Réaction #1009217

ord-b1fd4efb8cc54120aad5c56ed9eee5b8

Équation de réaction

Cc1cc(N2CCOCC2)nc(Cl)c1C(=O)NCc1cccc(F)c1
2-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide
C1CCNC1
pyrrolidine
CCN(CC)CC
NEt3
Cc1cc(N2CCOCC2)nc(N2CCCC2)c1C(=O)NCc1cccc(F)c1
N-[(3-Fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-2-pyrrolidin-1-yl-pyridine-3-carboxylic acid amide
Rendement 59.0%

Solvants

Conditions de réaction

Température
140°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThen the mixture was filtered through celite and
  2. 2
    Concentrationconcentrated in vacuo
  3. 3
    AutrePurification of the residue by CC (hexane/EtOAc 2:1)
  4. 4
    Autrefollowed by crystallization (hexane/EtOAc)

Mode opératoire

To a solution of 254 mg (0.7 mmol) 2-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide (synthesis is described in section a) of example 9) in MeCN (0.5 ml) were added 115 μl (1.4 mmol) pyrrolidine and 290 μl (2.1 mmol) NEt3. The RM was heated in the microwave to 120° C. for 30 min and subsequently to 140° C. for 45 min. Then the mixture was filtered through celite and concentrated in vacuo. Purification of the residue by CC (hexane/EtOAc 2:1), followed by crystallization (hexane/EtOAc) provided 164 mg (0.41 mmol, 59%) N-[(3-Fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-2-pyrrolidin-1-yl-pyridine-3-carboxylic acid amide (example 24). [M+H]+ 399.2.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09278103B2uspto-grants-2016_03