HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodo-1-tritylimidazole → HCID 178505534, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| Reactant | 5-Bromo-2-fluoropyridine | HCID 2783168 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178505534 | HCID 178505534 | 46% |
Reaction Steps
To a solution of 4-Iodo-1-trityl-1H-imidazole (1 eq) in THF at room temperature was added ethylmagnesium bromide (1.2 eq) under dry conditions. After stirring for 90 minutes, zinc chloride (1.2 eq) was added to the reaction mixture. After stirring for another 90 minutes, tetrakis(triphenylphosphine)palladium (10%) and 5-bromo-2-fluoropyridine (1.2 eq) were added to the reaction mixture. Subsequent reaction conditions and work up are as described previously, in Example 73 to afford the solid 2-Fluoro-5-(1H-imidazol-4-yl)-pyridine (46%). MH+(164).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06756359B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-b50cd01093f94198a5b30cef4e152629 |
| Source note | uspto-grants-2004_06 |