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Ethyl 4-piperidinecarboxylate → Ethyl 1-carbamothioylpiperidine-4-carboxylate

HRID 1028145
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HRID 1028145 반응식
[Si]([N:5]=[C:6]=[S:7])(C)(C)C.[NH:8]1[CH2:13][CH2:12][CH:11]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH2:10][CH2:9]1>O1CCCC1.C(OCC)(=O)C>[C:6]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH2:10][CH2:9]1)(=[S:7])[NH2:5]
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참가 물질

5

반응물 2

HCID 70770Ethyl 4-piperidinecarboxylateHCID 75297Isothiocyanatotrimethylsilane

생성물 1

HCID 23076419Ethyl 1-carbamothioylpiperidine-4-carboxylate수율 20.3%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of TMS-isothiocyanate (5.4 mL, 38 mmol) and ethyl piperidine-4-carboxylate (5.9 ml, 38 mmol) in tetrahydrofuran (127 ml) was stirred at room temperature for 3 days. The mixture was then diluted with 500 mL ethyl acetate and washed with 500 mL water and 500 mL brine. The aqueous fractions were further extracted with 500 mL ethyl acetate. The combined organic extracts were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by CombiFlash (40-100% ethyl acetate/hexanes) to provide 1.85 g (7.7 mmol, 20%) of ethyl 1-carbamothioylpiperidine-4-carboxylate as a white solid.

후처리

  1. washwashed with 500 mL water and 500 mL brine
  2. extractionThe aqueous fractions were further extracted with 500 mL ethyl acetate
  3. dry with materialThe combined organic extracts were dried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by CombiFlash (40-100% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-46960106a52a4a48b1398f104ccdfe19
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735417B2

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