HCID 12397258, Verbindung → HCID 54332840, Verbindung
Reaktionsgleichung
[CH2:1]([O:8]C1C=CC(C=O)=NC=1CS(C)(=O)=O)C1C=CC=CC=1.C1OC2C=CC(C([N+]#[C-])(C)C)=CC=2O1.[OH:36][C:37]1[CH:38]=[CH:39][C:40]([CH:48]([CH2:50][NH:51][CH:52]([CH3:61])[CH2:53][C:54]2[CH:59]=[CH:58][C:57]([OH:60])=[CH:56][CH:55]=2)[OH:49])=[N:41][C:42]=1[CH2:43][S:44]([CH3:47])(=[O:46])=[O:45]>>[OH:36][C:37]1[CH:38]=[CH:39][C:40]([CH:48]([CH2:50][NH:51][CH:52]([CH3:61])[CH2:53][C:54]2[CH:55]=[CH:56][C:57]3[O:60][CH2:1][O:8][C:58]=3[CH:59]=2)[OH:49])=[N:41][C:42]=1[CH2:43][S:44]([CH3:47])(=[O:46])=[O:45]Komponenten
4
Versuchsvorschrift
Reacting 5-benzyloxy-6-methanesulfonylmethyl-2-pyridinecarboxaldehyde with 3,4-methylenedioxyphenylisopropyl isocyanide followed by reduction of the intermediate amide and hydrogenation of the amine gives 5-hydroxy-6-methanesulfonylmethyl-α-[2-(3,4-methylenedioxyphenyl)-1-methylethylaminomethyl]-2-pyridinemethanol.
Quellen und Nachweise
- ORD-Eintrag
- ord-9a81e8849eb840599fc14ceb295f5fbe
- Quelldatensatz
- uspto-grants-1976_04
- Patentnummer
- US03952101
Notizen zur Reaktion
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