HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12557673, compound → HCID 54712699, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12557673 | HCID 12557673 | — |
| Reactant | methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide | HCID 54676532 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54712699 | HCID 54712699 | 40.7% |
Reaction Steps
A mixture of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (1.5 g) and 2-amino-5-chloro-2,4,6-cycloheptatrien-1-one (0.87 g) in xylene (37 ml) was refluxed for 24 hours. The reaction mixture was cooled to room temperature. The crystals were collected by filtration and recrystallized from N,N-dimethylformamide to give N-(5-chloro-1-oxo-2,4,6-cycloheptatrien-2-yl)-4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (0.89 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540692 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-a83a937ca36c4318a448c7744e506a25 |
| Source note | uspto-grants-1985_09 |