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Ethyl 4-(dimethylamino)-2-oxo-but-3-enoate → Ethyl 1-(2-methoxyethyl)-1H-pyrazole-5-carboxylate

HRID 2100361
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HRID 2100361 반응식
Cl.[CH3:2][O:3][CH2:4][CH2:5][NH:6]N.[CH2:8]([O:10][C:11](=[O:19])[C:12](=O)[CH:13]=[CH:14][N:15](C)C)[CH3:9]>C(O)C>[CH2:8]([O:10][C:11]([C:12]1[N:6]([CH2:5][CH2:4][O:3][CH3:2])[N:15]=[CH:14][CH:13]=1)=[O:19])[CH3:9]
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참가 물질

4

반응물 2

HCID 2777802Ethyl 4-(dimethylamino)-2-oxo-but-3-enoateHCID 71305269(2-Methoxyethyl)hydrazine hydrochloride

생성물 1

HCID 57799147Ethyl 1-(2-methoxyethyl)-1H-pyrazole-5-carboxylate

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
60 °C

실험 절차

2-Methoxyethylhydrazine hydrochloride (Ref: J. Med. Chem. (1967) 11 (1) 79-83) (1.07 g, 8.5 mmol) and ethyl-4-dimethylamino-2-oxo-but-3-enoate (1.5 g, 8.5 mmol) were dissolved in ethanol (10 ml) and heated at 60° C. for 7 hours. The solvent was evaporated in vacuo and the residue was partitioned between ethyl acetate (80 ml) and dilute sodium carbonate solution (40 ml). The organic layer was dried over anhydrous Na2SO4 and the solvent removed in vacuo to give a brown gum. This material was chromatographed on silica gel (30 g) using 40% to 20% heptane in ethyl acetate. The higher running product was collected to give 2-(2-methoxyethyl)-2H-pyrazole-3-carboxylic acid ethyl ester as 750 mg of a mobile yellow oil. The lower running product was collected to give 1-(2-methoxyethyl)-1H-pyrazole-3-carboxylic acid ethyl ester as 360 mg of a yellow oil.

후처리

  1. customThe solvent was evaporated in vacuo
  2. customthe residue was partitioned between ethyl acetate (80 ml) and dilute sodium carbonate solution (40 ml)
  3. dry with materialThe organic layer was dried over anhydrous Na2SO4
  4. customthe solvent removed in vacuo
  5. customto give a brown gum
  6. customThis material was chromatographed on silica gel (30 g)
  7. customwas collected

출처 및 근거

ORD 기록
ord-ca9d32ab03e44d54b52dc9c927f39d05
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572797B2

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