1215299-91-4Relevant academic research and scientific papers
A NOVEL 3-SUBSTITUTED 7-IMINO-2-THIOXO-3, 7-DIHYDRO-2H-THIAZOLO [4,5-DI PYRIMIDIN-6-YL - AND PROCESS FOR PREPARATION THEREOF
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Page/Page column 10, (2011/06/19)
The present invention relates to novel 3-substituted (7-imino-2-thioxo-3, 7-dihydro-2H-thiazolo [4,5-d] pyrimidin-6-yl of formula 1 wherein R is selected from a group consisting of hydrogen, alkyl having carbon no up to 10, allyl, cycloalkyl, aromatic, substituted aromatics (halogen, OH, COOH, OCH3, alkyl, etc), pyridyl, piperidine, piprazine, morphine. R1 is selected from a group consisting of NH2, NHR, N(R) 2(wherein R could be aliphatic or olefinic group up to 10 carbon), hetrocycles such as furan, thiophene, pyrole, prydyl, piprazine, morphine and R2 is O and S separately. Particularly the present invention relates to (7-Imino-3-substituated -2-thioxo-3,7-dihydro-2H-thiazolo[4,5- d]pyrimidin-6-yl)-urea( 15-21) and Furan-2-carboxylic acid (7-imino-3 -substituted -2-thioxo-3,7- dihydro-2H-thiazolo[4,5-d]pyrimidin-6-yl)-amide. The compounds of present invention are useful in the treatment of central nervous disorders including, Parkinson disease, Huntington's disease, attention disorder, cognition, Alzheimer disease, depression and hypertension.
Synthesis of novel 7-imino-2-thioxo-3,7-dihydro-2H-thiazolo [4,5-d] pyrimidine derivatives as adenosine A2A receptor antagonists
Luthra, Pratibha Mehta,Mishra, Chandra Bhushan,Jha, Pawan Kumar,Barodia, Sandeep Kumar
supporting information; experimental part, p. 1214 - 1218 (2010/06/15)
Novel bicyclic thiazolopyrimidine compounds (15-26) were synthesized to develop adenosine A2A receptor (A2AR) antagonist for the treatment of Parkinson's disease (PD). The binding affinity of the compounds (15-26) with A2A
