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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361320Generated: October 30, 2026

Methyl iodide → HCID 66971294, compound

https://huagongshe.com/reaction/1361320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 66971267HCID 66971267—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66971294HCID 6697129494.6%

Reaction Steps

To a solution of (3S)-1-Boc-3-[(4,4-dimethylcyclohexyl)(3-hydroxy-2,2-dimethylpropanoyl)amino]pyrrolidine (800 mg, 2.02 mmol) prepared in Step B of Example A8 in THF was added NaH (73 mg, 3.03 mmol) and iodomethane (430 mg, 3.03 mmol) at 0° C., and the solution was stirred at rt for 2 h. After the reaction finished, the solution was concentrated in vacuo, extracted with 1N-HCl and EtOAc. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by column chromatography (eluent: EtOAc/Hex=1/2) to give the title compound (784 mg, 94.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879852B2
Source datasetuspto-grants-2011_02
ORD IDord-337ec102a7bc4b4197a8c0d62e4cccb0
Source noteuspto-grants-2011_02