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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046561Generated: November 2, 2026

Water → HCID 57993617, compound

https://huagongshe.com/reaction/1046561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
ReactantCyclopropanesulfonyl chlorideHCID 2760919—
Reactanttert-Butyl {[1-(2-aminoethyl)piperidin-4-yl]methyl}carbamateHCID 34178247—
SolventDichloromethaneHCID 6344—
ProductHCID 57993617HCID 5799361778.2%

Reaction Steps

At 15° C., to a solution of tert-butyl (1-(2-aminoethyl)piperidin-4-yl)methylcarbamate (2.00 g, 7.78 mmol) and DIPEA (3.00 g, 23.3 mmol) in CH2Cl2 (40 mL) was added slowly cyclopropylsulfonyl chloride (3.40 g, 25.0 mmol) under Ar. The reaction mixture was stirred at room temperature for 2 hrs. Water (30 mL) was added, and the mixture was extracted with CH2Cl2 (3×30 mL). The combined extract was washed with saturated NaHCO3 (40 mL) and dried over anhydrous Na2SO4. After filtration the solvent was removed in vacuo, and the residue was applied to flash column chromatography (3-7% CH3OH in CH2Cl2) to provide tert-butyl (1-(2-(cyclopropanesulfonamido)ethyl)piperidin-4-yl)methylcarbamate as pale yellow oil (2.2 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569344B2
Source datasetuspto-grants-2013_10
ORD IDord-cef54450f0884f7eb538a0543337a279
Source noteuspto-grants-2013_10