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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856874Generated: October 27, 2026

Diethyl Ether → n-Hydroxy-1-[4-(4-chlorophenyl)-piperazine-1-sulfonyl]-piperidine-2-(rs)-carboxamide

https://huagongshe.com/reaction/1856874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTrifluoroacetic acidHCID 6422—
Reactantn-Tert-butyldimethylsiloxy-1-[4-(4-chlorophenyl)piperazine-1-sulfonyl]piperidine-2-(rs)-carboxamideHCID 22615606—
SolventDichloromethaneHCID 6344—
Productn-Hydroxy-1-[4-(4-chlorophenyl)-piperazine-1-sulfonyl]-piperidine-2-(rs)-carboxamideHCID 1034109467%

Reaction Steps

Trifluoroacetic acid (few drops) was added to a solution of N-tert-butyldimethylsiloxy-1-[4-(4-chlorophenyl)piperazine-1-sulfonyl]piperidine-2-(RS)-carboxamide (63 mg, 0.12 mmol), [prepared as described in Step 2 above], in methylene chloride (2 ml) and the reaction mixture was stirred at RT for 45 min. The organics were removed in vacuo and the residue was dissolved in methylene chloride (25 ml) and the washed with sat. sodium bicarbonate, brine, and dried over MgSO4. The solvent was removed in vacuo to give a foam which was redissolved in a minimum amount of methylene chloride. Diethyl ether was added and the resulting white precipitates were filtered to give N-hydroxy-1-[4-(4-chlorophenyl)-piperazine-1-sulfonyl]-piperidine-2-(RS)-carboxamide (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-b8281121a1a2465781bfcf728bfb2e4c
Source noteuspto-grants-2000_11