HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Pyridinecarboxaldehyde → 7-Iodo-1-pyridin-2-yl-[1,2,4]triazolo[4,3-a]quinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Edukt | Iodo benzene diacetate | HCID 12217721 | — |
| Edukt | (6-Iodo-quinolin-2-yl)-hydrazine | HCID 53403040 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 7-Iodo-1-pyridin-2-yl-[1,2,4]triazolo[4,3-a]quinoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07919621B2 |
| Quelldatensatz | uspto-grants-2011_04 |
| ORD ID | ord-0de7e5fe627a46139bccc5c89a4503f6 |
| Quellennotiz | uspto-grants-2011_04 |