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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418906Generated: November 1, 2026

Diethylamine → HCID 21842266, compound

https://huagongshe.com/reaction/1418906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantHCID 21842258HCID 21842258—
ProductHCID 21842266HCID 2184226616%

Reaction Steps

125 ml of this crude solution of 8-fluoro-3-(5-iodomethyl-oxazol-2-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one were treated with 11.3 ml (0.109 mol) of diethylamine and stirred at room temperature for 20 hrs. The suspension obtained was completely freed from the solvents, the residue was partitioned between ethyl acetate and 1N aqueous hydrochloric acid and extracted. The aqueous-acidic phase was made basic and extracted with ethyl acetate. The organic phase was concentrated, the orange-brownish product was chromatographed over silica gel with ethyl acetate/methanol 17:3 as the eluent and recrystallized from hot ethyl acetate. There was obtained 0.75 g (16%) of 3-(5-diethylaminomethyloxazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one as light beige crystals; m.p. 182°-184°. A further 0.39 g of yellowish crystals was obtained from the mother liquor.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885986
Source datasetuspto-grants-1999_03
ORD IDord-5ba5950f47254d1bb692273af9912e0a
Source noteuspto-grants-1999_03