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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476710Generated: October 25, 2026

Potassium Carbonate → Diisopropyl(((2-((2-methoxyphenyl)carbamoyl)-3-((4-nitro-phenyl)thio)phenyl)amino)methyl)phosphonate

https://huagongshe.com/reaction/1476710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropyl bromomethylphosphonateHCID 4366885—
Reactant2-amino-N-(2-methoxyphenyl)-6-(4-nitrophenyl-thio)benzamideHCID 71811587—
SolventAcetonitrileHCID 6342—
ProductDiisopropyl(((2-((2-methoxyphenyl)carbamoyl)-3-((4-nitro-phenyl)thio)phenyl)amino)methyl)phosphonateHCID 7181171841%

Reaction Conditions

Temperature60 °C

Reaction Steps

Compound 25 (1.0 equiv.) was dissolved in MeCN (40 mL) and treated with anhydrous potassium carbonate (2.0 equiv.) at room temperature. To this mixture diisopropyl(bromomethyl)phosphonate (1.2 equiv.) was added via a micro syringe. After being stirred for 4 Hours at 60° C., the reaction mixture was concentrated under reduced pressure. The crude residue was diluted by ethyl acetate (50 mL), and washed with water (2×10 mL). Then it was dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (1:4 v/v ethyl acetate/petroleum ether) to provide a yellow solid (235.2 mg, 41% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402819B2
Source datasetuspto-grants-2016_08
ORD IDord-88db3d8f35ff41cca758454c7100483a
Source noteuspto-grants-2016_08