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2,6-Difluorobenzoyl isocyanate → 1-(2,6-Difluorobenzoyl)-3-(6-methyl-5-phenyl-2-pyridyl)urea

HRID 1980321
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인쇄 미리보기

반응식

HRID 1980321 반응식
[CH3:1][C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[F:15][C:16]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:17]=1[C:18]([N:20]=[C:21]=[O:22])=[O:19]>C(OCC)(=O)C>[F:15][C:16]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:17]=1[C:18]([NH:20][C:21]([NH:8][C:6]1[CH:5]=[CH:4][C:3]([C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)=[C:2]([CH3:1])[N:7]=1)=[O:22])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27333692,6-Difluorobenzoyl isocyanateHCID 135028556-Methyl-5-phenylpyridin-2-amine

생성물 1

HCID 132426531-(2,6-Difluorobenzoyl)-3-(6-methyl-5-phenyl-2-pyridyl)urea

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

6-Methyl-5-phenyl-2-pyridylamine (500 mg) and 2,6-difluorobenzoyl isocyanate (650 mg) were reacted in 25 ml ethyl acetate. A precipitate formed which was filtered, dried, and identified as the desired product by NMR, m.p. 206°-208° C.

후처리

  • customA precipitate formed which
  • filtrationwas filtered
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-8ff3a61095794189a178b61ee56fcf9f
    출처 데이터셋
    uspto-grants-1985_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04508722

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