HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339736Generated: October 29, 2026
Water → 3-(1-Piperazinyl)-1,2-benzisothiazole
https://huagongshe.com/reaction/339736
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 3-Chloro-1,2-benzisothiazole | HCID 598190 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-(1-Piperazinyl)-1,2-benzisothiazole | HCID 2772144 | — |
Reaction Steps
A mixture of piperazine (10.2 g, 0.118 mmol) and 3-chloro-1,2-benzisothiazole (4.0 g, 0.024 mmol) in t-BuOH (4 mL) was refluxed overnight. The reaction mixture was poured into water (100 mL) and extracted with toluene (200 mL). The organic phase was dried over MgSO4 and evaporated until about 20 mL remained, under vacuum. The resulting suspension was cooled at 0-5° C. overnight. The precipitate was filtered and dried under vacuum to provide 3-(piperazin-1-yl)benzo[d]isothiazole as an intermediate (3.36 g, 15.4 mmol, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895558B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-92b7a1a8a3144fe488139969106a72ca |
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| Source note | uspto-grants-2014_11 |
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