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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1517074Erstellt: 25. Oktober 2026

4-(1-Pyrrolidinyl)piperidine → [4-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone

https://huagongshe.com/reaction/1517074

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(1-Pyrrolidinyl)piperidineHCID 78703—
Edukt3-Methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acidHCID 57441124—
Edukt4-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid methyl esterHCID 67025389—
Edukt4-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acidHCID 86637421—
Produkt[4-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanoneHCID 57441144—

Reaktionsschritte

In analogy to the procedure described for example 1, 4-chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid [prepared from 4-chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid methyl ester (intermediate 3) by saponification in analogy to the procedure described for intermediate 1B] was reacted with 4-pyrrolidin-1-yl-piperidine to give the title compound as colorless solid. MS: 452.1 (MH+, 1Cl).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08227613B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-81be8d1fbdd3415c80457870a20c52a3
Quellennotizuspto-grants-2012_07