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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735207Generated: October 30, 2026

Methanol → 4,10-Dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine

https://huagongshe.com/reaction/1735207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Oxo-4,5-dihydropyrrolo[1,2-a]thieno[3,2-e][1,4]diazepineHCID 21837150—
SolventTetrahydrofuranHCID 8028—
Product4,10-Dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepineHCID 21836969—

Reaction Steps

To a suspension of 7.0 g of 5-oxo-4,5-dihydropyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine in 25 ml of anhydrous tetrahydrofuran is added 9 ml of 10M boranedimethylsulfide in tetrahydrofuran. The mixture is refluxed for 6 hours. The solution is cooled to room temperature and 25 ml of methanol added dropwise. The volatiles are removed under vacuum. To the residue is added 100 ml of 2N NaOH. The mixture is refluxed 5 hours and filtered. The solid is extracted with dichloromethane and the extract is washed with 2N citric acid, water and dried (Na2SO4). The solvent is removed to give a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536718
Source datasetuspto-grants-1996_07
ORD IDord-5bc6b2e9eb3649a69f222394e4eeefd6
Source noteuspto-grants-1996_07