Réaction #1009217
ord-b1fd4efb8cc54120aad5c56ed9eee5b8
Équation de réaction
2-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide
pyrrolidine
NEt3
→
N-[(3-Fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-2-pyrrolidin-1-yl-pyridine-3-carboxylic acid amide
Rendement 59.0%
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Température
140°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1FiltrationThen the mixture was filtered through celite and
- 2Concentrationconcentrated in vacuo
- 3AutrePurification of the residue by CC (hexane/EtOAc 2:1)
- 4Autrefollowed 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.