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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523903Generated: October 25, 2026

2-Aminopyridine → HCID 58545058, compound

https://huagongshe.com/reaction/523903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant2-Bromo-4-phenylpyridineHCID 104700—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 58545058HCID 5854505862.2%

Reaction Steps

2-Bromo-4-phenylpyridine (280 mg, 1.19 mmol), 2-aminopyridine (124 mg, 1.31 mmol), potassium tert-butoxide (201 mg, 1.79 mmol), (±)-BINAP (3 mg, 0.05 mmol) and Pd2(dba)3 (2.7 mg, 0.03 mmol) were stirred in toluene (2.5 mL) at 90° C. under Ar(g). After 17 h stirring, the reaction mixture was diluted with CH2Cl2 (2.5 mL) and silica was added. The solvent was removed under reduced pressure and the resulting dry loaded material purified by silica gel column chromatography, eluting with CH2Cl2/MeOH (100:2), to furnish I as a yellow solid (183 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340503B2
Source datasetuspto-grants-2016_05
ORD IDord-fdc5427ea8a34ef094ee382c86fbde1a
Source noteuspto-grants-2016_05