HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12538206, compound → HCID 54712701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12538206 | HCID 12538206 | — |
| Reactant | methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide | HCID 54676532 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54712701 | HCID 54712701 | 24.1% |
Reaction Steps
A solution of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (2.4 g) and 2-amino-4-methyl-2,4,6-cycloheptatrien-1-one (1.3 g) in xylene (50 ml) is refluxed for 7 hours. The reaction mixture is then allowed to stand at room temperature overnight. The resulting crystals (1.0 g) are collected by filtration and recrystallized from dioxane to give 4-hydroxy-2-methyl-N-(4-methyl-1-oxo-2,4,6-cycloheptatrien-2-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (0.8 g), m.p. 235°-242° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540692 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-1cc03cd0d9704892b4035548d4d9d5b9 |
| Source note | uspto-grants-1985_09 |