Pyridine → 2-Valerylamino-5-bromo-4-methyl-3-nitropyridine

HRID 53443

Reaktionsgleichung

Reaktionsgleichung von HRID 53443
[NH2:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6]([CH3:11])[C:5]([Br:12])=[CH:4][N:3]=1.N1C=CC=CC=1.[C:19](Cl)(=[O:24])[CH2:20][CH2:21][CH2:22][CH3:23].C(Cl)Cl>O>[C:19]([NH:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6]([CH3:11])[C:5]([Br:12])=[CH:4][N:3]=1)(=[O:24])[CH2:20][CH2:21][CH2:22][CH3:23]

Komponenten

6

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

A mixture comprising 10 g (43.1 mmol) of 2-amino-5-bromo-4-methyl-3-nitropyridine and 6.8 g of pyridine was heated to 110° C. in a nitrogen atmosphere. 5.7 g (47.4 mmol) of valeroyl chloride was dropwise added thereto and the mixture was stirred at 110° C. for 5 hours. The reaction mixture was brought to room temperature, followed by the addition of methylene chloride (50 ml) and water (50 ml). The organic phase was separated. The aqueous phase was further extracted with methylene chloride (50 ml). The organic phases were combined, dried over anhydrous magnesium sulfate and subjected to vacuum concentration to give a crude crystal. It was recrystallized from ethyl acetate to give 11 g of 2-valerylamino-5-bromo-4-methyl-3-nitropyridine (yield 81%).

Aufarbeitung

  1. customwas brought to room temperature
  2. customThe organic phase was separated
  3. extractionThe aqueous phase was further extracted with methylene chloride (50 ml)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationsubjected to vacuum concentration
  6. customto give a crude crystal
  7. customIt was recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-1da1f522f51f4cdfa04c306c6fee3dc0
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05618969

Verknüpfte Notizen

Wird geladen…