Réaction #531788

ord-4352c6a372534f1d85c587f7a1676115

Équation de réaction

c1ccc(C2=NC(c3cccc(C4N=C(c5ccccc5)NC5=C4CCc4c(-c6ccccc6)cc(-c6ccccc6)nc45)c3)C3=C(N2)c2nc(-c4ccccc4)cc(-c4ccccc4)c2CC3)cc1
1,3-bis(2,7,9-triphenyl-1,4,5,6-tetrahydropyrido[3,2-h]quinazolin-4-yl)benzene
c1ccc(-c2cc(-c3ccccc3)c3ccc4c(-c5cccc(-c6nc(-c7ccccc7)nc7c6ccc6c(-c8ccccc8)cc(-c8ccccc8)nc67)c5)nc(-c5ccccc5)nc4c3n2)cc1
1,3-bis(2,7,9-triphenylpyrido[3,2-h]quinazolin-4-yl)benzene

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated until total dissolution
  2. 2
    Températurethe reaction was refluxed for 6 hours with argon bubbling directly in the solution

Mode opératoire

A suspension of 1,3-bis(2,7,9-triphenyl-1,4,5,6-tetrahydropyrido[3,2-h]quinazolin-4-yl)benzene (5) (4.4 mmol) in 220 diethyleneglycol was heated until total dissolution. 1.2 g Pd/C was then slowly added, and the reaction was refluxed for 6 hours with argon bubbling directly in the solution. The reaction was then stopped, and the suspension cooled to room temperature.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08475686B2uspto-grants-2013_07