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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944671Generated: October 30, 2026

Ammonium Chloride → 2-(4-Cyclopropylpiperazin-1-yl)benzothiazole-6-carbonitrile

https://huagongshe.com/reaction/1944671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-CyclopropylpiperazineHCID 4742004—
Reactant2-Chloro-1,3-benzothiazole-6-carbonitrileHCID 21985859—
Solvent1-ButanolHCID 263—
Product2-(4-Cyclopropylpiperazin-1-yl)benzothiazole-6-carbonitrileHCID 5958878943%

Reaction Steps

A suspension of 2-chlorobenzothiazole-6-carbonitrile (3.5 g, 18 mmol), 1-cyclopropylpiperazine (3.63 g, 28.8 mmol) and ammonium chloride (0.96 g, 18 mmol) in butan-1-ol (112 mL) was heated at reflux for 48 h. The solvent was removed under reduced pressure and the residue was diluted with water (30 mL). The mixture was made alkaline with potassium carbonate and extracted with CH2Cl2 (3×20 mL). The combined organic extracts were concenrated to give a residue which was purified by column chromatography on silica gel (20% ethyl acetate in petroleum ether) to give 2.2 g (43 5) of 2-(4-cyclopropylpiperazin-1-yl)benzothiazole-6-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394842B2
Source datasetuspto-grants-2013_03
ORD IDord-ba2688646505410394d5387b3ab02438
Source noteuspto-grants-2013_03