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Ammonia → 4-Chloro-2,6-diphenyl-2H-pyrazolo[3,4-b]pyridine

HRID 2071648
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HRID 2071648 반응식
[C:1]1([N:7]2[CH:15]=[C:14]3[C:9]([N:10]=[C:11]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[CH:12]=[C:13]3O)=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)([Cl:25])=O.N>>[Cl:25][C:13]1[C:14]2[C:9](=[N:8][N:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[CH:15]=2)[N:10]=[C:11]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 222AmmoniaHCID 24813Phosphorus oxychlorideHCID 178515555HCID 178515555, 화합물

생성물 1

HCID 227568644-Chloro-2,6-diphenyl-2H-pyrazolo[3,4-b]pyridine

실험 절차

5.5 g. of 2,6-diphenyl-2H-pyrazolo[3,4-b]pyridin-4-ol (0.019 mol.) and 27.5 ml. of phosphorus oxychloride are refluxed with stirring for 90 minutes. The colled mixture is poured onto crushed ice, then made alkaline with concentrated aqueous ammonia while adding ice. The collected 4-chloro-2,6-diphenyl-2H-pyrazolo[3,4-b]pyridine is washed with water and dried at 80°; m.p. 175°-177°. A sample, recrystallized from ethanol, melts at 176°-178°; yield: 5 g. (86%).

후처리

  1. additionThe colled mixture is poured
  • customonto crushed ice
  • additionwhile adding ice
  • washThe collected 4-chloro-2,6-diphenyl-2H-pyrazolo[3,4-b]pyridine is washed with water
  • customdried at 80°
  • customA sample, recrystallized from ethanol, melts at 176°-178°
  • 출처 및 근거

    ORD 기록
    ord-478dc955b9eb4427856d5eaf6c96db29
    출처 데이터셋
    uspto-grants-1977_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04048184

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