Hydrochloric Acid → HCID 66984909, Verbindung

HRID 1950776Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1950776
Cl[C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([CH3:13])[N:5]=[C:4]([S:14][CH3:15])[N:3]=1.[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:22]=[C:23]([O:25][CH3:26])[CH:24]=1)[NH2:21].Cl>C(#N)C.C(OCC)(=O)C.C([O-])(O)=O.[Na+]>[CH3:26][O:25][C:23]1[CH:22]=[C:20]([NH:21][C:2]2[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([CH3:13])[N:5]=[C:4]([S:14][CH3:15])[N:3]=2)[CH:19]=[C:18]([O:17][CH3:16])[CH:24]=1

Komponenten

7

Versuchsvorschrift

A 200 mL RB flask was charged with ethyl 4-chloro-6-methyl-2-(methylthio)pyrimidine-5-carboxylate (2.76 g, 11.1 mmol) in 40 mL acetonitrile. To the solution was added 3,5-dimethoxy aniline (1.784 g, 11.4 mmol), and conc. HCl solution (494 uL, 5.6 mmol), the reaction mixture was stirred at 60˜70° C. for 2 hours. The mixture was diluted with ethyl acetate and saturated aqueous NaHCO3 solution. It was stirred for an additional 5 minutes. The separated organic layer was dried over MgSO4, and condensed under reduced pressure yielding the residue. The residue was recrystallized from acetonitrile, dried under reduced pressure providing pale yellow solids (2.92 g, 72%). MS m/z: 364.1 (M+H)+.

Aufarbeitung

  1. stirringIt was stirred for an additional 5 minutes
  2. dry with materialThe separated organic layer was dried over MgSO4, and condensed under reduced pressure
  3. customyielding the residue
  4. customThe residue was recrystallized from acetonitrile
  5. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-aa5ec20b622c4f8298cd02e34237f04f
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08404677B2

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