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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856861Generated: November 3, 2026

Methyl iodide → HCID 18727283, compound

https://huagongshe.com/reaction/1856861

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 numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-03446bcccf4345eaa98c4b5b3285c26f
Source noteuspto-grants-2000_11