HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245587Generated: October 30, 2026
(Pyridin-4-yl)boronic acid → 4-(1,3-Diethyl-5-methyl-1H-pyrazol-4-yl)pyridine
https://huagongshe.com/reaction/1245587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | 1,3-Diethyl-4-iodo-5-methylpyrazole | HCID 21912748 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(1,3-Diethyl-5-methyl-1H-pyrazol-4-yl)pyridine | HCID 21912786 | — |
Reaction Steps
A mixture of 17.05 g (64.6 mmol) of 1,3-diethyl-4-iodo-5-methylpyrazole (from Step D) and 11.9 g (105.4 mmol) of pyridine 4-boronic acid in 300 mL of dioxane was treated with a solution of 44 g (392 mmol) of potassium tert-butoxide in 100 mL of water. The resulting mixture was treated with 3.75 g (3.2 mmol) of tetrakis(triphenylphosphine)palladium(0), put under an argon atmosphere and heated at 100° C. for 18 h. The mixture was cooled and partitioned between 1 L of ether and 500 mL of water. The organic layer was separated, dried over MgSO4 and concentrated. Flash chromtography on a Biotage 75S afforded of the title compound. 1H-NMR (500 MHz) δ 1.19 (t, J=7.5, 3H), 1.48 (t, J=7.5, 3H), 2.27 (s, 3H), 2.67 (q, J=7.5, 2H), 4.09 (q, J=7.5, 2H), 7.18 (dd, J=2.0, 4.5, 2H), 8.60 (dd, J=2.0, 4.5, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125887B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-e00eabd55ed2499b9567c411eb08de03 |
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| Source note | uspto-grants-2006_10 |
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