HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533669Generated: October 26, 2026
Methylamine → N2-Methyl-6-(trifluoromethyl)pyridine-2,3-diamine
https://huagongshe.com/reaction/533669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | 2-Chloro-5-(trifluoromethyl)pyridin-3-amine | HCID 12919757 | — |
| Catalyst | acetylacetone copper(II) | HCID 21863952 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N2-Methyl-6-(trifluoromethyl)pyridine-2,3-diamine | HCID 68091056 | — |
Reaction Steps
To a pressure-resistant reaction container, 3-amino-2-chloro-5-trifluoromethylpyridine (5 g), copper (II) acetylacetone (1.31 g), acetylacetone (2.50 g), cesium carbonate (16.25 g), NMP (20 ml), and 40% of aqueous methylamine solution (15 ml) were added, and stirred at 100° C. for 3 hours, at 120° C. for 3 hours, then at 140° C. for 5 hours. After the mixture was allowed to cool to room temperature, saturated aqueous ammonium chloride solution was poured thereinto, and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to give 2.09 g of N2-methyl-6-trifluoromethylpyridin-2,3-diamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853238B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-d7e1ebc75d4a46fdbe5056a3cfaeaf67 |
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| Source note | uspto-grants-2014_10 |
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