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

HRID 1980312
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인쇄 미리보기

반응식

HRID 1980312 반응식
[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[C:3]=1[C:4]([N:6]=[C:7]=[O:8])=[O:5].[CH3:14][C:15]1[N:20]=[C:19]([NH2:21])[CH:18]=[CH:17][C:16]=1[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>C(OCC)(=O)C>[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[C:3]=1[C:4]([NH:6][C:7]([NH:21][C:19]1[CH:18]=[CH:17][C:16]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[C:15]([CH3:14])[N:20]=1)=[O:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 129127392,6-Dichlorobenzoyl isocyanateHCID 135028556-Methyl-5-phenylpyridin-2-amine

생성물 1

HCID 132426501-(2,6-Dichlorobenzoyl)-3-(6-methyl-5-phenyl-2-pyridyl)urea

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

2,6-Dichlorobenzoyl isocyanate (650 mg) was reacted with 6-methyl-5-phenyl-2-pyridylamine (500 mg) in 25 ml of ethyl acetate. A precipitate formed which was filtered and confirmed by NMR as the desired product, 219°-220° C.

후처리

  • customA precipitate formed which
  • filtrationwas filtered
  • customconfirmed by NMR as the desired product, 219°-220° C.
  • 출처 및 근거

    ORD 기록
    ord-3eef636f0cbf480d896d904fc2f6a5f8
    출처 데이터셋
    uspto-grants-1985_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04508722

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