HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802513Generated: October 29, 2026
Potassium Carbonate → HCID 59436060, compound
https://huagongshe.com/reaction/1802513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | HCID 21928082 | HCID 21928082 | — |
| Reactant | HCID 59435985 | HCID 59435985 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59436060 | HCID 59436060 | — |
Reaction Steps
To a solution of 9-bromo-5((2,6-dichloro-4-fluorophenyl){[2-(trimethylsilyl)ethoxy]methyl}amino)-2-{[2-(trimethylsilyl)ethoxy]methyl}benzo[c]-2,6-naphthyridin-1(2H)-one (Example 172, Step 1) (50 mg, 0.07 mmol) and 2-amino-1-pyrazin-2-ylethanol (14.6 mg, 0.11 mmol) in DMSO (1 ml) was added L-proline (2 mg, 0.014 mmol), potassium carbonate (29.7 mg, 0.14 mmol) and CuI (1.3 mg, 7.01 μmol). The solution was heated to 100° C. in a sealed tube for 16 h. After cooling to room temperature, the reaction was diluted with ethyl acetate and washed with water. The organic layer was dried with sodium sulfate, filtered and concentrated under reduced pressure to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349865B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8ceb9d0bc27740d9b7eec5c200975991 |
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| Source note | uspto-grants-2013_01 |
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