Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26523Generated: October 29, 2026

3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine → 3-methoxy-11H-s-triazolo[3,4-b][3]benzazepine

https://huagongshe.com/reaction/26523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapineHCID 21323525—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
Product3-methoxy-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323368—

Reaction Steps

To 0.522 g of 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazepine in 5 ml of methanol was added 3 ml of 2 N-sodium methoxide/methanol. The mixture was refluxed for 15 minutes and then the solvent was evaporated off. The residue was diluted with water and 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 isopropyl ether. By the above procedure was obtained 3-methoxy-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from ethyl acetate-n-hexane yielded colorless prisms, melting point: 160°-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-a9d49ac76bfe42409466037a002bccaa
Source noteuspto-grants-1979_04