反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][CH:15]=[CH:16][C:17]([N:19]2[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]2)=[O:18])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].C(N(CC)CC)C.[CH3:32][NH:33][C:34](=[O:37])[CH2:35]Cl>C1(C)C=CC=CC=1.C1(C)C=CC=CC=1.C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][CH:15]=[CH:16][C:17]([N:19]2[CH2:20][CH2:21][N:22]([CH2:35][C:34]([NH:33][CH3:32])=[O:37])[CH2:23][CH2:24]2)=[O:18])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 302 mg of 1-[5-(3,4,5-trimethoxyphenyl)-2,4-pentadienoyl]-piperazine in dry toluene (12 ml) were added in an atmosphere of argon 1.3 ml of triethylamine and subsequently a solution of 254 mg of N-methylchloroacetamide in dry toluene-chloroform (1:1, 2 ml). The mixture was refluxed for 8 hours. To the reaction mixture was added water, and extraction was made with methylene chloride. The organic layer was concentrated under reduced pressure, and the residue thus obtained was chromatographed on silica gel column. There was obtained 263 mg of 1-[5-(3,4,5-trimethoxyphenyl)-2,4-pentadienoyl]-4-(methylaminocarbonylmethyl)-piperazine. Spectrophotometric data of the product support the structure of the formula (V) shown below. ##STR5##
後処理
- temperatureThe mixture was refluxed for 8 hours
- additionTo the reaction mixture was added
- extractionwater, and extraction
- concentrationThe organic layer was concentrated under reduced pressure
- customthe residue thus obtained
- customwas chromatographed on silica gel column
出典と根拠
- ORDレコード
- ord-253f5fbbf2084f0f95c1c0e20c2f9ce3
- 出典データセット
- uspto-grants-1987_04
- 特許番号
- US04656172
関連ノート
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