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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56724Generated: October 26, 2026

(5-Chloro-2-(trifluoromethoxy)phenyl)boronic acid → tert-Butyl 4-[(2-{4-[5-chloro-2-(trifluoromethoxy)phenyl]-5-cyano-2-oxopyridin-1(2H)-yl}propanoyl)amino]benzoate

https://huagongshe.com/reaction/56724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Chloro-2-(trifluoromethoxy)phenyl)boronic acidHCID 53216719—
Reactanttert-Butyl 4-{[2-(4-bromo-5-cyano-2-oxopyridin-1(2H)-yl)propanoyl]amino}benzoateHCID 117622561—
Producttert-Butyl 4-[(2-{4-[5-chloro-2-(trifluoromethoxy)phenyl]-5-cyano-2-oxopyridin-1(2H)-yl}propanoyl)amino]benzoateHCID 117622836—

Reaction Steps

127 mg (purity 70%, 0.2 mmol) of tert-butyl 4-{[2-(4-bromo-5-cyano-2-oxopyridin-1(2H)-yl)propanoyl]amino}benzoate (racemate) and 58 mg (0.24 mmol) of 5-chloro-2-trifluoromethoxyphenylboronic acid in the presence of [1,1-bis(diphenylphosphino)ferrocene]palladium(II) chloride/dichloromethane monoadduct were reacted according to General Method 2A. Yield: 107 mg (purity 94%, 89% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434690B2
Source datasetuspto-grants-2016_09
ORD IDord-2a4ed281d9ff4df8ad39de456ba650f6
Source noteuspto-grants-2016_09