HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446737Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 57863434, compound
https://huagongshe.com/reaction/1446737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | (6-Methoxypyridin-3-yl)boronic acid | HCID 2734368 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | 1-[4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-benzyl]-3-(3-trifluoromethyl-phenyl)-urea | HCID 68539157 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | HCID 57863434 | HCID 57863434 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666879B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-e0fa3a5d91f84fd294873502d8f2062f |
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| Source note | uspto-grants-2010_02 |
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