1,4-Dioxane → 1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthalene

HRID 351667

Reaktionsgleichung

Reaktionsgleichung von HRID 351667
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](Br)=[CH:4][CH:3]=1.O1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([C:4]2[CH:5]=[CH:6][CH:11]=[C:2]([N:1]3[CH2:18][CH2:17][O:16][CH2:15][CH2:14]3)[CH:3]=2)=[CH:4][CH:3]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

The above intermediate (1.49 g, 3.51 mmol) and 1-amino-4-bromonaphthalene (0.69 g, 3.11 mmol) were dissolved in 20 mL anhydrous 1,4-dioxane in a sealable tube under inert gas atmosphere. The solution was degased and purged with nitrogen (2×). Tetrakis(triphenylphosphine)palladium(0) (0.21 g, 0.18 mmol) was added and the solution was degassed and purged with nitrogen again (2×). The tube was sealed and heated to 100° C. for 17 h. After cooling to room temperature the mixture was diluted with EtOAc, saturated aqueous potassium carbonate solution (10 mL) was added and the mixture was stirred for 1 h at room temperature. The mixture was filtered over diatomaceous earth and the layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered and evaporated to dryness. Purification of the residue by flash chromatography afforded 0.363 g (1.19 mmol, 38%) of title compound.

Aufarbeitung

  1. customThe solution was degased
  2. custompurged with nitrogen (2×)
  3. customthe solution was degassed
  4. custompurged with nitrogen again (2×)
  5. customThe tube was sealed
  6. temperatureAfter cooling to room temperature the mixture
  7. additionwas diluted with EtOAc, saturated aqueous potassium carbonate solution (10 mL)
  8. additionwas added
  9. filtrationThe mixture was filtered over diatomaceous earth
  10. customthe layers were separated
  11. extractionThe aqueous layer was extracted with EtOAc
  12. washThe combined organic layers were washed with brine
  13. dry with materialdried (Na2SO4)
  14. filtrationfiltered
  15. customevaporated to dryness
  16. customPurification of the residue by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-f8a3525846e6472391e56daff4f1a631
Quelldatensatz
uspto-grants-2004_06
Patentnummer
US06743788B2

Verknüpfte Notizen

Wird geladen…