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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Benzylamine → N-benzyl-3,5,6-trifluoropyridin-2-amine

HRID 1274662
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HRID 1274662 반응식
F[C:2]1[C:7]([F:8])=[CH:6][C:5]([F:9])=[C:4]([F:10])[N:3]=1.[CH2:11]([NH2:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C(#N)C>[CH2:11]([NH:18][C:2]1[C:7]([F:8])=[CH:6][C:5]([F:9])=[C:4]([F:10])[N:3]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
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참가 물질

4

반응물 2

HCID 7504BenzylamineHCID 1377492,3,5,6-Tetrafluoropyridine

생성물 1

HCID 22121263N-benzyl-3,5,6-trifluoropyridin-2-amine수율 84.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To 50 ml of acetonitrile were added 12.0 g of 2,3,5,6-tetrafluoropyridine and 18.0 g of benzylamine, and the mixture was stirred under reflux condition for 2 hours, and the solvent and the like were distilled off. To the residue was added 150 ml of ethyl acetate, and the mixture was washed twice with 150 ml of distilled water and 150 ml of 10% aqueous solution of citric acid. The ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 16.0 g of the title compound as a pale yellow oil.

후처리

  1. temperatureunder reflux condition for 2 hours
  2. distillationthe solvent and the like were distilled off
  3. additionTo the residue was added 150 ml of ethyl acetate
  4. washthe mixture was washed twice with 150 ml of distilled water and 150 ml of 10% aqueous solution of citric acid
  5. dry with materialThe ethyl acetate layer was dried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-4f7edaf7fa4e46d4b84306668461a03e
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06156903

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