Ethanol → 3-Amino-4-[N-(4-cyanophenyl)amino]pyridine

HRID 1655251

Reaktionsgleichung

Reaktionsgleichung von HRID 1655251
[Sn](Cl)Cl.[C:4]([C:6]1[CH:11]=[CH:10][C:9]([N:12]2C=C[C:15]([NH2:18])=[C:14]([N+:19]([O-])=O)[CH2:13]2)=[CH:8][CH:7]=1)#[N:5].[CH2:22](O)[CH3:23]>O>[NH2:19][C:14]1[CH:15]=[N:18][CH:22]=[CH:23][C:13]=1[NH:12][C:9]1[CH:8]=[CH:7][C:6]([C:4]#[N:5])=[CH:11][CH:10]=1

Komponenten

5

Edukt 3

HCID 702EthanolHCID 24479Stannous ChlorideHCID 19791284N-(4-cyanophenyl)-4-amino-3-nitropyridine

Produkt 1

HCID 105364203-Amino-4-[N-(4-cyanophenyl)amino]pyridine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

According to a modification of the method of Pharm. Helv. Acta, 1975, 50, 188., tin dichloride dibydrate (56.4 g, 250 mmol) was added to a suspension of N-(4-cyanophenyl)-4-amino-3-nitropyridine (12.0 g, 50 mmol) in 2N aqueous bydrochloric acid (35 ml), water (150 ml) and ethanol (75 ml) and the resulting mixture was heated to reflux for 10 minutes under nitrogen. The mixture was cooled in ice, poured into ice-cold 2N aqueous sodium bydroxide (400 ml) and filtered. The creamy-coloured solid was washed with 2N aqueous sodium hydroxide and water, and then dried in a vacuum desiccator. The product, 3-amino-4-(4'-cyanophenyl)aminopyridine, 9.31 g, gradually turns reddish brown on exposure to light and air.

Aufarbeitung

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux for 10 minutes under nitrogen
  3. temperatureThe mixture was cooled in ice
  4. filtrationfiltered
  5. washThe creamy-coloured solid was washed with 2N aqueous sodium hydroxide and water
  6. customdried in a vacuum desiccator

Quellen und Nachweise

ORD-Eintrag
ord-4daca26124c74bc5adf7081a98117dd3
Quelldatensatz
uspto-grants-1993_10
Patentnummer
US05250531

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