Reaktion #45713

Reaktionsgleichung

Tributylstannyl-1-methylpyrrole

2,6-di-tert-butylcresol

2-chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile

→

7-Fluoro-5-methyl-2-(1-methyl-1H-pyrrol-2-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrile

Lösungsmittel

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturunder heat under nitrogen atmosphere for 3 hours
2. 2
   TemperaturAfter cooling
3. 3
   Sonstigethe reaction liquid
4. 4
   Filtrationwas filtered
5. 5
   Sonstigethe solvent of the filtrate was evaporate away under reduced pressure
6. 6
   Wascheneluted with a mixed solvent of n-hexane/ethyl acetate (9:1, v/v→5
7. 7
   Sonstige1, v/v) to obtain a main product
8. 8
   WaschenAfter washing with isopropyl ether
9. 9
   Filtrationthe entitled compound (50 mg, 22%) was collected by filtration as a pale yellow solid

Vorschrift

Tributylstannyl-1-methylpyrrole (389 mg, 1.05 mmol), bis(triphenylphosphine)palladium(II) dichloride (49 mg, 0.07 mmol), and a catalytic amount of 2,6-di-tert-butylcresol (2 mg) were added to a toluene (20 ml) solution of 2-chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile (I-130) (200 mg, 0.70 mol), followed by stirring under heat under nitrogen atmosphere for 3 hours. After cooling, the reaction liquid was filtered, and the solvent of the filtrate was evaporate away under reduced pressure. The resulting residue was subjected to silica gel column chromatography, and eluted with a mixed solvent of n-hexane/ethyl acetate (9:1, v/v→5:1, v/v) to obtain a main product. After washing with isopropyl ether, the entitled compound (50 mg, 22%) was collected by filtration as a pale yellow solid.

Quelle