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HRID 16589作成日:2026年10月26日

Diisopropylethylamine → Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylate

https://huagongshe.com/reaction/16589

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
反応物Methyl 1-(iodomethyl)cyclopentanecarboxylateHCID 67231596—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
溶媒Sodium BicarbonateHCID 516892—
生成物Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylateHCID 6723246967.2%

反応条件

温度120 °C

反応手順

A mixture of Methyl 1-(iodomethyl)cyclopentanecarboxylate(5.52 g, 0.0206 mol, Step 1), tert-butyl(piperidin-4-ylmethyl)carbamate (8.83 g, 0.0412 mol) and iPr2NEt (10.76 mL, 0.0618 mol) in N-methylpyrrolidone (70 mL) was stirred at 120° C. for 24 h. After cooling, the reaction mixture was diluted with sat. NaHCO3 aq. (200 mL), extracted with AcOEt (200 mL) for three times, and the combined organic layer was washed with water (200 mL) and brine (200 mL). The organic layer was dried over Na2SO4, filtered and concentrated. Removal of the solvent gave a residue, which was chromatographed on a column of silica gel eluting with EtOAc/hexane (1:1) to give 4.91 g (67%) of title compound as a yellow syrup.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737163B2
出典データセットuspto-grants-2010_06
ORD IDord-7979378220074b7c996aa06eafdcf99f
出典メモuspto-grants-2010_06