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The title compound [MOM-SalB; systematic name: methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-2-(3-fur­yl)-9-meth­oxy­meth­oxy-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octa­hydro-1H-benzo[f]isochromene-7-carboxyl­ate], C23H30O8, is a deriv­ative of the κ-opioid salvinorin A with enhanced potency, selectivity, and duration of action. Superimposition of their crystal structures reveals, surprisingly, that the terminal C and O atoms of the MOM group overlap with the corresponding atoms in salvinorin A, which are separated by an additional bond. This counter-intuitive isosterism is possible because the MOM ether adopts the `classic anomeric' conformation (gauchegauche), tracing a helix around the planar acetate of salvinorin A. This overlap is not seen in the recently reported structure of the tetra­hydro­pyranyl ether, which is less potent. The classic anomeric conformation is strongly favoured in alk­oxy­methyl ethers, but not in substituted acetals, which may contribute to their reduced potency. This structure may prove useful in evaluating models of the activated κ-opioid receptor.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536812043449/qm2086sup1.cif
Contains datablocks global, I

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S1600536812043449/qm2086Isup2.hkl
Contains datablock I

cdx

Chemdraw file https://doi.org/10.1107/S1600536812043449/qm2086Isup3.cdx
Supplementary material

cml

Chemical Markup Language (CML) file https://doi.org/10.1107/S1600536812043449/qm2086Isup4.cml
Supplementary material

CCDC reference: 909888

Key indicators

  • Single-crystal X-ray study
  • T = 193 K
  • Mean [sigma](C-C) = 0.002 Å
  • Disorder in main residue
  • R factor = 0.040
  • wR factor = 0.108
  • Data-to-parameter ratio = 18.8

checkCIF/PLATON results

No syntax errors found



Alert level C STRVA01_ALERT_4_C Flack test results are meaningless. From the CIF: _refine_ls_abs_structure_Flack 0.200 From the CIF: _refine_ls_abs_structure_Flack_su 0.700 PLAT411_ALERT_2_C Short Inter H...H Contact H21A .. H15* .. 2.14 Ang. PLAT910_ALERT_3_C Missing # of FCF Reflections Below Th(Min) ..... 2
Alert level G REFLT03_ALERT_4_G ALERT: MoKa measured Friedel data cannot be used to determine absolute structure in a light-atom study EXCEPT under VERY special conditions. It is preferred that Friedel data is merged in such cases. From the CIF: _diffrn_reflns_theta_max 30.00 From the CIF: _reflns_number_total 6195 Count of symmetry unique reflns 3364 Completeness (_total/calc) 184.16% TEST3: Check Friedels for noncentro structure Estimate of Friedel pairs measured 2831 Fraction of Friedel pairs measured 0.842 Are heavy atom types Z>Si present no PLAT002_ALERT_2_G Number of Distance or Angle Restraints on AtSite 11 PLAT003_ALERT_2_G Number of Uiso or Uij Restrained Atom Sites .... 10 PLAT005_ALERT_5_G No _iucr_refine_instructions_details in CIF .... ? PLAT032_ALERT_4_G Std. Uncertainty on Flack Parameter Value High . 0.700 PLAT301_ALERT_3_G Note: Main Residue Disorder ................... 16 Perc. PLAT720_ALERT_4_G Number of Unusual/Non-Standard Labels .......... 9 PLAT791_ALERT_4_G Note: The Model has Chirality at C2 (Verify) S PLAT791_ALERT_4_G Note: The Model has Chirality at C4 (Verify) R PLAT791_ALERT_4_G Note: The Model has Chirality at C5 (Verify) R PLAT791_ALERT_4_G Note: The Model has Chirality at C8 (Verify) R PLAT791_ALERT_4_G Note: The Model has Chirality at C9 (Verify) R PLAT791_ALERT_4_G Note: The Model has Chirality at C10 (Verify) R PLAT811_ALERT_5_G No ADDSYM Analysis: Too Many Excluded Atoms .... ! PLAT860_ALERT_3_G Note: Number of Least-Squares Restraints ....... 181 PLAT916_ALERT_2_G Hooft y and Flack x Parameter values differ by . 0.20
0 ALERT level A = Most likely a serious problem - resolve or explain 0 ALERT level B = A potentially serious problem, consider carefully 3 ALERT level C = Check. Ensure it is not caused by an omission or oversight 16 ALERT level G = General information/check it is not something unexpected 0 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 4 ALERT type 2 Indicator that the structure model may be wrong or deficient 3 ALERT type 3 Indicator that the structure quality may be low 10 ALERT type 4 Improvement, methodology, query or suggestion 2 ALERT type 5 Informative message, check

Comment top

Salvinorin B methoxymethyl ether (1) is among the most potent and selective κ (kappa) opioids known, with subnanomolar affinity and potency (Wang et al., 2008). A semisynthetic derivative of the naturally occurring κ opioid salvinorin A (2), (1) was the first derivative reported to be more potent than (2) in vitro, and also showed greater potency and duration of action in mice (Wang et al., 2008). The extreme potency of (1) has been confirmed both in vitro (Munro et al., 2008, Prevatt-Smith et al., 2011) and in rats (Baker et al., 2009, Peet & Baker, 2011). The name MOM-SalB is widely used; the incorrect name `2-methoxymethylsalvinorin B', implying that the substituent is directly attached to C2, should be avoided.

In Figure 1, the structures of (1) and (2) have been drawn to emphasize their similarity, with O2, C21 and O3 superimposable. The terminal methyl group C22 is attached to O3 in (1) but C21 in (2), and might be expected to interact with different regions of the receptor. Extensive research has been done into the structure-activity relationships of (2), especially the role of the C2 acetate. The deacetyl analogue salvinorin B is at least 60-fold less potent than (2). Deoxygenation or demethylation of the acetate causes smaller reductions in potency (Cunningham et al., 2011). This suggests that the two extremities of the acetate (O3 and C22) engage in separate, synergistic interactions with the binding pocket (Munro et al., 2008). The structure-activity relationships of (1) have also been explored. Potency is dramatically reduced by replacement of O3 with sulfur or carbon (Munro et al., 2008); this similarity to (2) is consistent with the proposed common binding pose. The ethoxymethyl ether (3) appears to be even more potent and selective than (1), both in vitro (Munro et al., 2008, Prevatt-Smith et al., 2011) and in vivo (Baker et al., 2009, Peet & Baker, 2011). Similarly, 12-epi-(3) reportedly exhibits higher affinity than 12-epi-(1) (Béguin et al., 2012). Further extension or branching of the terminal alkyl chain reduces affinity (Munro et al., 2008). Thus, the ethoxymethyl substituent appears to confer optimal affinity and potency. Like (1), (3) is also metabolized more slowly than (2) (Hooker et al., 2009). Based on the above hypothesis that the C22 methyl groups in (1) and (2) address different regions of the binding pocket, ethoxyethyl ether (4) was designed in that hope that it would interact with both of these regions, maximizing affinity. However, upon testing, (4) proved to have much lower affinity and potency than (3) (Munro et al., 2008, Prevatt-Smith et al., 2011). Indeed, all derivatives tested to date featuring substituted acetals, such as (5), exhibit reduced affinity and potency (Munro et al., 2008, Prevatt-Smith et al., 2011). These surprising and disappointing results cast doubt on the proposed binding model. We therefore determined the structure of (1) by single-crystal X-ray diffraction to obtain conformational information (Figure 2).

Other than the disordered furan ring, the neoclerodane scaffold is almost perfectly superimposable (r.m.s. < 0.1 Å) upon that of (2), as expected (Ortega et al., 1982). However, the resulting relationship between the acetate and the MOM ether was unexpected. Both O3 and C22 in (1) overlap with their counterparts in (2), being separated by just 0.9 Å (O3) and 1.2 Å (C22) – less than their atomic radii. The overlapping van der Waals surfaces of O3 and C22 are shown in Figure 3. This result was surprising, given the different point of attachment of C22 in these two compounds (Figure 1). This counterintuitive result occurs because both bonds to the acetal carbon C21 in (1) are gauche (torsion angles: 69.8° (O2—C22) and 76.5° (C2—O3)), allowing the ether to trace a part helix around the planar acetate in (2). This is known as the `classic anomeric' conformation (Anderson, 2000, Brameld et al., 2008). Generally, solid-state conformations coincide closely with the bioactive conformation of the protein-bound ligand (Brameld et al., 2008). This is because both solid-state and bound conformations tend toward the free energy minimum. The similarity is greatest in high-affinity ligands, since any change in conformation during binding requires energy, and this `energetic penalty' reduces affinity (Brameld et al., 2008). As discussed above, structure-activity studies indicate that O3 and C22 contribute substantially to binding of both (2) and (1). The near-superimposability of these atoms in the crystal structures of these two high-affinity ligands suggests that they may represent similar bioactive conformations. Alkoxymethyl ethers invariably adopt the classic anomeric conformation, due to strong anomeric interactions involving both O atoms (Anderson, 2000, Brameld et al., 2008). Interestingly, however, substitution of the acetal carbon introduces steric interactions which greatly reduce this preference. With a methyl substituent, as in (4), the classic anomeric conformation predominates, but is not exclusive. With larger substituents this conformation is strongly disfavoured, and rarely occurs (Anderson, 2000). If the classic anomeric conformation seen in (1) is optimal for binding, acetal substitution would therefore be expected to reduce affinity by this conformational influence, even if the substituents do not themselves interact unfavourably with the receptor. This may contribute to the dramatic reductions in affinity and potency seen even with small acetal substituents (Munro et al., 2008, Prevatt-Smith et al., 2011).

The recently reported crystal structure of the tetrahydropyranyl (THP) ether (5) illustrates this point (Prevatt-Smith et al., 2011). The cyclic acetal does not adopt the classic anomeric conformation, and superimposition on (2) gives much poorer overlap than seen with (1) (Figure 4). Acetal oxygen O3 is separated from its counterpart in (2) by 2.5 Å, and is instead almost coincident with C22 (<0.2 Å). Furthermore, the THP ring is disordered, consisting of a mixture of two interconvertible chair conformations. Thus, the THP ether exhibits weaker conformational preferences than the MOM ether, and much poorer overlap with (2). This may partly account for its lower potency. Our results suggest a possible conformational basis for the high binding affinity of salvinorin B alkoxymethyl ethers such as (1) and (3), and for the reduced affinity of substituted acetal derivatives such as (4) and (5). As a structurally atypical and extremely potent agonist, the structure of (1) reported here may prove useful in modelling the activation of the κ opioid receptor.

Related literature top

For the preparation, see: Béguin et al. (2009). For amended characterization data, see: Munro et al. (2008). For structure–activity relationships in vitro, see: Béguin et al. (2012); Munro et al. (2008) Prevatt-Smith et al. (2011). For in vivo pharmacology, see: Baker et al. (2009); Peet & Baker (2011); Wang et al. (2008). For pharmacokinetics and PET imaging of the ethoxymethyl ether, see: Hooker et al. (2009). For structure–activity relationships of salvinorin A, see: Cunningham et al. (2011). For crystal structures of related compounds, see: Ortega et al. (1982); Prevatt-Smith et al. (2011); Tidgewell et al. (2006). For solid-state and bioactive conformations of acetals, see: Anderson (2000); Brameld et al. (2008).

Experimental top

Compound (1) was prepared as described previously, by treatment of salvinorin B with CH3OCH2Cl and i-Pr2NEt in anhydrous CH2Cl2, and purified by flash chromatography on silica gel (Béguin et al., 2009). Amended characterization data have been reported elsewhere (Munro et al., 2008). Dissolution of 200 mg in minimal boiling methanol (~3 ml) and slow cooling gave colourless needles, mp 165–167 °C (438–440 K).

Refinement top

The 3-furyl substituent was treated with a two-site disorder model consisting of [O8, C13, C14, C15, C16] and [O8*, C13*, C14*, C15*, C16*] with refined site occupancy factors of 0.66 (2) and 0.34 (2), respectively. These ten atoms were included in the least-squares refinement with rigid bond, similar Uij, common plane and 1,2-distance restraints. All H atoms were allowed to ride on their respective C atoms with C—H distances constrained to the SHELXTL (Sheldrick, 2008) default values for the specified functional groups at 193 K, i.e., 0.95, 0.98, 0.99 and 1.00 Å for the olefic, methyl, methylene and methine H atoms, respectively. The Uiso(H) values were set at 1.5Ueq(C) for the methyl H atoms and 1.2Ueq(C) for all others. The Flack parameter obtained [x = 0.2 (7)] was inconclusive. The absolute stereochemistry of salvinorin B has been established via the p-bromobenzoate (Tidgewell et al., 2006).

Computing details top

Data collection: APEX2 (Bruker, 2006); cell refinement: SAINT (Bruker, 2006); data reduction: SAINT (Bruker, 2006); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997) and pyMOL (DeLano, 2009); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. Structures of compounds discussed.
[Figure 2] Fig. 2. Crystal structure of (1) with 50% probability thermal displacement ellipsoids. Atom numbering follows the crystal structure of (2) (Ortega et al., 1982) (* = minor component of disorder) (Cross-eyed stereoview).
[Figure 3] Fig. 3. Superimposed structures of (1) in blue and (2) in black (CSD code BUJJIZ, Ortega et al., 1982). Spheres represent the van der Waals surfaces of O3 and C22, connected by dotted yellow lines (Cross-eyed stereoview).
[Figure 4] Fig. 4. Superimposed structures of (2) in black with (5) in blue (major component) and purple (minor component)(CCDC 837303, Prevatt-Smith et al., 2011). Spheres represent the van der Waals surface of O3, connected by dotted yellow lines (Cross-eyed stereoview).
Methyl (2S,4aR,6aR,7R,9S,10aS,10bR)- 2-(3-furyl)-9-methoxymethoxy-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a- octahydro-1H-benzo[f]isochromene-7-carboxylate top
Crystal data top
C23H30O8F(000) = 928
Mr = 434.47Dx = 1.355 Mg m3
Monoclinic, C2Melting point = 438–440 K
Hall symbol: C 2yMo Kα radiation, λ = 0.71073 Å
a = 27.8848 (7) ÅCell parameters from 9071 reflections
b = 6.2415 (2) Åθ = 3.0–29.5°
c = 12.8212 (3) ŵ = 0.10 mm1
β = 107.351 (1)°T = 193 K
V = 2129.9 (1) Å3Needle, colourless
Z = 40.25 × 0.13 × 0.07 mm
Data collection top
Bruker APEXII CCD
diffractometer
6195 independent reflections
Radiation source: fine-focus sealed tube5296 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.033
Detector resolution: 836.6 pixels mm-1θmax = 30.0°, θmin = 1.9°
ω scans, 2580 0.5° rotationsh = 3838
Absorption correction: multi-scan
(SADABS; Bruker, 2004)
k = 88
Tmin = 0.975, Tmax = 0.993l = 1818
27784 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.040Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.108H-atom parameters constrained
S = 1.04 w = 1/[σ2(Fo2) + (0.062P)2 + 0.2734P]
where P = (Fo2 + 2Fc2)/3
6195 reflections(Δ/σ)max = 0.001
330 parametersΔρmax = 0.28 e Å3
181 restraintsΔρmin = 0.16 e Å3
Crystal data top
C23H30O8V = 2129.9 (1) Å3
Mr = 434.47Z = 4
Monoclinic, C2Mo Kα radiation
a = 27.8848 (7) ŵ = 0.10 mm1
b = 6.2415 (2) ÅT = 193 K
c = 12.8212 (3) Å0.25 × 0.13 × 0.07 mm
β = 107.351 (1)°
Data collection top
Bruker APEXII CCD
diffractometer
6195 independent reflections
Absorption correction: multi-scan
(SADABS; Bruker, 2004)
5296 reflections with I > 2σ(I)
Tmin = 0.975, Tmax = 0.993Rint = 0.033
27784 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.040181 restraints
wR(F2) = 0.108H-atom parameters constrained
S = 1.04Δρmax = 0.28 e Å3
6195 reflectionsΔρmin = 0.16 e Å3
330 parameters
Special details top

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > 2σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R-factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
O10.34600 (4)1.0459 (2)0.20598 (9)0.0363 (3)
O20.37399 (4)1.1271 (2)0.02768 (10)0.0382 (3)
O30.28986 (5)1.1470 (3)0.07126 (12)0.0533 (3)
O40.50180 (4)0.3453 (2)0.13791 (9)0.0347 (2)
O50.53410 (4)0.6752 (2)0.15051 (11)0.0434 (3)
O60.31648 (4)0.4502 (3)0.48120 (9)0.0436 (3)
O70.39036 (5)0.3347 (3)0.57679 (9)0.0458 (3)
O80.1529 (2)0.3841 (16)0.3150 (5)0.0598 (16)0.66 (2)
O8*0.1624 (5)0.306 (3)0.3130 (11)0.065 (3)0.34 (2)
C10.36787 (5)0.9006 (2)0.17700 (11)0.0249 (3)
C20.38017 (5)0.9135 (3)0.06823 (11)0.0283 (3)
H20.35580.82010.01420.034*
C30.43320 (5)0.8377 (3)0.07636 (12)0.0315 (3)
H3A0.43600.81630.00190.038*
H3B0.45760.94990.11260.038*
C40.44644 (5)0.6293 (3)0.14044 (11)0.0257 (3)
H40.42220.51710.10070.031*
C50.44100 (5)0.6503 (2)0.25776 (11)0.0228 (2)
C60.45549 (5)0.4362 (3)0.31852 (12)0.0267 (3)
H6A0.43960.31760.26900.032*
H6B0.49240.41760.33790.032*
C70.43961 (5)0.4217 (3)0.42203 (11)0.0274 (3)
H7A0.44980.28130.45760.033*
H7B0.45650.53550.47380.033*
C80.38318 (5)0.4474 (2)0.39397 (11)0.0244 (3)
H80.36780.33400.33910.029*
C90.36365 (5)0.6644 (2)0.34072 (11)0.0237 (2)
C100.38330 (5)0.6924 (2)0.23975 (11)0.0223 (2)
H100.36580.57800.18770.027*
C110.30621 (5)0.6350 (3)0.30016 (11)0.0291 (3)
H11A0.29060.76910.26450.035*
H11B0.29800.51990.24450.035*
C120.28354 (5)0.5783 (3)0.39194 (12)0.0320 (3)
H120.27660.71620.42450.038*0.66 (2)
H12*0.27440.71380.42310.038*0.34 (2)
C130.2346 (2)0.4602 (14)0.3521 (11)0.0399 (14)0.66 (2)
C140.2245 (3)0.2544 (13)0.3026 (9)0.0608 (16)0.66 (2)
H140.24860.16290.28650.073*0.66 (2)
C150.1763 (4)0.2117 (11)0.2826 (5)0.0577 (16)0.66 (2)
H150.16020.08300.25100.069*0.66 (2)
C160.1899 (2)0.5337 (15)0.3570 (8)0.0508 (17)0.66 (2)
H160.18470.66940.38530.061*0.66 (2)
C13*0.2374 (3)0.442 (2)0.351 (2)0.032 (2)0.34 (2)
C14*0.2354 (5)0.241 (2)0.2978 (16)0.044 (2)0.34 (2)
H14*0.26340.17180.28480.052*0.34 (2)
C15*0.1891 (5)0.165 (2)0.2686 (15)0.062 (3)0.34 (2)
H15*0.17690.04080.22640.075*0.34 (2)
C16*0.1910 (4)0.481 (3)0.3591 (14)0.042 (2)0.34 (2)
H16*0.18020.60400.38980.051*0.34 (2)
C170.36481 (6)0.4082 (3)0.49147 (12)0.0321 (3)
C180.49892 (5)0.5576 (3)0.14339 (12)0.0295 (3)
C190.47495 (5)0.8301 (3)0.32085 (12)0.0293 (3)
H19A0.50880.81350.31380.044*
H19B0.47660.82250.39820.044*
H19C0.46120.96920.29090.044*
C200.37823 (6)0.8467 (3)0.42559 (12)0.0314 (3)
H20A0.36620.81250.48810.047*
H20B0.36290.98100.39210.047*
H20C0.41490.86230.45050.047*
C210.33854 (7)1.1533 (4)0.07497 (15)0.0486 (5)
H21A0.34451.29250.10600.058*
H21B0.34331.03890.12440.058*
C220.27678 (9)1.3292 (5)0.0192 (2)0.0654 (6)
H22A0.24031.33320.03320.098*
H22B0.28771.45950.04820.098*
H22C0.29331.32060.05970.098*
C230.55100 (6)0.2564 (3)0.14724 (16)0.0407 (4)
H23A0.54920.09960.14740.061*
H23B0.57510.30560.21550.061*
H23C0.56200.30390.08510.061*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
O10.0463 (6)0.0288 (5)0.0338 (6)0.0112 (5)0.0120 (5)0.0024 (4)
O20.0313 (5)0.0392 (6)0.0420 (6)0.0014 (5)0.0073 (4)0.0178 (5)
O30.0365 (6)0.0615 (9)0.0539 (8)0.0058 (6)0.0015 (5)0.0023 (7)
O40.0311 (5)0.0329 (5)0.0440 (6)0.0031 (4)0.0170 (5)0.0081 (5)
O50.0319 (5)0.0406 (7)0.0629 (8)0.0012 (5)0.0221 (5)0.0062 (6)
O60.0355 (6)0.0683 (8)0.0309 (6)0.0052 (6)0.0160 (5)0.0144 (6)
O70.0433 (6)0.0649 (8)0.0291 (6)0.0023 (6)0.0105 (5)0.0140 (6)
O80.0397 (17)0.096 (4)0.0512 (16)0.019 (2)0.0254 (14)0.016 (2)
O8*0.047 (4)0.086 (7)0.072 (5)0.019 (4)0.032 (3)0.007 (4)
C10.0239 (6)0.0249 (6)0.0237 (6)0.0013 (5)0.0039 (5)0.0001 (5)
C20.0283 (6)0.0299 (7)0.0266 (6)0.0006 (6)0.0081 (5)0.0056 (6)
C30.0312 (7)0.0364 (7)0.0297 (7)0.0035 (6)0.0135 (6)0.0075 (6)
C40.0252 (6)0.0288 (7)0.0250 (6)0.0006 (5)0.0103 (5)0.0000 (5)
C50.0239 (6)0.0211 (6)0.0239 (6)0.0001 (5)0.0077 (5)0.0000 (5)
C60.0291 (7)0.0223 (6)0.0301 (7)0.0026 (5)0.0109 (5)0.0021 (5)
C70.0289 (6)0.0265 (6)0.0269 (6)0.0026 (5)0.0082 (5)0.0051 (5)
C80.0284 (6)0.0227 (6)0.0228 (6)0.0021 (5)0.0086 (5)0.0002 (5)
C90.0257 (6)0.0239 (6)0.0227 (6)0.0010 (5)0.0094 (5)0.0004 (5)
C100.0247 (6)0.0215 (6)0.0213 (6)0.0004 (5)0.0078 (5)0.0006 (5)
C110.0267 (6)0.0371 (7)0.0254 (7)0.0017 (6)0.0107 (5)0.0028 (6)
C120.0308 (7)0.0376 (8)0.0306 (7)0.0020 (6)0.0137 (6)0.0021 (6)
C130.045 (3)0.040 (2)0.037 (3)0.006 (2)0.015 (3)0.007 (2)
C140.060 (3)0.046 (2)0.083 (3)0.001 (3)0.033 (3)0.001 (2)
C150.064 (4)0.057 (3)0.063 (2)0.024 (3)0.035 (2)0.015 (2)
C160.043 (2)0.071 (4)0.042 (3)0.007 (2)0.0173 (18)0.008 (3)
C13*0.022 (3)0.043 (5)0.037 (5)0.005 (3)0.018 (3)0.003 (4)
C14*0.035 (3)0.031 (3)0.070 (4)0.011 (3)0.024 (3)0.017 (3)
C15*0.046 (5)0.049 (4)0.098 (6)0.022 (4)0.031 (4)0.010 (4)
C16*0.034 (4)0.067 (5)0.038 (4)0.007 (3)0.030 (3)0.012 (4)
C170.0345 (7)0.0362 (8)0.0271 (7)0.0030 (6)0.0114 (6)0.0015 (6)
C180.0281 (7)0.0346 (7)0.0285 (7)0.0012 (6)0.0126 (6)0.0014 (6)
C190.0300 (7)0.0259 (6)0.0309 (7)0.0046 (6)0.0073 (5)0.0023 (6)
C200.0402 (8)0.0281 (7)0.0273 (7)0.0001 (6)0.0121 (6)0.0041 (6)
C210.0445 (9)0.0660 (12)0.0357 (9)0.0152 (9)0.0126 (7)0.0210 (9)
C220.0532 (12)0.0669 (14)0.0752 (15)0.0227 (11)0.0176 (11)0.0014 (13)
C230.0338 (8)0.0450 (9)0.0468 (10)0.0088 (7)0.0172 (7)0.0058 (7)
Geometric parameters (Å, º) top
O1—C11.2112 (17)C9—C111.5404 (19)
O2—C211.400 (2)C9—C201.543 (2)
O2—C21.4225 (18)C9—C101.5586 (17)
O3—C211.373 (2)C10—H101.0000
O3—C221.420 (3)C11—C121.5340 (19)
O4—C181.3305 (19)C11—H11A0.9900
O4—C231.4513 (18)C11—H11B0.9900
O5—C181.2067 (19)C12—C13*1.500 (3)
O6—C171.3404 (18)C12—C131.501 (2)
O6—C121.4715 (19)C12—H121.0000
O7—C171.2040 (19)C12—H12*1.0000
O8—C161.377 (3)C13—C161.346 (3)
O8—C151.385 (3)C13—C141.423 (3)
O8*—C16*1.378 (3)C14—C151.320 (3)
O8*—C15*1.380 (3)C14—H140.9500
C1—C101.5214 (18)C15—H150.9500
C1—C21.5344 (18)C16—H160.9500
C2—C31.5263 (19)C13*—C16*1.349 (3)
C2—H21.0000C13*—C14*1.423 (3)
C3—C41.524 (2)C14*—C15*1.320 (3)
C3—H3A0.9900C14*—H14*0.9500
C3—H3B0.9900C15*—H15*0.9500
C4—C181.5198 (19)C16*—H16*0.9500
C4—C51.5617 (18)C19—H19A0.9800
C4—H41.0000C19—H19B0.9800
C5—C191.5340 (19)C19—H19C0.9800
C5—C61.5390 (19)C20—H20A0.9800
C5—C101.5778 (17)C20—H20B0.9800
C6—C71.5216 (19)C20—H20C0.9800
C6—H6A0.9900C21—H21A0.9900
C6—H6B0.9900C21—H21B0.9900
C7—C81.5147 (19)C22—H22A0.9800
C7—H7A0.9900C22—H22B0.9800
C7—H7B0.9900C22—H22C0.9800
C8—C171.5054 (18)C23—H23A0.9800
C8—C91.5415 (19)C23—H23B0.9800
C8—H81.0000C23—H23C0.9800
C21—O2—C2115.33 (14)O6—C12—C13106.9 (5)
C21—O3—C22112.85 (17)O6—C12—C11114.68 (11)
C18—O4—C23116.56 (13)C13*—C12—C11111.9 (9)
C17—O6—C12123.97 (11)C13—C12—C11113.2 (5)
C16—O8—C15106.2 (4)O6—C12—H12107.2
C16*—O8*—C15*111.6 (8)C13—C12—H12107.2
O1—C1—C10124.47 (12)C11—C12—H12107.2
O1—C1—C2120.59 (12)O6—C12—H12*108.8
C10—C1—C2114.89 (11)C13*—C12—H12*108.8
O2—C2—C3108.95 (11)C11—C12—H12*108.8
O2—C2—C1110.23 (12)C16—C13—C14105.5 (4)
C3—C2—C1113.35 (11)C16—C13—C12125.2 (5)
O2—C2—H2108.1C14—C13—C12129.3 (6)
C3—C2—H2108.1C15—C14—C13108.8 (4)
C1—C2—H2108.1C15—C14—H14125.6
C4—C3—C2112.05 (11)C13—C14—H14125.6
C4—C3—H3A109.2C14—C15—O8109.2 (4)
C2—C3—H3A109.2C14—C15—H15125.4
C4—C3—H3B109.2O8—C15—H15125.4
C2—C3—H3B109.2C13—C16—O8110.3 (4)
H3A—C3—H3B107.9C13—C16—H16124.8
C18—C4—C3109.94 (11)O8—C16—H16124.8
C18—C4—C5111.73 (11)C16*—C13*—C14*107.1 (6)
C3—C4—C5111.70 (11)C16*—C13*—C12128.0 (8)
C18—C4—H4107.8C14*—C13*—C12124.9 (8)
C3—C4—H4107.8C15*—C14*—C13*110.3 (8)
C5—C4—H4107.8C15*—C14*—H14*124.8
C19—C5—C6109.92 (11)C13*—C14*—H14*124.8
C19—C5—C4110.34 (10)C14*—C15*—O8*104.9 (9)
C6—C5—C4109.16 (11)C14*—C15*—H15*127.6
C19—C5—C10113.43 (11)O8*—C15*—H15*127.6
C6—C5—C10108.71 (10)C13*—C16*—O8*105.6 (7)
C4—C5—C10105.12 (10)C13*—C16*—H16*127.2
C7—C6—C5113.11 (11)O8*—C16*—H16*127.2
C7—C6—H6A109.0O7—C17—O6117.96 (13)
C5—C6—H6A109.0O7—C17—C8124.09 (14)
C7—C6—H6B109.0O6—C17—C8117.89 (12)
C5—C6—H6B109.0O5—C18—O4123.31 (13)
H6A—C6—H6B107.8O5—C18—C4125.31 (14)
C8—C7—C6109.78 (11)O4—C18—C4111.38 (12)
C8—C7—H7A109.7C5—C19—H19A109.5
C6—C7—H7A109.7C5—C19—H19B109.5
C8—C7—H7B109.7H19A—C19—H19B109.5
C6—C7—H7B109.7C5—C19—H19C109.5
H7A—C7—H7B108.2H19A—C19—H19C109.5
C17—C8—C7111.86 (11)H19B—C19—H19C109.5
C17—C8—C9110.35 (11)C9—C20—H20A109.5
C7—C8—C9113.75 (11)C9—C20—H20B109.5
C17—C8—H8106.8H20A—C20—H20B109.5
C7—C8—H8106.8C9—C20—H20C109.5
C9—C8—H8106.8H20A—C20—H20C109.5
C11—C9—C8103.83 (11)H20B—C20—H20C109.5
C11—C9—C20110.78 (11)O3—C21—O2113.10 (14)
C8—C9—C20110.59 (11)O3—C21—H21A109.0
C11—C9—C10108.70 (10)O2—C21—H21A109.0
C8—C9—C10107.52 (10)O3—C21—H21B109.0
C20—C9—C10114.80 (11)O2—C21—H21B109.0
C1—C10—C9114.89 (11)H21A—C21—H21B107.8
C1—C10—C5109.55 (10)O3—C22—H22A109.5
C9—C10—C5117.10 (10)O3—C22—H22B109.5
C1—C10—H10104.6H22A—C22—H22B109.5
C9—C10—H10104.6O3—C22—H22C109.5
C5—C10—H10104.6H22A—C22—H22C109.5
C12—C11—C9113.17 (11)H22B—C22—H22C109.5
C12—C11—H11A108.9O4—C23—H23A109.5
C9—C11—H11A108.9O4—C23—H23B109.5
C12—C11—H11B108.9H23A—C23—H23B109.5
C9—C11—H11B108.9O4—C23—H23C109.5
H11A—C11—H11B107.8H23A—C23—H23C109.5
O6—C12—C13*103.5 (10)H23B—C23—H23C109.5
C21—O2—C2—C3114.88 (14)C20—C9—C11—C1260.11 (16)
C21—O2—C2—C1120.16 (14)C10—C9—C11—C12172.88 (12)
O1—C1—C2—O214.32 (18)C17—O6—C12—C13*130.8 (6)
C10—C1—C2—O2167.98 (11)C17—O6—C12—C13134.9 (4)
O1—C1—C2—C3136.74 (15)C17—O6—C12—C118.6 (2)
C10—C1—C2—C345.56 (16)C9—C11—C12—O632.17 (18)
O2—C2—C3—C4168.32 (12)C9—C11—C12—C13*149.7 (8)
C1—C2—C3—C445.19 (17)C9—C11—C12—C13155.2 (4)
C2—C3—C4—C18178.41 (12)O6—C12—C13—C16116.8 (10)
C2—C3—C4—C556.95 (16)C11—C12—C13—C16115.9 (10)
C18—C4—C5—C1965.23 (14)O6—C12—C13—C1463.2 (12)
C3—C4—C5—C1958.40 (14)C11—C12—C13—C1464.0 (12)
C18—C4—C5—C655.66 (14)C16—C13—C14—C151.4 (9)
C3—C4—C5—C6179.29 (11)C12—C13—C14—C15178.7 (12)
C18—C4—C5—C10172.13 (12)C13—C14—C15—O81.2 (9)
C3—C4—C5—C1064.24 (13)C16—O8—C15—C140.6 (8)
C19—C5—C6—C772.79 (14)C14—C13—C16—O81.0 (9)
C4—C5—C6—C7166.06 (11)C12—C13—C16—O8179.0 (11)
C10—C5—C6—C751.90 (14)C15—O8—C16—C130.3 (9)
C5—C6—C7—C859.29 (15)O6—C12—C13*—C16*112 (2)
C6—C7—C8—C17173.22 (12)C11—C12—C13*—C16*123.9 (19)
C6—C7—C8—C960.92 (15)O6—C12—C13*—C14*67.1 (19)
C17—C8—C9—C1163.99 (13)C11—C12—C13*—C14*57 (2)
C7—C8—C9—C11169.34 (11)C16*—C13*—C14*—C15*3.1 (17)
C17—C8—C9—C2054.87 (14)C12—C13*—C14*—C15*178 (2)
C7—C8—C9—C2071.79 (14)C13*—C14*—C15*—O8*5.8 (16)
C17—C8—C9—C10179.08 (11)C16*—O8*—C15*—C14*6.7 (16)
C7—C8—C9—C1054.26 (14)C14*—C13*—C16*—O8*1.1 (16)
O1—C1—C10—C96.55 (19)C12—C13*—C16*—O8*178 (2)
C2—C1—C10—C9171.04 (11)C15*—O8*—C16*—C13*4.9 (17)
O1—C1—C10—C5127.68 (14)C12—O6—C17—O7167.27 (17)
C2—C1—C10—C554.72 (14)C12—O6—C17—C815.2 (2)
C11—C9—C10—C168.63 (14)C7—C8—C17—O710.3 (2)
C8—C9—C10—C1179.56 (11)C9—C8—C17—O7138.04 (17)
C20—C9—C10—C156.05 (15)C7—C8—C17—O6172.30 (14)
C11—C9—C10—C5160.70 (11)C9—C8—C17—O644.60 (18)
C8—C9—C10—C548.89 (14)C23—O4—C18—O53.4 (2)
C20—C9—C10—C574.63 (15)C23—O4—C18—C4176.09 (12)
C19—C5—C10—C158.93 (13)C3—C4—C18—O536.7 (2)
C6—C5—C10—C1178.48 (11)C5—C4—C18—O587.90 (17)
C4—C5—C10—C161.70 (13)C3—C4—C18—O4143.75 (13)
C19—C5—C10—C974.18 (14)C5—C4—C18—O491.63 (15)
C6—C5—C10—C948.42 (15)C22—O3—C21—O269.8 (2)
C4—C5—C10—C9165.19 (11)C2—O2—C21—O376.5 (2)
C8—C9—C11—C1258.63 (15)

Experimental details

Crystal data
Chemical formulaC23H30O8
Mr434.47
Crystal system, space groupMonoclinic, C2
Temperature (K)193
a, b, c (Å)27.8848 (7), 6.2415 (2), 12.8212 (3)
β (°) 107.351 (1)
V3)2129.9 (1)
Z4
Radiation typeMo Kα
µ (mm1)0.10
Crystal size (mm)0.25 × 0.13 × 0.07
Data collection
DiffractometerBruker APEXII CCD
diffractometer
Absorption correctionMulti-scan
(SADABS; Bruker, 2004)
Tmin, Tmax0.975, 0.993
No. of measured, independent and
observed [I > 2σ(I)] reflections
27784, 6195, 5296
Rint0.033
(sin θ/λ)max1)0.703
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.040, 0.108, 1.04
No. of reflections6195
No. of parameters330
No. of restraints181
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.28, 0.16

Computer programs: APEX2 (Bruker, 2006), SAINT (Bruker, 2006), SHELXTL (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997) and pyMOL (DeLano, 2009).

 

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