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1,3-Dichloro-5,5-dimethylhydantoin → 2-Amino-5-chloro-3-fluoro-N-methoxy-N-methyl-benzamide

HRID 1497228
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HRID 1497228 반응식
[NH2:1][C:2]1[C:13]([F:14])=[CH:12][CH:11]=[CH:10][C:3]=1[C:4]([N:6]([O:8][CH3:9])[CH3:7])=[O:5].[Cl:15]N1C(C)(C)C(=O)N(Cl)C1=O>C(O)(=O)C>[NH2:1][C:2]1[C:13]([F:14])=[CH:12][C:11]([Cl:15])=[CH:10][C:3]=1[C:4]([N:6]([O:8][CH3:9])[CH3:7])=[O:5]
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참가 물질

4

반응물 2

HCID 83601,3-Dichloro-5,5-dimethylhydantoinHCID 815074922-Amino-3-fluoro-N-methoxy-N-methyl-benzamide

생성물 1

HCID 866830482-Amino-5-chloro-3-fluoro-N-methoxy-N-methyl-benzamide수율 86.6%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a solution of 2-amino-3-fluoro-N-methoxy-N-methyl-benzamide (765 mg, 3.86 mmol) in acetic acid (18 ml) was added 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione (783 mg, 2.7 mmol) at room temperature. The orange solution was stirred over night and was then poured carefully onto ice/saturated NaHCO3-solution. The mixture was extracted with EtOAc and the combined extracts were washed with brine, dried with Na2SO4 and evaporated. The remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 90:10-80:20) to afford the title compound (544 mg, 61%) as light brown solid. MS (ESI): 233.0 (M+H)+.

후처리

  1. additionwas then poured carefully onto ice/saturated NaHCO3-solution
  2. extractionThe mixture was extracted with EtOAc
  3. washthe combined extracts were washed with brine
  4. dry with materialdried with Na2SO4
  5. customevaporated
  6. customThe remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 90:10-80:20)

출처 및 근거

ORD 기록
ord-4c743107b2644a8f9409bbc09f1e76cb
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199938B2

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