반응식
[CH:1]1([C:4]([N:6]2[CH2:11][CH2:10][CH:9]([C:12]([O:14]CC)=[O:13])[CH2:8][CH2:7]2)=[O:5])[CH2:3][CH2:2]1.[OH-].[Na+]>C(O)C>[CH:1]1([C:4]([N:6]2[CH2:7][CH2:8][CH:9]([C:12]([OH:14])=[O:13])[CH2:10][CH2:11]2)=[O:5])[CH2:2][CH2:3]1참가 물질
4
실험 절차
To a solution of the compound (6.3 g) obtained in step 4 in ethanol (30 mL) was added 4N aqueous sodium hydroxide solution (35 mL), and the mixture was stirred at room temperature for 22 hr. The reaction mixture was concentrated under reduced pressure, and made acidic with 6N hydrochloric acid. The resultant product was extracted with ethyl acetate, the organic layer was washed with brine and dried, and the solvent was evaporated under reduced pressure to give 1-(cyclopropylcarbonyl)piperidine-4-carboxylic acid (5.21 g, 95%) as a pale yellow powder.
후처리
- concentrationThe reaction mixture was concentrated under reduced pressure
- extractionThe resultant product was extracted with ethyl acetate
- washthe organic layer was washed with brine
- customdried
- customthe solvent was evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-6cd70335563140fd9ea2cbe21af12742
- 출처 데이터셋
- uspto-grants-2013_06
- 특허 번호
- US08470816B2
연결된 노트
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