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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903229Generated: October 31, 2026

Sodium hydride → HCID 86739312, compound

https://huagongshe.com/reaction/1903229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(Chloromethyl)-1-methylpiperidine--hydrogen chloride (1/1)HCID 12644392—
Reactant3-Phenylquinolin-2-thioneHCID 13200206—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86739312HCID 86739312—

Reaction Steps

Sodium hydride (0.96 g. of a 50% w/w dispersion in mineral oil) was added to a solution of 3-phenylquinolin-2-thione (2.37 g.) in dimethylformamide (100 ml.) at ambient temperature. When all the hydrogen had evolved, 2-chloromethyl-1-methylpiperidine hydrochloride (1.84 g.) was added and the mixture was stirred at ambient temperature for 16 hr. The mixture was then poured into water (750 ml.) and extracted with ethyl acetate (2×150 ml.). The ethyl acetate extract was washed with water (2×50 ml.) and then dried (MgSO4). The solvent was evaporated and the residue was chromatographed on basic alumina (150 g. Brockmann Grade III), eluted with increasing concentrations of chloroform in petroleum ether. The eluate obtained with 20% v/v chloroform in petroleum ether was evaporated. The residue was dissolved in diethyl ether (50 ml.) and ethereal hydrogen chloride was added until precipitation was complete. The solid was collected by filtration and crystallised from ethanol-diethyl ether to give 2-[(1-methyl-2-piperidylmethylthio]-3-phenylquinoline hydrochloride, m.p. 198°-200°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435405
Source datasetuspto-grants-1984_03
ORD IDord-fe938d146f3044e8bcdf151173172381
Source noteuspto-grants-1984_03