MobiusDick
Bluelighter
When you look at thiophene rings of sufentanil and the oxo-1,4-dihydrotetrazol ring of alfentanil, you realize that there is not always the appearance of a geometric match because of differences in molecular size, unshared electron pairs and steric hindrance, for something to fit in a receptor or, reuptake or vesicular transporter which typically binds a phenyl group.
It would be interesting to try to put a methylenedioxy ring on molecules similar to these and the N-methyl isopropylamine in an analogous position as 3,4 in MDMA to see what you have.
I suppose seeing if these two types of group can make a methamphetamine analogue might be the first step.
Also, although I realize that morpholine and piperidine or piperazine are different because of unshared electrons, these molecules in place of piperidine might be interesting too when producing analogues.
MobiusDick
MobiusDick
It would be interesting to try to put a methylenedioxy ring on molecules similar to these and the N-methyl isopropylamine in an analogous position as 3,4 in MDMA to see what you have.
I suppose seeing if these two types of group can make a methamphetamine analogue might be the first step.
Also, although I realize that morpholine and piperidine or piperazine are different because of unshared electrons, these molecules in place of piperidine might be interesting too when producing analogues.
MobiusDick
MobiusDick
