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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1892303생성일: 2026년 10월 26일

N'-(6-Chloropyridazin-3-yl)-2-(quinolin-6-yl)acetohydrazide → 6-((6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline

https://huagongshe.com/reaction/1892303

반응식

참여 물질

역할이름HCID투입량
반응물N'-(6-Chloropyridazin-3-yl)-2-(quinolin-6-yl)acetohydrazideHCID 86652010—
용매Acetic AcidHCID 176—
생성물6-((6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinolineHCID 2496836753%

반응 단계

A solution of N′-(6-chloropyridazin-3-yl)-2-(quinolin-6-yl)acetohydrazide (8 g crude, 25.5 mmol) in 250 mL of acetic acid was heated at 50° C. for 5 h. After the reaction was complete, the solvent was evaporated and the residue was taken up in EtOAc. The formed solid (mainly dicyclohexyl urea) was filtered off and the filtrate was evaporated to afford the title compound as yellow solid (4 g, 53%). 1H-NMR (400 MHz, MeOH-d4) δ ppm 8.82 (d, 1H), 8.33 (d, 1H), 8.25 (d, 1H), 8.0 (d, 1H), 7.93 (s, 1H), 7.83 (d, 1H), 7.53 (m, 1H), 7.42 (d, 1H), 4.79 (s, 2H). LCMS (method B): [MH]+=296.0, tR=1.876 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507676B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-55a162630bb24c119dc8d38339224876
출처 메모uspto-grants-2013_08