-Hs, o- to NH-Ar, J = 12.6 Hz), 7.21(s, br, 1H, NH), 6.90 (d, 2H, Ar-Hs, o- to OCH3, J = 12.0Hz), 3.83 (s, 3H, OCH3), 2.58 (s, 3H, S-CH3), 2.50 (s, 3H,CH3); EIMS m/z 286 (M+., 100), 271 (33), 270 (25), 238(13); Anal. Calcd. for C14H14N4OS: (286.35): C, 58.72; H,4.93; N, 19.72. Found: C, 58.97; H, 4.98; N, 19.57.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,1208170-17-5, 4-Chloro-6-methyl-2-(methylthio)pyrimidine-5-carbonitrile, and friends who are interested can also refer to it.

Reference:
Article; Farghaly, Ahmed M.; AboulWafa, Omaima M.; Elshaier, Yaseen A. M.; Badawi, Waleed A.; Haridy, Haridy H.; Mubarak, Heba A. E.; Medicinal Chemistry Research; vol. 28; 3; (2019); p. 360 – 379;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia