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1-Propanol → HCID 86642063, Verbindung

HRID 215800
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 215800
[Li]CCCC.[F:6][C:7]1[CH:8]=[N:9][C:10]2[C:15]([CH:16]=1)=[CH:14][C:13]([O:17][CH3:18])=[CH:12][CH:11]=2.CN([CH:22]=[O:23])C.C(O)CC>C1COCC1>[F:6][C:7]1[CH:8]=[N:9][C:10]2[C:15]([C:16]=1[CH:22]=[O:23])=[CH:14][C:13]([O:17][CH3:18])=[CH:12][CH:11]=2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 10311-PropanolHCID 6228DimethylformamideHCID 113098403-fluoro-6-methoxyquinolineHCID 178418339Butyllithium

Produkt 1

HCID 86642063HCID 86642063, VerbindungAusbeute 51 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of DIPA (15.5 mL) in THF (300 mL), cooled to −78° C., was added n-BuLi (2.35N in hexanes, 44 mL). The reaction mixture was stirred 5 min at this temperature before warming to 0° C. The reaction mixture was stirred 15 min before cooling to −78° C. 3-fluoro-6-methoxy-quinoline (prepared as described in FR 2004/01105, 15 g) in THF (50 mL+10 mL rinse) was added and the mixture was stirred 3 h at −78° C. DMF (3 mL) was added quickly. After 45 min., 1-propanol (8 mL) was added and the mixture was warmed to rt. The mixture was partitioned between water (100 mL) and EA (200 mL). The aq. layer was extracted with EA (200 mL). The combined org. layers were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue triturated in Hept to give an orange solid (9.0 g, 51% yield).

Aufarbeitung

  1. stirringThe reaction mixture was stirred 15 min
  2. temperaturebefore cooling to −78° C
  3. stirringthe mixture was stirred 3 h at −78° C
  4. waitAfter 45 min.
  5. temperaturethe mixture was warmed to rt
  6. customThe mixture was partitioned between water (100 mL) and EA (200 mL)
  7. extractionThe aq. layer was extracted with EA (200 mL)
  8. washlayers were washed with brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated to dryness
  12. customThe residue triturated in Hept

Quellen und Nachweise

ORD-Eintrag
ord-b88e9cdc528f463283c88b61a42a56c7
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08193179B2

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