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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844968Generated: October 31, 2026

Cyanogen Bromide → HCID 178497384, compound

https://huagongshe.com/reaction/1844968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant3,5-Diamino-2-methylbenzoic acidHCID 135524—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178497384HCID 178497384—

Reaction Steps

3.4 g (20.5 mmol) of methyl 3,4-diaminobenzoate was dissolved in a mixture of 50 mL of ethanol and 10 mL of H2O. To this stirring solution 2.6 g (24.5 mmol) of BrCN was added in one portion, and the resulting mixture was heated under reflux for 1.0 h. The reaction mixture was cooled to room temperature, concentrated to 10 mL, then washed with ethyl acetate (20 mL). The EtOAc layer was extracted with water (20 mL). The combined water extracts were neutralized with saturated NaHCO3 solution to ˜pH 8, and the resulting suspension was extracted with EtOAc (50 mL). The organic layer was washed with water and brine solution, dried with Na2SO4, and evaporated to give 2-amino-1H-benzoimidazole-5-carboxylic acid methyl ester, which was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946259B2
Source datasetuspto-grants-2015_02
ORD IDord-af66bb1bd2bb4979a3c5ae1706e48897
Source noteuspto-grants-2015_02