5-Methoxy-6-(trifluoromethyl)indoline → HCID 10837468, Verbindung

HRID 1603807Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1603807
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[C:15]3[O:14][CH2:13][CH2:12][C:11]=3[CH:10]=[C:9]([NH:16][C:17](=[O:25])OC3C=CC=CC=3)[CH:8]=2)[CH:2]=1.[CH3:26][O:27][C:28]1[CH:29]=[C:30]2[C:34](=[CH:35][C:36]=1[C:37]([F:40])([F:39])[F:38])[NH:33][CH2:32][CH2:31]2>CN(C=O)C>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[C:15]3[O:14][CH2:13][CH2:12][C:11]=3[CH:10]=[C:9]([NH:16][C:17]([N:33]3[C:34]4[C:30](=[CH:29][C:28]([O:27][CH3:26])=[C:36]([C:37]([F:39])([F:40])[F:38])[CH:35]=4)[CH2:31][CH2:32]3)=[O:25])[CH:8]=2)[CH:2]=1

Komponenten

4

Edukt 2

HCID 112067135-Methoxy-6-(trifluoromethyl)indolineHCID 18005145HCID 18005145, Verbindung

Produkt 1

HCID 10837468HCID 10837468, VerbindungAusbeute 26 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Phenyl N-[2,3-dihydro-7-(pyrid-3-yl)benzofuran-5-yl]carbamate (D65) (0.20 g, 0.00060mole) in dry DMF (10 ml) was treated under argon with 5-methoxy-6 trifluoromethyl indoline (D11) (0.13 g, 0.00060 mole) and heated under reflux for 18 hours. The reaction was allowed to cool to ambient temperature and the solvent was removed in vacuo. The residue was dissolved in dichloromethane, washed with deionised water and 10% sodium hydroxide solution, dried (Na2SO4) and evaporated in vacuo. The resulting brown oil was purified by flash column chromatography on silica gel, eluting with 2% methanol/dichloromethane, followed by recrystallisation from ethyl acetate 60-80° petroleum ether to afford the title compound (0.07 g, 26%) as a beige solid.

Aufarbeitung

  1. temperatureheated
  2. temperatureunder reflux for 18 hours
  3. customthe solvent was removed in vacuo
  4. dissolutionThe residue was dissolved in dichloromethane
  5. washwashed with deionised water and 10% sodium hydroxide solution
  6. dry with materialdried (Na2SO4)
  7. customevaporated in vacuo
  8. customThe resulting brown oil was purified by flash column chromatography on silica gel
  9. washeluting with 2% methanol/dichloromethane
  10. customfollowed by recrystallisation from ethyl acetate 60-80° petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-5b68f605669e4833aec4f968db261665
Quelldatensatz
uspto-grants-1999_11
Patentnummer
US05990133

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