1,4-Oxathian-2-one → N-[4-(4-Dimethylaminomethyl-2-pyridyloxy)-cis-2-butenyl]-2-(2-hydroxyethylthio)acetamide
Reaktionsgleichung
[CH3:1][N:2]([CH2:4][C:5]1[CH:10]=[CH:9][N:8]=[C:7]([O:11][CH2:12]/[CH:13]=[CH:14]\[CH2:15][NH2:16])[CH:6]=1)[CH3:3].[O:17]1[CH2:22][CH2:21][S:20][CH2:19][C:18]1=[O:23]>>[CH3:1][N:2]([CH2:4][C:5]1[CH:10]=[CH:9][N:8]=[C:7]([O:11][CH2:12]/[CH:13]=[CH:14]\[CH2:15][NH:16][C:18](=[O:23])[CH2:19][S:20][CH2:21][CH2:22][OH:17])[CH:6]=1)[CH3:3]Komponenten
3
Versuchsvorschrift
Following a procedure similar to that described in Example 68, but using 4-(4-dimethylaminomethyl-2-pyridyloxy)-cis-2-butenylamine and 1,4-oxathian-2-one as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained in a 53% yield.
Quellen und Nachweise
- ORD-Eintrag
- ord-f37fbe5f088f4ce5998302782341a4c9
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05616579
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