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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26508Generated: October 26, 2026

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

https://huagongshe.com/reaction/26508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2,11-dihydro-3H-s-triazolo[3,4-b][3]benzazepine-3-thioneHCID 13072423—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
Product3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—

Reaction Steps

To 3 ml of methanol was added 0.215 g of 2,11-dihydro-3H-s-triazolo[3,4-b][3]benzazepine-3-thione and, under stirring, 0.6 ml of 2N-sodium methoxide/methanol was added. Then, 0.07 ml of methyl iodide was added dropwise. After 20 minutes, the reaction mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over Na2SO4. The solvent was then evaporated off and the residue was treated with ether. In this manner, 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine were obtained as crystals. Recrystallization from methanol yielded colorless needles melting at 168°-169° C. This was identical with the products obtained in Examples 1 and 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-bab0281336fd44af883de71d8461ae1f
Source noteuspto-grants-1979_04