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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619245Generated: November 1, 2026

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

https://huagongshe.com/reaction/1619245

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-cyclopropyl-piperazine (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 concentrated 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 numberUS08772285B2
Source datasetuspto-grants-2014_07
ORD IDord-3cc136eb8c884c6b9ef4577dc0b9be1b
Source noteuspto-grants-2014_07