HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925224Generated: November 2, 2026
3-(1-Piperazinyl)-1,2-benzisothiazole → Ziprasidone
https://huagongshe.com/reaction/1925224
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(1-Piperazinyl)-1,2-benzisothiazole | HCID 2772144 | — |
| Reactant | HCID 10588416 | HCID 10588416 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ziprasidone | HCID 60854 | — |
Reaction Steps
To de-ionized water (1.5 Lit), was added 5-(2-bromoethyl)-6-chloro-oxindole (75 g) and 1-(1,2-benzisothiazol-3-yl)piperazine (132 g) at 30-35° C. The mixture was slowly heated under stirring to 98-100° C. over 60-80 minutes. The resultant mass was stirred for 4-5 hours at 98-100° C. After completion of reaction as monitored by HPLC, the suspended solid material was filtered at 98-100° C. The wet cake so obtained was suspended in de-ionized water (1.5 Lit) and heated to 90-95° C. and further maintained at this temperature for 30 minutes. The solid suspension was filtered at 90-95° C. The wet cake was further added to isopropyl alcohol (1.5 Lit) and the resultant mass was heated to reflux and maintained at reflux for 1 hour. The mass was further cooled to 30-35° C. and stirred for 2 hours at 30-35° C. The solids were filtered and washed with isopropyl alcohol (75 ml) and dried under vacuum at 50-55° C. for 7-8 hours till moisture content was not more than 1.0% w/w.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178674B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-ee123f7104a94b718f887157f63435ce |
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| Source note | uspto-grants-2012_05 |
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