N-(5-bromothiazolo[5,4-b]pyridin-2-yl)benzamide synthesis

Yield:1107694-72-3 76%

Reaction Conditions:

with sodium ethanolate in 1-methyl-pyrrolidin-2-one at 120; for 8 h;

Steps:

13.2

A solution of N-(6-bromo-2-chloropyridin-3-ylcarbamothioyl)benzamide (1.5 g, 4.0 mmol) and sodium ethoxide (0.54 g, 8.0 mmol) in l-methyl-2-pyrrolidinone (10 mL) was heated to 120 °C for 8 hours. After cooling the reaction mixture to room temperature the mixture was poured into water. The resulting solid was collected by filtration, then washed sequentially with water and diethyl ether. The filter cake was dried to give N-(5-bromothiazolo[5,4-b]pyridin-2-yl)benzamide (1.02 g, 76%). ¹H NMR (400 MHz, de-DMSO): 13.2 (br s, 1H), 8.16-8.10 (m, 3H), 7.72 (d, 1H), 7.70 (t, 1H), 7.59 (t, 2H). MS (EI) for C₁₃H₈BrN₃OS: 336 (MH⁺).

References:

WO2010/135524,2010,A1 Location in patent:Page/Page column 208