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4-[3-(Trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridine → 1-(3-Pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine

HRID 1248014
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인쇄 미리보기

반응식

HRID 1248014 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]([O:10]C2C=CC([N+]([O-])=O)=CC=2)=O)[CH:2]=1.[F:20][C:21]([F:35])([F:34])[C:22]1[CH:23]=[C:24]([C:28]2[CH2:29][CH2:30][NH:31][CH2:32][CH:33]=2)[CH:25]=[CH:26][CH:27]=1>C(O)C>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]([N:31]2[CH2:30][CH:29]=[C:28]([C:24]3[CH:25]=[CH:26][CH:27]=[C:22]([C:21]([F:20])([F:34])[F:35])[CH:23]=3)[CH2:33][CH2:32]2)=[O:10])[CH:2]=1
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참가 물질

4

반응물 2

HCID 111280344-[3-(Trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridineHCID 20280550p-Nitrophenyl 3-pyridylacetate

생성물 1

HCID 202805321-(3-Pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine수율 52.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 11.3 g of p-nitrophenyl 3-pyridylacetate and 10 g of 4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine in 150 ml of ethanol is stirred 1 hour at room temperature, then concentrated under reduced pressure. The residue is dissolved in diethyl ether, the solution is washed with water, then with sodium hydroxide and again with water, dried on anhydrous sodium sulfate and concentrated. Thus, 1-(3-pyridylacetyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine (8 g) is obtained as an oil which is used for the subsequent reaction.

후처리

  1. concentrationconcentrated under reduced pressure
  2. dissolutionThe residue is dissolved in diethyl ether
  3. washthe solution is washed with water
  4. dry with materialwith sodium hydroxide and again with water, dried on anhydrous sodium sulfate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f7a8c886b30c4963a05c64b547a0290b
출처 데이터셋
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04521428

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