反応式
[CH3:1][N:2]([CH3:18])[CH2:3][C@H:4]([CH3:17])[C@:5]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH3:16])[CH:10]=1)([OH:8])[CH2:6][CH3:7].S(=O)(=O)(O)O.CS(O)(=O)=O.[C:29]1([CH3:39])[CH:34]=[CH:33][C:32]([S:35](O)(=[O:37])=[O:36])=[CH:31][CH:30]=1.[OH-].[Na+]>C1CCCCC1.O1CCCC1>[CH3:39][C:29]1[CH:34]=[CH:33][C:32]([S:35]([O:8][C@:5]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH3:16])[CH:10]=2)([CH2:6][CH3:7])[C@@H:4]([CH3:17])[CH2:3][N:2]([CH3:1])[CH3:18])(=[O:37])=[O:36])=[CH:31][CH:30]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 20 °C
実験手順
Accordingly the compound (2S,3R)-1-(dimethylamino)-3-(3-methoxyphenyl)-2-methyl pentan-3-ol of Formula-V was charged in the solvent tetrahydrofuran and under stirring charged concentrated sulfuric acid at temperature of 20-30° C. The reaction mixture is stirred and charged methanesulfonic acid or para toluenesulfonic acid and solvent cyclohexane. Stirred and raised the temperature to reflux. Maintained the reaction mass at reflux temperature for 3-5 hours with simultaneous removal of water. Cooled the reaction mass to 20° C. and quenched with water. The pH of the quenched reaction solution was adjusted to 8-9 using dilute sodium hydroxide solution. The reaction solution was extracted with cyclohexane. Separated the organic layer and concentrated under reduced pressure to get the compound (2S,3R)-1-(dimethylamino)-3-(3-methoxyphenyl)-2-methyl pentan-3-yl methane sulfonate of Formula IXA or (2S,3R)-1-(dimethylamino)-3-(3-methoxyphenyl)-2-methyl-pentan-3-yl 4-methylbenzenesulfonate of Formula IXB.
後処理
- stirringThe reaction mixture is stirred
- stirringStirred
- temperatureraised the temperature
- temperatureto reflux
- temperatureMaintained the reaction mass
- temperatureat reflux temperature for 3-5 hours
- customwith simultaneous removal of water
- customquenched with water
- customThe pH of the quenched reaction solution
- extractionThe reaction solution was extracted with cyclohexane
- customSeparated the organic layer
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-ea248a4580344c1b8f17e9ed117ceaeb
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08853456B2
関連ノート
読み込み中…