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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425598Generated: October 28, 2026

Methanesulfonyl chloride → Tert-butyl 4-(2-(methylsulfonamido)ethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2425598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 1514400—
SolventPyridineHCID 1049—
ProductTert-butyl 4-(2-(methylsulfonamido)ethyl)piperazine-1-carboxylateHCID 4721520870%

Reaction Steps

Methanesulfonyl chloride (0.7 mL, 9.0 mmol) was added to a cooled solution of 4-(2-amino-ethyl)-piperazine-1-carboxylic acid tert-butyl ester (1.33 g, 5.8 mmol) in pyridine (25.0 mL). The reaction was stirred for 12 h and partitioned between partitioned between aqueous sodium bicarbonate and methylene chloride. The organic phase was washed with 1M hydrochloric acid, aqueous sodium bicarbonate, brine, dried over anhydrous magnesium sulfate and concentrated. Purification of the crude residue by chromatography over silica gel using 0-5% methanol in methylene chloride gave 4-(2-methanesulfonylamino-ethyl)-piperazine-1-carboxylic acid tert-butyl ester (0.70 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964724B2
Source datasetuspto-grants-2011_06
ORD IDord-5a98f90cd4f145a2ac2ef9b16cb413e7
Source noteuspto-grants-2011_06