Ammonia → 2-(4-Chlorobenzoylamino)-3-(2-quinolon-4-yl)propionamide

HRID 483187노트

반응식

HRID 483187 반응식
[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([C:6]([NH:8][CH:9]([CH2:13][C:14]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[NH:17][C:16](=[O:24])[CH:15]=2)[C:10]([OH:12])=O)=[O:7])=[CH:4][CH:3]=1.C([N:29](CC)CC)C.ClC(OCC(C)C)=O.N>CN(C)C=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([NH:8][CH:9]([CH2:13][C:14]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[NH:17][C:16](=[O:24])[CH:15]=2)[C:10]([NH2:29])=[O:12])=[O:7])=[CH:25][CH:26]=1

참가 물질

6

실험 절차

1.8 Grams of 2-(4-chlorobenzoylamino)-3-(2-quinolon-4-yl)propionic acid was dissolved in 80 ml of N,N-dimethylformamide. To this solution was added 0.6 g of triethylamine. Then, under ice-cooled condition with stirring, 0.8 g of isobutyl chloroformate was added to the above-mentioned mixture. At the same temperature condition, 10 ml of N,N-dimethylformamide solution containing 0.4 g of ammonia was added dropwise to the reaction mixture, and stirred for 3 hours. After the removal of N,N-dimethylformamide by distillation, water was added to the residue and the crystals precipitated were collected by filtration, and were washed with an aqueous solution of sodium hydroxide. Recrystallized from dimethylformamide-water to obtain 0.7 g of 2-(4-chlorobenzoylamino)-3-(2-quinolon-4-yl)propionamide in the form of light yellowish powdery product.

후처리

  1. temperatureThen, under ice-cooled condition
  2. additionwas added dropwise to the reaction mixture
  3. stirringstirred for 3 hours
  4. customAfter the removal of N,N-dimethylformamide
  5. distillationby distillation, water
  6. additionwas added to the residue
  7. customthe crystals precipitated
  8. filtrationwere collected by filtration
  9. washwere washed with an aqueous solution of sodium hydroxide
  10. customRecrystallized from dimethylformamide-water

출처 및 근거

ORD 기록
ord-af07915151fb4bf68ed53ee5cf365a44
출처 데이터셋
uspto-grants-1986_03
특허 번호
US04578381

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