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Piperidine → 3-(6-Morpholin-4-yl-pyridin-3-yl)-acrylic acid methyl ester

HRID 2265939
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인쇄 미리보기

반응식

HRID 2265939 반응식
[CH3:1][O:2][C:3](=[O:13])[CH:4]=[CH:5][C:6]1[CH:7]=[N:8][C:9](Br)=[CH:10][CH:11]=1.[NH:14]1[CH2:19][CH2:18]C[CH2:16][CH2:15]1.CC[O:22]C(C)=O>>[CH3:1][O:2][C:3](=[O:13])[CH:4]=[CH:5][C:6]1[CH:7]=[N:8][C:9]([N:14]2[CH2:19][CH2:18][O:22][CH2:16][CH2:15]2)=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 8082PiperidineHCID 8857Ethyl AcetateHCID 714275823-(6-Bromopyridin-3-yl)acrylic acid methyl ester

생성물 1

HCID 687853973-(6-Morpholin-4-yl-pyridin-3-yl)-acrylic acid methyl ester수율 21%

실험 절차

3-(6-Bromo-pyridin-3-yl)-acrylic acid methyl ester (100 mg, 0.413 mmol) was added to piperidine (1 ml) and the mixture was stirred for 1.5 hrs at room temperature. The reaction mixture was diluted with EtOAc and then washed three times with H2O, brine, dried. Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was column-chromatographed to yield 3-(6-Morpholin-4-yl-pyridin-3-yl)-acrylic acid methyl ester (40 mg, 21%).

후처리

  1. washwashed three times with H2O, brine
  2. customdried
  3. filtrationNa2SO4, filtered
  4. concentrationconcentrated under reduced pressure
  5. customThe obtained residue was column-chromatographed

출처 및 근거

ORD 기록
ord-b194ff5c54cf4669b917b6e0d033b93d
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858621B2

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