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Hydrochloric Acid → HCID 135848110, 화합물

HRID 498070
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인쇄 미리보기

반응식

HRID 498070 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]2[N:12]([C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([CH3:22])[N:17]=3)[N:13]=[C:14]([CH3:15])[C:3]=12.Cl.C([OH:26])C>>[CH3:15][C:14]1[C:3]2[C:2](=[O:26])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[NH:5][C:4]=2[N:12]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([CH3:22])[N:17]=2)[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 22320337HCID 22320337, 화합물

생성물 1

HCID 135848110HCID 135848110, 화합물수율 82%

실험 절차

To a solution of 4-chloro-3-methyl-1-(6-methyl-2-pyridinyl)-1H-pyrazolo[3,4-b]quinoline (2.00 g, 6.48 mmol) in ethanol (90 mL), 6N hydrochloric acid (3 mL, 18.0 mmol) was added and the mixture was heated under reflux for 4 hours. The reaction solution was allowed to cool to room temperature, and the resulting crystals were collected by filtration. The crystals were washed with ethanol, air dried, and recrystallized from ethanol to give the title compound (1.55 g, 82% yield).

후처리

  1. temperaturethe mixture was heated
temperature
under reflux for 4 hours
  • filtrationthe resulting crystals were collected by filtration
  • washThe crystals were washed with ethanol, air
  • customdried
  • customrecrystallized from ethanol
  • 출처 및 근거

    ORD 기록
    ord-31c94a7da8404d2791999d6ed6f7299b
    출처 데이터셋
    uspto-grants-2005_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06949648B2

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