HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644530Generated: October 28, 2026
1,3-Propanediol → 1-Phenyl-7-(4-pyridyl)-5-trifluoromethylbenzimidazole
https://huagongshe.com/reaction/644530
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | 7-Iodo-1-phenyl-5-(trifluoromethyl)-1H-benzimidazole | HCID 19426024 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-Phenyl-7-(4-pyridyl)-5-trifluoromethylbenzimidazole | HCID 11209965 | — |
Reaction Steps
A mixture of 7-iodo-1-phenyl-5-trifluoromethylbenzimidazole (3.0 g, 7.5 mmol), pyridine 4-boronic acid (1.38 g, 11.2 mmol), 1,3-propanediol (2.7 ml, 37.3 mmol), potassium carbonate (5.2 g, 37.3 mmol) and bis(triphenylphosphin)palladium dichloride (200 mg, 0.28 mmol) in a mixture of dimethoxyethane (30 ml) and water (15 ml) was stirred at reflux for 5 days. The cooled reaction mixture was concentrated under reduced pressure, and the concentrate was partitioned between water and ethyl acetate. The organic phase was dried and concentrated under reduced pressure, and the concentrate was purified by column chromatography on silica gel eluting with a mixture of ligroin and ethyl acetate (1:1 v/v). The product was isolated as a yellowish solid by evaporation of solvent from the eluate (1.55 g, 61%) m/z, 340.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700638B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-50c58617b5e141fcb663f8f867085a07 |
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| Source note | uspto-grants-2010_04 |
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