Hydrochloric Acid → 1-{2-Chloro-5-[(R)-1-(4-chloro-3,5-dimethyl-phenyl)-propylamino]-benzyl}-azetidine-3-carboxylic acid
反応式
C([O:5][C:6]([CH:8]1[CH2:11][N:10]([CH2:12][C:13]2[CH:18]=[C:17]([NH:19][C@@H:20]([C:23]3[CH:28]=[C:27]([CH3:29])[C:26]([Cl:30])=[C:25]([CH3:31])[CH:24]=3)[CH2:21][CH3:22])[CH:16]=[CH:15][C:14]=2[Cl:32])[CH2:9]1)=[O:7])(C)(C)C.Cl>C(Cl)Cl>[Cl:32][C:14]1[CH:15]=[CH:16][C:17]([NH:19][C@@H:20]([C:23]2[CH:28]=[C:27]([CH3:29])[C:26]([Cl:30])=[C:25]([CH3:31])[CH:24]=2)[CH2:21][CH3:22])=[CH:18][C:13]=1[CH2:12][N:10]1[CH2:9][CH:8]([C:6]([OH:7])=[O:5])[CH2:11]1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of INT 58 (206 mg, 0.431 mmol) in CH2Cl2 (5 mL) was treated with HCl (4 M in dioxane, 0.43 mL, 1.726 mmol) and stirred at room temperature overnight. The mixture contained some starting material, so another portion of HCl (4 M in dioxane, 0.50 ml, 2.00 mmol) was added and stirring continued for 4 hours. Excess of HCl gas was removed by a stream of argon. The mixture was neutralized with 10% sodium bicarbonate solution then treated with 10% ammonium chloride solution and extracted first with CH2Cl2 then with EtOAc. The combined organic layers were dried over sodium sulfate, filtered and concentrated. The title compound was purified by preparative UPLC (H2O/CH3CN).
後処理
- stirringstirring
- waitcontinued for 4 hours
- customExcess of HCl gas was removed by a stream of argon
- additionthen treated with 10% ammonium chloride solution
- extractionextracted first with CH2Cl2
- dry with materialThe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe title compound was purified by preparative UPLC (H2O/CH3CN)
出典と根拠
- ORDレコード
- ord-b4d472d77a394a3093326a0ebdecb420
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08791100B2
反応ノート
読み込み中…