Pyridine → 7-Chloro-1-(2-chloroethyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, ethyl ester
反応式
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:20])[C:7]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:8][N:9]2[CH2:12][CH2:13]O)=[CH:4][C:3]=1[F:21].N1C=CC=CC=1.C([O-])([O-])=O.[Na+].[Na+].S(Cl)([Cl:36])=O>>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:20])[C:7]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:8][N:9]2[CH2:12][CH2:13][Cl:36])=[CH:4][C:3]=1[F:21]参加物
実験手順
27 g of the foregoing ester product were added, portionwise, to an agitated and cooled solution of pyridine (8.1 cm3) in thionyl chloride (54 cm3). The addition was carried out at such a rate that the temperature of the mixture remained between 0° and 5° C. After returning to room temperature, the solution was heated for 1 hour under reflux and the excess of reagent was then removed by distillation under reduced pressure. The residue was added, with agitation, to 100 cm3 of iced water. The suspension obtained was neutralised by the addition of 10% aqueous Na2CO3. The precipitate obtained was filtered off, washed with water and recrystallised from ethanol (480 cm3). 22.4 g of 7-chloro-1-(2-chloroethyl)-3-ethoxycarbonyl-6-fluoro-4-oxo-1,4-dihydro-quinoline, m.p. 222° C., were obtained; yield 80%.
後処理
- additionThe addition
- customremained between 0° and 5° C
- customAfter returning to room temperature
- temperaturethe solution was heated for 1 hour
- temperatureunder reflux
- customthe excess of reagent was then removed by distillation under reduced pressure
- additionThe residue was added, with agitation, to 100 cm3 of iced water
- customThe suspension obtained
- customThe precipitate obtained
- filtrationwas filtered off
- washwashed with water
- customrecrystallised from ethanol (480 cm3)
出典と根拠
- ORDレコード
- ord-9a9ba1ca650e4991835d4b9a579c1720
- 出典データセット
- uspto-grants-1981_09
- 特許番号
- US04292317
反応ノート
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