反応式
[C:1]([C:3]([CH:16]1[CH2:21][CH2:20][CH2:19][NH:18][CH2:17]1)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)#[N:2].Br[CH2:23][CH2:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[C:1]([C:3]([CH:16]1[CH2:21][CH2:20][CH2:19][N:18]([CH2:23][CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH2:17]1)([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)#[N:2]参加物
実験手順
A mixture containing 3-(R,S)-(1-cyano-1,1-diphenylmethyl)piperidine (0.3 g--see EP-A-0178947), 1-bromo-3-phenylpropane (0.238 g), anhydrous potassium carbonate (0.4 g) and acetonitrile (10 ml) was heated under reflux for 5 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×20 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated vacuo to give a gum which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 2%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as a gum, yield 0.4g.
後処理
- temperaturewas heated
- temperatureunder reflux for 5 hours
- customThe mixture was partitioned between dichloromethane (30 ml) and 10% aqueous potassium carbonate (30 ml)
- customthe layers separated
- extractionthe aqueous layer extracted with dichloromethane (2×20 ml)
- dry with materialThe combined dichloromethane extracts were dried (MgSO4)
- concentrationconcentrated vacuo
- customto give a gum which
- customwas purified by column chromatography on silica eluting with dichloromethane
- additioncontaining methanol (0% up to 2%)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-d567ec4934e94bc8972791d5770869a0
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05422358
関連ノート
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