Reaktionsgleichung
S1C=CC=C1.CC(N(O)C(N)=[O:12])C#C.[F:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23]2S[C:26]([C:28]#[C:29][CH:30]([N:32]([OH:36])[C:33]([NH2:35])=[O:34])[CH3:31])=[CH:25][CH:24]=2)=[CH:18][CH:17]=1>>[F:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23]2[O:12][C:26](/[CH:28]=[CH:29]/[CH:30]([N:32]([OH:36])[C:33]([NH2:35])=[O:34])[CH3:31])=[CH:25][CH:24]=2)=[CH:18][CH:17]=1Komponenten
4
Versuchsvorschrift
The desired compound is prepared according to the method of Example 2, except substituting furan for thiophene, and substituting N-(3-butyn-2-yl)N-hydroxyurea, prepared as in Example 3, step 2, for (R) N-(3-butyn-2-yl)N-hydroxyurea.
Quellen und Nachweise
- ORD-Eintrag
- ord-197e8b32c35b4a61b27832d814391a99
- Quelldatensatz
- uspto-grants-1996_04
- Patentnummer
- US05506261
Verknüpfte Notizen
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