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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244625Generated: November 2, 2026

1,3-Benzothiazole-6-carboxamide → Benzothiazole-6-carbonitrile

https://huagongshe.com/reaction/2244625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzothiazole-6-carboxamideHCID 43236343—
SolventPhosphorus oxychlorideHCID 24813—
ProductBenzothiazole-6-carbonitrileHCID 10607144—

Reaction Steps

A solution of 1,3-benzothiazole-6-carboxamide (1.96 g) in POCl3 (10 ml) was refluxed for 4 hours. The reaction solution was concentrated, and water was slowly added thereto at 0° C. It was extracted with EtOAc, and the organic layer was dried over anhydrous MgSO4, and then filtered, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=80:20 to 60:40) to obtain 1,3-benzothiazole-6-carbonitrile as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678820B2
Source datasetuspto-grants-2010_03
ORD IDord-b14312c2312c4a159b95755553149be9
Source noteuspto-grants-2010_03