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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391121Generated: October 31, 2026

Ethyl 6-Iodoimidazo[1,2-b]pyridazine-2-carboxylate → 6-iodo-N-methylimidazo[1,2-b]pyridazine-2-carboxamide

https://huagongshe.com/reaction/2391121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-Iodoimidazo[1,2-b]pyridazine-2-carboxylateHCID 51063906—
ReactantMethylamine tetrahydrofuranHCID 66615946—
SolventMethanolHCID 887—
Product6-iodo-N-methylimidazo[1,2-b]pyridazine-2-carboxamideHCID 5744102671.6%

Reaction Steps

To a suspension of ethyl 6-iodoimidazo[1,2-b]pyridazine-2-carboxylate (4.5 g, 14.8 mmol) in methanol (13.5 mL) was added dropwise a solution of methylamine/tetrahydrofuran (2 mol/L, 37.1 mL, 74.2 mmol), and the mixture was stirred at room temperature for 96 hr. The solvent was evaporated under reduced pressure, and the residue was washed with ethyl acetate, saturated brine and water to give the title compound (3.2 g, 71%) as a dark brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273741B2
Source datasetuspto-grants-2012_09
ORD IDord-a17c1c8fd0b049f4b8e3af9036254cab
Source noteuspto-grants-2012_09