Discovery of 2-Cyanoacetamide

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference of 107-91-5, A common heterocyclic compound, 107-91-5, name is 2-Cyanoacetamide, molecular formula is C3H4N2O, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

General procedure: A substituted alkyl methyl ketone or cyclic ketone (1 equiv) and ethyl formate or ethyl acetic(1 equiv) was added dropwise to absolute ether solution of sodium metal (1 equiv) for 1 h whilemaintained below 20 C. After the addition, the reaction was allowed to stir in an ice bath untilthe sodium metal had disappeared. The precipitate was filtered, washed with absolute ether anddried to give the corresponding compound which was directly used for the next step without further purification. To a solution of previous product (1 equiv), and cyanoacetamide (1.05 equiv) in water was stirred6 min at room temperature. The mixture was added dropwise piperidine acetate solution (0.3 equiv),which was prepared from piperidine (1 equiv), acetic acid (1 equiv) and water (5 equiv). The solutionwas heated to reflux for 2 h. Then, the reactor was cooled to room temperature, and adjusted to pH 4 by 4 N hydrochloric acid. The resulting solid was filtered, respectively washed with water and ether,and dried to give the corresponding compound which was purified by recrystallizing using menthol as solvent. 4,6-Dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (1a): 58% yield, white solid, m.p. 264-266 C(lit. [24] 294 C), 1H-NMR (DMSO-d6, 600 MHz): delta 12.31 (br, 1H), 6.16 (s, 1H), 2.30 (s, 3H), 2.22 (s, 3H).

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Brief introduction of 107-91-5

According to the analysis of related databases, 107-91-5, the application of this compound in the production field has become more and more popular.

Reference of 107-91-5, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 107-91-5 as follows.

Add 13.8 g (0.1 mol) to a 250 mL three-necked bottlePotassium carbonate, dissolved in 100 mL of water, added 11.0 g (0.1 mol)Acetylacetone, 8.4 g (0.1 mol) of cyanoacetamide was added in portions at room temperature.During the feeding process, the temperature slowly rises by about 10 C.A large amount of solid precipitated out as the reaction proceeded. After 24 h, the reaction was stopped by TLC (MeOH: DCM = 1: 20) and filtered.The filter cake was washed three times with water.Dry to give 14 g of a white solid.The solid was recrystallized from 1 L of methanol.13.0 g of a white needle-like solid was obtained in a yield of 87.8%.

According to the analysis of related databases, 107-91-5, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Shenyang Pharmaceutical University; Chen Guoliang; Wang Lihui; Zhou Qifan; Du Fangyu; Dong Xiaoyu; Yang Jingyu; Wu Chunfu; (48 pag.)CN109320499; (2019); A;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Introduction of a new synthetic route about 107-91-5

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2-Cyanoacetamide, and friends who are interested can also refer to it.

Reference of 107-91-5, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 107-91-5 name is 2-Cyanoacetamide, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

Pentadione (10 g, 0.1 mol), cyanoacetamide (8.4 g, 0.1 mol) and sodium hydroxide (4 g, 0.1 mol) were added to anhydrous ethanol and stirred overnight at room temperature. The reaction was monitored by TLC and the reaction was stopped. The precipitated solid material was filtered off with suction, washed with a little water, ethanol and diethyl ether and dried to give 4,6-dimethyl-3-cyanopyridone, 142 g, 95.8%.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2-Cyanoacetamide, and friends who are interested can also refer to it.

Reference:
Patent; Sichuan University; Puluo Pharmaceutical Co., Ltd.; Yu Luoting; Wei Yuquan; (24 pag.)CN107573327; (2018); A;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts