HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397596Generated: October 29, 2026
3-Amino-5-methylisoxazole → 1-{[5-(4-hydroxy-2H-1,2-benzothiazin-3-yl)-1,2,4-oxadiazol-3-yl]methyl}ethanone
https://huagongshe.com/reaction/2397596
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Amino-5-methylisoxazole | HCID 66172 | — |
| Reactant | 1,2-Benzisothiazole-2(3H)-acetamide, N-(5-methyl-3-isoxazolyl)-3-oxo-, 1,1-dioxide | HCID 2425592 | — |
| Reactant | Isoxicam | HCID 54677972 | — |
| Product | 1-{[5-(4-hydroxy-2H-1,2-benzothiazin-3-yl)-1,2,4-oxadiazol-3-yl]methyl}ethanone | HCID 135748576 | — |
Reaction Steps
A novel process for preparing 4-hydroxy-3-(5-methyl-3-isoxazolylcarbamoyl)-2-methyl-2H-1,2-benzothiazine 1,1-dioxide (I), starting with 3-amino-5-methylisoxazole (II) is disclosed. Compound I exhibits anti-inflammatory properties and is useful for treating inflammation. In the process of the invention an intermediate obtained, 2,3-dihydro-N-(5-methyl-3-isoxazolyl)-3-oxo-1,2-benzisothiazole-2-actamide 1,1-dioxide (IV) undergoes rearrangement to provide 1-{[5-(4-hydroxy-2H-1,2-benzothiazin-3-yl)-1,2,4-oxadiazol-3-yl]methyl}ethanone, S,S-dioxide (V), which is methylated, according to conventional procedures. The methylated intermediate VI, upon further treatment, undergoes a second rearrangement to obtain the desired anti-inflammatory compound I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04022796 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-3fc3b8d8200641638062677b92c0948f |
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| Source note | uspto-grants-1977_05 |
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