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Morpholine → 4-(3-Fluorobenzyl)-N-(2-(5-morpholino-1H-indol-3-yl)ethyl)benzamide

HRID 1777681
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1777681
C1(P(C2CCCCC2)C2C=CC=CC=2C2C(N(C)C)=CC=CC=2)CCCCC1.CC([O-])(C)C.[Na+].[NH:35]1[CH2:40][CH2:39][O:38][CH2:37][CH2:36]1.Br[C:42]1[CH:43]=[C:44]2[C:48](=[CH:49][CH:50]=1)[NH:47][CH:46]=[C:45]2[CH2:51][CH2:52][NH:53][C:54](=[O:69])[C:55]1[CH:60]=[CH:59][C:58]([CH2:61][C:62]2[CH:67]=[CH:66][CH:65]=[C:64]([F:68])[CH:63]=2)=[CH:57][CH:56]=1>O1CCOCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[F:68][C:64]1[CH:63]=[C:62]([CH:67]=[CH:66][CH:65]=1)[CH2:61][C:58]1[CH:57]=[CH:56][C:55]([C:54]([NH:53][CH2:52][CH2:51][C:45]2[C:44]3[C:48](=[CH:49][CH:50]=[C:42]([N:35]4[CH2:40][CH2:39][O:38][CH2:37][CH2:36]4)[CH:43]=3)[NH:47][CH:46]=2)=[O:69])=[CH:60][CH:59]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8083MorpholineHCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 23676156Sodium t-butoxideHCID 86699393HCID 86699393, Verbindung

Produkt 1

HCID 679741904-(3-Fluorobenzyl)-N-(2-(5-morpholino-1H-indol-3-yl)ethyl)benzamideAusbeute 6,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845palladium(II) acetateKatalysatorHCID 312751,4-DioxaneLösungsmittel2×

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of palladium acetate (0.004 g; 0.017 mmol) and 2′-(dicyclohexylphosphino)-N,N-dimethylbiphenyl-2-amine (0.028 g; 0.071 mmol) in dioxane (0.5 mL) was degassed and sonicated for 30 minutes. This solution was then added to a degassed mixture of sodium 2-methylpropan-2-olate (0.024 g; 0.248 mmol), morpholine (0.031 mL; 0.354 mmol) and N-(2-(5-bromo-1H-indol-3-yl)ethyl)-4-(3-fluorobenzyl)benzamide (0.080 g; 0.177 mmol) in dioxane (2 mL). The resulting mixture was stirred at 100° C. for 18 hours and evaporated to dryness. The residue was partitioned between water and ethyl acetate and the organic layer was dried and concentrated under reduced pressure. The crude material was purified twice by flash chromatography on silica gel (eluent 65 to 100% ethyl acetate in heptane and 20 to 100% ethyl acetate in dichloromethane) and by preparative HPLC (method 2) to afford 0.0052 g (6%) of the title compound as a white solid.

Aufarbeitung

  1. customwas degassed
  2. customsonicated for 30 minutes
  3. customevaporated to dryness
  4. customThe residue was partitioned between water and ethyl acetate
  5. customthe organic layer was dried
  6. concentrationconcentrated under reduced pressure
  7. customThe crude material was purified twice by flash chromatography on silica gel (eluent 65 to 100% ethyl acetate in heptane and 20 to 100% ethyl acetate in dichloromethane) and by preparative HPLC (method 2)

Quellen und Nachweise

ORD-Eintrag
ord-8144a93adc7045fdafee546652036d8e
Quelldatensatz
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09266832B2

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