Reaktionsgleichung
CC1N=[CH:4][C:5]([C:8]([NH:10][C@@H:11]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])[C:12]([OH:14])=[O:13])=[O:9])=[N:6]C=1.[CH3:22][N:23]1[C:27](C)=[CH:26]C(C(O)=O)=N1>>[CH3:22][N:23]1[C:27]([CH3:26])=[CH:4][C:5]([C:8]([NH:10][C@@H:11]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])[C:12]([OH:14])=[O:13])=[O:9])=[N:6]1Komponenten
3
Versuchsvorschrift
Example 50 can be prepared according to the procedure described for the preparation of Example 49, replacing 5-methylpyrazine-2-carboxylic acid from Example 49a with -(1,5-dimethyl-1H-pyrazole-3-carboxylic acid in Example 50a to produce (S)-2-(1,5-dimethyl-1H-pyrazole-3-carboxamido)non-8-enoic acid. All subsequent steps should proceed in a similar fashion to Example 49 to produce Example 50.
Aufarbeitung
- customExample 50 can be prepared
- customdescribed for the preparation of Example 49
Quellen und Nachweise
- ORD-Eintrag
- ord-e5018ae99c9740fe814ab91d692c6a32
- Quelldatensatz
- uspto-grants-2014_02
- Patentnummer
- US08642538B2
Verknüpfte Notizen
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