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Sodium Hydroxide → 2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid

HRID 1428771
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반응식

HRID 1428771 반응식
[CH2:1]([S:3]([NH:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]([CH3:20])[C:15]([O:17]CC)=[O:16])=[CH:10][C:9]=1[F:21])(=[O:5])=[O:4])[CH3:2].[OH-].[Na+]>O1CCCC1.O>[CH2:1]([S:3]([NH:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]([CH3:20])[C:15]([OH:17])=[O:16])=[CH:10][C:9]=1[F:21])(=[O:5])=[O:4])[CH3:2]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 70816333Ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate

생성물 1

HCID 708165692-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid수율 100.6%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate (60 mg, 0.189 mmol) in tetrahydrofuran and water co-solvent, sodium hydroxide (19 mg) was added at room temperature. The mixture was stirred for overnight and extracted with ethyl acetate, dried over magnesium sulfate, the solvent was evaporated in vacuo. It was purified by column chromatography to give 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid (55 mg).

후처리

  1. extractionextracted with ethyl acetate
  2. dry with materialdried over magnesium sulfate
  3. customthe solvent was evaporated in vacuo
  4. customIt was purified by column chromatography

출처 및 근거

ORD 기록
ord-8e4f8cc61a81493fa721fb6894976bc4
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08937092B2

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