Реакция #2009328

ord-25b2c3e642614ff2aad6730fb1e15bc9

Уравнение реакции

Cc1c(Cc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)c(OC(F)F)nc2c(Cl)ccc(OCC(=O)OC(C)(C)C)c12
{8-chloro-2-difluoromethoxy-4-methyl-3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzyl]quinolin-5-yloxy}acetic acid tert-butyl ester
Clc1cc[nH]n1
3-chloro-1H-pyrazole
Cc1c(Cc2ccc(-n3ccc(Cl)n3)cc2)c(OC(F)F)nc2c(Cl)ccc(OCC(=O)OC(C)(C)C)c12
title compound
Cc1c(Cc2ccc(-n3ccc(Cl)n3)cc2)c(OC(F)F)nc2c(Cl)ccc(OCC(=O)OC(C)(C)C)c12
{8-chloro-3-[4-(3-chloropyrazol-1-yl)benzyl]-2-difluoromethoxy-4-methylquinolin-5-yloxy}acetic acid tert-butyl ester

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

The title compound was prepared by the method of Preparation 18a using {8-chloro-2-difluoromethoxy-4-methyl-3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzyl]quinolin-5-yloxy}acetic acid tert-butyl ester and 3-chloro-1H-pyrazole.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08173812B2uspto-grants-2012_05