Water → 1-(diphenylmethyl)-4-fluoro-1H-indole-2,3-dione

HRID 1965358노트

반응식

HRID 1965358 반응식
[C:1]1([CH:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:8]2[C:16]3[C:11](=[C:12]([F:17])[CH:13]=[CH:14][CH:15]=3)[C:10](I)=[CH:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.I([O-])(=O)(=O)=[O:26].[Na+].[OH2:31]>C(#N)C.C(OCC)(=O)C.O.[Ru](Cl)(Cl)Cl>[C:1]1([CH:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:8]2[C:16]3[C:11](=[C:12]([F:17])[CH:13]=[CH:14][CH:15]=3)[C:10](=[O:31])[C:9]2=[O:26])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

7

실험 절차

To a solution of 1-(diphenylmethyl)-3-iodo-4-fluoroindole (8.85 g, 20.7 mmol) in a mixture of acetonitrile (25 mL) and water (5 mL) was added ruthenium (III) chloride monohydrate (0.30 g, 1.45 mmol) and sodium periodate (13.3 g, 62.2 mmol). The reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was diluted with ethyl acetate (100 mL), washed with water (3×25 mL), saturated aqueous ammonium chloride (3×25 mL) and brine (3×25 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was crystallized from acetonitrile to afford 1-(diphenylmethyl)-4-fluoro-1H-indole-2,3-dione (1.73 g, 25%) as an orange solid: mp 168-171° C.; 1H NMR (300 MHz, DMSO-d6) δ 7.49-7.41 (m, 1H), 7.38-7.28 (m, 10H), 6.86 (dd, J=8.8, 8.8 Hz, 1H), 6.80 (s, 1H), 6.45 (d, J=8.1 Hz, 1H); 13C NMR (75 MHz, DMSO-d6) δ 178.3, 157.8, 157.7 (d, 1JC-F=261.0 Hz), 150.6 (d, 3JC-F=6.0 Hz), 139.7 (d, 2JC-F=10.0 Hz), 137.0, 128.5, 128.3, 127.8, 110.7 (d, 2JC-F=19.5 Hz), 108.8 (d, 4JC-F=2.9 Hz), 106.4 (d, JC-F=18.2 Hz), 28.7; MS (ES+) m/z 332.2 (M+23).

후처리

  1. washwashed with water (3×25 mL), saturated aqueous ammonium chloride (3×25 mL) and brine (3×25 mL)
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was crystallized from acetonitrile

출처 및 근거

ORD 기록
ord-3cd0e585dfcd4e738a2980b43dec6ac8
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08415370B2

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