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2-(1H-1,2,4-triazol-1-yl)pyridine-3-carbonitrile → (2-(1H-1,2,4-triazol-1-yl)pyridin-3-yl)methanamine

HRID 1171074
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1171074
[N:1]1([C:6]2[N:13]=[CH:12][CH:11]=[CH:10][C:7]=2[C:8]#[N:9])[CH:5]=[N:4][CH:3]=[N:2]1>O.N.CO.[Ni]>[N:1]1([C:6]2[C:7]([CH2:8][NH2:9])=[CH:10][CH:11]=[CH:12][N:13]=2)[CH:5]=[N:4][CH:3]=[N:2]1
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Komponenten

5

Edukt 1

HCID 247024322-(1H-1,2,4-triazol-1-yl)pyridine-3-carbonitrile

Produkt 1

HCID 16785127(2-(1H-1,2,4-triazol-1-yl)pyridin-3-yl)methanamineAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 935NickelKatalysatorHCID 962WaterLösungsmittelHCID 21705897Ammonia methanolLösungsmittel

Versuchsvorschrift

A catalytic amount of Raney 2800 nickel in water (Aldrich; withdrawn as a wet slurry with the tip of a spatula) was added under air to a translucent slurry of 2-[1,2,4]triazol-1-yl-nicotinonitrile (1.053 g, 6.16 mmol), as prepared in the previous step, in 2 M NH3/MeOH (50 mL). The flask was then sealed with a septum, the air was removed from the system, and the flask was flushed with H2 gas under balloon pressure. The reaction was stirred at rt under H2 for 11 h (TLC showed no starting material remained), and the bulk of the Raney nickel was then removed with a magnet. The translucent white reaction mixture was then diluted with DCM (50 mL), filtered, and the translucent filtrate was concentrated under vacuum to provide the title compound as a beige crystalline solid (988 mg, 92%).

Aufarbeitung

  1. customwithdrawn as a wet slurry with the tip of a spatula)
  2. customThe flask was then sealed with a septum
  3. customthe air was removed from the system
  4. customthe flask was flushed with H2 gas under balloon pressure
  5. customwas then removed with a magnet
  6. additionThe translucent white reaction mixture was then diluted with DCM (50 mL)
  7. filtrationfiltered
  8. concentrationthe translucent filtrate was concentrated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-0a1a887a954a4216be2b7e5eee342312
Quelldatensatz
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07829584B2

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