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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502207Generated: October 31, 2026

2-Methylindolizine → (5E)-4-methylidene-5-{(2E)-2-[(2-methylindolizin-3-yl)carbonyl]but-2-en-1-ylidene}-2-phenyl-4,5-dihydro-6H-1,3-oxazin-6-one

https://huagongshe.com/reaction/1502207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylindolizineHCID 582630—
Reactant(2E)-2-[(E)-(4-methylidene-6-oxo-2-phenyl-4H-1,3-oxazin-5(6H)-ylidene)methyl]but-2-enoyl chlorideHCID 117776641—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(5E)-4-methylidene-5-{(2E)-2-[(2-methylindolizin-3-yl)carbonyl]but-2-en-1-ylidene}-2-phenyl-4,5-dihydro-6H-1,3-oxazin-6-oneHCID 8965579569%

Reaction Steps

A solution of 2-methylindolizine (11.5 g; 87.7 mmol) in 35 mL of THF is added dropwise to a suspension of (2E)-2-[(E)-(4-methylidene-6-oxo-2-phenyl-4H-1,3-oxazin-5(6H)-ylidene)methyl]but-2-enoyl chloride (25 g; 87.7 mmol) in 140 mL of THF at 0° C. under nitrogen. After 18 h of stirring at ambient temperature, the reaction medium is diluted in ethyl acetate, and the solution is washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over sodium sulphate and concentrated to dryness. The residue obtained is purified by flash chromatography on silica (DCM) to give 22.75 g (69%) of a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206177B2
Source datasetuspto-grants-2015_12
ORD IDord-b98f1d3088e24120a923de8bddbca45f
Source noteuspto-grants-2015_12