Reaktionsgleichung
Cl[C:2]1[N:10]=[C:9]([F:11])[N:8]=[C:7]2[C:3]=1[N:4]=[CH:5][N:6]2[CH:12]([CH3:14])[CH3:13].[CH3:15][N:16]1[CH:20]=[C:19]([NH2:21])[CH:18]=[N:17]1.CCN(C(C)C)C(C)C>C(O)CCC>[F:11][C:9]1[N:8]=[C:7]2[C:3]([N:4]=[CH:5][N:6]2[CH:12]([CH3:14])[CH3:13])=[C:2]([NH:21][C:19]2[CH:18]=[N:17][N:16]([CH3:15])[CH:20]=2)[N:10]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 6-chloro-2-fluoro-9-isopropyl-9H-purine (215 mg, 1 mmol), 1-methyl-1H-pyrazol-4-amine (116 mg, 1.2 mmol) in nBuOH (5 mL, 0.2 M) and DIPEA (0.7 mL, 4 mmol) was stirred at ambient temperature for 2 days. LCMS showed major title product with M+1=276.2 amu. This crude product was used in the following step with no isolation.
Quellen und Nachweise
- ORD-Eintrag
- ord-7096dd6408b54c18815ec14bb39a7a09
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09290496B2
Verknüpfte Notizen
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