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Sodium Hydroxide → 5-Amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

HRID 561094
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반응식

HRID 561094 반응식
[NH2:1][C:2]1[C:11]([F:12])=[C:10]([F:13])[C:9]([F:14])=[C:8]2[C:3]=1[C:4](=[O:23])[C:5]([C:18]([O:20]CC)=[O:19])=[CH:6][N:7]2[CH:15]1[CH2:17][CH2:16]1.[OH-].[Na+]>>[NH2:1][C:2]1[C:11]([F:12])=[C:10]([F:13])[C:9]([F:14])=[C:8]2[C:3]=1[C:4](=[O:23])[C:5]([C:18]([OH:20])=[O:19])=[CH:6][N:7]2[CH:15]1[CH2:16][CH2:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14798Sodium HydroxideHCID 14127986Ethyl 5-amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

생성물 1

HCID 139109475-Amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid수율 77%

실험 절차

A solution of 6 (1.85 g, 5.7 mmol) in a mixture of AcOH—H2O—H2SO4 (8:6:1 v/v, 75 mL) was heated at reflux for 2 h. The reaction mixture was poured into ice water and adjusted to pH 4 with 1M NaOH solution. A precipitate formed and was collected by filtration, washed successively with water and ethanol and then dried to give 7 (1.3 g, 77%) as a light yellow solid.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 2 h
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customA precipitate formed
  • filtrationwas collected by filtration
  • washwashed successively with water and ethanol
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-8136ff04c59840e2b31b05552b340087
    출처 데이터셋
    uspto-grants-2011_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08063221B2

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