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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175132Generated: October 26, 2026

Sodium Carbonate → 2,3-difluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridine

https://huagongshe.com/reaction/2175132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant5-Bromo-2,3-difluoropyridineHCID 14549654—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product2,3-difluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridineHCID 5769136578.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-bromo-2,3-difluoropyridine (1.9 g, 9.79 mmol) and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (2.038 g, 9.79 mmol), Na2CO3 (2.076 g, 19.59 mmol) and Pd(PPh3)4 (1.131 g, 0.979 mmol) in DMF (8 ml) was bubbled with N2 for 10 min and was then heated to 80° C. for 10 h. After being cooled to rt, the mixture was filtered and the filtrate was diluted with EA, washed with water and brine, dried over anhydrous MgSO4. Filtered and concentrated. The residue was purified by silica gel chromatography eluted with Hex/EA (from 100% to 20%) to afford the title compound as a white solid (1.5 g, 57.4% yield). 1H-NMR (400 MHz, DMSO-d6) δ ppm 8.29 (d, 3H), 7.99 (d, 1H), 3.87 (s, 3H). LCMS (method B): [M+H]+=196, tR=1.91 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062045B2
Source datasetuspto-grants-2015_06
ORD IDord-46595d96c8624a0ba7db52cae7e5df53
Source noteuspto-grants-2015_06