Sodium Carbonate → 6-(2,4-Dimethoxy-pyrimidin-5-yl)-pyridine-2-carbonitrile
Reaktionsgleichung
I[C:2]1[C:3]([O:10][CH3:11])=[N:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.[C:12]([C:14]1[N:19]=[C:18](B2OC(C)(C)C(C)(C)O2)[CH:17]=[CH:16][CH:15]=1)#[N:13].C([O-])([O-])=O.[Na+].[Na+].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>C(O)CC.CC([O-])=O.CC([O-])=O.[Pd+2]>[CH3:9][O:8][C:5]1[N:4]=[C:3]([O:10][CH3:11])[C:2]([C:18]2[N:19]=[C:14]([C:12]#[N:13])[CH:15]=[CH:16][CH:17]=2)=[CH:7][N:6]=1Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
5-Iodo-2,4-dimethoxy-pyrimidine (500 mg, 1.88 mmol) was dissolved in degassed n-PrOH (40 ml) and then 6-cyano-pyridine-2-boronic acid pinacol ester (650 mg, 2.82 mmol), Na2CO3 (598 mg, 5.64 mmol), PPh3 (164 mg, 0.62 mmol) and Pd(OAc)2 (42 mg, 0.19 mmol) were added. The suspension was stirred at reflux for 3 hours. The solvent was evaporated and the crude was partitioned between water and ethyl acetate. The organic phase was dried (Na2SO4) and evaporated. The crude was triturated with iPrOH to give 200 mg of the title compound (44% yield).
Aufarbeitung
- temperatureat reflux for 3 hours
- customThe solvent was evaporated
- customthe crude was partitioned between water and ethyl acetate
- dry with materialThe organic phase was dried (Na2SO4)
- customevaporated
- customThe crude was triturated with iPrOH
Quellen und Nachweise
- ORD-Eintrag
- ord-9c661d50fd2d4b33b0dcf9a476560655
- Quelldatensatz
- uspto-grants-2010_06
- Patentnummer
- US07727988B2
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