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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635966Generated: October 31, 2026

(Pyridin-4-yl)boronic acid → 4-(1,3-Diethyl-5-methyl-1H-pyrazol-4-yl)pyridine

https://huagongshe.com/reaction/1635966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant1,3-Diethyl-4-iodo-5-methylpyrazoleHCID 21912748—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-(1,3-Diethyl-5-methyl-1H-pyrazol-4-yl)pyridineHCID 21912786—

Reaction Conditions

Temperature100 °C

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 t-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 chromatography on a Biotage 75S afforded 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511994B2
Source datasetuspto-grants-2003_01
ORD IDord-2b792dacc4c84ac39ae634bb478dbd51
Source noteuspto-grants-2003_01