Dimethyl Sulfoxide → Methyl 4-(piperidin-2-yl)butanoate hydrochloride

HRID 1645246ノート

反応式

HRID 1645246 の反応式
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

6

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

  1. temperaturewhile maintaining the internal temperature below −65° C
  2. temperaturewhile maintaining the temperature below −65° C
  3. stirringAfter the reaction mixture was stirred at −78° C. for 45 min
  4. temperatureto warm to room temperature
  5. stirringstirring
  6. waitwas continued for an additional hour
  7. washThe reaction mixture was washed with H2O and brine
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated
  10. dissolutionThe residue was dissolved in Et2O
  11. filtrationfiltered
  12. concentrationthe filtrate was concentrated
  13. 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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