HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4'-{3-[(3R)-3-hydroxy-3-methylpyrrolidinyl]propoxy}[1,1'-biphenyl]-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-{3-[(3R)-3-Aminopyrrolidinyl]propoxy}[1,1'-biphenyl]-4-carbonitrile | HCID 9923147 | — |
| Reactant | (3R)-3-Methylpyrrolidin-3-ol | HCID 55288331 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4'-{3-[(3R)-3-hydroxy-3-methylpyrrolidinyl]propoxy}[1,1'-biphenyl]-4-carbonitrile | HCID 69355600 | 40% |
Reaction Steps
4′-{3-[(3R)-3-Aminopyrrolidinyl]propoxy}[1,1′-biphenyl]-4-carbonitrile (177 mg, 0.65 mmol), (3R)-3-methyl-3-pyrrolidinol (75 mg, 0.74 mmol), potassium carbonate (153 mg) and potassium iodide (184 mg) in 10 mL of DMF were heated at 110° C. for 10 hours. The mixture was evaporated under reduced pressure and the residue was purified by chromatography (CHCl3:MeOH:NH4OH, 9:1:0.1) to provide the title compound (40% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06620839B2 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-841be8ca02c743fc89a4f6cbfe8d3850 |
| Source note | uspto-grants-2003_09 |