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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500570Generated: October 31, 2026

7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-3,4-dihydro-2H-isoquinolin-1-one → 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-3,4-dihydro-2H-isoquinolin-1-one hydrochloride

https://huagongshe.com/reaction/1500570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-3,4-dihydro-2H-isoquinolin-1-oneHCID 11978938—
ReactantEthanol hydrochlorideHCID 21887872—
Reactant7-(4-chlorobutoxy)-3,4-dihydro-2H-isoquinolin-1-oneHCID 66885683—
SolventEthyl AcetateHCID 8857—
Product7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-3,4-dihydro-2H-isoquinolin-1-one hydrochlorideHCID 66885207—

Reaction Steps

By a similar method as in Example 1, 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-3,4-dihydro-2H-isoquinolin-1-one was prepared from 7-(4-chlorobutoxy)-3,4-dihydro-2H-isoquinolin-1-one, and after it was made into an ethyl acetate solution, 1N hydrochloric acid ethanol solution was added thereto, precipitated crystals were separated by filtration, recrystallized from ethyl acetate and thereby 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-3,4-dihydro-2H-isoquinolin-1-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-48307d02275b4c8f8210a2f2563a09c5
Source noteuspto-grants-2015_12