Reacción #1939206

ord-53538d9e34484c9b8eacbe363c44205d

Ecuación de reacción

C[C@H](N)c1c(F)ccc(F)c1F.Cl
(S)-1-(2,3,6-trifluorophenyl)ethanamine hydrochloride
Cc1c(C)n(Cc2ccc(-c3ccccc3C(=O)OC(C)(C)C)cc2)c2ccc(C(=O)O)cc12
1-((2′-(tert-butoxycarbonyl)-[1,1′-biphenyl]-4-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid
→
Cc1c(C)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)c2ccc(C(=O)N[C@@H](C)c3c(F)ccc(F)c3F)cc12
title compound
Cc1c(C)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)c2ccc(C(=O)N[C@@H](C)c3c(F)ccc(F)c3F)cc12
(S)-4′-((2,3-dimethyl-5-((1-(2,3,6-trifluorophenyl)ethyl)carbamoyl)-1H-indol-1-yl)methyl)-[1,1′-biphenyl]-2-carboxylic acid

Reactantes

C[C@H](N)c1c(F)ccc(F)c1F.Cl
(S)-1-(2,3,6-trifluorophenyl)ethanamine hydrochloride
Cc1c(C)n(Cc2ccc(-c3ccccc3C(=O)OC(C)(C)C)cc2)c2ccc(C(=O)O)cc12
1-((2′-(tert-butoxycarbonyl)-[1,1′-biphenyl]-4-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

The title compound was prepared following the same general protocol as described in Step 8-9, Example 1, using the (S)-1-(2,3,6-trifluorophenyl)ethanamine hydrochloride and the 1-((2′-(tert-butoxycarbonyl)-[1,1′-biphenyl]-4-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid. ESI-MS (m/z): 557 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08957093B2uspto-grants-2015_02