Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943740Generated: November 1, 2026

Tetrahydrofuran → HCID 66936733, compound

https://huagongshe.com/reaction/1943740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Indole-4-boronic acid, pinacol esterHCID 11322471—
Reactant7-bromo-1H,2H,3H-pyrido[2,3-b][1,4]oxazineHCID 66789061—
SolventWaterHCID 962—
ProductHCID 66936733HCID 66936733139.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 3 ml of tetrahydrofuran (THF)/0.5 ml of distilled water, 7-bromo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine (80.0 mg, 0.37 mmol), 4-(4,4,5,5,-tetramethyl-[1,3,2]dioxaborolane-2-yl)-1H-indole (109 mg, 0.45 mmol), potassium carbonate (103 mg, 0.74 mmol) and tetrakis triphenylphosphine palladium (172 mg, 0.15 mmol) were added and stirred at 80° C. for 4 hours. After completion of the reaction, the mixture was extracted with ethyl acetate, and the combined organic layer was dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on amine silica eluting with a solvent of dichloromethane:methanol=40:1. The fractions containing the product were collected and evaporated to obtain 7-(1H-indol-4-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine as white solid (130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394792B2
Source datasetuspto-grants-2013_03
ORD IDord-05a591a6f3ba4285915111af68f57a83
Source noteuspto-grants-2013_03