Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:14])[CH2:4][CH2:5][C:6]1[C:11]([OH:12])=[CH:10][CH:9]=[C:8](I)[N:7]=1.[CH2:15]([OH:20])[CH2:16][CH2:17][C:18]#[CH:19]>>[CH3:1][O:2][C:3](=[O:14])[CH2:4][CH2:5][C:6]1[C:11]([OH:12])=[CH:10][CH:9]=[C:8]([C:19]#[C:18][CH2:17][CH2:16][CH2:15][OH:20])[N:7]=1Komponenten
3
Versuchsvorschrift
Under the conditions of example 5 A, 5 g of 3-(3-hydroxy-6-iodo-2-pyridyl)-propionic acid methyl ester is reacted with 1.37 g of 4-pentyn-1-ol, worked up, and the crude product is chromatographed on silica gel with hexane/0-4% methanol. 1.2 g of 3-[3-hydroxy-6-(5-hydroxy-1-pentynyl)-2-pyridyl]-propionic acid methyl ester is obtained as colorless oil.
Aufarbeitung
- customthe crude product is chromatographed on silica gel with hexane/0-4% methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-3041615f29b8409b826be1c81f949e26
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05624943
Verknüpfte Notizen
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