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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378072Generated: November 2, 2026

Pyrrolidine → HCID 22914635, compound

https://huagongshe.com/reaction/1378072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantHCID 22914351HCID 22914351—
SolventDimethylformamideHCID 6228—
ProductHCID 22914635HCID 2291463582.1%

Reaction Steps

A suspension of 1.50 g (0.0043 mol) of 3-(5-chloromethyl-1,2,4-oxadiazol-3-yl) -8-fluoro-5-methyl-5,6-dihydro-4H-imidazo [1,5-a][1,4]benzodiazepin-6-one in 15 ml of dimethylformamide was treated with 1.5 g (0.022 mol) of pyrrolidine. After stirring at room temperature for 65 hrs. the yellow-orange solution obtained was freed completely from solvent. The residue was chromatographed over silica gel with dichloromethane/methanol 19:1 as the eluent. The product was recrystallized from methanol/ether. There were obtained 1.35 g (82%) of 8-fluoro-5-methyl-3-(5-pyrrolidin-1-ylmethyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one as white crystals; m.p. 158°-160°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-b93c299ab1db4c338dddeec13103a023
Source noteuspto-grants-1997_09