Reaktion #6911

ord-5b2ee72421e84c96a53e63a90b2cd355

Reaktionsgleichung

CC(C)(C)C(=O)NC1CCN(c2ccc3cc(C(=N)NO)ccc3n2)C1
product
CC(C)(C)C(=O)NC1CCN(c2ccc3cc(C(=N)NO)ccc3n2)C1
N-(1-{6-[(Hydroxyamino)(imino)methyl]quinolin-2-yl}pyrrolidin-3-yl)-2,2-dimethylpropanamide
CC(C(=O)O)c1ccc(C(F)(F)F)cc1
4-trifluoromethylphenylpropionic acid
ClCCCl
EDC
CC(C)(C)C(=O)NC1CCN(c2ccc3cc(-c4noc(CCc5ccc(C(F)(F)F)cc5)n4)ccc3n2)C1
2,2-Dimethyl-N-{1-[6-(5-{2-[4-(trifluoromethyl)phenyl]ethyl}-1,2,4-oxadiazol-3-yl)quinolin-2-yl]pyrrolidin-3-yl}propanamide

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    Temperaturthe mixture was heated at 110° C. for 2 hr
  2. 2
    TemperaturThe mixture was cooled to r.t.
  3. 3
    Sonstigequenched with water
  4. 4
    Extraktionextracted with excess EtOAc
  5. 5
    SonstigeThe combined extracts were dried over a drying agent
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigethe solvent removed under vacuum
  8. 8
    SonstigeThe residue was purified by preparative TLC
  9. 9
    Wascheneluting with EtOAc
  10. 10
    Sonstigeto afford the product, MS

Vorschrift

To a mixture of the product of Step E, (66 mg) in anhydrous diglyme (2 mL) was added 4-trifluoromethylphenylpropionic acid (1.1 eq.) and EDC (2 eq.). The reaction mixture was heated to 50° C. overnight. After approximately 18 h, the mixture was heated at 110° C. for 2 hr. The mixture was cooled to r.t., quenched with water and extracted with excess EtOAc. The combined extracts were dried over a drying agent filtered and the solvent removed under vacuum. The residue was purified by preparative TLC eluting with EtOAc to afford the product, MS: m/z 538.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084156B2uspto-grants-2006_08