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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641592Generated: October 25, 2026

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

https://huagongshe.com/reaction/1641592

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 numberUS08115027B2
Source datasetuspto-grants-2012_02
ORD IDord-90bf8fde81d040c9b35eb024cdc57133
Source noteuspto-grants-2012_02