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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970385Generated: October 29, 2026

Potassium Bicarbonate → 7-Chloro-6-((E)-styryl)-4H-pyrido[3,2-b][1,4]oxazin-3-one

https://huagongshe.com/reaction/970385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BicarbonateHCID 516893—
ReactantStyrylboronic acidHCID 5702628—
Reactant6-Bromo-7-chloro-4H-pyrido[3,2-b][1,4]oxazin-3-oneHCID 85853694—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product7-Chloro-6-((E)-styryl)-4H-pyrido[3,2-b][1,4]oxazin-3-oneHCID 6856386768.3%

Reaction Steps

6-Bromo-7-chloro-4H-pyrido[3,2-b][1,4]oxazin-3-one (15a) (22 g, 83.7 mmole) and trans-2-phenylvinylboronic acid (17.33 g, 117 mmole) were dissolved in 1,4-dioxane (300 mL) and the solution was degassed with argon. (Ph3P)4Pd (1.9 g, 2 mole %) was added, followed by a solution of potassium hydrogen carbonate (21 g, 210 mmole) in H2O (100 mL). The reaction was heated at reflux under argon overnight, then was cooled to room temperature and diluted with ethyl acetate (1 L). The solution was washed sequentially with H2O and brine, dried (Na2SO4), and concentrated in vacuo. The residue was slurried with chloroform (120 mL), then diluted with diethyl ether (100 mL). The precipitated product was collected by filtration and washed with ether to provide the product (16.4 g, 68%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312212B2
Source datasetuspto-grants-2007_12
ORD IDord-5963729bff3d42fab5be1c4f08b003a4
Source noteuspto-grants-2007_12