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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903214Generated: November 2, 2026

Sodium hydride → HCID 3028230, compound

https://huagongshe.com/reaction/1903214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantCaptamine HydrochlorideHCID 25798—
Reactant2-Chloro-3-(propan-2-yl)quinolineHCID 13200203—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 3028230HCID 3028230—

Reaction Steps

2-Dimethylaminoethanethiol hydrochloride (3.4 g.) was added to a suspension of sodium hydride (2.32 g. of a 50% w/w dispersion in mineral oil) in dimethylformamide (25 ml.) at 0° to 5°. When all the hydrogen had evolved, 2-chloro-3-isopropylquinoline (4.0 g.) was added and the mixture heated at 80° for 5 hr. The reaction mixture was then poured into ice water (500 ml.) and extracted with ethyl acetate (3×120 ml.). The ethyl acetate extract was washed successively with water (100 ml.) and saturated brine (100 ml.) and then dried (MgSO4). The ethyl acetate solution was evaporated and the residual oil was chromatographed on basic alumina (70 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 residual oil was dissolved in diethyl ether, and ethereal hydrogen chloride was added until precipitation was complete. The solid residue was collected by filtration and crystallised from ethanol-diethyl ether to give 2-(2-dimethylaminoethylthio)-3-isopropylquinoline hydrochloride, m.p. 164°-7°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435405
Source datasetuspto-grants-1984_03
ORD IDord-650981ac49164f219e7c2ccb18a693dc
Source noteuspto-grants-1984_03