HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230953Generated: October 31, 2026
Potassium Phosphate, Tribasic → HCID 57761903, compound
https://huagongshe.com/reaction/230953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | [3-(3-Methoxy-3-oxopropyl)phenyl]boronic acid | HCID 4993880 | — |
| Reactant | HCID 57429019 | HCID 57429019 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57761903 | HCID 57761903 | — |
Reaction Steps
Purge a solution of 4-{4-chloro-6-[4-(3-trifluoromethyl-pyridin-2-yl)-piperazin-1-yl]-pyrimidin-2-yl}-morpholine (142 mg, 0.33 mmol), (3-(2-methoxycarbonylethyl)phenyl)boronic acid (Combi-Blocks, Inc., San Diego, Calif.; 104 mg, 0.5 mmol) and K3PO4 (2M, 331 μL) in dioxane with nitrogen for 10 minutes. Add Pd(PPh3)4 (19 mg, 0.017 mmol) and purge for an additional 5 minutes. Seal the contents in a reaction vial and heat at 80° C. for 16 hours. Partition the mixture between EtOAc and water, dry (Na2SO4) the organic layer and concentrate under reduced pressure. Filter the residue through a small pad of silica gel eluting with 50% EtOAc/hexanes. Concentrate under reduced pressure to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566712B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-85b1345fb92f4877b3a6ef0defd86eef |
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| Source note | uspto-grants-2009_07 |
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