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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423246Generated: November 1, 2026

Pyridine → HCID 178475153, compound

https://huagongshe.com/reaction/2423246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178514710HCID 178514710—
SolventDimethylformamideHCID 6228—
ProductHCID 178475153HCID 178475153—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 3-[3-(3,5-difluorophenyl)-2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-3-oxopropanoyl]benzenesulfonamide (hereinafter referred to as starting compound B, 500 mg), acetic anhydride (5 mL), pyridine (10 mL) and DMF (20 mL) was heated with stirring at 55° C. for 2 hours. The reaction mixture was concentrated under reduced pressure, diluted with ethyl acetate and washed with aqueous saturated sodium hydrogencarbonate solution and water successively. The solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform/methanol=10/1), and recrystallized from ethyl acetate/n-hexane to obtain N-({3-[3-(3,5-difluorophenyl)-2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-3-oxopropanoyl]phenyl}sulfonyl)acetamide (58 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960562B2
Source datasetuspto-grants-2011_06
ORD IDord-1efe7cf37d9143399b22e325f891ab6e
Source noteuspto-grants-2011_06