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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40194생성일: 2026년 10월 24일

Sodium Hydroxide → 8-((6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-ol

https://huagongshe.com/ko/reaction/40194

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물7-methoxy-N-[(6-phenyl[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl]-1,5-naphthyridin-4-amineHCID 25064730—
용매Hydrogen BromideHCID 260—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물8-((6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-olHCID 13598747879.6%

반응 조건

온도100 °C

반응 단계

In a 25 mL sealed tube was dissolved 7-methoxy-N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-1,5-naphthyridin-4-amine (prepared according to General Method D) (300 mg, 782 μmol) in 5 mL of concentrated HBr then stirred and heated at 100° C. for 48 h. The reaction mixture was diluted with DCM and H2O then neutralized with NaOH (1N) to neutral pH. The aqueous phase was extracted 3× with DCM then the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude mixture was purified by MPLC (ISCO) with DCM:MeOH:NH4OH (90:10:1) and then triturated with hot EtOH to afforded 8-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-ol (230 mg, 79.6% yield) as a tan solid. MS m/z=369.1 [M+1]+. Calc'd for C20H15N7O: 370.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-b9d493f86bcc489bb27580e06a09dbe6
출처 메모uspto-grants-2013_09