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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828164Generated: November 1, 2026

Hydrazine → HCID 22063889, compound

https://huagongshe.com/reaction/1828164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHCID 22063859HCID 22063859—
SolventEthanolHCID 702—
ProductHCID 22063889HCID 2206388973.8%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a stirred, hot solution of 2-{2-[5-(1,3-Dimethyl-2-oxo-2,3-dihydro-1H-benzoimidazol-5-yl)-4-m-tolyl-imidazol-1-yl]-ethyl}-isoindole-1,3-dione (90 mg, 0.18 mmoles) in 5 mL ethanol was added aqueous 35 wt % hydrazine (50 pL). The resulting mixture was heated at reflux for 4 hours. The mixture (white precipitate visible) was cooled to 23° C. and concentrated in vacuo. The residue was taken up in 3 N HCl and methanol and extracted with ethyl acetate. The ethyl acetate extract was washed with 3 N HCl. The combined acidic aqueous layers were extracted with ethyl acetate (2 times). The acidic aqueous layer was made basic (pH 10–11) with Na2CO3 and extracted with ethyl acetate (3 times). These ethyl acetate extracts were combined and dried (Na2SO4), filtered, and the filtrate was concentrated to give 48 mg of 5-[3-(2-Amino-ethyl)-5-m-tolyl-3H-imidazol-4-yl]-1,3-dimethyl-1,3-dihydro-benzoimidazol-2-one as an off white film/solid. MS (APCI) m/z 362 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056918B2
Source datasetuspto-grants-2006_06
ORD IDord-a75ec27aa14346599965099ed5863ebe
Source noteuspto-grants-2006_06