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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224287Generated: October 26, 2026

Imidazole → 2-(4-(Isoxazol-5-yl)benzyl)-7-(4-chlorophenyl)-8-(1H-imidazol-1-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one

https://huagongshe.com/reaction/2224287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-(4-(isoxazol-5-yl)benzyl)-8-chloro-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-oneHCID 59716540—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(4-(Isoxazol-5-yl)benzyl)-7-(4-chlorophenyl)-8-(1H-imidazol-1-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-oneHCID 5971662355%

Reaction Steps

A solution of 2-(4-(isoxazol-5-yl)benzyl)-8-chloro-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (149 mg, 0.34 mmol) and imidazole (69.5 mg, 1.02 mmol) in dry 1-methyl-2-pyrrolidinone (3 mL) was heated at 100° C. for 18 h. HPLC/MS analysis indicated 90% complete reaction. The reaction mixture was concentrated under vacuum with co-evaporation of toluene (5 mL×2) to obtain a dark yellow solid. The crude product was purified by silica gel column chromatography (ISCO) eluting with CH2Cl2/EtOAc to obtain pure title compound (87 mg, 55%) as a yellow solid. MS [M+H]+ 470; HPLC retention time=2.59 min; 1HNMR (400 MHz, CDCl3) δ 8.29 (d, 1H, J=0.5 Hz), 8.18 (s, 1H), 7.80-7.85 (m, 2H), 7.78 (s, 1H), 7.49 (d, 2H, J=7.0 Hz), 7.43 (d, 2H, J=7.0 Hz), 7.13-7.15 (m, 3H), 6.94 (m, 1H), 6.53 (d, 1H, J=0.5 Hz), 5.27 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-40e348f2831d44209f67e56bffb1694f
Source noteuspto-grants-2008_05