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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500563Generated: October 31, 2026

6-(3-Chloropropoxy)-3,4-dihydroquinolin-2(1H)-one → 6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3,4-dihydro-1H-quinolin-2-one hydrochloride

https://huagongshe.com/reaction/1500563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(3-Chloropropoxy)-3,4-dihydroquinolin-2(1H)-oneHCID 11042828—
Reactant6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3,4-dihydro-1H-quinolin-2-oneHCID 11978817—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
Product6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3,4-dihydro-1H-quinolin-2-one hydrochlorideHCID 66884601—

Reaction Steps

By a similar method as in Example 1, 6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3,4-dihydro-1H-quinolin-2-one was prepared from 6-(3-chloropropoxy)-3,4-dihydro-1H-quinolin-2-one, and after it was made into a methanol solution, 0.5N hydrochloric acid methanol solution was added thereto, precipitated crystals were separated by filtration, recrystallized from a mixed solvent of ethyl acetate-diethyl ether and thereby 6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3,4-dihydro-1H-quinolin-2-one hydrochloride was obtained in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206167B2
Source datasetuspto-grants-2015_12
ORD IDord-d92526a8e8c3417aa28ac00b89e91f1b
Source noteuspto-grants-2015_12