24-Sep News Sources of common compounds: 199522-66-2

According to the analysis of related databases, 199522-66-2, the application of this compound in the production field has become more and more popular.

Reference of 199522-66-2, 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. 199522-66-2, name is N1-(5-Bromopyrid-2-yl)ethane-1,2-diamine, molecular formula is C7H10BrN3, 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 2: 3-[2-(5-Bromo-pyridin-2-ylamino)-ethyl]-3H-quinazolin-4-one (compound 75) A suspension of primary amine 73 (1.17 g, 5.40 mmol) and isatoic anhydride 74 (880 mg, 5.40 mmol) in methanol (25 mL) was stirred for 3 h at 50 C. and then concentrated. The resulting oily residue was dissolved in 88% formic acid (20 mL) and refluxed overnight. After removal of formic acid, the solid residue was purified through column chromatography on silica gel (5% methanol in dichloromethane) to give 1.24 g (3.6 mmol, 67% yield) of 75. 13C NMR (300 MHz, CDCl3): 161.6, 156.8, 147.7, 147.6, 147.2, 139.8, 134.5, 127.4, 126.8, 126.3, 121.6, 110.1, 107.0, 46.3, 40.1. LRMS=347.1 (M+1).

According to the analysis of related databases, 199522-66-2, the application of this compound in the production field has become more and more popular.

Reference:
Patent; MethylGene, Inc.; US2005/288282; (2005); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem