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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
SolventDichloromethaneHCID 6344—
Product3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepin-11-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-861eaf04c4be4f87b7b525d31013af3e
Source noteuspto-grants-1979_04