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Ethanol → 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

HRID 1655249
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인쇄 미리보기

반응식

HRID 1655249 반응식
C(C1[CH:8]=[CH:7][C:6]([N:9]2[C:17]3[CH:16]=[CH:15][N:14]=[CH:13][C:12]=3[N:11]=[C:10]2[CH3:18])=[CH:5][CH:4]=1)#N.[OH-:19].[Na+].[CH2:21]([OH:23])[CH3:22]>>[CH3:18][C:10]1[N:9]([C:6]2[CH:7]=[CH:8][C:22]([C:21]([OH:19])=[O:23])=[CH:4][CH:5]=2)[C:17]2[CH:16]=[CH:15][N:14]=[CH:13][C:12]=2[N:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 106811874-(2-Methyl-1H-imidazo[4,5-c]pyridin-1-yl)benzonitrile

생성물 1

HCID 104674374-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

반응 조건

온도
0 °C

실험 절차

A mixture of 1-(4-cyanophenyl)-2-methylimidazo[4,5-c]pyridine (12.0 g, 51.3 mmol) and 40% aqueous sodium hydroxide (55 ml) in absolute ethanol (55 ml) was heated at reflux for 11/2 hours. The solvent was removed under reduced pressure, and the brown residue was dissolved in water. The solution was chilled to 0° C. by the addition of ice. Glacial acetic acid (ca 33 ml) was added slowly. The buff solid which precipitated was filtered off, washed with water, and dried in vacuo at 70° C. Yield 9.14 g (70%).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 11/2 hours
  3. customThe solvent was removed under reduced pressure
  4. dissolutionthe brown residue was dissolved in water
  5. additionGlacial acetic acid (ca 33 ml) was added slowly
  6. customThe buff solid which precipitated
  7. filtrationwas filtered off
  8. washwashed with water
  9. customdried in vacuo at 70° C

출처 및 근거

ORD 기록
ord-7ad95d7932b4408498a72336f7a94e31
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05250531

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