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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814456Generated: November 3, 2026

Ethyl isocyanate → HCID 22502549, compound

https://huagongshe.com/reaction/1814456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
Reactant1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinolineHCID 135719042—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22502549HCID 22502549—

Reaction Steps

1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinoline (333 mg) was dissolved in tetrahydrofuran (5 ml), ethyl isocyanate (800 ml) was added thereto, and then the mixture was stirred at room temperature for 3 hr. The reaction mixture was evaporated. The resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), and then recrystallized from ethyl acetate/hexane, to give the free compound of the title compound. The free compound was converted into a hydrochloride in a conventional manner, which was then recrystallized (from ethanol/isopropyl ether), to give the hydrochloride of the title compound as yellow crystals (313 mg, yield; 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-28216833a9004aa5bf2222fc9541a695
Source noteuspto-grants-2005_04