Structural investigation of methyl 3-(4-fluoro-benzo-yl)-7-methyl-2-phenyl-indolizine-1-carboxyl-ate, an inhibitory drug towards Mycobacterium tuberculosis.

The title compound, C24H18FNO3, crystallizes in the monoclinic centrosymmetric space group P21/n and its mol-ecular conformation is stabilized via C-H⋯O intra-molecular inter-actions. The supra-molecular network mainly comprises C-H⋯O, C-H⋯F and C-H⋯π inter-actions, which contribute towards the formation of the crystal structure. The different inter-molecular inter-actions have been further analysed via Hirshfeld surface analysis and fingerprint plots. © Hasija et al. 2020.

Chemical context

Indolizine represents an inter­esting heterocyclic scaffold in which the nitro­gen atom belongs to both of the fused six- and five-membered rings. It is a well-known pharmacophore endowed with various promising pharmacological properties. For instance, indolizines have been found to exhibit analgesic (Vaught et al., 1990 ▸), anti­cancer (Butler, 2008 ▸; Sandeep et al., 2016a ▸,b ▸), anti­diabetic (Mederski et al., 2012 ▸), anti­histaminic (Cingolani et al., 1990 ▸), anti-microbial (Hazra et al., 2011 ▸) and anti­viral (Mishra & Tiwari, 2011 ▸) activity. It has also been found to act as cyclo-oxygenase (COX-2) inhibitor (Chandrashekharappa et al., 2018b ▸) and to have larvicidal activity against Anopheles arabiensis (Chandrashekharappa et al., 2018a ▸).

The title compound, comprising a substituted indolizine unit, displays a modest activity against susceptible H37Rv strains of Mycobacterium tuberculosis (Venugopala et al., 2019 ▸). Besides the tremendous scope of the pharmacological studies on indolizine-based compounds, the substitution of fluorine on the benzoyl ring, the presence of flexible moieties and of competitive hydrogen-bond acceptors (namely, oxygen O2 in the ester group at C6 and O3 in the carbonyl group at C8) make the structural study of the title compound of extreme relevance. In addition, it is of importance to observe the cooperative inter­play of weak inter­actions that contribute towards the consolidation of the crystal lattice. In the present paper, we report the mol­ecular and crystal structure of the title compound, highlighting its mol­ecular conformation and analysing the different inter­molecular inter­actions via Hirshfeld surface analysis and fingerprint plots.

Structural commentary

The title compound crystallizes in the centrosymmetric monoclinic P2 space group. The mol­ecular structure comprises one methyl­indolizine heterocyclic moiety (N1/C1–C9) consisting of fused six- and five-membered rings (N1/C1–C5, centroid Cg1 and N1/C5–C8, centroid Cg2). The heterocycle is substituted at the carbon atoms C6, C7 and C8 with a meth­oxy carbonyl group, a phenyl ring (C12–C17, centroid Cg3), and a fluoro­benzoyl ring [C18/O3/C19–C24/F1, centroid Cg4], respectively (Fig. 1 ▸). The mol­ecular structure possesses three conformational degrees of freedom due to the free rotation with respect to the C6—C10, C7—C12, and C8—C18 single bonds. The mol­ecular conformation is stabilized by the presence of intra­molecular C1—H1⋯O3 [C1⋯O3 = 2.853 (3) Å] and C4—H4⋯O2 [C4⋯O2 = 2.927 (2) Å] inter­actions (Table 1 ▸) and by π–π stacking [Cg3⋯Cg4 = 3.5084 (13) Å]. The dihedral angle between the mean plane through ring Cg3 (coloured in green in Fig. 2 ▸) and the mean plane of the indolizine skeleton (coloured in red) is 59.05 (9)°, while the dihedral angle between the mean plane through the phenyl ring and that through the fluoro­benzoyl ring (coloured in blue) is as small as 19.04 (10),° showing the nearly parallel position of the rings. The torsion angles N1—C8—C18—C19 and C8—C18—C19—C24 are −161.74 (19) and 46.2 (3)°, respectively.

Figure 1

Ellipsoid plot of the title compound drawn with 50% probability ellipsoids. Dotted lines indicate intra­molecular C—H⋯O inter­actions. Cg1, Cg3 and Cg4 represent the centroids of the six-membered rings N1/C1–C5, C12–C17 and C18/O3/C19–C24/F1, respectively, while Cg2 represents the five-membered ring N1/C5–C8.

Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C1—H1⋯O3	0.95	2.26	2.853 (3)	120
C4—H4⋯O2	0.95	2.38	2.927 (2)	116
C21—H21⋯O3i	0.95	2.54	3.399 (3)	149
C2—H2⋯O1ii	0.95	2.63	3.531 (4)	157
C15—H15⋯O3iii	0.95	2.76	3.519 (4)	137
C1—H1⋯C15ii	0.95	2.74	3.6064 (3)	152
C11—H11A⋯C5iv	0.98	2.74	3.4906 (1)	133
C11—H11B⋯F1v	0.98	2.67	3.0585 (3)	104
C23—H23⋯O3vi	0.95	2.67	3.4875 (3)	143

Symmetry codes: (i) ; (ii) ; (iii) ; (iv) ; (v) ; (vi) .

Figure 2

Dihedral angles between the mean plane passing through the C12–C17 ring (green) and the C18/O3/C19–C24/F1 ring (blue) and through the indolizine skeleton (red).

Supra­molecular features

The list of all intra- and inter­molecular inter­actions along with their geometrical parameters have been reported in Table 1 ▸. The inter­actions included for investigation are based on the distance criteria of vdW + 0.4 Å (Dance, 2003 ▸). In the crystal, the mol­ecules are primarily assembled through concomitant C2/15—H2/15⋯O1ii/O3iii inter­actions [C2⋯O1ii = 3.531 (4) Å, 157°; C15⋯O3iii = 3.519 (4) Å, 137°; symmetry codes: (ii) x, y − 1, z; (iii) x, y + 1, z] and C1—H1⋯π(C15)ii [C1⋯C15 = 3.6064 (3) Å, 152°], forming ribbons along the [010] direction, as shown by the green shading in Fig. 3 ▸. Two adjacent ribbons are connected to each other via C11—H11B⋯F1v [C11⋯F1 = 3.0585 (3) Å, 104°; symmetry code: (v) x − , −y + , z − ] (Fig. 3 ▸) and C21—H21⋯O3i [C21⋯O3 = 3.399 (3) Å, 149°; symmetry code: (i) −x + , y + , −z + ] (Fig. 4 ▸) inter­actions in a zigzag fashion along [001], resulting in the formation of a mol­ecular sheet parallel to the ac plane. Analogous C—H⋯F inter­actions have been investigated, showing that where the angularity is in the range 90 to 140°, the σ-hole on fluorine is directed towards the electron density of the C—H bond (Hathwar et al., 2020 ▸), underlining the importance of inter­actions with low angularity. The mol­ecular sheets are closely stacked along the a-axis direction via weak inter­actions such as C9—H9C⋯π(C1) [C9⋯C1vii = 3.7431 (5) Å; symmetry code: (vii) −x + 1, −y, −z], C11—H11A⋯π(C5) [C11⋯C5iv = 3.4906 (4) Å; symmetry code: (iv) −x, −y + 1, −z], C11—H11C⋯π(C8) [C11⋯C8viii = 3.6590 (5) Å; symmetry code: (viii) −x + 1, −y + 1, −z] (Fig. 4 ▸), giving rise to a layered supra­molecular structure. From this analysis, it can be stated that the formation of the crystal structure is mainly governed by several C—H⋯O and C—H⋯π inter­actions, while the C—H⋯F inter­actions play a secondary but supporting role in its overall consolidation.

Figure 3

Crystal packing of title compound showing the formation of mol­ecular sheets parallel to the bc plane via C—H⋯O, C—H⋯π and C—H⋯F inter­actions.

Figure 4

Stacking of mol­ecular sheets along the a-axis direction, primarily via C—H⋯π and C—H⋯F inter­actions, resulting in a layered supra­molecular architecture.

Database survey

A search for the 2-phenyl­indolizine skeleton in the CSD (version 5.40, update of August 2019; Groom et al., 2016 ▸) was carried out. Out of the 39 hits for unsubstituted phenyl rings attached to indolizine, the majority of entries gave reports of varied synthetic procedures and methodologies to obtain these compounds, underlining their importance. The near-infrared emissive properties of KIVLIN, KIVLOT, KIVLUZ (Gayton et al., 2019 ▸) and KENFAN (McNamara et al., 2017 ▸) have also been reported.

Structural details of compounds such as CAJTAI (Aslanov et al., 1983 ▸), EMUTOV (Liu, et al., 2003 ▸), FEDQAH (Liu, et al., 2005 ▸), GIYLOP (Sonnenschein & Schneider, 1997 ▸), ODEFIN (Qian et al., 2006 ▸), PNOIZA, PNOIZB, PNOIZE, PNOIZF (Tafeenkov & Aslanov, 1980 ▸), ROLKIM (Tafeenkov & Au, 1996 ▸) and TIGXOX (Liu, et al., 2007 ▸) have also been deposited. Almost all of these mol­ecules are substituted at the C8 position with electron-withdrawing substituents such as –COMe, –CH2CN, –CN, –N=O, –CH=C(Ph)(CN), etc.

In particular, the papers reporting TIGXOX (Liu et al., 2007 ▸), FEDQAH (Liu et al., 2005 ▸) and ODEFIN (Qian et al., 2006 ▸) discuss the structural features of mol­ecules comprising the 2-phenyl indolizine skeleton, showing high fluorescent efficiency. In these reports, the respective dihedral angles between the mean plane of the indolizine skeleton and the plane of the phenyl ring are ca 53, 39 and 49 and 45°, comparable to that reported in the title compound.

Hirshfeld surface analysis and fingerprint plots

The significance of the cumulative effect of the inter­actions involved in the crystal structure can be visualized qualitatively through Hirshfeld surface analysis (Spackman et al., 2009 ▸). The Hirshfeld surfaces and the two-dimensional fingerprint plots were calculated using CrystalExplorer (Version 17.5; Wolff et al., 2012 ▸) and are shown in Figs. 5 ▸ and 6 ▸, respectively. The red spots on the HS surface illustrate the presence of supra­molecular inter­actions such as C—H⋯O, C—H⋯π and C—H⋯F whereas the blue regions indicate the lack of contact distances shorter than the sum of the van der Waals radii. The fingerprint plots represent the individual contributions of the different inter­actions. Fig. 6 ▸ shows that the major contribution comes from H⋯H (47.1%), O⋯H/H⋯O (13.1%), C⋯H/ H⋯C (21.4%), H⋯F/F⋯H (9.0%), C⋯C (1.9%) and N⋯H/H⋯N (1.7%) contacts. The relatively high percentage of C⋯H/H⋯C contacts indicates how the contribution of all of the C—H⋯π inter­actions plays an important role in consolidating the crystal packing.

Figure 5

The Hirshfeld surface of title compound mapped over d norm. Dashed lines indicate hydrogen bonds.

Figure 6

The fingerprint plots of the title compound showing the different contributions deriving from the O⋯H/H⋯O, N⋯H/H⋯N, C⋯H/H⋯C, H⋯F/F⋯H, C⋯C and H⋯H contacts.

Synthesis and crystallization

All chemicals were obtained from Sigma–Aldrich and used without further purification. A mixture of methyl 3-phenyl­propiolate (1) (160 mg, 1 mmol), 4-methyl­pyridine (2) (93 mg, 1 mmol), 2-bromo-1-(4-fluoro­phen­yl)ethan-1-one (3) (217 mg, 1 mmol), and tri­ethyl­amine (0.101 mg, 1 mmol) in 4.5 mL of aceto­nitrile were added to a 10 mL microwave tube under a nitro­gen atmosphere (Fig. 7 ▸). A microwave initiator was used to irradiate the reaction mixture at 373 K for about 5 min. The reaction was monitored via TLC. The solvent was then removed under reduced pressure, the crude residue was diluted with water and the aqueous layer was extracted twice with ethyl acetate, and the combined organic solvent was washed with a brine solution. The organic layer was removed under reduced pressure and the remaining residue was subjected to column chromatography using 60–120 mesh silica gel with an ethyl acetate and hexane solvent system to afford 0.3414 g (88% yield) of the title compound (Venugopala et al., 2019 ▸). Suitable single crystals of the compound were grown by the slow evaporation of acetone at ambient conditions.

Figure 7

The reaction scheme for the synthesis of the title compound.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. The hydrogen atoms were placed in idealized positions and refined using a riding model with U iso(H) =1.2U eq(C) or 1.5U eq(C-meth­yl).

Table 2

Experimental details

Crystal data
Chemical formula	C24H18FNO3
M r	387.39
Crystal system, space group	Monoclinic, P21/n
Temperature (K)	173
a, b, c (Å)	7.3246 (11), 9.8460 (13), 25.837 (4)
β (°)	93.318 (3)
V (Å3)	1860.2 (5)
Z	4
Radiation type	Mo Kα
μ (mm−1)	0.10
Crystal size (mm)	0.32 × 0.18 × 0.04
Data collection
Diffractometer	Bruker Kappa Duo APEXII
Absorption correction	Multi-scan (SADABS; Bruker, 2008 ▸)
T min, T max	0.855, 1.000
No. of measured, independent and observed [I > 2σ(I)] reflections	27523, 4296, 2641
R int	0.090
(sin θ/λ)max (Å−1)	0.652
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S	0.050, 0.131, 1.00
No. of reflections	4296
No. of parameters	265
H-atom treatment	H-atom parameters constrained
Δρmax, Δρmin (e Å−3)	0.29, −0.30

Computer programs: APEX2 (Bruker, 2012 ▸), SAINT (Bruker, 2008 ▸), SHELXS97 (Sheldrick, 2008 ▸), X-SEED (Barbour, 2001 ▸), Mercury (Macrae et al., 2020 ▸), SHELXL2014 (Sheldrick, 2015 ▸) and PLATON (Spek, 2020 ▸).

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2056989020003837/xi2021sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989020003837/xi2021Isup2.hkl

Click here for additional data file.

Supporting information file. DOI: 10.1107/S2056989020003837/xi2021Isup3.cml

CCDC reference: 1865697

Additional supporting information: crystallographic information; 3D view; checkCIF report

C24H18FNO3	F(000) = 808
Mr = 387.39	Dx = 1.383 Mg m−3
Monoclinic, P21/n	Mo Kα radiation, λ = 0.71073 Å
a = 7.3246 (11) Å	Cell parameters from 27523 reflections
b = 9.8460 (13) Å	θ = 2.2–27.6°
c = 25.837 (4) Å	µ = 0.10 mm−1
β = 93.318 (3)°	T = 173 K
V = 1860.2 (5) Å3	Block, yellow
Z = 4	0.32 × 0.18 × 0.04 mm

Bruker Kappa Duo APEXII diffractometer	2641 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	Rint = 0.090
0.5° φ scans and ω scans	θmax = 27.6°, θmin = 2.2°
Absorption correction: multi-scan (SADABS; Bruker, 2008)	h = −9→9
Tmin = 0.855, Tmax = 1.000	k = −12→12
27523 measured reflections	l = −33→33
4296 independent reflections

Refinement on F2	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.050	H-atom parameters constrained
wR(F2) = 0.131	w = 1/[σ2(Fo2) + (0.0555P)2 + 0.455P] where P = (Fo2 + 2Fc2)/3
S = 1.00	(Δ/σ)max < 0.001
4296 reflections	Δρmax = 0.29 e Å−3
265 parameters	Δρmin = −0.30 e Å−3
0 restraints	Extinction correction: SHELXL-2014/7 (Sheldrick 2015, Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methods	Extinction coefficient: 0.0044 (8)

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

	x	y	z	Uiso*/Ueq
F1	0.4480 (2)	0.70181 (14)	0.32107 (5)	0.0563 (4)
O1	0.2787 (2)	0.69998 (15)	0.00174 (6)	0.0381 (4)
O2	0.1668 (2)	0.53237 (14)	−0.04937 (5)	0.0302 (4)
O3	0.5350 (2)	0.21447 (15)	0.16777 (5)	0.0336 (4)
N1	0.3494 (2)	0.26669 (16)	0.06884 (6)	0.0230 (4)
C1	0.3588 (3)	0.1276 (2)	0.07210 (8)	0.0293 (5)
H1	0.4025	0.0857	0.1035	0.035*
C2	0.3057 (3)	0.0502 (2)	0.03060 (8)	0.0294 (5)
H2	0.3148	−0.0459	0.0330	0.035*
C3	0.2368 (3)	0.1106 (2)	−0.01642 (8)	0.0269 (5)
C4	0.2282 (3)	0.2488 (2)	−0.01917 (7)	0.0252 (5)
H4	0.1830	0.2906	−0.0505	0.030*
C5	0.2850 (3)	0.3307 (2)	0.02346 (7)	0.0232 (4)
C6	0.2913 (3)	0.4722 (2)	0.03281 (7)	0.0232 (4)
C7	0.3565 (3)	0.4924 (2)	0.08437 (7)	0.0225 (4)
C8	0.3910 (3)	0.3647 (2)	0.10738 (7)	0.0229 (4)
C9	0.1754 (3)	0.0225 (2)	−0.06142 (8)	0.0356 (5)
H9A	0.1001	0.0760	−0.0865	0.053*
H9B	0.1035	−0.0537	−0.0491	0.053*
H9C	0.2826	−0.0125	−0.0781	0.053*
C10	0.2478 (3)	0.5806 (2)	−0.00470 (7)	0.0248 (5)
C11	0.1182 (3)	0.6340 (2)	−0.08794 (8)	0.0315 (5)
H11A	0.0323	0.6988	−0.0739	0.047*
H11B	0.0606	0.5902	−0.1188	0.047*
H11C	0.2285	0.6822	−0.0974	0.047*
C12	0.3881 (3)	0.6250 (2)	0.11063 (7)	0.0250 (5)
C13	0.5610 (3)	0.6581 (2)	0.13180 (7)	0.0287 (5)
H13	0.6610	0.5989	0.1269	0.034*
C14	0.5889 (3)	0.7767 (2)	0.15993 (8)	0.0363 (6)
H14	0.7076	0.7984	0.1743	0.044*
C15	0.4445 (4)	0.8634 (2)	0.16707 (8)	0.0387 (6)
H15	0.4631	0.9443	0.1867	0.046*
C16	0.2724 (4)	0.8320 (2)	0.14543 (8)	0.0390 (6)
H16	0.1729	0.8918	0.1502	0.047*
C17	0.2443 (3)	0.7144 (2)	0.11693 (8)	0.0326 (5)
H17	0.1263	0.6945	0.1016	0.039*
C18	0.4633 (3)	0.3265 (2)	0.15900 (7)	0.0253 (5)
C19	0.4534 (3)	0.4247 (2)	0.20269 (7)	0.0257 (5)
C20	0.6087 (3)	0.4441 (2)	0.23563 (8)	0.0324 (5)
H20	0.7157	0.3924	0.2307	0.039*
C21	0.6082 (3)	0.5381 (2)	0.27542 (8)	0.0385 (6)
H21	0.7144	0.5534	0.2975	0.046*
C22	0.4491 (4)	0.6086 (2)	0.28191 (8)	0.0374 (6)
C23	0.2923 (3)	0.5899 (2)	0.25163 (8)	0.0328 (5)
H23	0.1843	0.6393	0.2579	0.039*
C24	0.2955 (3)	0.4967 (2)	0.21143 (8)	0.0283 (5)
H24	0.1883	0.4820	0.1897	0.034*

	U11	U22	U33	U12	U13	U23
F1	0.0812 (12)	0.0445 (9)	0.0415 (8)	0.0051 (8)	−0.0116 (7)	−0.0201 (7)
O1	0.0596 (11)	0.0203 (8)	0.0333 (8)	−0.0034 (7)	−0.0062 (7)	0.0057 (7)
O2	0.0413 (9)	0.0238 (8)	0.0248 (7)	0.0018 (7)	−0.0048 (6)	0.0033 (6)
O3	0.0420 (9)	0.0259 (8)	0.0323 (8)	0.0073 (7)	−0.0035 (7)	0.0032 (7)
N1	0.0271 (10)	0.0201 (9)	0.0219 (8)	0.0005 (7)	0.0025 (7)	0.0018 (7)
C1	0.0363 (13)	0.0213 (11)	0.0304 (11)	0.0029 (9)	0.0019 (9)	0.0052 (9)
C2	0.0369 (13)	0.0192 (11)	0.0324 (11)	0.0007 (9)	0.0036 (9)	−0.0004 (9)
C3	0.0282 (11)	0.0251 (12)	0.0280 (11)	−0.0045 (9)	0.0057 (9)	−0.0019 (9)
C4	0.0282 (11)	0.0248 (11)	0.0228 (10)	−0.0010 (9)	0.0020 (8)	0.0008 (8)
C5	0.0235 (10)	0.0234 (11)	0.0228 (10)	0.0005 (8)	0.0032 (8)	0.0033 (8)
C6	0.0255 (11)	0.0214 (10)	0.0228 (10)	0.0001 (8)	0.0020 (8)	0.0010 (8)
C7	0.0239 (11)	0.0206 (10)	0.0233 (10)	0.0014 (8)	0.0028 (8)	0.0005 (8)
C8	0.0260 (11)	0.0207 (10)	0.0219 (9)	0.0001 (8)	0.0021 (8)	−0.0014 (8)
C9	0.0460 (14)	0.0281 (12)	0.0326 (12)	−0.0038 (10)	0.0005 (10)	−0.0039 (10)
C10	0.0268 (11)	0.0243 (11)	0.0237 (10)	0.0000 (9)	0.0033 (8)	0.0015 (9)
C11	0.0382 (13)	0.0302 (12)	0.0256 (10)	0.0028 (10)	−0.0036 (9)	0.0077 (9)
C12	0.0373 (12)	0.0183 (10)	0.0197 (9)	−0.0001 (9)	0.0028 (9)	0.0029 (8)
C13	0.0375 (12)	0.0237 (11)	0.0253 (10)	−0.0035 (9)	0.0056 (9)	0.0008 (9)
C14	0.0494 (15)	0.0283 (12)	0.0311 (12)	−0.0106 (11)	0.0033 (11)	−0.0014 (10)
C15	0.0653 (17)	0.0199 (12)	0.0311 (12)	−0.0025 (11)	0.0026 (11)	−0.0030 (10)
C16	0.0589 (16)	0.0251 (12)	0.0333 (12)	0.0136 (11)	0.0062 (11)	0.0012 (10)
C17	0.0407 (13)	0.0267 (12)	0.0301 (11)	0.0059 (10)	−0.0009 (10)	0.0018 (9)
C18	0.0254 (11)	0.0259 (11)	0.0247 (10)	−0.0020 (9)	0.0026 (8)	0.0024 (9)
C19	0.0344 (12)	0.0223 (11)	0.0202 (9)	−0.0025 (9)	0.0000 (9)	0.0045 (8)
C20	0.0371 (13)	0.0289 (12)	0.0305 (11)	0.0013 (10)	−0.0046 (10)	0.0022 (10)
C21	0.0498 (16)	0.0324 (13)	0.0316 (12)	−0.0036 (11)	−0.0130 (11)	0.0016 (10)
C22	0.0614 (17)	0.0235 (12)	0.0268 (11)	−0.0004 (11)	−0.0024 (11)	−0.0027 (9)
C23	0.0420 (14)	0.0298 (12)	0.0269 (11)	0.0020 (10)	0.0058 (10)	0.0018 (9)
C24	0.0346 (12)	0.0274 (12)	0.0228 (10)	−0.0028 (9)	0.0010 (9)	0.0018 (9)

F1—C22	1.367 (2)	C11—H11A	0.9800
O1—C10	1.206 (2)	C11—H11B	0.9800
O2—C10	1.353 (2)	C11—H11C	0.9800
O2—C11	1.442 (2)	C12—C13	1.389 (3)
O3—C18	1.236 (2)	C12—C17	1.389 (3)
N1—C1	1.373 (3)	C13—C14	1.384 (3)
N1—C5	1.389 (2)	C13—H13	0.9500
N1—C8	1.408 (2)	C14—C15	1.380 (3)
C1—C2	1.354 (3)	C14—H14	0.9500
C1—H1	0.9500	C15—C16	1.384 (3)
C2—C3	1.419 (3)	C15—H15	0.9500
C2—H2	0.9500	C16—C17	1.382 (3)
C3—C4	1.364 (3)	C16—H16	0.9500
C3—C9	1.499 (3)	C17—H17	0.9500
C4—C5	1.409 (3)	C18—C19	1.491 (3)
C4—H4	0.9500	C19—C24	1.387 (3)
C5—C6	1.414 (3)	C19—C20	1.393 (3)
C6—C7	1.403 (3)	C20—C21	1.383 (3)
C6—C10	1.465 (3)	C20—H20	0.9500
C7—C8	1.407 (3)	C21—C22	1.375 (3)
C7—C12	1.483 (3)	C21—H21	0.9500
C8—C18	1.456 (3)	C22—C23	1.364 (3)
C9—H9A	0.9800	C23—C24	1.388 (3)
C9—H9B	0.9800	C23—H23	0.9500
C9—H9C	0.9800	C24—H24	0.9500
C10—O2—C11	115.09 (16)	H11A—C11—H11C	109.5
C1—N1—C5	121.17 (17)	H11B—C11—H11C	109.5
C1—N1—C8	129.22 (17)	C13—C12—C17	119.06 (19)
C5—N1—C8	109.56 (16)	C13—C12—C7	120.09 (18)
C2—C1—N1	120.09 (19)	C17—C12—C7	120.76 (19)
C2—C1—H1	120.0	C14—C13—C12	120.5 (2)
N1—C1—H1	120.0	C14—C13—H13	119.7
C1—C2—C3	120.92 (19)	C12—C13—H13	119.7
C1—C2—H2	119.5	C15—C14—C13	120.1 (2)
C3—C2—H2	119.5	C15—C14—H14	120.0
C4—C3—C2	118.41 (18)	C13—C14—H14	120.0
C4—C3—C9	121.74 (19)	C14—C15—C16	119.7 (2)
C2—C3—C9	119.85 (18)	C14—C15—H15	120.2
C3—C4—C5	121.33 (19)	C16—C15—H15	120.2
C3—C4—H4	119.3	C17—C16—C15	120.4 (2)
C5—C4—H4	119.3	C17—C16—H16	119.8
N1—C5—C4	118.07 (18)	C15—C16—H16	119.8
N1—C5—C6	107.26 (16)	C16—C17—C12	120.2 (2)
C4—C5—C6	134.66 (18)	C16—C17—H17	119.9
C7—C6—C5	107.94 (17)	C12—C17—H17	119.9
C7—C6—C10	125.01 (18)	O3—C18—C8	121.78 (18)
C5—C6—C10	126.97 (17)	O3—C18—C19	118.57 (17)
C6—C7—C8	108.49 (17)	C8—C18—C19	119.64 (17)
C6—C7—C12	126.51 (17)	C24—C19—C20	119.31 (19)
C8—C7—C12	124.99 (17)	C24—C19—C18	122.16 (18)
C7—C8—N1	106.72 (16)	C20—C19—C18	118.54 (19)
C7—C8—C18	131.69 (18)	C21—C20—C19	120.6 (2)
N1—C8—C18	121.52 (17)	C21—C20—H20	119.7
C3—C9—H9A	109.5	C19—C20—H20	119.7
C3—C9—H9B	109.5	C22—C21—C20	117.8 (2)
H9A—C9—H9B	109.5	C22—C21—H21	121.1
C3—C9—H9C	109.5	C20—C21—H21	121.1
H9A—C9—H9C	109.5	C23—C22—F1	118.3 (2)
H9B—C9—H9C	109.5	C23—C22—C21	123.6 (2)
O1—C10—O2	121.96 (18)	F1—C22—C21	118.1 (2)
O1—C10—C6	125.95 (18)	C22—C23—C24	117.9 (2)
O2—C10—C6	112.09 (17)	C22—C23—H23	121.0
O2—C11—H11A	109.5	C24—C23—H23	121.0
O2—C11—H11B	109.5	C19—C24—C23	120.7 (2)
H11A—C11—H11B	109.5	C19—C24—H24	119.6
O2—C11—H11C	109.5	C23—C24—H24	119.6
C5—N1—C1—C2	0.4 (3)	C7—C6—C10—O2	−172.44 (18)
C8—N1—C1—C2	177.53 (19)	C5—C6—C10—O2	11.1 (3)
N1—C1—C2—C3	−1.2 (3)	C6—C7—C12—C13	−121.3 (2)
C1—C2—C3—C4	1.2 (3)	C8—C7—C12—C13	57.4 (3)
C1—C2—C3—C9	−178.8 (2)	C6—C7—C12—C17	62.2 (3)
C2—C3—C4—C5	−0.4 (3)	C8—C7—C12—C17	−119.0 (2)
C9—C3—C4—C5	179.56 (19)	C17—C12—C13—C14	1.7 (3)
C1—N1—C5—C4	0.4 (3)	C7—C12—C13—C14	−174.86 (18)
C8—N1—C5—C4	−177.26 (17)	C12—C13—C14—C15	−0.2 (3)
C1—N1—C5—C6	179.55 (18)	C13—C14—C15—C16	−0.8 (3)
C8—N1—C5—C6	1.9 (2)	C14—C15—C16—C17	0.2 (3)
C3—C4—C5—N1	−0.4 (3)	C15—C16—C17—C12	1.3 (3)
C3—C4—C5—C6	−179.2 (2)	C13—C12—C17—C16	−2.2 (3)
N1—C5—C6—C7	−1.1 (2)	C7—C12—C17—C16	174.28 (19)
C4—C5—C6—C7	177.8 (2)	C7—C8—C18—O3	−157.8 (2)
N1—C5—C6—C10	175.82 (18)	N1—C8—C18—O3	19.0 (3)
C4—C5—C6—C10	−5.3 (4)	C7—C8—C18—C19	21.5 (3)
C5—C6—C7—C8	0.0 (2)	N1—C8—C18—C19	−161.76 (18)
C10—C6—C7—C8	−177.05 (19)	O3—C18—C19—C24	−134.5 (2)
C5—C6—C7—C12	178.88 (19)	C8—C18—C19—C24	46.2 (3)
C10—C6—C7—C12	1.9 (3)	O3—C18—C19—C20	45.5 (3)
C6—C7—C8—N1	1.2 (2)	C8—C18—C19—C20	−133.8 (2)
C12—C7—C8—N1	−177.78 (18)	C24—C19—C20—C21	−2.6 (3)
C6—C7—C8—C18	178.3 (2)	C18—C19—C20—C21	177.43 (19)
C12—C7—C8—C18	−0.7 (3)	C19—C20—C21—C22	1.4 (3)
C1—N1—C8—C7	−179.3 (2)	C20—C21—C22—C23	0.6 (3)
C5—N1—C8—C7	−1.9 (2)	C20—C21—C22—F1	−179.8 (2)
C1—N1—C8—C18	3.2 (3)	F1—C22—C23—C24	178.97 (19)
C5—N1—C8—C18	−179.35 (17)	C21—C22—C23—C24	−1.4 (3)
C11—O2—C10—O1	−1.0 (3)	C20—C19—C24—C23	1.7 (3)
C11—O2—C10—C6	179.33 (17)	C18—C19—C24—C23	−178.30 (19)
C7—C6—C10—O1	7.9 (3)	C22—C23—C24—C19	0.2 (3)
C5—C6—C10—O1	−168.6 (2)

D—H···A	D—H	H···A	D···A	D—H···A
C1—H1···O3	0.95	2.26	2.853 (3)	120
C4—H4···O2	0.95	2.38	2.927 (2)	116
C21—H21···O3i	0.95	2.54	3.399 (3)	149
C2—H2···O1ii	0.95	2.63	3.531 (4)	157
C15—H15···O3iii	0.95	2.76	3.519 (4)	137
C1—H1···C15ii	0.95	2.74	3.6064 (3)	152
C11—H11A···C5iv	0.98	2.74	3.4906 (1)	133
C11—H11B···F1v	0.98	2.67	3.0585 (3)	104
C23—H23···O3vi	0.95	2.67	3.4875 (3)	143