Reaktionsgleichung
[NH2:1][C:2]1[N:7]=[C:6]2[N:8](C(OC(C)(C)C)=O)[N:9]=[CH:10][C:5]2=[C:4]([C:18]2[O:19][CH:20]=[CH:21][CH:22]=2)[N:3]=1.CNC>CO.O>[O:19]1[CH:20]=[CH:21][CH:22]=[C:18]1[C:4]1[N:3]=[C:2]([NH2:1])[N:7]=[C:6]2[NH:8][N:9]=[CH:10][C:5]=12Komponenten
5
Versuchsvorschrift
A solution of tert-butyl 6-amino-4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidine-1-carboxylate (204 mg, 0.68 mmol) in MeOH (2 mL) was treated with dimethylamine in water (0.5 mL, 40%), refluxed for 1 h, cooled and the resulting solid filtered and washed with water to give the title compound (95 mg, 70%) as a cream solid.
Aufarbeitung
- temperaturerefluxed for 1 h
- temperaturecooled
- filtrationthe resulting solid filtered
- washwashed with water
Quellen und Nachweise
- ORD-Eintrag
- ord-0aaf967e9712498692b57d3cf2a03587
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07087754B2
Verknüpfte Notizen
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