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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40181생성일: 2026년 10월 25일

Ammonia → 7-methoxy-N-((6-(3-methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-1,5-naphthyridin-4-amine

https://huagongshe.com/reaction/40181

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물(+-)-2-ButanolHCID 6568—
반응물(6-(3-Methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamineHCID 57691076—
반응물8-Chloro-3-methoxy-1,5-naphthyridineHCID 59427340—
용매MethanolHCID 887—
생성물7-methoxy-N-((6-(3-methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-1,5-naphthyridin-4-amineHCID 4548787080%

반응 조건

온도120 °C

반응 단계

(6-(3-methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamine (548 mg, 2225 μmol) and 8-chloro-3-methoxy-1,5-naphthyridine (576 mg, 2959 μmol) were charged in a microwave vial. 2-butanol (7 mL) was added and the reaction mixture was stirred at 120° C. under micro-waves irradiation for 8 h. 2M NH3 in MeOH was added. Purification by MPLC (DCM/MeOH+1% NH4OH: 100/0 to 90/10) afforded the title compound (720 mg, 80% yield). MS m/z=405.1 [M+H]+. Calc'd for C19H16N8OS: 404.46

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e067184bd6044a3eb214bfc7983350bf
출처 메모uspto-grants-2013_09