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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645776Generated: October 30, 2026

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

https://huagongshe.com/reaction/645776

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 flash 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 numberUS07705007B2
Source datasetuspto-grants-2010_04
ORD IDord-bcefdefdb3f6428c843d20fe551f97f5
Source noteuspto-grants-2010_04