Acetonitrile → N-(2-tert-butoxybenzyl)-6-(4-(2-methoxyphenyl)cyclohexyl)-N-(pyridin-2-ylmethyl)hexan-1-amine
반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N:8]([CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=1.CO[CH:30]1[CH2:35][CH:34]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=2)[CH2:33][CH2:32]N1.[C:42]([O-:45])([O-])=O.[K+].[K+].[CH3:48]C#N>>[C:24]([O:23][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=1[CH2:16][N:8]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=1)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH:39]1[CH2:38][CH2:37][CH:36]([C:34]2[CH:33]=[CH:32][CH:48]=[CH:30][C:35]=2[O:45][CH3:42])[CH2:41][CH2:40]1)([CH3:27])([CH3:26])[CH3:25]참가 물질
실험 절차
The compound 10 (0.377 g, 0.85 mmol), 2-methoxy-4-phenylpiperidine (0.262 g, 1.54 mmol) and K2CO3 (0.118 g, 0.85 mmol) were added to 50 mL CH3CN, and the solution was refluxed under argon atmosphere for 6 h and stirred overnight. Then the solvent was evaporated to dryness. Purification was carried out on a silica gel TLC plate that was developed in 4% methanolic NH3 (7 M NH3 in methanol)/96% CH2Cl2. The product was obtained as pale yellow oil (58%). 1H NMR (CDCl3) δ 8.491 (d, 1H, Ar), 7.262 (m, 1H, Ar), 7.583 (m, 2H, Ar), 7.216 (d, 1H, Ar), 7.160 (m, 1H, Ar), 7.112 (m, 2H, Ar), 7.024 (m, 2H, Ar), 6.917 (t, 1H, Ar), 6.839 (d, 1H, Ar), 3.806 (s, 3H, —OCH3), 3.744 (s, 2H, —CH2—), 3.667 (s, 2H, —CH2—), 3.043 (d, 2H, —CH2—), 2.958 (m, 1H, —CH—), 2.459 (t, 2H, —CH2—), 2.326 (m, 2H, —CH2—), 2.061 (m, 2H, —CH2—), 1.790 (m, 4H, —CH2—CH2—), 1.531 (m, 4H, —CH2—CH2—), 1.360 (s, 9H, —C(CH3)3—), 1.298 (m, 2H, —CH2—), 1.228 (m, 2H, —CH2—). Mass Spec.=543.78 (M+H)+.
후처리
- temperaturethe solution was refluxed under argon atmosphere for 6 h
- customThen the solvent was evaporated to dryness
- customPurification
출처 및 근거
- ORD 기록
- ord-8bceeb1c7350482e8ae5f3fd694f4063
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08747810B2
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