8 Sep 2021 News Brief introduction of 34552-13-1

Statistics shows that 34552-13-1 is playing an increasingly important role. we look forward to future research findings about 2-Chloro-5-methylpyridin-3-amine.

Electric Literature of 34552-13-1, 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.34552-13-1, name is 2-Chloro-5-methylpyridin-3-amine, molecular formula is C6H7ClN2, molecular weight is 142.59, as common compound, the synthetic route is as follows.

Step A: 2,6-Dichloro-5-methylpyridin-3-amine. NCS (32.9 g, 246 mmol) was added in portions to a solution of 2-chloro-5-methylpyridin-3-amine (35.0 g, 245 mmol) and acetonitrile (250 mL). The resulting mixture was heated at 35 C. for 16 hours before cooling to room temperature. The resulting suspension was filtered, and the filtrate concentrated to dryness under reduced pressure. The residue was purified by flash chromatography (eluent:petroleum ether/ethyl acetate; 1:0 to 4:1, gradient elution) to afford the title compound (45 g, 99%). MS (ESI): mass calcd. For C6H6Cl2N2 176.0 m/z found 176.8 [M+H]+. 1H NMR (400 MHz, DMSO-d6) delta 7.07 (s, 1H), 5.65 (br s, 2H), 2.53 (s, 3H).

Statistics shows that 34552-13-1 is playing an increasingly important role. we look forward to future research findings about 2-Chloro-5-methylpyridin-3-amine.

Reference:
Patent; Janssen Pharmaceutica NV; Barbay, J. Kent; Chai, Wenying; Hirst, Gavin C.; Kreutter, Kevin D.; Kummer, David A.; McClure, Kelly J.; Nishimura, Rachel T.; Shih, Amy Y.; Venable, Jennifer D.; Venkatesan, Hariharan; Wei, Jianmei; (501 pag.)US2020/55874; (2020); A1;,
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