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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366472Generated: October 31, 2026

Methyl iodide → HCID 18727283, compound

https://huagongshe.com/reaction/366472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18727281HCID 18727281—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 18727283HCID 1872728363%

Reaction Steps

Anhydrous potassium carbonate (152 mg, 1.1 mmol) and iodomethane (0.034 ml, 0.5 mmol) were added to a solution of tert-butyl 2-(R)-{[4-(4-chlorobenzoyl)piperidine-1-sulfonyl]amino}-3-methylbutyrate (100 mg, 0.22 mmol) in DMF (1.5 ml) at RT. After 3 h, the reaction mixture was diluted with ethyl acetate (30 ml) and then washed with 0.1M HCl and brine, and dried over MgSO4. The solvent was removed in vacuo and the residue was chromatographed (]PTLC, SiO2, 25% ethyl acetate/hexane) to give tert-butyl 2-(R)-{methyl-[4-(4-chlorobenzoyl)piperidine-1-sulfonyl]amino}-3-methylbutyrate as a colorless oil (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130220
Source datasetuspto-grants-2000_10
ORD IDord-12b8ccbb44cf47508c91059518784551
Source noteuspto-grants-2000_10