HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Cesium fluoride → HCID 90118179, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Cesium fluoride | HCID 25953 | — |
| Edukt | 2-(Tributylstannyl)pyrimidine | HCID 2763251 | — |
| Edukt | 2,4-Dichloro-6-(4-isopropoxyphenyl)pyridine | HCID 90118079 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Produkt | HCID 90118179 | HCID 90118179 | — |
Reaktionsschritte
To a 2 dram vial equipped with a stir bar was added 2,4-dichloro-6-(4-isopropoxyphenyl)pyridine (50 mg, 0.18 mmol), 2-(tributylstannyl)pyrimidine (65 mg, 0.18 mmol), CuI (8 mg, 0.04 mmol), CsF (81 mg, 0.53 mmol), and Pd(PPh3)4 (10 mg, 8.9 μmol). The vial was capped with a septum screw-cap and then placed under N2 atmosphere. To the vial was added degassed DMF (1 mL). The vial was placed in a 80° C. heating block with stirring for 1 hour. The mixture was allowed to cool to room temperature, and the reaction mixture was then directly subjected to C18 chromatography (water:MeOH w/0.1% TFA) to afford 2-(4-chloro-6-(4-isopropoxyphenyl)pyridin-2-yl)pyrimidine as an amber solid. This material was carried forward into step 2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09334279B2 |
| Quelldatensatz | uspto-grants-2016_05 |
| ORD ID | ord-a20a0a571a7445be80c3fdf900ddb2c7 |
| Quellennotiz | uspto-grants-2016_05 |