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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075691Erstellt: 25. Oktober 2026

2-Pyridinecarboxaldehyde → 7-Iodo-1-pyridin-2-yl-[1,2,4]triazolo[4,3-a]quinoline

https://huagongshe.com/reaction/2075691

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-PyridinecarboxaldehydeHCID 14273—
EduktIodo benzene diacetateHCID 12217721—
Edukt(6-Iodo-quinolin-2-yl)-hydrazineHCID 53403040—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-Iodo-1-pyridin-2-yl-[1,2,4]triazolo[4,3-a]quinolineHCID 67090963—

Reaktionsschritte

To (6-Iodo-quinolin-2-yl)-hydrazine (2.99 g, 10.5 mmol) suspended in CH2Cl2 (30 mL) was added 2-pyridinecarboxaldehyde (1.2 mL, 12.6 mmol). The reaction was stirred at room temperature for 2 hours, followed by the addition of iodobenzene diacetate (3.39 g, 10.5 mmol). The reaction was stirred overnight at room temperature, during which time a precipitate formed. The mixture was concentrated to half the volume, and the precipitate was filtered and washed with minimal CH2Cl2 to give the desired product, 5k. The filtrate was concentrated and suspended in EtOH. After stirring overnight at room temperature, the mixture was filtered and rinsed with EtOH to obtain additional product, 5k.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07919621B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-0de7e5fe627a46139bccc5c89a4503f6
Quellennotizuspto-grants-2011_04