HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2187379Erstellt: 26. Oktober 2026
Potassium Carbonate → Ethyl 5-(4-chloro-3-methyl-[1,8]-naphthyridin-2-yl)pentanoate
https://huagongshe.com/reaction/2187379
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethyl 4-pentenoate | HCID 74786 | — |
| Edukt | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Edukt | 2,4-Dichloro-3-methyl-1,8-naphthyridine | HCID 22082661 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Katalysator | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 5-(4-chloro-3-methyl-[1,8]-naphthyridin-2-yl)pentanoate | HCID 18475432 | — |
Reaktionsschritte
To a solution of ethyl 4-pentenoate (2.5 g, 20 mmol) in 60 mL THF was added 9-BBN (0.5 M in THF, 47 mL, 23 mmol) gradually at room temperature. After stirring for 10 hours, it was treated with Pd(OAc)2 (0.4 g, 2.0 mmol), 1,1′-bis(diphenylphosphino)-ferrocene (DPPF) (1.1 g, 2.0 mmol), K2CO3 (powder, 8.1 g, 58 mmol), 2,4-dichloro-3-methyl-naphthyridine (L) (3.6 g, 20 mmol) and 50 mL DMF. The reaction mixture was purged with argon for 5 minutes and then refluxed at 75° C. for 24 hours. It was cooled to room temperature and treated with 10 mL ethanolamine and stirred for 30 minutes. The mixture was diluted with 400 mL H2O and extracted with EtOAc(×3). The combined organic layers were washed with brine and dried. After solvent removal, the residue was purified by silica gel chromatography using EtOAc/hexanes (1:1) to give the desired product 3-3 as a liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06410526B1 |
|---|
| Quelldatensatz | uspto-grants-2002_06 |
|---|
| ORD ID | ord-f61ba7ed573a42e384bb8cb7db67a911 |
|---|
| Quellennotiz | uspto-grants-2002_06 |
|---|