Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201566Generated: October 29, 2026

Potassium Phosphate, Tribasic → HCID 87056128, compound

https://huagongshe.com/reaction/2201566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamideHCID 68239402—
ReactantHCID 117771590HCID 117771590—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductHCID 87056128HCID 8705612810%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a degassed mixture of 6-bromo-3-(2-fluorophenyl)pyrido[2,3-d]pyrimidin-4(3H)-one (100 mg, 0.313 mmol), and 2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide (100 mg, 0.199 mmol) in N, N-dimethyl-formamide (5 mL) were added Pd(dppf)Cl2 (15 mg) and K3PO4 (135 mg, 0.637 mmol) under N2. The mixture was heated to 80° C. overnight. The reaction mixture was cooled to RT and filtered. The filtrate was concentrated, and the residue was purified by prep-HPLC to give 2-(4-fluorophenyl)-5-(3-(2-fluorophenyl)-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-6-yl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide (11.78 mg, yield: 10%). 1H-NMR (CDCl3, 400 MHz) δ 9.12 (d, J=2.0 Hz, 1H), 8.77 (d, J=2.0 Hz, 1H), 8.33 (s, 1H), 7.94 (t, J=6.8 Hz, 3H), 7.68 (s, 1H), 7.54˜7.59 (m, 1H), 7.47 (t, J=6.8 Hz, 1H), 7.33˜7.39 (m, 2H), 7.21 (t, J=8.4 Hz, 2H), 6.04 (d, J=4.4 Hz, 1H), 3.27 (s, 3H), 3.01 (d, J=4.8 Hz, 3H), 2.83 (s, 3H). MS (M+H)+: 616.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-77bc2050eedb497e9be20e3e56815862
Source noteuspto-grants-2016_06