N,N'-Dimethylethylenediamine → 4-(cyclopropylsulfonyl)-1H-pyrazolo[3,4-b]pyridine

HRID 1802889노트

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HRID 1802889 반응식
I[C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[NH:8][N:9]=[CH:10][C:3]=12.CNCCNC.[CH:17]1([S:20]([O-:22])=[O:21])[CH2:19][CH2:18]1.[Na+].C(=O)([O-])[O-].[K+].[K+]>CS(C)=O.[Cu]I>[CH:17]1([S:20]([C:2]2[CH:7]=[CH:6][N:5]=[C:4]3[NH:8][N:9]=[CH:10][C:3]=23)(=[O:22])=[O:21])[CH2:19][CH2:18]1

참가 물질

7

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온도
100 °C

실험 절차

To a solution of 4-iodo-1H-pyrazolo[3,4-b]pyridine (5.2 g) in dimethyl sulfoxide (70 mL) were added N,N′-dimethylethylenediamine (114 μL), copper (I) iodide (202 mg), sodium cyclopropanesulfinate (8.16 g) and potassium carbonate (5.06 g) at room temperature under argon atmosphere, and the mixture was stirred at 100° C. for 16 hr. The reaction mixture was filtered, water was added to the filtrate, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (0.42 g, yield 9%) as yellow crystals from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). MS: 224 (MH+).

후처리

  1. filtrationThe reaction mixture was filtered
  2. additionwater was added to the filtrate
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe ethyl acetate layer was washed with saturated brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0a58d9542a994a4c8bc0e0482c449355
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08349886B2

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