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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27081Generated: October 31, 2026

Water → 2-(5-Chloropyrid-2-yl)-3-(4-ethoxycarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one

https://huagongshe.com/reaction/27081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-Piperazinecarboxylic acid, ethyl ester, hydrochloride (1:1)HCID 90438—
Reactant2-(5-Chloropyrid-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-oneHCID 23343656—
SolventAcetonitrileHCID 6342—
Product2-(5-Chloropyrid-2-yl)-3-(4-ethoxycarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-oneHCID 13728649—

Reaction Conditions

Temperature20 °C

Reaction Steps

Triethylamine (3.03 g.) is added to a suspension of 2-(5-chloropyrid-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one (3.8 g.) and 1-ethoxycarbonylpiperazine hydrochloride (4.86 g.) in acetonitrile (50 cc.), and the mixture is stirred for 18 hours at a temperature of about 20° C. Water (100 cc.) is then added and the insoluble product is filtered off and washed with water (10 cc.). After drying, a product (4 g.) is obtained which, after recrystallisation from acetonitrile (30 cc.), gives 2-(5-chloropyrid-2-yl)-3-(4-ethoxycarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one (2.8 g.) melting at 160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220646
Source datasetuspto-grants-1980_09
ORD IDord-5f6592c6a4384358a914cfdad510b3b6
Source noteuspto-grants-1980_09