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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403424Generated: November 1, 2026

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

https://huagongshe.com/reaction/2403424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantTriethylamineHCID 8471—
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 methanesulfonic acid (0.21 ml). After stirring for 24 hours, the reaction mixture was diluted with dichloromethane, washed with sodium bicarbonate solution, dried (MgSO4) 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 numberUS08802670B2
Source datasetuspto-grants-2014_08
ORD IDord-90c3dcb8887e43caadcff9ee20e74cb3
Source noteuspto-grants-2014_08