Ethyl 2-formyl-3-oxopropanoate → 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester

HRID 491851

반응식

HRID 491851 반응식
[CH2:1]([O:3][C:4](=[O:10])[CH:5]([CH:8]=O)[CH:6]=O)[CH3:2].Cl.[NH:12]([C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][C:22]=1[CH3:23])[C:17]([OH:19])=[O:18])[NH2:13]>CCO>[CH2:1]([O:3][C:4]([C:5]1[CH:8]=[N:13][N:12]([C:14]2[CH:15]=[C:16]([C:17]([OH:19])=[O:18])[CH:20]=[CH:21][C:22]=2[CH3:23])[CH:6]=1)=[O:10])[CH3:2]

참가 물질

4

실험 절차

A solution of 2-formyl-3-oxo-propionic acid ethyl ester (S. H. Bertz et al., J. Org. Chem., 1982, 47, 2216) (1.44 g, 10 mmol) in EtOH (10 mL) was cooled in an ice bath. A slurry of 3-hydrazino-4-methyl-benzoic acid hydrochloride (2.02 g, 10 mmol) in EtOH (50 mL) was added and the reaction was stirred overnight. The EtOH was removed under reduced pressure and the residue partitioned between water and CH2Cl2. The layers were separated and the organic layer washed with brine. The organic layer was dried over Na2SO4, filtered, and concentrated. Hexanes were added and the solution concentrated. The resulting solid was collected by vacuum filtration, washed with hexanes and dried under vacuum to provide 1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester (1.86 g, 68%) as a yellow solid: ESI MS m/z 275 [C14H14N2O4+H]+.

후처리

  1. customThe EtOH was removed under reduced pressure
  2. customthe residue partitioned between water and CH2Cl2
  3. customThe layers were separated
  4. washthe organic layer washed with brine
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. additionHexanes were added
  9. concentrationthe solution concentrated
  10. filtrationThe resulting solid was collected by vacuum filtration
  11. washwashed with hexanes
  12. customdried under vacuum

출처 및 근거

ORD 기록
ord-c22620a1782542e7943f04f163d8a864
출처 데이터셋
uspto-grants-2009_05
특허 번호
US07531560B2

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