55966-68-2

Upstream product

• 75-21-8 oxirane 
• 94-09-7 p-aminoethylbenzoate 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 141-43-5 ethanolamine 
• 26815-64-5 ethyl 4-benzoate 
• 59081-60-6 N-(4-ethoxycarbonylphenyl)aminoacetic acid 

Downstream Products

• 170799-53-8 diethyl N-<4-pyrimidin-5-yl)ethyl>amino>benzoyl>-L-glutamate 
• 170799-61-8 ethyl 4-pyrimidin-5-yl)ethyl>amino>benzoate 
• 149325-84-8 4-pyrimidin-5-yl)ethyl>amino>benzoic acid 
• 170799-66-3 ethyl 4-amino>benzoate 
• 170799-70-9 ethyl 4-<2-<(2-cyano-3-oxocyclopentan-1-yl)ethyl>amino>benzoate 
• 170799-71-0 ethyl 4-benzoate 

Relevant academic research and scientific papers

Highly Efficient Mechanochemical N-Arylation of Amino Alcohols and Diamines with Cu0 Powder

Cu0-catalysed arylations have rightly acquired great importance over the last decade. This paper reports the N-arylation of amino alcohols and diamines with iodobenzene derivatives in a planetary ball mill and an investigation into the procedure. This newly developed solvent-free protocol is fast, efficient and occurs under the mechanochemical activation of metallic copper powder. It does not require additional ligands and gives excellent yields. This paper aims to broaden the scope of mechanochemical Cu0-activation and so a new one-pot, two-step synthesis that combines CuAAC and N-arylation has been successfully performed and reported herein.

Novel 6-5 fused ring heterocycle antifolates with potent antitumor activity: Bridge modifications and heterocyclic benzoyl isosters of 2,4-diamino-6,7-dihydro-5H-cyclopenta[d]pyrimidine antifolate

Structural modifications of an extremely potent inhibitor of dihydrofolate reductase (DHFR) activity and tumor cell growth, N-[4-[3-(2,4-diamino-6,7-dihydro-5H-cyclopenta[d]pyrimidin-5-yl)propyl ]benzoyl]-L-glutamic acid (1), have led to the synthesis of