Reaktion #485684

ord-5133ad4cd19948dd9c9e3d30fccc94ad

Reaktionsgleichung

CN(C)[P+](On1nnc2ccccc21)(N(C)C)N(C)C.F[P-](F)(F)(F)(F)F
benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate
O=C(O)C(CC1CCCC1)c1ccc(Cl)c(Cl)c1
3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
Nc1ncco1
2-aminooxazole
O=C(Nc1ncco1)C(CC1CCCC1)c1ccc(Cl)c(Cl)c1
3-cyclopentyl-2-(3,4-dichlorophenyl)-N-oxazol-2-yl-propionamide
Ausbeute 47.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was partitioned between water and ethyl acetate
  2. 2
    WaschenThe organic layer was washed sequentially with a 1N aqueous hydrochloric acid solution, water
  3. 3
    TrocknenThe organic layer was dried over magnesium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated in vacuo

Vorschrift

A solution of benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (102 mg, 0.23 mmol), 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (prepared as in Example 38A, 60 mg, 0.21 mmol), N,N-diisopropylethylamine (73 μL, 0.42 mmol), and 2-aminooxazole (27 mg, 0.31 mmol) in dry N,N-dimethylformamide (1 mL) was stirred at 25° C. under nitrogen for 15 h. The reaction mixture was partitioned between water and ethyl acetate. The organic layer was washed sequentially with a 1N aqueous hydrochloric acid solution, water, and a saturated aqueous sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-oxazol-2-yl-propionamide (34.9 mg, 47%) as a white solid: mp 134-136° C.; EI-HRMS m/e calcd for C17H18Cl2N2O2 (M+) 352.0745, found 352.0750.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06610846B1uspto-grants-2003_08