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n-[(3r)-1-(4-Chlorophenyl)-2-oxopyrrolidin-3-yl](phenylmethoxy)carboxamide → (3R)-3-amino-1-(4-chlorophenyl)pyrrolidin-2-one

HRID 855593
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HRID 855593 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:12][CH2:11][C@@H:10]([NH:13]C(OCC3C=CC=CC=3)=O)[C:9]2=[O:24])=[CH:4][CH:3]=1>C(O)C.C1CCCCC=1.[OH-].[Pd+2].[OH-]>[NH2:13][C@@H:10]1[CH2:11][CH2:12][N:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)[C:9]1=[O:24]
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참가 물질

5

반응물 1

HCID 21060625n-[(3r)-1-(4-Chlorophenyl)-2-oxopyrrolidin-3-yl](phenylmethoxy)carboxamide

생성물 1

HCID 58714338(3R)-3-amino-1-(4-chlorophenyl)pyrrolidin-2-one

시약·촉매·용매 3

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매HCID 8079Cyclohexene용매

실험 절차

To a solution of N-[(3R)-1-(4-chlorophenyl)-2-oxopyrrolidin-3-yl](phenylmethoxy)carboxamide (0.2 g, 0.58 mmol) in ethanol (10 ml) and cyclohexene (4 ml) was added palladium hydroxide (40 mg). The reaction was refluxed vigorously overnight. Palladium was removed by filtration and the filtrate was concentrated to yield (3R)-3-amino-1-(4-chlorophenyl)pyrrolidin-2-one.

후처리

  1. temperatureThe reaction was refluxed vigorously overnight
  2. customPalladium was removed by filtration
  3. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-0a684f1cf84a4e88a54813af546225ac
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262198B2

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