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Ethyl Acetate → 3-(4-Trifluoromethoxyphenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione

HRID 605565
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HRID 605565 반응식
C([N:8]1[CH:13]2[CH2:14][CH2:15][CH2:16][CH:9]1[C:10](=[O:29])[N:11]([C:18]1[CH:23]=[CH:22][C:21]([O:24][C:25]([F:28])([F:27])[F:26])=[CH:20][CH:19]=1)[C:12]2=[O:17])C1C=CC=CC=1.C(OCC)(=O)C>[Pd].C(O)C>[F:28][C:25]([F:26])([F:27])[O:24][C:21]1[CH:22]=[CH:23][C:18]([N:11]2[C:12](=[O:17])[CH:13]3[NH:8][CH:9]([CH2:16][CH2:15][CH2:14]3)[C:10]2=[O:29])=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8857Ethyl AcetateHCID 670460419-Benzyl-3-(4-trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione

생성물 1

HCID 670459993-(4-Trifluoromethoxyphenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매2회

실험 절차

A mixture of 9-benzyl-3-(4-trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione (120 mg, 0.3 mmol), 10% Pd/C (20 mg, 0.02 mmol Pd), ethyl acetate (8 mL), and ethanol (2 mL) were stirred vigorously under an atmosphere of H2. After 2 h, more ethanol (2 mL) was added. After an additional 16 h, the reaction was filtered through Celite and concentrated to give 3-(4-trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione: MS (ESI): 315.4 (M+H).

후처리

  1. waitAfter an additional 16 h
  2. filtrationthe reaction was filtered through Celite
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0caf3b2582a34f4c8694732358ff1cf5
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915253B2

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