반응 #61219

ord-b90a12c4f7ff48cb872cf782cb15a5a0

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The flask was fitted with a septum
  2. 2
    온도the reaction maintained
  3. 3
    workup.STIRRINGwith stirring at 50-60° C. for four hours
  4. 4
    기타The solution was evaporated
  5. 5
    기타the residue purified by column chromatography

실험 절차

To a 50 mL round-bottom flask were added N-(5-chloro-4-fluoro-2-iodo-phenyl)-methanesulfonamide (0.30 g, 1.0 mmol), bis(triphenylphosphine) palladium(II) chloride (35 mg, 0.05 mmol) and copper (I) iodide (19 mg, 0.1 mmol). The flask was fitted with a septum and stirred under argon. Tetrahydrofuran (5 mL) and triethylamine (0.28 mL, 2.0 mmol) were then added via syringe. 1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol (0.14 g, 1.0 mmol) in tetrahydrofuran (1 mL) was added via syringe and the reaction maintained with stirring at 50-60° C. for four hours. The solution was evaporated and the residue purified by column chromatography using dichloromethane as solvent to yield the title compound as a brown oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07427682B2uspto-grants-2008_09