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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473206Generated: October 31, 2026

Potassium Phosphate, Tribasic → 2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)-N-(oxetan-3-yl)quinazoline-8-carboxamide

https://huagongshe.com/reaction/473206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant3-OxetanamineHCID 9833923—
Reactant8-Bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazolineHCID 66609469—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)-N-(oxetan-3-yl)quinazoline-8-carboxamideHCID 66610325266.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a mixture of 8-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline from Example 35 step B (200 mg, 0.5 mmol), palladium acetate (6 mg, 0.025 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (29 mg, 0.05 mmol), oxetan-3-amine (55 mg, 0.75 mmol) and K3PO4 (320 mg, 1.5 mmol) was added toluene (2 mL). The vial was evacuated and flushed with carbon monoxide (2×) and the mixture was heated at 110° C. overnight under an atmosphere of carbon monoxide. The mixture was diluted with DCM/MeOH and concentrated under reduced pressure onto Celite. The residue was purified by silica gel chromatography eluting with 10-100% EtOAc/hexanes to afford 2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)-N-(oxetan-3-yl)quinazoline-8-carboxamide (56 mg, 26%). LC-MS (ESI) m/z 421 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633207B2
Source datasetuspto-grants-2014_01
ORD IDord-28eb8dc552b449a88083d3772cb8802a
Source noteuspto-grants-2014_01