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Hydrogen Peroxide → 2-(6-Bromopyridin-2-yl)-2-methylpropanamide

HRID 385912
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인쇄 미리보기

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HRID 385912 반응식
[Br:1][C:2]1[N:7]=[C:6]([C:8]([CH3:12])([CH3:11])[C:9]#[N:10])[CH:5]=[CH:4][CH:3]=1.OO.C(=O)([O-])[O-:16].[K+].[K+]>CS(C)=O>[Br:1][C:2]1[N:7]=[C:6]([C:8]([CH3:12])([CH3:11])[C:9]([NH2:10])=[O:16])[CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 784Hydrogen PeroxideHCID 11430Potassium CarbonateHCID 579696582-(6-Bromopyridin-2-yl)-2-methylpropanenitrile

생성물 1

HCID 595255632-(6-Bromopyridin-2-yl)-2-methylpropanamide

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

반응 조건

온도
70 °C

실험 절차

To a solution of 2-(6-bromopyridin-2-yl)-2-methylpropanenitrile (Example 367, Step 1) (200 mg, 0.89 mmol) in dimethylsulfoxide (4 mL) was added hydrogen peroxide (0.42 mL, 4.8 mmol) and potassium carbonate (1.23 g, 8.89 mmol). The reaction was then stirred overnight at 70° C. The resulting slurry was cooled to ambient temperature, filtered and directly purified by reverse phase HPLC (10-100% acteonitrile/water+0.05% TFA modifier) to yield the title compound.

후처리

  1. temperatureThe resulting slurry was cooled to ambient temperature
  2. filtrationfiltered
  3. customdirectly purified by reverse phase HPLC (10-100% acteonitrile/water+0.05% TFA modifier)

출처 및 근거

ORD 기록
ord-78b45d5989f648298460c2852aeefe9f
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367706B2

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