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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461833Generated: November 1, 2026

Benzoyl chloride → HCID 19979516, compound

https://huagongshe.com/reaction/1461833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 14823474HCID 14823474—
SolventDiethyl EtherHCID 3283—
ProductHCID 19979516HCID 1997951655.8%

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 numberUS05077405
Source datasetuspto-grants-1991_12
ORD IDord-b75c2738cce34789865f1f6b1178ae46
Source noteuspto-grants-1991_12