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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529218Generated: November 4, 2026

Potassium Phosphate, Tribasic → 4-[3-(6-Amino-pyridin-3-ylethynyl)-2-ethyl-pyridin-4-yl]-2-chloro-benzoic acid methyl ester

https://huagongshe.com/reaction/1529218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant3-Chloro-4-(methoxycarbonyl)benzeneboronic acidHCID 23005335—
Reactant5-(4-Chloro-2-ethyl-pyridin-3-ylethynyl)-pyridin-2-ylamineHCID 58235313—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-[3-(6-Amino-pyridin-3-ylethynyl)-2-ethyl-pyridin-4-yl]-2-chloro-benzoic acid methyl esterHCID 58235323—

Reaction Steps

The title compound is synthesized according to general procedure GP3 starting from 2.0 g (7.8 mmol) 5-(4-Chloro-2-ethyl-pyridin-3-ylethynyl)-pyridin-2-ylamine (A-30) using 2.5 g (11.6 mmol) 3-chloro-4-methoxycarbonylphenyl boronic acid, 335 mg (0.39 mmol) Pd2(dba)3, 555 mg (1.2 mmol) X-Phos and 2.7 g (11.6 mmol) K3PO4 in a mixture of 100 mL DME and 20 mL water. The reaction mixture is stiffed under reflux for 4 days. The DME is removed under reduced pressure and the aqueous is extracted with ethyl acetate. The organic phase is dried over Na2SO4, filtered and the solvent removed under vacuum. The product is purified by chromatography on silica gel using an DCM/MeOH-gradient. Yield: 0.59 g (19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090564B2
Source datasetuspto-grants-2015_07
ORD IDord-0876d95a32a5447b8d447ca84a74121c
Source noteuspto-grants-2015_07