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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33922생성일: 2026년 10월 23일

Piperidine → 4-(4-((Quinolin-2-yl)methoxy)phenyl)-3-(pyridin-4-yl)but-3-en-2-one

https://huagongshe.com/ko/reaction/33922

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-PyridinylacetoneHCID 80552—
반응물4-(2-quinolinylmethoxy)BenzaldehydeHCID 14578960—
용매TolueneHCID 1140—
생성물4-(4-((Quinolin-2-yl)methoxy)phenyl)-3-(pyridin-4-yl)but-3-en-2-oneHCID 68578495—

반응 단계

A mixture of 4-((quinolin-2-yl)methoxy)benzaldehyde (2.5 g, 9.5 mmol), 1-(pyridin-4-yl)propan-2-one (1.3 g, 9.5 mmol) and piperidine (162 mg, 1.9 mmol) in toluene (50 mL) was heated at reflux for 18 h, concentrated, and the residue chromatographed on silica eluting with a gradient of ethyl acetate in hexanes giving impure title substance (2.4 g) as a yellow solid which was chromatographed again on silica eluted with 1% and 2% methanol in dichloromethane containing 0.5% concentrated ammonium hydroxide giving a 3:1 mixture of the title substance contaminated with the pyridyl starting material. Yield 2.0 g, 55%. The title substance appeared to be a 10:1 mixture of two isomers by NMR. 1H NMR (CDCl3, 400 mHz, partial) δ 2.35 (s, 3H, major isomer), 2.23 (s, 3H, minor isomer). HPLC-MS 6.09 min, m/e 381 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429665B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-cdc2826d4e884d9da32a0d7456f0a126
출처 메모uspto-grants-2008_09