N&PD Moderators: Skorpio
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Smyth2
Bluelighter
[1] Chang, A.-C., Burgess, J. P., Mascarella, S. W., Abraham, P., Kuhar, M. J., Carroll, F. I. (1 April 1997). "Synthesis and Transporter Binding Properties of 2,3-Diphenyltropane Stereoisomers. Comparison to 3β-Phenyltropane-2β-carboxylic Acid Esters". Journal of Medicinal Chemistry. 40 (8): 1247–1251. doi:10.1021/jm960703k.
[2] Serge Petit, et al. EP0273199 (1988 to Sanofi Aventis France).
[3] Jacques Dreux & Serge Petit, US4785007 (1988 to Sanofi Aventis France).
[4] Jacques Prof. Dreux & Serge Petit, EP0203308 (1986 to Sanofi Aventis France).
[5] Petit, S., Nallet, J., Guillard, M., Dreux, J., Chermat, R., Poncelet, M., Bulach, C., Simon, P. (October 1990). "Synthèses et activités psychotropes de 3,4-diarylpiperidin-2-ones: corrélation structure-activité". European Journal of Medicinal Chemistry. 25 (8): 641–652. doi:10.1016/0223-5234(90)90129-Q.
[6] Petit, S., Nallet, J., Guillard, M., Dreux, J., Chermat, R., Poncelet, M., Bulach, C., Simon, P., Fontaine, C., Barthelmebs, M., Imbs, J. (January 1991). "Synthèses et activités psychotropes de 3,4-diarylpipéridines. Corrélation structure-activité et recherche d'une activité antihypertensive". European Journal of Medicinal Chemistry. 26 (1): 19–32. doi:10.1016/0223-5234(91)90209-6.Smyth2
Bluelighter
I saw the synthesis that you posted for this class of agents a while ago.
ALLISON_WUNDERLANDE
1-(3,4-dimethylphenyl)-2-methylamino-1-carbomethoxypropane
Aw!
If you want opioid activity why not develop like ketobemidone instead of like pethidine:
Smyth2
Bluelighter
Rectify
Bluelighter
Yes, that is a good idea (the benzylic-(C=O)-CH2CH3), but really opioids are not my thing at all, and I have a hunch that Bz-(C=O)-O-CH3's are more fun.
If you want opioid activity why not develop like ketobemidone instead of like pethidine: