HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyano-4-methylpyridine → 7-Chloro-2-(4-methyl-2-pyridyl)-4H-1,3-benzothiazine-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyano-4-methylpyridine | HCID 88739 | — |
| Reactant | 4-Chloro-2-sulfanylbenzoic acid | HCID 20456974 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 7-Chloro-2-(4-methyl-2-pyridyl)-4H-1,3-benzothiazine-4-one | HCID 59750318 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399759B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-d0f82fae872948b2939335fcaae87a27 |
| Source note | uspto-grants-2008_07 |