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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925222Generated: October 28, 2026

Ziprasidone Hydrochloride → Ziprasidone

https://huagongshe.com/reaction/1925222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantZiprasidone HydrochlorideHCID 219099—
Reactant3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 2772144—
Reactant5-(2-Chloroethyl)-6-chlorooxindoleHCID 10609474—
SolventSodium CarbonateHCID 10340—
ProductZiprasidoneHCID 60854—

Reaction Conditions

Temperature20 °C

Reaction Steps

U.S. Pat. No. 5,312,925 discloses a process for the preparation of ziprasidone hydrochloride, which involves heating to reflux a mixture of 5-(2-chloroethyl)-6-chloro-oxindole and 1-(1,2-benzisothiazol-3-yl)piperazine in aqueous sodium carbonate for 14 hours, followed by cooling to 20° C. and filtration. The wet product is re-slurried in isopropyl alcohol and filtered, washed with fresh isopropyl alcohol followed by drying under vacuum to get ziprasidone base. The base is then treated with aqueous hydrochloric acid in the presence of water at a temperature of about 60-65° C. for 3 to 24 hours, followed by filtration, washing with water and drying under vacuum to get ziprasidone hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178674B2
Source datasetuspto-grants-2012_05
ORD IDord-b3fe1195cc804f14a815670a0b6e0aac
Source noteuspto-grants-2012_05