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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378032Generated: October 31, 2026

HCID 53739287, compound → HCID 54124626, compound

https://huagongshe.com/reaction/1378032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53739287HCID 53739287—
SolventEthanolHCID 702—
SolventMethylamineHCID 6329—
ProductHCID 54124626HCID 54124626—

Reaction Steps

9 g (19.9 mmol) of (S)-12,12a-dihydro-1-(3-phthalimidomethyl-1,2,4-oxadiazol-5-yl)-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one in 20 ml of ethanol and 65 ml of methylamine (33%) in ethanol were stirred at 70° for 2 hours. The solution was concentrated and the residue was triturated with 70 ml of methylene chloride. The suspension obtained was filtered. After drying the filter residue there was obtained (S)-1-(3-aminomethyl-1,2,4-oxadiazol-5-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, which was used without further crystallization as the starting material for the Example described hereinafter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-0969d485cf7f498989746bebd14f80b9
Source noteuspto-grants-1997_09