2-Amino-5-fluoropyridine → 7-Chloro-6-fluoro-1-(5-fluoro-pyridin-2-yl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic Acid Ethyl Ester
반응식
[CH2:1]([O:3][C:4](=[O:21])[C:5]([C:10](=[O:20])[C:11]1[CH:16]=[C:15]([F:17])[C:14]([Cl:18])=[CH:13][C:12]=1Cl)=[CH:6]OCC)[CH3:2].[NH2:22][C:23]1[CH:28]=[CH:27][C:26]([F:29])=[CH:25][N:24]=1>C(O)C>[CH2:1]([O:3][C:4]([C:5]1[C:10](=[O:20])[C:11]2[C:12](=[CH:13][C:14]([Cl:18])=[C:15]([F:17])[CH:16]=2)[N:22]([C:23]2[CH:28]=[CH:27][C:26]([F:29])=[CH:25][N:24]=2)[CH:6]=1)=[O:21])[CH3:2]참가 물질
실험 절차
A solution of 0.747 g of 2-(2,4-dichloro-5-fluoro-benzoyl)-3-ethoxy-acrylic acid ethyl ester (2.23 mmol) and 0.250 g of 2-amino-5-fluoropyridine (2.23 mmol) in 5 ml ethanol was stirred at reflux for 25 hrs. The reaction was monitored by TLC. The ethanol was evaporated and the last traces of ethanol were distilled from an azeotrope with a mixture of 10 ml heptane and 10 ml ethyl acetate. The yellow oil was dissolved in 10 ml of THF, reacted with 120 mg of a 50% NaH suspension in oil and stirred at reflux over night. The solvent was evaporated, the residue dissolved in dichloromethane/methanol 9:1, washed with water and brine, dried over Mg sulfate, filtered and evaporated. The residue was digested in ethyl acetate, and the solid filtered.
후처리
- temperatureat reflux for 25 hrs
- customThe ethanol was evaporated
- distillationthe last traces of ethanol were distilled from an azeotrope with a mixture of 10 ml heptane and 10 ml ethyl acetate
- dissolutionThe yellow oil was dissolved in 10 ml of THF
- customreacted with 120 mg of a 50% NaH suspension in oil
- temperatureat reflux over night
- customThe solvent was evaporated
- dissolutionthe residue dissolved in dichloromethane/methanol 9:1
- washwashed with water and brine
- dry with materialdried over Mg sulfate
- filtrationfiltered
- customevaporated
- filtrationthe solid filtered
출처 및 근거
- ORD 기록
- ord-63c5a3fbb13d45b4a5eeaff8c6ec595a
- 출처 데이터셋
- uspto-grants-2010_10
- 특허 번호
- US07820823B2
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