Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[N:3]=1.[CH:10]1([N+:16]#[C-:17])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1.[CH:18](=O)[CH3:19]>Cl(O)(=O)(=O)=O>[CH:10]1([NH:16][C:17]2[N:3]3[C:4]([CH3:9])=[CH:5][C:6]([CH3:8])=[CH:7][C:2]3=[N:1][C:18]=2[CH3:19])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Compound (19) was prepared according to the general synthesis instructions from 1.0 ml of 2-amino-4,6-dimethylpyridine solution (0.1 M, DCM), 0.575 ml of cyclohexyl isocyanide solution (0.2 M, DCM), 0.500 ml of acetaldehyde solution (0.3 M, DCM) and 10 μl of perchloric acid (w=20%).
Quellen und Nachweise
- ORD-Eintrag
- ord-793046b5752c4850a3b36506c79c4a06
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06849642B2
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