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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381198Generated: November 3, 2026

Hydrochloric Acid → o-Carbamoyl-alpha-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochloride monohydrate

https://huagongshe.com/reaction/1381198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantVeratroyl chlorideHCID 77070—
Reactanto-Carbamoyl-alpha-(1-piperazinyl)acetanilideHCID 13646249—
ReactantEthanol hydrochlorideHCID 21887872—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Producto-Carbamoyl-alpha-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochloride monohydrateHCID 23323531—

Reaction Steps

6.15 Grams of o-carbamoyl-α-(1-piperazinyl)acetanilide and 2.4 g of triethylamine were dissolved in 50 ml of methylene chloride, then to this solution was added dropwise a methylene chloride solution of 5.4 g of 3,4-dimethoxybenzoyl chloride under ice-cooled condition with stirring. The reaction was carried out at the same temperature for 1 hour, then the reaction mixture was washed with water, 5%-sodium bicarbonate aqueous solution, and an aqueous solution of potassium carbonate, then dried. Methylene chloride was removed by distillation, the residue was purified by a silica gel column chromatography, the product obtained was converted into a hydrochloride by adding hydrochloric acid-ethanol, then recrystallized from water-acetone to obtain 5.1 g of o-carbamoyl-α-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochloride monohydrate in the form of colorless needle-like crystals. Melting point: 122.0°-125.0° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585774
Source datasetuspto-grants-1986_04
ORD IDord-00d273adfece4b1690b591384941da89
Source noteuspto-grants-1986_04