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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242026Generated: November 1, 2026

Cesium carbonate → ethyl 1-{[6-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl)methyl}-4-oxo-1,4-dihydrocinnoline-3-carboxylate

https://huagongshe.com/reaction/242026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantEthyl 1-[(6-bromopyridin-3-yl)methyl]-4-oxo-1,4-dihydrocinnoline-3-carboxylateHCID 86660005—
CatalystHCID 178418851HCID 178418851—
SolventTetrahydrofuranHCID 8028—
Productethyl 1-{[6-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl)methyl}-4-oxo-1,4-dihydrocinnoline-3-carboxylateHCID 86660008—

Reaction Steps

Ethyl 1-[(6-bromopyridin-3-yl)methyl]-4-oxo-1,4-dihydrocinnoline-3-carboxylate [(Example 83, Step 1), 748 mg, 1.93 mmol] and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (682 mg, 3.28 mmol, 1.7 equiv) were suspended in tetrahydrofuran (15 mL) and treated with an aqueous solution (1.5 mL) of cesium carbonate (1.26 g, 3.85 mmol, 2 equiv). The mixture was sparged under nitrogen, treated with bis(tri-tert-butylphosphine)palladium(0) (197 mg, 0.385 mmol, 0.2 equiv) and placed in an oil bath preheated to 80° C. for 1 hour. The mixture was cooled to ambient temperature, poured into sodium bicarbonate (75 mL, aqueous saturated) and extracted with ethyl acetate (2×100 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel gradient chromatography (100:0 to 0:100; hexanes:ethyl acetate), providing the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653079B2
Source datasetuspto-grants-2014_02
ORD IDord-2342a89225d248a7905aa8e04b7e012e
Source noteuspto-grants-2014_02