Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20075Erstellt: 24. Oktober 2026

Acetic Acid → 4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridine

https://huagongshe.com/de/reaction/20075

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt3,4-DiaminopyridineHCID 5918—
Edukt1-Benzyl-4-piperidoneHCID 19220—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridineHCID 2229324598,2%

Reaktionsschritte

A mixture of 3,4-diaminopyridine (1.1 g, 10.1 mmol), 1-benzyl-4-piperidone (3.2 g, 16.9 mmol) sodium triacetoxyborohydride (4.0 g, 18.9 mmol), and acetic acid (10.7 mL) in dichloroethane (10 mL) was stirred for about 6 days at room temperature. The reaction was concentrated to near dryness, and partitioned between chloroform (5×50 mL) and 1N sodium hydroxide (50 mL). The organic phase was dried over magnesium sulfate and concentrated to give the title compound (2.8 g). MS 283 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745427B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-83011ce417e94bfbb3e2412d8e518bc5
Quellennotizuspto-grants-2010_06