Reaktion #1725899

ord-fcc58ed6a7ff4dfda5d8a052d4b88b56

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was refluxed
  2. 2
    Temperaturcooled
  3. 3
    SonstigeThe orange crystalline solid which separated
  4. 4
    Filtrationwas filtered
  5. 5
    Waschenwashed with ether
  6. 6
    Sonstigecrystallized for acetone/ether
  7. 7
    SonstigeYield

Vorschrift

To a solution of 5.0 g (11.7 mmol) of compound 8c in 20 ml of acetone, 3.3 g (23.4 mmol) of methyl iodide were added and the mixture was refluxed under stirring for 6 hour, then cooled. The orange crystalline solid which separated was filtered, washed with ether and crystallized for acetone/ether. Yield, 5.6 g (85%), m.p. 163°-165° C. U.V. (buffer pH 7.4) 270, 215 nm. NMR (DMSO-d6) δ7.68-7.06 (ms, 7H, C5N4N+ +C6H3 +NH), 4.56 (s, 3H, --N+ --CH3), 3.42 (q, 2H, J=7 Hz, --N--CH2). 3.19 (t, 2H, J=7 Hz, CH2), 1.32 [s, 18H, 2--C(CH3)3 ]. Anal. Calcd for C25H33IN2O5 : C, 52.82; H, 5.85; N, 4.92. Found: C, 52.76; H, 5.87; N, 4.90.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04880816uspto-grants-1989_11