Hydrochloric Acid → HCID 68294367, 화합물
반응식
[C:1]([C:3]1([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[C:18]([Cl:23])[CH:17]=2)[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)#N.Cl.[OH-:25].[Na+].CC(OC(OC(OC(C)(C)C)=O)=O)(C)C.[OH2:42]>O1CCOCC1>[C:12]([O:11][C:9]([N:6]1[CH2:7][CH2:8][C:3]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[C:18]([Cl:23])[CH:17]=2)([C:1]([OH:42])=[O:25])[CH2:4][CH2:5]1)=[O:10])([CH3:14])([CH3:15])[CH3:13]참가 물질
실험 절차
A solution of 356 (4.54 g, 12.78 mmol) and concentrated HCl (106.5 mL, 1278 mmol) was heated to reflux and stirred over the weekend. The reaction mixture was then cooled to RT, transferred to separatory funnel, and washed with Et2O (1×200 mL). The aqueous layer was concentrated in a rotovap under high vacuum. The resulting solids were dissolved in 10% NaOH (20.45 g, 51.12 mmol). To the solution was added dioxane (30 mL) followed by Boc2O (2.929 g, 13.42 mmol). After stirring overnight, the reaction was diluted with H2O (100 mL) and washed with ether (1×100 mL). The aqueous layer was acidified with solid KHSO4 and then extracted with DCM (200 mL). The combined extracts were dried (MgSO4), filtered, concentrated and dried under high vacuum to afford 1.98 g (41%) of 1-(tert-butoxycarbonyl)-4-(3,4-dichlorophenyl)piperidine-4-carboxylic acid (358) as a white foam.
후처리
- temperatureto reflux
- customtransferred to separatory funnel
- washwashed with Et2O (1×200 mL)
- concentrationThe aqueous layer was concentrated in a rotovap under high vacuum
- stirringAfter stirring overnight
- washwashed with ether (1×100 mL)
- extractionextracted with DCM (200 mL)
- dry with materialThe combined extracts were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customdried under high vacuum
출처 및 근거
- ORD 기록
- ord-7cfba998ecea47a3972c8a073ccc2597
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09133187B2
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