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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378192Generated: October 31, 2026

Dihexylamine → HCID 54093883, compound

https://huagongshe.com/reaction/1378192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDihexylamineHCID 8920—
Reactant(S)-8-chloro-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]-imidazo[1,5-a][1,4]benzodiazepin-9-oneHCID 53954665—
SolventDimethylformamideHCID 6228—
ProductHCID 54093883HCID 5409388356.5%

Reaction Steps

1.13 g (3 mmol) of (S)-8-chloro-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one were stirred at room temperature overnight with 1.7 g (9 mmol) of dihexylamine and 15 ml of N,N-dimethylformamide. By evaporation of the reaction mixture and chromatography of the residue on silica gel while eluting with ethyl acetate there was obtained 0.89 g (56%) of (S)-8-chloro-1-(5-dihexylaminomethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, which was converted into the hydrochloride (amorphous).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-0e10f4e1e71e42f5a574c35cd9bb6e72
Source noteuspto-grants-1997_09