Synthetic Route of 2419-56-9, As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 2419-56-9, Name is H-Glu(OtBu)-OH, SMILES is [H][C@](N)(CCC(=O)OC(C)(C)C)C(O)=O, belongs to amides-buliding-blocks compound. In a article, author is Fisk, Heidi, introduce new discover of the category.
Synthesis of Vicinal Bromoamine Compounds via Three Components Reaction of beta,beta-Dicyanostyrene/Amide/N-Bromo-succinimide
Vicinal bromoamine derivative belongs to an important class of difunctionalization compounds. New synthetic method and new vicinal bromoamine derivatives are eagerly desired. Thus, a new one-pot protocol for the synthesis of vicinal bromoamines from beta, beta-dicyanostyrene derivatives/amides/N-bromo-succinimide was developed. In the presence of anhydrous K2CO3, beta, beta-dicyanostyrenes reacted smoothly with amides and N-bromo-succinimide (NBS) to generate the vicinal bromoamine compounds in good to excellent yield (up to 93% yield) at room temperature without the protection of inert gas in CH2Cl2. 13 different structural beta, beta-dicyanostyrene derivatives reacted with 7 different structural amides (acrylamide, acetamide, valeramide, isobutyramide, benzamide, 4-nitrobenzamide, ethylurethanm) and NBS have been investigated in this work. The results indicated that the method is not only widely subjected to beta, beta-dicyanostyrene, but also suitable for the different type of amide. The structures of all the products were confirmed by their nuclear magnetic resonance spectroscopy (NMR), infrared spectra (IR) and high resolution mass spectrometry (HRMS), and the possible reaction mechanism was proposed.
Synthetic Route of 2419-56-9, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 2419-56-9.