Adamantyl cannabinoids: A novel class of cannabinergic ligands

Article abstract of DOI:10.1021/jm058175c

Structure-activity relationship studies have established that the aliphatic side chain plays a pivotal role in determining the cannabinergic potency of tricyclic classical cannabinoids. We have now synthesized a series of analogues in which a variety of a

Full text of DOI:10.1021/jm058175c

4576
J. Med. Chem. 2005, 48, 4576-4585
Adamantyl Cannabinoids: A Novel Class of Cannabinergic Ligands
Dai Lu,† Zhaoxing Meng,† Ganesh A. Thakur,† Pusheng Fan,† John Steed,‡ Cindy L. Tartal,‡ Dow P. Hurst,‡
Patricia H. Reggio,‡ Jeffrey R. Deschamps,| Damon A. Parrish,| Clifford George,| Torbjo¨rn U. C. Ja¨rbe,§
Richard J. Lamb, and Alexandros Makriyannis*,†
Center for Drug Discovery, Northeastern University, 360 Huntington Avenue, 116 Mugar Life Sciences Building, Boston,
Massachusetts 02115, Department of Chemistry and Biochemistry, University of North CarolinasGreensboro, Greensboro,
North Carolina 27402, Naval Research Laboratory, Code 6030, Washington, D.C. 20375, Department of Psychology, Temple
University, Philadelphia, Pennsylvania 19122, and Departments of Psychiatry and Pharmacology, University of Texas Health
Science Center at San Antonio, San Antonio, Texas 78229
Received January 21, 2005
Structure-activity relationship studies have established that the aliphatic side chain plays a
pivotal role in determining the cannabinergic potency of tricyclic classical cannabinoids. We
have now synthesized a series of analogues in which a variety of adamantyl substituents were
introduced at the C3 position of ∆8-THC. Our lead compound, (-)-3-(1-adamantyl)-∆8-
tetrahydrocannabinol (1a, AM411), was found to have robust affinity and selectivity for the
CB1 receptor as well as high in vivo potency. The X-ray crystal structure of 1a was determined.
Exploration of the side chain conformational space using molecular modeling approaches has
allowed us to develop cannabinoid side chain pharmacophore models for the CB1 and CB2
receptors. Our results suggest that although a bulky group at the C3 position of classical
cannabinoids could be tolerated by both CB1 and CB2 binding sites, the relative orientation of
that group with respect to the tricyclic component can lead to receptor subtype selectivity.
Introduction
inergic potency.13-19 Earlier work from our laboratory
has explored the pharmacophoric requirements of the
side chain within the classical tetrahydrocannabinol
(THC) template. This included conformational restric-
tion through the inclusion of multiple bonds within the
chain, the addition of C1′ cyclic substituents,17,18 and
the incorporation of the first one or two side chain
carbons into a six-membered ring fused with the phe-
nolic A ring.19 This led to a series of cannabinergic
ligands possessing enhanced affinity and selectivity for
both CB1 and CB2 receptors.
To add to our present understanding of the possible
conformation of the side chain adopted during interac-
tion with the active site, we have developed novel
analogues carrying bulky and/or rigid aliphatic substit-
uents at the 3-position of the phenolic A ring. Here we
describe the synthesis of a carefully designed series of
analogues, in which a variety of adamantyl substituents
were introduced at the C3 position of the phenolic ring
of ∆8-THC (Figure 1). Exploration of the allowable
conformational space for these side chains provided us
with insights regarding the pharmacophoric features
required for CB1 and CB2 selectivities. We also used
computational modeling studies to outline steric differ-
ences between the different side chain substitutions that
define receptor subtype recognition. Our results shed
new light on the bioactive conformation of the classical
cannabinoid side chain as well as the side chain subsites
within the CB1 and CB2 receptors. Our lead compound
1a (AM411), the first pharmacologically active20,21 clas-
sical cannabinoid to be crystallized, was found to possess
substantial CB1 selectivity and high in vivo potency.
Chemistry. Generally, the synthesis of adamantyl
congeners of ∆8-THC (1a-e) was achieved by condensa-
tion of the chiral monoterpenoid alcohol (+)-cis/trans-
p-mentha-2,8-dien-1-ol with an appropriately 5-substi-
∆9-Tetrahydrocannabinol (∆9-THC), the active ingre-
dient of marijuana (Cannabis sativa),1 binds almost
equally to the two known G-protein-coupled cannabinoid
receptors CB12,3 and CB2.4 CB1 is found in the central
nervous system (CNS), as well as in a number of organs
in the periphery, while CB2 is principally associated
with the immune system.5 The search for cannabinoids
possessing a high degree of pharmacological potency and
selectivity has led to the synthesis and testing of a large
number of novel analogues6-9 from which structure-
activity relationships (SAR) could be established. Four
pharmacophores associated with cannabimimetic activ-
ity10 were recognized within the classical and nonclas-
sical cannabinoid prototypes. These include a phenolic
hydroxyl, a lipophilic alkyl side chain, a northern
aliphatic hydroxyl group also found in the metabolites
of the plant-derived cannabinoids, and a southern
aliphatic hydroxyl first introduced in the nonclassical
class of cannabinoids developed by Pfizer and repre-
sented by the well-known ligand CP-55,940, (-)-3-[2-
hydroxy-4-(1,1-dimethylheptyl)phenyl]-4-(3-hydroxypro-
pyl)cyclohexan-1-ol.
The significance of the aliphatic side chain was first
demonstrated by Adams, who showed that substitution
of the n-pentyl side chain of ∆9-THC with a 1′,1′-
dimethylheptyl group led to a 100-fold increase in
potency.11,12 Subsequent work has established that the
side chain plays a pivotal role in modulating cannab-
* Corresponding author. Phone: 617-373-4200; Fax: 617-373-7493;
E-mail: a.makriyannis@neu.edu.
† Northeastern University.
‡ University of North CarolinasGreensboro.
| Naval Research Laboratory.
§ Temple University.
University of Texas Health Science Center at San Antonio.
10.1021/jm058175c CCC: $30.25 © 2005 American Chemical Society
Published on Web 06/16/2005

Adamantyl Cannabinoids
Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14 4577
Table 1. Affinities (Ki) of ∆8-THC Analogues for CB1 and CB2
Cannabinoid Receptorsa
Figure 1. (-)-∆8-THC and target compounds (1a-e) used to
examine the effects of steric bulk and rigidity at the side chain
of classical cannabinoids.
Scheme 1a
a Affinities for CB1 and CB2 were determined using rat brain
(CB1) or mouse spleen (CB2) membranes and [3H]CP-55,940 as
the radioligand following previously described procedures.27 Ki
values were obtained from three independent experiments run in
duplicate and are expressed as the mean of the three values, 95%
confidence limits are indicated in parentheses.
Scheme 2a
a Reagents and conditions: (a) BBr3, CH2Cl2, 0 °C to rt; (b)
p-TSA, CHCl3, 65 °C, 6 h.
tuted resorcinol. Following a well-established pro-
tocol,19,22,23 condensation (Scheme 1) of resorcinol de-
rivatives 2a-e with (+)-cis/trans-p-mentha-2,8-dien-
1-ol catalyzed by p-toluenesulfonic acid monohydrate
afforded the corresponding tetrahydrocannabinol ana-
logues 1a-e (Table 1) in 40-84% yield.
The dimethylated resorcinol 3a was synthesized by
following a previously reported procedure.24 Alkylation
of 2,6-dimethoxyphenol with 1-adamantanol in the
presence of methanesulfonic acid gave 4 as the pre-
dominant isomer (Scheme 2). This was converted to the
phosphate ester 5 using diethylphosphonate in a 75%
yield, and then treatment of 5 with Li/NH3 at -78 °C
gave the 5-alkylresorcinol dimethyl ether 3a in a 70%
yield. The 5-alkylresorcinol dimethyl ether 3b was
prepared from commercially available 3,5-dimethoxya-
niline. Diazotization of 3,5-dimethoxyaniline followed by
its exposure to cuprous bromide gave 1-bromo-3,5-
dimethoxybenzene (6) in 56% yield. Addition of 2-ada-
mantanone to the organomagnesium reagent derived
a Reagents and conditions: (a) 1-adamantanol, CH3SO3H, 80
°C to rt; (b) H(O)P(OEt)2, Et3N, CCl4, 0 °C to rt; (c) Li/NH3, Et2O/
THF, -78 °C; (d) NaNO2, HBr; (e) CuBr, HBr; (f) Mg, THF,
2-adamantanone; (g) Li/NH3, THF, -60 °C; (h) Mg, Et2O, 2-ada-
mantanone; (i) p-TSA, CH2Cl2, reflux; (j) H2/Pd-C, EtOH, rt; (k)
Mg, Et2O, 1-bromoadamantane, heating.
from 6 gave carbinol 7 (68% yield), which when further
treated with lithium in liquid ammonia gave 3b in 78%
yield. The remaining three 5-alkylresorcinol dimethyl
ethers 3c, 3d, and 3e were synthesized from com-
mercially available 3,5-dimethoxybenzyl chloride. The

4578 Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14
Lu et al.
Figure 2. AM1 conformational search results for compounds 1a-c are illustrated here. All accessible conformers for each ligand
are shown superimposed at their aromatic rings and contoured at their van der Waals radii. (Top Row) For each conformer
superposition in this view, the aromatic ring has been turned perpendicular to the plane of the page with the adamantyl substituent
closest to the viewer and the carbocyclic ring furthest from the viewer. (Bottom Row) A bottom view of each conformer superposition
for compounds 1a-c is shown here. In this view, the aromatic ring of each conformer is oriented perpendicular to the plane of the
page, with the long axis of each molecule horizontal. C4 is closest to the viewer and the phenolic hydroxyl is furthest from the
viewer.
corresponding Grignard reacted with 2-adamantanone
to give carbinol 8 in 80% yield. This was further
dehydrated to 3c in 83% yield under acidic conditions
and catalytically reduced to provide the 5-alkylresorci-
nol dimethyl ether 3d in nearly quantitative yield.
Intermediate 3e was obtained through a Wurtz-like
coupling reaction25,26 between 1-bromoadamantane and
the Grignard reagent derived from 3,5-dimethoxybenzyl
chloride. Generally, the above reaction produced rela-
tively low yields of product with the best result (24%
yield) being obtained when high concentrations of
reactants were used. Resorcinols 2a-e were obtained
from 3a-e, respectively, by demethylation (85-95%
yields).
is positioned further from the aromatic A ring by the
introduction of a methylene link 1e, affinity for CB1
receptor is reduced and there is no CB1/CB2 selectivity.
Similarly, introduction of a methylene link in the
2-adamantyl position 1d further reduced affinity and
again eliminated CB1/CB2 selectivity. The compound
with the highest CB2 selectivity was one in which the
adamantyl group was linked at its 2-position to the
aromatic ring through a styrene double bond. This
compound 1c also exhibited improved CB2 affinity (8.9
nM).
Examination of the CB1 and CB2 affinities for the
five analogues included in this study indicated that both
receptor subtypes are capable of accommodating bulky
groups in the 3-position of the tricyclic cannabinoid
structure. However, compounds 1a-e also exhibited
differences in their relative affinities for the two receptor
subtypes. We postulated that these observed differences
in the relative ability of each ligand to interact with the
CB1 and CB2 sites could be accounted for by examining
their respective allowable conformational spaces. There-
fore, we first used computer modeling to calculate the
accessible conformers of compounds 1a-e. Then the van
der Waals volume maps and the Unique Volume Maps
for the CB1 selective 1a, the CB2 selective 1c, and the
nonselective 1d were analyzed.
Computational Study. Conformational Analysis
Results. Spartan conformational analysis identified
four accessible conformers for 1a, six accessible con-
formers for 1b, 1c, and 1d and two accessible conform-
ers for 1e (see Supporting Information for further
details). Figures 2 and 3 illustrate the conformational
analysis results with accessible conformers superim-
posed at their benzene rings. Two graphical representa-
tions for each of the resultant superimposed structures
have been illustrated. In the first (shown at the top of
Figures 2 and 3), the fused ring structure is vertical and
is oriented perpendicular to the plane of the page with
the adamantyl group closest to the viewer and the
carbocyclic C ring furthest from the viewer. In this
Results and Discussion
Receptor Binding Studies. The compounds re-
ported in this study are ∆8-THC analogues in which the
C3 five carbon side chain of ∆8-THC was replaced with
bulky adamantyl substituents. As with earlier work, we
used (-)-∆8-THC as our prototype, favoring it over the
less stable and almost equipotent isomer (-)-∆9-THC.
The abilities of 1a-e to displace radiolabeled CP-55,-
940 from purified rat forebrain synaptosomes27 and
mouse spleen membranes28 were determined. Inhibition
constant values (Ki)29 calculated from the respective
displacement curves are listed in Table 1 and serve as
indicators for the affinities of these ∆8-THC analogues
for the CB1 and CB2 receptors. As can be seen in Table
1, the range of Ki values of the five analogues indicates
that structural modifications of the C3 adamantyl
substituents on the ∆8-THC template can have profound
effects on CB1/CB2 affinities and selectivities. Interest-
ingly, replacing the linear side chain of ∆8-THC with
bulky adamantyl groups did not abolish binding affinity.
The 3-(1-adamantyl)-∆8-THC analogue 1a exhibited
robust affinity (6.8 nM) for CB1 exceeding that of ∆8-
THC and has significant CB1/CB2 selectivity. Con-
versely, the 3-(2-adamantyl)-∆8-THC analogue 1b is
more CB2-selective. When the 1-adamantyl group of 1a

Adamantyl Cannabinoids
Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14 4579
Figure 3. AM1 conformational search results for compounds 1d,e are illustrated here. All accessible conformers for each ligand
are shown superimposed at their aromatic rings and contoured at their van der Waals radii. (Top Row) For each conformer
superposition in this view, the aromatic ring has been turned perpendicular to the plane of the page with the adamantyl substituent
closest to the viewer and the carbocyclic ring furthest from the viewer. (Bottom Row) A bottom view of each conformer superposition
for compounds 1d,e is shown here. In this view, the aromatic ring of each conformer is oriented perpendicular to the plane of the
page, with the long axis of each molecule horizontal. C4 is closest to the viewer and the phenolic hydroxyl is furthest from the
viewer.
orientation the top face of the molecule is to the left of
the fused ring system and the bottom face is to the right
of the fused ring system. In the second representation
(shown at the bottom of Figures 2 and 3), the fused ring
structure is oriented along the horizontal direction and
perpendicular to the plane of the page such that the C1
phenolic hydroxyl is furthest from the viewer and C4 is
closest (see numbering system for ∆8-THC in Figure 1).
In this orientation, the top face of the molecule is above
the plane of the fused ring structure and the bottom
face is below the plane.
Experimental results reported in Table 1 indicate that
the change in the attachment point for C3 to the
adamantyl group from compound 1a to 1b resulted in
a shift from CB1 to CB2 selectivity. It is clear from
Figure 2 (1a and 1b) that the site of attachment for C3
to the adamantyl group has a significant effect on the
volume of space that the adamantyl group can occupy.
Attachment of C3 to a bridgehead position (C1′) on the
adamantyl group as in 1a resulted in the adamantyl
group orienting symmetrically such that the plane of
the aromatic A ring bisects the adamantyl group.
Attachment of C3 to a nonbridgehead atom (C2′) as in
1b resulted in the adamantyl group being able to occupy
more space clearly extending into the top and bottom
faces of the ligand.
It is clear from Figures 2 and 3 that the introduction
of a methylene spacer (C1′′) between C3 and the
adamantyl group in compounds 1c, 1d, and 1e also led
to the adamantyl group being able to occupy more
volume in the top and bottom faces of the molecules. In
compounds 1c and 1d, attachment of the adamantyl
group to the methylene spacer and C3 was via the
nonbridgehead C2′ position. Although rotation about the
C3-C1′′ bond was possible for both 1c and 1d, rotation
about the C1′′-C2′ bond was restricted for compound
1c due to the presence of the C1′′-C2′ double bond. As
is indicated in Table 1, this structural variation had a
profound effect on affinity, as 1c showed the highest
CB2 selectivity in the series and 1d exhibited the
poorest affinity (both for CB1 and CB2) in the series.
Compound 1e was the only compound for which several
conformers were above the 2.00 kcal/mol cutoff for
accessibility in this study. Conformers that placed the
adamantyl group in the plane of the fused ring system
(C2-C3-C1′′-C1′ ) -179.8° and 0.8°) were highest in
energy (3.48 and 3.63 kcal/mol, respectively).
Table 1 indicates that in the progression from 1a to
1b to 1c, CB2 selectivity increases. Modeling studies
indicate that the major change in going from 1a to 1b
to 1c is an ability to place the adamantyl group further
into the top and bottom faces of the molecules. This is
illustrated in Figure 2 by the wider arc in the form of a
donut transcribed by the adamantyl group in the
allowed conformers of each compound as one moves from
1a to 1b to 1c. On the other hand, the CB1 selectivity
of 1a can be associated with the conformationally
allowable space of the 1-adamantyl group represented
by the smaller symmetrical sphere attached to the C3
carbon of the tricyclic cannabinoid structure.
Unique Volume Map Calculations. When inter-
preted together with receptor binding data, our confor-
mational analysis results suggested that there is a
difference in the requirements for a C3 adamantyl group
interaction with the respective hydrophobic pockets
within CB1 or CB2. To illustrate the key conformational
differences between the CB1 selective 3-(1-adamantyl)-
THC 1a and the CB2 selective 3-(2-adamantylidene)-
methyl-THC 1c, we used a modification of the Active
Analog Approach30 to calculate the volume of space that
is unique to the CB2 selective analogue 1c using all
accessible conformers of 1a and 1c identified by AM1
Conformational Search calculations. In Figure 4a, the
global minimum energy conformer of 1a is shown in
green tube display and in the same orientation as shown
in the top row of Figure 2. The purple grid shows the
union of the van der Waals volume maps of all accessible
conformers of 1a superimposed at their aromatic rings.
The global minimum energy conformer of compound 1c
is illustrated in green tube display in Figures 4b and
4c. The yellow grid area in Figure 4b represents that
region of the van der Waals space of all conformers of

4580 Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14
Lu et al.
Figure 4. In each of the volume map calculations illustrated here, the view is such that the aromatic ring of subject molecules
has been turned perpendicular to the plane of the page with the adamantyl substituent closest to the viewer and the carbocyclic
ring furthest from the viewer. (a) This figure illustrates the union of the van der Waals volume of all accessible conformers of the
CB1 selective compound 1a (purple grid). The global minimum energy conformer of 1a is shown in green tube display here. (b)
This figure illustrates the Unique Volume Map calculated using all conformers of the CB1 selective compound 1a and of the CB2
selective compound 1c. The global minimum energy conformer of compound 1c is shown here in green tube display. The yellow
grid area shows the region of space into which conformers of 1c protrude that is not shared with the accessible conformers of 1a.
(c) This figure illustrates the Unique Volume Map calculated using all conformers of the CB2 selective compound 1c and of the
nonselective compound 1d. The global minimum energy conformer of 1c is shown here in green tube display. The red grid area
shows the region of space into which conformers of 1c protrude that is not shared with the accessible conformers of 1d.
1c that is not occupied by the conformers of 1a. This
Unique Volume Map provides an illustration of the
extent to which the adamantyl group can be placed
away from the plane of the aromatic ring in the most
CB2 selective analogue 1c. This map can be interpreted
as encompassing that region of space occupied by
adamantyl-THC analogues in order to selectively inter-
act with the CB2 receptor.
In compounds 1c and 1d, a methylene spacer is
located between C3 and the adamantyl group, and the
attachment of the adamantyl group to the methylene
spacer is via a nonbridgehead (C2′) position. Although
rotation about the C3-C1′′ bond is possible for both 1c
and 1d, rotation about the C1′′-C2′ bond in 1c is
restricted by the C1′′-C2′ double bond. The Unique
Volume Map illustrated in Figure 4c shows that region
of space (red grid) that is unique to the CB2 selective
compound 1c when compared to the nonselective com-
pound 1d. This map can also be interpreted to indicate
unique regions in both the top and bottom faces of the
molecule associated with favorable interaction with the
CB2 subsite for the side chain of this class of com-
pounds.
Figure 5. Thermal ellipsoid plot of 1a is shown with the
Crystal Structure of 3-(1-Adamantanyl)-6,6,9-
aromatic C ring facing the viewer (top) and with the aromatic
trimethyl-6a,7,10,10a-tetrahydro-6H-benzo[c]-
C ring perpendicular to the paper (bottom). Ellipsoids are at
the 30% probability level. Oxygen is shown in red color.
chromen-1-ol (1a). The three-dimensional structure of
1a (Figure 5) was determined by X-ray crystallography,
which showed a great deal of correspondence with the
computationally determined one. Detail of the structural
data is shown in the Experimental Section and with the
Supporting Information.
In the crystal structure, the pyran and the cyclohex-
ene rings exist in half-chair conformations, of which the
O(5)-C(4A)-C(10B)-C(10A)-C(6A) atoms are in a
slightly twisted plane, and C(6) is away from the plane
by about 24° (Figure 5, Table 2). The phenolic ring also
has a slight twist, with the adamantyl group bisecting
the aromatic ring.
affinities for CB1 and CB2 and cannot be considered
suitable models for the pharmacophoric requirements
at the CB1/CB2 sites. Conversely, compound 1a exhibits
high affinity for the CB1 receptor and high in vivo
potency. Therefore, the crystal structure of 1a may
provide the best available model for understanding
ligand interactions with the CB1 cannabinoid receptor.
In Vivo Cannabinergic Activity. We have tested
the in vivo cannabinergic properties of 1a in rats using
a drug discrimination assay as described earlier.33
Compound 1a was evaluated at three time intervals
after administration (30, 90, and 270 min post) in doses
ranging from 0.03 to 1.8 mg/kg. The ED50 values are
listed in Table 3. The outcome of the in vivo assay
suggested that 1a is a full agonist that is more potent
Prior to the determination of the crystal structure of
1a, the crystal structures of naturally occurring canna-
bidiol31 and ∆9-tetrahydrocannabinolic acid b32 were
reported. However, those two molecules have only weak

Adamantyl Cannabinoids
Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14 4581
inoid ∆8-THC in lieu of the native n-pentyl chain.
Testing of the five ligands included in this study for
their affinities for the CB1 and CB2 receptors revealed
that the bulky adamantyl group can easily be accom-
modated within the CB1 and CB2 binding sites. The
results also revealed that variations in the adamantyl
substituents can lead to higher affinities and selectivi-
ties for each of the two receptors depending on the
relative orientation of the adamantyl group with respect
to the tricyclic cannabinoid structure. Computational
modeling suggested that the differences in affinities and
selectivities can be explained on the basis of the allow-
able conformational space of each substituent.
Table 2. Some Torsion Angles [deg] for Crystalline 1a
atom and bond connectiona
torsion angles [deg]
O(5)-C(4A)-C(10B)-C(10A)
O(5)-C(4A)-C(10B)-C(1)
C(4A)-C(10B)-C(10A)-C(6A)
C(1)-C(10B)-C(10A)-C(6A)
C(4)-C(4A)-C(10B)-C(10A)
C(10B)-C(4A)-O(5)-C(6)
C(4)-C(4A)-O(5)-C(6)
3.1(2)
-175.61(13)
4.8(2)
-176.52(14)
-177.14 (15)
24.2(2)
-155.58(13)
6.4(3)
C(7)-C(8)-C(9)-C(10)
C(8)-C(9)-C(10)-C(10A)
C(10B)-C(10A)-C(10)-C(9)
C(6A)-C(10A)-C(10)-C(9)
C(4A)-C(10B)-C(10A)-C(6A)
C(4A)-C(10B)-C(10A)-C(10)
10.1(2)
-168.92(13)
-45.85(17)
4.8(2)
126.48(16)
The 3-(1-adamantyl) group of the CB1 selective
analogue 1a orients within a compact spherical space
in the direct proximity of the tricyclic ring. Conversely,
in the CB2 selective analogues 1b and 1c, the allowable
adamantyl group conformations exist within a donut
like space that extends beyond that of the spherical
conformational space of 1a. Finally, ligands capable of
occupying both spaces (1d, 1e) exhibit no CB1/CB2
selectivity. The crystal structure of our lead compound
1a was compatible with the computationally determined
3D-structure. Compound 1a was shown to be a long
acting CB1 receptor agonist. Coupled with its favorable
physical properties, the compound’s potency and selec-
tivity support its potential as a useful pharmacological
lead.
a The atom numbering system is illustrated in Figure 5.
Complete data of torsion angles are available in Supporting
Information.
Table 3. Drug Discrimination Test with 1aa
drug
time (h)
ED50 (mg/kg)
∆9-THC
1a
0.5
0.5
1.5
4.5
1.16 (0.73-1.58)
0.68 (0.47-0.90)
0.44 (0.06-0.82)
0.41 (0.09-0.72)
1a
1a
a ED50 values (( 95% C.L.) for 1a and ∆9-THC for animals
trained to discriminate between 3 mg/kg ∆9-THC and vehicle,
injected ip 30 min prior to training session onset. The doses
examined were: 1a (0.03, 0.1, 0.3, 0.56, 1, and 1.8 mg/kg);
∆9-THC (0.1, 0.3, 1, 1.8, and 3 mg/kg).
than ∆9-THC in this assay, with perhaps a slower onset
time and a longer duration of action as compared to
∆9-THC.34,35 Figure 6 shows that the CB1-selective
Experimental Section
Chemistry. (+)-cis/trans-p-Mentha-2,8-dien-1-ol was sup-
plied by Firmenich Inc., Princeton, NJ. All other reagents and
solvents were purchased from Aldrich, Milwaukee, WI, unless
specified otherwise and were used without further purification.
All anhydrous reactions were performed under a static argon
or nitrogen atmosphere in flame-dried glassware using scru-
pulously dry solvents. Organic phases were dried over Na2-
SO4 and rotary evaporated under reduced pressure, and flash
column chromatography employed silica gel 60 (230-400
mesh, Selecto Scientific Inc., Suwanee, GA). All compounds
were demonstrated to be homogeneous by analytical thin-layer
chromatography (TLC) on precoated silica gel TLC aluminum
plates (Whatman, UV254, layer thickness 250 µm), and chro-
matograms were visualized under ultraviolet light or by
phosphomolybdic acid straining. Melting points were deter-
mined on a capillary Electrothermal melting point apparatus
and are uncorrected. 1H NMR spectra were recorded on a
Bruker DMX-500 spectrometer operating at 500 MHz. All
NMR spectra were recorded using CDCl3 as solvent unless
otherwise stated and chemical shifts are reported in ppm
(parts per million) relative to tetramethylsilane as internal
standard. Multiplicities are indicated as br (broadened), s
(singlet), d (doublet), t (triplet), q (quartet), m (multiplet), bs
(broadened singlet), and coupling constants (J) are reported
in hertz (Hz). Low- and high-resolution mass spectra were
performed at the School of Chemical Sciences, University of
Illinois at Urbana-Champaign, or were recorded on a Hewlett-
Packard 6890 GC/MS instrument at the School of Pharmacy,
University of Connecticut. Elemental analyses were obtained
at Baron Consulting Co., Milford, CT.
Figure 6. Generalization test results for 1a alone and in
combination with SR141716A at three postinjection intervals
for rats trained to discriminate between 3 mg/kg ∆9-THC and
vehicle (n ) 8). The generalization test results represent the
mean percentage of lever presses on the ∆9-THC appropriate
lever out of the total number of lever presses emitted during
a six trial test probe (Y-axis); time in hours since injection
(X-axis).
antagonist SR141716A36 (1 mg/kg) antagonized the
discriminative stimulus effects of 1.8 mg/kg 1a 30 min
postinjection. The antagonism was reduced at 1.5 and
4.5 h post administration. A two-way repeated ANOVA
indicated no significant Dose × Time interaction [F )
6.88 (2, 14); p ) 0.052] with regard to the rate of
responding (responses/second) associated with the tests
evaluating antagonism of 1a by SR141716A.
General Procedure A: Preparation of 5-Alkylresorci-
nols (2a-e) from 5-Alkyl-1,3-dimethoxybenzenes (3a-e).
4.1 mL of 1.0 M boron tribromide in dichloromethane was
added dropwise to a stirred solution of 2.0 mmol of 5-alkyl-
1,3-dimethoxybenzene in 20 mL of dichloromethane at 0 °C.
The reaction mixture was then stirred at 0 °C for 2 h and
allowed to warm to room temperature over a period of time
ranging between 6 h to 16 h. Upon completion, the reaction
mixture was cooled in an ice bath and cold water was added
cautiously. The organic layer was separated and washed with
Summary
Our study focused on introducing bulky adamantyl
substituents in the 3-position of the classical cannab-

4582 Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14
Lu et al.
H2O, brine, and dried. Filtration, solvent removal, and puri-
fication by flash column chromatography (33% acetone-
petroleum ether) provided 5-alkylresorcinol in a yield of 85 to
95%.
1.84, d, J ) 2.0 Hz, 6H), 1.80-1.69 (m, 10H), 1.38 (s, 3H), 1.11
(s, 3H); MS m/z 378 (M+). Anal. (C26H34O2) C, H.
1-Bromo-3,5-dimethoxybenzene (6). 7.4 g (107 mmol) of
sodium nitrate in 15 mL of distilled water was added in small
portions to a solution of 10.0 g (65.3 mmol) 3,5-dimethoxya-
niline in 30 mL of 48% hydrobromic acid at 0 °C until the
stable presence of diazonium salt was observed with starch-
potassium iodide test paper. In the meantime, a mixture of
5.2 g (36 mmol) of cuprous bromide in 5.2 mL of 48%
hydrobromic acid was heated to boiling in another flask. The
prepared diazonium salt solution was added in small portions
to the cuprous bromide-hydrobromic acid solution, which was
maintained at its boiling point. After the addition, the total
reaction mixture was stirred and heated for an additional 30
min, and the resulting crude product was purified by steam
distillation. 7.84 g of 6 was collected in 55.8% yield as a white
General Procedure B: Synthesis of (-)-3-Alkyl-∆8-
tetrahydrocannabinol (1a-e). A mixture of 1.0 mmol of
the 5-alkylresorcinol, 1.1 mmol of (+)-cis/trans-p-mentha-2,8-
dien-1-ol and 0.1 mmol of p-toluenesulfonic acid monohydrate
in 5-10 mL of anhydrous chloroform was stirred and heated
at 65 °C for 6 h. Upon completion, the reaction mixture was
cooled and diluted with 10 mL of dichloromethane and stirred
with 10 mL of saturated aqueous NaHCO3 solution for 15 min.
The organic layer was then separated and washed with H2O,
brine, and dried over Na2SO4. Filtration, concentration and
purification by flash column chromatography (10% ethyl
acetate-petroleum ether) provided the 3-alkyl-∆8-tetrahydro-
cannabinol in a yield of 43 to 84%.
1
solid, mp 63-64 °C; H NMR δ 6.67 (d, J ) 2.0 Hz, 2H), 6.39
(t, J ) 2.0 Hz, 1H), 3.78 (s, 6H); MS m/z 216, 218 (M+).
4-(1-Adamantanyl)-2,6-dimethoxyphenol (4). A mixture
of 5.0 g (32 mmol) of 2,6-dimethoxyphenol and 5.0 g (33 mmol)
of 1-adamantanol in 15 mL of 99% methanesulfonic acid was
stirred at 80 °C for 3 h and then at room temperature
overnight. The reaction mixture was poured onto ice and water
and then extracted with dichloromethane. The extract was
washed with H2O, saturated aqueous NaHCO3, H2O, brine,
and dried over Na2SO4. Evaporation of solvent followed by
flash column chromatography (30% acetone-petroleum ether)
provided 6.0 g of 4 in 64% yield as a white solid, mp 111-112
5-(2-Hydroxy-2-adamantyl)-1,3-dimethoxybenzene (7).
A solution of 690 mg (4.6 mmol) of 2-adamantanone in 10 mL
of anhydrous THF was added dropwise to a THF solution of
20 mmol of Grignard reagent prepared from 1.0 g (4.6 mmol)
of 1-bromo-3,5-dimethoxybenzene 6 and 110 mg (4.6 mmol) of
magnesium chips. The reaction mixture was stirred and heated
in a 90 °C oil bath for 2 h and then treated with 20 mL of
saturated aqueous NH4Cl at room temperature with stirring.
THF was then removed and the residue was extracted with
ether. The ether layer was separated and washed with H2O,
brine, and dried. Filtration, removal of solvent, and purifica-
tion by flash column chromatography (30% acetone-petroleum
ether) afforded 830 mg of 7 in 63.6% yield as a white solid,
1
°C; H NMR δ 6.59 (s, 2H), 5.39 (s, 1H), 3.90 (s, 6H), 2.09 (br
s, 3H), 1.89 (d, J ) 2.2 Hz, 6H), 1.79 (d, J ) 12.2 Hz, 3H),
1.77 (d, J ) 12.2 Hz, 3H); MS m/z 288 (M+).
4-(1-Adamantanyl)-2,6-dimethoxyphenyl Diethyl Phos-
phate (5). To a solution of 5.5 g (19 mmol) of 4 in 30 mL of
freshly distilled CCl4 was added 3.1 g (22 mmol) of diethyl
phosphonate at 0 °C followed by dropwise addition of 3 mL of
triethylamine. The mixture was stirred at 0 °C for 1 h and
then at room temperature overnight. The mixture was diluted
with 70 mL of dichloromethane, washed with H2O, 4 N NaOH,
H2O, 1 N HCl, H2O, brine, and dried. Removal of solvent and
purification using flash column chromatography (25% acetone-
petroleum ether) afforded 7.8 g of 5 in 96.8% yield as a white
solid, mp 78-80 °C; 1H NMR (CDCl3) δ 6.58 (s, 2H), 4.34-
4.22 (m, especially two q, J ) 8.5 Hz, 4H), 3.86 (s, 3H), 3.85
(s, 3H) 2.09 (br s, 3H), 1.87 (bs, 6H), 1.80 (d, J ) 13.7 Hz, 3H),
1.76 (d, J ) 13.7 Hz, 3H), 1.42-1.34 (m, especially two t, J )
6.8 Hz, 6H); MS m/z 424 (M+).
1
mp 104-105 °C; H NMR δ 6.70 (d, J ) 2.2 Hz, 2H), 6.39 (t,
J ) 2.2 Hz, 1H), 3.80 (s, 6H), 2.48 (bs, 2H), 2.39-2.37 (m, 2H),
1.89 (bs, 1H) 1.73-1.70 (m, 8H), 1.53 (bs, 2H); MS m/z 288
(M+).
5-(2-Adamantyl)-1,3-dimethoxybenzene (3b). A solution
of 600 mg (2 mmol) of 7 in 6 mL of anhydrous THF was added
dropwise to a flask containing a mixture of 120 mg of lithium
and 16 mL of liquid NH3 at -60 °C. The reaction mixture was
stirred vigorously for 2 h at -60 °C. The reaction was warmed
to room temperature, and then quenched by the addition of
480 mg of NH4Cl powder. Then, 25 mL of ether was added to
the reaction mixture to extract the product. After the NH3 had
evaporated, the ether solution was separated and washed with
H2O, brine, and dried. Filtration, solvent removal and purifica-
tion by flash column chromatography (10% acetone-petroleum
ether) afforded 420 mg of 3b in 78% yield as a white solid, mp
72-73 °C; 1H NMR δ 6.52 (d, J ) 2.0 Hz, 2H), 6.30 (t, J ) 2.0
Hz, 1H), 3.79 (s, 6H), 2.93 (s, 1H), 2.41 (bs, 2H), 2.00-1.85
(m, 7H), 1.76 (m, 3H), 1.56 (d, J ) 8.5 Hz, 2H); MS m/z 272
(M+).
5-(1-Adamantyl)-1,3-dimethoxybenzene (3a). A solution
of 7.8 g (18.4 mmol) of 5 in 20 mL of Et2O and 4 mL of THF
was added dropwise to 50 mL of liquid NH3 at -78 °C as a
total 0.3 g of Li metal was added at a rate to maintain a blue
color solution. After 1 h, excess Li was treated with NH4Cl
powder, and 100 mL of water-saturated Et2O was added
cautiously. The mixture was brought up to room temperature,
and the residual liquid NH3 was allowed to evaporate. The
residual mixture was washed with H2O, 4 N NaOH, H2O,
brine, and dried. Removal of solvent afforded 3.90 g of a yellow
oil which upon chromatographic purification gave 3.62 g of 3a
5-(2-Adamantanyl)resorcinol (2b). 330 mg of 2b was
prepared from 400 mg of 3b following general procedure A in
92% yield as a white solid, mp 159-160 °C; 1H NMR (CD3-
COCD3) δ 7.97 (s, 2H), 6.36 (d, J ) 2.0 Hz, 2H), 6.18 (t, J )
2.0 Hz, 1H), 2.83 (s, 1H), 2.35 (bs, 2H), 2.05-1.87 (m, 7H),
1.77 (bs, 3H), 1.56 (d, J ) 12.5 Hz, 2H); MS m/z 244 (M+).
1
in 70% yield as a white solid, mp 47-48 °C; H NMR δ 6.55
(d, J ) 2.3 Hz, 2H), 6.30 (t, J ) 2.3 Hz, 1H), 3.79 (s, 6H), 2.10
(br s, 3H), 1.90 (d, J ) 2.6 Hz, 6H), 1.81 (d, J ) 12.5 Hz, 3H),
1.77 (d, J ) 12.5 Hz, 3H); MS m/z 272 (M+).
3-(2-Adamantanyl)-6,6,9-trimethyl-6a,7,10,10a-tetrahy-
dro-6H-benzo[c]chromen-1-ol (1b). 55 mg of 1b was pre-
pared from 80 mg of 2b following general procedure B in 48.5%
yield as a white solid, mp 103-105 °C; 1H NMR δ 6.43 (d, J )
2.1 Hz, 1H), 6.25 (d, J ) 2.1 Hz, 1H), 5.42 (d, J ) 4.0 Hz, 1H),
4.67 (s, 1H), 3.20 (dd, J ) 16.5, J ) 4.0 Hz, 1H), 2.84 (s, 1H),
2.70 (m, 1H), 2.34 (br d, J ) 6 Hz, 2H), 2.15 (m, 1H), 1.96-
1.74 (m, 13H), 1.70 (s, 3H), 1.52 (m, 2H), 1.38 (s, 3H), 1.15 (s,
3H); MS m/z 378 (M+). Anal. (C26H34O2) C, H.
5-(1-Adamantanyl)resorcinol (2a). 2.7 g of 2a was pre-
pared from 3.6 g (13.3 mmol) of 3a following general procedure
1
A in 85% yield as a white solid, mp 186-188 °C; H NMR δ
6.42 (d, J ) 2.1 Hz, 2H), 6.18 (t, J ) 2.1 Hz, 1H), 5.40 (s, 2H),
2.07 (bs, 3H), 1.85 (d, J ) 2.4 Hz, 6H), 1.79 (d, J ) 12.3 Hz,
3H), 1.74 (d, J ) 12.3 Hz, 3H); MS m/z 244 (M+).
3-(1-Adamantanyl)-6,6,9-trimethyl-6a,7,10,10a-tetrahy-
dro-6H-benzo[c]chromen-1-ol (1a). 3.0 g of 1a was prepared
from 2.3 g (9.4 mmol) of 2a following general procedure B in
5-(2-Hydroxy-2-adamantyl)methyl-1,3-dimethoxyben-
zenene (8). A solution of 2.72 g (18 mmol) 2-adamantanone
in 15 mL of anhydrous ether was added dropwise to an ether
solution of 20 mmol of Grignard reagent prepared from 3.72 g
(20 mmol) of 3,5-dimethoxybenzyl chloride and 0.5 g (20.8
mmol) of magnesium chips. The reaction mixture was stirred
for 1 h, and then quenched with 15 mL of saturated aqueous
NH4Cl. The ether layer was separated and washed with H2O,
1
84% yield as a white solid, mp 205-206 °C; H NMR δ 6.43
(d, J ) 1.5 Hz, 1H), 6.27 (d, J ) 1.5 Hz, 1H), 5.42 (d, J ) 3.65
Hz, 1H), 4.84 (s 1H), 3.20 (dd, J ) 17.0 Hz, J ) 4 Hz, 1H),
2.70 (dt, J ) 11 Hz, J ) 5.0 Hz, 1H), 2.13 (dd, J ) 13.0 Hz, J
) 5.0 Hz, 1H), 2.04 (br s, 3H), 1.86-1.82 (m, 8H, especially

Adamantyl Cannabinoids
Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14 4583
brine, and dried. Filtration, removal of solvent and purification
by flash column chromatography (30% acetone-petroleum
ether) afforded 4.30 g of 8 in 79.7% yield as a white solid, mp
75-77 °C; 1H NMR δ 6.40 (d, J ) 2.2 Hz, 2H), 6.37 (t, J ) 2.2
Hz, 1H), 3.78 (s, 6H), 2.94 (s, 2H), 2.17-2.03 (m, 4H), 1.92
(bs, 1H), 1.81-1.70 (m, 6H), 1.59-1.52 (m, 4H); MS m/e 284
(M+-H2O).
solvent removal and purification by flash column chromatog-
raphy (10% acetone-petroleum ether) afforded 210 mg of 3e
1
in 24% yield as colorless oil; H NMR δ 6.33 (t, J ) 2.1 Hz,
1H), 6.25 (d, J ) 2.1 Hz, 2H), 3.78 (s, 6H), 2.31 (s, 2H), 1.93
(bs, 3H), 1.67-1.64 (m, 2H), 1.58-1.55 (m, 4H), 1.49 (bs, 6H);
MS m/z 286 (M+).
5-(1-Adamantyl)methylresorcinol (2e). 150 mg of 2e was
prepared from 190 mg of 3e following general procedure A in
89.3% yield as a white solid, mp 163-164 °C; 1H NMR δ 6.20
(t, J ) 1.6 Hz, 1H), 6.15 (d, J ) 1.6 Hz, 2H), 4.72 (bs, 2H),
2.25 (bs, 2H), 1.92 (bs, 3H), 1.67-1.55 (m, 6H), 1.47 (bs, 6H);
MS m/z 258 (M+).
5-(2-Adamantylidene)methyl-1,3-dimethoxybenzene
(3c). A mixture of 2.0 g of 8 and 0.2 g of p-toluenesulfonic acid
monohydrate in 20 mL of dichloromethane was stirred and
heated at 45 °C overnight. The reaction mixture was then
treated with 10% aqueous NaHCO3 solution. The organic layer
was separated and washed with H2O, brine, and dried.
Filtration, concentration and purification by flash column
chromatography (15% acetone-petroleum ether) afforded 1.70
3-(1-Adamantyl)methyl-6,6,9-trimethyl-6a,7,10,10a-tet-
rahydro-6H-benzo[c]chromen-1-ol (1e). 85 mg of 1e was
prepared from 130 mg of 2e following the general procedure
1
1
g of 3c in 83% yield as a white solid, mp 51-52 °C; H NMR
B in 43.4% yield as a white solid, mp 84-85 °C; H NMR δ
δ 6.37 (d, J ) 1.8 Hz, 2H), 6.32 (t, J ) 1.8 Hz, 1H), 6.12 (s,
1H), 3.78 (s, 6H), 3.18 (bs, 1H), 2.47 (br s, 1H), 1.99-1.85 (m,
12H); MS m/z 284 (M+).
6.17 (d, J ) 1.5 Hz, 1H), 6.01 (d, J ) 1.5 Hz, 1H), 5.42 (d, J )
4.2 Hz, 1H), 4.64 (bs, 1H), 3.20 (dd, J ) 17.0 Hz, J ) 3.5 Hz,
1H), 2.70 (dt, J ) 10.5, J ) 4.5 Hz, 1H), 2.23 (d, J ) 12.5 Hz,
1H), 2.18 (d, J ) 12.5 Hz, 1H), 2.17-2.12 (m, 1H), 1.92 (bs,
3H), 1.82 (m, 2H), 1.70 (s, 3H), 1.64 (br d, J ) 12.5 Hz, 3H),
1.58 (br d, J ) 12.5 Hz, 3H), 1.50 (m, 1H), 1.47 (bs, 6H), 1.37
(s, 3H), 1.10 (s, 3H); MS m/z 392 (M+). Anal. (C27H36O2‚1/2H2O)
C, H.
5-(2-Adamantylidene)methylresorcinol (2c). 320 mg of
2c was prepared from 400 mg of 3c following general procedure
A in 88% yield as a white solid, mp 144-146 °C; 1H NMR (CD3-
COCD3) δ 8.07 (bs, 2H), 6.21 (d, J ) 1.8 Hz, 2H), 6.20 (t, J )
1.8 Hz, 1H), 6.06 (s, 1H), 3.20 (bs, 1H), 2.44 (bs, 1H), 1.97-
1.79 (m, 12H); MS m/z 256 (M+).
Radioligand Binding Assay. Forebrain synaptosomal
membranes were prepared from frozen rat brains by the
method of Dodd et al.27 and were used to assess the affinities
of the novel analogues for the CB1 binding sites, while
affinities for the CB2 sites were measured using a membrane
preparation from frozen mouse spleen using a similar proce-
dure.28 The displacement of specifically tritiated CP-55,940
from these membranes was used to determine the IC50 values
for the test compounds. The assay was conducted in a 96-well
microfilter plate. The samples were filtered using a Packard
Filtermate Harvester and Whatman GF/B unifilter-96 plates,
and 0.5% BSA was incorporated into the wash buffer. Radio-
activity was detected using MicroScint 20 scintillation cocktail
added to the dried filter plates and was counted using a
Packard Instruments Top Count. Data were collected from
three independent experiments between 100% and 0% specific
binding for [3H]CP-55,940, determined using 0 and 100 nM
CP-55,940. The normalized data from three independent
experiments were combined and analyzed using a four-
parameter logistic equation to yield IC50 values which were
converted to Ki values using the assumptions of Cheng and
Prusoff.29
Computational Study. Conformational Analyses. The
structures of 1a-e were built in the Spartan molecular
modeling program (V4.1.1; Wavefunction, Inc., Irvine, CA)
initially in the global minimum energy conformation of (-)-
∆8-THC.37 Each structure was then energy minimized using
the AM1 semiempirical method as encoded in Spartan. AM1
conformational searches were performed for each side chain
rotateable bond. This search included a 12-fold rotation about
the C3-C1′ bond for 1a, the C3-C2′ bond for 1b, and the C3-
C1′′ bond for 1c. For 1d and 1e, 12-fold rotations were
performed about the C3-C1′′ bond and about the C1′′-C2′
bond in 1d and the C1′′-C1′ bond in 1e. The results of these
conformational searches were used to identify the global
minimum energy conformer of each compound and to deter-
mine the energy separation between the global minimum
energy conformer and other minimum energy conformers
identified by the AM1 conformational analysis. For each
compound, conformers were considered accessible at biological
temperature if their energies were less than 2.0 kcal/mol above
the global minimum energy. Conformational analysis results
are graphically represented in Figures 2 and 3.
3-(2-Adamantylidene)methyl-6,6,9-trimethyl-6a,7,10,-
10a-tetrahydro-6H-benzo[c]chromen-1-ol (1c). 120 mg of
1c was prepared from 144 mg of 2c following general procedure
B in 40% yield as a white solid, mp 98-100 °C; 1H NMR δ
6.30 (d, J ) 1.3 Hz, 1H), 6.12 (d, J ) 1.3 Hz, 1H), 5.99 (s, 1H),
5.43 (br d, J ) 4.5 Hz, 1H), 4.70 (s, 1H), 3.23 (bs, 1H), 3.18
(dd, J ) 16.5, J ) 4.5 Hz, 1H), 2.71 (td, 1H), 2.43 (bs, 1H),
2.14 (m, 1H), 1.98-1.79 (m, 15H), 1.76 (s, 3H), 1.37 (s, 3H),
1.10 (s, 3H); MS m/z 390 (M+). Anal. (C27H34O2‚H2O) C, H.
5-(2-Adamantyl)methyl-1,3-dimethoxybenzene (3d). A
mixture of 800 mg 3c and 100 mg of 10% Pd-C in 25 mL of
anhydrous ethanol was hydrogenated on Parr hydrogenation
shaker at 45 psi. Upon completion of hydrogenation, filtration
of palladium catalyst, and solvent removal, 785 mg of 3d was
collected in a yield of 98% as a low melting point solid, mp
31-32 °C; 1H NMR δ 6.34 (d, J ) 2.2 Hz, 2H), 6.29 (t, J ) 2.2
Hz, 1H), 3.77 (s, 6H), 2.67 (d, J ) 7.5 Hz, 2H), 1.99 (d, J )
12.0 Hz, 2H), 1.93 (t, J ) 8.0 Hz, 1H), 1.85-1.79 (m, 4H), 1.72-
1.67 (m, 6H), 1.56 (d, J ) 12.0 Hz, 2H); MS m/z 286 (M+).
5-(2-Adamantyl)methylresorcinol (2d). 370 mg of 2d
was prepared from 520 mg of 3d following general procedure
A in 79% yield as white solid, mp 147-149 °C; 1H NMR δ 6.12
(d, J ) 1.5 Hz, 2H), 6.07 (t, J ) 1.5 Hz, 1H), 2.59 (d, J ) 8.0
Hz, 2H), 2.06 (d, J ) 12.5 Hz, 2H), 1.91 (t, J ) 7.8 Hz, 1H),
1.86-1.84 (m, 4H), 1.76-1.71 (m, 4H), 1.65 (bs, 2H), 1.57 (d,
J ) 12.5 Hz, 2H); MS m/z 258 (M+).
3-(2-Adamantyl)methyl-6,6,9-trimethyl-6a,7,10,10a-tet-
rahydro-6H-benzo[c]chromen-1-ol (1d). 300 mg of 1d was
prepared from 341 mg of 2d following general procedure B in
1
57% yield as a white solid, mp 94-96 °C; H NMR δ 6.25 (d,
J ) 2.4 Hz, 1H), 6.09 (d, J ) 2.4 Hz, 1H), 5.42 (d, J ) 4.3 Hz,
1H), 4.65 (s, 1H), 3.19 (dd, J ) 16.5, J ) 4.0 Hz, 1H), 2.68 (td,
J ) 10.6, J ) 4.6 Hz, 1H), 2.56 (m, 2H), 2.13 (m, 1H), 1.98 (d,
J ) 12.5 Hz, 1H), 1.95 (t, J ) 7.5 Hz, 1H), 1.91-1.78 (m, 8H),
1.71-1.67 (m, 9H, especially 1.69, s, CH3), 1.53 (br d, J ) 12.5
Hz, 2H), 1.37 (s, 3H), 1.10 (s, 3H); MS m/z 392 (M+). Anal.
(C27H36O2) C, H.
5-(1-Adamantyl)methyl-1,3-dimethoxybenzene (3e). A
solution of 645 mg (3 mmol) of 1-bromoadamantane in 15 mL
of anhydrous ether was added dropwise to a 20 mL ether
solution of Grignard reagent prepared from 560 mg (3 mmol)
of 3,5-dimethoxybenzyl chloride and 77 mg (3.2 mmol) of
magnesium chips. The reaction mixture was stirred and
refluxed for 3 h. Then, the ether was gradually removed with
an argon gas stream, and the highly concentrated residue was
heated at 90 °C for 8 h. The reaction mixture was then treated
with 15 mL of saturated aqueous NH4Cl solution at room
temperature and extracted with ether. The ether layer was
separated, washed with H2O, brine, and dried. Filtration,
Unique Volume Map Calculation. To illustrate the key
conformational differences between the CB1 selective 3-(1-
adamantyl)-THC 1a and the CB2 selective 3-(2-adamantyl)-
methyl-THC 1c, we used a modification of the Active Analog
Approach30 to calculate the volume of space that is unique to
the CB2 selective analogue 1c. All accessible conformers
identified for 1a and 1c were superimposed at their aromatic

4584 Journal of Medicinal Chemistry, 2005, Vol. 48, No. 14
Lu et al.
rings. Using the DEF MAP, SET MAP, and COMBINE MAP
facilities within the Chem-X molecular modeling suite of
programs (v2000.1; Oxford Molecular, Inc.) and a density of 4
points per Å, the van der Waals (VdW's) volume map of each
of the conformers identified for 1a and for 1c was calculated.
The UNION of the VdW’s volume maps of the CB1-selective
compound 1a was calculated and is illustrated as a purple grid
in Figure 4a. Similarly, the UNION of the VdW’s volume maps
of the CB2-selective compound 1c was calculated. Using a
logical NOT operation, the region of space that the conformers
of 1c did not share with that of 1a was then calculated. This
Unique Volume Map is illustrated as a yellow grid in Figure
4b. A similar protocol was followed to calculate the volume
unique to the CB2 selective compound 1c relative to the
nonselective compound 1d (red grid, Figure 4c).
Crystallography of 3-(1-Adamantanyl)-6,6,9-trimethyl-
6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-ol (1a). The
molecular formula of 1a is C26H34O2, and the formula weight
is 378.55. An irregular colorless crystal of 1a with dimensions
0.11 × 0.34 × 0.42 mm2 was grown from a two-phase solvent
system (hexane (top) and dichloromethane (bottom)). Crystal-
lographic data were collected on a Bruker three-circle platform
diffractometer equipped with a SMART 1000 CCD detector.
The crystals were irradiated using graphite monochromated
Mo KR radiation (λ ) 0.71073). An MSC X-Stream low-
temperature device was used to keep the crystals at a constant
-180 °C during data collection. Data collection was performed
and the unit cell was initially refined using SMART v5.625
(Bruker 2001a, SMART v5.625. Bruker AXS Inc., Madison,
WI). Data reduction was performed using SAINT v6.26A
(Bruker, 2002, SAINT v6.26A. Bruker AXS Inc., Madison, WI)
and XPREP v6.12 (Bruker, 2001b, XPREP v6.12. Bruker AXS
Inc., Madison, WI). Corrections were applied for Lorentz,
polarization, and absorption effects using SADABS v2.03
(Bruker, 2000, SADABS v2.03, Bruker AXS Inc., Madison, WI).
The structure was solved and refined with the aid of the
programs in the SHELXTL-plus v6.12 system of programs
(Bruker, 2000, SHELXTL v6.12. Bruker AXS Inc., Madison,
WI). The full-matrix least-squares refinement on F2 included
atomic coordinates and anisotropic thermal parameters for all
non-H atoms. The H atoms were included using a riding model.
The crystal of 1a was orthorhombic and space group P212121
with cell dimensions: a ) 11.863(5) Å, b ) 13.186(6) Å, c )
13.788(6) Å, and volume of 2157.0(17) Å3, Z ) 4. Calculated
density was 1.166 mg/mm3. Absorption coefficient was 0.071
mm-1. Final R indices were 0.0437 for 4321 observed (I > 2σI)
reflections and 0.0547 for all 4996 reflections. Goodness-of-fit
equals to 1.017, 256 parameters. Complete data for bond
lengths and angles are available in the Supporting Information.
or vehicle (N) administrations was nonsystematic, with no
more than two consecutive D or N trials. There was ap-
proximately an equal number of D and N training sessions
throughout the study. To avoid the influence of odor cues left
in a chamber by a preceding subject,38 the order in which D
and N training sessions were conducted for animals trained
in the same chamber was randomized. Training sessions were
conducted Monday through Friday and lasted 20 min. Training
continued until animals reached the acquisition criterion of
selecting the injection-appropriate (D or N) lever on at least 8
out of 10 consecutive training days. Correct selection was
defined as total presses before the first reinforcement being
equal or less than 14 (i.e., an animal did not press the wrong
lever more than 4 times before pressing 10 times on the
appropriate lever).
Testing. After animals reached acquisition criterion, test
sessions were conducted on average 3 times every two weeks;
on interim days, training sessions were conducted. A drug
training session preceded half the test sessions; the other half
was preceded by a vehicle session. Tests were conducted only
if responding during the preceding training sessions had been
correct. During testing, animals were reinforced for 10 presses
on either lever until 20 min had elapsed or 6 reinforcers had
been delivered, whichever occurred first. A repeated tests
procedure34,35 was used to assess the time course of 1a. Thus,
rats were injected with a specified dose of 1a and first put
into the experimental chamber 30 min postadministration with
above-described reinforcement contingencies in effect. The
second test took place 90 min post, and the third (final) test
occurred 270 min after administration. Between these trials
animals waited in their respective home cages. Doses were
examined in a mixed order. Each dose of ∆9-THC was
examined once (30 min post). For each dose tested, the
percentage of responding on the drug-appropriate lever was
calculated from the ratio of the number of presses on the ∆9-
THC-associated lever to the total number of lever presses in
a test session. Additionally, response rate (responses per
second) was calculated and analyzed with two-way repeated
analysis of variance (ANOVA; Sigma Stat., V, 3; SPSS,
Chicago, IL). Nonlinear regression analysis of dose-generaliza-
tion data was performed using Prism 3 software (GraphPad
Software, San Diego, CA) to provide ED50 ((95% confidence
limits, 95% C.L.).
Drugs. (-)-∆9-THC, dissolved in ethanol (200 mg/mL), was
kindly provided by NIDA (batch 7074-91) and stored at -20
°C until used. Upon arrival, 1a was also dissolved in ethanol,
appropriate amounts were withdrawn, the ethanol was evapo-
rated under a stream of nitrogen, and the residue was then
dissolved in a solution of 5% propylene glycol and 3% Tween-
80 and stored at -20 °C. Shortly before being used, the solute
was diluted with normal (0.9%) saline after the solute had been
sonicated for 20-30 min. This procedure was followed for
preparing suspensions of ∆9-THC as well. SR141716A (Sanofi
Recherche´, France) was stored at room temperature in crystal-
line form and dissolved in the propylene glycol/Tween-80 (5%/
3%) mixture before being diluted with saline (92%). Drugs were
administered ip 2 mL/kg.
Methods for in Vivo Study of Compound 1a. Ap-
paratus. Drug discrimination training and testing were
conducted in 8 operant chambers (ENV-001, Med. Associates,
St Albans/Georgia, VT), constructed of Plexiglas and alumi-
num, equipped with two response levers, house and lever
lights, and a grid floor. Each chamber was enclosed within
sound- and light-attenuating boxes equipped with an exhaust
fan. These chambers were connected to an IBM-compatible PC.
Animals. Adult male Sprague-Dawley rats (n ) 8; Taconic
Farms, Germantown, NY) were individually housed in a colony
room with an average temperature of 20 °C and a 12-h light/
dark cycle (rats were trained and tested during the light
phase). Purina Rat Chow was restricted to approximately 12
g/day, thus maintaining body weights between 330 and 400 g.
Training. Rats were magazine trained, and shaped to lever
press for food reinforcement until they responded 10 times for
each reinforcer (FR 10). Each reinforcement consisted of two
45 mg Noyes pellets. The rats were then trained in a two-choice
task to respond on drug- or vehicle-appropriate levers once
daily. The position of drug-appropriate levers was randomly
assigned among subjects so that it was to the right of the food
cup for half the subjects. Animals were administered 3 mg/kg
∆9-THC or vehicle (2 mL/kg) intraperitoneally 30 min before
session onset. Presses on the wrong lever were recorded, but
had no programmed consequences. The schedule of drug (D)
Acknowledgment. This work was supported by
grants from the National Institute on Drug Abuse
DA03801, DA09158, and DA07215 (Northeastern Uni-
versity), and DA09064 and DA00253 (Temple Univer-
sity). We are grateful to Richard Duclos for assistance
with the manuscript.
Supporting Information Available: Crystal structure
data for analogue 1a, detailed conformational analysis results
for compounds 1a-e, and elemental analysis results for
compounds 1a-e. This material is available free of charge via
the Internet at http://pubs.acs.org.
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