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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879717Generated: November 1, 2026

Methyl iodide → HCID 61360573, compound

https://huagongshe.com/reaction/1879717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 61699309HCID 61699309—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 61360573HCID 6136057370%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 6-chloro-N-(cyclopropylmethyl)pyrazin-2-amine (0.60 g) in tetrahydrofuran (5 mL) was added dropwise n-butyllithium (3.06 mL, 1.6 M hexane solution) at −78° C. The mixture was stirred at −78° C. for 5 min, and iodomethane (1.02 mL) was added dropwise thereto. The mixture was stirred at −78° C. for 30 min, and further stirred at 0° C. for 1 hr. Saturated aqueous sodium thiosulfate solution (10 mL) was added, and the mixture was extracted with ethyl acetate. The aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography (solvent gradient: 5→15% ethyl acetate/hexane) to give the title compound (0.46 g, 70%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318722B2
Source datasetuspto-grants-2012_11
ORD IDord-016bc03cf2b14c829ad7bd49b43d4b87
Source noteuspto-grants-2012_11