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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270123Generated: October 26, 2026

5-amino-1-methyl-1H-imidazole-4-carbonitrile → 7-Methoxy-2-methoxymethylbenzofuran-4-carboxylic acid (5-cyano-3-methyl-3H-imidazol-4-yl)-amide

https://huagongshe.com/reaction/2270123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-amino-1-methyl-1H-imidazole-4-carbonitrileHCID 11051635—
Reactant7-Methoxy-2-methoxymethylbenzofuran-4-carboxylic acid 4-nitrophenyl esterHCID 69838008—
SolventWaterHCID 962—
Product7-Methoxy-2-methoxymethylbenzofuran-4-carboxylic acid (5-cyano-3-methyl-3H-imidazol-4-yl)-amideHCID 1029100174.8%

Reaction Steps

Prepared from 7-methoxy-2-methoxymethylbenzofuran-4-carboxylic acid 4-nitro-phenyl ester (250 mg) and 5-amino-1-methyl-1-H-imidazole-4-carbonitrile (171 mg). The reaction was stirrred for 1 hour and 40 minutes. Water (1 ml) was added and the solvent removed in vacuo. Purification by column chromatography on silica eluting with 10% methanol in dichloromethane afforded the title compound as a pale yellow solid (178 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331556B2
Source datasetuspto-grants-2001_12
ORD IDord-e86141202ea64ac1b453ce12c9b51f70
Source noteuspto-grants-2001_12