HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802481Generated: November 3, 2026
2-Methyl-3-butyn-2-ol → HCID 25226754, compound
https://huagongshe.com/reaction/1802481
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 59435999 | HCID 59435999 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 25226754 | HCID 25226754 | — |
Reaction Steps
A solution of 9-bromo-5-{[2,6-dichloro-4-(1H-pyrazol-5-yl)phenyl]amino}benzo[c]-2,6-naphthyridin-1(2H)-one (125 mg, 0.25 mmol) in DMF (3 mL) was degassed with nitrogen. Triethylamine (0.07 ml, 0.50 mmol), 2-methylbut-3-yn-2-ol (42.0 mg, 0.499 mmol), Pd(Ph3P)4 (28.8 mg, 0.025 mmol) and copper(I) iodide (9.50 mg, 0.050 mmol) were added and the reaction was heated to 75° C. for 16 h. After cooling to room temperature, the reaction was diluted with ethyl acetate and extracted with water. The organic layer was dried with sodium sulfate, filtered and concentrated under reduced pressure. The residue was dissolved in THF/MeOH, filtered and purified by reverse phase HPLC 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-ebe2f557d24947f88f0c2104b980e793 |
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| Source note | uspto-grants-2013_01 |
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