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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404152Generated: October 26, 2026

2-Aminopyridine → (5-Benzyloxy-pyridin-2-yl)-pyridin-2-yl-amine

https://huagongshe.com/reaction/404152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant5-(Benzyloxy)-2-bromopyridineHCID 16094696—
ReactantHCID 178418922HCID 178418922—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product(5-Benzyloxy-pyridin-2-yl)-pyridin-2-yl-amineHCID 8666014391.4%

Reaction Steps

Compound I (370 mg, 1.40 mmol), 2-aminopyridine (145 mg, 1.54 mmol), tBuOK (235 mg, 2.10 mmol), (±)-BINAP (35 mg, 0.01 mmol) and Pd2(dba)3 (32 mg, 0.006 mmol) were stirred in toluene (5 mL) at 90° C. under Ar(g) for 17 h. The reaction mixture was then diluted with CH2Cl2 (5 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 colourless oil (355 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748458B2
Source datasetuspto-grants-2014_06
ORD IDord-950f928aefd640b18761458fd45fa7d6
Source noteuspto-grants-2014_06