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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238637Generated: October 31, 2026

N-bromobutanimide → HCID 68686099, compound

https://huagongshe.com/reaction/2238637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-aminopyridine-3-carboxylateHCID 351633—
ReactantHCID 18506912HCID 18506912—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68686099HCID 6868609950.7%

Reaction Steps

137.2 mg of the 4-[(E)-2-ethoxyvinyl]-2-(methylthio)pyrimidine [25-2] was dissolved in a mixture solvent of 5 mL of 1,4-dioxane and 2 mL of water, and 124.1 mg of N-bromosuccinimide was added thereto. After stirring at room temperature for 1 hour, 106 mg of the 2-aminonicotinic acid methylester [25-1] was added, and stirred at 85° C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and the residue was purified by preparative thin layer chromatography, to obtain 106.1 mg of methyl 3-[2-(methylthio)-4-pyrimidinyl]imidazo[1,2-a]pyridine-8-carboxylate [25-3].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718801B2
Source datasetuspto-grants-2010_05
ORD IDord-1769578a4a444457b1559b73e869bd17
Source noteuspto-grants-2010_05