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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509310Generated: October 31, 2026

Sodium Carbonate → tert-butyl 4-(2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)benzylcarbamate

https://huagongshe.com/reaction/1509310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(tert-Butoxycarbonylaminomethyl)phenylboronic acid, pinacol esterHCID 3415442—
Reactant6-bromo-7-phenyl-1H-pyrido[2,3-b][1,4]oxazin-2(3H)-oneHCID 86683650—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventSodium BicarbonateHCID 516892—
Producttert-butyl 4-(2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)benzylcarbamateHCID 6725558778.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a reaction tube was added 6-bromo-7-phenyl-1H-pyrido[2,3-b][1,4]oxazin-2(3H)-one (0.19 g, 0.623 mmol) and tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzylcarbamate (0.25 g, 0.750 mmol) in 1,4-Dioxane (10 ml), followed by a solution of sodium carbonate (0.198 g, 1.868 mmol) in water (2.5 ml) to give a suspension. This was degassed followed by the addition of PdCl2(dppf)-CH2Cl2 adduct (0.051 g, 0.062 mmol). The resulting mixture was heated at 80° C. for 20 h. The reaction mixture was cooled down to room temperature and diluted with saturated sodium bicarbonate solution (30 ml) and extracted with ethyl acetate (20 mlX3). The combined organic phase was washed with water, brine and concentrated to give product (0.21 g) used for next step without further purification. LCMS (Method D): RT=1.25 min, M+H+=433.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-c62d6b3890a34cb1adc4aeb9c3d838ad
Source noteuspto-grants-2015_12