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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552485Generated: October 30, 2026

Sodium Carbonate → 4-(3-Fluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide

https://huagongshe.com/reaction/552485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantHCID 25208982HCID 25208982—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4-(3-Fluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amideHCID 2520941471%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of 150 mg (0.48 mmol) of 4-Bromo-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide, 71 mg (0.5 mmol, 1.05 equiv.) of 3-Fluorophenyl-boronic acid in 2 ml of dioxane were added 0.5 ml of 2M sodium carbonate solution and the mixture was purged with Argon for 10 min. Then 25 mg (0.096 mmol, 0.2 equiv.) of Triphenylphosphine and 10.8 mg (0.048 mmol, 0.1 equiv.) of Palladium acetate were added and the mixture was stirred under Argon atmosphere for 24 h at 90° C. The reaction was allowed to cool to r.t., taken up in two times in ethyl acetate and evaporated to dryness. The residue was separated by flash chromatography on silicagel (heptane/ethyl acetate 4:1) to yield the title compound (111 mg, 71%) as a yellow solid, MS (ISP): m/e=328.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951824B2
Source datasetuspto-grants-2011_05
ORD IDord-7b4b6f8c219549e3baa96fd0b71e4735
Source noteuspto-grants-2011_05