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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404147Generated: October 25, 2026

2-Aminopyridine → HCID 58545058, compound

https://huagongshe.com/reaction/404147

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 numberUS08748458B2
Source datasetuspto-grants-2014_06
ORD IDord-12d4c056b99b495e824f039e45e5457c
Source noteuspto-grants-2014_06