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5-Nitro-2-(2,2,2-trifluoroethoxy)pyridine → 6-(2,2,2-Trifluoroethoxy)pyridin-3-amine

HRID 2092662
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HRID 2092662 반응식
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:10][CH2:11][C:12]([F:15])([F:14])[F:13])=[N:8][CH:9]=1)([O-])=O.[H][H]>CO.[Pd]>[F:15][C:12]([F:13])([F:14])[CH2:11][O:10][C:7]1[N:8]=[CH:9][C:4]([NH2:1])=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6137185-Nitro-2-(2,2,2-trifluoroethoxy)pyridineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 5431566-(2,2,2-Trifluoroethoxy)pyridin-3-amine수율 93%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

5-Nitro-2-(2,2,2-trifluoro-ethoxy)-pyridine (20.5 g, obtained in example 108, step 1) was dissolved in methanol (160 mL). Palladium on activated charcoal (1.96 g, 10% Pd) was added and an atmosphere of hydrogen was introduced at RT. The mixture was stirred under hydrogen for 72 hours. The reaction mixture was filtered over dicalite speed plus (Acros Organics), washed with ethyl acetate and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, gradient of heptane in ethyl acetate) to give the title compound as a brown liquid (16.49 g, 91%). MS (m/e): 193.1 [MH+].

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후처리

  1. filtrationThe reaction mixture was filtered over dicalite speed plus (Acros Organics)
  2. washwashed with ethyl acetate
  3. customthe solvent was evaporated
  4. customThe residue was purified by flash chromatography (silica gel, gradient of heptane in ethyl acetate)

출처 및 근거

ORD 기록
ord-dd6002a99ab8485c86ce701f21034f46
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08440710B2

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