Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260480Generated: October 31, 2026

Methyl iodide → HCID 483539, compound

https://huagongshe.com/reaction/260480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 22401505HCID 22401505—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 483539HCID 483539—

Reaction Steps

To a partial suspension of N-[(imidazol-2-yl)methyl] 3-phenylsulfonyl-5-chloroindole-2-carboxamide (Example 35) (42 mg, 0.1 mmol) in 1:1 methanol/tetrahydrofuran (4 mL) was added iodomethane (0.05 mL, 0.8 mmol). The reaction was stirred for three days at room temperature. The solvents were removed under reduced pressure, aq. NaHCO3 added and the product extracted into ethyl acetate/methanol. The organic layer was dried (Na2SO4), filtered, and the solvents evaporated. The residue was purified by chromatography and the product eluted with 3% methanol/chloroform. Appropriate fractions were combined, the solvents evaporated, and the residue triturated with methylene chloride to give pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527819
Source datasetuspto-grants-1996_06
ORD IDord-6e51df6542b84bc78dc09e296c44b14d
Source noteuspto-grants-1996_06