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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206389Generated: November 3, 2026

Potassium di-tert-butyl phosphate → HCID 72550900, compound

https://huagongshe.com/reaction/2206389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium di-tert-butyl phosphateHCID 23674467—
ReactantHCID 72550899HCID 72550899—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 72550900HCID 7255090054.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of chiral 2-iodoethyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-3-methoxybenzoate (Example 11, 20 mg, 0.026 mmol) in dimethyl formamide (2 mL) was added potassium di-tert-butylphosphate (Accela ChemBio, 21.8 mg, 0.088 mmol). The reaction mixture was heated at 60° C. for 6 h. The mixture was diluted with ethyl acetate, washed with water and then brine, dried over anhydrous sodium sulfate and concentrated. The crude material was purified by flash chromatography to give chiral 2-(di-tert-butoxyphosphoryloxy)ethyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-3-methoxybenzoate (12 mg, 54% yield). MS (ES+) m/z calcd. for C41H50Cl2F2N3O8PNa: [(M+Na)+]: 874. found: 874.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371280B2
Source datasetuspto-grants-2016_06
ORD IDord-08a5ccafb5394e6ab1401295db3c988d
Source noteuspto-grants-2016_06