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Sodium Bicarbonate → HCID 58742216, 화합물

HRID 1514441
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HRID 1514441 반응식
[CH3:1][C:2]1[S:3][C:4]([C:8]2[CH:13]=[CH:12][N:11]=[C:10](SC)[N:9]=2)=[C:5]([CH3:7])[N:6]=1.O[O:17][S:18]([O-:20])=O.[K+].[C:22]([O-])(O)=O.[Na+]>CO>[CH3:1][C:2]1[S:3][C:4]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([S:18]([CH3:22])(=[O:20])=[O:17])[N:9]=2)=[C:5]([CH3:7])[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 23707502Potassium hydroxy sulfiteHCID 587422264-(2,4-Dimethyl-thiazol-5-yl)-2-methylsulfanyl-pyrimidine

생성물 1

HCID 58742216HCID 58742216, 화합물수율 75%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 4-(2,4-dimethyl-thiazol-5-yl)-2-methylsulfanyl-pyrimidine (342 mg, 1.44 mmol) in MeOH (12 ml) was cooled at 0° C., then an aqueous solution of oxone (2.65 g, 4.32 mmol in 12 ml of water) was slowly added. After stirring 2 hours at room temperature, the mixture was basified with 5% NaHCO3 and the product was extracted with ethyl acetate. The organic phase was dried (Na2SO4) and evaporated to give 288 mg of the title compound that was used in the next step without further purification (75% yield).

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후처리

  1. extractionthe product was extracted with ethyl acetate
  2. dry with materialThe organic phase was dried (Na2SO4)
  3. customevaporated

출처 및 근거

ORD 기록
ord-c64d34ced7b444a792caf48cbc990fa2
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222266B2

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