Reaktion #69082

ord-064840ed9e5840418937556be1917095

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe titled compound precipitated almost immediately
  2. 2
    Sonstigewas obtained as a white crystalline solid
  3. 3
    Filtrationafter suction filtration
  4. 4
    Waschenby washing with acetone
  5. 5
    Sonstigeair-dried (11.81 g, 98%, m.p. 212-214° C.)

Vorschrift

To a suspension of 2,4-diamino-6-ethyl-5-(3-(6-fluoroquinolin-4-yloxy)propoxy)pyrimidine (10.02 g, 28 mmol) in methanol (40 mL) was added 5.3 mL of concentrated HCl. The titled compound precipitated almost immediately and was obtained as a white crystalline solid after suction filtration followed by washing with acetone and air-dried (11.81 g, 98%, m.p. 212-214° C.). 1H NMR (400 MHz, DMSO-d6): 1.05 (3H, t, J=7.4 Hz), 2.40 (2H, m), 2.48 (2H, m), 3.98 (2H, t, J=5.8 Hz), 4.68 (2H, t, J=5.5 Hz), 7.50 (bs, 2H), 7.60 (1H, d, J=6.5 Hz), 7.90 (1H, s), 8.04 (1H, dt, J=9.0, 2.6 Hz), 8.10 (1H, dd, J=8.9, 2.3 Hz), 8.33 (1H, s), 8.43 (1H, dd, J=9.3, 4.8 Hz), 9.17 (1H, d, J=6.4 Hz), 12.70 (1H, s).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530491B2uspto-grants-2013_09