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HRID 417969作成日:2026年10月26日

Triethylamine → 2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417969

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Piperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2)HCID 12212341—
反応物2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
溶媒DimethylformamideHCID 6228—
生成物AmmoniaHCID 222—
生成物2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylateHCID 42635622158.1%

反応手順

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 740 mg, 2.4 mmol) was dissolved in DMF (20 mL). NEt3 (1.2 mL, 8.6 mmol) and 4-(4-chlorophenyl)piperazine dihydrochloride (691 mg, 2.6 mmol) were added and the reaction mixture was stirred at room temperature for 24 hours, and the reaction mixture was then concentrated in vacuo. The resulting residue was dissolved in EtOAc (50 mL) and washed with 1M aq Na2CO3 solution (5×50 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by normal phase column chromatography (eluting with DCM, followed by a 100:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylate (696 mg, 79%) as a colourless oil which crystallized on standing to give a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093248B2
出典データセットuspto-grants-2012_01
ORD IDord-f07f9e367e1041eab2c25ceface38d43
出典メモuspto-grants-2012_01