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1-(3-Mercapto-1-oxopropyl)-L-proline → 1-[3-[[(ethoxy)carbonyl]thio]propanoyl]-L-proline

HRID 262561
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인쇄 미리보기

반응식

HRID 262561 반응식
C[CH2:2][O:3][CH2:4][CH3:5].ClC([O-])=[O:8].[SH:10][CH2:11][CH2:12][C:13]([N:15]1[CH2:22][CH2:21][CH2:20][C@H:16]1[C:17]([OH:19])=[O:18])=[O:14]>C(=O)(O)[O-].[Na+]>[CH2:4]([O:3][C:2]([S:10][CH2:11][CH2:12][C:13]([N:15]1[CH2:22][CH2:21][CH2:20][C@H:16]1[C:17]([OH:19])=[O:18])=[O:14])=[O:8])[CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 999781-(3-Mercapto-1-oxopropyl)-L-prolineHCID 21319165Ether chloroformate

생성물 1

HCID 537685991-[3-[[(ethoxy)carbonyl]thio]propanoyl]-L-proline

시약·촉매·용매 1

HCID 516892Sodium Bicarbonate용매

실험 절차

Ether chloroformate (1.2 g.) is added to a solution of 3-mercaptopropanoyl-L-proline [2.03 g.) in normal sodium bicarbonate (30 ml.) and the mixture is stirred vigorously at 5° for one hour, and for two hours at room temperature. After acidification with concentrated hydrochloric acid, the mixture is extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate, and concentrated to dryness to yield 1-[3-[[(ethoxy)carbonyl]thio]propanoyl]-L-proline.

후처리

  1. extractionAfter acidification with concentrated hydrochloric acid, the mixture is extracted with ethyl acetate
  2. washThe organic phase is washed with water
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-1a6654ee32314ac58843c323a8ad00b9
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04154840

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