1-(2-Methoxyphenyl)-4-(1-(4-phenylphenyl)cyclohex-1-en-4-yl)piperazine → HCID 178489564、化合物
反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]1[CH2:14][CH2:13][N:12]([CH:15]2[CH2:20][CH2:19][C:18]([C:21]3[CH:26]=[CH:25][C:24]([C:27]4[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=4)=[CH:23][CH:22]=3)=[CH:17][CH2:16]2)[CH2:11][CH2:10]1>C(O)(=O)C.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]1[CH2:10][CH2:11][N:12]([C@H:15]2[CH2:20][CH2:19][C@H:18]([C:21]3[CH:22]=[CH:23][C:24]([C:27]4[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=4)=[CH:25][CH:26]=3)[CH2:17][CH2:16]2)[CH2:13][CH2:14]1参加物
実験手順
1-(2-Methoxyphenyl)-4-(1-(4-phenylphenyl)cyclohex-1-en-4-yl)piperazine (2.7 g, 5.4 mmol) was hydrogenated at 50 psi (about 3.5×105N.m-2) above atmospheric pressure at 45° C. in acetic acid (50 ml), using 10% Pd/C (2.4 g) as a catalyst for three days. The volatiles were evaporated in vacuo and the residue was partitioned between dichloromethane (150 ml) and sat. NaHCO3 (200 ml). The organic layer was separated and washed with brine and evaporated in vacuo. The residues were recrystallised from dichloromethane and again from methanol. The white solid was dissolved in ether and acidified to pH 1 with ethereal HCl. The volatiles were removed in vacuo to give the title compound as the one and a half hydrochloride; three quarters hydrate (0.281 g), m.p. 220°-225° C.
後処理
- customfor three days
- customThe volatiles were evaporated in vacuo
- customthe residue was partitioned between dichloromethane (150 ml) and sat. NaHCO3 (200 ml)
- customThe organic layer was separated
- washwashed with brine
- customevaporated in vacuo
- customThe residues were recrystallised from dichloromethane and again from methanol
- dissolutionThe white solid was dissolved in ether
- customThe volatiles were removed in vacuo
出典と根拠
- ORDレコード
- ord-d55d7cc28e1a48f58fe03a4724d0e591
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05622951
反応ノート
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