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HRID 417972作成日:2026年10月26日

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

https://huagongshe.com/reaction/417972

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-(p-Tolyl)piperazine dihydrochlorideHCID 83112—
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-methylphenyl)piperazine-1-carboxylateHCID 4263562660.4%

反応手順

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 866 mg, 2.8 mmol) was dissolved in DMF (25 mL). NEt3 (1.5 mL, 10.8 mmol) and 4-(4-methyl-phenyl)piperazine dihydrochloride (724 mg, 2.9 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 200:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)-ethyl 4-(4-methylphenyl)piperazine-1-carboxylate (293 mg, 30%) as a yellow oil.

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-e4104e0f421c4ee984101e92ab38cb83
出典メモuspto-grants-2012_01