Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403665Generated: October 29, 2026

3-(Carboxymethyl)benzeneboronic acid → [2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(pyridin-4-ylcarbamoyl)-biphenyl-3-yl]-acetic acid

https://huagongshe.com/reaction/1403665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Carboxymethyl)benzeneboronic acidHCID 22480132—
Reactant{1-[2-Bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67408319—
CatalystHCID 178418397HCID 178418397—
SolventDimethoxyethane ethanolHCID 20074477—
Product[2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(pyridin-4-ylcarbamoyl)-biphenyl-3-yl]-acetic acidHCID 68245521—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a solution of {1-[2-bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]ethyl}-carbamic acid tert-butyl ester (1951 μmol) in a mixture of DME/EtOH/2N Na2CO3: 1/1/1 (10 ml) were added 3-carboxymethylphenylboronic acid (1.5 eq) and Pd tetrakis (0.05 eq). The reaction mixture was heated in the microwave at 160° C. for 15 minutes. The reaction mixture was cooled to RT, filtered over celite and washed with EtOAc and MeOH. The solvents were removed under reduced pressure. The compound was purified by column chromatography (silicagel, DCM/MeOH gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912209B2
Source datasetuspto-grants-2014_12
ORD IDord-7ff7fb8da371437fbade0991adf50876
Source noteuspto-grants-2014_12