Reaktion #41446

ord-1dcee2700c794235bf9cec9a0d7abf27

Reaktionsgleichung

CC(C)C(=O)Cl
2-methylpropanoyl chloride
NC(=O)C(Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
2-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-2-phenylacetamide
CC(C)(C)[O-].[K+]
potassium 2-methylpropan-2-olate
CC(C)C(=O)NC(=O)C(Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
N-[2-[1-(4-fluorophenyl)indazol-5-yl]oxy-2-phenyl-acetyl]-2-methyl-propanamide

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGStirring
  2. 2
    workup.WAITwas continued for 30 min at 0° C
  3. 3
    EinengenThen the sample was concentrated in vacuo
  4. 4
    Sonstigepurified by semi-prep
  5. 5
    SonstigeHPLC go give white solid material, 14 mg (59%)

Vorschrift

A stirred solution of 2-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-2-phenylacetamide (137b, 20 mg, 60 μmol) in THF (2 ml) was cooled to 0° C., and potassium 2-methylpropan-2-olate (18.6 mg, 170 μmol) was added. The mixture was stirred at 0° C. for 10 min, and a solution of 2-methylpropanoyl chloride (30 mg, 280 μmol) in THF (0.5 ml) was added. Stirring was continued for 30 min at 0° C. Then the sample was concentrated in vacuo and purified by semi-prep. HPLC go give white solid material, 14 mg (59%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728030B2uspto-grants-2010_06