Cesium carbonate → 6-(3-Fluoro-1-azetidinyl)-2-methyl-3-nitropyridine

HRID 510481Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 510481
Cl[C:2]1[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=1.C([O-])([O-])=O.[Cs+].[Cs+].[F:18][CH:19]1[CH2:22][NH:21][CH2:20]1>CN(C=O)C.CCOC(C)=O>[F:18][CH:19]1[CH2:22][N:21]([C:2]2[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=2)[CH2:20]1

Komponenten

6

Edukt 3

HCID 10796Cesium carbonateHCID 2531236-Chloro-2-methyl-3-nitropyridineHCID 36035423-Fluoroazetidine

Produkt 1

HCID 895591516-(3-Fluoro-1-azetidinyl)-2-methyl-3-nitropyridineAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution of 6-chloro-2-methyl-3-nitropyridine (0.5 g, 2.9 mmol) in DMF (5 mL) was added Cs2CO3 (1.9 g, 5.8 mmol) followed 3-fluoroazetidine (0.64 g, 5.8 mmol) and the reaction mixture was heated for 2 h at 80° C. The reaction mixture was then diluted with EtOAc and the organic layer was washed with saturated aqueous sodium bicarbonate solution. The organic layer was then dried over sodium sulphate and concentrated. The crude material obtained was purified by column chromatography (silica: 100-200 mesh, MeOH:DCM 2-3%) to afford the title compound (0.6 g, 92%). LCMS (ES+) 211.95 (M+H)+, RT 2.33 minutes (method 1).

Aufarbeitung

  1. washthe organic layer was washed with saturated aqueous sodium bicarbonate solution
  2. dry with materialThe organic layer was then dried over sodium sulphate
  3. concentrationconcentrated
  4. customThe crude material obtained
  5. customwas purified by column chromatography (silica: 100-200 mesh, MeOH:DCM 2-3%)

Quellen und Nachweise

ORD-Eintrag
ord-091cf670ef17446db971cfd83348d3b7
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09096614B2

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