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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16552Generated: October 28, 2026

2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-4-chlorobenzhydrylamine

https://huagongshe.com/reaction/16552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzimidazoleHCID 78572—
Reactant4-Chlorobenzhydrylamine hydrochlorideHCID 16219096—
ProductN-(Benzimidazol-2-yl)-4-chlorobenzhydrylamineHCID 11660016—

Reaction Steps

The title compound was prepared from 2-chlorobenzimidazole and 4-chlorobenzhydrylamine HCl by Procedure A. The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 180-184° C.). MS(ES+)m/z 334 ([M+1]+, 100). 1NMR (DMSO-d6) δ 6.18 (d, 1H), 6.80-6.90 (m, 2H), 7.08-7.14 (m, 2H), 7.20-7.40 (m, 9H), 7.66 (d, 1 H), 10.6 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737167B2
Source datasetuspto-grants-2010_06
ORD IDord-fb47033a3ca14588b0ba2abc8b5a6d00
Source noteuspto-grants-2010_06