Cyclohexylamine, N-methyl-, hydrochloride → HCID 67277979, Verbindung

HRID 1696234Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1696234
Cl[C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[NH:8][CH:9]=[CH:10][C:3]=12.Cl.[CH3:12][NH:13][CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1>C(Cl)(Cl)Cl>[CH:14]1([N:13]([CH3:12])[C:2]2[C:3]3[CH:10]=[CH:9][NH:8][C:4]=3[N:5]=[CH:6][CH:7]=2)[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1

Komponenten

4

Reaktionsbedingungen

Temperatur
180 °C

Versuchsvorschrift

4-Chloro-1H-pyrrolo[2,3-b]pyridine (224 mg) and N-methylcyclohexanamine hydrochloride (1.1g) was combined and stirred at 180° C. for 5 hours under nitrogen atmosphere. After cooled, the reaction mixture was dissolved in chloroform (20ml), washed with saturated aqueous sodium hydrogencarbonate (10ml) and brine, dried over MgSO4, and evaporated in vacuo to give crude red oil. The residue was purified by flash column chromatography over NH-silica gel with a EtOAc as eluant. The fractions containing the object compound were combined, and evaporated under reduced pressure. The residue was washed with ether to give N-cyclohexyl-N-methyl-1H-pyrrolo[2,3-b]pyridin-4-amine (49.8 mg) as a pale yellow solid.

Aufarbeitung

  1. temperatureAfter cooled
  2. washwashed with saturated aqueous sodium hydrogencarbonate (10ml) and brine
  3. dry with materialdried over MgSO4
  4. customevaporated in vacuo
  5. customto give crude red oil
  6. customThe residue was purified by flash column chromatography over NH-silica gel with a EtOAc as eluant
  7. additionThe fractions containing the object compound
  8. customevaporated under reduced pressure
  9. washThe residue was washed with ether

Quellen und Nachweise

ORD-Eintrag
ord-3482f81051cf47b092af7c10e5835dde
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08163767B2

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