Hydrochloric Acid → 3-(4-carboxy-2-oxo-2H-pyridin-1-ylmethyl)-7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid methyl ester
반응식
[CH3:1][O:2][C:3]([C:5]1[N:6]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:7]2[C:12]([C:13](=[O:27])[C:14]=1[CH2:15][N:16]1[CH:21]=[CH:20][C:19]([C:22]([O:24]C)=[O:23])=[CH:18][C:17]1=[O:26])=[CH:11][CH:10]=[C:9]([Cl:28])[CH:8]=2)=[O:4].[OH-].[Na+].Cl>O1CCCC1>[CH3:1][O:2][C:3]([C:5]1[N:6]([C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)[C:7]2[C:12]([C:13](=[O:27])[C:14]=1[CH2:15][N:16]1[CH:21]=[CH:20][C:19]([C:22]([OH:24])=[O:23])=[CH:18][C:17]1=[O:26])=[CH:11][CH:10]=[C:9]([Cl:28])[CH:8]=2)=[O:4]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 25 °C
실험 절차
A solution of 7-chloro-3-(4-methoxycarbonyl-2-oxo-2H-pyridin-1-ylmethyl)-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid methyl ester (0.22 g, 459 μmol) in tetrahydrofuran (10 mL) at 25° C. was treated with a 1N aqueous sodium hydroxide solution (0.7 mL, 459 μmol). The reaction was stirred at 25° C. for 2 h. At this time, the reaction was acidified with a 1N aqueous hydrochloric acid solution and then concentrated in vacuo to afford 3-(4-carboxy-2-oxo-2H-pyridin-1-ylmethyl)-7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid methyl ester. The material was used without further purification.
후처리
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-94c2035d25f14872ad6df4bbdd28150e
- 출처 데이터셋
- uspto-grants-2013_06
- 특허 번호
- US08471027B2
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