Triethylamine → HCID 9846314, Verbindung

HRID 47530Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 47530
Cl.Cl.[NH:3]1[CH2:8][CH2:7][CH:6]([N:9]2[CH2:14][CH2:13][CH:12]([N:15]3[C:19]4[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=4[NH:17][C:16]3=[O:24])[CH2:11][CH2:10]2)[CH2:5][CH2:4]1.Cl[C:26]([O:28][CH2:29][CH3:30])=[O:27].C(N([CH2:36][CH3:37])CC)C.[C:38](=O)([O-:40])[OH:39].[Na+]>C(Cl)(Cl)Cl>[CH2:29]([O:28][C:26]([N:3]1[CH2:4][CH2:5][CH:6]([N:9]2[CH2:10][CH2:11][CH:12]([N:15]3[C:19]4[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=4[N:17]([C:38]([O:40][CH2:36][CH3:37])=[O:39])[C:16]3=[O:24])[CH2:13][CH2:14]2)[CH2:7][CH2:8]1)=[O:27])[CH3:30]

Komponenten

6

Versuchsvorschrift

1-[1-(Piperidin-4-yl)piperidin-4-yl]-1,3-dihydro-2H-benzimidazol-2-one-dihydrochloride (37.3 mg) was dissolved in 3 ml of chloroform, and to which 21 μl of ethyl chloroformate and 84 μl of triethylamine were successively added under cooling with ice, followed by overnight stirring at room temperature. To the reaction liquid saturated aqueous sodium hydrogencarbonate solution was added and extracted with chloroform. The organic layer was washed with saturated. brine, dried over anhydrous sodium sulfate and then the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (chloroform/methanol=10/1) to provide 41.7 mg of the title compound as a colorless oil.

Aufarbeitung

  1. temperatureunder cooling with ice
  2. additionwas added
  3. extractionextracted with chloroform
  4. washThe organic layer was washed with saturated
  5. dry with materialbrine, dried over anhydrous sodium sulfate
  6. distillationthe solvent was distilled off
  7. customThe resulting residue was purified by silica gel column chromatography (chloroform/methanol=10/1)

Quellen und Nachweise

ORD-Eintrag
ord-4cff432082f54af1baff8ac907c5a989
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06699880B1

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