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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinamideHCID 936—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant3-Aminocarbonyl-2-chloro-6-methyl-4-(trifluoromethyl)pyridineHCID 19960052—
SolventWaterHCID 962—
Product3-Amino-2-chloro-6-methyl-4-(trifluoromethyl)pyridineHCID 19960079—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620974
Source datasetuspto-grants-1997_04
ORD IDord-d1e9210922024c1794abea3aecf6bd64
Source noteuspto-grants-1997_04