HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Hydroxymethyl)benzeneboronic acid | HCID 2734706 | — |
| Reactant | 5-Cyano-7-(3-hydroxymethylphenyl)-1-phenylbenzimidazole | HCID 11393198 | — |
| Reactant | 5-Cyano-7-iodo-1-phenylbenzimidazole | HCID 67485627 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole | HCID 67485006 | — |
Reaction Steps
5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole was prepared from 5-cyano-7-iodo-1-phenylbenzimidazole (1.0 g, 2.90 mmol), 4-hydroxymethylphenylboronic acid (440 mg, 2.90 mmol), tetrakis(triphenylphosphine)palladium(0) (330 mg, 2.90 mmol) and potassium carbonate (2M in water, 2.9 ml, 800 mg, 5.8 mmol) in toluene (8.0 ml) and ethanol (2.0 ml) using the method described for 5-cyano-7-(3-hydroxymethylphenyl)-1-phenylbenzimidazole. 5-Cyano-7-(4-hydroxymethylphenyl)-1-phenylbenzimidazole was obtained as a white solid (711 mg) m/z, 326.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700638B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-3ac02db958504ecb8d09ec5b60bffbc2 |
| Source note | uspto-grants-2010_04 |