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Methyl iodide → HCID 11348311, 화합물

HRID 1374423
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HRID 1374423 반응식
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([CH2:22][OH:23])[CH2:13][CH2:14][C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:24]I>C(#N)C.[Ag]=O>[CH2:1]([O:8][C:9]([NH:11][C@H:12]([CH2:22][O:23][CH3:24])[CH2:13][CH2:14][C:15]([O:17][C:18]([CH3:19])([CH3:20])[CH3:21])=[O:16])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 15043091HCID 15043091, 화합물

생성물 1

HCID 11348311HCID 11348311, 화합물수율 71.2%

시약·촉매·용매 2

HCID 92152Silver(II) oxide촉매HCID 6342Acetonitrile용매

실험 절차

To a solution of tert-butyl (4S)-4-{[(benzyloxy)carbonyl]amino}-5-hydroxypentanoate (4.0 g, 12.4 mmol) in acetonitrile (80 ml) were added silveroxide (14.3 g, 61.7 mmol) and methyliodide (7.7 ml, 124 mmol), and the mixture was stirred for 19 hours. After removal of the insoluble materials, the solvent was removed in vacuo and the residue was purified with silica gel chromatography to give tert-butyl (4S)-4-{[(benzyloxy)carbonyl]amino}-5-methoxypentanoate (2.98 g, 71%).

후처리

  1. customAfter removal of the insoluble materials
  2. customthe solvent was removed in vacuo
  3. customthe residue was purified with silica gel chromatography

출처 및 근거

ORD 기록
ord-c74257373f7041299672e9a930d1814e
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07163936B2

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