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Sodium Iodide → 2(S)-benzyloxycarbonylamino-4,4-dimethylpentanoic acid 3-methyloxetan-3-ylmethyl ester

HRID 907615
ノート
印刷プレビュー

反応式

HRID 907615 の反応式
[CH3:1][C:2]1([CH2:6]OS(C2C=CC(C)=CC=2)(=O)=O)[CH2:5][O:4][CH2:3]1.C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:24]([O:31][C:32]([NH:34][C@@H:35]([CH2:39][C:40]([CH3:43])([CH3:42])[CH3:41])[C:36]([OH:38])=[O:37])=[O:33])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.[I-].[Na+]>O.CN(C=O)C.C(OCC)(=O)C>[CH3:1][C:2]1([CH2:6][O:37][C:36](=[O:38])[C@@H:35]([NH:34][C:32]([O:31][CH2:24][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[O:33])[CH2:39][C:40]([CH3:43])([CH3:42])[CH3:41])[CH2:5][O:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 5238Sodium IodideHCID 10796Cesium carbonateHCID 5461213(3-Methyloxetan-3-yl)methyl 4-methylbenzenesulfonateHCID 70202524-Methyl-N-((phenylmethoxy)carbonyl)-L-leucine

生成物 1

HCID 673918222(S)-benzyloxycarbonylamino-4,4-dimethylpentanoic acid 3-methyloxetan-3-ylmethyl ester収率 89.6%

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

Toluene-4-sulfonic acid 3-methyloxetan-3-ylmethyl ester (18.6 g, 66 mmol) was added to a solution of cesium carbonate (13.04 g, 39 mmol) in water (15 ml) and stirred until the solution became clear. The solution was lyophilized overnight to give flaky white solid. The solid was dissolved in DMF (50 ml) and 2(S)-benzyloxycarbonylamino-4,4-dimethylpentanoic acid (15.99 g, 66 mmol) and sodium iodide (2 g, 13.2 mmol) were added. After 48 h, the solution was diluted with 500 ml of ethyl acetate, washed with water, saturated solution of sodium bicarbonate solution (50 ml) and brine. The ethyl acetate layer was separated and dried over MgSO4. The solvent was evaporated and the crude was column chromatographed on a silica gel column using 20:80 EtOAc:Hexane as eluent to give 2(S)-benzyloxycarbonylamino-4,4-dimethylpentanoic acid 3-methyloxetan-3-ylmethyl ester (21.5 g) as a white solid.

後処理

  1. customto give flaky white solid
  2. waitAfter 48 h
  3. washwashed with water, saturated solution of sodium bicarbonate solution (50 ml) and brine
  4. customThe ethyl acetate layer was separated
  5. dry with materialdried over MgSO4
  6. customThe solvent was evaporated
  7. customchromatographed on a silica gel column

出典と根拠

ORDレコード
ord-9de4de9080bd4bc3b358f416417ba9ed
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08013186B2

反応ノート

読み込み中…

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