HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381194Generated: November 3, 2026
Triethylamine → m-Methoxycarbonyl-alpha-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide
https://huagongshe.com/reaction/1381194
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | methyl 3-[(chloroacetyl)amino]benzoate | HCID 2304955 | — |
| Reactant | 1-(3,4-Dimethoxybenzoyl)piperazine hydrochloride | HCID 17517625 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | m-Methoxycarbonyl-alpha-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide | HCID 13646256 | — |
Reaction Steps
5 Grams of methyl m-(α-chloroacetylamino)benzoate, 7.56 g of N-(3,4-dimethoxybenzoyl)piperazine monohydrochloride, 7.76 g of triethylamine and 30 ml of acetonitrile were mixed together and reacted at 45° to 50° C. for 5 hours. After completion of the reaction, the reaction mixture was ice-cooled, and the crystals formed were removed by filtration. The mother liquor was concentrated to dryness, and extracted by adding 1 N-sodium hydroxide aqueous solution and chloroform. The chloroform layer was washed with water, dried and removed by distillation. The oily substance obtained was purified by a silica gel column chromatography to obtain 10.08 g of m-methoxycarbonyl-α-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide in the form of colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04585774 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-02233a38139a4016aff92bdd247a9359 |
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| Source note | uspto-grants-1986_04 |
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