HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Meloxicam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | O-Methyl Meloxicam | HCID 23331598 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Meloxicam | HCID 54677470 | — |
Reaction Steps
0.5 ml of 48% hydrobromic acid and 1 ml of glacial acetic acid were added to 0.2 gm (0.55 millimols) of 4-methoxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-caboxamide-1,1-dioxide. After standing for 24 hours, the reaction mixture was heated for two hours on a water bath and was subsequently evaporated in vacuo to dryness. The residue was dissolved in methylene chloride, and the solution was washed with water. After drying and evaporating of the organic phase, 4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide was obtained with a yield of 0.1 gm (52% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04233299 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-d7329cedddb3408a8e1d2fb81ea7303b |
| Source note | uspto-grants-1980_11 |