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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446737Generated: November 1, 2026

Potassium Phosphate, Tribasic → HCID 57863434, compound

https://huagongshe.com/reaction/1446737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant1-[4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-benzyl]-3-(3-trifluoromethyl-phenyl)-ureaHCID 68539157—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 57863434HCID 5786343456%

Reaction Conditions

Temperature40 °C

Reaction Steps

Load a 5 mL septum capped vial with the following: small magnetic stir bar, 1-[4-(7-chloro-imidazo[1,2-a]pyridin-3-yl)-benzyl]-3-(3-trifluoromethyl-phenyl)-urea (208 mg, 0.46 mmol), 6-methoxy-pyridin-3-yl boronic acid (0.51 mmols, 1.1 Eq), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (23.6 mg), Pd(OAc)2 (5 mg), K3PO4 (218 mg, 1.03 mmol), dioxane:H2O 2:1 (3 mL). Deoxygenate the reaction with N2 and heat to 40° C. for 24 hours. Cool the mixture and pour into a separatory funnel containing CH2Cl2 (45 mL) and H2O (2 mL). Extract the CH2Cl2 and evaporate under reduced pressure. Mix the residue with CH2Cl2 and a small amount of acetone. Filter the resulting solid and rinse with a small amount of CH2Cl2 and air dry. Vacuum oven dry the solid at 40° C. to give the title compound in 56% yield: MS(ES), m/z 518 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666879B2
Source datasetuspto-grants-2010_02
ORD IDord-e0fa3a5d91f84fd294873502d8f2062f
Source noteuspto-grants-2010_02