HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26518Generated: October 26, 2026
Acetic Acid → 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine
https://huagongshe.com/reaction/26518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323406 | — |
| Product | 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine | HCID 21323525 | — |
Reaction Steps
To a solution of 0.23 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 2 ml of acetic acid was added 0.2 ml of concentrated sulfuric acid and 0.5 ml of 30% hydrogen peroxide was added dropwise under stirring. After 20 hours, a solution of sodium sulfite was added and the solvent was evaporated off. To the residue was added a saturated aqueous solution of sodium hydrogen carbonate and the mixture was extracted with chloroform. The chloroform layer was washed with water and dried over Na2SO4. The solvent was then evaporated off and the residue was treated with ethanol. By the above procedure was obtained 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine as crystals. m.p. 110°-111° C. Based on its infrared absorption spectrum and other data, this compound was identified with the compound obtained in Example 23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04150139 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-1eef57295dfd4dcdab4e36d92a195c96 |
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| Source note | uspto-grants-1979_04 |
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