돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725541생성일: 2026년 10월 26일

8-Quinolinamine, 6-bromo- → 5-Acetyl-4-[(6-bromoquinolin-8-yl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one

https://huagongshe.com/reaction/1725541

반응식

참여 물질

역할이름HCID투입량
반응물8-Quinolinamine, 6-bromo-HCID 93637—
반응물5-acetyl-2-ethylnitro6-phenylpyridazin-3(2H)-oneHCID 10732015—
용매EthanolHCID 702—
생성물5-Acetyl-4-[(6-bromoquinolin-8-yl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-oneHCID 6848564985.3%

반응 단계

To a stirred solution of 80 mg (0.279 mmol) of 5-acetyl-2-ethyl-4-nitro-6-phenylpyridazin-3(2H)-one (Dal Piaz, V et al, J. Med. Chem. 1997, 40, 1417) in ethanol (4 mL), 8-amino-6-bromoquinoline (93 mg, 0.417 mmol) was added. The resulting mixture was stirred at room temperature or one day. The solvent was evaporated and the residue purified by column chromatography (silica gel, hexane/ethyl acetate 3:1) to yield the title compound (110 mg, 85.3% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07491722B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-11ca5e69572648439f9b95e2087dbef5
출처 메모uspto-grants-2009_02