HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Meloxicam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Amino-5-methylthiazole | HCID 351770 | — |
| Reactant | 2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-phenyl-, 1,1-dioxide | HCID 54684780 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Meloxicam | HCID 54677470 | 24% |
Reaction Steps
1.0 gm (3 millimols) of 4-hydroxy-2-methyl-N-phenyl-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide were refluxed with 1.15 gm (10 millimols) of 2-amino-5-methyl-thiazole and 0.1 gm of p-toluenesulfonic acid in 250 ml of xylene for 72 hours. After cooling, the reaction mixture was washed with 2N hydrochloric acid and with water, dried and evaporated in vacuo. The residue was purified column-chromatographically (Merck-silica gel 60; particle size: 0.2-0.5 mm; eluant: chloroform/ethanol, 95:5), yielding 0.25 gm (24% of theory) of 4-hydroxy-2-methyl-N-(5-methy-2-thiazolyl)-2H-1,2-benzothiazine-3-caboxamide-1,1-dioxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04233299 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-f432adac9e5044f6adb1fdcf037a7279 |
| Source note | uspto-grants-1980_11 |