Methanol → HCID 19358875, Verbindung
Reaktionsgleichung
Cl[C:2]1[C:7]([N+:8]([O-])=O)=[C:6](Cl)[N:5]=[CH:4][N:3]=1.C([O:19][CH2:20][CH2:21][NH:22][CH2:23]C1C=CC=CC=1)C1C=CC=CC=1.[CH2:30]([C:32]1[NH:33][CH:34]=[C:35]([CH3:37])[N:36]=1)[CH3:31].[Sn](Cl)Cl.C(N1C=CN=C1)(N1C=CN=C1)=[O:42].CO.[OH-].[Na+]>[Pd]>[CH2:30]([C:32]1[N:36]2[C:35]([C:37](=[O:42])[NH:8][C:7]3[C:2]([N:22]([CH2:21][CH2:20][OH:19])[CH3:23])=[N:3][CH:4]=[N:5][C:6]=32)=[CH:34][N:33]=1)[CH3:31]Komponenten
9
Edukt 7
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Prepared by treatment of 4,6-dichloro-5-nitropyrimidine with N-(2-(benzyloxy)ethylbenzylamine, followed by reaction with 2-ethyl-4-methylimidazole, reduction with tin (II) chloride, cyclization with carbonyldiimidazole, and hydrogenation with palladium on carbon in methanol containing 1.1 eq. NaOH at 50 psi and 500 for 24 hours.
Quellen und Nachweise
- ORD-Eintrag
- ord-df9484a66de844869a75e5fdcee19583
- Quelldatensatz
- uspto-grants-2000_02
- Patentnummer
- US06025489
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