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4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-6-methoxy-7-benzyloxyquinoline → HCID 136029933, 화합물

HRID 1510104
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인쇄 미리보기

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HRID 1510104 반응식
[F:1][C:2]1[C:10]([O:11][C:12]2[C:21]3[C:16](=[CH:17][C:18]([O:24]CC4C=CC=CC=4)=[C:19]([O:22][CH3:23])[CH:20]=3)[N:15]=[CH:14][CH:13]=2)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:32])[NH:6]2>[Pd]>[F:1][C:2]1[C:10]([O:11][C:12]2[C:21]3[C:16](=[CH:17][C:18]([OH:24])=[C:19]([O:22][CH3:23])[CH:20]=3)[N:15]=[CH:14][CH:13]=2)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:32])[NH:6]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 592007474-(4-fluoro-2-methyl-1H-indol-5-yloxy)-6-methoxy-7-benzyloxyquinoline

생성물 1

HCID 136029933HCID 136029933, 화합물수율 84.4%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

4-(4-Fluoro-2-methyl-1H-indol-5-yloxy)-6-methoxy-7-benzyloxyquinoline (600 mg) was mixed with HCONH4 (600 mg) and Pd/C (10%, 100 mg) followed by refluxing 30 min. The reaction was filtered while it was hot and the filtrate was evaporated and washed with water followed by filtration to give 4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-6-methoxy-7-hydroxyquinoline (400 mg).

후처리

  1. temperatureby refluxing 30 min
  2. filtrationThe reaction was filtered while it
  • customthe filtrate was evaporated
  • washwashed with water
  • filtrationfollowed by filtration
  • 출처 및 근거

    ORD 기록
    ord-6c1a8a71c276453f8465a3665428d815
    출처 데이터셋
    uspto-grants-2012_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08211911B2

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