8-(1-tert-butyl-1,2,3,6-tetrahydropyridin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one hydrochloride → 8-(1-tert-butylpiperidin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one
反応式
Cl.[C:2]([N:6]1[CH2:11][CH:10]=[C:9]([C:12]2[CH:13]=[C:14]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=3[Cl:37])[N:15]3[C:20]([CH:21]=2)=[C:19]([C:22]2[C:27]([Cl:28])=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:29])[C:18](=[O:30])[CH:17]=[CH:16]3)[CH2:8][CH2:7]1)([CH3:5])([CH3:4])[CH3:3]>CO.C(OCC)(=O)C.[Pt]=O>[C:2]([N:6]1[CH2:11][CH2:10][CH:9]([C:12]2[CH:13]=[C:14]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=3[Cl:37])[N:15]3[C:20]([CH:21]=2)=[C:19]([C:22]2[C:27]([Cl:28])=[CH:26][CH:25]=[CH:24][C:23]=2[Cl:29])[C:18](=[O:30])[CH:17]=[CH:16]3)[CH2:8][CH2:7]1)([CH3:5])([CH3:3])[CH3:4]参加物
4
反応物 1
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 8-(1-tert-butyl-1,2,3,6-tetrahydropyridin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one hydrochloride (Example 19, 24 mg) in methanol/ethyl acetate=1/5 was added platinum oxide (9 mg). The solution was hydrogenated under hydrogen (1 atm) for 1 h. The mixture was filtered though celite and concentrated. The residue was purified by silica gel (methylene chloride/methanol/2N ammonia=10/1/0.2) to give the title compound.
後処理
- filtrationThe mixture was filtered though celite and
- concentrationconcentrated
- customThe residue was purified by silica gel (methylene chloride/methanol/2N ammonia=10/1/0.2)
出典と根拠
- ORDレコード
- ord-4dd558562d2d4992965cd65f1b1dfbc2
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07879875B2
反応ノート
読み込み中…