HCID 22891997, Verbindung → HCID 69940044, Verbindung

HRID 993435Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 993435
[CH2:1]([O:8]C([N:11]1[CH2:16][CH2:15][CH:14]([CH2:17][N:18]2[C:22]([CH2:23][N:24]3[CH:28]=[C:27]([C:29]([N:31]4[CH2:36][CH2:35][O:34][CH2:33][CH2:32]4)=[O:30])[C:26]([C:37]4[C:46]5[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=5)[CH:40]=[CH:39][CH:38]=4)=[N:25]3)=[CH:21][N:20]=[CH:19]2)[CH2:13][CH2:12]1)=O)C1C=CC=CC=1.[H][H]>CO.[C+4].[OH-].[Pd+2].[OH-].[OH-].[OH-].[OH-].[OH-]>[OH2:8].[NH3:11].[CH3:1][OH:8].[NH:11]1[CH2:12][CH2:13][CH:14]([CH2:17][N:18]2[C:22]([CH2:23][N:24]3[CH:28]=[C:27]([C:29]([N:31]4[CH2:36][CH2:35][O:34][CH2:33][CH2:32]4)=[O:30])[C:26]([C:37]4[C:46]5[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=5)[CH:40]=[CH:39][CH:38]=4)=[N:25]3)=[CH:21][N:20]=[CH:19]2)[CH2:15][CH2:16]1

Komponenten

6

Versuchsvorschrift

227 mg (0.36 mmol) of the compound prepared in Example 158 was dissolved in methanol, 20 mg of palladium hydroxide carbon was added thereto, and the mixture was reacted under 1 atm of hydrogen for 2 hours. After the reaction was completed, the mixture was filtered and the solvent therein was removed. The residue was subjected to silica gel column chromatography(eluent: ammonia water/methanol=15/85, v/v) to give 120 mg (0.26 mmol, Yield 74%) of the title compound.

Aufarbeitung

  1. filtrationthe mixture was filtered
  2. customthe solvent therein was removed

Quellen und Nachweise

ORD-Eintrag
ord-609d34d020a544c09ff8a043d3d4ad85
Quelldatensatz
uspto-grants-2002_10
Patentnummer
US06472526B1

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