Tetrahydrofuran → N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid

HRID 1665688노트

반응식

HRID 1665688 반응식
[OH-].[Na+].C([O:5][C:6](=[O:23])[CH2:7][C:8]([NH:10][C:11]1[CH:15]=[C:14]([C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[O:13][N:12]=1)=[O:9])C.C1COCC1>O>[F:22][C:19]1[CH:20]=[CH:21][C:16]([C:14]2[O:13][N:12]=[C:11]([NH:10][C:8](=[O:9])[CH2:7][C:6]([OH:23])=[O:5])[CH:15]=2)=[CH:17][CH:18]=1

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 57875802N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid ethyl ester

생성물 1

HCID 57875816N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid수율 90.9%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

NaOH (34 mg, 8.5 mmol) was added to a solution of N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid ethyl ester (292 mg, 1.0 mmol) in the mixture of THF (13 mL) and H2O (13 mL) and stirred for 1 hr at room temperature. The reaction mixture was concentrated and the obtained residue was diluted with water, acidified with concentrated HCl, and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried over Na2SO4 and concentrated to afford 40 mg (90.9% Yield) of N-[5-(4-fluoro-phenyl)-isoxazol-3-yl]-malonamic acid.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additionthe obtained residue was diluted with water
  3. extractionextracted with ethyl acetate
  4. washThe ethyl acetate layer was washed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-bfdb5dd771a44f1695541b673278d3d2
출처 데이터셋
uspto-grants-2011_10
특허 번호
US08039463B2

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