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Sodium Thiosulfate → Methyl cis(+/-)-3-acetyl-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)thiophene-2-carboxylate

HRID 43948
ノート
印刷プレビュー

反応式

HRID 43948 の反応式
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[CH2:23]([O:30][C:31]([NH:33][C@H:34]1[CH2:39][CH2:38][N:37]([C:40]2[S:44][C:43]([C:45]([O:47][CH3:48])=[O:46])=[C:42]([CH:49]([OH:51])[CH3:50])[CH:41]=2)[CH2:36][C@H:35]1[O:52][CH3:53])=[O:32])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.S([O-])([O-])(=O)=S.[Na+].[Na+]>ClCCl>[C:49]([C:42]1[CH:41]=[C:40]([N:37]2[CH2:38][CH2:39][C@H:34]([NH:33][C:31]([O:30][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)=[O:32])[C@H:35]([O:52][CH3:53])[CH2:36]2)[S:44][C:43]=1[C:45]([O:47][CH3:48])=[O:46])(=[O:51])[CH3:50]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24477Sodium ThiosulfateHCID 159087TriacetoxyperiodinaneHCID 68405949Methyl 5-((3R*,4S*)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-3-(1-hydroxyethyl)thiophene-2-carboxylate

生成物 1

HCID 86648832Methyl cis(+/-)-3-acetyl-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)thiophene-2-carboxylate収率 49.5%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

The Dess-Martin reagent (305 mg, 0.72 mmol) was added to a solution of methyl 5-((3R*,4S*)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-3-(1-hydroxyethyl)thiophene-2-carboxylate obtained in Example (246d) (215 mg, 0.48 mmol) in dichloromethane (5 mL) at room temperature, followed by stirring for one hour. Aqueous sodium thiosulfate solution was added to the reaction solution, followed by stirring at room temperature. Then, the mixture was extracted with chloroform. The combined organic layers were dried over anhydrous magnesium sulfate. Following filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/1) to obtain 106 mg of the title compound as a yellow oily substance (50%).

後処理

  1. stirringby stirring at room temperature
  2. extractionThen, the mixture was extracted with chloroform
  3. dry with materialThe combined organic layers were dried over anhydrous magnesium sulfate
  4. filtrationfiltration
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/1)

出典と根拠

ORDレコード
ord-ebe057d8dbae4ce8905e4d95bb7252b6
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08536197B2

反応ノート

読み込み中…

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