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Lawesson's reagent → tert-Butyl 2-thioxo-1,4'-bipiperidin-1'-carboxylate

HRID 2366552
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HRID 2366552 반응식
O=[C:2]1[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[CH:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:30])=CC=1>C1(C)C=CC=CC=1>[S:30]=[C:2]1[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[CH:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]1
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참가 물질

4

반응물 2

HCID 87949Lawesson's reagentHCID 66524582Tert-butyl 2-oxo-1,4'-bipiperidine-1'-carboxylate

생성물 1

HCID 86082829tert-Butyl 2-thioxo-1,4'-bipiperidin-1'-carboxylate수율 128.7%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of tert-butyl 2-oxo-1,4′-bipiperidin-1′-carboxylate (2.8 g) and Lawesson's reagent (2.0 g) in toluene (30 mL) was refluxed for one hour. Toluene was distilled off under reduced pressure, and the residue was diluted with dichloromethane, and washed with an aqueous 1N sodium hydroxide solution and saturated saline solution. This dichloromethane solution was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1 to 1/2) to obtain the title compound (1.9 g, 64%) as a white powder.

후처리

  1. distillationToluene was distilled off under reduced pressure
  2. additionthe residue was diluted with dichloromethane
  3. washwashed with an aqueous 1N sodium hydroxide solution and saturated saline solution
  4. dry with materialThis dichloromethane solution was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1 to 1/2)

출처 및 근거

ORD 기록
ord-ff1f1615cd8d44d88f9328bf4a1ecd50
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08697865B2

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