HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699446Generated: October 25, 2026
Potassium Iodide → 4-(1-Piperazinyl)isoquinoline
https://huagongshe.com/reaction/1699446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(5,6,7,8-Tetrahydronaphthalen-1-yl)piperazine | HCID 98698 | — |
| Reactant | 2-(3-Chloroprop-1-yl)-3,3-dimethyl-2,3-dihydro-1,2-benzoisothia-zole 1,1-dioxide | HCID 70162324 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(1-Piperazinyl)isoquinoline | HCID 11769830 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06346622B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-aee5bd8e029843db9cf1beeb61ee1bf1 |
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| Source note | uspto-grants-2002_02 |
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