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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243155Generated: October 31, 2026

Methyl iodide → HCID 11418800, compound

https://huagongshe.com/reaction/2243155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 11177293HCID 11177293—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11418800HCID 1141880061.9%

Reaction Steps

To a suspension of NaH (16.3 nmg, 410 μmol, 60% dispersion in mineral oil) in THF (300 μL) at 0° C. was added a solution of 4-cyano-N-[2-ethyl-1-(1-phenyl-1H-pyrazol-5-yl)butyl]benzenesulfonamide (example 37, 140 mg, 340 μmol) in THF (600 μL). The reaction mixture was warmed to room temperature, and after 20 min iodomethane (45 μL, 714 μmol) was added. The mixture was allowed to stir overnight. TLC indicated that the reaction was not complete. Additional aliquots of NaH and iodomethane were added until the reaction was driven to completion. The mixture was then quenched with H2O and extracted with EtOAc twice. The organic extracts were dried (MgSO4) and concentrated. Column chromatography (EtOAc/hexanes, 1:1) provided 89 mg (57% yield) of the title compound as a glassy yellow solid. mp 37.8-54° C.; Mass Spectrum (ES): 481.1;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674813B2
Source datasetuspto-grants-2010_03
ORD IDord-139ea5fdca5342b98ad636af045802d6
Source noteuspto-grants-2010_03