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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403666Generated: October 30, 2026

3-(2-Carboxyethyl)phenylboronic acid → 3-[2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(pyridin-4-ylcarbamoyl)-biphenyl-3-yl]-propionic acid

https://huagongshe.com/reaction/1403666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Carboxyethyl)phenylboronic acidHCID 3856118—
Reactant{1-[2-Bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67408319—
CatalystHCID 178418397HCID 178418397—
SolventDimethoxyethane ethanolHCID 20074477—
Product3-[2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(pyridin-4-ylcarbamoyl)-biphenyl-3-yl]-propionic acidHCID 67422360—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a solution of {1-[2-bromo-4-(pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester (3122 μmol) in a mixture of DME/EtOH/2N Na2CO3: 1/1/1 (20 ml) were added 3-carboxyethylphenylboronic 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-9477462d13dd46b28fd25ddc06e5751a
Source noteuspto-grants-2014_12