Ethyl 2-[(2'-cyanobiphenyl-4-yl)methyl]-3-oxohexanoate → 4'-[(5-Oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile
Reaktionsgleichung
[N:1]1[N:2]=[C:3]([NH2:6])[NH:4][CH:5]=1.[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH:22]([C:28](=O)[CH2:29][CH2:30][CH3:31])[C:23](OCC)=[O:24])=[CH:17][CH:16]=1)#[N:8]>ClC1C=CC(Cl)=CC=1Cl>[O:24]=[C:23]1[C:22]([CH2:21][C:18]2[CH:19]=[CH:20][C:15]([C:10]3[C:9]([C:7]#[N:8])=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:16][CH:17]=2)=[C:28]([CH2:29][CH2:30][CH3:31])[N:2]2[N:1]=[CH:5][N:4]=[C:3]2[NH:6]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 4H-1,2,4-triazol-3-amine (2.4 g) and ethyl 2-[(2′-cyanobiphenyl-4-yl)methyl]-3-oxohexanoate (10 g) in 1,2,4-trichlorobenzene (50 mL) was stirred at 180° C. for 6 hr. After evaporation of the solvent under reduced pressure, the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (4 g, 38%).
Aufarbeitung
- customAfter evaporation of the solvent under reduced pressure
- customthe residue was purified by silica gel column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-89635ed5af6d42d6a908ff74c26e7cac
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09115136B2
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