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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655338Generated: October 26, 2026

Triphenylphosphine → 5-methyl-3-{3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]benzyl}-3H-oxazolo[4,5-b]pyridin-2-one

https://huagongshe.com/reaction/655338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant5-Methyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 10012075—
Reactant{3-[5-(4-Methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanolHCID 59484860—
SolventDimethylformamideHCID 6228—
Product5-methyl-3-{3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]benzyl}-3H-oxazolo[4,5-b]pyridin-2-oneHCID 58486104—

Reaction Steps

67 mg (0.44 mmol) of 5-methyl-3H-oxazolo[4,5-b]pyridin-2-one and 125 mg (0.44 mmol) of {3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanol are suspended in 5 ml of DMF with 222 mg (0.67 mmol) of polymer-bound triphenylphosphine (about 3 mmol of triphenylphosphine per g), and the mixture is shaken at room temperature for 30 min. 156 mg (0.67 mmol) of di-tert-butyl azodicarboxylate are added. The reaction mixture is shaken at room temperature for 15 h. The reaction mixture is filtered, the residue is evaporated, and the residue is purified by column chromatography on silica gel, giving 67 mg of “A125”; HPLC: Rt=2.26 min (method B); ESI: 418 (M+H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071593B2
Source datasetuspto-grants-2011_12
ORD IDord-51384a395767447e990e66c19e294b6d
Source noteuspto-grants-2011_12