HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092289Generated: October 31, 2026
Methylamine → 6-bromo-N-methylpyridin-2-amine
https://huagongshe.com/reaction/1092289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-bromo-N-methylpyridin-2-amine | HCID 13470315 | — |
Reaction Steps
30 g (0.13 mol) of 2,6-dibromopyridine are added to a solution of 225 ml (2.39 mol) of methylamine in ethanol (33% by weight, Aldrich) precooled to 0° C. The reaction is heated at 80° C. with stirring for 20 hours, in a glass system equipped with a manometer. The reaction is monitored by TLC control. The reaction medium is cooled to 0° C. and the assembly is opened. The slightly brown solution thus obtained is concentrated under vacuum to a volume of 60 ml, and water (240 ml) is then added, followed by addition of aqueous sodium carbonate solution (2N, 240 ml). The beige-coloured precipitate formed is filtered off, washed with water and dissolved in dichloromethane (200 ml). The solution is dried over magnesium sulfate and the solvent is evaporated off. The addition of heptane allows the precipitation of 17.5 g (74%) of 6-methylamino-2-bromopyridine in the form of a beige-coloured powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129416B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-59ed87edd533465c98251b19568dd3d9 |
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| Source note | uspto-grants-2012_03 |
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