Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944684Generated: October 31, 2026

3-Chloropropanesulphonyl chloride → 2-(4-Cyclopropylpiperazin-1-yl)-6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)benzothiazole

https://huagongshe.com/reaction/1944684

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-Cyclopropylpiperazin-1-yl)benzothiazol-6-ylamineHCID 59588804—
SolventDimethylformamideHCID 6228—
Product2-(4-Cyclopropylpiperazin-1-yl)-6-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)benzothiazoleHCID 23728969—

Reaction Steps

To a solution of 2-(4-cyclopropylpiperazin-1-yl)benzothiazol-6-ylamine (500 mg, 1.82 mmol) in DMF (10 mL) was added NaH (220 mg, 5.46 mmol) at 0° C. The mixture was allowed to warm to rt and then stirred for 30 min. A solution of 3-chloropropane-1-sulfonyl chloride (450 mg, 2.55 mmol) in DMF (2 mL) was added and the reaction mixture was stirred for 2 h. The resulting mixture was extracted with ethyl acetate (3×20 mL). The combined organic extracts were dried (Na2SO4) and concentrated under reduced pressure to give a residue which was purified by column chromatography on silica gel (elute: 2% dichloromethane in methanol). This afforded 217 mg (31%) of 2-(4-cyclopropylpiperazin-1-yl)-6-(1,1-dioxo-1λ6-isothiazolidin-2-yl)benzothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394842B2
Source datasetuspto-grants-2013_03
ORD IDord-c5709ec0db384e128554a653a3531937
Source noteuspto-grants-2013_03