Some scientific research about 3,3′,3”-(1,3,5-Triazinane-1,3,5-triyl)tris(N,N-dimethylpropan-1-amine)

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In an article, author is Truax, Nathanyal J., once mentioned the application of 15875-13-5, Recommanded Product: 3,3′,3”-(1,3,5-Triazinane-1,3,5-triyl)tris(N,N-dimethylpropan-1-amine), Name is 3,3′,3”-(1,3,5-Triazinane-1,3,5-triyl)tris(N,N-dimethylpropan-1-amine), molecular formula is C18H42N6, molecular weight is 342.57, MDL number is MFCD00059766, category is pyrrolines. Now introduce a scientific discovery about this category.

Synthesis of Benzo[a]carbazoles and an Indolo[2,3-a]carbazole from 3-Aryltetramic Acids

A simple and flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed. The key step involves the BF3-mediated electrophilic substitution of indoles with N-alkyl-substituted 3-aryltetramic acids, which provides access to indole-substituted 3-pyrrolin-2-ones. Scholl-type oxidative cyclizations of these materials led to the formation of the corresponding 3-pyrrolin-2-one-fused benzo [a]carbazoles and indolo[2,3-a]carbazoles. This work represents the first synthesis of the benzo [a]pyrrolo[3,4-c]carbazol-3(8H)-one ring system, while the indolo[2,3-a]pyrrolo[3,4-c]carbazol-5-one ring system is found in a number of biologically active compounds including the protein kinase C (PKC) inhibitor, staurosporine.

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Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem