Water → 2-(2-Methoxypyrimidine-4-yl)-6-(2-fluoroethoxy)benzothiophene

HRID 454812Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 454812
Cl[C:2]1[N:7]=[C:6]([C:8]2[S:9][C:10]3[CH:16]=[C:15]([O:17][CH2:18][CH2:19][F:20])[CH:14]=[CH:13][C:11]=3[CH:12]=2)[CH:5]=[CH:4][N:3]=1.[CH3:21][OH:22].C[O-].[Na+].O>O1CCCC1>[CH3:21][O:22][C:2]1[N:7]=[C:6]([C:8]2[S:9][C:10]3[CH:16]=[C:15]([O:17][CH2:18][CH2:19][F:20])[CH:14]=[CH:13][C:11]=3[CH:12]=2)[CH:5]=[CH:4][N:3]=1

Komponenten

5

Edukt 3

HCID 962WaterHCID 23694274Sodium methanolate methanolHCID 866465562-(2-Chloropyrimidine-4-yl)-6-(2-fluoroethoxy)benzothiophene

Produkt 1

HCID 469475492-(2-Methoxypyrimidine-4-yl)-6-(2-fluoroethoxy)benzothiopheneAusbeute 75,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

2-(2-Chloropyrimidine-4-yl)-6-(2-fluoroethoxy)benzothiophene (105b, 80 mg, 0.26 mmol) obtained in Preparation Example 20 was dissolved in anhydrous tetrahydrofuran (4 mL). A 0.5 M sodium methoxide methanol solution (NaOMe in MeOH, 1.0 mL, 0.5 mmol) was added to the reaction mixture and stirred at room temperature for 18 hours. To the reaction mixture was added water, and organic compounds were extracted with ethyl acetate and evaporated after a treatment with sodium sulfate. Column chromatography was performed to give the target compound 2-(2-methoxypyrimidine-4-yl)-6-(2-fluoroethoxy)benzothiophene (1-34, 60 mg, 70%) as a yellow solid.

Aufarbeitung

  1. extractionwere extracted with ethyl acetate
  2. customevaporated after a treatment with sodium sulfate

Quellen und Nachweise

ORD-Eintrag
ord-f475f210ea684d1ba8a3c1ee54f2b3ca
Quelldatensatz
uspto-grants-2013_07
Patentnummer
US08497260B2

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