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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545885Generated: October 29, 2026

6-Methoxy-3-pyridinylamine → HCID 59263506, compound

https://huagongshe.com/reaction/545885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium MethoxideHCID 10942334—
Reactant4'-bromo-1'-pentylspiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1'H)oneHCID 59263339—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 59263506HCID 5926350654%

Reaction Steps

To an oven-dried 2-neck 25 mL round bottom flask equipped with a condenser was charged with 4′-bromo-1′-pentylspiro-(6,7-dihydrofuro-[2,3-f][1,3]benzodioxole-7,3′-indole)-2′-(1′H)-one (50.5 mg, 0.12 mmol), 5-amino-2-methoxypyridine (22.3 mg, 0.18 mmol), Pd2(dba)3 (10 mole %), BINAP (10 mole %) and sodium methoxide (12.9 mg, 0.24 mmol). The flask was flushed with nitrogen for 5 min followed by the addition of degassed toluene (5.00 mL). The reaction mixture was heated at reflux for 16 h. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate (20.0 mL) and washed with saturated ammonium chloride (10.0 mL), brine (10.0 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness. The brown residue was subjected to column chromatography eluting with ethyl acetate-hexane (20% to 50%) to yield the title compound (30.0 mg) in 54% yield: MS (ES+), m/z 474.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935721B2
Source datasetuspto-grants-2011_05
ORD IDord-6819f924696f442180fc708505edbce3
Source noteuspto-grants-2011_05