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4-Sulfanylidene-1,3-thiazolidin-2-one → HCID 178518187, 화합물

HRID 1620756
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HRID 1620756 반응식
[NH2:1][C@H:2]1[C@H:7]([OH:8])[CH2:6][CH2:5][O:4][CH2:3]1.S=[C:10]1[CH2:14][S:13][C:12](=[O:15])[NH:11]1>C(O)C>[O:15]=[C:12]1[N:11]=[C:10]([NH:1][C@H:2]2[C@H:7]([OH:8])[CH2:6][CH2:5][O:4][CH2:3]2)[CH2:14][S:13]1
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참가 물질

4

반응물 2

HCID 15395954-Sulfanylidene-1,3-thiazolidin-2-oneHCID 72207589(3R,4R)-3-Aminotetrahydro-2H-pyran-4-ol

생성물 1

HCID 178518187HCID 178518187, 화합물수율 73.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 2-amino-1,5-anhydro-2,4-dideoxy-threo-pentitol (527 mg) in ethanol (100 mL) was added 4-thioxo-1,3-thiazolidin-2-one (590 mg), and the mixture was heated under reflux for 15 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, ethyl acetate) to give the title compound (700 mg).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 15 hr
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. customthe residue was purified by silica gel column chromatography (NH, ethyl acetate)

출처 및 근거

ORD 기록
ord-831048285ab54fbf96293076f12e765d
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772277B2

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