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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 881985생성일: 2026년 10월 25일

Dimethylformamide → Tert-butyl 4-(1-(3-(cyclopropylmethoxy)-5-methoxybenzamido)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/881985

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylateHCID 22647295—
반응물3-(2-Cyclopropylethyl)-5-methoxybenzoic acidHCID 89463753—
용매WaterHCID 962—
생성물Tert-butyl 4-(1-(3-(cyclopropylmethoxy)-5-methoxybenzamido)ethyl)piperidine-1-carboxylateHCID 89464457—

반응 단계

To a solution of 3-(2-cyclopropylethyl)-5-methoxybenzoic acid (2.4 g, 10.7 mmol) and tert-butyl 4-(1-aminoethyl)piperidine-1-carboxylate (2.4 g, 10.7 mmol) in DMF (40 ml), was added triethyl amine (4.47 ml). After stirring for 10 minutes at room temperature TBTU (5.15 g, 16.1 mmol) was added in portions. The reaction mixture was stirred at room temperature for 2 hours. 100 ml H2O was added and the product was extracted into ethyla acetate. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by using normal phase chromatography eluting with petroleum ether containing 10% ethyl acetate to give tert-butyl 4-(1-(3-(cyclopropylmethoxy)-5-methoxybenzamido)ethyl)piperidine-1-carboxylate (3.0 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993757B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-f87213cc2a164907857dba4e43b554d0
출처 메모uspto-grants-2015_03