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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743049Generated: October 26, 2026

Ethanimidic acid, ethyl ester, hydrochloride (1:1) → HCID 178432147, compound

https://huagongshe.com/reaction/1743049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
Reactant4-[1-(1H-imidazol-1-yl)-2-methylpropyl]-1,2-benzenediamineHCID 14518426—
SolventEthanolHCID 702—
ProductHCID 178432147HCID 17843214744%

Reaction Steps

A mixture of 6.2 parts of 4-[1-(1H-imidazol- 1-yl)-2-methylpropyl]-1,2-benzenediamine, 6.5 parts of ethyl ethanimidate hydrochloride and 80 parts of ethanol was stirred for 3 hours at reflux temperature. After evaporation to dry, the residue was taken up in water and sodium carbonate. The product was extracted three times with 120 parts of trichloromethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in a mixture of 2-propanone and ethanol. The salt was filtered off and crystallized from a mixture of ethanol and 2-propanone. The product was filtered off and dried, yielding 4 parts (44%) of 5-[1-(1H-imidazol-1yl)-2-methylpropyl]-2-methyl-1H-benzimidazole dihydrochloride.monohydrate; mp. 214.8° C. (comp. 22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05342957
Source datasetuspto-grants-1994_08
ORD IDord-0b37ebf56ed44e989e82d9dd4109a216
Source noteuspto-grants-1994_08