HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343590Generated: October 30, 2026
Piperazine → 3-(1-Piperazinyl)-1,2-benzisothiazole
https://huagongshe.com/reaction/343590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 3-Chloro-1,2-benzisothiazole | HCID 598190 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 3-(1-Piperazinyl)-1,2-benzisothiazole | HCID 2772144 | 47.3% |
Reaction Steps
304.2 g (3.53 mol) of piperazine, 7.5 g of chlorobenzene, 39.8 g (0.235 mol) of 3-chloro-1,2-benzisothiazole were placed in a four-neck 1000 ml flask equipped with a stirrer, a thermometer, a dropping funnel and a condenser, which was heated to stir at about 120° C. for 20 hours. After excess piperazine was removed with water, the reaction mixture was made acidic with hydrochloric acid, extracted into an aqueous layer, which was made alkaline with aqueous sodium hydroxide to obtain 24.4 g (m.p. 89° to 90 ° C.) of 3-(1-piperazinyl)-1,2-benzisothiazole as crystals. Yield from 3-chloro-1,2-benzisothiazole was 47.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861511 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-82f7375813bf4f68bd2f3e88e2354922 |
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| Source note | uspto-grants-1999_01 |
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