반응 #710543

ord-53e25d3de96844c2932dadfc8b8c4d5b

반응 방정식

O
water
Fc1ccc(CBr)cc1
4-Fluorobenzyl bromide
CC(C)CNS(=O)(=O)c1ccc(Br)cc1
4-bromo-N-isobutyl-benzenesulfonamide
[H-].[Na+]
NaH
CC(C)CN(Cc1ccc(F)cc1)S(=O)(=O)c1ccc(Br)cc1
4-bromo-N-(4-fluoro-benzyl)-N-isobutyl-benzenesulfonamide
수율 78.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타reaction
  2. 2
    온도heated at 90° C. for 2 hours
  3. 3
    workup.WAITThe reaction was left
  4. 4
    온도to cool to room temperature
  5. 5
    추출extracted with DCM
  6. 6
    여과filtered through a phase separator
  7. 7
    농축concentrated
  8. 8
    기타purified by silica gel column chromatography (0-25% DCM in cyclohexane)

실험 절차

To a solution of 4-bromo-N-isobutyl-benzenesulfonamide (0.25 g, 856 μmol) in anhydrous dimethylacetamide (5 mL) was added NaH (60% dispersion in mineral oil, 37.7 mg, 942 μmol) and the mixture was stirred at room temperature for 15 minutes. 4-Fluorobenzyl bromide (117 μL, 942 μmol) was added and reaction heated at 90° C. for 2 hours. The reaction was left to cool to room temperature, water added and then extracted with DCM, filtered through a phase separator, concentrated and purified by silica gel column chromatography (0-25% DCM in cyclohexane) to give 4-bromo-N-(4-fluoro-benzyl)-N-isobutyl-benzenesulfonamide (267 mg, 78%) 1H NMR (300 MHz, CDCl3): δ 7.65-7.66 (m, 4 H), 7.23 (m, 2 H), 6.99 (t, 2 H), 4.27 (s, 2 H), 2.89 (d, 2 H), 1.64 (dt, 1 H), 0.74 (d, 6 H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09302985B2uspto-grants-2016_04