Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 86675960 | HCID 86675960 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71743116 | HCID 71743116 | — |
Reaction Steps
In a microwaveable vessel, 1.03 g of N-(2,6-dichloropyridin-3-yl)-4-methoxy-3,5-dimethylbenzamide were dissolved in 15 ml of dry tetrahydrofuran, and 30 mg of copper(I) iodide, 57 mg of 1,10-phenanthroline and 1.54 g of cesium carbonate were added. In a microwave sunthesizer, the reaction mixture was then heated at 140° C. for 2 h. For work-up, the mixture was added to 10 ml of a 0.5 M aqueous hydrochloric acid solution. The mixture was extracted twice with ethyl acetate. The collected organic phases were combined and the solvent was removed under reduced pressure. This gave 0.88 g (98%) of the product, which was reacted further without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580816B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-d026dacb5f244ee68a2ac913d357a14e |
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| Source note | uspto-grants-2013_11 |
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