Chloroacetic Acid → 2-(Carboxymethylthio)-1-(3,5-difluorobenzyl)imidazole

HRID 2107636노트

반응식

HRID 2107636 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:12]=[C:13]([F:15])[CH:14]=1)[CH2:5][N:6]1[CH:10]=[CH:9][N:8]=[C:7]1[SH:11].Cl[CH2:17][C:18]([OH:20])=[O:19].[OH-].[K+].Cl>CN(C)C=O.O>[C:18]([CH2:17][S:11][C:7]1[N:6]([CH2:5][C:4]2[CH:3]=[C:2]([F:1])[CH:14]=[C:13]([F:15])[CH:12]=2)[CH:10]=[CH:9][N:8]=1)([OH:20])=[O:19]

참가 물질

7

실험 절차

1-(3,5-Difluorobenzyl)-2-mercaptoimidazole (2.26 g, 0.010 mole) and chloroacetic acid (0.95 g, 0.010 mole) were dissolved in a mixture of dimethylformamide (10 ml) and water (0.5 ml), and potassium hydroxide (1.12 g, 0.020 mole) in water (10 ml) was added dropwise with stirring at ambient temperature over 30 minutes. Stirring at ambient temperature was continued for five hours. The solution was then diluted with water (10 ml) and acidified with concentrated hydrochloric acid. A trace of precipitate formed. The mixture was filtered and the pH of the filtrate was adjusted to 5.5 with concentrated ammonium hydroxide and the mixture was extracted with three portions of methylene chloride. Concentration of the combined extracts gave a clear, heavy oil which was triturated with boiling ether. A white crystalline solid formed which was filtered and recrystallized from ethyl acetate hexane to give 1.18 g (42% yield) of 2-(carboxymethylthio)-1-(3,5-difluorobenzyl)imidazole, mp 101°-103° C.

후처리

  1. additionwas added dropwise
  2. stirringStirring at ambient temperature
  3. waitwas continued for five hours
  4. customA trace of precipitate formed
  5. filtrationThe mixture was filtered
  6. extractionthe mixture was extracted with three portions of methylene chloride
  7. customConcentration of the combined extracts gave a clear, heavy oil which
  8. customwas triturated with boiling ether
  9. customA white crystalline solid formed which
  10. filtrationwas filtered
  11. customrecrystallized from ethyl acetate hexane

출처 및 근거

ORD 기록
ord-6c77deba5e074acc849903a760f8dcba
출처 데이터셋
uspto-grants-1990_06
특허 번호
US04935438

반응 노트

불러오는 중…