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Dimethylformamide → 1-(3-Chloro-2-pyridyl)-3-methyl-pyrazole-4-carbaldehyde

HRID 1517597
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HRID 1517597 반응식
[CH3:1][C:2]1[C:6]([CH:7]=[O:8])=[CH:5][NH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].FN1C=C[CH:19]=[CH:18][CH:17]1[Cl:22].[CH3:23][N:24]([CH3:27])C=O>O>[Cl:22][C:17]1[C:23]([N:4]2[CH:5]=[C:6]([CH:7]=[O:8])[C:2]([CH3:1])=[N:3]2)=[N:24][CH:27]=[CH:19][CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 866535441-Fluoro-2-chloropyridineHCID 1784345503-methyl-1H-pyrazole-4-carbaldehyde

생성물 1

HCID 582685431-(3-Chloro-2-pyridyl)-3-methyl-pyrazole-4-carbaldehyde수율 52%

시약·촉매·용매 1

HCID 962
Water
용매

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온도
40 °C

실험 절차

To a solution of 3-methyl-pyrazole-4-carbaldehyde (0.5 g, 4.5 mmol) in dry dimethylformamide (15 mL) is added potassium carbonate (2.5 g, 18 mmol,) at room temperature. The reaction mixture is stirred at 40° C. for 30 min and then 1-fluoro-2-chloropyridine (0.77 g, 6 mmol,) is added. The reaction mixture is heated at 70° C. for 16 h. After completion, the reaction mixture is cooled to room temperature, diluted with water and then extracted with ethyl acetate. The organic layer is dried over sodium sulfate, filtered and concentrated under reduce pressure. The crude mixture is purified by chromatography on silica gel eluting with hexane/ethyl acetate (75:25, 65:35) to yield 0.525 g (52%) of the title compound. MS (m/z): 222 (M+1).

후처리

  1. temperatureThe reaction mixture is heated at 70° C. for 16 h
  2. temperatureAfter completion, the reaction mixture is cooled to room temperature
  3. extractionextracted with ethyl acetate
  4. dry with materialThe organic layer is dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude mixture is purified by chromatography on silica gel eluting with hexane/ethyl acetate (75:25, 65:35)

출처 및 근거

ORD 기록
ord-b20cf038e506491fad97d4ca41cc6b6b
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232289B2

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