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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469157Generated: November 1, 2026

Methyl iodide → HCID 178463214, compound

https://huagongshe.com/reaction/1469157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178463215HCID 178463215—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178463214HCID 17846321497.4%

Reaction Steps

To a stirred solution of methyl 5-bromo-3-(((trans)-4-((tert-butoxycarbonyl)amino)cyclohexyl)(ethyl)amino)-2-methylbenzoate (3 g, 6.41 mmol, see, e.g., WO2012142504) in THF (30 mL), NaH (0.184 g, 7.69 mmol) was added at 0° C. and stirred it at same temperature for 20 min. Then methyl iodide (9.10 g, 64.10 mmol) was added at 0° C. and reaction was stirred for overnight at room temperature. On completion, reaction was quenched with ice water and extracted with dichloromethane. The combined organic layers were washed with water, dried, concentrated under reduced pressure. The crude compound was purified by column chromatography to afford the crude title compound that was used without further purification (3 g, 97.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006242B2
Source datasetuspto-grants-2015_04
ORD IDord-133d22cad3ac4e9baad725a2d6d1aaf3
Source noteuspto-grants-2015_04