Continuously updated synthesis method about 312736-49-5

The synthetic route of 312736-49-5 has been constantly updated, and we look forward to future research findings.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 312736-49-5, name is 3,5-Dichloropyrazine-2-carboxylic acid belongs to pyrazines compound, it is a common compound, a new synthetic route is introduced below. Product Details of 312736-49-5

To a solution of 2,6-dichloropyrazine-3-carboxylic acid (9 g, 46.6 mmol) in dichloromethane (250 mL) at room temperature (RT) was added oxalyl chloride (5.2 mL, 61.5 mmol) dropwise followed by careful addition of DMF (3 drops) and then the reaction mixture was stirred at RT for 3 hr. Then it was concentrated in a rotavap and the residue was taken in toluene (150 mL) and added dropwise to a mixture of 3-dimethylaminoacrylic acid ethyl ester (8.5 g, 59.4 mmol) and triethylamine (9.7 mL, 69.5 mmol) and the resulting reaction mixture was stirred at 90 C. for 16 hr. Then the reaction mixture was cooled, filtered, and the filtrate was concentrated. The residue obtained was purified by column chromatography (silica gel 60-120 mesh) eluting with 0-40% EtOAc in petroleum ether to obtain the product as pale yellow solid.Yield: 6.7 g (45%).1H NMR (300 MHz, DMSO-d6): 8.8 (s, 1H), 8.0 (s, 1H), 3.8 (q, 5 Hz, 2H), 3.4 (s, 3H), 3.0 (s, 3H), 0.9 (t, 5 Hz, 3H). LC/MS (M+H)+ 318, 320

The synthetic route of 312736-49-5 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Sudhakar, Anantha; US2011/105497; (2011); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem