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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618104Generated: November 1, 2026

Methyl iodide → HCID 68314590, compound

https://huagongshe.com/reaction/1618104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 67194237HCID 67194237—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68314590HCID 68314590—

Reaction Steps

To a stirred solution of 7-bromo-2-(1-cyclohexylpiperidin-4-yl)-5-fluoro-2,3-dihydro-1H-isoindol-1-one (70 mg, 0.177 mmol) and methyliodide (1.1 equiv., 0.195 mmol, 0.012 mL) in anhydrous tetrahydrofuran (3.5 mL) under nitrogen at −78° C., 1M sodium bis(trimethylsilyl)amide in tetrahydrofuran (1.2 equiv., 0.212 mL) was slowly added. The reaction mixture was stirred for 90 min and quenched by adding dropwise a 10% ammonium hydroxide solution. Dichloromethane was added, the layers were separated, and the aqueous layer was extracted twice dichloromethane. Organic layers were collected, dried and evaporated. Crude (58 mg) was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765972B2
Source datasetuspto-grants-2014_07
ORD IDord-179b5fa91aac4518be1e93519329ff85
Source noteuspto-grants-2014_07