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Tetrahydrofuran → 3-Pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate

HRID 2074327
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HRID 2074327 반응식
C1COCC1.C([O:13][C:14]1[CH:35]=[CH:34][C:17]([O:18][CH:19]2[CH2:24][CH2:23][N:22]([C:25]([O:27][C:28]3[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=3)=[O:26])[CH2:21][CH2:20]2)=[CH:16][CH:15]=1)C1C=CC=CC=1.[H][H]>[C].[Pd].CC(O)C>[OH:13][C:14]1[CH:35]=[CH:34][C:17]([O:18][CH:19]2[CH2:24][CH2:23][N:22]([C:25]([O:27][C:28]3[CH:29]=[N:30][CH:31]=[CH:32][CH:33]=3)=[O:26])[CH2:21][CH2:20]2)=[CH:16][CH:15]=1
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참가 물질

6

반응물 3

HCID 8028TetrahydrofuranHCID 670670553-Pyridyl 4-[4-(benzyloxy)phenoxy]-1-piperidinecarboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 670670763-Pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate수율 83.5%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매
HCID 3776
Isopropanol
용매

실험 절차

10% Palladium-carbon (catalytic amount) was added to a THF (75 ml)/2-propanol (75 ml) solution containing 3-pyridyl 4-[4-(benzyloxy)phenoxy]-1-piperidinecarboxylate (3.7 g), and in a hydrogen gas atmosphere, this was stirred at room temperature under normal pressure for 24 hours. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure, and the resulting solid was washed with EtOAc/hexane, and dried under reduced pressure to obtain 3-pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate (2.4 g).

후처리

  1. customThe catalyst was removed by filtration
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. washthe resulting solid was washed with EtOAc/hexane
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-ecd666eb161f46589aef3084b9d3481a
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07919495B2

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