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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607559Generated: November 1, 2026

Isopropenyl acetate → 4-Methyl-7-(2-oxopropyl)-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one

https://huagongshe.com/reaction/1607559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantMethoxytri-n-butylstannaneHCID 11964040—
Reactant7-Bromo-4-methyl-4H-pyrido[3,2-b][1,4]oxazin-3-oneHCID 15925984—
Catalystpalladium(II) acetateHCID 167845—
SolventBenzeneHCID 241—
Product4-Methyl-7-(2-oxopropyl)-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-oneHCID 15925985—

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Methyl-7-bromo-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one (3 g) (0.012 mole) in 80 ml of benzene is treated with 365 mg tri-o-tolylphosphine, 138 mg palladium acetate, 1.87 g (0.018 mole) of isopropenyl acetate and 5.9 g (0.18 mole) of tributyltin methoxide. The mixture is heated to 70° C. for 25 hours. The reaction mixture is then quenched with 20 ml sat. ammonium chloride and diluted with 50 ml ethyl acetate. The organic phase separates, dried over sodium sulfate and concentrated to dryness. The residue is dissolved in methylene chloride, washed with sat. KF solution, filtered through a cotton plug, dried over sodium sulfate and concentrated to dryness to obtain crude product. This is chromatographed using 200×60 mm SiO2,EtOAc (100%) as eluent. The desired product is identified by NMR and used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866074
Source datasetuspto-grants-1989_09
ORD IDord-24f915ae5032459f8d4bfa33df49624f
Source noteuspto-grants-1989_09