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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26511Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/26511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323409—

Reaction Steps

To 4.6 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 60 ml of tetrahydrofuran was added 2.4 g of paraformaldehyde together with 4.0 ml of a 40% solution of trimethylbenzylammonium hydroxide in methanol. After refluxing the mixture for 30 minutes, the solvent was evaporated off. The residue was diluted with water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over Na2SO4. The solvent was then evaporated off and the residual crystals were collected by filtration, washed with isopropyl alcohol and dried. The above procedure provided 11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from ethyl acetate yielded colorless needles melting at 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-22b338e3d06e4891a3d85666cc0ffccb
Source noteuspto-grants-1979_04