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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609684Generated: October 27, 2026

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

https://huagongshe.com/reaction/609684

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]pipeidine-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 numberUS05998412
Source datasetuspto-grants-1999_12
ORD IDord-0e7d7b255f104cd4baea464201f5f657
Source noteuspto-grants-1999_12