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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288729Generated: November 1, 2026

Water → 1-(t-Butoxycarbonyl)4-(1-(6-chloronaphth-2-ylsulphonyl)piperazin-4-ylcarbonyl)piperidine

https://huagongshe.com/reaction/2288729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantSuccinimido 1-t-butoxycarbonylpiperidine-4-carboxylateHCID 15578030—
Reactant1-(6-Chloronaphth-2-ylsulphonyl)piperazine hydrochlorideHCID 22709766—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-(t-Butoxycarbonyl)4-(1-(6-chloronaphth-2-ylsulphonyl)piperazin-4-ylcarbonyl)piperidineHCID 1211202081%

Reaction Steps

Triethylamine (2.92 ml) was added to a mixture of 1-(6-chloronaphth-2-ylsulphonyl)piperazine hydrochloride (6.93 g) in dichloromethane (100 ml). 1-(1-(t-butoxycarbonyl)piperidin-4-ylcarbonyloxy)-2,5-dioxopyrrolidine (6.25 g) was added and the mixture stirred overnight. The mixture was evaporated to give a solid which was suspended in ethyl acetate (200 ml). Water (50 ml) was added and the ethyl acetate phase separated, washed with water (4×50 ml), brine (50 ml), dried (MgSO4) and evaporated. The residue was purified by flash chromatography on silica gel using a 75:25 mixture of ethyl acetate/hexane as eluent to give 1-(t-butoxycarbonyl)-4-(1-(6-chloronaphth-2-ylsulphonyl)piperazin-4-ylcarbonyl)piperidine (8.1 g);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090813
Source datasetuspto-grants-2000_07
ORD IDord-2016414e00734b129bf01f4b014f0f99
Source noteuspto-grants-2000_07