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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777446Generated: November 1, 2026

Potassium Carbonate → HCID 86680487, compound

https://huagongshe.com/reaction/1777446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(5-Acetylthiophen-2-yl)boronic acidHCID 4143377—
Reactant5-Bromo-1-methylpyridin-2(1H)-oneHCID 13024027—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86680487HCID 8668048762%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-1-methylpyridin-2(1H)-one (0.2 g, 1.06 mmol) in 1,4-dioxane (5 mL) and water (2 mL), (5-acetylthiophen-2-yl)boronic acid (0.2 g, 1.27 mmol), tetrabutyl ammonium bromide (0.034 g, 0.16 mmol), K2CO3 (0.4 mL, 3.19 mmol) and Pd(PPh3)2Cl2 (0.18 g, 1.59 mmol) were added under argon. The mixture was purged with argon for 10 min and heated to 100° C. for 1 h. The reaction mixture was filtered through Celite® reagent, the filtrate concentrated, the residue extracted with EtOAc (2×100 mL), and washed with water (100 mL). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to obtain crude product. The crude product was purified by Biotage IsoleraOne® column purifier (80% ethyl acetate in hexane) and obtained as yellow viscous liquid (0.15 g, 62% yield). 1H NMR (400 MHz, CDCl3): δ 7.69-7.58 (m, 3H), 7.08 (d, 1H), 6.65 (d, 1H), 3.61 (s, 3H), 2.54 (s, 3H); LC-MS m/z calculated for M+H+ 234.05. found 234.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266873B2
Source datasetuspto-grants-2016_02
ORD IDord-6c08ae5e4dda4043a8f5a001ab9a9d89
Source noteuspto-grants-2016_02