Dichloromethane → 1-(2-Amino-4-methylphenyl)-5-bromoindoline hydrochloride

HRID 4034

반응식

HRID 4034 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][C:12]=1[N+:18]([O-])=O)[CH2:6][CH2:5]2.[Cl:21]CCl>C(O)C.[Pt]>[ClH:21].[NH2:18][C:12]1[CH:13]=[C:14]([CH3:17])[CH:15]=[CH:16][C:11]=1[N:7]1[C:8]2[C:4](=[CH:3][C:2]([Br:1])=[CH:10][CH:9]=2)[CH2:5][CH2:6]1

참가 물질

5

실험 절차

To a warm solution of 4-(5-bromo-1-indolinyl)-3-nitrotoluene (10 g, 0.03 mole) in dichloromethane (40 ml) and ethanol (160 ml) was added 1% platinum-on-carbon (2.0 gm). The mixture was shaken under hydrogen (57 psi) for 3.5 hours. The mixture was filtered and concentrated. The residue was dried under vacuum at 55° C. Purification was accomplished by flash chromatography over silica gel (100 g), eluted with a mixture of hexane:dichloromethane (3:1, 2 l and 1:1, 1 l). The fractions containing pure product were pooled and concentrated. The residue was dissolved in ether (250 ml) and added to a methanol/hydrogen chloride solution, and the mixture was stirred at 0° C. for 10 minutes. The precipitate was filtered and dried to afford 4.0 g (39%) of product, mp 195°-200° C. dec.

후처리

  1. filtrationThe mixture was filtered
  2. concentrationconcentrated
  3. customThe residue was dried under vacuum at 55° C
  4. customPurification
  5. washeluted with a mixture of hexane:dichloromethane (3:1, 2 l and 1:1, 1 l)
  6. additionThe fractions containing pure product
  7. concentrationconcentrated
  8. dissolutionThe residue was dissolved in ether (250 ml)
  9. additionadded to a methanol/hydrogen chloride solution
  10. stirringthe mixture was stirred at 0° C. for 10 minutes
  11. filtrationThe precipitate was filtered
  12. customdried

출처 및 근거

ORD 기록
ord-b9a65ccb0ddb418c83d873e96b8bd48d
출처 데이터셋
uspto-grants-1988_02
특허 번호
US04723007

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