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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287556Generated: November 1, 2026

1-Hydroxybenzotriazole → 1,2-Dimethylbenzimidazole

https://huagongshe.com/reaction/2287556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-1,2-dimethyl-1H-benzimidazoleHCID 15462176—
Reactant3-[4-(Methylcarbamoyl)phenyl]prop-2-enoic acidHCID 53412022—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1,2-DimethylbenzimidazoleHCID 312693337.1%

Reaction Steps

To a mixture of 4-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-1,2-dimethyl-1H-benzimidazole (100 mg), 4-(methylcarbamoyl)cinnamic acid (55.4 mg) and dimethylformamide (1 ml) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (61.2 mg) and 1-hydroxybenzotriazole (49.7 mg), and the mixture was stirred for 3 hours at ambient temperature. To the mixture was added water, and the mixture was extracted with dichloromethane. The separated organic layer was washed with saturated sodium bicarbonate solution and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin layer chromatography (dichloromethane-methanol) to give 4-[2,6-dichloro-3-[N-methyl-N-[4-(methyl-carbamoyl)cinnamoylglycyl]amino]benzyloxy]]-1,2-dimethyl-1H-benzimidazole (121 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083961
Source datasetuspto-grants-2000_07
ORD IDord-9859af679dcd4eda823c0c64825cf3c1
Source noteuspto-grants-2000_07