SYNTHESIS AND DOPAMINE RECEPTOR AFFINITIES OF ENANTIOMERS OF 2-SUBSTITUTED APOMORPHINES AND THEIR N-N-PROPYL ANALOGS

Syntheses of (R)-(-)-2-methoxyapomorphine (R-8), its antipode (R-8), and its (R)-(-)-N-n-propyl R-9 derivative are described. The dopaminergic receptor affinities of these compounds and their 2-unsubstituted counterparts (R)-(-)-apomorphine (R(-)-APO, R-1), (S)-(+)-apomorphine (S(+)-APO, S–1), and (R)-(-)-N-n-propylnorapomorphine (R(-)-NPA, R-2), as well as those of (R)-(-)-2-chloroapomorphine (R(-)-2-Cl-APO, R-6), (R)-(-)-2-bromoapomorphine (R(-)-2-Br-APO, R-6), were determined with tissue membrane preparations of corpus striatum from rat brain. Contribution of both an N-n-propyl and a 2-hydroxy in {R)-(-)-2-hydroxy-N-n-propylnorapomorphine (R(-)-2-OH-NPA, R-7) or a methoxy group in (R)-(-)-2-methoxy-N-n-propylnorapomorphine (R(-)-2-OCH3-NPA, R-9) produced the highest D2 affinity (0.053 and 0.17 nM) and D2 over D1 selectivity (17 300 and 10500 times) of the compounds evaluated. The structure-affinity relationships of these 2-substituted aporphines suggest that secondary binding sites of D2 receptors interact with 2-substituents on the A ring of aporphines through H-bonding. © 1990, American Chemical Society. All rights reserved.