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

HRID 43948
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HRID 43948 반응식
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]
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참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-ebe057d8dbae4ce8905e4d95bb7252b6
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08536197B2

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