Hydrochloric Acid → 9-Fluoro-4-methyl-1-oxo-8-pyrrolidinyl-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylic acid
反応式
[F:1][C:2]1[C:3]([N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)=[CH:4][C:5]2[N:14]=[CH:13][C:12]3[N:11]([CH3:15])[CH:10]=[C:9]([C:16]([O:18]CC)=[O:17])[C:8](=[O:21])[C:7]=3[C:6]=2[CH:22]=1.[OH-].[K+].Cl>C(O)C>[F:1][C:2]1[C:3]([N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)=[CH:4][C:5]2[N:14]=[CH:13][C:12]3[N:11]([CH3:15])[CH:10]=[C:9]([C:16]([OH:18])=[O:17])[C:8](=[O:21])[C:7]=3[C:6]=2[CH:22]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 70 °C
実験手順
A suspension of 0.8 g of ethyl 9-fluoro-4-methyl-1-oxo-8-pyrrolidinyl-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylate in a mixture of 60 Cm3 of aqueous ethanol at 50% and 2.8 cm3 of a 1 N aqueous potassium hydroxide solution was heated, with stirring, for 2 hours at a temperature of 70° C. After concentration under reduced pressure (5.2 kPa) at 60° C., the residue was dissolved in 100 cm3 of water; the light insoluble material was removed by filtration. The solution obtained was neutralized with 2.8 cm3 of a 1 N aqueous hydrochloric acid solution. The insoluble material formed was dewatered, washed 3 times with 20 cm of water, twice with 15 cm3 of ethanol and dried under vacuum at 100° C. 0.65 g of 9-fluoro-4-methyl-1-oxo-8-pyrrolidinyl-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylic acid was obtained in the form of yellow crystals, which melted at 365° C.
後処理
- temperaturewas heated
- concentrationAfter concentration under reduced pressure (5.2 kPa) at 60° C.
- dissolutionthe residue was dissolved in 100 cm3 of water
- customthe light insoluble material was removed by filtration
- customThe solution obtained
- customThe insoluble material formed
- washwashed 3 times with 20 cm of water
- dry with materialtwice with 15 cm3 of ethanol and dried under vacuum at 100° C
出典と根拠
- ORDレコード
- ord-f540022aa6204cf1898db23e4fed415d
- 出典データセット
- uspto-grants-2003_05
- 特許番号
- US06566362B2
反応ノート
読み込み中…