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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725541Generated: October 26, 2026

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

https://huagongshe.com/reaction/1725541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Quinolinamine, 6-bromo-HCID 93637—
Reactant5-acetyl-2-ethylnitro6-phenylpyridazin-3(2H)-oneHCID 10732015—
SolventEthanolHCID 702—
Product5-Acetyl-4-[(6-bromoquinolin-8-yl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-oneHCID 6848564985.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491722B2
Source datasetuspto-grants-2009_02
ORD IDord-11ca5e69572648439f9b95e2087dbef5
Source noteuspto-grants-2009_02