HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248755Generated: October 25, 2026
1-(5-Isoquinolinylsulfonyl)piperazine → HCID 13116936, compound
https://huagongshe.com/reaction/1248755
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(5-Isoquinolinylsulfonyl)piperazine | HCID 3545 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13116936 | HCID 13116936 | 74.1% |
Reaction Steps
In 100 ml of ethanol were added 2.77 g of 1-(5-isoquinolinesulfonyl)piperazine, i.e., Compound (35), 1.66 g of anhydrous potassium carbonate and 5.45 g of ethyl bromide, and the reaction was carried out at an external temperature of 70° C. for 24 hours. After the reaction solution was filtered, the filtrate was condensed and the residue was dissolved in 50 ml of chloroform, and the solution was extracted twice with a 2N aqueous hydrochloric acid solution. The aqueous hydrochloric acid layer was rendered alkaline, extracted twice with 50 ml of chloroform, and the chloroform layer extracted was washed with water and dried with anhydrous magnesium sulfate. After the chloroform was distilled therefrom, the residue obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: 2% methanol-chloroform) to give 2.26 g of 1-(5-isoquinolinesulfonyl)-4-ethylpiperazine, i.e., Compound (42) in a yield of 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04525589 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-2257dfdddf1a41f7a102c66b0c1f0f49 |
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| Source note | uspto-grants-1985_06 |
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