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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761513Generated: October 29, 2026

Dimethylformamide → HCID 178502018, compound

https://huagongshe.com/reaction/1761513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-MethylimidazoleHCID 12749—
ReactantHCID 178419604HCID 178419604—
SolventWaterHCID 962—
ProductHCID 178502018HCID 17850201834.2%

Reaction Steps

A mixture of 9.18 parts of methyl [5-[bromo(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]carbamate monohydrobromide, 12.3 parts of 2-methyl-1H-imidazole and 56.4 parts of N,N-dimethylformamide was stirred for 17 hours at room temperature. The reaction mixture was diluted with 300 parts of water. The precipitated product was filtered off and dissolved in dichloromethane. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane, methanol and methanol, saturated with ammonia, (90:5:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 27 parts of ethyl acetate. The product was filtered off, washed with 1,1'-oxybisethane and dried, yielding 2.6 parts (34.2%) of methyl [5-[(4-fluorophenyl)(2-methyl-1H-imidazol-1-yl)methyl]-1H-benzimidazol-2-yl]carbamate; mp. >300° C. (compound 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826862
Source datasetuspto-grants-1989_05
ORD IDord-0caadf18b61a4089954f0ab8e4567f4d
Source noteuspto-grants-1989_05