Reaktion #62933

ord-136dcb68c9ac44ea8f5cae799bab2e17

Reaktionsgleichung

O=C1CCCc2ncccc21
7,8-dihydro-5(6H)-quinolinone
CN(C)C(N(C)C)N(C)C
tris(dimethylamino)-methane
N=C(N)N.O=C(O)O
guanidine carbonate
Nc1ncc2c(n1)-c1cccnc1CC2
title compound
Ausbeute 77.0%
Nc1ncc2c(n1)-c1cccnc1CC2
5,6-Dihydropyrido[2,3-h]quinazolin-2-amine
Ausbeute 77.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe solution is refluxed for 2 hours
  2. 2
    Temperaturcooled
  3. 3
    Einengenconcentrated
  4. 4
    workup.DISSOLUTIONThe residue is dissolved in 1 l of methanol
  5. 5
    TemperaturThe reaction mixture is refluxed, under nitrogen, for 2 hours
  6. 6
    EinengenThe mixture is concentrated to a green solid
  7. 7
    Waschenthe solid is washed with 500 ml of water
  8. 8
    Filtrationfiltered
  9. 9
    Sonstigevacuum dried
  10. 10
    Sonstigeto give 69.1 g of crude product
  11. 11
    SonstigeRecrystallization from acetonitrile

Vorschrift

To a refluxing solution, under nitrogen, of 45.0 g (0.306 mol) of 7,8-dihydro-5(6H)-quinolinone, (Example 1), in 750 ml of toluene is added dropwise a solution of 49.8 g (0.343 mol) of tris(dimethylamino)-methane in 250 ml of toluene. The solution is refluxed for 2 hours, cooled and concentrated. The residue is dissolved in 1 l of methanol and treated with 66.2 g (0.367 mol) of guanidine carbonate. The reaction mixture is refluxed, under nitrogen, for 2 hours. The mixture is concentrated to a green solid, the solid is washed with 500 ml of water, filtered and vacuum dried to give 69.1 g of crude product. Recrystallization from acetonitrile affords 6.8 g (77%) of the title compound as a light brown solid; mp 220°-226° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04762843uspto-grants-1988_08