THE REACTION OF SOME HETEROCYCLIC FORMAMIDINES WITH TRIMETHYLSILYLETHYNYLLITHIUM
Ключевые слова:
[bis(trimethylsilylethynyl)methylamino]heterocycles, [(dimethylamino)methyleneamino]protected heterocyclic amines, trimethylsilylethynyllithiumАннотация
The reaction of a 2-[(dimethylamino)methyleneamino]pteridine, two 2-[(di-methylamino)methyleneamino]pyrimidines, and a 2-[(dimethylamino)methylene-amino]pyrido[2,3-d]pyrimidine with trimethylsilylethynylithium in the presence of benzyl chloroformate leads to the corresponding 2-[bis(trimethylsilylethynyl)-methylamino]-substituted heterocycles. A series of such substrates was prepared
and some of the factors which permit this transformation were delineated. An
X-ray crystal structure was determined of one of the products – 2-[bis(trimethyl-
silylethynyl)methylamino]-5,6,7,8-tetrahydro-3-(2,2-dimethylpropanoyloxymethyl)-
quinazolin-4-one.
How to Cite
Ajana, W.; Helliwell, M.; Collison, D.; Garner, C. D.; Joule, J. A. Chem. Heterocycl. Compd. 2001, 37, 1375. [Khim. Geterotsikl. Soedin. 2001, 1506.]
For this article in the English edition, see DOI https://doi.org/10.1023/A:1017999117482