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Hydrazine hydrate (1:1) → 5-Chloro-2-(methylthio)pyrimidine-4-carbohydrazide

HRID 2267417
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HRID 2267417 반응식
[Cl:1][C:2]1[C:3]([C:10]([OH:12])=O)=[N:4][C:5]([S:8][CH3:9])=[N:6][CH:7]=1.O.[NH2:14][NH2:15]>C1COCC1.O>[Cl:1][C:2]1[C:3]([C:10]([NH:14][NH2:15])=[O:12])=[N:4][C:5]([S:8][CH3:9])=[N:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 7257115-Chloro-2-(methylsulfanyl)pyrimidine-4-carboxylic acid

생성물 1

HCID 432447685-Chloro-2-(methylthio)pyrimidine-4-carbohydrazide수율 58%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

5-Chloro-2-(methylthio)pyrimidine-4-carboxylic acid (4.0 g, 19.6 mmol) and 1,1-carbonyl diimidazole (6.35 g, 39.2 mmol) were dissolved in 80 mL THF and stirred at room temperature. After 3 h, the solution was cooled with an ice bath and hydrazine hydrate (1.90 mL, 39.2 mmol) was added in one quick portion. The solution was allowed to stir for 5 h, gradually warming to room temperature. The reaction mixture was diluted with excess H2O and extracted with EtOAc several times. These organics were combined and washed with 2 N HCl. The combined aqueous layers were then basified carefully with 5 N NaOH, and extracted once again with EtOAc. This second set of organic layers were combined, dried over magnesium sulfate and concentrated under vacuum to give 2.46 g (58% yield) of product as a white solid. MS (M+H)+ 219.

후처리

  1. temperaturethe solution was cooled with an ice bath
  2. stirringto stir for 5 h
  3. temperaturegradually warming to room temperature
  4. extractionextracted with EtOAc several times
  5. washwashed with 2 N HCl
  6. extractionextracted once again with EtOAc
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-84ebdd80ab9c40b5881f57ffd5c516e8
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858785B2

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