(Tetrahydrofuran-3-yl)methanamine → 4-(2-chloro-4-pyridinyl)-N-[(tetrahydro-3-furanyl)methyl]-2-pyrimidinamine
Reaktionsgleichung
Cl[C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([Cl:14])[CH:9]=2)[CH:5]=[CH:4][N:3]=1.[O:15]1[CH2:19][CH2:18][CH:17]([CH2:20][NH2:21])[CH2:16]1>>[Cl:14][C:10]1[CH:9]=[C:8]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH:21][CH2:20][CH:17]3[CH2:18][CH2:19][O:15][CH2:16]3)[N:7]=2)[CH:13]=[CH:12][N:11]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 2-chloro-4-(2-chloro-4-pyridinyl)pyrimidine (i.e., the product of Example 6, Step A) and tetrahydro-3-furanmethanamine (i.e., the product of Step C) in the same fashion as described in Example 9, Step A.
Quellen und Nachweise
- ORD-Eintrag
- ord-b06fbe0c3c90455aa7102f5ce9ff5c00
- Quelldatensatz
- uspto-grants-2011_09
- Patentnummer
- US08026359B2
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