Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][C:12]([O-:14])=O)[CH:6]=[C:7]([O:9][CH3:10])[CH:8]=1.[NH2:15][C:16]1[C:21]([CH:22]=O)=[CH:20][N:19]=[C:18]([S:24][CH3:25])[N:17]=1.[C:26](=O)([O-])[O-].[K+].[K+]>CN(C=O)C.O>[CH3:10][O:9][C:7]1[CH:6]=[C:5]([C:11]2[C:12](=[O:14])[N:15]([CH3:26])[C:16]3[N:17]=[C:18]([S:24][CH3:25])[N:19]=[CH:20][C:21]=3[CH:22]=2)[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 2-(3,5-dimethoxyphenyl)acetate (6) (440 mg, 2.40 mmol), 4-amino-2-(methylthio)pyrimidine-5-carbaldehyde (4) (605 mg, 2.88 mmol) and potassium carbonate (662 mg, 4.8 mmol) in DMF (30 mL) was stirred at 110° C. for 3 hours. The reaction was monitored by LCMS. The reaction mixture was diluted with H2O (30 mL), and extracted by EtOAc (3×40 mL). The combined organic layers were washed with water and brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by column chromatography (silica gel, petroleum ether/EtOAc=2:1) to afford 6-(3,5-dimethoxyphenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one (7) (683 mg, 83%) as a white solid. MS (ES+) C17H17N3O5S requires: 343. found: 344 [M+H]+.
Aufarbeitung
- extractionextracted by EtOAc (3×40 mL)
- washThe combined organic layers were washed with water and brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by column chromatography (silica gel, petroleum ether/EtOAc=2:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-9f38157d1275451eb51109fea4fbfcb4
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09340514B2
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