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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794998Generated: November 3, 2026

Toluene → HCID 11294580, compound

https://huagongshe.com/reaction/1794998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Iodo-6-[3,5-bis(trifluoromethyl)benzyl]-6,7,8,9-tetrahydro-5H-10-oxa-1,6-diazabenzocyclooctene-5-oneHCID 11478095—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11294580HCID 1129458080.5%

Reaction Steps

Phenylboronic acid (417 mg), tetrakis(triphenylphosphine)palladium (132 mg), toluene (10 mL), 1,4-dioxane (5 mL), and a 2 mol/L aqueous solution of sodium carbonate (10 mL) were added to 5-[3,5-bis(trifluoromethyl)benzyl]-7-iodo6-oxo-2,3,4,5-tetrahydro-6H-pyrido[2,3-b][1,5]oxazocine (compound of Reference Example 3; 1.00 g). While heated, the mixture was stirred for 7 hours under a stream of argon gas. The reaction mixture was diluted with ethyl acetate, and the diluted mixture was washed with a 2 mol/L aqueous solution of sodium carbonate, and was then dried on anhydrous sodium sulfate. The solvent was removed by distillation to obtain a residue, and then the residue was recrystallized from isopropanol to obtain 5-[3,5-bis(trifluoromethyl)benzyl]-6-oxo-7-phenyl-2,3,4,5-tetrahydro-6H-pyrido[2,3-b][1,5]oxazocine (729 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026309B2
Source datasetuspto-grants-2006_04
ORD IDord-1f9ab8b83f6b438a8d98cb69959cc5e1
Source noteuspto-grants-2006_04