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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835325Generated: November 2, 2026

Methyl iodide → HCID 10231535, compound

https://huagongshe.com/reaction/1835325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 86584821HCID 86584821—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10231535HCID 1023153518%

Reaction Steps

To a solution of 70 mg (0.12 mmol) acetic acid (5-{[2-(3,5-bis-trifluoromethyl-phenyl)-2-methyl-propionyl]-methyl-amino}-4-o-tolyl-pyridin-2-ylcarbamoyl)-methyl ester in 4 ml tetrahydrofuran at room temperature under argon were added dropwise 0.13 ml (0.12 mmol) of a 1 M solution of potassium hexamethyldisilazide in tetrahydrofuran. Stirring was continued for 1 h at room temperature and 17 mg (0.12 mmol) methyl iodide were added. After stirring overnight, saturated ammonium chloride solution was added and the aqueous layer was extracted with diethyl ether. The diethyl ether layer was dried with sodium sulfate, evaporated, and the residue was purified by flash-chromatography to give 12 mg (18%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770637B2
Source datasetuspto-grants-2004_08
ORD IDord-815b56faf5ee4024b2d152725652edd6
Source noteuspto-grants-2004_08