반응 #1483071

ord-2fced6258af3412ca0e81b9001da9f94

반응 방정식

COC(=O)c1ccc2cc[nH]c2c1
1H-indole-6-carboxylic acid methyl ester
O=[N+]([O-])c1cccc(CBr)c1
3-nitrobenzyl bromide
O=C([O-])[O-].[K+].[K+]
K2CO3
COC(=O)c1ccc2ccn(Cc3cccc([N+](=O)[O-])c3)c2c1
1-(3-nitrobenzyl)-1H-indole-6-carboxylic acid methyl ester
수율 76.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with water (3×50 ml)
  2. 2
    건조The organic layer was dried (MgSO4)
  3. 3
    여과filtered
  4. 4
    농축concentrated
  5. 5
    기타The remaining residue was recrystallized with ethyl acetate/hexane

실험 절차

To a solution of 1H-indole-6-carboxylic acid methyl ester (1.0 g, 5.7 mmol) and 3-nitrobenzyl bromide (1.48 g, 6.8 mmol) in DMF (15 mL) was added K2CO3 (1.6 g, 11.4 mmol). After stirring at room temperature for 16 hr, the solution was diluted with ethyl acetate (100 ml) and washed with water (3×50 ml). The organic layer was dried (MgSO4), filtered and concentrated. The remaining residue was recrystallized with ethyl acetate/hexane to provide 1.34 g (76% yield) of 1-(3-nitrobenzyl)-1H-indole-6-carboxylic acid methyl ester as light orange crystals. 1H NMR (300 MHz, DMSO) δ 8.13 (m, 2H), 8.03 (s, 1H), 7.81 (d, 1H, J=3.0 Hz), 7.67-7.54 (m, 4H, J=9.0 Hz), 6.65 (d, 1H, J=3.0 Hz), 5.73 (s, 2H), 3.81 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08900565B2uspto-grants-2014_12