Category: 873-40-5

Application of 873-40-5,Some common heterocyclic compound, 873-40-5, name is 2,3,5-Trichloropyrazine, molecular formula is C4HCl3N2, 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.

2, 3, 5-trichloropyrazine (70.50 g, 384.36 mmol, 1 equiv) and ammonia solution(25% wt, 364.00 g, 400 mL, 2.68 mol, 6.14 equiv) were added to a l-L sealed reactor. The mixture was heated to 80 C and stirred for 24 h, and the reaction was completed. The reaction mixture was cooled to 30 C and filtered to give a brown filter cake. The brown filter cake was dissolved in acetone(50 mL), and filtered. To the filtrate was added petroleum ether (300 mL). The suspension was stirred for 4 h, and filtered to give the crude product. The crude product was slurried in combined solvents of petroleum ether and acetone (10/1, 200 mL) and filtered to give the product Y7d (51.00 g, 307.91 mmol, 80% yield) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) d = 7.63 (s, 1H).

The synthetic route of 873-40-5 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; NOVARTIS AG; FEI, Zhongbo; LU, Gang; WAN, Yinbo; WANG, Jianhua; WU, Quanbing; ZHANG, Hao; (116 pag.)WO2020/65453; (2020); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Application of 873-40-5, The chemical industry reduces the impact on the environment during synthesis 873-40-5, name is 2,3,5-Trichloropyrazine, I believe this compound will play a more active role in future production and life.

2, 3, 5-trichloropyrazine (70.50 g, 384.36 mmol, 1 equiv) and ammonia solution (25% wt, 364.00 g, 400 mL, 2.68 mol, 6.14 equiv) were added to a l-L sealed reactor. The mixture was heated to 80 C and stirred for 24 h, and the reaction was completed. The reaction mixture was cooled to 30 C and filtered to give a brown filter cake. The brown filter cake was dissolved in acetone (50 mL), and filtered. To the filtrate was added petroleum ether (300 mL). The suspension was stirred for 4 h, and filtered to give the crude product. The crude product was slurried in combined solvents of petroleum ether and acetone (10/1, 200 mL) and filtered to give the product Y7d (51.00 g, 307.91 mmol, 80% yield) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) d = 7.63 (s, 1H). The advantage of this (also generalized) method is that no column chromatography is required to obtain Y7d.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 2,3,5-Trichloropyrazine, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; NOVARTIS AG; FEI, Zhongbo; ZHANG, Hao; JIA, Huanqing; WANG, Hui; WANG, Jianhua; LI, Wei; LIN, Xiaohui; MIN, Zhongcheng; (91 pag.)WO2020/65452; (2020); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 873-40-5, name is 2,3,5-Trichloropyrazine, This compound has unique chemical properties. The synthetic route is as follows., Product Details of 873-40-5

28.5 g (152.65 mmol) of 2,3,5-trichloropyrazine, 23.8 g (152.65 mmol) of 2-chlorophenylboronic acid, 63.3 g (457.9 mmol) of K2CO3 and 800 ml / 200 ml of THF/H2O were added under nitrogen atmosphere and stirred. 5.3 g (4.58 mmol) of Pd (PPh3) 4 was added at 40 DEG C, and the mixture was stirred at 80 DEG C for 12 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane. The organic layer was dried over MgSO4 and filtered under reduced pressure. The filtered organic layer was distilled under reduced pressure, and 12 g (yield: 30%) of 2,5-dichloro-3- (2-chlorophenyl) pyrazine was obtained by column chromatography.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 873-40-5.

Reference:
Patent; Doosan Co., Ltd; Kim Tae-hyeong; Bae Hyeong-chan; Son Hyo-seok; Baek Yeong-mi; Park Ho-cheol; (53 pag.)KR101920101; (2018); B1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

873-40-5, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 873-40-5, name is 2,3,5-Trichloropyrazine, This compound has unique chemical properties. The synthetic route is as follows.

General procedure: Under nitrogen gas stream 2,3,5-trichloropyrazine of 28g (152.65mmol),2-chlorophenylboronic acid of 23.8g (152.65mmol),Put THF / H2O and K2CO3 of 800ml / 200ml 63.3g (457.9mmol) and stirred. At 40 into the Pd (PPh3) 4 of 5.3g (4.58mmol) was stirred at 80 for 12 hours.After completion of the reaction, which was then extracted with dichloromethane. The organic layer was dried over MgSO4 filtered under reduced pressure. The filtered organic layer was evaporated under reduced pressure to a back by column chromatography the desired compound 2,5-dichloro-3- (2-chlorophenyl) pyrazine 12g (yield: 30%) was obtained.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.

Reference:
Patent; Doosan Corporation; Kim, Tae Hyung; Bae, Hyung Chan; Son, Hyo Suk; Baek, Young Mi; Patk, Ho Chul; (54 pag.)KR101488560; (2015); B1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem