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ethyl (1R,3R,4S)-2-[(S)-1-phenylethyl]-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylate → HCID 10535139, 화합물

HRID 347803
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HRID 347803 반응식
C1([C@@H]([N:9]2[C@@H:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[C@H:13]3[CH2:20][C@@H:10]2[CH:11]=[CH:12]3)C)C=CC=CC=1>C(OCC)(=O)C.[OH-].[OH-].[Pd+2]>[C@@H:10]12[CH2:20][C@@H:13]([CH2:12][CH2:11]1)[C@H:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[NH:9]2
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참가 물질

4

반응물 1

HCID 10730826ethyl (1R,3R,4S)-2-[(S)-1-phenylethyl]-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylate

생성물 1

HCID 10535139HCID 10535139, 화합물수율 25%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 8857Ethyl Acetate용매

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온도
45 °C

실험 절차

To a solution of ethyl (1R, 3R, 4S)-2-[(S)-1-phenylethyl]-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylate (3.84 g, 14.2 mmol) in ethyl acetate (28 ml) was added 20 wt % Pd(OH)2 (4.97 g), and the mixture was stirred under a hydrogen atmosphere at 45° C. 64 hours. After a filtration through Celite, the solvent was concentrated. The residue was purified by silica gel column chromatography (1%–5% methanol/chloroform), to give ethyl (1S, 3R, 4R)-2-azabicyclo[2.2.1]heptane-3-carboxylate (0.595 g, 25%).

후처리

  1. custom64 hours
  2. filtrationAfter a filtration through Celite
  3. concentrationthe solvent was concentrated
  4. customThe residue was purified by silica gel column chromatography (1%–5% methanol/chloroform)

출처 및 근거

ORD 기록
ord-d7b5cdf74ea5440e82f03564ec2c1922
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07176217B2

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