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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975865Generated: October 25, 2026

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

https://huagongshe.com/reaction/975865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
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 boranedimethylsulfide 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 numberUS05610156
Source datasetuspto-grants-1997_03
ORD IDord-7d9917f11d534c95ba40f9ed0ad0c1dc
Source noteuspto-grants-1997_03