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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737374Generated: November 1, 2026

Diallylamine → 3-(4-diallylaminomethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1737374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiallylamineHCID 31279—
Reactant3-(4-chloromethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 21842296—
SolventTetrahydrofuranHCID 8028—
Product3-(4-diallylaminomethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 2184223866%

Reaction Steps

A suspension of 1.0 g (0.00275 mol) of 3-(4-chloromethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one in 50 ml of tetrahydrofuran was treated wth 4.1 ml (0.033 mol) of diallylamine. After stirring at reflux for 18 hrs. the solution obtained was completely freed from the solvents. The residue was chromatographed over silica gel with dichloromethane/methanol 19:1 as the eluent and recrystallized from hot isopropyl ether. There was obtained 0.76 g (66%) of 3-(4-diallylaminomethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one as white crystals; m.p. 125-127°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962450
Source datasetuspto-grants-1999_10
ORD IDord-632ed42dba034b6ca368d4947c0c44ea
Source noteuspto-grants-1999_10