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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585782Generated: November 1, 2026

Piperazine → 3-(1-Piperazinyl)-1,2-benzisothiazole

https://huagongshe.com/reaction/1585782

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 numberUS05939548
Source datasetuspto-grants-1999_08
ORD IDord-1b6d9aaea37f41cabbd16452011ff879
Source noteuspto-grants-1999_08