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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431583Generated: October 27, 2026

Potassium Phosphate, Tribasic → 5'-Methoxy-5-morpholino-2,3'-bipyridin-3-amine

https://huagongshe.com/reaction/1431583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant5-Methoxypyridine-3-boronic AcidHCID 2763087—
Reactant2-Chloro-5-morpholinopyridin-3-amineHCID 59631039—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5'-Methoxy-5-morpholino-2,3'-bipyridin-3-amineHCID 59631309—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Chloro-5-morpholinopyridin-3-amine (0.26 g, 1.2 mmol), 5-methoxypyridin-3-ylboronic acid (0.24 g, 1.6 mmol), tricyclohexylphosphine (42.7 mg, 0.15 mmol), and tris(dibenzylideneacetone)dipalladium (0) (68.4 mg, 0.075 mmol) were added to a flask then degassed and backfilled with argon. To the flask, 1,4-dioxane (5.0 mL) and aq. 1.3M potassium phosphate tribasic (2.3 mL, 3 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 basic alumina (0-100% EtOAc in hexanes) to afford a brown solid as 5′-methoxy-5-morpholino-2,3′-bipyridin-3-amine. Mass Spectrum (pos.) m/e: 287.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-162e5d7f851049d29b3dbd3f52cc2f76
Source noteuspto-grants-2015_01