3-Methyl-4-pyridinamine → 2-(5-Bromo-2-pyrrolidin-1-ylphenyl)-4-(3-methyl-4-pyridylamino)pteridine
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:19]2[CH2:23][CH2:22][CH2:21][CH2:20]2)=[C:6]([C:8]2[NH:17][C:16](=O)[C:15]3[C:10](=[N:11][CH:12]=[CH:13][N:14]=3)[N:9]=2)[CH:7]=1.[NH2:24][C:25]1[CH:30]=[CH:29][N:28]=[CH:27][C:26]=1[CH3:31].BrC1C=CC(F)=C(C2N=C(NC3C=CN=CC=3)C3C(=NC=CN=3)N=2)C=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:19]2[CH2:23][CH2:22][CH2:21][CH2:20]2)=[C:6]([C:8]2[N:17]=[C:16]([NH:24][C:25]3[CH:30]=[CH:29][N:28]=[CH:27][C:26]=3[CH3:31])[C:15]3[C:10](=[N:11][CH:12]=[CH:13][N:14]=3)[N:9]=2)[CH:7]=1Komponenten
4
Versuchsvorschrift
The title product was synthesized by reaction of the 2-(5-bromo-2-pyrrolidin-1-yl-phenyl)pteridin-4-one 110 and 4-amino-3-methylpyridine following the procedure described for 4-(4-pyridylamino)-2-(5-bromo-2-fluorophenyl)pteridine 1 (LCMS analysis).
Quellen und Nachweise
- ORD-Eintrag
- ord-21295f404408445a956eb92576208a57
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09290502B2
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