Reaktionsgleichung
[NH2:1][C:2]1[C:3]([C:19]2[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:26])=[CH:4][C:5]2[CH:10]=[N:9][C:8]([NH:11][CH2:12][CH2:13][CH2:14][N:15]([CH3:17])[CH3:16])=[N:7][C:6]=2[N:18]=1.[C:27]([N:31]=[C:32]=[O:33])([CH3:30])([CH3:29])[CH3:28]>>[C:27]([NH:31][C:32]([NH:1][C:2]1[C:3]([C:19]2[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:26])=[CH:4][C:5]2[CH:10]=[N:9][C:8]([NH:11][CH2:12][CH2:13][CH2:14][N:15]([CH3:17])[CH3:16])=[N:7][C:6]=2[N:18]=1)=[O:33])([CH3:30])([CH3:29])[CH3:28]Komponenten
3
Versuchsvorschrift
Following the procedure of Example 21, 1.62 g of 7-amino-6-(2,6-dichlorophenyl)-2-(3-dimethylamino-propylamino)-pyrido[2,3-d]pyrimidine from Example 27 was reacted with 0.48 g of t-butyl isocyanate to give the title compound; mp gradually dec above 130° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-7013e5535a2f460db3dcc240ffdb06ae
- Quelldatensatz
- uspto-grants-1999_09
- Patentnummer
- US05952342
Verknüpfte Notizen
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