反应 #1005946

ord-12dec7615c6340958af75a8559742ac1

反应方程式

NCc1ccc(N2CCC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)cc1C(F)(F)F
1-{4-[3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]-2-(trifluoro-methyl)phenyl}methanamine
O=C(Cl)c1ccc(Cl)nc1
6-chloronicotinic acid chloride
ClCCl
methylene chloride
c1ccncc1
pyridine
O=C(Cc1ccc(Cl)nc1)NCc1ccc(N2CCC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)cc1C(F)(F)F
title compound
O=C(Cc1ccc(Cl)nc1)NCc1ccc(N2CCC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)cc1C(F)(F)F
6-chloro-N-{4-[3-(3,5-dichlorophenyl)-3-(trifluoro-methyl)-pyrrolidin-1-yl]-2-(trifluoromethyl)benzyl}pyridine-3-carboxyamide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The solvent was evaporated off under reduced pressure
  2. 2
    其他the residue was then purified by a column chromatography

实验过程

1-{4-[3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]-2-(trifluoro-methyl)phenyl}methanamine (0.1 g) and 6-chloronicotinic acid chloride (0.04 g) were dissolved in methylene chloride (5 mL), and then pyridine (0.03 g) was added thereto. The resulting mixture was stirred at room temperature for one hour. The solvent was evaporated off under reduced pressure, and the residue was then purified by a column chromatography to obtain the title compound (0.1 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09271499B2uspto-grants-2016_03