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Pyridine → 4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzonitrile

HRID 32250
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 32250
[C:1]([CH:5]1[CH2:10][CH2:9][CH:8]([C:11]2[CH:19]=[CH:18][C:14]([CH:15]=[N:16]O)=[CH:13][C:12]=2[N:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][CH3:29])[CH2:22][CH2:21]2)[CH2:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2].C1(S(Cl)(=O)=O)C=CC=CC=1.N1C=CC=CC=1>O1CCCC1>[C:1]([CH:5]1[CH2:6][CH2:7][CH:8]([C:11]2[CH:19]=[CH:18][C:14]([C:15]#[N:16])=[CH:13][C:12]=2[N:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][CH3:29])[CH2:22][CH2:21]2)[CH2:9][CH2:10]1)([CH3:4])([CH3:3])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 7369Benzenesulfonyl chlorideHCID 740205524-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehydeoxime

Produkt 1

HCID 114064144-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzonitrileAusbeute 74,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

A mixture of the crude product of 4-(4-t-butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehydeoxime produced in Example (101c) (269 mg), benzenesulfonyl chloride (0,11 mL, 0.862 mmol), pyridine (0.11 ml, 1.36 mmol) and tetrahydrofuran (15 mL) was refluxed for 4 hours and 30 minutes. After then distilling off tetrahydrofuran partially in the reaction mixture under reduced pressure, chloroform was added and the mixture was further refluxed for 1 hour. The reaction mixture was concentrated under reduced pressure, the obtained residue was poured into ice water, and then ethyl acetate and saturated aqueous solution of ammonium chloride were added and extraction was performed with ethyl acetate. The separated organic layer was washed twice with saturated aqueous ammonium chloride and once with brine, and then dried over anhydrous sodium sulfate. The desiccant was filtered off, and the filtrate was concentrated under reduced pressure to give a residue, which was purified by NH silica gel column chromatography (ethyl acetate/hexane, followed by ethyl acetate/methanol), to give 192 mg of the title compound as an ochre oil.

Aufarbeitung

  1. temperaturewas refluxed for 4 hours and 30 minutes
  2. distillationAfter then distilling off tetrahydrofuran partially in the reaction mixture under reduced pressure, chloroform
  3. additionwas added
  4. temperaturethe mixture was further refluxed for 1 hour
  5. concentrationThe reaction mixture was concentrated under reduced pressure
  6. additionthe obtained residue was poured into ice water
  7. additionethyl acetate and saturated aqueous solution of ammonium chloride were added
  8. extractionextraction
  9. washThe separated organic layer was washed twice with saturated aqueous ammonium chloride and once with brine
  10. dry with materialdried over anhydrous sodium sulfate
  11. filtrationThe desiccant was filtered off
  12. concentrationthe filtrate was concentrated under reduced pressure
  13. customto give a residue, which
  14. customwas purified by NH silica gel column chromatography (ethyl acetate/hexane, followed by ethyl acetate/methanol)

Quellen und Nachweise

ORD-Eintrag
ord-9bdfb2d1875f4134bab94f34c5f24598
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07425554B2

Notizen zur Reaktion

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