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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378193Generated: November 2, 2026

3,3-Dimethylpiperidine → HCID 22914495, compound

https://huagongshe.com/reaction/1378193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-DimethylpiperidineHCID 70942—
Reactant3-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 22914314—
SolventDimethylformamideHCID 6228—
ProductHCID 22914495HCID 2291449592.8%

Reaction Steps

1.15 g (3.5 mmol) of 3-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one were stirred at room temperature for 1 hour with 1 g (8.8 mmol) of 3,3-dimethylpiperidine and 10 ml of N,N-dimethylformamide. By evaporation of the reaction mixture and chromatography of the residue on silica gel while eluting with ethyl acetate/ethanol 9/1 there were obtained 1.32 g (92%) of 3-[5-(3,3-dimethylpiperidin-1-yl)methyl-1,2,4-oxadiazol-3-yl]-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one of m.p. 167°-168°, which was converted into the hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-1bdf515edb224ae1a5b8961a2faa0f56
Source noteuspto-grants-1997_09