Réaction #41923

ord-20c47747d4944f5c96f2dc4f1765c73b

Conditions de réaction

Température
145°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe tube was sealed
  2. 2
    TempératureAfter cooling
  3. 3
    Filtrationthe mixture was filtered
  4. 4
    Lavagewashed with methylene chloride (50 ml)
  5. 5
    LavageThe filtrate was washed with deionized water (3×50 ml)
  6. 6
    Séchagewith brine (50 ml), dried over magnesium sulfate
  7. 7
    Concentrationthen concentrated
  8. 8
    Autredried in vacuo
  9. 9
    AutreFlash column chromatography (Silica gel, 0-100% methylene chloride in hexane) gave a solid which
  10. 10
    Lavagewashed with diethyl ether
  11. 11
    Filtrationfiltered
  12. 12
    Autredried in vacuo

Mode opératoire

Ethyl 2-(4-hydroxy-6-iodo-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate (0.200 g, 0.46 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.048 g, 0.087 mmol), Copper cyamide (0.194 g, 2.2 mmol) and Tris(dibenzylideneacetone)dipalladium (0.020 g, 0.022 mmol) in 1,4-dioxane (2 ml) were combined in a 10 ml tube. Tetraethylammonium cyamide (0.085 g, 0.54 mmol) and 1,4-dioxane (1 ml) were added and the tube was sealed and heated to 145° C. for 15 min under Argon in a microwave (Personal Chemistry 300 W). After cooling, the mixture was filtered and washed with methylene chloride (50 ml). The filtrate was washed with deionized water (3×50 ml), then with brine (50 ml), dried over magnesium sulfate then concentrated and dried in vacuo. Flash column chromatography (Silica gel, 0-100% methylene chloride in hexane) gave a solid which washed with diethyl ether, filtered and dried in vacuo to give ethyl 2-(6-cyano-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate (0.135 g, 90% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07728130B2uspto-grants-2010_06