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Potassium Iodide → {(Z)-4-[(R)-2-(1-ethoxyethoxymethyl)-6-oxo-piperidin-1-yl]-but-2-enyloxy}-acetic acid ethyl ester

HRID 489146
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HRID 489146 반응식
[H-].[Na+].[CH2:3]([O:5][CH:6]([O:8][CH2:9][C@@H:10]1[NH:15][C:14](=[O:16])[CH2:13][CH2:12][CH2:11]1)[CH3:7])[CH3:4].[I-].[K+].[CH2:19]([O:21][C:22](=[O:30])[CH2:23][O:24][CH2:25]/[CH:26]=[CH:27]\[CH2:28]Cl)[CH3:20]>CN(C=O)C>[CH2:19]([O:21][C:22](=[O:30])[CH2:23][O:24][CH2:25]/[CH:26]=[CH:27]\[CH2:28][N:15]1[C:14](=[O:16])[CH2:13][CH2:12][CH2:11][C@@H:10]1[CH2:9][O:8][CH:6]([O:5][CH2:3][CH3:4])[CH3:7])[CH3:20]
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참가 물질

6

반응물 4

HCID 4875Potassium IodideHCID 24758Sodium hydrideHCID 57473593((Z)-4-chloro-but-2-enyloxy)-acetic acid ethyl esterHCID 58961293(R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one

생성물 1

HCID 69022257{(Z)-4-[(R)-2-(1-ethoxyethoxymethyl)-6-oxo-piperidin-1-yl]-but-2-enyloxy}-acetic acid ethyl ester수율 31%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

Sodium hydride (60% dispersion in oil, 402 mg, 10.0 mmol) was added to a solution of (R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one (2.02 g, 10.0 mmol) in DMF (15 mL) at 0° C. After 1 h, a solution of potassium iodide (1.66 g, 10.0 mmol) and ((Z)-4-chloro-but-2-enyloxy)-acetic acid ethyl ester (prepared according to PCT 2003/007941, 3.09 g, 16.0 mmol) in DMF (10 mL) was added via cannula. The reaction was allowed to warm to rt. After 18 h at rt, the reaction was quenched by the addition of saturated aqueous NaHCO3 (100 mL) and the mixture was extracted with EtOAc (3×100 mL). The combined organic phase was washed with brine (3×100 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (10% EtOAc/CH2Cl2 →60% EtOAc/CH2Cl2, gradient) afforded 1.10 g (31%) of {(Z)-4-[(R)-2-(1-ethoxyethoxymethyl)-6-oxo-piperidin-1-yl]-but-2-enyloxy}-acetic acid ethyl ester.

후처리

  1. waitAfter 18 h at rt
  2. customthe reaction was quenched by the addition of saturated aqueous NaHCO3 (100 mL)
  3. extractionthe mixture was extracted with EtOAc (3×100 mL)
  4. washThe combined organic phase was washed with brine (3×100 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification of the residue by flash column chromatography on silica gel (10% EtOAc/CH2Cl2 →60% EtOAc/CH2Cl2, gradient)

출처 및 근거

ORD 기록
ord-d85cf0681c604d598763ad0c311f89d5
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06977260B2

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