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Sodium Hydroxide → HCID 178474713, 화합물

HRID 425405
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HRID 425405 반응식
[CH3:1][C:2]([CH3:33])([CH3:32])[CH2:3][C:4]1[N:5]=[C:6]([C:15](O)([CH3:30])[CH2:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]3[CH:28]=[CH:27][C:26]([F:29])=[CH:25][N:24]=3)=[CH:19][CH:18]=2)[N:7](S(N(C)C)(=O)=O)[CH:8]=1.[OH-:34].[Na+].S(=O)(=O)(O)O.[C:41](#[N:43])[CH3:42]>>[CH3:32][C:2]([CH3:33])([CH3:1])[CH2:3][C:4]1[N:5]=[C:6]([C:15]([NH:43][C:41](=[O:34])[CH3:42])([CH3:30])[CH2:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]3[CH:28]=[CH:27][C:26]([F:29])=[CH:25][N:24]=3)=[CH:19][CH:18]=2)[NH:7][CH:8]=1
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참가 물질

4

반응물 3

HCID 14798Sodium HydroxideHCID 22284053Sulfuric acid acetonitrileHCID 667058194-(2,2-dimethylpropyl)-2-{2-[4-(5-fluoropyridin-2-yl)phenyl]-1-hydroxy-1-methylethyl}-N,N-dimethyl-1H-imidazole-1-sulfonamide

생성물 1

HCID 178474713HCID 178474713, 화합물

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온도
140 °C

실험 절차

4-(2,2-dimethylpropyl)-2-{2-[4-(5-fluoropyridin-2-yl)phenyl]-1-hydroxy-1-methylethyl}-N,N-dimethyl-1H-imidazole-1-sulfonamide (for synthesis see Example 15) (20 mg, 0.042 mmol) was dissolved in sulfuric acid/acetonitrile (1:1) (2 mL). After stirring at 140° C. overnight, the reaction mixture was cooled to ambient temperature, neutralized with aqueous sodium hydroxide and extracted with chloroform. The combined organic extracts were dried (magnesium sulfate), filtered, and concentrated in vacuo to afford the title compound. (M+H) found: 409.

후처리

  1. temperaturethe reaction mixture was cooled to ambient temperature
  2. extractionextracted with chloroform
  3. dry with materialThe combined organic extracts were dried (magnesium sulfate)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-98c2204cb25e4b9da72d60267874743d
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106070B2

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