Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431585Generated: October 27, 2026

Potassium Phosphate, Tribasic → 4-(3-Amino-5-morpholinopyridin-2-yl)benzonitrile

https://huagongshe.com/reaction/1431585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant4-Cyanophenylboronic acidHCID 2734326—
Reactant2-Chloro-5-morpholinopyridin-3-amineHCID 59631039—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-(3-Amino-5-morpholinopyridin-2-yl)benzonitrileHCID 59631436—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Chloro-5-morpholinopyridin-3-amine (0.25 g, 1.2 mmol), 4-cyanophenylboronic acid (0.21 g, 1.4 mmol), tricyclohexylphosphine (39.4 mg, 0.14 mmol), and tris(dibenzylideneacetone)dipalladium (0) (64.8 g, 0.07 mmol) were added to a flask then degassed and backfilled with argon. To the flask, 1,4-dioxane (3.0 mL) and aq. 1.3M potassium phosphate tribasic (2.7 mL, 3.5 mmol) were added by syringe. The resulting reaction was heated to 90° C. and monitored with TLC and LC-MS. After 19 h, the reaction was cooled to rt then poured into water. After extracting twice with EtOAc and twice with DCM, the combined organic extractions were dried over anhydrous magnesium sulfate. After filtration and concentration, the residue was purified on silica gel (0-30% of a premixed solution of 89:9:1 DCM:MeOH:ammonium hydroxide in DCM) to afford a light yellow solid as 4-(3-amino-5-morpholinopyridin-2-yl)benzonitrile. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.91 (5H, m), 6.67 (1H, d, J=2.4 Hz), 5.19 (2H, s), 3.82 (4H, m), 3.21 (4H, m). Mass Spectrum (pos.) m/e: 281.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-5e23f2f538ce4d8597229a17374e690b
Source noteuspto-grants-2015_01