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3-Chloro-3-phenyl-2-propenal → Phenyl(7-phenylpyrazolo[1,5-a]pyrimidin-3-yl)methanone

HRID 1247946
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인쇄 미리보기

반응식

HRID 1247946 반응식
Cl[C:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[CH:3][CH:4]=O.[NH2:12][C:13]1[C:17]([C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:19])=[CH:16][NH:15][N:14]=1>C(O)(=O)C>[C:20]1([C:18]([C:17]2[CH:16]=[N:15][N:14]3[C:2]([C:6]4[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=4)=[CH:3][CH:4]=[N:12][C:13]=23)=[O:19])[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 383893-Chloro-3-phenyl-2-propenalHCID 178509267HCID 178509267, 화합물

생성물 1

HCID 13475886Phenyl(7-phenylpyrazolo[1,5-a]pyrimidin-3-yl)methanone

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 0.01 mole of 3-chloro-3-phenyl-2-propenal and 0.01 mole of (3-amino-1H-pyrazol-4-yl)phenyl-methanone in 25 ml of acetic acid was refluxed for 6 hours. The solvent was removed in vacuo and the product isolated as described in Example 1, giving the desired product as crystals, mp 163°-165° C.

후처리

  1. temperaturewas refluxed for 6 hours
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customThe solvent was removed in vacuo
  • customthe product isolated
  • 출처 및 근거

    ORD 기록
    ord-ce205ec633b54248a0728969eba33ce2
    출처 데이터셋
    uspto-grants-1985_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04521422

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