A kind of 2-(1-dimethylamino-2-cyanoethyl) pyrrole derivative and its synthesis method
A technology of pyrrole derivatives and synthesis methods, applied in the direction of organic chemistry and the like, can solve the problems of complex preparation, high price, environmental pollution and the like, and achieve the effects of high yield, simple operation and high efficiency
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Embodiment 1
[0030]
[0031] In a 10mL reaction flask, add N-methylpyrrole 2a (R 1 =CH 3 ; 2 =H) (41 mg, 0.5 mmol), 3-dimethylaminoacrylonitrile 3 (96 mg, 1.0 mmol), p-toluenesulfonic acid monohydrate (190 mg, 1.0 mmol) and 2 mL of solvent dichloromethane at 28 °C The reaction was stirred for 6h. After the reaction is completed, the reaction solution is poured into a separatory funnel, and 10 mL of saturated aqueous sodium bicarbonate solution is added thereto, shaken, left to stand, and the oil-water phase is separated, and the water phase is extracted with dichloromethane (2 × 5 mL), and the organic Mutually. The organic phases were combined, dried over anhydrous sodium sulfate, and filtered. The volatile components were removed, and then separated by silica gel column chromatography (the eluent was dichloromethane / ethyl acetate, v / v=50:1) to obtain the target product (1a) (75mg, yield 85% ). The target product was confirmed by NMR and high-resolution mass spectrometry.
[0032...
Embodiment 2
[0035] The reaction steps and operations are the same as those in Example 1, except that the reaction time is 1 h. The reaction was stopped, and the target product 1a (41 mg, yield 46%) was obtained after post-treatment.
Embodiment 3
[0037] The reaction steps and operations are the same as those in Example 1, except that the reaction time in the reaction is 24 hours. The reaction was stopped, and the target product 1a (74 mg, yield 84%) was obtained after post-treatment.
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