HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12557655, compound → HCID 54712702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12557655 | HCID 12557655 | — |
| Reactant | methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide | HCID 54676532 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54712702 | HCID 54712702 | 34.1% |
Reaction Steps
A solution of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (1.5 g) and 2-amino-7-methoxy-2,4,6-cycloheptatrien-1-one (0.8 g) in xylene (25 ml) is refluxed for 6.5 hours. The reaction mixture is then allowed to stand at room temperature overnight. The crystals that have separated out are collected by filtration and recrystallized from dimethylformamide to give 4-hydroxy-2-methyl-N-(7-methoxy-1-oxo-2,4,6-cycloheptatrien-2-yl)-2H-1,2 -benzothiazine-3-carboxamide 1,1-dioxide (0.7 g), m.p. 243°-247° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540692 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-f54448515f25433e96db9b86b7a113c9 |
| Source note | uspto-grants-1985_09 |