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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622656Generated: October 30, 2026

Sodium Carbonate → 4-(2-Amino-5-chloropyridin-3-yl)phenol

https://huagongshe.com/reaction/1622656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Bromo-5-chloropyridin-2-amineHCID 2763971—
Reactant4-(tert-Butyldimethylsilyloxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 11107815—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(2-Amino-5-chloropyridin-3-yl)phenolHCID 66748004—
Product3-(4-{[Tert-butyl(dimethyl)silyl]oxy}phenyl)-5-chloropyridin-2-amineHCID 66748550—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of sodium carbonate (4.09 g), tetrakis(triphenylphosphine)palladium(0) (0.668 g), 4-(tert-butyldimethylsilyloxy)phenylboronic acid (6.32 g) and 3-bromo-5-chloropyridin-2-amine (4.00 g) in DME (100 ml) and water (20 mL) was stirred at 80° C. overnight. Silica gel was added and the mixture was concentrated in vacuo. The residue was purified by column chromatography (silica gel, eluted with EtOAc in hexane) to give 4-(2-amino-5-chloropyridin-3-yl)phenol (3.05 g) as a pale yellow solid and 3-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-5-chloropyridin-2-amine (1.55 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778934B2
Source datasetuspto-grants-2014_07
ORD IDord-523b41db07f645babf70e2fe2ff6b833
Source noteuspto-grants-2014_07