Martinez-Viturro, Carlos M.; Dominguez, Domingo published an article in Tetrahedron Letters. The title of the article was 《Synthesis of aza analogues of the anticancer agent batracylin》.Recommanded Product: 70298-88-3 The author mentioned the following in the article:
Three series of pyrido-fused pyrimido[2,1-a]isoindol-7-ones were prepared from readily available (aminopyridinyl)(aryl)methanones by reduction followed by a Mitsunobu reaction with phthalimide and acid-catalyzed cyclodehydration. This approach provided a wide variety of aza analogs of the antitumor agent batracylin. After reading the article, we found that the author used 2,2-Dimehtyl-N-pyridin-3-yl-propionamide(cas: 70298-88-3Recommanded Product: 70298-88-3)
2,2-Dimehtyl-N-pyridin-3-yl-propionamide(cas: 70298-88-3) belongs to anime. Milder oxidation, using reagents such as NaOCl, can remove four hydrogen atoms from primary amines of the type RCH2NH2 to form nitriles (R―C≡N), and oxidation with reagents such as MnO2 can remove two hydrogen atoms from secondary amines (R2CH―NHR′) to form imines (R2C=NR′). Tertiary amines can be oxidized to enamines (R2C=CHNR2) by a variety of reagents.Recommanded Product: 70298-88-3
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics