Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium pentafluoropropionate | HCID 2733305 | — |
| Reactant | 2-Chloro-5-iodopyridine | HCID 4397176 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86708231 | HCID 86708231 | — |
Reaction Steps
28 g of sodium pentafluoropropionate and 14 g of copper iodide were added to a mixture of 7.2 g of 2-chloro-5-iodopyridine, 75 mL of NMP and 75 mL of xylene under room temperature, and the mixture was heated to 150° C. and heated and stirred for 5.5 hours. After cooling the mixture to 80° C., 180 mL of a 40% aqueous methylamine solution was added in 4 parts every 2 hours, and the mixture was heated and stirred for 8.5 hours. After the reaction, the mixture was ice-cooled to 0° C., a 28% aqueous ammonia solution and a saturated aqueous sodium bicarbonate solution were added, and the mixture was extracted with MTBE. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was applied to a silica gel column chromatography to obtain 4.6 g of methyl-(5-pentafluoroethyl-pyridin-2-yl)-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09392791B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-521aa56110924bca9f89cd62e5626127 |
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| Source note | uspto-grants-2016_07 |
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