Reacción #44831

ord-21faa14c17de4db8a6d3eec40b762b9a

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe product was isolated by preparative LCMS

Procedimiento

The title compound was prepared from 2-chlorobenzimidazole and 4,4′-dichlorobenzhydrylamine (prepared by Procedure B from 4,4′-dichlorobenzophenone) by Procedure A. The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 176-180° C.). MS(ES+) m/z 368 ([M+1]+, 100). 1NMR (DMSO-d6) δ6.19 (d, 1H), 6.82-6.90 (m, 2H), 7.10-7.16 (m, 2H), 7.40 (s, 8H), 7.69 (d, 1H), 10.6 (s, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07737167B2uspto-grants-2010_06