Реакция #1715

ord-6d542e3dbdd248a898a4ea74dbd0c2eb

Уравнение реакции

CCCCN1CCC(CN)CC1
N-(1-butyl-4-piperidinyl)methylamine
Cc1nc2cc(Cl)cc(C(=O)O)c2o1
5-Chloro-2-methylbenzoxazole-7-carboxylic acid
O=C(Cl)C(=O)Cl
oxalyl chloride
CCCCN1CCC(CNC(=O)c2cc(Cl)cc3nc(C)oc23)CC1
title compound
CCCCN1CCC(CNC(=O)c2cc(Cl)cc3nc(C)oc23)CC1
N-[(1-Butyl-4-piperidinyl)methyl]5-chloro-2-methylbenzoxazole-7-carboxamide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

5-Chloro-2-methylbenzoxazole-7-carboxylic acid (Ger. Offen. 2,225,544) is converted to its acid chloride by treatment with oxalyl chloride. The acid chloride is treated with N-(1-butyl-4-piperidinyl)methylamine in the presence of triethylamine to afford the title compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726187uspto-grants-1998_03