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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365195Generated: November 2, 2026

Triethylamine → 3-(Methanesulfonyl-methyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2365195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl 3-(methylamino)pyrrolidine-1-carboxylateHCID 45089533—
SolventDichloromethaneHCID 6344—
Product3-(Methanesulfonyl-methyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66617696—

Reaction Steps

To a solution of 3-methylamino-pyrrolidine-1-carboxylic acid tert-butyl ester (0.50 g) in dichloromethane (10 ml) was added triethylamine (0.38 ml) followed by methanesulfonyl chloride (0.21 ml). After stirring for 24 hours the reaction mixture was diluted with dichloromethane, washed with sodium bicarbonate solution, dried (Mg2SO4) and the solvent removed in vacuo. The residue was purified by flash chromatography to yield 3-(methanesulfonyl-methyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.52 g). Treatment of this compound with HCl in dichloromethane/methanol yielded N-Methyl-N-pyrrolidin-3-yl-methanesulfonamide hydrochloride salt (0.41 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697693B2
Source datasetuspto-grants-2014_04
ORD IDord-d5864e4cd26045ab9b83398b3b99b631
Source noteuspto-grants-2014_04