2-Hydrazinylpyridine-4-carbonitrile → HCID 178439127, Verbindung
Reaktionsgleichung
[NH:1]([C:3]1[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=1)[NH2:2].[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([CH3:27])([CH3:26])[C:19](=O)[CH2:20][C:21](OC)=[O:22])=[CH:14][CH:13]=1>>[Cl:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]([C:19]2[CH:20]=[C:21]([OH:22])[N:1]([C:3]3[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=3)[N:2]=2)([CH3:27])[CH3:26])=[CH:16][CH:17]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 2-hydrazinylpyridine-4-carbonitrile (PREPARATION 2) and methyl 4-(4-chlorophenyl)-4-methyl-3-oxopentanoate according to the procedure for the preparation of Example 158, part A.
Quellen und Nachweise
- ORD-Eintrag
- ord-5079804b131744ea9121746a2ea8144e
- Quelldatensatz
- uspto-grants-2015_03
- Patentnummer