6-Chloro-3-nitropyridin-2-ylamine → 6-Chloropyridine-2,3-diamine

HRID 413259Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 413259
[Cl:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([N+:9]([O-])=O)=[CH:4][CH:3]=1>C(O)(=O)C.CO.[Zn]>[Cl:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[CH:4][CH:3]=1

Komponenten

5

Edukt 1

HCID 27240356-Chloro-3-nitropyridin-2-ylamine

Produkt 1

HCID 106306156-Chloropyridine-2,3-diamine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23994ZincKatalysatorHCID 176Acetic AcidLösungsmittelHCID 887MethanolLösungsmittel

Versuchsvorschrift

Add zinc (4.0 g) to a solution of 6-chloro-3-nitropyridin-2-yl-amine (1.0 g, 5.76 mmol) in acetic acid (1.5 mL) and methanol (40 mL). Stir the resulting mixture is at room temperature for 18 hours, and filter through a pad of celite. Evaporate the filtrate to dryness under reduced pressure. Treat the resulting residue with 1N aqueous NaOH and extract with EtOAc. Wash the EtOAc extract with water and saturated aqueous NaCl. Separate the organic layer, dry over Na2SO4, filter and concentrate. Purify by flash column chromatography (50% EtOAc-hexane) to obtain 6-chloro-pyridine-2,3-diamine.

Aufarbeitung

  1. filtrationfilter through a pad of celite
  2. customEvaporate the filtrate to dryness under reduced pressure
  3. additionTreat the resulting residue with 1N aqueous NaOH
  4. extractionextract with EtOAc
  5. washWash the EtOAc
  6. extractionextract with water and saturated aqueous NaCl
  7. customSeparate the organic layer
  8. dry with materialdry over Na2SO4
  9. filtrationfilter
  10. concentrationconcentrate
  11. customPurify by flash column chromatography (50% EtOAc-hexane)

Quellen und Nachweise

ORD-Eintrag
ord-999fc0ff5cc34071aab4b79ed9e9932f
Quelldatensatz
uspto-grants-2003_05
Patentnummer
US06566367B2

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