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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456113Generated: October 28, 2026

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

https://huagongshe.com/reaction/1456113

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 10M borane-dimethylsulfide in tetrahydrofuran. The mixture is refluxed for 6 hours, cooled to room temperature and 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 numberUS05843944
Source datasetuspto-grants-1998_12
ORD IDord-c5116ab3939c4defb65d01ce07a18c3c
Source noteuspto-grants-1998_12