Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278584Generated: October 26, 2026

Diisopropylamine → 1-(4-Diisopropylaminomethylbenzoyl)-4-(2-naphthalenesulfonyl)piperazine

https://huagongshe.com/reaction/278584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Chloromethylbenzoyl)-4-(2-naphthalenesulfonyl)piperazineHCID 11059046—
SolventDimethylformamideHCID 6228—
Product1-(4-Diisopropylaminomethylbenzoyl)-4-(2-naphthalenesulfonyl)piperazineHCID 10951109—

Reaction Steps

A solution of 1-(4-chloromethylbenzoyl)-4-(2-naphthalenesulfonyl)piperazine (300 mg), potassium carbonate (200 mg) and diisopropylamine (4 ml) in DMF (6 ml) was stirred at 100° C. for 10 hours and concentrated. To the residue was added ethyl acetate, and the mixture was washed with water, and extracted with 1 N hydrochloric acid. The extract was made alkaline with sodium hydroxide solution and extracted with dichloromethane. The extract was dried and concentrated. The residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:2) to give the title compound (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359134B1
Source datasetuspto-grants-2002_03
ORD IDord-ea30e577eb3b4cd98b6b058a1effae5e
Source noteuspto-grants-2002_03