HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridine → HCID 58790088, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridine | HCID 57516658 | — |
| Edukt | HCID 58790408 | HCID 58790408 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | HCID 58790088 | HCID 58790088 | 15,3% |
Reaktionsbedingungen
| Temperatur | 100 °C |
|---|
Reaktionsschritte
To a solution of the tributyltin derivative 6 (1.88 g, 4.1 mmol) (scheme 2) in toluene (39 mL) was added 5-bromo-1-(2-morpholinoethyl)pyrimidin-2(1H)-one (413, 1.29 g, 4.5 mmol) and Pd(PPh3)4 (474 mg, 0.41 mmol). The reaction mixture was stirred at 100° C. for 16 h. The mixture was filtered and the solvent was evaporated. The residue was triturated in hexanes, then triturated in EtOAc to produce title compound 414 (236 mg, 15% yield). MS (m/z): 377.0 (M+H). 1H NMR (DMSO-d6) δ (ppm): 9.18 (d, J=3.5 Hz, 1H), 8.76 (d, J=3.3 Hz, 1H), 8.64 (d, J=5.1 Hz, 1H), 8.05 (s, 1H), 7.57 (d, J=5.1 Hz, 1H), 4.06 (t, J=5.9 Hz, 2H), 3.54 (t, J=4.5 Hz, 4H), 2.64 (t, J=5.9 Hz, 2H), 2.49-2.43 (m, 4H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08093264B2 |
| Quelldatensatz | uspto-grants-2012_01 |
| ORD ID | ord-d76c378b771d43b2b6eb81dff81323c1 |
| Quellennotiz | uspto-grants-2012_01 |