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2-Chloronicotinonitrile → 2-Chloro-N'-hydroxynicotinimidamide

HRID 2415762
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HRID 2415762 반응식
C[O-].[Na+].Cl.[NH2:5][OH:6].[Cl:7][C:8]1[C:13]([C:14]#[N:15])=[CH:12][CH:11]=[CH:10][N:9]=1>CO>[Cl:7][C:8]1[C:13]([C:14](=[N:5][OH:6])[NH2:15])=[CH:12][CH:11]=[CH:10][N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 810792-ChloronicotinonitrileHCID 443297Hydroxyamine hydrochlorideHCID 10942334Sodium Methoxide

생성물 1

HCID 406339952-Chloro-N'-hydroxynicotinimidamide수율 100.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Sodium methoxide (150 mi of 0.25M solution in methanol, 37.5 mmol) was added to a solution of hydroxylamine hydrochloride (2.8 g, 39.7 mmol) in methanol (150 mL), and the reaction was stirred at room temperature for 30 minutes. The mixture was filtered, then 2-chloro-3-cyanopyridine (5.0 g, 36.1 mmol) was added, the reaction was stirred at room temperature for 16 hours and then heated to reflux for 2 hours. The reaction was cooled to room temperature, concentrated in vacuo to approximately 50 mL and filtered. The filtrate was concentrated to dryness in vacuo, the residue was triturated with dichloromethane and filtered to give the title compound as a white solid (6.2 g).

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후처리

  1. filtrationThe mixture was filtered
  2. stirringthe reaction was stirred at room temperature for 16 hours
  3. temperatureheated
  4. temperatureto reflux for 2 hours
  5. temperatureThe reaction was cooled to room temperature
  6. concentrationconcentrated in vacuo to approximately 50 mL
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated to dryness in vacuo
  9. customthe residue was triturated with dichloromethane
  10. filtrationfiltered

출처 및 근거

ORD 기록
ord-92c9310b65c64afaa27b14d92b4dd2c6
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06821972B2

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