Reaktion #1584850

ord-0fbbb22fccd4481b8eaf2fb12366883b

Reaktionsgleichung

O=C(n1ccnc1)n1ccnc1
CDI
O=C(O)c1ncccc1F
3-fluoro-pyridine-2-carboxylic acid
C[CH2][K].O=C(O)CC(=O)O
ethyl potassium malonate
[Cl-].[Cl-].[Mg+2]
MgCl2
CCOC(=O)CC(=O)c1ncccc1F
3-(3-Fluoro-pyridin-2-yl)-3-oxo-propionic acid ethyl ester

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to room temperature
  2. 2
    workup.STIRRINGThe mixture was stirred at room temperature for 1 h
  3. 3
    workup.ADDITIONthis reaction mixture was then added to the above suspension
  4. 4
    workup.STIRRINGstirred at room temperature for 18 h
  5. 5
    workup.ADDITIONwas added
  6. 6
    Extraktionthe mixture was extracted with ethyl acetate
  7. 7
    WaschenThe organic layer was washed with brine
  8. 8
    Trocknendried over Na2SO4
  9. 9
    Einengenconcentrated

Vorschrift

To a solution of ethyl potassium malonate (2) (452 mg, 2.66 mmol) in tetrahydrofuran (5 mL) was added MgCl2 (202 mg, 2.13 mL). The mixture was stirred at 50° C. for 4 h and then cooled to room temperature. In another flask a solution of 3-fluoro-pyridine-2-carboxylic acid (1) (250 mg, 1.77 mmol) in tetrahydrofuran (5 mL) was taken and CDI (carbonyldiimidazole) (489 mg, 3.01 mmol) was added at 10° C. The mixture was stirred at room temperature for 1 h, this reaction mixture was then added to the above suspension and stirred at room temperature for 18 h. After completion of the reaction, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09199987B2uspto-grants-2015_12