HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide → HCID 178481148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide | HCID 54676532 | — |
| Reactant | HCID 178507571 | HCID 178507571 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178481148 | HCID 178481148 | 90.4% |
Reaction Steps
A mixture of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (2.95 g) and 2-amino-7-hydroxy-2,4,6-cycloheptatrien-1-one (1.5 g) in xylene (103 ml) was refluxed for 52 hours. The reaction mixture was cooled to room temperature. The crystals were collected by filtration and washed successively with N,N-dimethylformamide and chloroform to give 4-hydroxy-N-(7-hydroxy-1-oxo-2,4,6-cycloheptatrien-2-yl)-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (3.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540692 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-f88f88313e9d4841aeb4886ac77e1894 |
| Source note | uspto-grants-1985_09 |