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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378130Generated: November 2, 2026

HCID 54137505, compound → HCID 53735413, compound

https://huagongshe.com/reaction/1378130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54137505HCID 54137505—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 53735413HCID 5373541360%

Reaction Steps

1.8 g (4 mmol) of (S)-1-(3-diallylaminomethyl-1,2,4-oxadiazol-5-yl)-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepin-9-one were dissolved in 50 ml of methanol and hydrogenated at normal pressure and room temperature in the presence of 60 mg of 5% palladium-charcoal. The catalyst was separated and the solution was evaporated. By chromatography of the residue on silica gel while eluting with methylene chloride/methanol 19.5/0.5 there was obtained 1 g (60%) of (S)-1-(3-dipropylaminomethyl-1,2,4-oxadiazol-5-yl)-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepin-9-one, which was converted into the hydrochloride of m.p. 198°-201°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-d2ef968543044135b5c8b8845b11a0da
Source noteuspto-grants-1997_09