Reaktion #66707

ord-cc4c99025821491089fd53ccd157da18

Reaktionsgleichung

Cl.N=C(N)N
guanidine HCl
C[O-].[Na+]
sodium methoxide
CCc1c(OC(C#N)C(N(C)C)N(C)C)cc(C)c2sccc12
3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrile
Cl.Nc1ccccc1
aniline HCl
N=C(N)N
guanidine
CCc1c(OC(C#N)=CNc2ccccc2)cc(C)c2sccc12
2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile
Ausbeute 55.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 2.0 hours
  2. 2
    Temperaturthe reaction mixture was heated
  3. 3
    Temperaturto reflux for 5 hours
  4. 4
    Temperaturcooled
  5. 5
    SonstigeSolvent was removed in vacuo
  6. 6
    Sonstigechromatographed (5% MeOH/methylene chloride/1% Na4OH)

Vorschrift

3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrile (590 mg, 2 mmol) and aniline HCl (1.1 g, 9 mmol) in 5 mL absolute ethanol were heated at reflux for 2.0 hours. In a separate flask, guanidine HCl (0.850 mg., 9 mmol) and sodium methoxide solution (1.83 ml, 9 mmol, 4.9 molar solution in methanol) were mixed in 1 ml Ethanol. The guanidine solution was added to the reaction mixture via pipette, and the reaction mixture was heated to reflux for 5 hours, then cooled. Solvent was removed in vacuo, and the residue was, chromatographed (5% MeOH/methylene chloride/1% Na4OH) to give 368 mg 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile, 61%. Also present was 50 mg of 5-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-pyrimidine-2,4-diamine, 9%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524725B2uspto-grants-2013_09