Potassium Carbonate → 4-[(4-fluorobenzyl)oxy]-1-{4-[(1E)-3-hydroxy-1-propen-1-yl]phenyl}pyridin-2(1H)-one

HRID 254409

Reaktionsgleichung

Reaktionsgleichung von HRID 254409
[F:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][NH:11][C:10](=[O:14])[CH:9]=2)=[CH:4][CH:3]=1.Br[C:18]1[CH:23]=[CH:22][C:21](/[CH:24]=[CH:25]/[CH2:26][OH:27])=[CH:20][CH:19]=1.C(=O)([O-])[O-].[K+].[K+].O.N>C(OCC)(=O)C.CN(C=O)C>[F:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][O:7][C:8]2[CH:13]=[CH:12][N:11]([C:18]3[CH:23]=[CH:22][C:21](/[CH:24]=[CH:25]/[CH2:26][OH:27])=[CH:20][CH:19]=3)[C:10](=[O:14])[CH:9]=2)=[CH:4][CH:3]=1

Komponenten

7

Edukt 4

HCID 11430Potassium CarbonateHCID 11183465(2E)-3-(4-bromophenyl)prop-2-en-1-olHCID 12896473Azane;hydrateHCID 220499004-(4-Fluorobenzyloxy)-1h-pyridin-2-one

Produkt 1

HCID 668728494-[(4-fluorobenzyl)oxy]-1-{4-[(1E)-3-hydroxy-1-propen-1-yl]phenyl}pyridin-2(1H)-oneAusbeute 50,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
155 °C

Versuchsvorschrift

A mixture of 4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one (1.10 g, 5.0 mmol), (2E)-3-(4-bromophenyl)-2-propen-1-ol (1.28 g, 6 mmol), cuprous iodide (476 mg, 3 mmol), potassium carbonate (829 mg, 6 mmol) and DMF (20 mL) was stirred overnight at 155° C. The reaction liquid was cooled to room temperature, then poured into ammonia water, and ethyl acetate was added for extraction. The organic layer was washed with water and saturated saline, and dried with anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, followed by purification by flash column chromatography (KP-Sil, hexane:ethyl acetate=1:1 to 0:1) to obtain the entitled compound (881 mg).

Aufarbeitung

  1. customThe reaction liquid
  2. temperaturewas cooled to room temperature
  3. additionwas added for extraction
  4. washThe organic layer was washed with water and saturated saline
  5. dry with materialdried with anhydrous magnesium sulfate
  6. concentrationThe solvent was concentrated under reduced pressure
  7. customfollowed by purification by flash column chromatography (KP-Sil, hexane:ethyl acetate=1:1 to 0:1)

Quellen und Nachweise

ORD-Eintrag
ord-d8bc3e29064449df8c43fa1906e3655b
Quelldatensatz
uspto-grants-2011_01
Patentnummer
US07875633B2

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