Reaktion #163978

ord-d82f1772d69546239fba981cd12dae9e

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe T3P charged vessel was washed with 2-MeTHF (0.6 vol)
  2. 2
    Temperaturthe resulting suspension was heated to 47.5+/−5.0° C.
  3. 3
    TemperaturOnce complete, the resulting mixture was cooled to 20° C.+/−5° C
  4. 4
    workup.ADDITIONto dilute the mixture
  5. 5
    WaschenThe reaction mixture was washed with water (10.0 vol) 2 times and 2-MeTHF (16.5 vol)
  6. 6
    workup.ADDITIONwas charged to the reactor
  7. 7
    SonstigeOnce complete, the reaction was quenched with 1.2N HCl/H2O (10.0 vol)
  8. 8
    Waschenwashed with 0.1N HCl/H2O (10.0 vol)
  9. 9
    Filtrationfiltered
  10. 10
    Sonstigeto remove any particulates
  11. 11
    Sonstigeplaced in a second reactor

Vorschrift

4-Oxo-1,4-dihydroquinoline-3-carboxylic acid, 26, (1.0 eq) and 5-amino-2,4-di-tert-butylphenyl methyl carbonate, 32, (1.1 eq) were charged to a reactor. 2-MeTHF (4.0 vol, relative to the acid) was added followed by T3P® 50% solution in 2-MeTHF (1.7 eq). The T3P charged vessel was washed with 2-MeTHF (0.6 vol). Pyridine (2.0 eq) was then added, and the resulting suspension was heated to 47.5+/−5.0° C. and held at this temperature for 8 hours. A sample was taken and checked for completion by HPLC. Once complete, the resulting mixture was cooled to 20° C.+/−5° C. 2-MeTHF was added (12.5 vol) to dilute the mixture. The reaction mixture was washed with water (10.0 vol) 2 times and 2-MeTHF (16.5 vol) was charged to the reactor. This solution was charged with 30% w/w NaOMe/MeOH (1.7 equiv) to perform the methanolysis. The reaction was stirred at 25.0° C.+/−5.0° C. for no less than 1.0 hour, and checked for completion by HPLC. Once complete, the reaction was quenched with 1.2N HCl/H2O (10.0 vol), and washed with 0.1N HCl/H2O (10.0 vol). The organic solution was polish filtered to remove any particulates and placed in a second reactor.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08835639B2uspto-grants-2014_09