HRID472394

反应详情

EQUATION

反应方程式

HRID 472394 的结构方程式

PROCEDURE

实验过程

N(8)-(2-Methanesulfonyl-phenyl)-N(2)-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-[1,2,4]triazolo[1,5-a]pyridine-2,8-diamine was prepared from (2-chloro-[1,2,4]triazolo[1,5-a]pyridin-8-yl)-(2-methanesulfonyl-phenyl)-amine (75.0 mg, 0.232 mmol) and 4-(2-pyrrolidin-1-yl-ethoxy)-phenylamine (58.0 mg, 0.281 mmol) (prepared as described in J. Med. Chem., 2006, 49, 4451-4454) with 2,2′-bis-dicyclohexylphosphanyl-biphenyl (25.0 mg, 0.0457 mmol) as the ligand in a manner analogous to Example 2d. Product isolated as a yellow foam (0.064 g, 56%). 1H NMR (400 MHz, CDCl3, δ, ppm): 8.46 (s, 1H), 8.11 (d, J=6.7 Hz, 1H), 7.98 (dd, J=7.9, 1.1 Hz, 1H), 7.57-7.50 (m, 2H), 7.48 (d, J=9.0 Hz, 2H), 7.28-7.24 (m, 1H), 7.14-7.09 (m, 1H), 6.93 (d, J=9.0 Hz, 2H), 6.79 (t, J=6.4 Hz, 1H), 6.68 (s, 1H), 4.10 (t, J=6.1 Hz, 2H), 3.14 (s, 3H), 2.90 (t, J=5.9 Hz, 2H), 2.68-2.58 (m, 4H), 1.86-1.76 (m, 4H). MS=493 (MH)+.