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1-Iodopropane → (Rac)-2-cyclopentylaminomethyl-pentanoic acid ethyl ester

HRID 2111259
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HRID 2111259 반응식
[CH2:1]([O:3][C:4](=[O:13])[CH2:5][CH2:6][NH:7][CH:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)[CH3:2].C[Si]([N-][Si](C)(C)C)(C)C.[Li+].I[CH2:25][CH2:26][CH3:27]>O1CCCC1>[CH2:1]([O:3][C:4](=[O:13])[CH:5]([CH2:6][NH:7][CH:8]1[CH2:12][CH2:11][CH2:10][CH2:9]1)[CH2:25][CH2:26][CH3:27])[CH3:2]
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참가 물질

5

반응물 3

HCID 336431-IodopropaneHCID 2733832Lithium hexamethyldisilazaneHCID 23053028Ethyl 3-(cyclopentylamino)propanoate

생성물 1

HCID 57635032(Rac)-2-cyclopentylaminomethyl-pentanoic acid ethyl ester수율 48.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a mixture of 2.0 g (0.0108 mole) of 3-cyclopentylamino-propanoic acid ethyl ester and 10 mL of anhydrous tetrahydrofuran, at −78 degrees, was added 24.0 mL (0.0236 mole) of lithium bis(trimethylsilyl)amide. The mixture was stirred for 1 hour and then a solution of 2.0 g (0.0119 mole) of iodopropane in 2.0 mL of tetrahydrofuran was added slowly. The mixture was stirred at room temperature for 24 hours and then quenched by the addition of water. The mixture was concentrated under reduced pressure and then extracted three times with 50 mL of ethyl acetate. The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 1.2 g of (rac)-2-cyclopentylaminomethyl-pentanoic acid ethyl ester, which was used without further purification in subsequent steps.

후처리

  1. stirringThe mixture was stirred at room temperature for 24 hours
  2. customquenched by the addition of water
  3. concentrationThe mixture was concentrated under reduced pressure
  4. extractionextracted three times with 50 mL of ethyl acetate
  5. dry with materialThe combined extracts were dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-a1cd2d3b2b4c4bef99b253234cb7ce22
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07517873B2

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