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 an aqueous methylamine solution (40%) 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 methyl tert-butyl ether (hereinafter, referred to as MTBE). The combined 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 | US09156838B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-74986d6f50054eff9f88e4f3020022d5 |
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| Source note | uspto-grants-2015_10 |
|---|