HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53514Generated: October 26, 2026
Nicotinamide → 3-Amino-2-chloro-6-methyl-4-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/53514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nicotinamide | HCID 936 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Aminocarbonyl-2-chloro-6-methyl-4-(trifluoromethyl)pyridine | HCID 19960052 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Amino-2-chloro-6-methyl-4-(trifluoromethyl)pyridine | HCID 19960079 | — |
Reaction Steps
To a solution of 6.6 g of sodium hydroxide in 60 ml of water at 5° C. was added 9.3 g of bromine. When a clear solution was obtained, 9.2 g of 3-aminocarbonyl-2-chloro-6-methyl-4-(trifluoromethyl)pyridine was added quickly, maintaining the temperature below 5° C. The resulting mixture was stirred until the 3-(aminocarbonyl)pyridine dissolved (~30 min). The cooling bath was removed and the mixture was then warmed to 75° C. for 30 min. After cooling to room temperature, the 3-aminopyridine product was extracted with ethyl acetate, dried (magnesium sulfate), filtered, and evaporated to give 4.9 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05620974 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-d1e9210922024c1794abea3aecf6bd64 |
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| Source note | uspto-grants-1997_04 |
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