Dimethylformamide → 1-Benzyl-7-chloro-5-methyl-1,5-dihydroimidazo[4,5-d]pyridazin-4-one

HRID 501432노트

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HRID 501432 반응식
[C:1](=[O:4])([O-])[O-].[K+].[K+].CI.CN(C)C=O.[CH2:14]([N:21]1[C:25]2[C:26]([Cl:31])=[N:27][NH:28][C:29](=O)[C:24]=2[N:23]=[CH:22]1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>O.C(OCC)(=O)C>[CH2:14]([N:21]1[C:25]2[C:26]([Cl:31])=[N:27][N:28]([CH3:29])[C:1](=[O:4])[C:24]=2[N:23]=[CH:22]1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1

참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 574728331-Benzyl-7-chloro-1,5-dihydroimidazo[4,5-d]pyridazin-4-one

생성물 1

HCID 574728321-Benzyl-7-chloro-5-methyl-1,5-dihydroimidazo[4,5-d]pyridazin-4-one수율 25.7%

시약·촉매·용매 2

HCID 962Water용매HCID 8857Ethyl Acetate용매

실험 절차

0.604 g of potassium carbonate and 0.297 ml of methyl iodide were added to a 30 ml N,N-dimethylformamide solution of 1.035 g of 1-benzyl-7-chloro-1,5-dihydroimidazo[4,5-d]pyridazin-4-one (J. A. Carbon Journal of the American Chemical Society, 80, pp. 6083, 1958), and the mixture was stirred at room temperature for 15 hours. 300 ml of ethyl acetate and 100 ml of water were added to the solution, and the organic layer was washed twice with 100 ml of water and then with 100 ml of a saturated sodium chloride solution. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography. Thus, 0.280 g of the title compound was obtained from the fraction eluted with ethyl acetate.

후처리

  1. washthe organic layer was washed twice with 100 ml of water
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-9c0c6ae43fd34ef1b22b194146871b42
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07772226B2

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