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Chloroform → 12-Chloro-9-fluoro-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide

HRID 513762
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HRID 513762 반응식
CN1C(C)(C)C(=O)N(C)C1=O.[F:12][C:13]1[CH:30]=[C:29]2[C:16]([S:17](=[O:32])(=[O:31])[NH:18][C:19]3[C:28]2=[CH:27][CH:26]=[C:25]2[C:20]=3[N:21]=[CH:22][CH:23]=[CH:24]2)=[CH:15][CH:14]=1.C(Cl)(Cl)[Cl:34]>>[Cl:34][C:26]1[CH:27]=[C:28]2[C:19](=[C:20]3[C:25]=1[CH:24]=[CH:23][CH:22]=[N:21]3)[NH:18][S:17](=[O:31])(=[O:32])[C:16]1[C:29]2=[CH:30][C:13]([F:12])=[CH:14][CH:15]=1
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참가 물질

4

반응물 3

HCID 6212ChloroformHCID 617941,3-Dimethyl-5,5-dimethylhydantoinHCID 167599219-fluoro-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide

생성물 1

HCID 6818318212-Chloro-9-fluoro-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide수율 69%

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온도
70 °C

실험 절차

1,3-dimethyl-5,5-dimethylhydantoin (0.73 g, 36.7 mmol) was added to a solution of 9-fluoro-5H-6-thia-4,5-diaza-chrysene 6,6-dioxide 187 (1.0 g, 33.3 mmol) in chloroform (40 ml) and the reaction was heated at 70° C. until the starting material was consumed (LCMS). After cooling, the mixture was concentrated in vacuo. The residue was dissolved in EtOAc and the organic phase was washed with sodium metabisulfate, water and brine. The organic phase was dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with DCM/MeOH (99:1) as the eluent to give the title compound (0.8 g, 69%).

후처리

  1. customwas consumed (LCMS)
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated in vacuo
  4. dissolutionThe residue was dissolved in EtOAc
  5. washthe organic phase was washed with sodium metabisulfate, water and brine
  6. dry with materialThe organic phase was dried (Na2SO4)
  7. concentrationconcentrated in vacuo
  8. customThe crude residue was purified by column chromatography with DCM/MeOH (99:1) as the eluent

출처 및 근거

ORD 기록
ord-8bc46504056948c28e1870549b252ddf
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102688B2

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