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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27073Generated: October 26, 2026

Phenyl chloroformate → 2-(7-Chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-1-isoindolinone

https://huagongshe.com/reaction/27073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
Reactant2-(7-Chloro-1,8-naphthyridin-2-yl)-3-hydroxyisoindolin-1-oneHCID 19900408—
SolventPyridineHCID 1049—
Product2-(7-Chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-1-isoindolinoneHCID 2334363780.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

Phenyl chloroformate (126 g.) is added to a suspension of 2-(7-chloro-1,8-naphthyridin-2-yl)-3-hydroxy-isoindolin-1-one (86.5 g.) in pyridine (980 cc.), whilst keeping the temperature at about 25° C. The reaction mixture is stirred for 3 hours at a temperature of about 20° C. and then poured into ice-water (9,000 cc.). The product which crystallises is filtered off, washed with water (6×500 cc.) and then with acetonitrile (3×200 cc.). After drying, 2-(7-chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one (96.7 g.), which melts at 235° C. with decomposition, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220646
Source datasetuspto-grants-1980_09
ORD IDord-6572f0c54f304f6b8594fe20750711f6
Source noteuspto-grants-1980_09