Category: 26364-65-8

Name is 2-Cyanoimino-1,3-thiazolidine, as a common heterocyclic compound, it belongs to thiazolidine compound, and cas is 26364-65-8, its synthesis route is as follows.,26364-65-8

General procedure: Thiazolidin-2-ylidene-cyanamide (0.317 g, 2.50 mmol) inacetonitrile (20 mL) was dropwise added to a stirred solutionof substituted benzyl bromide (2.5 mmol) and 14 mL NaOHaqueous solution (1 M). The mixture is stirred at room temperaturefor 8-10 h. The soild was collected by filtration,washed with n-hexane and dried in vacuo.

With the complex challenges of chemical substances, we look forward to future research findings about 2-Cyanoimino-1,3-thiazolidine

Reference£º
Article; Jia, Ai-Quan; Ma, Sen; Wang, Jun-Ling; Zhang, Qian-Feng; Journal of Chemical Crystallography; (2020);,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

2-Cyanoimino-1,3-thiazolidine, cas is 26364-65-8, it is a common heterocyclic compound, the thiazolidine compound, its synthesis route is as follows.

In a dry 50 mL single-mouth flask, 10 mmol of 2-cyanoimino-1,3-thiazolidine and 5 mL of acetone were added.In an ice bath, 0.32 mL of a 50% aqueous solution of NaOH was added, and the temperature was controlled at 0C to 5C.Add dropwise a solution of 5-(2,4-difluorophenyl)-2-furanoyl chloride in acetone to control the rate ofThe temperature was kept at 0C-5C; after the addition was completed, the reaction was performed at 0C-5C for 1-2 hours and TLC test.After the reaction is completed, a 4mol/L hydrochloric acid solution is added to adjust the pH to neutrality.Dichloromethane extraction was added and the dichloromethane layer was successively saturated with sodium bicarbonate,Saturated brine and water were washed three times. The dichloromethane layer was dried over anhydrous magnesium sulfate and filtered.The compound was isolated using a silica gel column (eluent: a 2:1 volume ratio of petroleum ether to ethyl acetate).Yield 75%, 26364-65-8

With the rapid development of chemical substances, we look forward to future research findings about 2-Cyanoimino-1,3-thiazolidine

Reference£º
Patent; South China Agricultural University; Cui Zining; Xiang Xuwen; Tao Hui; Jiang Shan; Zhang Lianhui; (19 pag.)CN107674070; (2018); A;,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

26364-65-8, 2-Cyanoimino-1,3-thiazolidine is a thiazolidine compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,26364-65-8

General procedure: Thiazolidin-2-ylidene-cyanamide (0.317 g, 2.50 mmol) inacetonitrile (20 mL) was dropwise added to a stirred solutionof substituted benzyl bromide (2.5 mmol) and 14 mL NaOHaqueous solution (1 M). The mixture is stirred at room temperaturefor 8-10 h. The soild was collected by filtration,washed with n-hexane and dried in vacuo.

As the paragraph descriping shows that 26364-65-8 is playing an increasingly important role.

Reference£º
Article; Jia, Ai-Quan; Ma, Sen; Wang, Jun-Ling; Zhang, Qian-Feng; Journal of Chemical Crystallography; (2020);,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.26364-65-8,2-Cyanoimino-1,3-thiazolidine,as a common compound, the synthetic route is as follows.,26364-65-8

Add 0.01 mol (1.28 g) to a 250 mL three-necked bottle2-cyanoimido-1,3-thiazolidine, 100 mL DMF as solvent,0.011 mol (1.52 g) of potassium carbonate as an acid binding agent, and the temperature was raised to 80 C.Stir for half an hour, then add 0.01mol (2.73g)5-(Chloromethyl)-3-(2-(2,2-difluoroethoxy)phenyl)-1,2,4-oxadiazole,Insulation reaction for 4h,TLC traces to the disappearance of the starting point and cools to room temperature.After adding 100 mL of water, stirring was continued, and a solid was precipitated and suction filtered to obtain a crude product, which was recrystallized from methanol.The compound of formula I [5-((2-cyanoimino-1,3-thiazolyl)methyl)-3-(2-(2,2-difluoroethoxy)phenyl-1,2 , 4-oxadiazole] 3.0g, yield 82.1%,

26364-65-8 2-Cyanoimino-1,3-thiazolidine 3700797, athiazolidine compound, is more and more widely used in various fields.

Reference£º
Patent; Qingdao University of Science and Technology; Xu Liangzhong; Liu Liancai; Hu Rao; Cui Huanqi; Wang Minghui; (7 pag.)CN108794462; (2018); A;,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

2-Cyanoimino-1,3-thiazolidine, cas is 26364-65-8, it is a common heterocyclic compound, the thiazolidine compound, its synthesis route is as follows.

General procedure: Thiazolidin-2-ylidene-cyanamide (0.317 g, 2.50 mmol) inacetonitrile (20 mL) was dropwise added to a stirred solutionof substituted benzyl bromide (2.5 mmol) and 14 mL NaOHaqueous solution (1 M). The mixture is stirred at room temperaturefor 8-10 h. The soild was collected by filtration,washed with n-hexane and dried in vacuo., 26364-65-8

As the rapid development of chemical substances, we look forward to future research findings about 26364-65-8

Reference£º
Article; Jia, Ai-Quan; Ma, Sen; Wang, Jun-Ling; Zhang, Qian-Feng; Journal of Chemical Crystallography; (2020);,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

2-Cyanoimino-1,3-thiazolidine, cas is 26364-65-8, it is a common heterocyclic compound, the thiazolidine compound, its synthesis route is as follows.

Add 0.01 mol to a 250 mL three-necked flask5-chloromethyl-3-(2,6-difluorophenyl)-1,2,4-oxadiazole,0.01mol2-(cyanoimino)thiazolidine,80mL DMF, stirring reaction at 80 C for 4h, TLC detection reaction is completed,Add distilled water, suction filtration, and dryness.Obtained 2.57g of a white solid.The yield was 80%., 26364-65-8

As the rapid development of chemical substances, we look forward to future research findings about 26364-65-8

Reference£º
Patent; Qingdao University of Science and Technology; Xu Liangzhong; Sun Jianxin; Cui Huanqi; Wang Minghui; (8 pag.)CN109320471; (2019); A;,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

2-Cyanoimino-1,3-thiazolidine, cas is 26364-65-8, it is a common heterocyclic compound, the thiazolidine compound, its synthesis route is as follows.

General procedure: Thiazolidin-2-ylidene-cyanamide (0.317 g, 2.50 mmol) inacetonitrile (20 mL) was dropwise added to a stirred solutionof substituted benzyl bromide (2.5 mmol) and 14 mL NaOHaqueous solution (1 M). The mixture is stirred at room temperaturefor 8-10 h. The soild was collected by filtration,washed with n-hexane and dried in vacuo., 26364-65-8

As the rapid development of chemical substances, we look forward to future research findings about 26364-65-8

Reference£º
Article; Jia, Ai-Quan; Ma, Sen; Wang, Jun-Ling; Zhang, Qian-Feng; Journal of Chemical Crystallography; (2020);,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

A common heterocyclic compound, the thiazolidine compound, name is 2-Cyanoimino-1,3-thiazolidine,cas is 26364-65-8, mainly used in chemical industry, its synthesis route is as follows.

Add 0.01 mol (1.28 g) to a 250 mL three-necked bottle2-cyanoimido-1,3-thiazolidine, 100 mL DMF as solvent,0.011 mol (1.52 g) of potassium carbonate as an acid binding agent, and the temperature was raised to 80 C.Stir for half an hour, then add 0.01mol (2.73g)5-(Chloromethyl)-3-(2-(2,2-difluoroethoxy)phenyl)-1,2,4-oxadiazole,Insulation reaction for 4h,TLC traces to the disappearance of the starting point and cools to room temperature.After adding 100 mL of water, stirring was continued, and a solid was precipitated and suction filtered to obtain a crude product, which was recrystallized from methanol.The compound of formula I [5-((2-cyanoimino-1,3-thiazolyl)methyl)-3-(2-(2,2-difluoroethoxy)phenyl-1,2 , 4-oxadiazole] 3.0g, yield 82.1%,

26364-65-8, As the rapid development of chemical substances, we look forward to future research findings about 26364-65-8

Reference£º
Patent; Qingdao University of Science and Technology; Xu Liangzhong; Liu Liancai; Hu Rao; Cui Huanqi; Wang Minghui; (7 pag.)CN108794462; (2018); A;,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

26364-65-8, 2-Cyanoimino-1,3-thiazolidine is a thiazolidine compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,26364-65-8

General procedure: Thiazolidin-2-ylidene-cyanamide (0.317 g, 2.50 mmol) inacetonitrile (20 mL) was dropwise added to a stirred solutionof substituted benzyl bromide (2.5 mmol) and 14 mL NaOHaqueous solution (1 M). The mixture is stirred at room temperaturefor 8-10 h. The soild was collected by filtration,washed with n-hexane and dried in vacuo.

The synthetic route of 26364-65-8 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Jia, Ai-Quan; Ma, Sen; Wang, Jun-Ling; Zhang, Qian-Feng; Journal of Chemical Crystallography; (2020);,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.26364-65-8,2-Cyanoimino-1,3-thiazolidine,as a common compound, the synthetic route is as follows.,26364-65-8

General procedure: Thiazolidin-2-ylidene-cyanamide (0.317 g, 2.50 mmol) inacetonitrile (20 mL) was dropwise added to a stirred solutionof substituted benzyl bromide (2.5 mmol) and 14 mL NaOHaqueous solution (1 M). The mixture is stirred at room temperaturefor 8-10 h. The soild was collected by filtration,washed with n-hexane and dried in vacuo.

The synthetic route of 26364-65-8 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Jia, Ai-Quan; Ma, Sen; Wang, Jun-Ling; Zhang, Qian-Feng; Journal of Chemical Crystallography; (2020);,
Thiazolidine – Wikipedia
Thiazolidine – ScienceDirect.com