65550-99-4Relevant academic research and scientific papers
Synthesis of Pyrazolyldithiocarbonates
Graubaum, H.
, p. 88 - 94 (1993)
The reaction of 3-amino-pyrazole 1 with carbondisulfide and alkylating agents in basic conditions to yield different dithiocarbonates 2 - 8 was studied.The dithiocarbonates 2a react with isocyanates to form 1-acyl-5-acylamino-pyrazoles 9 - 10.Acyl migrati
Synthesis of Purine Analogues: Photocatalyst-Free Visible-Light-Enhanced Annulation Approach to Pyrazolo[1,5- A[[1,3,5]triazine-2,4-diamines
Guo, Wei,Xie, Zhen,Cai, Liuhuan,Liu, Gongping,Deng, Ling,Mei, Weijie,Zou, Xiaoying,Zhong, Yumei,Zhuo, Xiaoya,Zheng, Lvyin,Fan, Xiaolin
supporting information, p. 8365 - 8380 (2021/06/28)
A new photocatalyst-free visible-light-enhanced strategy for the synthesis of pyrazolo[1,5-a][1,3,5]triazine-2,4-diamines via the formation of electron donor-acceptor (EDA) complexes is reported. The in situ generated pyrazolthiourea intermediates from 1H-pyrazol-3-amines and isothiocyanates undergo formal [4 + 2] annulation with 1,1,3,3-tetramethylguanidines (TMG) to deliver the corresponding products involved in three C-N bond formations in a one-pot protocol. The formation of EDA complex from pyrazolthiourea and TMG is confirmed by UV-vis spectroscopy and 1H NMR experiments. Moreover, this mild reaction proceeds in the absence of any external transition metals, oxidants, bases, and ligands. This efficient methodology for the synthesis of purine analogues pyrazolo[1,5-a][1,3,5]triazine-2,4-diamines provides potential synthetic applications in the field of drug research and development.
