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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031521Generated: October 28, 2026

Benzoyl chloride → HCID 19979516, compound

https://huagongshe.com/reaction/1031521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 14823474HCID 14823474—
SolventDiethyl EtherHCID 3283—
ProductHCID 19979516HCID 19979516—

Reaction Steps

A mixture of 3-{4[4,4-bis(4-fluorophenyl)butyl]-1-piperazinyl}-6-fluoro-1H-indazole (3.7 g, 0.008 mol) of Example 36 and benzoyl chloride (18.2 g, 0.129 mol) was warmed on a steam bath under N2 for 2 hours. The reaction was cooled to room temperature and the only residue was diluted with ether. The product was isolated by vacuum filtration and the filter cake was washed well with ether affording 4.2 g of a solid. The product was recrystallized twice from ethanol to provide 2.7 g (50%) of 1-benzoyl-3-{4-[4,4-bis(4-fluorophenyl)butyl]-1-piperazinyl-6-fluoro-1H-indazole hydrochloride, mp 236°-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954503
Source datasetuspto-grants-1990_09
ORD IDord-1d720873a12e44b599e167e1fad02e21
Source noteuspto-grants-1990_09