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Thiosemicarbazide → 5-(2,2,3,3-Tetrafluoro-1-methylcyclobutyl)-1,3,4-thiadiazol-2-amine

HRID 717225
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HRID 717225 반응식
[F:1][C:2]1([F:12])[C:5]([F:7])([F:6])[CH2:4][C:3]1([CH3:11])[C:8](Cl)=O.[NH2:13][NH:14][C:15]([NH2:17])=[S:16]>O1CCOCC1>[F:1][C:2]1([F:12])[C:5]([F:7])([F:6])[CH2:4][C:3]1([C:8]1[S:16][C:15]([NH2:17])=[N:14][N:13]=1)[CH3:11]
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참가 물질

4

반응물 2

HCID 2723789ThiosemicarbazideHCID 533989902,2,3,3-Tetrafluoro-1-(methyl)cyclobutanecarbonyl chloride

생성물 1

HCID 866298495-(2,2,3,3-Tetrafluoro-1-methylcyclobutyl)-1,3,4-thiadiazol-2-amine

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

A mixture of 2,2,3,3-tetrafluoro-1-methylcyclobutanecarbonyl chloride (ABCR) (2 g, 9.78 mmol) and thiosemicarbazide (Aldrich) (0.891 g, 9.78 mmol) in 10 mL of dioxane was heated at 90° C. for 12 h. The solvent was evaporated under reduced pressure. The residue was dissolved in dichloromethane and washed with saturated NaHCO3. The organic extract was dried over Na2SO4 and concentrated. The residue was purified by flash chromatography on SiO2 (2% methanol in dichloromethane) to give the title compound. MS (ESI+) m/z 242 (M+H)+.

후처리

  1. customThe solvent was evaporated under reduced pressure
  2. dissolutionThe residue was dissolved in dichloromethane
  3. washwashed with saturated NaHCO3
  4. extractionThe organic extract
  5. dry with materialwas dried over Na2SO4
  6. concentrationconcentrated
  7. customThe residue was purified by flash chromatography on SiO2 (2% methanol in dichloromethane)

출처 및 근거

ORD 기록
ord-cec3a18d108d4608890470a4b1e454e7
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09193713B2

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