Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854587Generated: October 29, 2026

2-Bromopyridine → HCID 58626645, compound

https://huagongshe.com/reaction/854587

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 58626662HCID 58626662—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTolueneHCID 1140—
ProductHCID 58626645HCID 58626645—

Reaction Conditions

Temperature100 °C

Reaction Steps

3-[2-Methyl-4-(2-{5-methyl-2-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-oxazol-4-yl}-ethoxy)-phenyl]-propionic acid methyl ester (167 mg; 0.328 mmol) is dissolved in anhydrous toluene (1 mL), degassed, and filled with nitrogen three times. [1,1′-Bis-(diphenylphosphino)ferrocene]dichloropalladium(II) (15 mg, 0.02 mmol), 2-bromopyridine (67 ul, 0.7 mmol), and sodium carbonate (150 uL, 10 M aqueous, 1.5 mmol) are added, and the degassing procedure is repeated. The reaction is heated to 100° C. and monitored by HPLC. Upon complete consumption of starting material, the reaction is allowed to cool to room temperature and diluted with ethyl acetate. Celite is added and the mixture is filtered and rinsed with more ethyl acetate and water. The solution is further diluted with water and the two phases are separated. The organic layer is washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259175B2
Source datasetuspto-grants-2007_08
ORD IDord-617b46b34dc248e9b4b0e693782267ed
Source noteuspto-grants-2007_08