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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053143Generated: October 25, 2026

Phenylboronic Acid → (3-[(4-Chloro-biphenyl-3-carbonyl)-amino]-phenyl)-acetic acid ethyl ester

https://huagongshe.com/reaction/2053143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant[3-(5-Bromo-2-chlorobenzoylamino)phenyl]acetic acid ethyl esterHCID 59654675—
Product(3-[(4-Chloro-biphenyl-3-carbonyl)-amino]-phenyl)-acetic acid ethyl esterHCID 59654748—

Reaction Conditions

Temperature80 °C

Reaction Steps

[3-(5-Bromo-2-chloro-benzoylamino)-phenyl]-acetic acid ethyl ester (198 mg, 0.50 mmol) was coupled to phenylboronic acid using Method E, except that the reaction mixture was heated at 80° C. for 25 min. The crude product was purified by column chromatography using 20% EtOAc in heptane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326732B2
Source datasetuspto-grants-2008_02
ORD IDord-a58417df8caf4b50af8825d314ab4482
Source noteuspto-grants-2008_02