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Methyl isothiocyanate → 1-[3-[[(methylamino)thiocarbonyl]thio]propanoyl]-L-proline

HRID 2419432
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반응식

HRID 2419432 반응식
[CH3:1][N:2]=[C:3]=[S:4].[SH:5][CH2:6][CH2:7][C:8]([N:10]1[CH2:17][CH2:16][CH2:15][C@H:11]1[C:12]([OH:14])=[O:13])=[O:9]>N1C=CC=CC=1.[OH-].[Na+]>[CH3:1][NH:2][C:3]([S:5][CH2:6][CH2:7][C:8]([N:10]1[CH2:17][CH2:16][CH2:15][C@H:11]1[C:12]([OH:14])=[O:13])=[O:9])=[S:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11167Methyl isothiocyanateHCID 999781-(3-Mercapto-1-oxopropyl)-L-proline

생성물 1

HCID 132083091-[3-[[(methylamino)thiocarbonyl]thio]propanoyl]-L-proline

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 14798Sodium Hydroxide용매

실험 절차

Methylisothiocyanate (4 g) is added to a solution of 3-mercaptopropanoyl-L-proline (10.1 g) in a mixture of pyridine (250 ml) and 0.5 N sodium hydroxide (100 ml). The solution is kept at 40° for two hours and concentrated to dryness in vacuo. The residue is dissolved in water (100 ml), acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The organic phase is concentrated to dryness to yield 1-[3-[[(methylamino)thiocarbonyl]thio]propanoyl]-L-proline.

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후처리

  1. concentrationconcentrated to dryness in vacuo
  2. dissolutionThe residue is dissolved in water (100 ml)
  3. extractionextracted with ethyl acetate
  4. concentrationThe organic phase is concentrated to dryness

출처 및 근거

ORD 기록
ord-9623c066c7254c6d89890beb8e4da7db
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04105776

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