Dimethyl Sulfoxide → Methyl 4-(piperidin-2-yl)butanoate hydrochloride
反応式
CS(C)=O.C(Cl)(=O)C([Cl:8])=O.C(OC([N:18]1[CH2:23][CH2:22][CH2:21][CH2:20][CH:19]1[CH2:24][CH2:25][CH2:26][C:27]([O:29][CH3:30])=[O:28])=O)(C)(C)C.CCN(CC)CC>C(Cl)Cl>[ClH:8].[NH:18]1[CH2:23][CH2:22][CH2:21][CH2:20][CH:19]1[CH2:24][CH2:25][CH2:26][C:27]([O:29][CH3:30])=[O:28]参加物
反応条件
- 温度
- -78 °C
実験手順
A solution of DMSO (21.24 ml, 299 mmol) in CH2Cl2 (600 ml) was dropwise added to a solution of oxalyl chloride (15.0 ml, 171 mmol) in CH2Cl2 (300 ml) in 30 min while maintaining the internal temperature below −65° C. A solution of 3 (46.7 g, 142 mmol) in CH2Cl2 (300 ml) was added dropwise in 15 min. while maintaining the temperature below −65° C. The reaction mixture was stirred an additional 45 minutes at −78° C., after which Et3N (99.0 ml, 712 mmol) was added. After the reaction mixture was stirred at −78° C. for 45 min, the reaction mixture was allowed to warm to room temperature and stirring was continued for an additional hour. The reaction mixture was washed with H2O and brine, dried (Na2SO4) and concentrated. The residue was dissolved in Et2O, filtered and the filtrate was concentrated and crystallized (Et2O/heptane) to result in 4 (30.9 g, 67%). The mother liquor was concentrated and crystallized (Et2O/heptane) and gave extra 4 (2.27 g, 5%).
後処理
- temperaturewhile maintaining the internal temperature below −65° C
- temperaturewhile maintaining the temperature below −65° C
- stirringAfter the reaction mixture was stirred at −78° C. for 45 min
- temperatureto warm to room temperature
- stirringstirring
- waitwas continued for an additional hour
- washThe reaction mixture was washed with H2O and brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- dissolutionThe residue was dissolved in Et2O
- filtrationfiltered
- concentrationthe filtrate was concentrated
- customcrystallized (Et2O/heptane)
出典と根拠
- ORDレコード
- ord-3221b3f1f5fe40e893bcc6eea6794c83
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08124624B2
反応ノート
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