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2-(Dimethylamino)-6-(trifluoromethyl)nicotinonitrile synthesis

3synthesis methods
386704-06-9 Synthesis
2-CHLORO-6-(TRIFLUOROMETHYL)NICOTINONITRILE

386704-06-9
127 suppliers
$11.00/250mg

2-(Dimethylamino)-6-(trifluoromethyl)nicotinonitrile

935518-01-7
4 suppliers
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Yield:935518-01-7 100%

Reaction Conditions:

at 150; for 48 h;

Steps:

14.i; 69

To 2-chloro-6-(trifluoromethyl)nicotinonitrile (0.8g, 3.8 mmol) was added hexamethylphosphoramide (6 mol eq, 4.16 mL) and the mixture was heated at 150°C for 48h. The reaction mixture was cooled at room temperature, water and brine were added and the mixture was extracted with EtOAc (4x35 mL). The recombined organic phases were dried over sodium sulfate and evaporated to dryness to obtain 28d as yellow oil (l .Olg, quantitative yield). 1HNM (DMSO, 200 MHz) δ 1.33 (s, 3H), 1.38 (s, 3H), 7.41 (d, 1H, J=6), 7.55 (d, 1H, J=6).

References:

WO2011/120604,2011,A1 Location in patent:Page/Page column 104; 137