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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523919Generated: October 30, 2026

2-Aminopyridine → (4-Benzyloxy-pyridin-2-yl)-pyridin-2-yl-amine

https://huagongshe.com/reaction/523919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant4-(Benzyloxy)-2-bromopyridineHCID 15389199—
ReactantHCID 178418922HCID 178418922—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product(4-Benzyloxy-pyridin-2-yl)-pyridin-2-yl-amineHCID 5854505573%

Reaction Steps

Compound I (2.325 mg, 8.80 mmol), 2-aminopyridine (911 mg, 9.68 mmol), tBuOK (1.481 g, 13.20 mmol), (±)-BINAP (219 mg, 0.35 mmol) and Pd2(dba)3 (201 mg, 0.22 mmol) were stirred in toluene (35 mL) at 90° C. under Ar(g) for 17 h. The reaction mixture was then diluted with CH2Cl2 (20 mL) and silica was added followed by the removal of the solvent under reduced pressure. The resulting dry loaded material was purified by silica gel column chromatography eluting with hexane/EtOAc (60:40 then 50:50) to furnish II as a yellow oil (1.773 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340503B2
Source datasetuspto-grants-2016_05
ORD IDord-26ba17396cc246e3af65201915259b2b
Source noteuspto-grants-2016_05