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][CH2:20][CH3:21])[CH2:13][C:14](OCC)=[O:15]>>[OH:15][C:14]1[N:1]([C:3]2[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=2)[N:2]=[C:12]([CH2:19][CH2:20][CH3:21])[CH:13]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared in 44% yield from 2-hydrazinylpyridine-4-carbonitrile (PREPARATION 2) and ethyl 3-oxohexanoate according to the procedure for the preparation of Example 3, part A. [M+H] Calc'd for C12H12N4O, 229. Found, 229.
Quellen und Nachweise
- ORD-Eintrag
- ord-658423a5b2f54b7d80fc58c558720160
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09107916B2
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