反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[F:29])=[C:6]([CH2:8][C:9]2[N:14]=[C:13]([C:15]([O:17]CC)=[O:16])[CH:12]=[CH:11][CH:10]=2)[CH:7]=1.[OH-].[Na+:31]>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[F:29])=[C:6]([CH2:8][C:9]2[N:14]=[C:13]([C:15]([O-:17])=[O:16])[CH:12]=[CH:11][CH:10]=2)[CH:7]=1.[Na+:31]参加物
実験手順
Ethyl 6-[(5-chloro-2-{[(4-chloro-2-fluorophenyl)methyl]oxy}phenyl)methyl]-2-pyridinecarboxylate (2 g) was dissolved in ethanol (15 ml) at reflux. 2M Sodium hydroxide (3.4 ml) was added and the solution heated under reflux for 30 minutes. No residual starting material by HPLC. The solution was filtered and the filter washed with a mixture of hot ethanol (5 ml) and water (5 ml). The combined filtrate and wash were re-heated to reflux, and water (15 ml) added dropwise over ˜5 minutes and the clear solution allowed to cool slowly to room temperature. The product crystallised rapidly at ˜35° C. The resulting thick suspension was cooled to 20-25° C. and stirred for 1 hour. The product was isolated and washed with 1:3 ethanol:water (20 ml) and then dried overnight at 50° C. in vacuo to give the title compound (1.94 g).
後処理
- temperatureat reflux
- temperaturethe solution heated
- temperatureunder reflux for 30 minutes
- filtrationThe solution was filtered
- washthe filter washed with a mixture of hot ethanol (5 ml) and water (5 ml)
- washThe combined filtrate and wash
- temperaturewere re-heated
- temperatureto reflux
- additionwater (15 ml) added dropwise over ˜5 minutes
- customThe product crystallised rapidly at ˜35° C
- temperatureThe resulting thick suspension was cooled to 20-25° C.
- customThe product was isolated
- washwashed with 1:3 ethanol
- dry with materialwater (20 ml) and then dried overnight at 50° C. in vacuo
出典と根拠
- ORDレコード
- ord-b2973bc9068e45339ab308432797ce78
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07759369B2
関連ノート
読み込み中…