《Ortho-functionalization of aminopyridines; regioselective lithiation of 3-pivaloylaminopyridines》 was published in Synthesis in 1982. These research results belong to Gungor, T.; Marsais, F.; Queguiner, G.. Application of 70298-88-3 The article mentions the following:
3-Pivaloylaminopyridine (I) was selectively lithiated in the 4-position. Treatment of the lithio derivative with RCHO (R = Ph, 4-MeC6H4, 2-MeOC6H4, 3,4-methylenedioxyphenyl, 2-thienyl, Me) gave the alcs. II. I-4-d was also prepared The results came from multiple reactions, including the reaction of 2,2-Dimehtyl-N-pyridin-3-yl-propionamide(cas: 70298-88-3Application of 70298-88-3)
2,2-Dimehtyl-N-pyridin-3-yl-propionamide(cas: 70298-88-3) belongs to anime. Aniline, ethanolamines, and several other amines are major industrial commodities used in making rubber, dyes, pharmaceuticals, and synthetic resins and fibres and for a host of other applications. Most of the numerous methods for the preparation of amines may be broadly divided into two groups: (1) chemical reduction (replacement of oxygen with hydrogen atoms in the molecule) of members of several other classes of organic nitrogen compounds and (2) reactions of ammonia or amines with organic compounds.Application of 70298-88-3
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics