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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699446Generated: October 25, 2026

Potassium Iodide → 4-(1-Piperazinyl)isoquinoline

https://huagongshe.com/reaction/1699446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantTriethylamineHCID 8471—
Reactant1-(5,6,7,8-Tetrahydronaphthalen-1-yl)piperazineHCID 98698—
Reactant2-(3-Chloroprop-1-yl)-3,3-dimethyl-2,3-dihydro-1,2-benzoisothia-zole 1,1-dioxideHCID 70162324—
SolventDimethylformamideHCID 6228—
Product4-(1-Piperazinyl)isoquinolineHCID 1176983043%

Reaction Conditions

Temperature100 °C

Reaction Steps

1.1 g (5.2 mmol) of 1-(5-tetralinyl)piperazine, 1.5 ml of triethylamine and a trace of potassium iodide were added to a solution of 1.64 g (6.0 mmol) of 2-(3-chloroprop-1-yl)-3,3-dimethyl-2,3-dihydro-1,2-benzoisothiazole 1,1-dioxide in 40 ml of DMF. The reaction mixture was stirred at 100° C. for four hours and then poured in ice-water, and the resulting precipitate was filtered off with suction. Purification took place by recrystallization from isopropanol to result in 1 g (43%) of the product (melting point 140° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346622B1
Source datasetuspto-grants-2002_02
ORD IDord-aee5bd8e029843db9cf1beeb61ee1bf1
Source noteuspto-grants-2002_02