2-Pyridinemethanamine → 2-[2-Pyridylmethylamino]-4-[benzimidazol-1-yl]pyrimidine
Reaktionsgleichung
CS([C:5]1[N:10]=[C:9]([N:11]2[C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=3[N:13]=[CH:12]2)[CH:8]=[CH:7][N:6]=1)(=O)=O.[NH2:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=1>>[N:23]1[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=1[CH2:21][NH:20][C:5]1[N:10]=[C:9]([N:11]2[C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=3[N:13]=[CH:12]2)[CH:8]=[CH:7][N:6]=1Komponenten
3
Versuchsvorschrift
2-Methanesulfonyl-4-[benzimidazol-1-yl]pyrimidine was reacted with 2-(aminomethyl)pyridine according to the procedure described in EXAMPLE 1, Step C to afford the title compound. Mass Spectrum (ESI): m/e 303.0 (M+1). 1H NMR (500 MHz, CDCl3): δ 8.63 (m, 2H); 8.46 (d, J=5.3 Hz, 1H); 8.12 (br s, 1H); 7.86 (m, 1H); 7.70 (m, 1H); 7.38 (m, 3H); 7.24 (m, 1H); 6.85 (d, J=5.3 Hz, 1H); 6.50 (br s, 1H); 4.87 (d, J=5.4 Hz, 2H).
Quellen und Nachweise
- ORD-Eintrag
- ord-6e4818bb240849b6b96e184ef0bd393f
- Quelldatensatz
- uspto-grants-2002_12
- Patentnummer
- US06498165B1
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