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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731338Generated: November 3, 2026

2-Amino-4-methylpyridine → 6-(3,7-dimethylimidazo[1,2-a]pyridin-2-yl)-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/1731338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylpyridineHCID 1533—
Reactant6-(2-Bromopropanoyl)-2-methyl-2H-1,4-benzoxazin-3(4H)-oneHCID 20228676—
SolventAcetonitrileHCID 6342—
Product6-(3,7-dimethylimidazo[1,2-a]pyridin-2-yl)-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 2022866545.3%

Reaction Steps

A solution of 6-(2-bromopropionyl)-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (1.5 g) and 2-amino-4-picoline (1.6 g) in acetonitrile (60 ml) was refluxed for 2.5 hours and the reaction mixture was evaporated under reduced pressure. A mixture of ethyl acetate and 5% hydrochloric acid was added to the residue and the resultant mixture was stirred at ambient temperature for 30 minutes. The precipitate was collected by filtration and suspended in water. The mixture was adjusted to pH 7.5 with 20% aqueous potassium carbonate. The resultant mixture was extracted with chloroform and the extract was washed with brine and dried over magnesium sulfate. The solvent was removed in vacuo to afford a crystalline residue, which was recrystallized from a mixture of ethyl acetate and tetrahydrofuran to give 6-(3,7-dimethylimidazo[1,2-a]pyridin-2-yl)-2-methyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (0.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621084
Source datasetuspto-grants-1986_11
ORD IDord-3cbc8c6064be40f5b780eacded30f601
Source noteuspto-grants-1986_11