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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627498Generated: October 30, 2026

1-Methylimidazole → HCID 82895561, compound

https://huagongshe.com/reaction/627498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantChlorotriethylsilaneHCID 13819—
ReactantN-Methoxy-N-methylpyrimidine-5-carboxamideHCID 66575045—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 82895561HCID 82895561—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-BuLi (1.6 M in hexane, 3.71 mL, 5.94 mmol) was added to a solution of 1-methylimidazole (0.452 mL, 5.7 mmol) in THF (10 mL) at −78° C. The mixture was stirred at −78° C. for 30 min. Chlorotriethylsilane (0.957 mL, 5.7 mmol) was added slowly. The mixture was stirred at −78° C. for 30 min. A second portion of n-BuLi (1.6 M in hexane, 3.71 mL, 5.94 mmol) was added. The mixture was stirred at −78° C. for 30 min. Crude N-methoxy-N-methylpyrimidine-5-carboxamide (794 mg, 4.75 mmol, Intermediate 28, step a) was added via cannula as a solution in THF (5 mL). The mixture was stirred at −78° C. for 5 min and was removed from the cold bath and stirred at room temperature overnight. Saturated aqueous NH4Cl was added and the phases were separated. The aqueous phase was extracted twice with DCM. The organic phase was dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, gradient 10-100% EtOAc-heptanes, then 0-10% MeOH-EtOAc) to afford impure title compound, which was further purified by flash column chromatography (silica gel, 4-5% MeOH-DCM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-242ea66578c14de7a36bcbe831767051
Source noteuspto-grants-2016_04