반응 #43546

ord-dbc008b6d4344431a0479a5e6a29980f

반응 방정식

O
water
O=C1Nc2ccc(F)cc2C1=O
5-Fluoro-1H-indole-2,3-dione
[H-].[Na+]
sodium hydride
COc1ccc(CCl)cc1
p-methoxybenzyl chloride
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
수율 80.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe solution was then stirred ca 2 hours
  2. 2
    추출followed by extraction into ethyl acetate
  3. 3
    세척The organic layer was washed twice with water
  4. 4
    건조dried over MgSO4

실험 절차

5-Fluoro-1H-indole-2,3-dione (956 mg, 5.79 mmol, 1 eq) was added as a solution in dry DMF to a stirred slurry of sodium hydride (278 mg, 11.6 mmol, 2 eq) in dry DMF drop wise over 15 minutes under an inert atmosphere with adequate pressure release to accommodate H2 evolution. The resulting mixture was stirred for 1 hour and p-methoxybenzyl chloride was added via syringe to the reaction. The solution was then stirred ca 2 hours and worked up by addition of water followed by extraction into ethyl acetate. The organic layer was washed twice with water and then dried over MgSO4. Column chromatography with ethyl acetate/hexane afforded 5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione as a red solid (1.3 g, 80% yield). 1H NMR (CDCl3) δ (ppm): 7.3-7.24 (m, 3H), 7.20 (td, J=8.7, 2.7 Hz, 1H), 6.9-6.86 (m, 2H), 6.76 (dd, J=8.6, 3.6 Hz, 1H), 3.81 (s, 2H), 3.78 (s, 3H). LC/MS=286.1 (M+1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732449B2uspto-grants-2010_06