HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37216Generated: October 25, 2026
Ethanimidic acid, ethyl ester, hydrochloride (1:1) → HCID 178432147, compound
https://huagongshe.com/reaction/37216
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanimidic acid, ethyl ester, hydrochloride (1:1) | HCID 2724290 | — |
| Reactant | 4-[1-(1H-imidazol-1-yl)-2-methylpropyl]-1,2-benzenediamine | HCID 14518426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178432147 | HCID 178432147 | 44% |
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 convened 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420147 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-0ce4a9a0b859482abf544ddf922c98a5 |
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| Source note | uspto-grants-1995_05 |
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