Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26501Generated: October 26, 2026

3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine → 11H-s-triazolo[3,4-b][3]benzazepine

https://huagongshe.com/reaction/26501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product11H-s-triazolo[3,4-b][3]benzazepineHCID 21223435—

Reaction Steps

To 1.15 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 20 ml of ethanol was added 6 ml of Raney nickel (wet) and the mixture was refluxed for 15 minutes under stirring. The Raney nickel was filtered off and the solvent was removed from the filtrate. To the residue was added water. By this procedure was obtained 11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from ethanol-n-hexane yielded colorless needles, m.p. 157°-158° C. The infrared absorption spectrum was identical with the spectrum of the same compound obtained by reacting 2-hydrazino-3-benzazepine with ortho-formic acid ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-0e51d84098784866b6379c338ba69455
Source noteuspto-grants-1979_04