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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844963Generated: October 26, 2026

Benzyl Bromide → 2-amino-1-benzyl-1H-benzoimidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1844963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactantmethyl 2-amino-1H-benzo[d]imidazole-4-carboxylateHCID 24730367—
SolventDimethyl SulfoxideHCID 679—
Product2-amino-1-benzyl-1H-benzoimidazole-4-carboxylic acid methyl esterHCID 6694032055%

Reaction Steps

To a solution of 0.1 g (0.52 mmol) of 2-amino-1H-benzoimidazole-4-carboxylic acid methyl ester (intermediate A) in DMSO (1 mL) was added 0.089 g (0.52 mmol) of benzyl bromide, the reaction mixture was stirred at room temperature for 3 h. The conversion was monitored by LCMS. After usual work up, the residue was purified by column chromatography eluting with DCM/methanol (v/v=10:1) to afford 0.08 g (55%) of 2-amino-1-benzyl-1H-benzoimidazole-4-carboxylic acid methyl ester. LCMS: 281 (M+1)+; 1H NMR (DMSO-d6, 400 MHz): δ 7.49 (dd, 1H), 7.29 (t, 2H), 7.25 (m, 2H), 7.16(m, 2H), 7.05 (bs, 2H), 6.85 (t, 1H), 5.28 (s, 2H), 3.79 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946259B2
Source datasetuspto-grants-2015_02
ORD IDord-35d29f11ad5d4d4daf296e8fd7e8748b
Source noteuspto-grants-2015_02