Sodium Hydroxide → 5-Amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-2-phenylquinoline-3-carboxylic acid

HRID 561154ノート

反応式

HRID 561154 の反応式
[NH2:1][C:2]1[C:11]([F:12])=[C:10]([F:13])[C:9]([O:14][CH3:15])=[C:8]2[C:3]=1[C:4](=[O:30])[C:5]([C:25]([O:27]CC)=[O:26])=[C:6]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[N:7]2[CH:16]1[CH2:18][CH2:17]1.[OH-].[Na+]>CCO>[NH2:1][C:2]1[C:11]([F:12])=[C:10]([F:13])[C:9]([O:14][CH3:15])=[C:8]2[C:3]=1[C:4](=[O:30])[C:5]([C:25]([OH:27])=[O:26])=[C:6]([C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)[N:7]2[CH:16]1[CH2:17][CH2:18]1

参加物

4

実験手順

A solution of ethyl 5-amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-2-phenylquinoline-3-carboxylate (980 mg, 2.36 nmol) and 1M aq. NaOH (5 mL) in EtOH (15 mL) was stirred at 50° C. for 24 h. After the reaction mixture was concentrated in vacuo, the residue was dissolved in water and 2M HCl was added to pH<3. The crude product was extracted with EtOAc, washed with brine, dried over MgSO4 and the solvent was removed in vacuo. The crude product was purified by column chromatography (Hexane:EtOAc 5:1→1:1) to yield 5-amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-2-phenylquinoline-3-carboxylic acid (574 mg, 63%) as a yellow amorphous solid.

後処理

  1. concentrationAfter the reaction mixture was concentrated in vacuo
  2. dissolutionthe residue was dissolved in water
  3. addition2M HCl was added to pH<3
  4. extractionThe crude product was extracted with EtOAc
  5. washwashed with brine
  6. dry with materialdried over MgSO4
  7. customthe solvent was removed in vacuo
  8. customThe crude product was purified by column chromatography (Hexane:EtOAc 5:1→1:1)

出典と根拠

ORDレコード
ord-da13fc96bdc147d3b447094618053b06
出典データセット
uspto-grants-2011_11
特許番号
US08063221B2

反応ノート

読み込み中…