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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801645Generated: October 30, 2026

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

https://huagongshe.com/reaction/1801645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-chlorobutyl)-3,4-dihydroquinolin-2(1H)-oneHCID 20469712—
ReactantEthanol hydrochlorideHCID 21887872—
Reactant1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-oneHCID 66884891—
SolventEthanolHCID 702—
Product1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one hydrochlorideHCID 66884890—

Reaction Steps

By a similar method as in Example 1, 1-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-3,4-dihydro-1H-quinolin-2-one was prepared from 1-(4-chlorobutyl)-3,4-dihydro-1H-quinolin-2-one, and after it was made into an ethanol solution, 1N hydrochloric acid ethanol solution was added thereto, precipitated crystals were separated by filtration and thereby 1-[(4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl]-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 numberUS08349840B2
Source datasetuspto-grants-2013_01
ORD IDord-1149565dcf304e97834b0961f4d063b8
Source noteuspto-grants-2013_01