反应 #2195503

ord-4b746b76f9b94869b66e53419165a4e7

反应方程式

Cc1c(C(=O)O)nn(-c2ccc(Cl)cc2Cl)c1-c1ccc(Cl)cc1
5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid
Cl.NN1CCC(F)(F)CC1
product
Cl.NN1CCC(F)(F)CC1
4,4-Difluoropiperidin-1-amine hydrochloride
Cc1c(C(=O)NN2CCC(F)(F)CC2)nn(-c2ccc(Cl)cc2Cl)c1-c1ccc(Cl)cc1.Cl
title compound
Cc1c(C(=O)NN2CCC(F)(F)CC2)nn(-c2ccc(Cl)cc2Cl)c1-c1ccc(Cl)cc1.Cl
5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-N-(4,4-difluoropiperidin-1-yl)-4-methyl-1H-pyrazole-3-carboxamide hydrochloride

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Form the acid chloride from 3.6 mmol of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid and react it with 2.6 mmol of the product of Example 28 using the general procedure set forth in Example 39, to yield the title compound as a white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07514068B2uspto-grants-2009_04