The important role of 2,3-Dichloropyridine

According to the analysis of related databases, 2402-77-9, the application of this compound in the production field has become more and more popular.

Application of 2402-77-9, Adding some certain compound to certain chemical reactions, such as: 2402-77-9, name is 2,3-Dichloropyridine,molecular formula is C5H3Cl2N, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 2402-77-9.

Reaction performed under nitrogen atmosphere. To a solution of n-butyllithium (27.6 ml, 69 mmol, 2.5 M in hexanes) in dry Et2O (150 ml) cooled at -78 0C, was added 2,2,6,6-tetramethylpiperidine (11.64 ml, 69 mmol) dropwise. The resulting reaction mixture was stirred at -78 0C for 10 min. and then a solution of 2,3-dichloropyridine (10 g, 67.57 mmol) in dry THF (75 ml) was added dropwise. The mixture was stirred at -78 0C for 30 minutes and then a solution of iodine (25.38 g, 100 mmol) in dry THF (75 ml) was added. The mixture was allowed to warm to room temperature overnight, quenched with Na2S2O3 (aqueous sat. solution) and extracted twice with EtOAc. The combined organic extracts were washed with NaHCO3 (aqueous sat. solution), dried (Na2SO4) and evaporated in vacuo. The crude residue was precipitated with heptane, filtered off and dried to yield compound D16 (8.21 g, 44%) as a pale cream solid. LCMS: MW (theor): 273; [MH+]: did not ionise; RT (min): 2.73 (Method 21).

According to the analysis of related databases, 2402-77-9, the application of this compound in the production field has become more and more popular.

Reference:
Patent; ORTHO-MCNEIL-JANSSEN PHARMACEUTICALS, INC.; ADDEX PHARMA S.A.; WO2009/62676; (2009); A2;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem