15-Sep News Introduction of a new synthetic route about 1446507-38-5

At the same time, in my other blogs, there are other synthetic methods of this type of compound,1446507-38-5, 6-(6-(Trifluoromethyl)pyridin-2-yl)-1,3,5-triazine-2,4(1H,3H)-dione, and friends who are interested can also refer to it.

Synthetic Route of 1446507-38-5, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 1446507-38-5, name is 6-(6-(Trifluoromethyl)pyridin-2-yl)-1,3,5-triazine-2,4(1H,3H)-dione. A new synthetic method of this compound is introduced below.

POCl3 (175.0 mL) is charged into the reaction vessel at 20-35 C., and 6-(6-trifluoromethyl-pyridin-2-yl)-1H-1,3,5-triazine-2,4-dione (35.0 g, 0.1355 mol) was added in portions at below 50 C. The reaction mixture was de-gassed 5-20 minutes by purging with N2 gas. Phosphorous pentachloride (112.86 g, 0.542 mol) was added while stirring at below 50 C., the resulting slurry was heated to reflux (105-110 C.) and maintained for 3-4 h. The reaction mixture was cooled to 50-55 C., concentrated at below 55 C. then cooled to 20-30 C. The reaction mixture was rinsed with ethyl acetate and the ethyl acetate layer was slowly added to cold water (temperature 5 C.) while stirring and maintaining the temperature below 10 C. The mixture was stirred 3-5 minutes at a temperature between 10 to 20 C. and the ethyl acetate layer was collected. The reaction mixture was rinsed with sodium bicarbonate solution and dried over anhydrous sodium sulphate. The material was dried 2-3 h under vacuum at below 45 C. to provide 2, 4-dichloro-6-(6-trifluoromethyl-pyridin-2-yl)-1, 3, 5-triazine.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,1446507-38-5, 6-(6-(Trifluoromethyl)pyridin-2-yl)-1,3,5-triazine-2,4(1H,3H)-dione, and friends who are interested can also refer to it.

Reference:
Patent; Agios Pharmaceuticals, Inc.; Agresta, Samuel V.; (34 pag.)US2018/311249; (2018); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

The origin of a common compound about 1446507-38-5

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 1446507-38-5, 6-(6-(Trifluoromethyl)pyridin-2-yl)-1,3,5-triazine-2,4(1H,3H)-dione.

Electric Literature of 1446507-38-5, 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. 1446507-38-5, name is 6-(6-(Trifluoromethyl)pyridin-2-yl)-1,3,5-triazine-2,4(1H,3H)-dione, molecular formula is C9H5F3N4O2, The 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.

Step 3: Preparation of 2,4-dichloro-6-(6-trfluomethyl-pyridin-2-yl)-1,3,5-triazine. To a solution of 6-(6-trifluomethyl-pyridin-2-yl)-1 ,3 ,5-triazine-2,4(1 H,3H)-dione (3.37 g, 0.013 mol) in POC13 (48 mL) was added PC15 (23 g, 0.1 mol). The mixture was stirred at 100C for 2 hr and then concentrated. The residue was dissolved inEtOAc and then washed with Sat. aq. NaHCO3. The organic layer was dried over anhydrous Na2504 and thenconcentrated to give the desired product.?H NMR (400 MHz, CDC13): 8.76 (d, J= 7.9 Hz, 1H), 8.19 (t, J 7.9 Hz, 1H), 7.97 (d, J 7.8 Hz, 1H).LC-MS: m/z 294.9 (M+H).

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 1446507-38-5, 6-(6-(Trifluoromethyl)pyridin-2-yl)-1,3,5-triazine-2,4(1H,3H)-dione.

Reference:
Patent; AGIOS PHARMACEUTICALS, INC.; KONTEATIS, Zenon D.; POPOVICI-MULLER, Janeta; TRAVINS, Jeremy M.; ZAHLER, Robert; CAI, Zhenwei; ZHOU, Ding; WO2015/3640; (2015); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem