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Sodium hydride → Ethyl 3-amino-2-(2-oxopentyl)pyrazol-4-carboxylate

HRID 274565
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HRID 274565 반응식
[H-].[Na+].[NH2:3][C:4]1[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:7][NH:6][N:5]=1.Br[CH2:15][C:16](=[O:20])[CH2:17][CH2:18][CH3:19]>CN(C=O)C>[NH2:3][C:4]1[N:5]([CH2:15][C:16](=[O:20])[CH2:17][CH2:18][CH3:19])[N:6]=[CH:7][C:8]=1[C:9]([O:11][CH2:12][CH3:13])=[O:10]
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참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 100578691-Bromopentan-2-oneHCID 178469928HCID 178469928, 화합물

생성물 1

HCID 20092995Ethyl 3-amino-2-(2-oxopentyl)pyrazol-4-carboxylate수율 45.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a mixture of sodium hydride (60% dispersion in mineral oil, 0.8 g) in DMF (50 ml) was added ethyl 3-amino-pyrazol-4-carboxylate (2.0 g) and the reaction mixture was stirred at room temperature for 15 minutes. After addition of 1-bromo-2-pentanone (4.0 g), the mixture was stirred at room temperature for 13 hours. The reaction mixture was concentrated to dryness, and the residue was dissolved in ethyl acetate-water. The organic layer was washed with water, dried and concentrated to dryness. The resulting yellow syrup was purified by column chromatography on silica gel to give pale yellow prisms (1.4 g, 45%).

후처리

  1. stirringthe mixture was stirred at room temperature for 13 hours
  2. concentrationThe reaction mixture was concentrated to dryness
  3. dissolutionthe residue was dissolved in ethyl acetate-water
  4. washThe organic layer was washed with water
  5. customdried
  6. concentrationconcentrated to dryness
  7. customThe resulting yellow syrup was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-f983fe279efb4c8381f2729c0fd64fb7
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05389641

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