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Ethyl Acetoacetate → 2-hexylthio-7-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one

HRID 1252092
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HRID 1252092 반응식
[NH2:1][C:2]1[S:3][C:4]([S:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])=[N:5][N:6]=1.[C:14](OCC)(=[O:19])[CH2:15][C:16]([CH3:18])=O>O>[CH2:8]([S:7][C:4]1[S:3][C:2]2=[N:1][C:16]([CH3:18])=[CH:15][C:14](=[O:19])[N:6]2[N:5]=1)[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]
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참가 물질

4

반응물 2

HCID 8868Ethyl AcetoacetateHCID 1579472Sbb043676

생성물 1

HCID 141007692-hexylthio-7-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one수율 82%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Seven (7.0) grams of the thus obtained 2-amino-5-hexylthio-1,3,4-thiadiazole and 4.3 g of ethyl acetoacetate were mixed with 8 g of polyphosphoric acid, and the mixture was heated to 130°-150° C. and stirred for 30 minutes. After cooling, water was added to the reaction mixture, and the resulting mixture was extracted with chloroform. The organic layer was washed with a sodium hydrogen carbonate aqueous solution and water respectively, dried over anhydrous sodium sulfate. The solvent was distilled off. The residue was purified by developing on a silica gel column, and eluting with an ethylacetate/n-hexane (1:1) mixture, and thus 7.5 g of 2-hexylthio-7-methyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. Refraction index nD20 : 1.6003. Yield 82%.

후처리

  1. temperaturethe mixture was heated to 130°-150° C.
  2. temperatureAfter cooling
  3. extractionthe resulting mixture was extracted with chloroform
  4. washThe organic layer was washed with a sodium hydrogen carbonate aqueous solution and water respectively
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationThe solvent was distilled off
  7. customThe residue was purified
  8. washeluting with an ethylacetate/n-hexane (1:1) mixture

출처 및 근거

ORD 기록
ord-d164c1f2beaf416fac28f004e5ce573a
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04742063

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