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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846783Generated: October 30, 2026

4-(4-Fluorobenzoyl)piperidine → HCID 15096985, compound

https://huagongshe.com/reaction/846783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
ReactantN-(2-Chloroethyl)-3-pyridinecarboxamideHCID 10535514—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 15096985HCID 1509698516.5%

Reaction Steps

To a stirred solution of 11.2 parts of (4-fluorophenyl) (4-piperidinyl)methanone in 80 parts of 4-methyl-2-pentanone were added 5 parts of N-(2-chloroethyl)-3-pyridinecarboxamide and the whole was stirred and refluxed overnight. The reaction mixture was filtered and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 4-methyl-2-pentanone and 2,2'-oxybispropane, yielding 1.6 parts (16.5%) of N-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-3-pyridinecarboxamide; mp. 118.3° C. (intermediate 114).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137896
Source datasetuspto-grants-1992_08
ORD IDord-28bf01667d6b41febae99bdff2429407
Source noteuspto-grants-1992_08