Reacción #1183187

ord-27a9d8e2e98440bbaaa97e09defd4a7d

Ecuación de reacción

CCn1cc(C(O)(C(C)c2ccc(Br)cc2Cl)C(F)(F)F)ccc1=O
5-[2-(4-bromo-2-chloro-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-1-ethyl-1H-pyridin-2-one
CCn1cc(C(O)(C(C)c2ccc(Br)cc2Cl)C(F)(F)F)ccc1=O
5-[2-(4-Bromo-2-chloro-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-1-ethyl-1H-pyridin-2-one
COC(=O)c1ccc(B(O)O)cc1OC
3-methoxy-4-methoxycarbonylphenylboronic acid
CCn1cc(C(O)(C(C)c2ccc(-c3ccc(C(=O)OC)c(OC)c3)cc2Cl)C(F)(F)F)ccc1=O
title compound
CCn1cc(C(O)(C(C)c2ccc(-c3ccc(C(=O)OC)c(OC)c3)cc2Cl)C(F)(F)F)ccc1=O
3′-Chloro-4′-[2-(1-ethyl-6-oxo-1,6-dihydro-pyridin-3-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-3-methoxy-biphenyl-4-carboxylic acid methyl ester

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

In analogy to Example 150, step 2, 5-[2-(4-bromo-2-chloro-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-1-ethyl-1H-pyridin-2-one (Example 183, step 2) was reacted with 3-methoxy-4-methoxycarbonylphenylboronic acid to give the title compound as an off-white solid. MS (m/e)=524.2 [M+H+].

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08138189B2uspto-grants-2012_03