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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1803972Erstellt: 26. Oktober 2026

(R)-4-Methyloxazolidin-2-one → (R)-3-{6-[4-(4-chlorobenzoyl)piperidine-1-carbonyl]pyridin-3-yl}-4-methyloxazolidin-2-one

https://huagongshe.com/reaction/1803972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-4-Methyloxazolidin-2-oneHCID 2734858—
Edukt(5-Bromopyridin-2-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanoneHCID 58484577—
Produkt(R)-3-{6-[4-(4-chlorobenzoyl)piperidine-1-carbonyl]pyridin-3-yl}-4-methyloxazolidin-2-oneHCID 5475511983,4%

Reaktionsschritte

By reaction and treatment in the same manner as in Preparation Example 31 and using (5-bromopyridin-2-yl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone (2.4 g) described in Preparation Example 35 and (R)-4-methyloxazolidin-2-one (728 mg) described in Preparation Example 25, the title compound (2.1 g) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08354401B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-5dc47467ef784151ab188b492d73ec0b
Quellennotizuspto-grants-2013_01