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HRID 417954作成日:2026年10月26日

Formaldehyde → (1-Methylpiperidin-4-yl)methyl 4-(4-methylphenyl)-piperazine-1-carboxylate

https://huagongshe.com/reaction/417954

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物WaterHCID 962—
反応物Piperidin-4-ylmethyl 4-(4-methylphenyl)piperazine-1-carboxylateHCID 42635252—
溶媒Formic AcidHCID 284—
生成物(1-Methylpiperidin-4-yl)methyl 4-(4-methylphenyl)-piperazine-1-carboxylateHCID 4263525343%

反応条件

温度95 °C

反応手順

(1-piperidin-4-yl)methyl 4-(4-methylphenyl)piperazine-1-carboxylate (Example 3; 9.75 g, 30.7 mmol) was dissolved in formic acid (3 mL), 35% aqueous formaldehyde solution (3 mL) and water (20 mL). The reaction mixture was heated at 95° C. for 45 minutes, and then cooled to room temperature. The reaction mixture was quenched by slowly pouring it onto 1M aq Na2CO3 solution (400 mL) and extracted with EtOAc (4×150 mL). The combined organic layers were washed with brine (75 mL), dried (MgSO4) and concentrated in vacuo. The residue was recrystallised from heptane and then purified by reverse phase column chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-30%). The resulting residue was dissolved in DCM (70 mL) and stirred with solid K2CO3 for 20 minutes, filtered and concentrated in vacuo. The residue was recrystallised from heptane to give (1-methylpiperidin-4-yl)methyl 4-(4-methylphenyl)-piperazine-1-carboxylate (4.38 g, 43.0%) as 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-babba1304fc948e1b2aba3bed884d7fa
出典メモuspto-grants-2012_01