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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409366Generated: October 28, 2026

Sodium Carbonate → {1-[3'-Hydroxy-5-(pyridin-4-ylcarbamoyl)-biphenyl-2-yl]-ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2409366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(3-hydroxyphenyl)boronic AcidHCID 2734359—
Reactant{1-[2-Bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67408319—
CatalystHCID 178418397HCID 178418397—
SolventDimethoxyethane ethanolHCID 20074477—
Product{1-[3'-Hydroxy-5-(pyridin-4-ylcarbamoyl)-biphenyl-2-yl]-ethyl}-carbamic acid tert-butyl esterHCID 68245743—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of {1-[2-bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester (2087 μmol) and 3-hydroxyphenylboronic acid (1.55 eq) in a mixture of DME/EtOH:1/1 (8 ml) were added Na2CO3 (4 eq) and Pd tetrakis (0.05 eq.). The reaction mixture was flushed with Ar and was heated in the microwave at 130° C. for 1.5 hours. The reaction mixture was cooled to RT, diluted with 1N NaHCO3 and extracted with EtOAc. The organic layer was extracted with 1N NaHCO3 and the combined aqueous layers were acidified with citric acid and 1N HCl. The aqueous layer was extracted with EtOAc, the organic layer was dried over MgSO4 and the solvent was removed under reduced pressure. The compound was purified by recrystallization from EtOAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815873B2
Source datasetuspto-grants-2014_08
ORD IDord-c8195834f72541f892c98e3806f9b93e
Source noteuspto-grants-2014_08