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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1517073Erstellt: 27. Oktober 2026

4-(1-Pyrrolidinyl)piperidine → [6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone

https://huagongshe.com/reaction/1517073

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(1-Pyrrolidinyl)piperidineHCID 78703—
Edukt3-Methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acidHCID 57441124—
Edukt6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid methyl esterHCID 57441125—
Edukt6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acidHCID 86637420—
Produkt[6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanoneHCID 44547211—

Reaktionsschritte

In analogy to the procedure described for example 1, 6-chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid [prepared from 6-chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid methyl ester (intermediate 2) 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 light brown solid. MS: 452.1 (MH+, 1Cl).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08227613B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-62cfcf0d424047f9a85b9bde9e2565c1
Quellennotizuspto-grants-2012_07