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ChemicalBook--->CAS DataBase List--->380381-36-2

380381-36-2

380381-36-2 Structure

380381-36-2 Structure
IdentificationBack Directory
[Name]

2-DiMethylaMino-5-iodopyridine
[CAS]

380381-36-2
[Synonyms]

2-DiMethylaMino-5-iodopyridine
5-Iodo-N,N-diMethylpyridin-2-aMine
(5-Iodo-pyridin-2-yl)-dimethyl-amine
2-Pyridinamine, 5-iodo-N,N-dimethyl-
[Molecular Formula]

C7H9IN2
[MOL File]

380381-36-2.mol
[Molecular Weight]

248.06
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[Appearance]

White to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

2-DiMethylaMino-5-iodopyridine(380381-36-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

(5-Iodo-pyridin-2-yl)-methyl-amine

280116-78-1

Iodomethane

74-88-4

2-DiMethylaMino-5-iodopyridine

380381-36-2

2-(N-monomethylamino)-5-iodopyridine (99, 1.00 g, 4.27 mmol), potassium carbonate (2.95 g, 21.36 mmol) and iodomethane (145 mg, 8.546 mmol) were dissolved in dimethylacetamide (30 mL). The reaction mixture was heated at 90°C for 24 hours. Upon completion of the reaction, the reaction was terminated by the addition of water. The organic phase was extracted with ethyl acetate, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography to afford 2-(N,N-dimethylamino)-5-iodopyridine (100, 603 mg, 57%).1H NMR (400 MHz, CDCl3) δ 3.08 (s, 6H), 6.34 (d, J = 8.4 Hz, 1H), 7.60 (dd, J = 8.8, 2.4 Hz, 1H), 8.27 (d, J = 2.4 Hz, 1H); 13C NMR (100 MHz, CDCl3) δ 38.1, 105.9, 107.1, 139.2, 148.3, 157.7.

[References]

[1] Patent: US2010/261727, 2010, A1. Location in patent: Page/Page column 23-24
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