Reaktion #11243

ord-79ef9e4d9baf47909d82b5c863d6a907

Reaktionsgleichung

COCCOc1ccccc1/C=C/c1cc2cc(OCc3ccccc3)ccc2[nH]1
( 852 )
COCCOc1ccccc1/C=C/c1cc2cc(OCc3ccccc3)ccc2[nH]1
5-(Benzyloxy)-2-{(E)-2-[2-(2-methoxyethoxy)phenyl]ethenyl}-1H-indole
O=C1C=CC(=O)N1
maleimide
COCCOc1ccccc1-c1cc2[nH]c3ccc(OCc4ccccc4)cc3c2c2c1C(=O)NC2=O
( 854 )
Ausbeute 46.0%
COCCOc1ccccc1-c1cc2[nH]c3ccc(OCc4ccccc4)cc3c2c2c1C(=O)NC2=O
9-(Benzyloxy)-4-[2-(2-methoxyethoxy)phenyl]pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 46.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigegave the adduct (CIII
  2. 2
    SonstigeAr=2-(2-methoxyethoxy)phenyl, R10═H (853), which was used without further purification

Vorschrift

Reaction of (852) with maleimide using the procedure described in method 4a gave the adduct (CIII; Ar=2-(2-methoxyethoxy)phenyl, R10═H (853), which was used without further purification. Aromatisation of (853) with MnO2 using the procedure described in example 79 gave (854) (46%) as an orange solid, mp 157–159° C., which was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07094798B1uspto-grants-2006_08