Hydrochloric Acid → HCID 67006469, 화합물
반응식
[CH3:1][N:2]1[CH:7]2[CH2:8][CH2:9][CH:3]1[CH2:4][C:5](=[CH:10][C:11]1[CH:12]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([C:23]#[N:24])[CH:18]=3)[CH:14]=[CH:15][CH:16]=1)[CH2:6]2.[ClH:25]>CO.[OH-].[OH-].[Pd+2]>[ClH:25].[ClH:25].[CH3:1][N:2]1[CH:7]2[CH2:8][CH2:9][CH:3]1[CH2:4][CH:5]([CH2:10][C:11]1[CH:12]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([CH2:23][NH2:24])[CH:18]=3)[CH:14]=[CH:15][CH:16]=1)[CH2:6]2참가 물질
5
실험 절차
To a solution of 3′-[(8-methyl-8-azabicyclo[3.2.1]oct-3-ylidene)methyl]-3-biphenylcarbonitrile (1.21 g, 3.85 mmol) in MeOH (192 mL) was added HCl (3.85 mL, 1N, 3.85 mmol). This mixture was then applied to an H-cube hydrogenation apparatus using 20% Pd(OH)2 cartridge at a flow rate of 1 mL/min. and H2 (1 atm) at 20° C. until reaction complete by monitoring with LC-MS. The reaction mixture was concentrated to afford 1.31 g (87%) of the title compound. LC-MS m/z 321 (M+H)+.
후처리
- customat 20° C.
- customuntil reaction complete
- concentrationThe reaction mixture was concentrated
출처 및 근거
- ORD 기록
- ord-56f51836efb544abb875602333eb949e
- 출처 데이터셋
- uspto-grants-2011_11
- 특허 번호
- US08067408B2
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