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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696271Generated: October 30, 2026

Pyrazole → Methyl 1-cyclopentyl-6-oxo-5-(1H-pyrazol-1-yl)-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1696271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-bromo-1-cyclopentyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 15946267—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductMethyl 1-cyclopentyl-6-oxo-5-(1H-pyrazol-1-yl)-1,6-dihydropyridine-3-carboxylateHCID 66845814—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 5-bromo-1-cyclopentyl-6-oxo-1,6-dihydropyridine-3-carboxylate (300 mg, 1.00 mmol), pyrazole (23 mg, 0.34 mmol), K2CO3 (99 mg, 0.72 mmol), CuI (9.1 mg, 0.048 mmol), N1—N2-dimethylethane-1,2-diamine (5 uL, 0.048 mmol) in toluene (3 mL) was heated to 100° C. for 17 h. The mixture was brought to RT and quenched with saturated NH4Cl, brine, dried over MgSO4 and chromatographed on silica gel using 3:1 hexanes:ethylacetate to afford the title compound as a white solid. MS m/z: 288 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163766B2
Source datasetuspto-grants-2012_04
ORD IDord-56e05bbe622245f98387b43e6a95e409
Source noteuspto-grants-2012_04