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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975348Generated: October 26, 2026

Diisopropylethylamine → 1-(4-Chloroacetylaminobenzoyl)-4-[2-(4-chlorophenyl)ethyl]piperazine

https://huagongshe.com/reaction/1975348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[2-(4-Chlorophenyl)ethyl]piperazineHCID 12235714—
Reactant4-Chloroacetylaminobenzoic acid chlorideHCID 13305693—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chloroacetylaminobenzoyl)-4-[2-(4-chlorophenyl)ethyl]piperazineHCID 18946330—

Reaction Steps

2.34 g of 1-[2-(4-chlorophenyl)ethyl]piperazine and 1.57 g of Hunig base (=N-ethyldiisopropylamine) are introduced into 40 ml of tetrahydrofuran. 2.36 g of 4-chloroacetylaminobenzoic acid chloride [see J. Med. Chem. 28 (1985) 910] are added thereto in small portions. After 30 minutes at 40°, the solution is concentrated by evaporation. The residue is chromatographed over silica gel, and recrystallisation is carried out from acetone, yielding 1-(4-chloroacetylaminobenzoyl)-4-[2-(4-chlorophenyl)ethyl]piperazine having a melting point of 146°-147°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286728
Source datasetuspto-grants-1994_02
ORD IDord-f8283adfc9f047c78a33b75bc3011bc8
Source noteuspto-grants-1994_02