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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645975생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/645975

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
반응물Methyl 1-(iodomethyl)cyclopentanecarboxylateHCID 67231596—
용매N-methyl-2-pyrrolidoneHCID 13387—
용매Sodium BicarbonateHCID 516892—
생성물Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylateHCID 6723246967.2%

반응 조건

온도120 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705020B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-0990d942ab5f43558b3462a30abdd717
출처 메모uspto-grants-2010_04