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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365306Generated: October 30, 2026

2-(1-Piperazinylmethyl)quinoline → HCID 15487637, compound

https://huagongshe.com/reaction/365306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1-Piperazinylmethyl)quinolineHCID 4375313—
Reactant5-(2-Chloroethoxy)-1,3-dihydro-3,3-dimethyl-2H-indol-2-oneHCID 13084687—
SolventChloroformHCID 6212—
ProductHCID 15487637HCID 1548763718.6%

Reaction Conditions

Temperature150 °C

Reaction Steps

5-(2-Chloroethoxy)-3,3-dimethyl-2,3-dihydroindol-2-one (182 mg, 3.0 mmol) and N--(2-quinolylmethyl)piperazine (690 mg, 3.0 mmol) were mixed, followed by stirring at 150° C. for 3 hours under an argon gas stream. The resulting mixture was allowed to cool down, and was then dissolved in chloroform. The thus-obtained solution was washed with water and then dried over anhydrous sodium sulfate. After the solution was concentrated under reduced pressure, the residue was purified by chromatography on a silica gel column while using chloroform-methanol (10:1) as an eluent. Fractions containing the target compound were collected and then concentrated under reduced pressure. The concentrate was crystallized from n-hexane and was then recrystallized from ethyl acetate-ethyl ether, whereby 240 mg of the title compound were obtained as pale yellow powder (yield: 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127360
Source datasetuspto-grants-2000_10
ORD IDord-76bf6ae4bfc84ee9875c60f7aa491d23
Source noteuspto-grants-2000_10