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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358023Generated: October 25, 2026

2-Butanone, 3-bromo- → 6-Methyl-8-phenylmethoxy-2,3-dimethylimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/358023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanone, 3-bromo-HCID 13142—
Reactant3-Amino-6-methyl-4-phenylmethoxypyridazineHCID 15591911—
SolventMethanolHCID 887—
Product6-Methyl-8-phenylmethoxy-2,3-dimethylimidazo[1,2-b]pyridazineHCID 15591912—

Reaction Steps

A mixture of (0.01 mole) 3-amino-6-methyl-4-phenylmethoxypyridazine, [prepared following the methodology of Becket, et al. J. Pract. Chem., 311, 285(1969) and references cited therein], and (0.012 mole) 2-bromo-3-butanone in methanol is heated for 24 hours in a bath maintained at 100°. The mixture is cooled to room temperature and partitioned between aqueous sodium bicarbonate and methylene chloride. The layers are separated and the aqueous phase extracted with methylene chloride. The organic extracts are combined and dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure to give 6-methyl-8-phenylmethoxy-2,3-dimethylimidazo[1,2-b]pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464372
Source datasetuspto-grants-1984_08
ORD IDord-1717a85a15664a429084898fa46e5458
Source noteuspto-grants-1984_08