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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440803Generated: October 26, 2026

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

https://huagongshe.com/reaction/1440803

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 numberUS05500435
Source datasetuspto-grants-1996_03
ORD IDord-6509b491760b4b74aebabb0e302e2966
Source noteuspto-grants-1996_03