Indole → 3-(1H-Indol-3-yl)-2-methyl-2,3-dihydro-isoindol-1-one
Reaktionsgleichung
O[CH:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[N:3]1[CH3:12].[NH:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14]1>>[NH:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:15]([CH:2]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[C:4](=[O:11])[N:3]2[CH3:12])=[CH:14]1Komponenten
3
Versuchsvorschrift
The product from example 20, step a) (650 mg, 3.98 mmol) and indole (780 mg, 6.67 mmol) were heated (neat) to 180° C. for 30 minutes. The reaction was cooled to rt and the product was recrystallized from ethanol/water to give 452 mg of the sub-title compound as a tan solid.
Aufarbeitung
- customthe product was recrystallized from ethanol/water
Quellen und Nachweise
- ORD-Eintrag
- ord-2d39dbcbab8e423ba7b3b57bd1a20e2a
- Quelldatensatz
- uspto-grants-2011_07
- Patentnummer
- US07981912B2
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