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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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[(Z)-4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-but-2-enyloxy]-acetic acid ethyl ester → [4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl ester

HRID 489161
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HRID 489161 반응식
[CH2:1]([O:3][C:4](=[O:20])[CH2:5][O:6][CH2:7]/[CH:8]=[CH:9]\[CH2:10][N:11]1[C:16](=[O:17])[CH2:15][CH2:14][CH2:13][C@@H:12]1[CH2:18][OH:19])[CH3:2].[H][H]>[Pd].CCO>[CH2:1]([O:3][C:4](=[O:20])[CH2:5][O:6][CH2:7][CH2:8][CH2:9][CH2:10][N:11]1[C:16](=[O:17])[CH2:15][CH2:14][CH2:13][C@@H:12]1[CH2:18][OH:19])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 69025613[(Z)-4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-but-2-enyloxy]-acetic acid ethyl esterHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 69020752[4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl ester수율 100.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

Palladium on carbon (10 wt. %, 15 mg) was added to a solution of [(Z)-4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-but-2-enyloxy]-acetic acid ethyl ester (290 mg, 1.02 mmol) in EtOH (3.0 mL). A hydrogen atmosphere was established by evacuating and refilling with hydrogen (3×) and the reaction mixture was stirred under a balloon of hydrogen for 3 h. The reaction mixture was filtered through celite, washing with EtOH, and the filtrate was concentrated in vacuo to afford 295 mg (quant. crude) of [4-((R)-2-hydroxymethyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl ester.

후처리

  1. customby evacuating
  2. filtrationThe reaction mixture was filtered through celite
  3. washwashing with EtOH
  4. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-a009cd72ec4b4e1184c3af1b489a3668
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06977260B2

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