HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255918Generated: October 27, 2026
Methylamine → 4-Chloro-6-methyl-2-methylaminopyridine
https://huagongshe.com/reaction/2255918
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2,4-Dichloro-6-methylpyridine | HCID 11959083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Chloro-6-methyl-2-methylaminopyridine | HCID 53883826 | 12% |
Reaction Steps
A mixture of 2,4-dichloro-6-methylpyridine (7.0 g) (West German Patent DE 2162238) and 33% w/v methylamine in ethanol (25 ml) was heated in a sealed tube at 100° C. for 8 hours. The solvent was removed by evaporation and the residual solid was purified by flash chromatography (Merck 9385 Silica, 100 g), using as eluant first an increasing gradient [20%-100% v/v] of diethyl ether in petrol (b.p. 60°-80° C.) and then an increasing gradient of up to 5% v/v methanol in dichloromethane. There was thus obtained 4-chloro-6-methyl-2-methylaminopyridine (0.8 g, 12% yield), m.p. 69°-70° C.; NMR: 2.2-2.3(3H,s, CH3), 2.7-2.8(3H,s,NHCH3), 6.25(1H,s, pyridine-3H), 6.4(1H,s, pyridine-5H), 6.55-6.7(1H,br,NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654298 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-27ab5f7bdb2745faa382f3784163ba52 |
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| Source note | uspto-grants-1997_08 |
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