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HRID 8138作成日:2026年10月24日

1-Phenylpiperazine → Methyl 4-{[(5-ethoxy-5-oxopentyl)(2-{[5-(4-phenylpiperazino)-pentyl]oxy}phenethyl)amino]methyl}benzoate

https://huagongshe.com/ja/reaction/8138

反応式

関与物質

役割名称HCID仕込み量
反応物1-PhenylpiperazineHCID 7096—
反応物TriethylamineHCID 8471—
反応物Methyl 4-{[{2-[(5-bromopentyl)oxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoateHCID 22015034—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-{[(5-ethoxy-5-oxopentyl)(2-{[5-(4-phenylpiperazino)-pentyl]oxy}phenethyl)amino]methyl}benzoateHCID 22015022—

反応手順

200.0 mg (0.355 mmol) of methyl 4-{[{2-[(5-bromopentyl)oxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoate from Ex. 107, 69.21 mg of N-phenylpiperazine and 71.95 mg (0.711 mmol) of triethylamine in 2 ml of tetrahydrofuran are heated at reflux for 18 hours. The reaction solution is washed with water, concentrated and chromatographed over silica gel using the mobile phase ethyl acetate/methanol 10/1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087644B1
出典データセットuspto-grants-2006_08
ORD IDord-e62791e523bc48a79da21cd90562ab8c
出典メモuspto-grants-2006_08