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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446735Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 57863432, compound

https://huagongshe.com/reaction/1446735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantHCID 68543228HCID 68543228—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 57863432HCID 5786343222.5%

Reaction Steps

Load in a 5 mL septum capped vial the following: small magnetic stir bar, 1-[4-(7-chloro-imidazo[1,2-a]pyridin-3-yl)-phenyl]-3-(3-trifluoromethyl-phenyl)-urea (250 mg, 0.58 mmol), 4-pyridyl boronic acid (77.4 mg, 0.63 mmols, 1.1 Eq), S-phos (236 mg), Pd(OAc)2 (60 mg), K3PO4 (237 mg, 1.12 mmol), 1,4-dioxane: H2O 2:1. Heat the reaction to 50° C. for 24 hours, cool and purify with a Varian SCX® (10 g) column that is pre-washed with water and methanol, and elute the product with 2 N NH3 in methanol. Evaporate the product containing fractions under reduced pressure and take up into CH2Cl2 and chromatograph using SiO2 eluting with a gradient of 0% to 10% of 2 M NH3 in MeOH with the balance CH2Cl2. Evaporate the fractions containing the product under reduced pressure, then vacuum oven dry at 40° C. to give the title compound as a yellow solid 61.8 mg (22.5%). MS (ES), m/z 474 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666879B2
Source datasetuspto-grants-2010_02
ORD IDord-01a92994e35b4af5b082468b5d464a20
Source noteuspto-grants-2010_02