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Bromine → 5-Bromo-1-phenyl-1H-pyrazolo[3,4-b]pyridin-6(7H)-one

HRID 1263489
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반응식

HRID 1263489 반응식
[Br:1]Br.[C:3]1([N:9]2[C:13]3[NH:14][C:15](=[O:18])[CH:16]=[CH:17][C:12]=3[CH:11]=[N:10]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)(=O)C.O>[Br:1][C:16]1[C:15](=[O:18])[NH:14][C:13]2[N:9]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:10]=[CH:11][C:12]=2[CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24408BromineHCID 1358542821-phenyl-7H-pyrazolo[5,4-b]pyridin-6-one

생성물 1

HCID 1358542805-Bromo-1-phenyl-1H-pyrazolo[3,4-b]pyridin-6(7H)-one수율 68%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

Bromine (76 μl, 1.47 mmol) was added to a solution of 1-phenyl-1,7-dihydropyrazolo[3,4-b]pyridin-6-one (0.31 g, 1.47 mmol) in acetic acid (7 ml) and the mixture was stirred for 30 min. The suspension was diluted with water, stirred for 10 min and then the precipitate filtered off, washing with water. The product was dried in a desiccator at 40° C. under vacuum for 17 h to give 5-bromo-1,7-dihydro-1-phenylpyrazolo[3,4-b]pyridin-6-one (0.29 g, 68%) as a brown solid. δH (400 MHz; DMSO) 7.32-7.37 (1H, m), 7.52-7.58 (2H, m), 8.12-8.24 (3H, m), 8.50 (1H, s); m/z (ES+) 290 (M+H+), 292 (M+H+).

후처리

  1. stirringstirred for 10 min
  2. filtrationthe precipitate filtered off
  3. washwashing with water
  4. customThe product was dried in a desiccator at 40° C. under vacuum for 17 h

출처 및 근거

ORD 기록
ord-952c512eebfc4b449c4344bdad50592d
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06541484B2

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