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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328288Generated: October 30, 2026

Pyridine → HCID 21444366, compound

https://huagongshe.com/reaction/328288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
Reactant4-Methylpiperazine-1-carbonyl chloride monohydrochlorideHCID 3016934—
Reactant2-(7-Chloro-1,8-naphthyridin-2-yl)-3-hydroxy-6-trifluoromethyl-1-isoindolinoneHCID 22754718—
SolventDichloromethaneHCID 6344—
ProductHCID 21444366HCID 2144436673.5%

Reaction Steps

Following the procedure of Example 28, but starting from 2-(7-chloro-1,8-naphthyridin-2-yl)-3-hydroxy-6-trifluoromethyl-1-isoindolinone (4.8 g.), 1-chlorocarbonyl-4-methyl-piperazine hydrochloride (15.1 g.), triethylamine (14.2 cc., equivalent to 10.2 g.) and pyridine (66 cc.) in methylene chloride (250 cc.), a crude product (7.8 g.) is obtained, which is triturated with water (50 cc.). The solid obtained is filtered off and washed with water (30 cc.). After recrystallisation from isopropanol (240 cc.), 2-(7-chloro1,8-naphthyridin-2-yl)-3-(4-methyl-piperazinyl)carbonyloxy-6-trifluoromethyl-1-isoindolinone (4.7 g.) melting at 219° C is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016274
Source datasetuspto-grants-1977_04
ORD IDord-02ca71111948424b80d514902a0b2243
Source noteuspto-grants-1977_04