Hydrochloric Acid → 5-((S)-1,3'-bipiperidin-4-yl)-2-chloro-N-((R)-1-(2,4-dichlorophenyl)ethyl)aniline
반응식
[Cl:1][C:2]1[CH:18]=[CH:17][C:16]([C:19]2[CH2:20][CH2:21][N:22]([C@H:25]3[CH2:30][CH2:29][CH2:28][NH:27][CH2:26]3)[CH2:23][CH:24]=2)=[CH:15][C:3]=1[NH:4][C@@H:5]([C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][C:8]=1[Cl:14])[CH3:6].Cl>C(O)C.[Pt](=O)=O>[N:22]1([C@H:25]2[CH2:30][CH2:29][CH2:28][NH:27][CH2:26]2)[CH2:21][CH2:20][CH:19]([C:16]2[CH:17]=[CH:18][C:2]([Cl:1])=[C:3]([CH:15]=2)[NH:4][C@@H:5]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][C:8]=2[Cl:14])[CH3:6])[CH2:24][CH2:23]1참가 물질
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of the crude 2-chloro-N-((1R)-1-(2,4-dichlorophenyl)ethyl)-5-(1-((3S)-3-piperidyl)-3,6-dihydro-2H-pyridin-4-yl)aniline (0.30 g, 0.63 mmol), platinum(IV) oxide (PtO2) (5% by weight, 0.045 g) in ethanol (3 mL) containing concentrated hydrochloric acid (conc. HCl) (0.20 mL, 2.20 mmol) in a Paar shaker flask was hydrogenated at 40 psi for 45 min. The reaction mixture was diluted with ethanol, and filtered through the Celite. The filtrate was concentrated in vacuo, and the resulting residue was diluted with dichloromethane (25 mL). The organic layer was washed with saturated aqueous sodium bicarbonate solution, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was used without further purification (0.27 g, 0.058 mmol). MS: (ES) m/z calculated for C24H31Cl3N3 [M+H]+466.2. found 466.
후처리
- filtrationfiltered through the Celite
- concentrationThe filtrate was concentrated in vacuo
- additionthe resulting residue was diluted with dichloromethane (25 mL)
- washThe organic layer was washed with saturated aqueous sodium bicarbonate solution
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was used without further purification (0.27 g, 0.058 mmol)
출처 및 근거
- ORD 기록
- ord-d54dae00a2494efaa5146ff02447b23f
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08835419B2
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