Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755313Generated: November 1, 2026

p-Toluenesulfonic acid → Methyl 4-(8-bromoimidazo[1,2-b]pyridazin-6-yl)benzoate

https://huagongshe.com/reaction/1755313

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Chloro-1,1-diethoxyethaneHCID 12128—
ReactantMethyl 4-(6-amino-5-bromopyridazin-3-yl)benzoateHCID 86682705—
SolventIsopropanolHCID 3776—
ProductMethyl 4-(8-bromoimidazo[1,2-b]pyridazin-6-yl)benzoateHCID 8668270636.2%

Reaction Steps

A solution of methyl 4-(6-amino-5-bromopyridazin-3-yl)benzoate (1.64 g, 5.32 mmol), 2-chloro-1,1-diethoxyethane (0.984 g, 6.39 mmol) and PTSA (1.215 g, 6.39 mmol) in isopropanol (50 mL) was heated to 80° C. for 40 h. After cooling to room temperature, the solution was concentrated in vacuo. The resulting mixture was treated with a saturated NaHCO3 solution (50 mL), extracted with dichloromethane (50 mL×3), dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=3:1) to give methyl 4-(8-bromoimidazo[1,2-b]pyridazin-6-yl)benzoate (640 mg, 36%) as a white solid. LC-MS: [M+H]+, 333.9, tR=1.637 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169259B2
Source datasetuspto-grants-2015_10
ORD IDord-adab5625d3314637a6929b3b18ce328b
Source noteuspto-grants-2015_10