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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33886생성일: 2026년 10월 24일

N-Dimethylaminomethylene-isonicotinamide → 2-[4-(5-Pyridin-4-yl-[1,2,4]triazol-1-yl)-phenoxymethyl]-quinoline

https://huagongshe.com/ko/reaction/33886

반응식

참여 물질

역할이름HCID투입량
반응물N-Dimethylaminomethylene-isonicotinamideHCID 12569643—
반응물4-(Quinolin-2-ylmethoxy)phenylhydrazineHCID 15225068—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물2-[4-(5-Pyridin-4-yl-[1,2,4]triazol-1-yl)-phenoxymethyl]-quinolineHCID 1166088021.8%

반응 단계

Isonicatinamide (4.15 g) was heated in 35 ml of N,N-Dimethylformamide diethyl acetal at reflux for 3 h. The reaction mixture was cooled to ambient temperature and concentrated to give 5.02 g of N-Dimethylaminomethylene-isonicotinamide. To a solution of [4-(Quinolin-2-ylmethoxy)-phenyl]-hydrazine (3.16 g) in methanol (30 mL) and acetic acid (2.5 mL) was added N-Dimethylaminomethylene-isonicotinamide (1.10 g) and the reaction mixture heated at reflux for 72 h. The reaction mixture was concentrated onto silica gel and purified by flash chromatography to provided the title compound (514 mg). 1H NMR (400 MHz, CDCl3) δ 8.60 (d, J=5.8 Hz, 2 H), 8.22 (d, J=8.7 Hz, 1 H), 8.10 (s, 1H), 8.07 (d, J=8.7 Hz, 1H), 7.85 (d, J=7.1 Hz, 1H), 7.76 (m, 1 H), 7.66 (d, J=8.3 Hz, 1 H), 7.56 (m, 1 H), 7.56 (m, 1H), 7.38 (d, J=6.2 Hz, 2 H), 7.26 (d, J=8.7Hz, 2H), 7.11 (d, J=9.1 Hz, 2H), 5.42 (s, 2H); MS: (M+H m/z=380.3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429665B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-fd40ee35efc44dc184a867c4e954f280
출처 메모uspto-grants-2008_09