반응 #512135

ord-48853fc76d1143189b398831ff2e41fb

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도To a cooled
  2. 2
    기타the temperature below 5° C
  3. 3
    기타was consumed
  4. 4
    workup.ADDITIONH2O (400 mL) was added slowly to the reaction mixture
  5. 5
    workup.ADDITIONfollowed by addition of IPAc (500 mL)
  6. 6
    workup.STIRRINGThe resulting mixture was stirred for 5 min.
  7. 7
    기타the organic layer was separated
  8. 8
    세척The organic layer was then washed with 20% brine (3×200 mL)
  9. 9
    건조dried over Na2SO4
  10. 10
    workup.ADDITIONtreated with activated carbon
  11. 11
    여과After filtration
  12. 12
    농축the filtrate was concentrated under reduced pressure

실험 절차

To a cooled (0° C.) suspension of KO-tBu (95%, 7.8 g, 66 mmol) in NMP (150 mL) was added a solution of 4-bromo-2-[4-(2-methyl-pyrrolidin-1-yl)-but-1-ynyl]-phenylamine (10 g, 33 mmol) in NMP (50 mL) dropwise keeping the temperature below 5° C. The resulting mixture was then stirred at room temperature for 3 hours under nitrogen. HPLC indicated that all the starting material was consumed. H2O (400 mL) was added slowly to the reaction mixture followed by addition of IPAc (500 mL). The resulting mixture was stirred for 5 min. and the organic layer was separated. The organic layer was then washed with 20% brine (3×200 mL), dried over Na2SO4 and treated with activated carbon. After filtration, the filtrate was concentrated under reduced pressure to give the title compound as a thick oil (6.2 g), which was used in the next coupling reaction without further purification. 1H NMR (400 MHz, CDCl3) δ 10.21 (s, 1H), 7.73 (s, 1H), 7.27 (s, 2H), 6.24 (s, 1H), 3.42-3.50 (m, 1H), 3.21-3.28 (m, 1H), 2.97-3.10 (m, 2H), 2.49-2.60 (m, 2H), 2.33 (q, J=8.78 Hz, 1H), 2.10-2.17 (m, 1H), 1.87-2.02 (m, 2H), 1.58-1.67 (m, 1H), 1.24 (d, J=6.2 Hz, 3H). 13C NMR (400 MHz, CDCl3) δ 140.89, 133.92, 129.91, 122.98, 121.77, 112.16, 111.75, 98.32, 60.47, 53.60, 53.34, 33.19, 26.30, 22.14, 19.56. [M+H]+ at m/z 307.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08106088B2uspto-grants-2012_01