Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021976Generated: October 27, 2026

2,6-Diaminopyridine → 3-(6-Amino-pyridin-2-ylamino)-5-bromo-1-methyl-1H-pyridin-2-one

https://huagongshe.com/reaction/1021976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DiaminopyridineHCID 8861—
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant3,5-Dibromo-1-methylpyridin-2(1H)-oneHCID 3614350—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product3-(6-Amino-pyridin-2-ylamino)-5-bromo-1-methyl-1H-pyridin-2-oneHCID 5974061748.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

A 50-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 1,4-dioxane (20 mL), 3,5-dibromo-1-methylpyridin-2(1H)-one (1.06 g, 4.0 mmol), pyridine-2,6-diamine (872 mg, 8.0 mmol), Pd2(dba)3 (732 mg, 0.80 mmol), XantPhos (462.4 mg, 0.80 mmol), and cesium carbonate (2.6 g, 8.0 mmol). After three cycles of vacuum/argon flush, the mixture was heated at 110° C. for 1 h. After this time the reaction was cooled to room temperature. It was then filtered and the filtrate was evaporated in vacuo. The residue was purified by silica-gel column chromatography eluting with 20:1 ethyl acetate/methanol to afford 221a (570 mg, 48%) as a white solid. MS-ESI: [M+H]+ 295.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716274B2
Source datasetuspto-grants-2014_05
ORD IDord-f2cf39ad27f344c4b4e262d91f2472d0
Source noteuspto-grants-2014_05