Реакция #11239

ord-e7283af0700a4001ac72fdbb3ed5f745

Уравнение реакции

C=C(c1ccccc1)c1cc2cc(OC)ccc2[nH]1
( 818 )
C=C(c1ccccc1)c1cc2cc(OC)ccc2[nH]1
Methyl 2-(1-phenylvinyl)-1H-indol-5-yl ether
O=C1C=CC(=O)N1
maleimide
COc1ccc2[nH]c3c(-c4ccccc4)cc4c(c3c2c1)C(=O)NC4=O
( 820 )
Выход 73.0%
COc1ccc2[nH]c3c(-c4ccccc4)cc4c(c3c2c1)C(=O)NC4=O
9-Methoxy-5-phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Выход 73.0%

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеprepared
  2. 2
    Другоеgave the adduct (XCVIII
  3. 3
    ДругоеR=phenyl, R′═H) (819), which was used without further purification

Методика

Reaction of (818) prepared as described in example 418 with maleimide at 180° C. using the procedure described in example 69 gave the adduct (XCVIII; R=phenyl, R′═H) (819), which was used without further purification. The crude Diels-Alder adduct was aromatised with MnO2 using the procedure described in example 79 to give (820) (73%), mp 281–285° C. 1H NMR δ [(CD3)2SO] 11.63 (br s, 1H), 11.15 (br s, 1H), 8.45 (d, J=2.5 Hz, 1H), 7.78–7.76 (m, 2H), 7.68 (s, 1H), 7.65–7.62 (m, 2H), 7.57–7.53 (m, 2H), 7.22 (dd, J=8.8, 2.5 Hz, 1H), 3.89 (s, 3H). Found: C, 72.06; H, 4.57; N, 7.69. C21H14N2O3.1/3H2O requires: C, 72.41; H, 4.24; N, 8.04.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07094798B1uspto-grants-2006_08