Sulfuric Acid → o-(1-Hydroxy-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)benzoic acid

HRID 249191

반응식

HRID 249191 반응식
[OH-].[Na+].[CH3:3][C:4]([NH:12][C:13]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[C:16](=[O:23])[O:15][N:14]=1)([CH:9]([CH3:11])[CH3:10])[C:5]([O:7]C)=O.[O:24]1CCCC1.S(=O)(=O)(O)O>O.C(Cl)Cl>[OH:15][N:14]1[C:5](=[O:7])[C:4]([CH:9]([CH3:11])[CH3:10])([CH3:3])[N:12]=[C:13]1[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=1[C:16]([OH:23])=[O:24]

참가 물질

7

반응 조건

온도
45 °C

실험 절차

Sodium hydroxide (0.58 g, 0.0145 mol) in water is added to a solution of methyl 2,3-dimethyl-2-[(1-oxo-2,3-benzoxazin-4-yl)amino]butyrate (2.0 g, 0.00689 mol) and tetrahydrofuran under a nitrogen atmosphere. The reaction mixture is stirred at 45° C. for 36 hours then at room temperature for 6 days. The reaction mixture is concentrated in vacuo to give an oil. The oil is dissolved into water. The aqueous solution is cooled with an ice-bath and concentrated sulfuric acid is added until a pH of about 1 is obtained then the solution is extracted with ethyl acetate. The combined ethyl acetate extracts are dried with anhydrous magnesium sulfate and concentrated in vacuo to give a pale yellow solid. The solid is added to boiling methylene chloride and after 2/3 of the methylene chloride has evaporated, the mixture is filtered to give the title compound as a white solid (1.44 g, 76%), mp 186°-188° C., identified by IR and NMR spectral analyses.

후처리

  1. waitat room temperature for 6 days
  2. concentrationThe reaction mixture is concentrated in vacuo
  3. customto give an oil
  4. temperatureThe aqueous solution is cooled with an ice-bath
  5. customis obtained
  6. extractionthe solution is extracted with ethyl acetate
  7. dry with materialThe combined ethyl acetate extracts are dried with anhydrous magnesium sulfate
  8. concentrationconcentrated in vacuo
  9. customto give a pale yellow solid
  10. additionThe solid is added
  11. customafter 2/3 of the methylene chloride has evaporated
  12. filtrationthe mixture is filtered

출처 및 근거

ORD 기록
ord-5c9c10f345e74325880a95d36a3d3ac8
출처 데이터셋
uspto-grants-1993_05
특허 번호
US05213607

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