p-Anisoyl chloride → 1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazine
反応式
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][N:8]([CH:11]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:7][CH2:6]1.C(N(CC)CC)C.[CH3:31][O:32][C:33]1[CH:41]=[CH:40][C:36]([C:37](Cl)=[O:38])=[CH:35][CH:34]=1>C(Cl)(Cl)Cl>[CH3:31][O:32][C:33]1[CH:41]=[CH:40][C:36]([C:37]([NH:1][CH2:2][CH2:3][CH2:4][N:5]2[CH2:6][CH2:7][N:8]([CH:11]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:9][CH2:10]2)=[O:38])=[CH:35][CH:34]=1参加物
実験手順
To a solution of 1-(3-aminopropyl)-4-benzhydrylpiperazine (1.55 g) and triethylamine (0.7 ml) in chloroform (15 ml) was dropwise added p-methoxybenzoyl chloride (0.85 g) at ambient temperature with stirring, which was continued for 20 minutes. The reaction mixture was washed successively with aqueous sodium bicarbonate and water. The organic layer was separated, dried and evaporated in vacuo. The resultant oily product was subjected to column chromatography on silica gel eluting with ethyl acetate. The fractions containing the desired compound were combined and evaporated in vacuo. The residue was crystallized from a mixture of ethyl acetate and hexane to give 1-[3-(4-methoxybenzoylamino)propyl]-4-benzhydrylpiperazine (1.1 g) as white crystals. mp: 126°-128° C.
後処理
- customat ambient temperature
- washThe reaction mixture was washed successively with aqueous sodium bicarbonate and water
- customThe organic layer was separated
- customdried
- customevaporated in vacuo
- additionThe fractions containing the desired compound
- customevaporated in vacuo
- customThe residue was crystallized from a mixture of ethyl acetate and hexane
出典と根拠
- ORDレコード
- ord-45435e028d2149abb3c42f25079f2be1
- 出典データセット
- uspto-grants-1986_05
- 特許番号
- US04591590
反応ノート
読み込み中…