HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215050Generated: October 30, 2026
Potassium Carbonate → HCID 10159980, compound
https://huagongshe.com/reaction/2215050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | HCID 10269984 | HCID 10269984 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 10159980 | HCID 10159980 | 63% |
Reaction Steps
An 8-mL amber vial was charged with 2-anilino-5-chloro-7-methyl-1-phenyl-1,6-naphthyridin-4(1H)-one (72 mg, 0.20 mmol), 4-methoxyphenylboronic acid (36 mg, 0.24 mmol), Pd(OAc)2 (1 mg, 0.02 mmol), Ph3P (5 mg, 0.02 mmol), K2CO3 (110 mg, 0.8 mmol, 2 M), and DME (2 mL). The mixture was heated to 90° C. 2 d. Water was added to the reaction mixture and it was extracted with CH2Cl2. The organic layer was dried over Na2SO4. The residue after concentration in vacuo was triturated with Et2O to provide 2-anilino-5-(4-methoxyphenyl)-7-methyl-1-phenyl-1,6-naphthyridin-4(1H)-one (54 mg, 63%): LCMS RT: 1.92 min, MH+: 434.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109196B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-d0e967c8044645f8a0debee6afa0ad5d |
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| Source note | uspto-grants-2006_09 |
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