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Sodium Thiosulfate → HCID 59909746、化合物

HRID 2084519
ノート
印刷プレビュー

反応式

HRID 2084519 の反応式
[CH:1]1([CH2:7][CH2:8][CH2:9][C@@H:10]([C:19]([NH:21][CH:22]([C:26]([O:28][CH3:29])=[O:27])[CH:23]([OH:25])[CH3:24])=[O:20])[CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.S([O-])([O-])(=O)=S.[Na+].[Na+].C(=O)([O-])O.[Na+]>ClCCl>[CH:1]1([CH2:7][CH2:8][CH2:9][C@@H:10]([C:19]([NH:21][CH:22]([C:26]([O:28][CH3:29])=[O:27])[C:23](=[O:25])[CH3:24])=[O:20])[CH2:11][C:12]([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 24477Sodium ThiosulfateHCID 159087TriacetoxyperiodinaneHCID 516892Sodium BicarbonateHCID 59909827HCID 59909827、化合物

生成物 1

HCID 59909746HCID 59909746、化合物収率 75.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒

実験手順

A solution of tert-butyl (3R)-6-cyclohexyl-3-({[2-hydroxy-1-(methoxycarbonyl)propyl]amino}carbonyl)hexanoate (Preparation 171) (6.48 g, 15.69 mmol) in dichloromethane (60 ml) was treated with Dess-Martin periodinane [1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one] (7.32 g, 17.26 mmol) and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. A solution of sodium thiosulphate (6 g in 50 ml water) and a saturated aqueous sodium hydrogen carbonate solution (50 ml) were then added to the mixture which was stirred for a further 10 minutes. The layers were separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were sequentially washed with water and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel eluting with a gradient system of pentane: ethyl acetate (100:0 to 90:10) to afford the title compound as a colourless oil (4.86 g)

後処理

  1. stirringwas stirred for a further 10 minutes
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with dichloromethane
  4. washThe combined organic layers were sequentially washed with water and brine
  5. dry with materialdried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. customthe solvent removed under reduced pressure
  8. customThe residue was purified by column chromatography on silica gel eluting with a gradient system of pentane: ethyl acetate (100:0 to 90:10)

出典と根拠

ORDレコード
ord-654bc111fa144634ad9379a7a446e231
出典データセット
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06716861B2

反応ノート

読み込み中…

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