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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097302Generated: October 30, 2026

Water → 3-[3-(2-Chloro-pyridin-4-yl)-imidazo[1,2-b]pyridazin-7-yl]-N-methyl-benzamide

https://huagongshe.com/reaction/1097302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloropyridine-4-boronic acidHCID 5151595—
Reactant3-(3-Bromo-imidazo-[1,2-b]-pyridazin-7-yl)-N-methyl-benzamideHCID 44473459—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-[3-(2-Chloro-pyridin-4-yl)-imidazo[1,2-b]pyridazin-7-yl]-N-methyl-benzamideHCID 44473460—

Reaction Steps

To a mixture of 3-(3-Bromo-imidazo-[1,2-b]-pyridazin-7-yl)-N-methyl-benzamide (Intermediate A) (1 eq, 0.353 mmol, 117 mg) and 2-chloropyridine-4-boronic acid (1.2 eq, 0.424 mmol, 66.7 mg) in DME (3 ml) are added water (1 ml) and Na2CO3 (2 eq, 0.707 mmol, 87.6 mg). PdCl2(PPh3)2 (0.1 eq, 0.035 mmol, 24.8 mg) is then added and the reaction mixture is heated using microwave radiation at 120° C. for 10 min. At the completion of this time the solvent is removed in vacuo and the reaction mixture is purified by flash column chromatography eluting with 9:1 DCM/MeOH to yield 3-[3-(2-Chloro-pyridin-4-yl)-imidazo[1,2-b]pyridazin-7-yl]-N-methyl-benzamide as a yellow solid; [M+H]+=364

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143253B2
Source datasetuspto-grants-2012_03
ORD IDord-f86c9039d8cf437c85e6f0bada8011d2
Source noteuspto-grants-2012_03