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1,1-dimethylethyl{(1R)-1-[3-hydroxy-1-(phenylmethyl)azetidin-3-yl]ethyl}carbamate → HCID 86621270, 화합물

HRID 605746
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HRID 605746 반응식
CC([N:5]([C@@H:9]([C:11]1([OH:22])[CH2:14][N:13](CC2C=CC=CC=2)[CH2:12]1)[CH3:10])[C:6](=[O:8])[O-:7])(C)C.[H][H]>CO.[Pd]>[OH:22][C:11]1([C@H:9]([NH:5][C:6](=[O:8])[O:7][C:11]([CH3:14])([CH3:12])[CH3:9])[CH3:10])[CH2:12][NH:13][CH2:14]1
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참가 물질

5

반응물 2

HCID 867612951,1-dimethylethyl{(1R)-1-[3-hydroxy-1-(phenylmethyl)azetidin-3-yl]ethyl}carbamateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86621270HCID 86621270, 화합물수율 211.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 1,1-dimethylethyl{(1R)-1-[3-hydroxy-1-(phenylmethyl)azetidin-3-yl]ethyl}carbamate (1.07 g, 3.5 mmol) in methanol was added wet 10% palladium on carbon (50% by mass, 250 mg). The resulting suspension was subjected to 1 atmosphere of hydrogen for 7 h, and an additional 250 mg of catalyst was added over the course of the reaction. The catalyst was then removed by filtration through celite. The filtrate was then concentrated in vacuo to provide 1,1-dimethylethyl [(1R)-1-(3-hydroxyazetidin-3-yl)ethyl]carbamate as a colorless syrup (800 mg, quantitative yield). MS (EI) for C10H20N2O3: 161 (M-tert-butyl+H).

후처리

  1. customThe catalyst was then removed by filtration through celite
  2. concentrationThe filtrate was then concentrated in vacuo

출처 및 근거

ORD 기록
ord-e3d3b7d6ba744fc3810430df5aef2814
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915250B2

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