Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

Ethenamine, N,N-dimethyl-2-(3-nitro-2-pyridinyl)- synthesis

4synthesis methods
-

Yield:65156-92-5 73%

Reaction Conditions:

in N,N-dimethyl-formamide at 90; for 4 h;Inert atmosphere;

Steps:

E.c (c)

(c)
(E)-N,N-Dimethyl-2-(3-nitropyridin-2-yl)ethenamine
A modified procedure of Cash et al. (Org. Biomol. Chem. 2005, 3. 3701-3706) was used. 2-Methyl-3-nitropyridine (0.7 g, 5.1 mmol) was dissolved in 15 ml dry DMF and stirred under nitrogen.
Dimethylformamiddimethylacetal (DMF-DMA) (1.35ml, 1.22g, 10.2 mmol) was added dropwise.
The reaction was heated to 90°C for 4 h.
After approximately 15 min a deep redish color appeared.
After evaporating the solvent (E)-N,N-Dimethyl-2-(3-nitropyridin-2-yl)ethenamine is obtained as a red oil (0.16 g, 0.8 mmol, 73%) which can be used without further purification. 1H NMR (300 MHz, CDCl3) 8.40 (pdd; 3J = 1.7 Hz; 3J = 4.4 Hz; 1H; H-6); 8.16 (pdd; 3J = 1.7 Hz; 3J = 8.3 Hz; 1H; H-4) ; 8.04 (d; 3JAX = 12.5 Hz; 1H; H-8) ; 6.76 (pdd; 3J = 4.4 Hz; 3J = 8.3 Hz; 1H; H-5); 6.15 (d; 3JAX = 12.5 Hz; 1H; H-7); 3.01 (s; 6H; CH3).

References:

EP2512469,2016,B1 Location in patent:Paragraph 0075; 0076