Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56652Generated: October 30, 2026

5-Chloro-2-cyanophenylboronic acid → tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]butanoate

https://huagongshe.com/reaction/56652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-cyanophenylboronic acidHCID 46738934—
Reactanttert-Butyl 2-(4-bromo-2-oxopyridin-1(2H)-yl)butanoateHCID 117622861—
CatalystHCID 178418397HCID 178418397—
Producttert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]butanoateHCID 117622863—

Reaction Steps

600 mg (purity 82%, 1.56 mmol) of tert-butyl 2-(4-bromo-2-oxopyridin-1(2H)-yl)butanoate (racemate) and 325 mg (1.8 mmol) of 5-chloro-2-cyanophenylboronic acid in the presence of tetrakis(triphenylphosphine)palladium(0) were reacted according to General Method 2A. Yield: 543 mg (purity 59%, 55% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434690B2
Source datasetuspto-grants-2016_09
ORD IDord-9a2de717170042578cf19f1175aeef13
Source noteuspto-grants-2016_09