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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940761Generated: November 1, 2026

Methanol → 5,6-Dihydro-4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepine

https://huagongshe.com/reaction/1940761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant5,6-dihydro-4H-[1,2,4]-triazolo-[4,3-a][1,5]benzodiazepin-5-oneHCID 21837128—
SolventTetrahydrofuranHCID 8028—
Product5,6-Dihydro-4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepineHCID 21837004—

Reaction Steps

A mixture of 7.0 g of 5,6-dihydro-4H-[1,2,4]-triazolo-[4,3-a][1,5]benzodiazepin-5-one in 25 ml of tetrahydrofuran is added 9 ml of 10 M borane-dimethylsulfide in tetrahydrofuran. The mixture is refluxed for 6 hours, cooled to room temperature and 25 ml of methanol added dropwise. The volatiles are removed under vacuum and to the residue is added 100 ml of 2N sodium hydroxide. The mixture is refluxed for 5 hours, chilled and extracted with dichloromethane. The extract is washed with 2N citric acid, water and dried (Na2SO4). The solvent is removed under vacuum to give a solid. The solid is purified by chromatography on silica gel to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700796
Source datasetuspto-grants-1997_12
ORD IDord-ddf6466d269c43499b4f23306d4dcec7
Source noteuspto-grants-1997_12