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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061561Generated: November 1, 2026

2-(5-amino-1,3-dihydrobenzimidazol-2-ylidene)-1-(3,5-difluorophenyl)-3-phenylpropane-1,3-dione → 1-(3,5-difluorophenyl)-2-[5-(methylamino)-1,3-dihydrobenzimidazol-2-ylidene]-3-phenylpropane-1,3-dione

https://huagongshe.com/reaction/1061561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-amino-1,3-dihydrobenzimidazol-2-ylidene)-1-(3,5-difluorophenyl)-3-phenylpropane-1,3-dioneHCID 178507259—
ReactantHCID 178519450HCID 178519450—
SolventEthanolHCID 702—
Product1-(3,5-difluorophenyl)-2-[5-(methylamino)-1,3-dihydrobenzimidazol-2-ylidene]-3-phenylpropane-1,3-dioneHCID 17848206148%

Reaction Steps

To a solution of 2-(5-amino-1,3-dihydro-2H-benzimidazol-2-ylidene)-1-(3,5-difluorophenyl)-3-phenylpropane-1,3-dione (400 mg) and ethanol (10 ml) was added hydroxymethylbenzotriazole (168 mg) at room temperature, and the reaction solution was stirred at room temperature for 20 hours. The reaction solution was filtered and the resulting solid matter was dissolved in THF (10 ml). Thereto was added sodium borohydride (78 mg) at room temperature and the reaction mixture was stirred at room temperature for 3 hours. The reaction solution was diluted with ethyl acetate (10 ml) and the organic layer was washed with saturated sodium hydrogen carbonate aqueous solution, water and saturated sodium chloride aqueous solution. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The obtained residue was subjected to silica gel column chromatography and eluted with chloroform-methanol (100:1 (v/v)) to obtain 1-(3,5-difluorophenyl)-2-[5-methylamino-1,3-dihydro-2H-benzimidazol-2-ylidene]-3-phenylpropane-1,3-dione (163 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960591B2
Source datasetuspto-grants-2005_11
ORD IDord-02663d104f344714a6380dbc7d9c46a6
Source noteuspto-grants-2005_11