HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20267116, compound → HCID 54712694, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20267116 | HCID 20267116 | — |
| Reactant | methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide | HCID 54676532 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54712694 | HCID 54712694 | 87.6% |
Reaction Steps
A mixture of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (0.36 g) and 2-amino-5-methoxy-2,4,6-cycloheptatrien-1-one (0.20 g) in xylene (9 ml) was refluxed for 40 hours. The reaction mixture was cooled to room temperature. The crystals were collected by filtration and washed with xylene to give 4-hydroxy-N-(5-methoxy-1-oxo-2,4,6-cycloheptatrien-2-yl)-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (0.45 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540692 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-0e9c630e318a418ebde8a3f24a9b2402 |
| Source note | uspto-grants-1985_09 |