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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26512Generated: October 26, 2026

m-Chloroperbenzoic acid → 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepine

https://huagongshe.com/reaction/26512

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
SolventDichloromethaneHCID 6344—
Product3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323529—

Reaction Steps

A solution of 4.6 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 100 ml of dichloromethane was stirred under ice-cooling and 5.2 g of m-chloroperbenzoic acid was added. The mixture was further stirred for 40 minutes, after which it was washed with a solution of sodium sulfite, a saturated solution of sodium hydrogen carbonate and water in the order mentioned, and followed by drying over Na2SO4. The solvent was then evaporated off and the crystalline residue was collected by filtration and washed with ethyl ether. The above procedure provided 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from methanol yielded colorless needles melting at 176°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-a31a8aea26db44ba9a6c67dae080060b
Source noteuspto-grants-1979_04