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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748103Generated: October 30, 2026

2-Cyano-4-methylpyridine → 7-Chloro-2-(4-methyl-2-pyridyl)-4H-1,3-benzothiazine-4-one

https://huagongshe.com/reaction/748103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyano-4-methylpyridineHCID 88739—
Reactant4-Chloro-2-sulfanylbenzoic acidHCID 20456974—
SolventPyridineHCID 1049—
Product7-Chloro-2-(4-methyl-2-pyridyl)-4H-1,3-benzothiazine-4-oneHCID 5975031832%

Reaction Steps

A mixture of 4-chloro-2-mercaptobenzoic acid (3.0 g, 15.9 mmol), 2-cyano-4-methylpyridine (1.9 g, 16.0 mmol) and pyridine (15 ml) was refluxed for 9 hrs as described in Example 9. After cooling, the precipitated crystals were collected by filtration, subjected to a silica gel column chromatography, eluted with ethyl acetate-methanol (5:1, v/v) and recrystallized from chlorobenzene-hexane to give the titled compound (1.47 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399759B2
Source datasetuspto-grants-2008_07
ORD IDord-d0f82fae872948b2939335fcaae87a27
Source noteuspto-grants-2008_07