Triethylamine → 1-(5-Amino-2,4-difluorophenyl)-8-chloro-7-dimethylamino-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid Hydrochloride

HRID 369228노트

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HRID 369228 반응식
[NH2:1][C:2]1[C:3]([F:26])=[CH:4][C:5]([F:25])=[C:6]([N:8]2[C:17]3[C:12](=[CH:13][C:14]([F:20])=[C:15](F)[C:16]=3[Cl:18])[C:11](=[O:21])[C:10]([C:22]([OH:24])=[O:23])=[CH:9]2)[CH:7]=1.Cl.[CH3:28][NH:29][CH3:30].C(N(CC)CC)C>C(#N)C>[ClH:18].[NH2:1][C:2]1[C:3]([F:26])=[CH:4][C:5]([F:25])=[C:6]([N:8]2[C:17]3[C:12](=[CH:13][C:14]([F:20])=[C:15]([N:29]([CH3:30])[CH3:28])[C:16]=3[Cl:18])[C:11](=[O:21])[C:10]([C:22]([OH:24])=[O:23])=[CH:9]2)[CH:7]=1

참가 물질

5

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온도
60 °C

실험 절차

1-(5-Amino-2,4-difluorophenyl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (100 mg), dimethylamine hydrochloride (94 mg) and triethylamine (140 mg) were added to acetonitrile (10 ml), and the mixture was heated and stirred overnight at 60° C. After the reaction mixture was allowed to cool, the solvent was distilled off under reduced pressure. Ethanol and concentrated hydrochloric acid were added to the residue, and the mixture was concentrated again under reduced pressure. Ethanol was added to the residue, and solids were collected by filtration. The solids were washed successively with ethanol and diethyl ether to obtain the title compound (70 mg) as a yellow powder.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto cool
  3. distillationthe solvent was distilled off under reduced pressure
  4. additionEthanol and concentrated hydrochloric acid were added to the residue
  5. concentrationthe mixture was concentrated again under reduced pressure
  6. additionEthanol was added to the residue, and solids
  7. filtrationwere collected by filtration
  8. washThe solids were washed successively with ethanol and diethyl ether

출처 및 근거

ORD 기록
ord-09325b36faca4258832515663e5e8d6d
출처 데이터셋
uspto-grants-2000_10
특허 번호
US06136823

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