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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403671Generated: October 29, 2026

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

https://huagongshe.com/reaction/1403671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminophenylboronic acidHCID 92269—
Reactant{1-[2-Bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67407943—
CatalystHCID 178418397HCID 178418397—
SolventCitric AcidHCID 311—
SolventWaterHCID 962—
SolventDimethoxyethane ethanolHCID 20074477—
Product{1-[3'-Amino-5-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-2-yl]-ethyl}-carbamic acid tert-butyl esterHCID 67422654—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of {1-[2-bromo-4-(3-fluoro-pyridine-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester (1094 μmol) and 3-aminophenylboronic acid (2 eq) in a mixture of DME/ethanol/1N Na2CO3: 1/1/1 (10 ml) was added Pd tetrakis (0.05 eq). The reaction mixture was heated in the microwave at 130° C. for 1.5 hours. The reaction mixture was cooled to RT and diluted with water and citric acid and extracted with EtOAc. The combined organic layers were washed with water and brine. The organic layer was dried over MgSO4 and the solvent was 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-3a40cbd91e8641e2ac9b571f4eeeb15b
Source noteuspto-grants-2014_12