Reaktion #41781

ord-bf6dc933770b47d2a8ca9040f0f8e650

Reaktionsgleichung

COS(=O)(=O)OC
dimethyl sulfate
COC(=O)c1cncc(Oc2ccc(NC(=O)C(F)(F)F)c([N+](=O)[O-])c2)c1
methyl5-[3-nitro-4-(2,2,2-trifluoroacetylamino)phenoxy]-pyridine-3-carboxylate
CC#N
acetonitrile
[Na+].[OH-]
sodium hydroxide
Cc1ccccc1
toluene
CNc1ccc(Oc2ccncc2C(=O)OC)cc1[N+](=O)[O-]
methyl-4-[4-(methylamino)-3-nitrophenoxy]pyridine-3-carboxylate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated
  2. 2
    Waschenwashed with water, brine
  3. 3
    Sonstigedried
  4. 4
    Sonstigeevaporated
  5. 5
    SonstigeThe crude was purified by column chromatography

Vorschrift

To the solution of the methyl5-[3-nitro-4-(2,2,2-trifluoroacetylamino)phenoxy]-pyridine-3-carboxylate (1 eq) in a mixture of toluene, acetonitrile and sodium hydroxide solution (50%) was added benzyltrimethylammonium chloride (1 eq) and dimethyl sulfate (1.2 eq). The biphasic mixture was stirred overnight at room temperature and evaporated. The mixture was taken up in ethyl acetate, washed with water, brine, dried and evaporated. The crude was purified by column chromatography to afford methyl-4-[4-(methylamino)-3-nitrophenoxy]pyridine-3-carboxylate. MS: MH+=303.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728010B2uspto-grants-2010_06