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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877847Generated: October 31, 2026

Methyl iodide → 6-chloro-N-cyclobutyl-N-methylpyrazin-2-amine

https://huagongshe.com/reaction/1877847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-chloro-N-cyclobutylpyrazin-2-amineHCID 62415214—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-N-cyclobutyl-N-methylpyrazin-2-amineHCID 8664899685%

Reaction Steps

To a solution of 6-chloro-N-cyclobutylpyrazin-2-amine (535 mg) in THF (30 mL) was added dropwise n-butyllithium (1.6 M hexane solution, 2.4 mL) under an argon stream at −78° C., and the mixture was stirred for 30 min. To the reaction mixture was added dropwise a solution of methyl iodide (542 μL) in THF (1 mL), and the mixture was stirred at room temperature for 1.5 hr. To the reaction mixture was added dropwise a saturated ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (solvent gradient: 5→33% ethyl acetate/hexane) to give the title compound (492 mg, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314088B2
Source datasetuspto-grants-2012_11
ORD IDord-32a06be896f2427894717aef001e7700
Source noteuspto-grants-2012_11