HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537435Generated: October 31, 2026
Potassium Carbonate → 5-iodo-2-(4-phenyl-1H-pyrazol-1-yl)pyridine
https://huagongshe.com/reaction/537435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenylpyrazole | HCID 139106 | — |
| Reactant | 2-Fluoro-5-iodopyridine | HCID 2783179 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-iodo-2-(4-phenyl-1H-pyrazol-1-yl)pyridine | HCID 68156673 | 94% |
Reaction Steps
A mixture of 2-fluoro-5-iodopyridine (368.3 mg, 1.652 mmol), 4-phenyl-1H-pyrazole (238.2 mg, 1.652 mmol), and potassium carbonate (457 mg, 3.30 mmol) in N,N-dimethylformamide (3.30 mL) was heated to 85° C. for 21 hours. The reaction was then concentrated and the crude residue diluted with water and ethyl acetate. The layers were separated and the aqueous was extracted two more times with ethyl acetate. The combined organics were dried over magnesium sulfate, filtered, and concentrated to give 5-iodo-2-(4-phenyl-1H-pyrazol-1-yl)pyridine (537.2 mg, 94%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 8.76 (s, 1H), 8.61 (d, J=1.8 Hz, 1H), 8.09 (dd, J=8.7, 2.2 Hz, 1H), 8.01 (s, 1H), 7.82 (d, J=8.6 Hz, 1H), 7.55-7.61 (m, 2H), 7.36-7.43 (m, 2H), 7.25-7.31 (m, 1H). MS (M+1): 348.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859591B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-1da442f6521f4130b827e6b41ceb748a |
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| Source note | uspto-grants-2014_10 |
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