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175461-33-3

175461-33-3 Structure

175461-33-3 Structure
IdentificationBack Directory
[Name]

2,6-dichloro-N-Methylpyridin-4-aMine
[CAS]

175461-33-3
[Synonyms]

2,6-dichloro-4-methylamino-pyridine
2,6-dichloro-N-Methylpyridin-4-aMine
2,6-dichloro-N-methyl-4-Pyridinamine
4-Pyridinamine, 2,6-dichloro-N-methyl-
[Molecular Formula]

C6H6Cl2N2
[MDL Number]

MFCD12024871
[MOL File]

175461-33-3.mol
[Molecular Weight]

177.03
Chemical PropertiesBack Directory
[Melting point ]

70 °C
[Boiling point ]

312.0±37.0 °C(Predicted)
[density ]

1.404±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

0.79±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-dichloro-N-Methylpyridin-4-aMine(175461-33-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4,6-Trichloropyridine

16063-69-7

Methylamine

74-89-5

2,6-dichloro-N-Methylpyridin-4-aMine

175461-33-3

GENERAL STEPS: 2,4,6-Trichloropyridine (20.0 g, 109.63 mmol) was dissolved in anhydrous ethanol (100 mL). An ethanol solution of 33% methylamine (81.9 mL, 657 mmol) was added slowly and dropwise at room temperature. The reaction mixture was stirred continuously at room temperature for 2 weeks. After completion of the reaction, the white precipitate was collected by filtration and washed with methyl tert-butyl ether and deionized water sequentially to afford 2,6-dichloro-4-methylaminopyridine (11.9 g, 61% yield) as white crystals.

[References]

[1] Patent: WO2008/92942, 2008, A2. Location in patent: Page/Page column 22
[2] Patent: WO2006/53166, 2006, A1. Location in patent: Page/Page column 57-58
[3] New Journal of Chemistry, 2016, vol. 40, # 11, p. 9194 - 9204
[4] Patent: WO2006/122137, 2006, A1. Location in patent: Page/Page column 71-72
[5] Patent: US2015/57260, 2015, A1. Location in patent: Paragraph 0300; 0331; 0551; 0552
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