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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381196Generated: October 27, 2026

Triethylamine → HCID 23323540, compound

https://huagongshe.com/reaction/1381196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl AnthranilateHCID 8635—
ReactantIsobutyl chloroformateHCID 62365—
Reactant[4-(4-Methoxybenzoyl)-1-piperazinyl]acetic acidHCID 20235785—
SolventDimethylformamideHCID 6228—
ProductHCID 23323540HCID 23323540—

Reaction Steps

2.5 Grams of [4-(4-methoxybenzoyl)-1-piperazinyl]acetic acid was dissolved in 30 ml of DMF, then 1.2 g of triethylamine was added thereto. Under an ice-cooled condition with stirring, 1.4 g of isobutyl chloroformate was added dropwise thereto and stirred for 30 minutes. Then, the reaction mixture was stirred at a room temperature, a DMF solution of 1.6 g of o-methoxycarbonylaniline was added dropwise to the reaction mixture and stirred for 6 hours. The reaction mixture obtained was concentrated to dryness, and the residue obtained was extracted with chloroform and 1 N-sodium hydroxide. The chloroform layer was washed with water, dried and then chloroform was removed by distillation. The residue obtained was crystallized by adding ethyl acetate, the crystals formed were collected by filtration. Recrystallized from ethanol to obtain 2.1 g of o-methoxycarbonyl-α-[4-(4-methoxybenzoyl)-1-piperazinyl]acetanilide in the form of colorless needle-like crystals. Melting point: 167.5°-169.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585774
Source datasetuspto-grants-1986_04
ORD IDord-2d34064b05f24288ae67ad4645622c16
Source noteuspto-grants-1986_04