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Sodium Hydroxide → 5-Amino-1-methyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxoquinoline-3-carboxylic acid

HRID 561140
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HRID 561140 반응식
[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:22])[C:5]([C:17]([O:19]CC)=[O:18])=[CH:6][N:7]2[CH3:16].[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:22])[C:5]([C:17]([OH:19])=[O:18])=[CH:6][N:7]2[CH3:16]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 59003029Ethyl 5-amino-1-methyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxoquinoline-3-carboxylate

생성물 1

HCID 590028475-Amino-1-methyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxoquinoline-3-carboxylic acid수율 97.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of ethyl 5-amino-1-methyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxoquinoline-3-carboxylate (203 mg, 0.650 mmol) and 1M aq. NaOH (2 mL) in EtOH (5 mL) was stirred at 50° C. for 1 h. The solvent was removed and the residue was dissolved in water. The solution was acidified to pH 7 with 2M HCl and the resulting precipitate was removed by filtration, washed with water, and dried to yield 5-amino-1-methyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxoquinoline-3-carboxylic acid (180 mg, 97%) as a pale yellow solid.

후처리

  1. customThe solvent was removed
  2. dissolutionthe residue was dissolved in water
  3. customthe resulting precipitate was removed by filtration
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-be6768affbee4e6cb39b6ce7802d7a83
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063221B2

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