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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16554Generated: October 28, 2026

2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-4,4'-difluorobenzhydrylamine

https://huagongshe.com/reaction/16554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzimidazoleHCID 78572—
Reactant4-Fluoro-alpha-(4-fluorophenyl)benzenemethanamineHCID 10955039—
ProductN-(Benzimidazol-2-yl)-4,4'-difluorobenzhydrylamineHCID 11624170—

Reaction Steps

The title compound was prepared from 2-chlorobenzimidazole and 4,4′-difluoro-benzhydrylamine (prepared by Procedure B from 4,4′-difluorobenzophenone) by Procedure A. The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 241-243° C.). MS(ES+) m/z 336 ([M+1]+, 100). 1NMR (DMSO-d6) δ 6.20 (d, 1H), 6.80-6.91 (m, 2H), 7.09-7.20 (m, 6H), 7.38-7.43 (m, 4H), 7.69 (d, 1H), 10.6 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737167B2
Source datasetuspto-grants-2010_06
ORD IDord-717e1b432dec4e4b906aaebcf91b3a05
Source noteuspto-grants-2010_06