HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203259Generated: October 30, 2026
Potassium Carbonate → HCID 73438318, compound
https://huagongshe.com/reaction/2203259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86714231 | HCID 86714231 | — |
| Reactant | HCID 90077584 | HCID 90077584 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 73438318 | HCID 73438318 | 41.8% |
Reaction Steps
9-chloro-1-(3-(trifluoromethyl)phenyl)pyrimidino[5,4-c][1,5]naphthyridine-2,4(1H,3H)-dione (300 mg, 0.77 mmol), (2-methoxypyrimidin-5-yl)boric acid (119 mg, 0.77 mmol), potassium carbonate (317 mg, 2.3 mmol) and tetrakis(triphenylphosphine)palladium(45 mg, 0.04 mmol) were added to 40 mL dioxane and 2 mL water. The resulting mixture was reacted under reflux in the nitrogen protection for 18 hrs, cooled to room temperature, filtered with Celite, and concentrated. 40 mL water was added. The resulting mixture was filtered to obtain a crude product, which was successively washed with ethyl acetate (30 mL) and methanol (10 mL) to produce 9-(2-methoxypyrimidin-5-yl)-1-(3-(trifluoromethyl)phenyl)pyrimidino[5,4-c][1,5]naphthyridine-2,4(1H,3H)-dione (150 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365572B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-168a50220b004c69be8e6031246bfdee |
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| Source note | uspto-grants-2016_06 |
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