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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067926Generated: October 31, 2026

Methyl iodide → Basimglurant

https://huagongshe.com/reaction/2067926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Chloro-4-[1-(4-fluoro-phenyl)-2-methyl-1H-imidazol-4-ylethynyl]-pyridineHCID 11278369—
SolventTetrahydrofuranHCID 8028—
ProductBasimglurantHCID 11438771—

Reaction Conditions

Temperature-75 °C

Reaction Steps

This compound was prepared according to the general procedure 3 described hereinabove. 2-chloro-4-[1-(4-fluoro-phenyl)-2-methyl-1H-imidazol-4-ylethynyl]-pyridine (200 mg, 0.607 mmol) was dissolved in 10 mL THF and cooled to −75° C. Lithiumdiisopropylamide (0.45 ml, 0.91 mmol) was added, and the mixture stirred for 15 min at −75° C. Iodomethane (0.05 ml, 0.85 mmol) was added and stirring was continued at −75° C. for 2 hrs. The reaction mixture was quenched with sat. NaHCO3− solution and extracted with water and ethyl acetate. The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (heptane/ethylacetate 90:10→20:80 gradient) and by recrystallization from ethyl acetate. The desired compound was obtained as a white solid (40 mg, 19%), MS: m/e=326.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293916B2
Source datasetuspto-grants-2012_10
ORD IDord-cced667fa4404edab14786f8a94e08ba
Source noteuspto-grants-2012_10