101970-40-5Relevant articles and documents
Design, synthesis and SAR study of 2-aminopyrimidines with diverse Michael addition acceptors for chemically tuning the potency against EGFRL858R/T790M
Chen, Wenteng,Liu, Shuangrong,Liu, Xingyu,Pan, Youlu,Shao, Jiaan
, (2020)
The covalent binding nature of irreversible kinase inhibitors potentially increases the severity of “off-target” toxicity. Based on our continual strategy of chemically tuning the Michael addition acceptors, herein, we further explore the relationship amo
IMIDAZOLO-5-YL-2-ANILINOPYRIMIDINES AS AGENTS FOR THE INHIBITION OF CELL PROLIFERATION
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Page/Page column 101, (2010/02/13)
Compounds of the formula (I), wherein variable groups are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti cell proliferation) effect in a warm blooded animal, such as man.
Nucleophilic substitutions on 3-chloro-4-fluoronitrobenzene
Ravi, R.,Sivaramakrishnan, H.,Nagarajan, K.
, p. 347 - 348 (2007/10/03)
Nucleophilic substitutions on 3-chloro-4-fluoronitrobenzene 5 with piperazines occur on the fluorine rather than on the chlorine atom as reported, to yield 3-chloro-4-piperazinylnitrobenzenes 8 and 9.