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Ammonium Hydroxide → 1-ethyl-3-methyl-4-chloro-1H-pyrazolo[3,4-b]quinoline

HRID 375848
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HRID 375848 반응식
[CH2:1]([N:3]1[C:7]([NH:8][C:9]2[C:10](=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:11](O)=O)=[CH:6][C:5]([CH3:18])=[N:4]1)[CH3:2].[NH4+].[OH-].O=P(Cl)(Cl)[Cl:23]>>[Cl:23][C:11]1[C:10]2[C:9](=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:8]=[C:7]2[N:3]([CH2:1][CH3:2])[N:4]=[C:5]([CH3:18])[C:6]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 14923Ammonium HydroxideHCID 24813Phosphorus oxychlorideHCID 19592214HCID 19592214, 화합물

생성물 1

HCID 195922341-ethyl-3-methyl-4-chloro-1H-pyrazolo[3,4-b]quinoline수율 95%

실험 절차

A mixture of N-(1-ethyl-3-methylpyrazol-5-yl) anthranilic acid (7.0 g), 28.57 mmol) and POCl3 (210 ml) was refluxed for 24 hours. The reaction mixture was cooled to room temperature, poured into ice-water and neutralized with concentrated NH4OH to a pH of 8.0. The product which slowly crystallized from the solution was collected by filtration, washed with water and dried to afford 6.7 g (95%) of 4-chloro-1-ethyl-3-methyl-1H-pyrazolo[3,4-b]quinoline.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • temperaturewas refluxed for 24 hours
  • customThe product which slowly crystallized from the solution
  • filtrationwas collected by filtration
  • washwashed with water
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-6200b5fb9d6f43bcb023ffcc03f6d07c
    출처 데이터셋
    uspto-grants-1996_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05488055

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