Reaktionsgleichung
CCOCC.[CH3:6][O:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][C:16]=1[O:17][CH3:18])[NH:13][C:12]([CH3:19])=[C:11]2[C:20](=[O:24])[C:21](Cl)=[O:22].[C:25]([CH:33]1[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]1)(=[O:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.C(=O)([O-])[O-].[K+].[K+]>C(Cl)(Cl)Cl.O>[C:25]([CH:33]1[CH2:38][CH2:37][N:36]([C:21](=[O:22])[C:20]([C:11]2[C:10]3[C:14](=[CH:15][C:16]([O:17][CH3:18])=[C:8]([O:7][CH3:6])[CH:9]=3)[NH:13][C:12]=2[CH3:19])=[O:24])[CH2:35][CH2:34]1)(=[O:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
The above ether suspension of 5,6-dimethoxy-2-methyl-3-indoleglyoxylyl chloride is added portionwise to a cooled stirring mixture of 4-benzoylpiperidine [Example 9(a)], 150 ml of water, 150 ml of chloroform and 25 g of potassium carbonate. The mixture is stirred for 16 hours at ambient temperature, the organic layer is separated and the solvent is removed, leaving a brown oil which is triturated with cyclohexane and then stirred for 16 hours with ether. A white solid results which is collected, dried and recrystallized thrice from methanol to give the compound, mp 188°-190° C., 4-benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidine.
Aufarbeitung
- additionis added portionwise to a cooled
- stirringThe mixture is stirred for 16 hours at ambient temperature
- customthe organic layer is separated
- customthe solvent is removed
- customleaving a brown oil which
- customis triturated with cyclohexane
- stirringstirred for 16 hours with ether
- customA white solid results which
- customis collected
- customdried
- customrecrystallized thrice from methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-b08f444901ae49b4bd339ed9754cb66e
- Quelldatensatz
- uspto-grants-1978_07
- Patentnummer
- US04101663
Verknüpfte Notizen
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