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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantmethyl 3-[(chloroacetyl)amino]benzoateHCID 2304955—
Reactant1-(3,4-Dimethoxybenzoyl)piperazine hydrochlorideHCID 17517625—
SolventAcetonitrileHCID 6342—
Productm-Methoxycarbonyl-alpha-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585774
Source datasetuspto-grants-1986_04
ORD IDord-02233a38139a4016aff92bdd247a9359
Source noteuspto-grants-1986_04