HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340791Generated: October 30, 2026
Potassium Carbonate → Ethyl 3-{[5-(biphenyl-4-yl)-1-(biphenyl-4-ylmethyl)-4,6-difluoro-1H-benzimidazol-2-yl]oxy}cyclopentanecarboxylate
https://huagongshe.com/reaction/340791
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,1'-Biphenyl-4-yl-boronic acid | HCID 151253 | — |
| Reactant | Ethyl 3-{[1-(biphenyl-4-ylmethyl)-4,6-difluoro-5-iodo-1H-benzimidazol-2-yl]oxy}cyclopentanecarboxylate | HCID 67408440 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 3-{[5-(biphenyl-4-yl)-1-(biphenyl-4-ylmethyl)-4,6-difluoro-1H-benzimidazol-2-yl]oxy}cyclopentanecarboxylate | HCID 67407206 | — |
Reaction Steps
A solution of ethyl 3-{[1-(biphenyl-4-ylmethyl)-4,6-difluoro-5-iodo-1H-benzimidazol-2-yl]oxy}cyclopentanecarboxylate (0.290 g, 0.481 mmol), biphenylboronic acid (0.105 g, 0.530 mmol), and Pd(PPh3)4 (22 mg, 0.019 mmol) in 4.8 mL of DMF was treated with a 1 M solution of K2CO3 (0.960 mL). The resulting yellow solution was heated at 120° C. for 45 min, and then diluted with EtOAc and H2O. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated. Purification of the resulting residue by flash chromatography (0-25% EtOac/hexanes) afforded the desired compound as a white solid. LCMS: calculated for C40H34F2N2O3 628.71, observed m/e 629.1 (M+H)+ (Rt 2.82/4 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895596B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3886c12536cc447783876bd4beb28eff |
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| Source note | uspto-grants-2014_11 |
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