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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693402Generated: October 30, 2026

Water → tert-Butyl 4-[(methanesulfonyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1693402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-[(methanesulfonyl)amino]piperidine-1-carboxylateHCID 47464928—

Reaction Steps

To a solution of 4-amino-1-Boc-piperidine (300 mg, 1.50 mmol) in dichloromethane (2.0 mL) was added a solution of methanesulfonyl chloride (348 μL, 4.49 mmol) in dichloromethane (1 mL) followed by a solution of pyridine (485 μL, 5.99 mmol) in dichloromethane (1 mL), and the reaction stirred at rt for 16 h. Water (10 mL) was added, the mixture separated and the organic layer washed with 1M HCl (10 mL), sodium bicarbonate solution (10 mL) then brine (2×10 mL). The solution was dried (MgSO4) and solvent removed in vacuo. The crude material was purified by chromatography using dichloromethane/methanol (95:5) as the eluent to give the title compound as an off-white powder. δH (CD3OD): 4.46-4.40 (1H, m), 4.09-3.97 (2H, m), 3.53-3.40 (1H, m), 3.0 (3H, s), 2.93-2.81 (2H, m), 2.01-1.93.(2H, m), 1.50-1.37 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158622B2
Source datasetuspto-grants-2012_04
ORD IDord-69786bca8fc44478939ac972ac533ff7
Source noteuspto-grants-2012_04