Ethyl (2-((2-hydroxypropyl)amino)-2-oxoacetyl)glycinate → Ethyl (2-oxo-2-((2-oxopropyl)amino)acetyl)glycinate

HRID 1795796

반응식

HRID 1795796 반응식
[CH2:1]([O:3][C:4]([CH2:6][NH:7][C:8]([C:10]([NH:12][CH2:13][CH:14]([OH:16])[CH3:15])=[O:11])=[O:9])=[O:5])[CH3:2].Br([O-])(=O)=O.[Na+]>O.C(OCC)(=O)C.[Cl-].[Na+].O.O.[Ru](Cl)(Cl)Cl>[CH2:1]([O:3][C:4]([CH2:6][NH:7][C:8]([C:10]([NH:12][CH2:13][C:14](=[O:16])[CH3:15])=[O:11])=[O:9])=[O:5])[CH3:2]

참가 물질

7

반응물 2

HCID 10537524Ethyl (2-((2-hydroxypropyl)amino)-2-oxoacetyl)glycinateHCID 23668195Sodium Bromate

생성물 1

HCID 10823329Ethyl (2-oxo-2-((2-oxopropyl)amino)acetyl)glycinate수율 92%

시약·촉매·용매 4

HCID 6093376Ruthenium trichloride hydrate촉매HCID 962Water용매2회HCID 8857Ethyl Acetate용매HCID 57417360Sodium chloride; water용매

실험 절차

To a stirred solution of N-(ethoxycarbonyl-methyl)-N′-(2-hydroxy-1-propyl)oxamide (8.0 g, 34.5 mmol), as prepared in the preceding step, in water (50 mL) under nitrogen at 50° C. was added ruthenium (III) chloride hydrate (75 mg, 0.35 mmol). The reaction flask was removed from the heating bath, and a solution of sodium bromate (5.2 g, 34.5 mmol) in water (40 mL) was added dropwise. The reaction mixture was allowed to cool to room temperature, and then diluted with ethyl acetate and brine. The aqueous layer was extracted with ethyl acetate (2×), then saturated with sodium chloride and extracted again (×2). The combined ethyl acetate layers were washed with brine, dried over Na2SO4, and treated with activated carbon. Evaporation of the solvent and drying under high vacuum provided the title compound as a white solid (7.3 g, 92%). 1H NMR (400 MHz, CDCl3) δ 7.99 (s(br), 1 H), 7.84 (s(br), 1 H), 4.24 (q, 2 H, J=7.1 Hz), 4.19 (d, 2 H, J=5.2 Hz), 4.10 (d, 2 H, J=5.7 Hz), 2.24 (s, 3 H), 1.30 (t, 3 H, J=7.1 Hz).

후처리

  1. customThe reaction flask was removed from the heating bath
  2. extractionThe aqueous layer was extracted with ethyl acetate (2×)
  3. extractionsaturated with sodium chloride and extracted again (×2)
  4. washThe combined ethyl acetate layers were washed with brine
  5. dry with materialdried over Na2SO4
  6. additiontreated with activated carbon
  7. customEvaporation of the solvent
  8. customdrying under high vacuum

출처 및 근거

ORD 기록
ord-3bb0b3c32a9c4621accba824fa8b7569
출처 데이터셋
uspto-grants-2006_04
특허 번호
US07030110B2

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