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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910139Generated: October 25, 2026

Water → 2-(3-isoquinolin-3-yl-ureido)-1H-benzoimidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1910139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantIsoquinolin-3-AmineHCID 311869—
Reactantmethyl 2-amino-1H-benzo[d]imidazole-4-carboxylateHCID 24730367—
SolventDimethylformamideHCID 6228—
Product2-(3-isoquinolin-3-yl-ureido)-1H-benzoimidazole-4-carboxylic acid methyl esterHCID 66940371—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirring mixture of 1.0 g (5.2 mmol) of 2-amino-3H-benzoimidazole-4-carboxylic acid methyl ester (Intermediate A) and 0.86 g (5.2 mmol) of CDI in 3.0 mL of DMF was added 0.75 g (5.2 mmol) of Isoquinolin-3-ylamine. The reaction mixture was heated at 60° C. for 30 min, and then cooled to room temperature. 5.0 mL of water was added. The resulting solid was filtered washed with water (10 ml) and ether (10 mL), and dried to provide the 2-(3-isoquinolin-3-yl-ureido)-1H-benzoimidazole-4-carboxylic acid methyl ester as a solid which was hydrolyzed as described in general procedure B to provide 0.75 g (40%) of 2-(3-isoquinolin-3-yl-ureido)-1H-benzoimidazole-4-carboxylic acid. LCMS: 348 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598353B2
Source datasetuspto-grants-2013_12
ORD IDord-d1acc2a7670640099f4c19a9e43e2ac9
Source noteuspto-grants-2013_12