Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736690Generated: October 25, 2026

4-Bromobenzaldehyde → 2-(4-bromophenyl)-1H-benzimidazole-4-carboxamide

https://huagongshe.com/reaction/736690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzaldehydeHCID 70741—
Reactant2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(4-bromophenyl)-1H-benzimidazole-4-carboxamideHCID 4454236517%

Reaction Steps

To a mixture of 2,3-diaminobenzamide dihydrochloride (synthesized as described in U.S. Pat. No. 6,737,421, column 11, EXAMPLE 2, step (e), 5 g, 22.3 mmol) and 4-bromobenzaldehyde (4.13 g, 22.3 mmol) in methanol (200 mL) was added 10% Pd/C (1.3 g). The mixture was refluxed overnight, then cooled and filtered though a pad of celite. The filtrate was concentrated under vacuum and purified by chromatography on a silica gel column with 0-10% methanol/dichloromethane to provide the title compound (1.2 g, 17%). MS (ESI) m/e 317 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595406B2
Source datasetuspto-grants-2009_09
ORD IDord-7130ff23e8874b5cb93e251389332c88
Source noteuspto-grants-2009_09