Cyclohexane → 2-(5-Amino-2-ethoxyphenyl)-5-methyl-7-(2-ethylheptyl)-3H-imidazo[5,1-f][1,2,4]-triazin-4-one
Reaktionsgleichung
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-])=O)=[CH:6][C:5]=1[C:13]1[NH:18][C:17](=[O:19])[C:16]2=[C:20]([CH3:32])[N:21]=[C:22]([CH2:23][CH:24]([CH2:30][CH3:31])[CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[N:15]2[N:14]=1)[CH3:2].C1CCCCC1.C(OCC)(=O)C>C(O)C.[Pd]>[NH2:10][C:7]1[CH:8]=[CH:9][C:4]([O:3][CH2:1][CH3:2])=[C:5]([C:13]2[NH:18][C:17](=[O:19])[C:16]3=[C:20]([CH3:32])[N:21]=[C:22]([CH2:23][CH:24]([CH2:30][CH3:31])[CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[N:15]3[N:14]=2)[CH:6]=1Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Analogously to the procedure of example 42A, 1.95 g (4.42 mmol) of the compound from example 49A are hydrogenated in 120 g of ethanol using 200 mg of 10% Pd/C. Chromatography on 400 ml of silica gel using cyclohexane and ethyl acetate in a gradient system from 90:10 to 40:60 gives 1.26 g (69.4% of theory).
Aufarbeitung
- customgives 1.26 g (69.4% of theory)
Quellen und Nachweise
- ORD-Eintrag
- ord-beb9284104874dccbc49023925c5f0f0
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07098207B2
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