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HCID 86646589, 화합물 → 3-(2-Cyclobutylacetyl)pyrrolidine-1-carboxylic acid tert butyl ester

HRID 1922172
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반응식

HRID 1922172 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH:10]([C:13](=[O:19])[CH:14]=[C:15]2[CH2:18][CH2:17][CH2:16]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H][H]>[Pd].C(OCC)(=O)C>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH:10]([C:13](=[O:19])[CH2:14][CH:15]2[CH2:18][CH2:17][CH2:16]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 86646589HCID 86646589, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 866465903-(2-Cyclobutylacetyl)pyrrolidine-1-carboxylic acid tert butyl ester수율 46%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

Add palladium on carbon (50 mg, catalytic) to 3-(2-cyclobutylidene-acetyl)pyrrolidine-1-carboxylic acid tert butyl ester (850 mg, 3.20 mmol) in ethyl acetate (25 mL) and stir under nitrogen at room temperature. Install a balloon of hydrogen gas and stir overnight. Filter the reaction over celite, rinse with ethyl acetate and concentrate to dryness to afford 391 mg (46%) of the desired compound. MS (m/z)=212.0 (M−55)

후처리

  1. filtrationFilter
  2. customthe reaction over celite
  3. washrinse with ethyl acetate
  4. concentrationconcentrate to dryness

출처 및 근거

ORD 기록
ord-92b29a1f4cbe496f8f5460dcbd3656ad
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08173821B2

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