5-Methoxyindole → 5-methoxy-3-(1-naphthoyl)-1H-indole

HRID 55924

Reaktionsgleichung

Reaktionsgleichung von HRID 55924
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[CH:6]2.C[Mg]Br.[C:15]1([C:25](Cl)=[O:26])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][CH:16]=1.[Cl-].[NH4+]>C(OCC)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[C:6]2[C:25]([C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][CH:16]=1)=[O:26]

Komponenten

6

Edukt 4

HCID 138725-MethoxyindoleHCID 25517Ammonium ChlorideHCID 701461-Naphthalenecarbonyl chlorideHCID 178418573HCID 178418573, Verbindung

Produkt 1

HCID 681592875-methoxy-3-(1-naphthoyl)-1H-indoleAusbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel3×

Versuchsvorschrift

To a cooled solution at 0° C. of 5-methoxy-1H-indole 3 (7.4 g, 50 mmol) in diethyl ether (150 ml) under nitrogen was added dropwise a solution of methylmagnesium bromide (3M) in diethyl ether (17.5 ml) and the mixture was stirred for 2 h at room temperature. The solution was then cooled at 0° C. and to this solution was added a solution of 1-naphthoylchloride (9.5 g, 50 mmol) in diethyl ether (100 ml) dropwise over a period of 15 min. After the addition was completed the solution was warmed up at room temperature and stirred for 2 h followed by slow addition of saturated ammonium chloride solution (375 ml) and stirred overnight. The white solid formed was filtered, washed by ether and dried under high vacuum to give 5-methoxy-3-(1-naphthoyl)-1H-indole 4 (11.3 g, 75%).

Aufarbeitung

  1. temperatureThe solution was then cooled at 0° C. and to this solution
  2. additionAfter the addition
  3. temperaturewas warmed up at room temperature
  4. stirringstirred for 2 h
  5. stirringstirred overnight
  6. customThe white solid formed
  7. filtrationwas filtered
  8. washwashed by ether
  9. customdried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-fe93391650c3489caaf5e02e57804c70
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434687B2

Verknüpfte Notizen

Wird geladen…