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Stannous chloride dihydrate → 2-(5-Amino-3-(trifluoromethyl)pyridin-2-yl)propanenitrile

HRID 576219
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HRID 576219 반응식
O.O.[Sn](Cl)Cl.[N+:6]([C:9]1[CH:10]=[C:11]([C:19]([F:22])([F:21])[F:20])[C:12]([CH:15]([CH3:18])[C:16]#[N:17])=[N:13][CH:14]=1)([O-])=O>CC(=O)OCC>[NH2:6][C:9]1[CH:10]=[C:11]([C:19]([F:22])([F:20])[F:21])[C:12]([CH:15]([CH3:18])[C:16]#[N:17])=[N:13][CH:14]=1
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참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 904165882-(5-Nitro-3-(trifluoromethyl)pyridin-2-yl)propanenitrile

생성물 1

HCID 904158462-(5-Amino-3-(trifluoromethyl)pyridin-2-yl)propanenitrile수율 85.3%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Tin(II) chloride dihydrate (135 mg, 0.600 mmol) was added to a solution of 2-(5-nitro-3-(trifluoromethyl)pyridin-2-yl)propanenitrile (73.6 mg, 0.300 mmol) in EA (15 mL). The mixture was at 50° C. for 3 h. Then the solution was concentrated and distributed between EA and saturated NaHCO3 solution. The combined organic extract was washed with brine, dried over MgSO4, filtered and concentrated. The resulting 2-(5-amino-3-(trifluoromethyl)pyridin-2-yl)propanenitrile (55 mg, 0.256 mmol, 85.0% yield) was used to next step without further purification. TLC (PE/EA=5:1, Rf=0.5): 1H NMR (400 MHz, CDCl3) δ: 8.25 (s, 1H), 7.17 (d, J=2.2 Hz, 1H), 4.15-4.28 (m, 1H), 1.66 (d, J=7.1 Hz, 3H); ES-LCMS m/z 216.0 (M+H).

후처리

  1. concentrationThen the solution was concentrated
  2. extractionThe combined organic extract
  3. washwas washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9e9cfe3ccc034a54967f2b208f675e2c
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09035063B2

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