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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30465생성일: 2026년 10월 23일

N-(2-Aminoethyl)piperidine → (4-Isopropyl-piperazin-1-yl)-[6-(2-piperidin-1-yl-ethylamino)-pyridin-3-yl]-methanone

https://huagongshe.com/ko/reaction/30465

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-Aminoethyl)piperidineHCID 33944—
반응물(6-Chloro-pyridin-3-yl)-(4-isopropyl-piperazin-1-yl)-methanoneHCID 43420904—
용매1-ButanolHCID 263—
생성물AmmoniaHCID 2222%
생성물(4-Isopropyl-piperazin-1-yl)-[6-(2-piperidin-1-yl-ethylamino)-pyridin-3-yl]-methanoneHCID 1171021237.1%

반응 단계

A solution of (6-chloro-pyridin-3-yl)-(4-isopropyl-piperazin-1-yl)-methanone (0.20 g, 0.75 mmol) and 1-(2-aminoethyl)-piperidine (0.16 mL, 1.13 mmol) in 1-butanol (10 mL) was heated at reflux temperature. After 18 h the reaction was concentrated, treated with 1 N aq. NaHCO3 (25 mL), and extracted with DCM (3×25 mL). The organic layers were combined, dried (Na2SO4), and concentrated. Chromatography of the residue (SiO2: 2-5% 2 M NH3 in MeOH/DCM) gave the title compound as an oil (0.050 g, 20%). MS (ESI): exact mass calcd. for C20H33N5O, 359.3; m/z found, 360.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 8.20 (d, J=1.8, 1H), 7.54 (dd, J=8.6, 2.3, 1H), 6.40 (d, J=9.0, 1H), 5.49 (br s, 1H), 3.65 (br s, 4H), 3.39-3.35 (m, 2H), 2.74-2.70 (m, 1H), 2.59-2.57 (m, 2H), 2.53 (br s, 4H), 2.42 (br s, 4H), 1.62-1.56 (m, 4H), 1.46-1.45 (m, 2H), 1.04 (d, 6.5, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423147B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ef3cb752837e487893a5fc6d81306e67
출처 메모uspto-grants-2008_09