The origin of a common compound about 133228-21-4

According to the analysis of related databases, 133228-21-4, the application of this compound in the production field has become more and more popular.

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. 133228-21-4, name is N,N-Dimethyl-1H-pyrazole-1-sulfonamide, This compound has unique chemical properties. The synthetic route is as follows., Computed Properties of C5H9N3O2S

Step B: Preparation of 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide. Under a nitrogen atmosphere, a solution of N,N-dimethyl-1H-pyrazole-1-sulfonamide (5.0 g, 28 mmol) (i.e. the product of Example 12, Step A) in tetrahydrofuran (50 mL) was cooled to -78 0C and then treated with n-butyllithium (2 M solution in cyclohexane, 15.0 mL, 30 mmol) dropwise. The reaction mixture formed a thick precipitate, and stirring was continued for 30 minutes after the addition. To the stirred suspension, a solution of hexachloroethane (7.1 g, 30 mmol) in tetrahydrofuran (20 mL) was added dropwise. After 30 minutes the resulting clear solution was warmed to ambient temperature and quenched with the addition of water (70 mL). The reaction mixture was extracted with dichloromethane and dried over MgSO4. The reaction mixture was filtered and concentrated under reduced pressure. The crude product was purified by silica gel chromatography (50 % hexanes in dichloromethane as eluant) to give 1.71 g of 5-chloro-iV,iV-dimethyl-lH-pyrazole- EPO 1 -sulfonamide. The S-chloro-MiV-dimethyl-lH-pyrazole-l-sulfonamide was heated to 110 C for 12 h with a catalytic amount of pyrazole to isomerize to the title compound. 1H NMR (CDCl3) 5 3.07 (s, 6H), 6.33 (s, IH), 7.60 (s, IH).

According to the analysis of related databases, 133228-21-4, the application of this compound in the production field has become more and more popular.

Reference:
Patent; E. I. DU PONT DE NEMOURS AND COMPANY; WO2007/14290; (2007); A2;,
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics