반응 #169026

ord-1293cbcf0ecc4210ac435f43d3cb5df8

반응 방정식

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
수율 55.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 2.0 hours
  2. 2
    온도the reaction mixture was heated
  3. 3
    온도to reflux for 5 hours
  4. 4
    온도cooled
  5. 5
    기타Solvent was removed in vacuo
  6. 6
    기타chromatographed (5% MeOH/methylene chloride/1% NH4OH)

실험 절차

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% NH4OH) 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%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08846705B2uspto-grants-2014_09