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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydroxylamine → HCID 72533800, 화합물

HRID 2246238
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HRID 2246238 반응식
[Cl:1][C:2]1[CH:9]=[C:8]([S:10]([CH3:13])(=[O:12])=[O:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[NH2:14][OH:15]>C(O)C>[Cl:1][C:2]1[CH:9]=[C:8]([S:10]([CH3:13])(=[O:12])=[O:11])[CH:7]=[CH:6][C:3]=1[C:4](=[N:14][OH:15])[NH2:5]
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참가 물질

4

반응물 2

HCID 787HydroxylamineHCID 591699432-Chloro-4-(methylsulfonyl)benzonitrile

생성물 1

HCID 72533800HCID 72533800, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The nitrile from Step B was dissolved into 100 mL of 1:1 ethanol/50% aqueous hydroxylamine then heated to reflux for 12 h. After evaporation of the solvent, the residue was dissolved into 400 mL of ethyl acetate then washed with saturated aqueous brine (150 mL). The organic phase was dried over magnesium sulfate, filtered, and evaporated in vacuo to yield the title compound, which was used without further purification. LC/MS 449.05 (M+1), 451.03 (M+3).

후처리

  1. temperaturethen heated
  2. temperatureto reflux for 12 h
  3. customAfter evaporation of the solvent
  4. dissolutionthe residue was dissolved into 400 mL of ethyl acetate
  5. washthen washed with saturated aqueous brine (150 mL)
  6. dry with materialThe organic phase was dried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-3d20213f5e024296a5989187f3f68b93
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07687492B2

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