Reaktionsgleichung
[NH:1]([C:3]1[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=1)[NH2:2].O=[C:12]([CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:13][C:14](OCC)=[O:15]>>[CH2:19]([C:12]1[CH:13]=[C:14]([OH:15])[N:1]([C:3]2[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=2)[N:2]=1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared in 53% yield from 2-hydrazinylpyridine-4-carbonitrile (PREPARATION 2) and ethyl 3-oxo-4-phenylbutanoate according to the procedure for the preparation of Example 3, part A. [M+H] Calc'd for C16H12N4O, 277. Found, 277.
Quellen und Nachweise
- ORD-Eintrag
- ord-1bd53c8ad02747dd85672b6dacfec08c
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09107916B2
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