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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079876Generated: October 30, 2026

Ethanol → HCID 18467278, compound

https://huagongshe.com/reaction/1079876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBenzoyl chlorideHCID 7412—
ReactantN-[2-[4-(6-fluoro1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimideHCID 18467209—
SolventDiethyl EtherHCID 3283—
ProductHCID 18467278HCID 18467278—

Reaction Conditions

Temperature175 °C

Reaction Steps

A mixture of 2-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]-1H-isoindol-1,3-(2H)-dione (6.0 g, 15 mmol) and benzoyl chloride (25 ml) was stirred at 175° C. under N2 for 2.0 hours. The reaction was cooled and diluted with anhydrous Et2O and the resultant hydrochloride salt was collected to yield 7.2 g. The compound was stirred in boiling absolute ethanol (300 ml) for 1 hour and then at ambient temperature overnight. The solid was collected and dried to afford 6.9 g. Recrystallization from MeOH gave 3.9 g of a light grey solid, m.p. 257°-260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580886
Source datasetuspto-grants-1996_12
ORD IDord-6b2232737d4f446395d2553445f61c08
Source noteuspto-grants-1996_12