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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915001Generated: October 26, 2026

Triethylamine → 4-t-Butylsulfinylamino-1-ethoxycarbonyl piperidine

https://huagongshe.com/reaction/915001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
Reactant2-Methylpropane-2-sulfinyl chlorideHCID 4686861—
SolventDichloromethaneHCID 6344—
Product4-t-Butylsulfinylamino-1-ethoxycarbonyl piperidineHCID 2274778086.6%

Reaction Steps

Ethyl 4-amino-1-piperidinecarboxylate (300 mg) and triethylamine (258 mg) were dissolved in 5 ml of dichloromethane. To the mixture, 2 ml of solution of t-butylsulfinyl chloride (222 mg) in dichloromethane was added and the mixture was stirred at room temperature for 4 hours. The solution was partitioned into an aqueous solution of potassium hydrogen sulfate and ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate anhydride. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography to give 378 mg of 4-t-butylsulfinylamino-1-ethoxycarbonyl piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265130B2
Source datasetuspto-grants-2007_09
ORD IDord-e0e5ee92ade94cb5aacd46048f215161
Source noteuspto-grants-2007_09