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Potassium Carbonate → HCID 18001243, Verbindung

HRID 478202
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 478202
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]2[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)=[CH:2]1.Cl.[Cl:17][CH2:18][CH2:19][CH2:20][N:21]1[CH2:26][CH2:25][CH:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH2:23][CH2:22]1.C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[ClH:17].[C:27]1([CH:24]2[CH2:23][CH2:22][N:21]([CH2:20][CH2:19][CH2:18][N:13]3[CH2:14][CH2:15][CH:10]([C:3]4[C:4]5[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=5)[NH:1][CH:2]=4)[CH2:11][CH2:12]3)[CH2:26][CH2:25]2)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 203688Piperidine, 1-(3-chloropropyl)-4-phenyl-, hydrochlorideHCID 7022353-(4-Piperidinyl)-1H-indole

Produkt 1

HCID 18001243HCID 18001243, VerbindungAusbeute 40 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a suspended solution of 4-(3-indolyl)piperidine (2.0 g, 10 mmol) and 1-(3-chloropropyl)-4-phenylpiperidine hydrochloride (3.1 g, 11.2 mmol) in DMF (60 mL) was added potassium carbonate (5.5 g, 40 mmol), and the mixture was stirred at 100° C. for 4 hours. After the precipitated salt was filtered off, the filtrate was concentrated, water (50 mL) was added to the filtrate, and the mixture was extracted with chloroform. After drying over anhydrous sodium sulfate, the chloroform layer was concentrated to afford a crude product. The crude product was purified by column chromatography on a silica gel (silica gel NH-DM 1020 produced by Fuji Silysia Chemical Ltd., eluent; chloroform) and was then recrystallized from ethyl acetate to afford a free form (1.6 g, yield: 40%) of the title compound as white crystals. After adding hydrochloric acid/methanol to a solution of the free form (1.6 g) in methanol, the mixture was concentrated and was then recrystallized from methanol/ether to afford the title compound (1.8 g) as white crystals.

Aufarbeitung

  1. filtrationAfter the precipitated salt was filtered off
  2. concentrationthe filtrate was concentrated
  3. additionwater (50 mL) was added to the filtrate
  4. extractionthe mixture was extracted with chloroform
  5. dry with materialAfter drying over anhydrous sodium sulfate
  6. concentrationthe chloroform layer was concentrated
  7. customto afford a crude product
  8. customThe crude product was purified by column chromatography on a silica gel (silica gel NH-DM 1020 produced by Fuji Silysia Chemical Ltd., eluent; chloroform)
  9. customwas then recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-0a2cf5f9c1ef416083e1abf734d75bb4
Quelldatensatz
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06642228B1

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