68302-95-4Relevant academic research and scientific papers
Continuous flow nucleophilic aromatic substitution with dimethylamine generated in situ by decomposition of DMF
Petersen, Trine P.,Larsen, Anders Foller,Ritzen, Andreas,Ulven, Trond
, p. 4190 - 4195 (2013/05/23)
A safe, practical, and scalable continuous flow protocol for the in situ generation of dimethylamine from DMF followed by nucleophilic aromatic substitution of a broad range of aromatic and heteroaromatic halides is reported.
Barriers to Rotation of the Dimethylamino Group in Some 2-Amino-4-(N,N-dimethylamino)pyrimidines
Wells, C. H. J.
, p. 274 - 275 (2007/10/02)
The free energy of activation for rotation about the exocyclic C-N bond of the dimethylamino group of some 6-substituted 2-amino-4-(N,N-dimethylamino)pyrimidines has been determined using 1H NMR line shape analysis.The results are discussed in terms of the relative electron-withdrawing and electron-releasing effects of the substituents.
N-pyrimidinyl-N-dialkylaminoalkyl ureas
-
, (2008/06/13)
Organic chemical compounds based upon the urea molecule are disclosed which have potent gastric secretion inhibitory properties. The urea is substituted with a 6 membered heterocyclic substituent containing 2 or 3 heteroatoms, and also with a substituted
