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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant3-Chloro-1,2-benzisothiazoleHCID 598190—
SolventChlorobenzeneHCID 7964—
Product3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 277214447.3%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861511
Source datasetuspto-grants-1999_01
ORD IDord-82f7375813bf4f68bd2f3e88e2354922
Source noteuspto-grants-1999_01