Acetic Acid → 1-Benzyl-4-[3-(1-cyano-1-methylethylamino)pyridyl]-piperazine
反応式
N[C:2]1C=[C:4]2[C:8](=[CH:9][CH:10]=1)N[C:6]([N:11]1[CH2:16][CH2:15][N:14]([C:17]3[C:22]([NH:23]C(C)C)=[CH:21][CH:20]=[CH:19][N:18]=3)[CH2:13][C:12]1=C=O)=[CH:5]2.[CH3:29]C(C)=O.C[Si]([C:37]#[N:38])(C)C.[OH-].[Na+].[C:41](O)(=O)[CH3:42]>CO.C(OCC)(=O)C.CCCCCC>[CH2:6]([N:11]1[CH2:12][CH2:13][N:14]([C:17]2[C:22]([NH:23][C:41]([C:37]#[N:38])([CH3:42])[CH3:29])=[CH:21][CH:20]=[CH:19][N:18]=2)[CH2:15][CH2:16]1)[C:5]1[CH:2]=[CH:10][CH:9]=[CH:8][CH:4]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
The 1-[5-Aminoindolyl -2-carbonyl -4-[3-(1-methylethyl amino)-2-pyridinyl]piperazine (EXAMPLE 7, 11.68 g, 43.51 mmol) is dissolved in 130 ml methanol and 130 ml acetic acid. Acetone (25.6 ml, 348.1 mmol) and trimethylsilylcyanide (46.4 ml, 348.1 mmol) are added and the mixture is stirred twenty hours. The solution is poured into cold aqueous sodium hydroxide solution, stirring vigorously, to give a basic solution. The aqueous solution is then extracted with ethyl acetate, the organic extract is washed with saline, dried over sodium sulfate and evaporated to dryness to give an oily residue of 12.6 g. Chromatography on a 400 g silica gel column with a step gradient of ethyl acetate/hexane (2/3 to 3/2, v/v), pooling and concentrating the appropriate fractions gives the title compound, NMR (300 MHz, CD3OD) 7.65, 7.29-7.17, 6.96-6.92, 3.51, 2.98, 2.55, 1.14 δ.
後処理
- stirringstirring vigorously
- customto give a basic solution
- extractionThe aqueous solution is then extracted with ethyl acetate
- extractionthe organic extract
- washis washed with saline
- dry with materialdried over sodium sulfate
- customevaporated to dryness
- customto give an oily residue of 12.6 g
- concentrationconcentrating the appropriate fractions
出典と根拠
- ORDレコード
- ord-a69ed5980bcc44098a9634312844006e
- 出典データセット
- uspto-grants-1997_02
- 特許番号
- US05599930
反応ノート
読み込み中…