88132-48-3Relevant academic research and scientific papers
Nucleophilic substitution of the acetoxy group in 3- methylbenzoylaminomethyl acetate
Labanauskas,Mazeikaite,Striela,Gedrimaite,Urbelis,Zilinskas
experimental part, p. 1672 - 1676 (2012/09/05)
Replacement of the acetoxy group in 3-methylbenzoylaminomethyl acetate with N- and S-nucleophiles generated from amines and thio compounds using sodium hydride gives the corresponding N-aminomethyl- and N-thiomethylbenzamides.
6-Hydroxy-4-[2-(di-n-propylamino)ethyl]indole: Synthesis and dopaminergic actions
Cannon,Lee,Ilhan,Koons,Long
, p. 386 - 389 (2007/10/02)
The title compound was proposed to be a biologically active metabolite of a dopaminergic agent, 4-[2-(di-n-propylamino)ethyl]indole. This proposed metabolite was synthesized by a multistep sequence beginning with methyl 3,5-dinitro o-toluate, and involvin
