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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33844생성일: 2026년 10월 24일

7-Chloro-2-(chloromethyl)quinoline → 7-Chloro-2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline hydrogen chloride

https://huagongshe.com/ko/reaction/33844

반응식

참여 물질

역할이름HCID투입량
반응물7-Chloro-2-(chloromethyl)quinolineHCID 10954844—
반응물Methyl 4-(2-quinolinylmethoxy)benzoateHCID 19934817—
반응물4-[1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl]PhenolHCID 135915213—
생성물7-Chloro-2-[4-(1-methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoline hydrogen chlorideHCID 11561731—

반응 단계

Following the procedure for the preparation of 4-(Quinolin-2-ylmethoxy)-benzoic acid methyl ester but substituting 4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenol and 7-chloro-2-chloromethyl-quinoline provided the title compound. 1H NMR (400 MHz, DMSO) δ 8.66 (d, J=6.6 Hz, 2H), 8.54 (s, 1 H), 8.47 (d, J=8.3, 2H), 8.04 (m, 2H), 7.70 (m, 2H), 7.65 (m, 1H), 7.36 (d, J=8.7 Hz, 2H), 7.12 (d, J=8.7, 2H), 5.38 (s, 2H), 3.90 (s, 3 H); MS: (M+H m/z=427.1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429665B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-691d24d58cb347c197930b510ed1a33c
출처 메모uspto-grants-2008_09