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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251135Generated: November 3, 2026

Ammonium Chloride → 1-(1-Ethylpiperazin-4-yl)-3-[(1-hydroxypropyl)thiazol-5-yl]isoquinoline dihydrochloride

https://huagongshe.com/reaction/1251135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(1-Ethylpiperazin-4-yl)-3-(2-formylthiazol-5-yl)isoquinolineHCID 22502491—
ReactantHCID 178420660HCID 178420660—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Ethylpiperazin-4-yl)-3-[(1-hydroxypropyl)thiazol-5-yl]isoquinoline dihydrochlorideHCID 22503441—

Reaction Steps

1-(1-Ethylpiperazin-4-yl)-3-(2-formylthiazol-5-yl)isoquinoline (205 mg) was dissolved in tetrahydrofuran (2 ml), 1M ethylmagnesium bromide/tetrahydrofuran solution (0.26 ml) was added thereto under ice-cooling. The resulting mixture was stirred overnight. An aqueous solution of saturated ammonium chloride was added to the reaction solution, which was then extracted with ethyl acetate. The resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (toluene/acetone system). The resulting product was converted into a hydrochloride in a conventional manner, and then solidified by adding ether thereto, to give the hydrochloride of the title compound as a brown amorphous (20 mg, yield; 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-e39fdfc5665940669006204d78adf4eb
Source noteuspto-grants-2002_01