Reaktion #1126929

ord-540611517fab4a80bbb2e45909c4695a

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
C/C=C/B(O)O
(E)-prop-1-enylboronic acid
CCO
EtOH
C/C=C/c1nc(N2CCOCC2)cc(C)c1C(=O)NCc1cccc(F)c1
(E)-N-(3-fluorobenzyl)-4-methyl-6-morpholino-2-(prop-1-enyl)-pyridine-3-carboxylic acid amide
Ausbeute 74.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
110°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwere added
  2. 2
    FiltrationSubsequently the RM was filtered through celite
  3. 3
    Einengenthe filtrate was concentrated in vacuo
  4. 4
    SonstigePurification of the residue by CC (hexane/EtOAc 3:1)

Vorschrift

To a solution of 400 mg (1.1 mmol) 2-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide in toluene (15 ml) were added 140 mg (1.7 mmol) (E)-prop-1-enylboronic acid, 1.1 g (3.3 mmol) CsCO3 and EtOH (1.5 ml). After degassing with argon for 15 min 370 mg (0.32 mmol) Pd(PPh3)4 were added and the RM was heated to 110° C. for 5 h. Subsequently the RM was filtered through celite and the filtrate was concentrated in vacuo. Purification of the residue by CC (hexane/EtOAc 3:1) provided 300 mg (0.8 mmol, 74%) (E)-N-(3-fluorobenzyl)-4-methyl-6-morpholino-2-(prop-1-enyl)-pyridine-3-carboxylic acid amide (example 9). [M+H]+ 370.2.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08552200B2uspto-grants-2013_10