HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26520Generated: October 26, 2026
Sodium Sulfite → 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepin-11-one
https://huagongshe.com/reaction/26520
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepin-11-one | HCID 21323350 | — |
Reaction Steps
Under ice-cooling and stirring, 0.224 g of m-chloroperbenzoic acid was added to a solution of 0.243 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 4 ml of dichloromethane. The mixture was stirred for 30 minutes, after which 0.035 g of m-chloroperbenzoic acid was further added. After additional stirring for 1 hour, the reaction mixture was shaken well with an aqueous solution of sodium sulfite and a saturated aqueous solution of sodium hydrogen carbonate. The dichloromethane layer was washed with water and dried over Na2SO4. The solvent was evaporated off and the crystalline precipitate was recovered by filtration and washed with ethyl acetate. The above procedure gave 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepin-11-one as crystals. Recrystallization from chloroform-methanol yielded colorless needles, m.p. 208°-211° C.
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-861eaf04c4be4f87b7b525d31013af3e |
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| Source note | uspto-grants-1979_04 |
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