Reaktion #1841058

ord-313014d3ee1c4c37a2ab55d6cb9d8965

Reaktionsgleichung

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
Ausbeute 59.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
140°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09168259B2uspto-grants-2015_10