Reaktion #1518609

ord-1a850de1115047968867626737605936

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared

Vorschrift

Prepared according to Procedure H using 1-(4-chloro-3-ethyl-5,7-difluoroquinolin-2-yl)piperidin-2-one (40.0 mg, 0.120 mmol) and 5-morpholinopyridin-3-amine in toluene to give 1-(3-ethyl-5,7-difluoro-4-((5-(4-morpholinyl)-3-pyridinyl)amino)-2-quinolinyl)-2-piperidinone. 1H NMR (400 MHz, chloroform-d) δ ppm 7.84 (2H, dd, J=7.2, 2.3 Hz), 7.46 (1H, ddd, J=9.6, 2.5, 1.4 Hz), 7.08 (1H, d, J=11.7 Hz), 6.97 (1H, ddd, J=13.5, 8.6, 2.5 Hz), 6.65 (1H, t, J=2.3 Hz), 4.24-4.39 (1H, m), 3.80 (4H, t, J=4.8 Hz), 3.50-3.60 (1H, m), 3.10-3.30 (4H, m), 2.38-2.64 (4H, m), 1.88-2.17 (4H, m), 1.01 (3H, t, J=7.4 Hz). Mass Spectrum (ESI) m/e=468.2 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08940724B2uspto-grants-2015_01