HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723131Generated: November 2, 2026
Ethanimidic acid, ethyl ester, hydrochloride (1:1) → HCID 178503472, compound
https://huagongshe.com/reaction/1723131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanimidic acid, ethyl ester, hydrochloride (1:1) | HCID 2724290 | — |
| Reactant | HCID 20026602 | HCID 20026602 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178503472 | HCID 178503472 | 79.3% |
Reaction Steps
(a-6) A mixture of 5.6 parts of (+)-4-[[2-(methylthio)-1H-imidazol-1-yl]-phenylmethyl]-1,2-benzendiamine, 2.8 parts of ethyl ethanimidate hydrochloride and 60 parts of methanol was stirred first overnight at room temperature and then for 2 hours at reflux temperature. After cooling, the reaction mixture was evaporated. The residue was treated with alkaline water and the product was extracted three times with dichloromethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (96:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 3.2 parts (79.3%) of (+)-2-methyl-5-[[2-(methylthio)-1H-imidazol-1-yl]phenylmethyl]-1H-benzimidazole as a residue (int. 144).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859684 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-0bb3cf263ffc4c2d896ad89b466b61f0 |
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| Source note | uspto-grants-1989_08 |
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