Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67544Generated: October 25, 2026

Water → 8-fluoro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo [1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/67544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantFlumazenilHCID 3373—
ReactantLithium borohydrideHCID 4148881—
ReactantHydrate;hydrochlorideHCID 21885828—
SolventTetrahydrofuranHCID 8028—
Product8-fluoro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo [1,5-a][1,4]benzodiazepin-6-oneHCID 20515340—

Reaction Conditions

Temperature40 °C

Reaction Steps

15.0 g (49.5 mmol) of ethyl 8-fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate are dissolved under argon in 450 ml of boiling absolute tetrahydrofuran (filtered over Alox) and added dropwise at 50° C. to a solution of 1.1 g (49.5 mmol) of lithium borohydride in 50 ml of absolute tetrahydrofuran. The mixture is stirred at 40° C. for 4 hours and at the boiling point for 2.5 hours. Subsequently, the mixture is decomposed at 40° C. with 20 ml of water and 20 ml of concentrated hydrochloric acid/water (1:1) and stirred at room temperature overnight. After removal of the tetrahydrofuran in vacuo, the residue is treated with 14 ml of concentrated ammonia. The mixture is left to crystallise in the cold and separated material is filtered off under suction and washed with water. After recrystallisation from ethanol, there is obtained 8-fluoro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[ 1,5-a][1,4]benzodiazepin-6-one of melting point 221°-223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346035
Source datasetuspto-grants-1982_08
ORD IDord-1b8f915592f24ebcb83f2f90a435e03d
Source noteuspto-grants-1982_08