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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092761Generated: November 2, 2026

Potassium Fluoride → Methyl 4-cyano-2-(1-methyl-1H-pyrazol-4-yl)nicotinate

https://huagongshe.com/reaction/2092761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantMethyl 2-chloro-4-cyanonicotinateHCID 58317566—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 4-cyano-2-(1-methyl-1H-pyrazol-4-yl)nicotinateHCID 5831764552.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of methyl 2-chloro-4-cyanonicotinate (730 mg, 3.71 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (927 mg, 4.46 mmol), trans-dichlorobis(triphenylphosphine)palladium (261 mg, 0.371 mmol) and potassium fluoride (2697 mg, 14.85 mmol) in DME (15 mL) was stirred at 120° C. for 1 h under microwave irradiation. The mixture was filtered through Celite, and the filtrate was diluted with H2O and EtOAc. The organic phase was washed with H2O and brine, dried over MgSO4, and evaporated. The residue was purified by chromatography on SiO2 to give the title compound as a pale yellow solid (470 mg, 52.3%). 1H NMR (500 MHz, CDCl3) δ ppm 3.97 (s, 3H), 4.03 (s, 3H), 7.41 (d, J=4.88 Hz, 1H), 7.82 (s, 1H), 7.91 (s, 1H), 8.79 (d, J=4.88 Hz, 1H). [M+H] calc'd for C12H10N4O2, 243; found, 243.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440689B2
Source datasetuspto-grants-2013_05
ORD IDord-f8dd578797384079ae69b0c775e5d9bd
Source noteuspto-grants-2013_05