1263407-24-4Relevant articles and documents
An improvement to the preparation of prasugrel hydrochloride
Ou, Wenhua,Yi, Weiyin,Liu, Feng,Pan, Xianhua,Peng, Xijiang
, p. 369 - 371 (2013/07/26)
An efficient synthesis of prasugrel, a thienopyridine ADP-receptor antagonists, is described. A thienopyridine intermediate was prepared by N-protection, boric acid substitution and N-substitution. After acid hydrolysis of the methyl ether and subsequent acetylation, prasugrel was obtained with a total yield of 50% after seven linear steps from 4,5,6,7-tetrahydrothieno [3,2-c]pyridine and 2-bromo-1-cyclopropyl-2-(2- fluorophenyl)ethan-1-one as raw materials.