HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448096Generated: October 31, 2026
Ethanimidic acid, ethyl ester, hydrochloride (1:1) → HCID 20298797, compound
https://huagongshe.com/reaction/1448096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanimidic acid, ethyl ester, hydrochloride (1:1) | HCID 2724290 | — |
| Reactant | 4-{[4-(Diphenylmethyl)piperazin-1-yl]methyl}-N~1~-ethylbenzene-1,2-diamine | HCID 3017880 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 20298797 | HCID 20298797 | — |
Reaction Steps
A mixture of 4.8 parts of 4-[4-(diphenylmethyl)-1-piperazinylmethyl]-N1 -ethyl-1,2-benzenediamine and 25 parts of acetic acid is stirred at room temperature till all solid enters solution. Then there are added 1.73 parts of ethyl ethanimidate hydrochloride and stirring is continued first for one hour at room temperature and further for one hour at reflux. The reaction mixture is evaporated and the residue is stirred in water. The whole is alkalized with a sodium hydroxide solution and the product is extracted with dichloromethane. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone. The product is filtered off and dried, yielding 2.7 parts of 5-[4-(diphenylmethyl)-1-piperazinylmethyl]-1-ethyl-2-methyl-1H-benzimidazole; mp. 152.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179505 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-2f1dc05ced344bc7b7dd306e03ca6692 |
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| Source note | uspto-grants-1979_12 |
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