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Dimethylformamide → (2S,4R)-2-(dimethylcarbamoyl)methyloxymethyl-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

HRID 703574
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HRID 703574 반응식
[CH3:1][N:2]([CH3:5])[CH:3]=[O:4].P(Cl)(Cl)(Cl)=O.C([CH2:14][O:15][CH2:16][C@@H:17]1[CH2:21][C@@H:20]([O:22][S:23]([CH3:26])(=[O:25])=[O:24])[CH2:19][N:18]1[C:27]([O:29][CH2:30][C:31]1[CH:36]=[CH:35][C:34]([N+:37]([O-:39])=[O:38])=[CH:33][CH:32]=1)=[O:28])(O)=O.Cl.CNC>O1CCCC1.CO.C(OCC)(=O)C.C(N(CC)CC)C>[CH3:1][N:2]([CH3:5])[C:3]([CH2:14][O:15][CH2:16][C@@H:17]1[CH2:21][C@@H:20]([O:22][S:23]([CH3:26])(=[O:24])=[O:25])[CH2:19][N:18]1[C:27]([O:29][CH2:30][C:31]1[CH:32]=[CH:33][C:34]([N+:37]([O-:39])=[O:38])=[CH:35][CH:36]=1)=[O:28])=[O:4]
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참가 물질

9

반응물 4

HCID 6228DimethylformamideHCID 10473Dimethylamine, hydrochlorideHCID 24813Phosphorus oxychlorideHCID 18631935(2S,4R)-2-(carboxymethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

생성물 1

HCID 86744485(2S,4R)-2-(dimethylcarbamoyl)methyloxymethyl-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

시약·촉매·용매

4
HCID 887Methanol용매HCID 8028Tetrahydrofuran용매2회HCID 8471Triethylamine용매HCID 8857Ethyl Acetate용매

실험 절차

To a mixture of dimethylformamide (3.9 ml) and tetrahydrofuran (30 ml) was dropwise added phosphorus oxychloride (3.75 ml) at 0°-10° C. and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added a solution of (2S,4R)-2-(carboxymethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (14.50 g) in tetrahydrofuran (15 ml) at 0°-10° C. and the mixture was stirred at the same temperature for 30 minutes. The resulting mixture was dropwise added to a mixture of dimethylamine hydrochloride (50 g) and triethylamine (100 ml) in methanol (200 ml) at 0°-10° C. with stirring. The mixture was stirred at the same temperature for 2 hours. The insoluble material was filtered off and the filtrate was concentrated under reduced pressure to give a syrup. The syrup was dissolved in ethyl acetate (200 ml), washed with water (200 ml), 1N hydrochloric acid (200 ml), saturated aqueous sodium hydrogen carbonate (200 ml) and brine (200 ml), in turn, dried over magnesium sulfate, and concentrated under reduced pressure to give (2S,4R)-2-(dimethylcarbamoyl)methyloxymethyl-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (12.03 g).

후처리

  1. customat 0°-10° C.
  2. stirringthe mixture was stirred at the same temperature for 30 minutes
  3. stirringwith stirring
  4. stirringThe mixture was stirred at the same temperature for 2 hours
  5. filtrationThe insoluble material was filtered off
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. customto give a syrup
  8. washwashed with water (200 ml), 1N hydrochloric acid (200 ml), saturated aqueous sodium hydrogen carbonate (200 ml) and brine (200 ml), in turn
  9. dry with materialdried over magnesium sulfate
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e3b3e852e32047a486dd1f0df75fbe4e
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04983596

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