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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1856869Erstellt: 26. Oktober 2026

N-tert-butoxy-1-[4-(4-chlorobenzoyl)piperidine-1-sulfonyl]piperidine-2-(R)-carboxamide → N-hydroxy-1-[4-(4-chlorobenzoyl)-piperidine-1-sulfonyl]piperidine-2-(R)-carboxamide

https://huagongshe.com/reaction/1856869

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-tert-butoxy-1-[4-(4-chlorobenzoyl)piperidine-1-sulfonyl]piperidine-2-(R)-carboxamideHCID 18727273—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktN-hydroxy-1-[4-(4-chlorobenzoyl)-piperidine-1-sulfonyl]piperidine-2-(R)-carboxamideHCID 1543491751%

Reaktionsschritte

A solution of N-tert-butoxy-1-[4-(4-chlorobenzoyl)piperidine-1-sulfonyl]piperidine-2-(R)-carboxamide (100 mg, 0.22 mmol), [prepared as described in Step 1 above], in 1,2-dichloroethane (10 ml) was cooled to -30° C. and HCl gas was bubbled through it for 10 min. The reaction vessel was then sealed and stirred at RT. After 2 days, the reaction mixture was vented with nitrogen and then concentrated in vacuo. The residue was chromatographed (PTLC, SiO2, 10% methanol/methylene chloride) to give N-hydroxy-1-[4-(4-chlorobenzoyl)piperidine-1-sulfonyl]piperidine-2-(R)-carboxamide as a white solid (51%), mp 84.4-86.4° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06143744
Quelldatensatzuspto-grants-2000_11
ORD IDord-e7a6b8ef7f8e476ab77def49b91ceac6
Quellennotizuspto-grants-2000_11