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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365303Generated: October 31, 2026

Thionyl Chloride → HCID 23291098, compound

https://huagongshe.com/reaction/365303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-(Quinolin-2-YL)acetic acidHCID 4711784—
SolventAcetoneHCID 180—
SolventChloroformHCID 6212—
ProductHCID 23291098HCID 23291098—

Reaction Steps

Thionyl chloride (6 ml) was added to a suspension of quinaldinic acid (3.463 g, 20 mmol) in chloroform (40 ml). After the resulting mixture was heated under reflux and stirring for 6 hours, the solvent was distilled off. The residue was dissolved in acetone (50 ml), followed by the addition of a solution of N-benzylpiperazine (10.576 g, 60 mmol) in acetone (50 ml). The thus-obtained mixture was stirred for 1 hour. A deposited precipitate was removed, and the solvent was distilled off. The residue was dissolved in ethyl ether. The resulting solution was washed with an aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was dissolved in methanol, followed by the addition of concentrated hydrochloric acid (5 ml) for acidification. The solvent was distilled off and the thus-obtained residue was crystallized from a mixed solvent of ethanol and methanol, whereby 7.166 g of the title compound were obtained as white powder (yield: 97.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127360
Source datasetuspto-grants-2000_10
ORD IDord-0debfc1f785f4189a107bae53f0f3f30
Source noteuspto-grants-2000_10