research communications
[2-Chloro-3-nitro-5-(trifluoromethyl)phenyl](piperidin-1-yl)methanone: structural characterization of a side product in benzothiazinone synthesis
aInstitut für Pharmazie, Wolfgang-Langenbeck-Str. 4, 06120 Halle (Saale), Germany, and bMax-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, Germany
*Correspondence e-mail: ruediger.seidel@pharmazie.uni-halle.de
1,3-Benzothiazin-4-ones (BTZs) are a promising new class of anti-tuberculosis drug candidates, some of which have reached clinical trials. The title compound, the benzamide derivative [2-chloro-3-nitro-5-(trifluoromethyl)phenyl](piperidin-1-yl)methanone, C13H12ClF3N2O3, occurs as a side product as a result of competitive reaction pathways in the nucleophilic attack during the synthesis of the BTZ 8-nitro-2-(piperidin-1-yl)-6-(trifluoromethyl)-1,3-benzothiazin-4-one, following the original synthetic route, whereby the corresponding benzoyl isothiocyanate is reacted with piperidine as secondary amine. In the title compound, the nitro group and the nearly planar amide group are significantly twisted out of the plane of the benzene ring. The piperidine ring adopts a chair conformation. The trifluoromethyl group exhibits slight rotational disorder with a refined ratio of occupancies of 0.972 (2):0.028 (2). There is structural evidence for intermolecular weak C—H⋯O hydrogen bonds.
Keywords: benzothiazinones; nitrobenzamides; anti-tuberculosis drugs; reaction mechanism; crystal structure.
CCDC reference: 2021003
1. Chemical context
1,3-Benzothiazin-4-ones (BTZs) are promising anti-tuberculosis drug candidates, some of which have already reached clinical trials (Mikušová et al., 2014; Makarov & Mikušová, 2020). Various methods for the synthesis of BTZs have been reported (Makarov et al., 2007; Moellmann et al., 2009; Makarov, 2011; Rudolph, 2014; Rudolph et al., 2016; Zhang & Aldrich, 2019). In the original synthesis, 2-chlorobenzoyl chloride derivatives are reacted with ammonium or alkali metal thiocyanates to form the corresponding 2-chlorobenzoyl isothiocyanates (Makarov et al., 2007; Moellmann et al., 2009). These are reactive species and are treated in situ with secondary to afford the corresponding thiourea derivatives, which undergo ring closure to give 1,3-thiazin-4-ones via an intramolecular nucleophilic The latter step is favoured when electron-withdrawing substituents are present on the benzene ring.
Fig. 1 depicts the synthesis following the original procedure for a BTZ previously reported by us (Rudolph, 2014; Rudolph et al., 2016; Richter, Rudolph et al., 2018). After treatment of 2-chloro-3-nitro-5-(trifluoromethyl)benzoic acid (1) with thionyl chloride and subsequently ammonium thiocyanate, the corresponding 2-chloro-3-nitro-5-(trifluoromethyl)benzoyl isothiocyanate (2) was reacted with piperidine. As illustrated, nucleophilic attack of the piperidine nitrogen atom at the isothiocyanate carbon atom leads to the anticipated 8-nitro-2-(piperidin-1-yl)-6-(trifluoromethyl)-1,3-benzothiazin-4-one (3). The alternative nucleophilic attack at the carbonyl carbon atom affords the side product (2-chloro-3-nitro-5-(trifluoromethyl)phenyl)(piperidin-1-yl)methanone (4), which was structurally characterized by X-ray crystallography in the present work. The ratio of 3 to 4 was found to vary depending on the reaction conditions. Temperatures at or below 283 K favour the formation of the anticipated 3, whereas substantial amounts of 4 form at elevated temperatures (Rudolph, 2014). Since BTZs are in clinical development [see, for example, Makarov & Mikušová (2020) or Mariandyshev et al. (2020)], this observation is not only important for the improvement of synthetic yields but also for the compilation of known synthetic side products for drug quality control.
It is interesting to note that dinitrobenzamide derivatives related to 4 have been found to have some anti-mycobacterial activity (Christophe et al., 2009; Trefzer et al., 2010; Tiwari et al., 2013), and the non-chlorinated analogue of 4 was reported to have anticoccidial activity (Welch et al., 1969).
2. Structural commentary
Fig. 2 shows the molecular structure of 4 in the solid state. Selected geometric parameters are listed in Table 1. The dihedral angle between the plane of the nitro group and the mean plane of the benzene ring is 38.1 (2)°, which can be attributed to the steric demand of the neighbouring chloro substituent at the benzene ring. The trifluoromethyl group exhibits rotational disorder over two sites with 97.2 (2)% occupancy for the major site. The plane of the amide group, as defined by C8, O3 and N2, is tilted out of the mean plane of the benzene ring by 79.6 (1)°. The Winkler–Dunitz parameters for the amide linkage τ (twist angle) = 1.2° and χN (pyramidalization at nitrogen) = 4.0° indicate an almost planar amide group (Winkler & Dunitz, 1971). In the IR spectrum (see supporting information), the band at 1639 cm−1 can be assigned to the C=O stretching vibration of the amide group. The molecule is axially chiral, although the centrosymmetric contains both enantiomers. The 13C NMR spectrum of 4 in methanol-d4 as well as chloroform-d at room temperature (see supporting information) displays five distinct signals in the aliphatic region, which are assigned to the piperidine carbon atoms, indicating that the rotation about the amide C—N bond is slow in solution under these conditions. The 13C NMR of the α-carbon atom C13 syn to the carbonyl oxygen atom of the amide group is shielded compared with that of the anti α-carbon atom C9. In chloroform-d, the observed shielding magnitude of ΔδC = 5.0 ppm is within the range expected for a benzoylpiperidine (Rubiralta et al., 1991). In the corresponding 1H NMR spectrum, the syn protons with respect to the amide carbonyl oxygen atom are deshielded compared with those in the anti position (ΔδH = 0.58 ppm). Complete assignments of 1H and 13C NMR data in chloroform-d by 13C,1H-HSQC and -HMBC NMR spectra can be found in the supporting information. Notably, the two separated methylene 1H NMR signals assigned to C10 in chloroform-d appear as one signal in methanol-d4.
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In the solid state, the piperidine ring in 4 adopts a low-energy chair conformation with some minor angular deviations from ideal tetrahedral values, resulting from planarity at N2 due to involvement in the amide linkage. The puckering parameters of the piperidine six-membered ring, as calculated with PLATON (Spek, 2020), are Q = 0.555 (2) Å, θ = 4.1 (2)° and φ = 161 (3)°. By way of comparison, the total puckering amplitude Q is 0.63 Å and the magnitude of distortion θ is 0° for an ideal cyclohexane chair (Cremer & Pople, 1975).
3. Supramolecular features
In general, the 4 appears to be dominated by close packing. According to Kitaigorodskii (1973), the Pbca is among those available for the densest packing of molecules of arbitrary shape. Nevertheless, the solid-state supramolecular structure features C—H⋯O contacts between an aromatic CH moiety and the amide oxygen atom of an adjacent molecule (Fig. 3a). The corresponding geometric parameters (Table 2) support the interpretation as a weak hydrogen bond (Thakuria et al., 2017). These interactions link the molecules into strands extending by 21 screw symmetry in the [010] direction. The α-methylene groups of the piperidine ring, on which the amide group should exert an electron-withdrawing effect, also form intermolecular C—H⋯O and C—H⋯π contacts, respectively, to the nitro group and the benzene ring of adjacent molecules (Fig. 3b–d). The corresponding geometric parameters (Table 2), however, reveal that these contacts may not have the same significance here as the aforementioned Caromatic—H⋯Oamide short contact (Wood et al., 2009). It is also worth noting that π–π stacking of the aromatic rings is not observed.
of4. Database survey
A search of the Cambridge Structural Database (CSD; version 5.41 with March 2020 updates; Groom et al., 2016) for related substituted N-benzoyl-piperidine compounds revealed about 30 structures, of which (2-chloro-3,5-dinitrophenyl)(piperidin-1-yl)methanone (CSD refcode: URALIJ; Luo et al., 2011) is structurally most related to 4. Similar to 4, the 3-nitro group with the neighbouring chloro substituent is tilted out of the mean plane of the benzene ring by 36.2°. At 75.8°, the dihedral angle between the amide plane and the mean plane of the benzene ring is comparable with that in 4. Likewise, the piperidine ring exhibits a chair conformation with a planar structure at the nitrogen atom. In contrast to 4, the solid-state supramolecular structure of URALIJ exhibits π–π stacking of the aromatic rings. Interestingly, a CSD search for the 2-chloro-3-nitro-5-(trifluoromethyl)phenyl moiety present in 4 led to only one structure, viz. 2-chloro-1,3-dinitro-5-(trifluoromethyl)benzene (JIHNUM; del Casino et al., 2018), also known as chloralin, which is active against Plasmodium, but which also shows toxicity in mice.
5. Anti-mycobacterial evaluation
The anti-mycobacterial activity of 4 was evaluated against Mycobacterium smegmatis mc2 155 and Mycobacterium abscessus ATCC19977, using broth microdilution assays [for the assay protocols, see the supporting information and Richter, Strauch et al. (2018)]. For both mycobacterial species, no growth inhibition was detectable up to a concentration of 100 µM. For M. smegmatis, the findings are consistent with the activity data for a related nitrobenzamide derivative reported by Tiwari et al. (2013). CT319, a 3-nitro-5-(trifluoromethyl)benzamide derivative, however, showed activity against M. smegmatis mc2 155 and other mycobacterial strains (Trefzer et al., 2010).
6. Synthesis and crystallization
Chemicals were purchased and used as received. The synthesis of 1 is described elsewhere (Welch et al., 1969). Solvents were of reagent grade and were distilled before use. The IR spectrum was measured on a Bruker TENSOR II FT–IR spectrometer at a resolution of 4 cm−1. NMR spectra were recorded at room temperature on an Agilent Technologies VNMRS 400 MHz NMR spectrometer (abbreviations: d = doublet, q = quartet, m = multiplet). Chemical shifts are referenced to the residual signals of methanol-d4 (δH = 3.35 ppm, δC = 49.3 ppm) or chloroform-d (δH = 7.26 ppm, δC = 77.2 ppm).
2.7 mL (37.0 mmol) of SOCl2 were added to a stirred solution of 1 (5.00 g,18.5 mmol) in toluene, and the mixture was heated to reflux for two h. The solvent was subsequently removed under reduced pressure, and the acid chloride thus obtained was used without purification. The residue was taken up in 6.5 mL of acetonitrile and a solution of 1.41 g (18.5 mmol) NH4SCN in 55 mL of acetonitrile was added dropwise with stirring to obtain 2 in situ. After stirring for 5 min at 313 K, the resulting NH4Cl precipitate was filtered off, and 3.7 mL (37.0 mmol) of piperidine were added. The mixture was refluxed overnight, and then the solvent was removed under reduced pressure. Water was added to the residue and, after extraction with dichloromethane, the organic phase was washed with 10% aqueous NaHCO3 and dried over MgSO4. After removal of the solvent, the crude product was subjected to flash on silica gel, eluting with ethyl acetate/n-heptane (gradient 10–50% v/v), to isolate 1.09 g (3.0 mmol, 16%) of 3 and a minor amount of the side product 4. 1H and 13C NMR spectroscopic and mass spectrometric data of 3 were in agreement with those in the literature (Rudolph, 2014; Rudolph et al., 2016). Crystals of 4 suitable for X-ray crystallography were obtained from a solution in ethyl acetate/heptane (1:1) by slow evaporation of the solvents at room temperature. NMR spectroscopic data for 4:
1H NMR (400 MHz, CD3OD) δ 8.42 (d, 4Jmeta = 2.2 Hz, 1H, Ar—H), 8.09 (d, 4Jmeta = 2.2 Hz, 1H, Ar—H), 3.88–3.71 (m, 2H, N—CH2), 3.33–3.21 (m, 2H, N—CH2), 1.76 (m, 4H, CH2), 1.64 (m, 2H, CH2) ppm; 13C NMR (101 MHz, CD3OD) δ 165.5, 150.7, 141.8, 132.3 (q, 2JC,F = 35 Hz), 129.2 (q, 3JC,F = 4 Hz), 128.1, 124.4 (q, 3JC,F = 4 Hz), 124.1 (q, 1JC,F = 273 Hz), 49.5, 44.3, 27.6, 26.7, 25.5 ppm.
1H NMR (400 MHz, CDCl3 δ) 8.07 (d, 4Jmeta = 2.0 Hz, 1H, C4—H), 7.73 (d, 4Jmeta = 2.0 Hz, 1H, C6—H), 3.83–3.68 (m, 2H, C13—CH2), 3.22 (ddd, 2Jgem = 13.2 Hz, 3Jvic = 7.1, 4.0 Hz, 1H, C9—CH2), 3.15 (ddd, 2Jgem = 13.2 Hz, 3Jvic = 7.1, 4.0 Hz, 1H, C9—CH2), 1.70 (m, 4H, C11, C12—CH2), 1.65–1.57 (m, 1H, C10—CH2), 1.56–1.47 (m, 1H, C10—CH2) ppm; 13C NMR (101 MHz, CDCl3 δ) 163.5 (C8, C=O), 148.9 (C3), 141.1 (C1), 131.2 (q, 2JC,F = 35 Hz, C5), 127.8 (q, 3JC,F = 4 Hz, C6), 127.6 (C2), 122.7 (q, 3JC,F = 4 Hz, C4), 122.4 (q, 1JC,F = 273 Hz, C7), 48.3 (C9), 43.3 (C13), 26.7 (C10), 25.7 (C12), 24.6 (C11) ppm.
7. Refinement
Crystal data, data collection and structure . The rotational disorder of the trifluoromethyl group was refined using a split model with similar distance restraints on the 1,2- and 1,3-distances and equal atomic displacement parameters for opposite fluorine atoms belonging to different disorder sites. of the ratio of occupancies by means of a free variable resulted in 0.972 (2):0.028 (2). Hydrogen-atom positions were calculated geometrically with Ca—H = 0.95 Å and Cm—H = 0.99 Å (a = aromatic and m = methylene), and refined with the appropriate riding model and Uiso(H) = 1.2 Ueq(C).
details are summarized in Table 3Supporting information
CCDC reference: 2021003
https://doi.org/10.1107/S2056989020010658/vm2238sup1.cif
contains datablocks global, I. DOI:Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S2056989020010658/vm2238Isup2.hkl
Supporting information file. DOI: https://doi.org/10.1107/S2056989020010658/vm2238Isup3.cdx
IR and NMR spectra, assay protocol for anti-mycobacterial activity. DOI: https://doi.org/10.1107/S2056989020010658/vm2238sup4.pdf
Supporting information file. DOI: https://doi.org/10.1107/S2056989020010658/vm2238Isup5.cml
Data collection: APEX3 (Bruker, 2017); cell
SAINT (Bruker, 2004); data reduction: SAINT (Bruker, 2004); program(s) used to solve structure: SHELXT2014/4 (Sheldrick, 2015a); program(s) used to refine structure: SHELXL2018/3 (Sheldrick, 2015b); molecular graphics: DIAMOND (Brandenburg, 2018); software used to prepare material for publication: enCIFer (Allen et al., 2004) and publCIF (Westrip, 2010).C13H12ClF3N2O3 | Dx = 1.581 Mg m−3 |
Mr = 336.70 | Cu Kα radiation, λ = 1.54178 Å |
Orthorhombic, Pbca | Cell parameters from 9968 reflections |
a = 18.0904 (7) Å | θ = 4.9–71.6° |
b = 7.8971 (3) Å | µ = 2.88 mm−1 |
c = 19.8043 (8) Å | T = 100 K |
V = 2829.28 (19) Å3 | Block, colourless |
Z = 8 | 0.59 × 0.50 × 0.44 mm |
F(000) = 1376 |
Bruker Kappa Mach3 APEXII diffractometer | 2784 independent reflections |
Radiation source: 0.2 × 2 mm2 focus rotating anode | 2699 reflections with I > 2σ(I) |
MONTEL graded multilayer optics monochromator | Rint = 0.041 |
Detector resolution: 66.67 pixels mm-1 | θmax = 72.2°, θmin = 4.9° |
φ– and ω–scans | h = −21→22 |
Absorption correction: gaussian (SADABS; Krause et al., 2015) | k = −9→9 |
Tmin = 0.297, Tmax = 0.586 | l = −24→24 |
49954 measured reflections |
Refinement on F2 | Primary atom site location: dual |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.043 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.115 | H-atom parameters constrained |
S = 1.15 | w = 1/[σ2(Fo2) + (0.0508P)2 + 2.7994P] where P = (Fo2 + 2Fc2)/3 |
2784 reflections | (Δ/σ)max < 0.001 |
209 parameters | Δρmax = 0.32 e Å−3 |
45 restraints | Δρmin = −0.32 e Å−3 |
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 | Occ. (<1) | |
C1 | 0.41556 (10) | 0.3250 (3) | 0.23581 (10) | 0.0230 (4) | |
C2 | 0.38370 (10) | 0.1651 (3) | 0.23833 (10) | 0.0224 (4) | |
C3 | 0.35007 (10) | 0.1004 (3) | 0.18023 (10) | 0.0227 (4) | |
C4 | 0.34763 (10) | 0.1927 (3) | 0.12111 (10) | 0.0243 (4) | |
H4 | 0.325215 | 0.146458 | 0.081847 | 0.029* | |
C5 | 0.37831 (10) | 0.3541 (3) | 0.11961 (10) | 0.0242 (4) | |
C6 | 0.41190 (11) | 0.4206 (3) | 0.17666 (10) | 0.0250 (4) | |
H6 | 0.432417 | 0.531321 | 0.175487 | 0.030* | |
C7 | 0.37425 (12) | 0.4549 (3) | 0.05572 (11) | 0.0298 (5) | |
C8 | 0.45848 (10) | 0.3906 (2) | 0.29575 (10) | 0.0232 (4) | |
C9 | 0.34929 (13) | 0.5683 (3) | 0.32422 (11) | 0.0327 (5) | |
H9A | 0.325497 | 0.503425 | 0.287381 | 0.039* | |
H9B | 0.351745 | 0.688568 | 0.310277 | 0.039* | |
C10 | 0.30335 (12) | 0.5528 (3) | 0.38813 (13) | 0.0404 (6) | |
H10A | 0.296350 | 0.431647 | 0.399304 | 0.048* | |
H10B | 0.254021 | 0.603627 | 0.380559 | 0.048* | |
C11 | 0.34134 (13) | 0.6421 (3) | 0.44689 (11) | 0.0373 (5) | |
H11A | 0.344826 | 0.764952 | 0.437412 | 0.045* | |
H11B | 0.311898 | 0.626777 | 0.488581 | 0.045* | |
C12 | 0.41843 (12) | 0.5691 (3) | 0.45695 (10) | 0.0294 (5) | |
H12A | 0.443955 | 0.632047 | 0.493365 | 0.035* | |
H12B | 0.414464 | 0.449164 | 0.470978 | 0.035* | |
C13 | 0.46343 (11) | 0.5807 (3) | 0.39245 (10) | 0.0277 (4) | |
H13A | 0.473754 | 0.701122 | 0.382205 | 0.033* | |
H13B | 0.511333 | 0.522352 | 0.398982 | 0.033* | |
N1 | 0.31581 (9) | −0.0681 (2) | 0.17845 (9) | 0.0253 (4) | |
N2 | 0.42423 (9) | 0.5038 (2) | 0.33544 (8) | 0.0249 (4) | |
O1 | 0.28104 (8) | −0.1161 (2) | 0.22819 (8) | 0.0324 (4) | |
O2 | 0.32229 (8) | −0.1493 (2) | 0.12611 (8) | 0.0341 (4) | |
O3 | 0.52198 (7) | 0.33806 (19) | 0.30471 (7) | 0.0288 (3) | |
F1 | 0.38438 (14) | 0.3603 (2) | 0.00122 (7) | 0.0711 (7) | 0.972 (2) |
F2 | 0.30831 (8) | 0.52847 (19) | 0.04797 (8) | 0.0418 (4) | 0.972 (2) |
F3 | 0.42321 (8) | 0.5801 (2) | 0.05379 (8) | 0.0470 (4) | 0.972 (2) |
F1' | 0.352 (3) | 0.612 (3) | 0.0688 (18) | 0.0711 (7) | 0.028 (2) |
F2' | 0.4387 (11) | 0.472 (6) | 0.0269 (18) | 0.0418 (4) | 0.028 (2) |
F3' | 0.325 (2) | 0.397 (5) | 0.0129 (15) | 0.0470 (4) | 0.028 (2) |
Cl1 | 0.38924 (3) | 0.05417 (6) | 0.31320 (2) | 0.02635 (16) |
U11 | U22 | U33 | U12 | U13 | U23 | |
C1 | 0.0194 (9) | 0.0250 (9) | 0.0246 (9) | 0.0021 (7) | 0.0012 (7) | −0.0019 (8) |
C2 | 0.0186 (8) | 0.0246 (9) | 0.0239 (9) | 0.0021 (7) | 0.0011 (7) | 0.0002 (8) |
C3 | 0.0166 (8) | 0.0219 (9) | 0.0296 (10) | 0.0011 (7) | 0.0009 (7) | −0.0021 (8) |
C4 | 0.0202 (9) | 0.0288 (10) | 0.0239 (9) | 0.0050 (8) | −0.0004 (7) | −0.0031 (8) |
C5 | 0.0219 (9) | 0.0261 (10) | 0.0247 (10) | 0.0056 (8) | 0.0021 (7) | 0.0011 (8) |
C6 | 0.0248 (10) | 0.0226 (9) | 0.0277 (10) | 0.0006 (8) | 0.0004 (8) | 0.0002 (8) |
C7 | 0.0350 (11) | 0.0292 (11) | 0.0251 (10) | 0.0056 (9) | 0.0005 (8) | −0.0002 (8) |
C8 | 0.0225 (9) | 0.0226 (9) | 0.0245 (9) | −0.0035 (8) | −0.0003 (7) | 0.0033 (8) |
C9 | 0.0335 (11) | 0.0298 (11) | 0.0347 (11) | 0.0094 (9) | −0.0117 (9) | −0.0088 (9) |
C10 | 0.0200 (10) | 0.0517 (15) | 0.0495 (14) | 0.0058 (9) | −0.0038 (9) | −0.0188 (11) |
C11 | 0.0324 (11) | 0.0474 (14) | 0.0322 (11) | 0.0039 (10) | −0.0011 (9) | −0.0114 (10) |
C12 | 0.0308 (11) | 0.0327 (11) | 0.0247 (10) | −0.0010 (9) | −0.0013 (8) | 0.0002 (8) |
C13 | 0.0267 (10) | 0.0306 (10) | 0.0257 (10) | −0.0070 (8) | −0.0028 (8) | −0.0018 (8) |
N1 | 0.0190 (8) | 0.0260 (9) | 0.0310 (9) | −0.0009 (6) | −0.0037 (7) | −0.0016 (7) |
N2 | 0.0213 (8) | 0.0277 (9) | 0.0257 (8) | −0.0010 (7) | −0.0042 (7) | −0.0030 (7) |
O1 | 0.0267 (7) | 0.0334 (8) | 0.0371 (8) | −0.0062 (6) | 0.0010 (6) | 0.0028 (7) |
O2 | 0.0348 (8) | 0.0320 (8) | 0.0356 (8) | −0.0010 (6) | −0.0045 (6) | −0.0098 (7) |
O3 | 0.0204 (7) | 0.0324 (8) | 0.0337 (8) | 0.0005 (6) | −0.0017 (6) | −0.0003 (6) |
F1 | 0.151 (2) | 0.0382 (9) | 0.0239 (7) | 0.0278 (10) | 0.0154 (9) | −0.0002 (6) |
F2 | 0.0336 (7) | 0.0457 (8) | 0.0460 (8) | 0.0053 (6) | −0.0056 (6) | 0.0175 (7) |
F3 | 0.0389 (8) | 0.0567 (10) | 0.0453 (8) | −0.0142 (7) | −0.0052 (6) | 0.0251 (7) |
F1' | 0.151 (2) | 0.0382 (9) | 0.0239 (7) | 0.0278 (10) | 0.0154 (9) | −0.0002 (6) |
F2' | 0.0336 (7) | 0.0457 (8) | 0.0460 (8) | 0.0053 (6) | −0.0056 (6) | 0.0175 (7) |
F3' | 0.0389 (8) | 0.0567 (10) | 0.0453 (8) | −0.0142 (7) | −0.0052 (6) | 0.0251 (7) |
Cl1 | 0.0267 (3) | 0.0273 (3) | 0.0250 (3) | −0.00271 (18) | 0.00002 (17) | 0.00364 (17) |
C1—C2 | 1.389 (3) | C8—N2 | 1.342 (3) |
C1—C6 | 1.395 (3) | C9—N2 | 1.465 (3) |
C1—C8 | 1.510 (3) | C9—C10 | 1.519 (3) |
C2—C3 | 1.398 (3) | C9—H9A | 0.9900 |
C2—Cl1 | 1.725 (2) | C9—H9B | 0.9900 |
C3—C4 | 1.380 (3) | C10—C11 | 1.525 (3) |
C3—N1 | 1.468 (3) | C10—H10A | 0.9900 |
C4—C5 | 1.390 (3) | C10—H10B | 0.9900 |
C4—H4 | 0.9500 | C11—C12 | 1.522 (3) |
C5—C6 | 1.386 (3) | C11—H11A | 0.9900 |
C5—C7 | 1.497 (3) | C11—H11B | 0.9900 |
C6—H6 | 0.9500 | C12—C13 | 1.518 (3) |
C7—F2' | 1.304 (14) | C12—H12A | 0.9900 |
C7—F3' | 1.314 (14) | C12—H12B | 0.9900 |
C7—F1 | 1.325 (3) | C13—N2 | 1.465 (2) |
C7—F3 | 1.328 (3) | C13—H13A | 0.9900 |
C7—F1' | 1.332 (14) | C13—H13B | 0.9900 |
C7—F2 | 1.336 (3) | N1—O2 | 1.225 (2) |
C8—O3 | 1.234 (2) | N1—O1 | 1.229 (2) |
C2—C1—C6 | 120.16 (18) | C10—C9—H9A | 109.5 |
C2—C1—C8 | 119.82 (17) | N2—C9—H9B | 109.5 |
C6—C1—C8 | 119.90 (17) | C10—C9—H9B | 109.5 |
C1—C2—C3 | 118.92 (18) | H9A—C9—H9B | 108.1 |
C1—C2—Cl1 | 117.93 (15) | C9—C10—C11 | 110.61 (19) |
C3—C2—Cl1 | 123.13 (16) | C9—C10—H10A | 109.5 |
C4—C3—C2 | 121.24 (18) | C11—C10—H10A | 109.5 |
C4—C3—N1 | 116.41 (17) | C9—C10—H10B | 109.5 |
C2—C3—N1 | 122.35 (18) | C11—C10—H10B | 109.5 |
C3—C4—C5 | 119.32 (18) | H10A—C10—H10B | 108.1 |
C3—C4—H4 | 120.3 | C12—C11—C10 | 109.74 (18) |
C5—C4—H4 | 120.3 | C12—C11—H11A | 109.7 |
C6—C5—C4 | 120.33 (18) | C10—C11—H11A | 109.7 |
C6—C5—C7 | 120.58 (19) | C12—C11—H11B | 109.7 |
C4—C5—C7 | 119.09 (18) | C10—C11—H11B | 109.7 |
C5—C6—C1 | 119.98 (19) | H11A—C11—H11B | 108.2 |
C5—C6—H6 | 120.0 | C13—C12—C11 | 111.01 (18) |
C1—C6—H6 | 120.0 | C13—C12—H12A | 109.4 |
F2'—C7—F3' | 111.1 (19) | C11—C12—H12A | 109.4 |
F1—C7—F3 | 107.69 (19) | C13—C12—H12B | 109.4 |
F2'—C7—F1' | 105.2 (19) | C11—C12—H12B | 109.4 |
F3'—C7—F1' | 104.0 (19) | H12A—C12—H12B | 108.0 |
F1—C7—F2 | 105.98 (19) | N2—C13—C12 | 111.35 (17) |
F3—C7—F2 | 105.59 (17) | N2—C13—H13A | 109.4 |
F2'—C7—C5 | 112.3 (15) | C12—C13—H13A | 109.4 |
F3'—C7—C5 | 113.2 (15) | N2—C13—H13B | 109.4 |
F1—C7—C5 | 112.43 (17) | C12—C13—H13B | 109.4 |
F3—C7—C5 | 112.80 (18) | H13A—C13—H13B | 108.0 |
F1'—C7—C5 | 110.3 (15) | O2—N1—O1 | 124.48 (17) |
F2—C7—C5 | 111.86 (17) | O2—N1—C3 | 117.04 (17) |
O3—C8—N2 | 124.72 (18) | O1—N1—C3 | 118.44 (16) |
O3—C8—C1 | 118.43 (18) | C8—N2—C13 | 120.26 (16) |
N2—C8—C1 | 116.85 (17) | C8—N2—C9 | 124.74 (16) |
N2—C9—C10 | 110.59 (18) | C13—N2—C9 | 114.89 (16) |
N2—C9—H9A | 109.5 | ||
C6—C1—C2—C3 | 1.9 (3) | C6—C5—C7—F1' | −47 (3) |
C8—C1—C2—C3 | −174.16 (17) | C4—C5—C7—F1' | 133 (3) |
C6—C1—C2—Cl1 | −179.32 (15) | C6—C5—C7—F2 | −99.4 (2) |
C8—C1—C2—Cl1 | 4.6 (2) | C4—C5—C7—F2 | 80.3 (2) |
C1—C2—C3—C4 | −0.5 (3) | C2—C1—C8—O3 | 77.8 (2) |
Cl1—C2—C3—C4 | −179.22 (14) | C6—C1—C8—O3 | −98.3 (2) |
C1—C2—C3—N1 | 179.37 (16) | C2—C1—C8—N2 | −102.6 (2) |
Cl1—C2—C3—N1 | 0.6 (3) | C6—C1—C8—N2 | 81.4 (2) |
C2—C3—C4—C5 | −0.9 (3) | N2—C9—C10—C11 | 55.5 (3) |
N1—C3—C4—C5 | 179.25 (16) | C9—C10—C11—C12 | −56.9 (3) |
C3—C4—C5—C6 | 0.9 (3) | C10—C11—C12—C13 | 55.8 (3) |
C3—C4—C5—C7 | −178.87 (18) | C11—C12—C13—N2 | −53.4 (2) |
C4—C5—C6—C1 | 0.5 (3) | C4—C3—N1—O2 | 36.6 (2) |
C7—C5—C6—C1 | −179.75 (18) | C2—C3—N1—O2 | −143.29 (19) |
C2—C1—C6—C5 | −1.9 (3) | C4—C3—N1—O1 | −141.34 (18) |
C8—C1—C6—C5 | 174.13 (18) | C2—C3—N1—O1 | 38.8 (3) |
C6—C5—C7—F2' | 70 (2) | O3—C8—N2—C13 | 3.0 (3) |
C4—C5—C7—F2' | −110 (2) | C1—C8—N2—C13 | −176.62 (17) |
C6—C5—C7—F3' | −163 (2) | O3—C8—N2—C9 | 179.0 (2) |
C4—C5—C7—F3' | 17 (2) | C1—C8—N2—C9 | −0.6 (3) |
C6—C5—C7—F1 | 141.5 (2) | C12—C13—N2—C8 | −130.0 (2) |
C4—C5—C7—F1 | −38.8 (3) | C12—C13—N2—C9 | 53.6 (2) |
C6—C5—C7—F3 | 19.5 (3) | C10—C9—N2—C8 | 129.2 (2) |
C4—C5—C7—F3 | −160.82 (18) | C10—C9—N2—C13 | −54.6 (2) |
D—H···A | D—H | H···A | D···A | D—H···A |
C6—H6···O3i | 0.95 | 2.59 | 3.526 (3) | 169 |
C9—H9A···O1ii | 0.99 | 2.45 | 3.361 (3) | 154 |
C9—H9B···O1iii | 0.99 | 2.58 | 3.369 (3) | 137 |
C13—H13A···Cg(C1–C6)iv | 0.99 | 2.92 | 3.447 (2) | 114 |
Symmetry codes: (i) −x+1, y+1/2, −z+1/2; (ii) −x+1/2, y+1/2, z; (iii) x, y+1, z; (iv) x+3/2, −y+1/2, −z. |
Acknowledgements
We thank Professor Christian W. Lehmann for providing access to the X-ray diffraction facility and Heike Schucht for technical assistance.
Funding information
We acknowledge the financial support within the funding programme Open Access Publishing by the German Research Foundation (DFG).
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