Stannous Chloride → Ethyl 6-amino-1H-indole-4-carboxylate
反応式
[CH2:1]([O:3][C:4](=[O:22])[C:5]1[CH:10]=[C:9]([N+:11]([O-])=O)[CH:8]=[C:7]([N+]([O-])=O)[C:6]=1[CH:17]=[CH:18][N:19](C)C)[CH3:2].Cl[Sn]Cl>C(O)C>[CH2:1]([O:3][C:4]([C:5]1[C:6]2[CH:17]=[CH:18][NH:19][C:7]=2[CH:8]=[C:9]([NH2:11])[CH:10]=1)=[O:22])[CH3:2]参加物
実験手順
A mixture of 2-(2-dimethylamino-vinyl)-3,5-dinitro-benzoic acid ethyl ester (11.3 g, 0.037 mol) and SnCl2 (83 g. 0.37 mol) in ethanol was heated at reflux for 4 h. The mixture was concentrated to dryness and the residue was poured into water and basified with sat. Na2CO3 solution to pH 8. The precipitate was filtered off and the filtrate was extracted with ethyl acetate (3×100 mL). The combined extracts were washed with water (2×100 mL) and brine (150 mL), dried over Na2SO4 and concentrated to dryness. The residue was purified by column chromatography on silica gel to give 6-amino-1H-indole-4-carboxylic acid ethyl ester (B-18) (3 g, 40%). 1H NMR (DMSO-d6) δ 10.76 (br s, 1H), 7.11-7.14 (m, 2H), 6.81-6.82 (m, 1H), 6.67-6.68 (m, 1H), 4.94 (br s, 2H), 4.32-4.25 (q, J=7.2 Hz, 2H), 1.35-1.31 (t, J=7.2, 3 H). ESI-MS 205.0 m/z (MH+).
後処理
- temperaturewas heated
- temperatureat reflux for 4 h
- concentrationThe mixture was concentrated to dryness
- additionthe residue was poured into water and basified with sat. Na2CO3 solution to pH 8
- filtrationThe precipitate was filtered off
- extractionthe filtrate was extracted with ethyl acetate (3×100 mL)
- washThe combined extracts were washed with water (2×100 mL) and brine (150 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated to dryness
- customThe residue was purified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-cadaadd4fc7a498dac18a8d6d37a65cc
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08741925B2
反応ノート
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