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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786911Generated: October 30, 2026

3-Methyl-4-((6-methylpyridin-3-yl)oxy)aniline → HCID 57597207, compound

https://huagongshe.com/reaction/1786911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-4-((6-methylpyridin-3-yl)oxy)anilineHCID 11424434—
ReactantHCID 86084730HCID 86084730—
SolventIsopropanolHCID 3776—
SolventSodium BicarbonateHCID 516892—
ProductHCID 57597207HCID 5759720786.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of ethyl (4-chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)acetate (140 mg) in isopropyl alcohol (0.6 mL) was added 3-methyl-4-[(6-methylpyridin-3-yl)oxy]aniline (188 mg), and the mixture was stirred in an oil bath at a temperature of 110° C. for 2 hrs. The reaction mixture was allowed to cool to room temperature, diluted with 5% aqueous sodium hydrogen carbonate solution (20 mL) and extracted with ethyl acetate (25 mL×3). The organic layer washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (basic silica gel, eluent:ethyl acetate/methanol=10/0→9/1). The object fraction was concentrated under reduced pressure. Diisopropyl ether was added to the residue, and the resultant precipitate was collected by filtration and dried under reduced pressure to give the title compound (210 mg) as white powder crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-385d48fc52af48e984fd4154ad554256
Source noteuspto-grants-2009_03