Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S2053229619005746/yf3175sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S2053229619005746/yf3175IVasup2.hkl | |
Structure factor file (CIF format) https://doi.org/10.1107/S2053229619005746/yf3175Vbsup3.hkl |
CCDC references: 1912496; 1912495
For both structures, data collection: APEX3 (Bruker, 2016); cell refinement: SAINT (Bruker, 2016); data reduction: SAINT (Bruker, 2016); program(s) used to solve structure: SIR92 (Altomare et al., 1994); program(s) used to refine structure: SHELXL2014 (Sheldrick, 2015); molecular graphics: PLATON (Spek, 2009); software used to prepare material for publication: SHELXL2014 (Sheldrick, 2015) and PLATON (Spek, 2009).
C22H20FNO3 | F(000) = 768 |
Mr = 365.39 | Dx = 1.361 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
a = 9.5920 (6) Å | Cell parameters from 4414 reflections |
b = 13.4325 (7) Å | θ = 2.2–28.3° |
c = 14.2186 (8) Å | µ = 0.10 mm−1 |
β = 103.290 (2)° | T = 100 K |
V = 1782.93 (18) Å3 | Needle, colourless |
Z = 4 | 0.30 × 0.10 × 0.10 mm |
Bruker D8 Venture diffractometer | 4414 independent reflections |
Radiation source: INCOATEC high brilliance microfocus sealed tube | 3808 reflections with I > 2σ(I) |
Multilayer mirror monochromator | Rint = 0.037 |
φ and ω scans | θmax = 28.3°, θmin = 2.2° |
Absorption correction: multi-scan (SADABS; Bruker, 2015) | h = −12→12 |
Tmin = 0.962, Tmax = 0.990 | k = −17→17 |
33534 measured reflections | l = −18→18 |
Refinement on F2 | Primary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.040 | H-atom parameters constrained |
wR(F2) = 0.112 | w = 1/[σ2(Fo2) + (0.050P)2 + 0.9921P] where P = (Fo2 + 2Fc2)/3 |
S = 1.06 | (Δ/σ)max = 0.001 |
4414 reflections | Δρmax = 0.52 e Å−3 |
246 parameters | Δρmin = −0.32 e Å−3 |
0 restraints |
Experimental. Spectroscopic data for compounds (IIIa), (IIIb), (IVa), (Va) and (Vb). IR spectra were recorded in KBr disks using a Bruker Tensor 27 spectrophotometer NMR spectra were recorded at 400 MHz (1H) and 100 MHz (13C) at 298 K, using the signals of the residual non-deuterated (7.26 ppm) and the 13C (77.16 ppm) signals of the solvent, respectively, as the internal references. The subscripts A and B applied to the diastereotopic protons are labels without further significance. The 13C NMR spectra were fully and unambiguously assigned using the DEPT spectra. Mass spectra were recorded using a Thermo model DSQ-II spectrometer, equipped with a direct inlet probe and operating at 70 eV. Compound (IIIa). IR (ATR, cm-1) 3385 (N—H), 2954 [C—H (arom.)], 1481 [C═C (arom.)], 1242 (C—N). NMR (CDCl3): δ(1H) 1.46 (d, J = 6.7 Hz, 3H, 11-CH3), 2.81–2.89 (m, 1H, 12-HB), 3.25–3.35 (m, 2H, 11-H, 12-HA), 4.01 (d, J = 14.7 Hz, 1H, 6-HB), 4.05 (br s, 1H, N—H), 4.88 (d, J = 14.7 Hz, 1H, 6-HA), 6.35 (dd, J = 8.8, 5.2 Hz, 1H, 4-H), 6.54 (td, J = 8.4, 3.0 Hz, 1H, 3-H), 6.69 (dd, J = 9.2, 3.0 Hz, 1H, 1-H), 7.00-7.05 (m, 2H, 7-H, 10-H), 7.06-7.11 (m, 2H, 8-H, 9-H); δ(13C) 24.8 (11-CH3), 40.5 (12-C), 44.5 (11-C), 51.4 (6-C), 113.3 (d, J = 22.4 Hz, 3-C), 114.1 (d, J = 22.1 Hz, 1-C), 119.6 (d, J = 8.9 Hz, 4-C), 126.9 (8-C), 128.0 (9-C), 130.3 (7-C, 10-C), 130.8 (d, J = 8.4 Hz, 12a-C), 135.3 (6a-C), 142.3 (10a-C), 144.8 (d, J = 2.7 Hz, 4a-C), 157.2 (d, J = 247.8 Hz, 2-C). GC-MS (70 eV) m/z (%) 241 (M+, 26), 226 (100), 211 (17), 150 (13), 117 (28), 91 (16). Compound (IIIb). IR (ATR, cm-1) 3383 (N—H), 2951 [C—H (arom.)], 1478 [C═C (arom.)], 1305 (C—N). NMR (CDCl3): δ(1H) 1.45 (d, J = 6.7 Hz, 3H, 11-CH3), 2.80–2.89 (m, 1H, 12-HB), 3.25-3.36 (m, 2H, 11-H, 12-HA), 3.98 (d, J = 14.8 Hz, 1H, 6-HB), 4.06 (br s, 1H, N—H), 4.93 (d, J = 14.8 Hz, 1H, 6-HA), 6.32 (d, J = 8.4 Hz, 1H, 4-H), 6.79 (dd, J = 8.4, 2.5 Hz, 1H, 3-H), 6.94 (d, J = 2.5 Hz, 1H, 1-H), 7.00–7.03 (m, 1H, 10-H), 7.04–7.06 (m, 1H, 7-H), 7.08–7.12 (m, 2H, 8-H, 9-H); δ(13C) 25.1 (11-CH3), 40.2 (12-C), 44.9 (11-C), 51.0 (6-C), 119.6 (4-C), 123.8 (2-C), 126.7 (3-C), 126.9 (8-C), 127.9 (9-C), 129.7 (12a-C), 130.4 (1-C, 10-C), 130.7 (7-C), 135.2 (6a-C), 144.7 (10a-C), 145.1 (4a-C). GC-MS (70 eV) m/z (%) 257 (M+, 35Cl, 46), 242 (35Cl, 100), 207 (43), 166 (15), 140 (13), 117 (59), 91 (25). Compound (IVa). IR (ATR, cm-1) 2935-2971 (C—H), 1723 [C═O (ester)], 1613 [C═O (ketone)], 1483 (C═C), 1142 (C-O). NMR (CDCl3): δ(1H) 1.03 (t, J = 7.2 Hz, 3H, 13-CH2-CH3), 1.41 (t, J = 7.1 Hz, 3H, O-CH2-CH3), 2.25–2.34 (m, 2H, 13-CH2-CH3), 4.15 (br s, 1H, 13-H), 4.39 (q, J = 7.1 Hz, 2H, O-CH2-), 5.00 (br s, 1H, 8-HB), 5.83 (br s, 1H, 8-HA), 7.23 (dd, J = 7.4, 1.1 Hz, 1H, 12-H), 7.28-7.38 (m, 3H, 1-H, 10-H, 11-H), 7.41 (dd, J = 7.0, 1.7 Hz, 1H, 9-H), 8.09 (dd, J = 8.4, 3.1 Hz, 1H, 3-H), 8.56 (s, 1H, 6-H); δ13C) 13.1 (13-CH2-CH3), 14.5 (O-CH2-CH3), 31.5 (13-CH2-CH3), 52.2 (13-C), 61.1 (O-CH2-), 61.2 (8-C), 109.1 (5-C), 111.9 (d, J = 22.5 Hz, 3-C), 128.0 (d, J = 22.9 Hz, 1-C), 128.1 (10-C), 129.1 (9-C), 129.2 (12-C), 129.8 (11-C), 131.8 (8a-C), 133.3 (d, J = 7.0 Hz, 3a-C), 135.1 (13a-C), 135.2 (d, J = 1.1 Hz, 3b-C), 140.5 (12a-C), 149.9 (6-C), 159.4 (d, J = 247.7 Hz, 2-C), 165.9 (COO), 173.1 (4-C).; GC-MS (70 eV) m/z (%) 365 (M+, 13), 337 (11), 336 (48), 293 (100), 264 (32). HRMS (Q-TOF-ESI) m/z found 366.1500; for C22H21FNO3 [M + H]+ requires 366.1505. Compound (Va). IR (ATR, cm-1) 2979 [C—H (arom.)], 1648 [C═O (amide)], 1461 [C═C (arom.)], 1382 (C—N). NMR (CDCl3): δ(1H) 1.44 (d, J = 6.7 Hz, 3H, 11-CH3), 1.83 (s, 3H, CO-CH3), 2.34 (dd, J = 15.4, 10.9 Hz, 1H, 12-HB), 3.36 (dd, J = 15.4, 7.2 Hz, 1H, 12-HA), 3.59 (dp, J = 11.4, 6.9 Hz, 1H, 11-H), 4.05 (d, J = 14.7 Hz, 1H, 6-HB), 5.87 (d, J = 14.7 Hz, 1H, 6-HA), 6.60 (dd, J = 9.2, 2.8 Hz, 1H, 1-H), 6.78 (td, J = 8.2, 2.8 Hz, 1H, 3-H), 6.90 (d, J = 7.5 Hz, 1H, 7-H ), 6.95–6.98 (m, 2H, 4-H, 8-H), 7.13–7.19 (m, 2H, 9-H, 10-H); δ(13C) 20.0 (11-CH3), 23.0 (CO-CH3), 32.1 (11-C), 44.9 (12-C), 52.3 (6-C), 114.5 (d, J = 22.2 Hz, 3-C), 117.9 (d, J = 22.1 Hz, 1-C), 124.4 (10-C), 126.3 (8-C), 128.3 (9-C), 129.6 (7-C), 130.2 (d, J = 8.9 Hz, 4-C), 134.0 (6a-C), 135.5 (d, J = 2.9 Hz, 4a-C), 142.0 (d, J = 8.1 Hz, 12a-C), 143.6 (10a-C), 161.8 (d, J = 248.1 Hz, 2-C), 170.1 (C═O). GC-MS (70 eV) m/z (%) 283 (M+, 80), 268 (33), 240 (85), 226 (100), 117 (60). HRMS (Q-TOF-ESI) m/z found 284.1445; for C18H19FNO [M + H]+ requires 284.1445. Compound (Vb). IR (ATR, cm-1) 2962 [C—H (arom.)], 1650 [C═O (amide)], 1488 [C═C (arom.)], 1386 (C—N), 764 (C-Cl). NMR (CDCl3): δ(1H) 1.44 (d, J = 6.8 Hz, 3H, 11-CH3), 1.82 (s, 3H, CO-CH3), 2.33 (dd, J = 15.4, 10.9 Hz, 1H, 12-HB), 3.34 (dd, J = 15.4, 7.3 Hz, 1H, 12-HA), 3.58 (dp, J = 10.9, 6.9 Hz, 1H, 11-H), 4.05 (d, J = 14.8 Hz, 1H, 6-HB), 5.87 (d, J = 14.8 Hz, 1H, 6-HA), 6.89 (d, J = 2.4 Hz, 1H, 1-H), 6.90 (d, J = 7.8 Hz, 1H, 7-H), 6.93 (d, J = 8.3 Hz, 1H, 4-H), 6.95–6.99 (m, 1H, 8-H), 7.07 (dd, J = 8.3, 2.4 Hz, 1H, 3-H), 7.13–7.19 (m, 2H, 9-H, 10-H); δ(13C) 20.0 (11-CH3), 23.0 (CO-CH3), 32.2 (11-C), 44.7 (12-C), 52.3 (6-C), 124.5 (10-C), 126.3 (8-C), 127.8 (3-C), 128.4 (9-C), 129.6 (7-C), 130.0 (4-C), 131.2 (1-C), 133.8 (2-C), 133.9 (6a-C), 138.1 (4a-C), 141.5 (12a-C), 143.5 (10a-C), 169.8 (C═O). GC-MS (70 eV) m/z (%) 299 (M+, 35Cl, 89), 284 (44), 256 (35Cl, 39), 242 (35Cl, 100), 117 (81). HRMS (Q-TOF-ESI) m/z found 300.1146, for C18H19ClNO [M + H]+ requires 300.1150. |
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 | ||
C1 | 0.76704 (13) | 0.48880 (9) | 0.50675 (9) | 0.0170 (2) | |
H1 | 0.8254 | 0.4940 | 0.4613 | 0.020* | |
C2 | 0.68911 (13) | 0.57064 (9) | 0.52398 (9) | 0.0168 (2) | |
F2 | 0.69784 (9) | 0.65521 (6) | 0.47303 (6) | 0.02351 (18) | |
C3 | 0.60800 (13) | 0.57020 (9) | 0.59120 (9) | 0.0157 (2) | |
H3 | 0.5601 | 0.6286 | 0.6044 | 0.019* | |
C3A | 0.59749 (12) | 0.48102 (9) | 0.64018 (8) | 0.0141 (2) | |
C4 | 0.50994 (13) | 0.48376 (9) | 0.71382 (9) | 0.0158 (2) | |
O4 | 0.45295 (11) | 0.56264 (7) | 0.73021 (7) | 0.0233 (2) | |
C5 | 0.50193 (13) | 0.39018 (9) | 0.76189 (9) | 0.0151 (2) | |
C6 | 0.56364 (12) | 0.30668 (9) | 0.73232 (8) | 0.0149 (2) | |
H6 | 0.5510 | 0.2453 | 0.7624 | 0.018* | |
N7 | 0.64019 (11) | 0.30533 (7) | 0.66429 (7) | 0.0145 (2) | |
C8 | 0.67867 (13) | 0.20682 (9) | 0.63070 (9) | 0.0157 (2) | |
H8A | 0.6443 | 0.2026 | 0.5596 | 0.019* | |
H8B | 0.6304 | 0.1539 | 0.6599 | 0.019* | |
C8A | 0.83772 (13) | 0.18999 (9) | 0.65748 (8) | 0.0155 (2) | |
C9 | 0.89680 (13) | 0.11852 (9) | 0.72634 (9) | 0.0183 (2) | |
H9 | 0.8361 | 0.0784 | 0.7548 | 0.022* | |
C10 | 1.04463 (14) | 0.10595 (10) | 0.75334 (10) | 0.0226 (3) | |
H10 | 1.0847 | 0.0561 | 0.7990 | 0.027* | |
C11 | 1.13337 (14) | 0.16613 (11) | 0.71357 (10) | 0.0251 (3) | |
H11 | 1.2344 | 0.1589 | 0.7334 | 0.030* | |
C12 | 1.07456 (14) | 0.23711 (10) | 0.64464 (10) | 0.0228 (3) | |
H12 | 1.1359 | 0.2781 | 0.6176 | 0.027* | |
C12A | 0.92672 (13) | 0.24873 (9) | 0.61487 (9) | 0.0179 (2) | |
C13 | 0.86567 (13) | 0.32007 (10) | 0.53351 (9) | 0.0187 (2) | |
H13 | 0.9500 | 0.3584 | 0.5226 | 0.022* | |
C13A | 0.76172 (13) | 0.39905 (9) | 0.55466 (9) | 0.0159 (2) | |
C13B | 0.66797 (12) | 0.39382 (9) | 0.61947 (8) | 0.0143 (2) | |
C51 | 0.42757 (13) | 0.37255 (9) | 0.84088 (9) | 0.0161 (2) | |
O51 | 0.45359 (11) | 0.30113 (7) | 0.89481 (7) | 0.0212 (2) | |
O52 | 0.32784 (10) | 0.44026 (7) | 0.84682 (7) | 0.0205 (2) | |
C52 | 0.24441 (14) | 0.41982 (10) | 0.91868 (10) | 0.0232 (3) | |
H52B | 0.2357 | 0.3469 | 0.9258 | 0.028* | |
H52A | 0.1468 | 0.4475 | 0.8960 | 0.028* | |
C53 | 0.31294 (17) | 0.46448 (11) | 1.01541 (11) | 0.0291 (3) | |
H53B | 0.3261 | 0.5362 | 1.0080 | 0.044* | |
H53C | 0.4062 | 0.4331 | 1.0407 | 0.044* | |
H53A | 0.2511 | 0.4533 | 1.0605 | 0.044* | |
C131 | 0.80444 (14) | 0.26574 (10) | 0.43672 (9) | 0.0215 (3) | |
H31A | 0.7204 | 0.2257 | 0.4430 | 0.026* | |
H31B | 0.7712 | 0.3159 | 0.3854 | 0.026* | |
C132 | 0.91372 (16) | 0.19764 (11) | 0.40648 (10) | 0.0276 (3) | |
H32A | 0.9404 | 0.1440 | 0.4540 | 0.041* | |
H32B | 0.9992 | 0.2362 | 0.4031 | 0.041* | |
H32C | 0.8718 | 0.1689 | 0.3429 | 0.041* |
U11 | U22 | U33 | U12 | U13 | U23 | |
C1 | 0.0159 (5) | 0.0211 (6) | 0.0143 (5) | −0.0012 (4) | 0.0038 (4) | 0.0017 (4) |
C2 | 0.0189 (5) | 0.0145 (5) | 0.0162 (6) | −0.0035 (4) | 0.0025 (4) | 0.0029 (4) |
F2 | 0.0312 (4) | 0.0169 (4) | 0.0253 (4) | −0.0015 (3) | 0.0123 (3) | 0.0063 (3) |
C3 | 0.0162 (5) | 0.0142 (5) | 0.0158 (5) | −0.0019 (4) | 0.0022 (4) | −0.0011 (4) |
C3A | 0.0138 (5) | 0.0148 (5) | 0.0134 (5) | −0.0015 (4) | 0.0024 (4) | −0.0006 (4) |
C4 | 0.0166 (5) | 0.0151 (5) | 0.0157 (5) | −0.0004 (4) | 0.0037 (4) | −0.0004 (4) |
O4 | 0.0324 (5) | 0.0149 (4) | 0.0270 (5) | 0.0051 (4) | 0.0158 (4) | 0.0018 (4) |
C5 | 0.0168 (5) | 0.0148 (5) | 0.0142 (5) | −0.0003 (4) | 0.0046 (4) | −0.0002 (4) |
C6 | 0.0153 (5) | 0.0148 (5) | 0.0146 (5) | 0.0002 (4) | 0.0034 (4) | 0.0009 (4) |
N7 | 0.0159 (5) | 0.0136 (5) | 0.0144 (5) | 0.0013 (4) | 0.0044 (4) | 0.0005 (4) |
C8 | 0.0164 (5) | 0.0146 (5) | 0.0164 (5) | 0.0011 (4) | 0.0041 (4) | −0.0018 (4) |
C8A | 0.0165 (5) | 0.0158 (5) | 0.0139 (5) | 0.0013 (4) | 0.0029 (4) | −0.0010 (4) |
C9 | 0.0207 (6) | 0.0172 (6) | 0.0172 (6) | 0.0009 (4) | 0.0045 (5) | 0.0015 (4) |
C10 | 0.0221 (6) | 0.0245 (6) | 0.0192 (6) | 0.0048 (5) | 0.0006 (5) | 0.0051 (5) |
C11 | 0.0166 (6) | 0.0321 (7) | 0.0251 (7) | 0.0035 (5) | 0.0014 (5) | 0.0043 (5) |
C12 | 0.0188 (6) | 0.0263 (7) | 0.0243 (6) | 0.0006 (5) | 0.0070 (5) | 0.0054 (5) |
C12A | 0.0187 (6) | 0.0196 (6) | 0.0161 (6) | 0.0036 (4) | 0.0056 (4) | 0.0024 (4) |
C13 | 0.0179 (6) | 0.0215 (6) | 0.0181 (6) | 0.0031 (4) | 0.0068 (5) | 0.0045 (5) |
C13A | 0.0154 (5) | 0.0178 (6) | 0.0142 (5) | 0.0010 (4) | 0.0025 (4) | 0.0014 (4) |
C13B | 0.0141 (5) | 0.0150 (5) | 0.0131 (5) | −0.0002 (4) | 0.0020 (4) | 0.0008 (4) |
C51 | 0.0176 (5) | 0.0135 (5) | 0.0178 (6) | −0.0010 (4) | 0.0052 (4) | −0.0020 (4) |
O51 | 0.0289 (5) | 0.0160 (4) | 0.0218 (5) | 0.0029 (4) | 0.0120 (4) | 0.0037 (3) |
O52 | 0.0208 (4) | 0.0199 (4) | 0.0246 (5) | 0.0043 (3) | 0.0127 (4) | 0.0046 (3) |
C52 | 0.0206 (6) | 0.0231 (6) | 0.0306 (7) | 0.0017 (5) | 0.0157 (5) | 0.0055 (5) |
C53 | 0.0349 (8) | 0.0291 (7) | 0.0284 (7) | 0.0013 (6) | 0.0182 (6) | 0.0024 (6) |
C131 | 0.0235 (6) | 0.0249 (6) | 0.0172 (6) | 0.0052 (5) | 0.0065 (5) | 0.0022 (5) |
C132 | 0.0310 (7) | 0.0310 (7) | 0.0224 (7) | 0.0128 (6) | 0.0090 (6) | 0.0014 (5) |
C1—C2 | 1.3826 (17) | C10—H10 | 0.9500 |
C1—C13A | 1.3915 (17) | C11—C12 | 1.3905 (19) |
C1—H1 | 0.9500 | C11—H11 | 0.9500 |
C2—F2 | 1.3602 (13) | C12—C12A | 1.3922 (18) |
C2—C3 | 1.3641 (17) | C12—H12 | 0.9500 |
C3—C3A | 1.4009 (16) | C12A—C13 | 1.5126 (17) |
C3—H3 | 0.9500 | C13—C13A | 1.5323 (17) |
C3A—C13B | 1.4168 (16) | C13—C131 | 1.5492 (18) |
C3A—C4 | 1.4856 (16) | C13—H13 | 1.0000 |
C4—O4 | 1.2387 (15) | C13A—C13B | 1.4296 (16) |
C4—C5 | 1.4413 (16) | C51—O51 | 1.2177 (15) |
C5—C6 | 1.3783 (16) | C51—O52 | 1.3366 (15) |
C5—C51 | 1.4813 (17) | O52—C52 | 1.4615 (15) |
C6—N7 | 1.3422 (15) | C52—C53 | 1.506 (2) |
C6—H6 | 0.9500 | C52—H52B | 0.9900 |
N7—C13B | 1.4029 (15) | C52—H52A | 0.9900 |
N7—C8 | 1.4819 (15) | C53—H53B | 0.9800 |
C8—C8A | 1.5022 (16) | C53—H53C | 0.9800 |
C8—H8A | 0.9900 | C53—H53A | 0.9800 |
C8—H8B | 0.9900 | C131—C132 | 1.5257 (18) |
C8A—C9 | 1.3951 (17) | C131—H31A | 0.9900 |
C8A—C12A | 1.3987 (17) | C131—H31B | 0.9900 |
C9—C10 | 1.3915 (18) | C132—H32A | 0.9800 |
C9—H9 | 0.9500 | C132—H32B | 0.9800 |
C10—C11 | 1.385 (2) | C132—H32C | 0.9800 |
C2—C1—C13A | 121.33 (11) | C12A—C12—H12 | 119.6 |
C2—C1—H1 | 119.3 | C12—C12A—C8A | 119.04 (11) |
C13A—C1—H1 | 119.3 | C12—C12A—C13 | 119.46 (11) |
F2—C2—C3 | 119.45 (11) | C8A—C12A—C13 | 121.41 (11) |
F2—C2—C1 | 117.88 (11) | C12A—C13—C13A | 116.33 (10) |
C3—C2—C1 | 122.64 (11) | C12A—C13—C131 | 112.46 (11) |
C2—C3—C3A | 118.03 (11) | C13A—C13—C131 | 111.69 (10) |
C2—C3—H3 | 121.0 | C12A—C13—H13 | 105.1 |
C3A—C3—H3 | 121.0 | C13A—C13—H13 | 105.1 |
C3—C3A—C13B | 120.75 (11) | C131—C13—H13 | 105.1 |
C3—C3A—C4 | 116.50 (10) | C1—C13A—C13B | 117.22 (11) |
C13B—C3A—C4 | 122.75 (10) | C1—C13A—C13 | 113.89 (10) |
O4—C4—C5 | 125.65 (11) | C13B—C13A—C13 | 128.80 (11) |
O4—C4—C3A | 119.94 (11) | N7—C13B—C3A | 117.17 (10) |
C5—C4—C3A | 114.40 (10) | N7—C13B—C13A | 123.21 (10) |
C6—C5—C4 | 119.45 (11) | C3A—C13B—C13A | 119.62 (11) |
C6—C5—C51 | 114.62 (10) | O51—C51—O52 | 122.84 (11) |
C4—C5—C51 | 125.90 (11) | O51—C51—C5 | 122.59 (11) |
N7—C6—C5 | 125.12 (11) | O52—C51—C5 | 114.55 (10) |
N7—C6—H6 | 117.4 | C51—O52—C52 | 115.54 (10) |
C5—C6—H6 | 117.4 | O52—C52—C53 | 111.68 (11) |
C6—N7—C13B | 120.56 (10) | O52—C52—H52B | 109.3 |
C6—N7—C8 | 117.54 (10) | C53—C52—H52B | 109.3 |
C13B—N7—C8 | 121.52 (10) | O52—C52—H52A | 109.3 |
N7—C8—C8A | 111.49 (10) | C53—C52—H52A | 109.3 |
N7—C8—H8A | 109.3 | H52B—C52—H52A | 107.9 |
C8A—C8—H8A | 109.3 | C52—C53—H53B | 109.5 |
N7—C8—H8B | 109.3 | C52—C53—H53C | 109.5 |
C8A—C8—H8B | 109.3 | H53B—C53—H53C | 109.5 |
H8A—C8—H8B | 108.0 | C52—C53—H53A | 109.5 |
C9—C8A—C12A | 120.15 (11) | H53B—C53—H53A | 109.5 |
C9—C8A—C8 | 120.43 (11) | H53C—C53—H53A | 109.5 |
C12A—C8A—C8 | 119.39 (11) | C132—C131—C13 | 112.84 (11) |
C10—C9—C8A | 120.06 (12) | C132—C131—H31A | 109.0 |
C10—C9—H9 | 120.0 | C13—C131—H31A | 109.0 |
C8A—C9—H9 | 120.0 | C132—C131—H31B | 109.0 |
C11—C10—C9 | 119.96 (12) | C13—C131—H31B | 109.0 |
C11—C10—H10 | 120.0 | H31A—C131—H31B | 107.8 |
C9—C10—H10 | 120.0 | C131—C132—H32A | 109.5 |
C10—C11—C12 | 120.00 (12) | C131—C132—H32B | 109.5 |
C10—C11—H11 | 120.0 | H32A—C132—H32B | 109.5 |
C12—C11—H11 | 120.0 | C131—C132—H32C | 109.5 |
C11—C12—C12A | 120.73 (12) | H32A—C132—H32C | 109.5 |
C11—C12—H12 | 119.6 | H32B—C132—H32C | 109.5 |
C13A—C1—C2—F2 | −178.82 (11) | C8—C8A—C12A—C13 | −7.65 (18) |
C13A—C1—C2—C3 | 2.94 (19) | C12—C12A—C13—C13A | −126.40 (13) |
F2—C2—C3—C3A | 177.96 (10) | C8A—C12A—C13—C13A | 57.14 (16) |
C1—C2—C3—C3A | −3.83 (18) | C12—C12A—C13—C131 | 103.00 (14) |
C2—C3—C3A—C13B | −0.68 (17) | C8A—C12A—C13—C131 | −73.46 (15) |
C2—C3—C3A—C4 | 179.16 (10) | C2—C1—C13A—C13B | 2.45 (18) |
C3—C3A—C4—O4 | −1.21 (17) | C2—C1—C13A—C13 | −174.51 (11) |
C13B—C3A—C4—O4 | 178.62 (11) | C12A—C13—C13A—C1 | 147.66 (11) |
C3—C3A—C4—C5 | 179.75 (10) | C131—C13—C13A—C1 | −81.38 (13) |
C13B—C3A—C4—C5 | −0.41 (16) | C12A—C13—C13A—C13B | −28.86 (18) |
O4—C4—C5—C6 | 176.15 (12) | C131—C13—C13A—C13B | 102.10 (14) |
C3A—C4—C5—C6 | −4.87 (16) | C6—N7—C13B—C3A | −7.68 (16) |
O4—C4—C5—C51 | −1.7 (2) | C8—N7—C13B—C3A | 164.99 (10) |
C3A—C4—C5—C51 | 177.25 (11) | C6—N7—C13B—C13A | 172.78 (11) |
C4—C5—C6—N7 | 4.14 (19) | C8—N7—C13B—C13A | −14.55 (17) |
C51—C5—C6—N7 | −177.75 (11) | C3—C3A—C13B—N7 | −173.58 (10) |
C5—C6—N7—C13B | 2.53 (18) | C4—C3A—C13B—N7 | 6.59 (16) |
C5—C6—N7—C8 | −170.43 (11) | C3—C3A—C13B—C13A | 5.97 (17) |
C6—N7—C8—C8A | −114.48 (12) | C4—C3A—C13B—C13A | −173.85 (11) |
C13B—N7—C8—C8A | 72.64 (13) | C1—C13A—C13B—N7 | 172.81 (11) |
N7—C8—C8A—C9 | 111.47 (12) | C13—C13A—C13B—N7 | −10.76 (19) |
N7—C8—C8A—C12A | −66.61 (14) | C1—C13A—C13B—C3A | −6.72 (17) |
C12A—C8A—C9—C10 | 0.45 (19) | C13—C13A—C13B—C3A | 169.71 (12) |
C8—C8A—C9—C10 | −177.62 (12) | C6—C5—C51—O51 | 21.28 (17) |
C8A—C9—C10—C11 | 1.6 (2) | C4—C5—C51—O51 | −160.76 (12) |
C9—C10—C11—C12 | −1.9 (2) | C6—C5—C51—O52 | −157.46 (11) |
C10—C11—C12—C12A | 0.1 (2) | C4—C5—C51—O52 | 20.51 (17) |
C11—C12—C12A—C8A | 2.0 (2) | O51—C51—O52—C52 | −3.85 (18) |
C11—C12—C12A—C13 | −174.58 (13) | C5—C51—O52—C52 | 174.88 (10) |
C9—C8A—C12A—C12 | −2.21 (18) | C51—O52—C52—C53 | 90.07 (14) |
C8—C8A—C12A—C12 | 175.88 (12) | C12A—C13—C131—C132 | −55.46 (15) |
C9—C8A—C12A—C13 | 174.27 (11) | C13A—C13—C131—C132 | 171.62 (11) |
D—H···A | D—H | H···A | D···A | D—H···A |
C3—H3···O51i | 0.95 | 2.32 | 3.1725 (16) | 149 |
C6—H6···O4ii | 0.95 | 2.46 | 3.3308 (15) | 153 |
C8—H8B···O4ii | 0.99 | 2.27 | 3.2255 (16) | 162 |
C131—H31A···O51iii | 0.99 | 2.52 | 3.4008 (17) | 148 |
C10—H10···Cg1iv | 0.95 | 2.72 | 3.5641 (15) | 148 |
Symmetry codes: (i) −x+1, y+1/2, −z+3/2; (ii) −x+1, y−1/2, −z+3/2; (iii) x, −y+1/2, z−1/2; (iv) −x+2, y−1/2, −z+3/2. |
C18H18ClNO | F(000) = 632 |
Mr = 299.78 | Dx = 1.314 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
a = 8.333 (5) Å | Cell parameters from 3774 reflections |
b = 20.800 (14) Å | θ = 2.5–28.4° |
c = 9.186 (6) Å | µ = 0.25 mm−1 |
β = 107.857 (17)° | T = 100 K |
V = 1515.5 (17) Å3 | Plate, colourless |
Z = 4 | 0.30 × 0.25 × 0.12 mm |
Bruker D8 Venture diffractometer | 3774 independent reflections |
Radiation source: INCOATEC high brilliance microfocus sealed tube | 3337 reflections with I > 2σ(I) |
Multilayer mirror monochromator | Rint = 0.066 |
φ and ω scans | θmax = 28.4°, θmin = 2.5° |
Absorption correction: multi-scan (SADABS; Bruker, 2015) | h = −10→11 |
Tmin = 0.947, Tmax = 0.970 | k = −27→27 |
50802 measured reflections | l = −12→12 |
Refinement on F2 | Primary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.038 | H-atom parameters constrained |
wR(F2) = 0.095 | w = 1/[σ2(Fo2) + (0.0355P)2 + 1.1112P] where P = (Fo2 + 2Fc2)/3 |
S = 1.07 | (Δ/σ)max = 0.001 |
3774 reflections | Δρmax = 0.43 e Å−3 |
192 parameters | Δρmin = −0.33 e Å−3 |
0 restraints |
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 | ||
C1 | 0.13803 (17) | 0.29721 (6) | 0.23168 (15) | 0.0147 (3) | |
H1 | 0.1058 | 0.2611 | 0.1658 | 0.018* | |
C2 | 0.04139 (16) | 0.31511 (6) | 0.32372 (15) | 0.0146 (3) | |
Cl2 | −0.13541 (5) | 0.26920 (2) | 0.31914 (4) | 0.02543 (11) | |
C3 | 0.08007 (16) | 0.36819 (6) | 0.41892 (14) | 0.0144 (2) | |
H3 | 0.0112 | 0.3802 | 0.4799 | 0.017* | |
C4 | 0.22308 (16) | 0.40329 (6) | 0.42235 (14) | 0.0128 (2) | |
H4 | 0.2522 | 0.4402 | 0.4860 | 0.015* | |
C4A | 0.32430 (15) | 0.38505 (6) | 0.33375 (14) | 0.0110 (2) | |
N5 | 0.47415 (13) | 0.42145 (5) | 0.34511 (12) | 0.0111 (2) | |
C6 | 0.46467 (17) | 0.47747 (6) | 0.24434 (15) | 0.0146 (3) | |
H6A | 0.5779 | 0.4854 | 0.2341 | 0.017* | |
H6B | 0.4331 | 0.5158 | 0.2933 | 0.017* | |
C6A | 0.33958 (16) | 0.46960 (6) | 0.08616 (14) | 0.0132 (2) | |
C7 | 0.22746 (17) | 0.51960 (7) | 0.02940 (16) | 0.0176 (3) | |
H7 | 0.2278 | 0.5559 | 0.0923 | 0.021* | |
C8 | 0.11457 (18) | 0.51757 (8) | −0.11792 (17) | 0.0235 (3) | |
H8 | 0.0407 | 0.5527 | −0.1561 | 0.028* | |
C9 | 0.11079 (19) | 0.46416 (8) | −0.20808 (16) | 0.0258 (3) | |
H9 | 0.0328 | 0.4619 | −0.3081 | 0.031* | |
C10 | 0.22197 (19) | 0.41372 (7) | −0.15153 (16) | 0.0215 (3) | |
H10 | 0.2179 | 0.3768 | −0.2136 | 0.026* | |
C10A | 0.33952 (17) | 0.41598 (7) | −0.00563 (15) | 0.0158 (3) | |
C11 | 0.46351 (17) | 0.36170 (6) | 0.05585 (15) | 0.0159 (3) | |
H11 | 0.5644 | 0.3804 | 0.1337 | 0.019* | |
C12 | 0.38781 (18) | 0.30976 (6) | 0.13671 (16) | 0.0161 (3) | |
H12A | 0.3172 | 0.2808 | 0.0570 | 0.019* | |
H12B | 0.4821 | 0.2837 | 0.2016 | 0.019* | |
C12A | 0.28266 (16) | 0.33200 (6) | 0.23513 (14) | 0.0126 (2) | |
C51 | 0.62253 (16) | 0.41006 (6) | 0.45647 (14) | 0.0119 (2) | |
O51 | 0.74656 (12) | 0.44425 (5) | 0.47193 (11) | 0.0172 (2) | |
C52 | 0.62918 (18) | 0.35294 (7) | 0.55875 (16) | 0.0197 (3) | |
H52C | 0.7403 | 0.3508 | 0.6360 | 0.030* | |
H52A | 0.6095 | 0.3135 | 0.4973 | 0.030* | |
H52B | 0.5420 | 0.3573 | 0.6095 | 0.030* | |
C111 | 0.5244 (2) | 0.32899 (7) | −0.06712 (18) | 0.0245 (3) | |
H11A | 0.4301 | 0.3061 | −0.1389 | 0.037* | |
H11B | 0.6143 | 0.2984 | −0.0187 | 0.037* | |
H11C | 0.5676 | 0.3616 | −0.1225 | 0.037* |
U11 | U22 | U33 | U12 | U13 | U23 | |
C1 | 0.0176 (6) | 0.0134 (6) | 0.0128 (6) | −0.0030 (5) | 0.0043 (5) | −0.0013 (5) |
C2 | 0.0121 (6) | 0.0169 (6) | 0.0146 (6) | −0.0038 (5) | 0.0036 (5) | 0.0019 (5) |
Cl2 | 0.01983 (18) | 0.0314 (2) | 0.02774 (19) | −0.01413 (14) | 0.01116 (14) | −0.00721 (15) |
C3 | 0.0130 (6) | 0.0182 (6) | 0.0129 (6) | 0.0006 (5) | 0.0055 (5) | 0.0010 (5) |
C4 | 0.0140 (6) | 0.0129 (6) | 0.0111 (5) | 0.0001 (5) | 0.0031 (4) | −0.0002 (4) |
C4A | 0.0113 (5) | 0.0110 (5) | 0.0100 (5) | −0.0009 (4) | 0.0023 (4) | 0.0025 (4) |
N5 | 0.0110 (5) | 0.0114 (5) | 0.0103 (5) | −0.0016 (4) | 0.0026 (4) | 0.0015 (4) |
C6 | 0.0177 (6) | 0.0113 (6) | 0.0132 (6) | −0.0025 (5) | 0.0024 (5) | 0.0013 (5) |
C6A | 0.0124 (6) | 0.0154 (6) | 0.0118 (6) | −0.0036 (5) | 0.0038 (5) | 0.0037 (5) |
C7 | 0.0172 (6) | 0.0170 (6) | 0.0190 (6) | −0.0011 (5) | 0.0060 (5) | 0.0045 (5) |
C8 | 0.0164 (7) | 0.0306 (8) | 0.0221 (7) | 0.0020 (6) | 0.0038 (5) | 0.0132 (6) |
C9 | 0.0200 (7) | 0.0405 (9) | 0.0132 (6) | −0.0096 (6) | −0.0004 (5) | 0.0065 (6) |
C10 | 0.0260 (7) | 0.0258 (7) | 0.0127 (6) | −0.0094 (6) | 0.0061 (5) | −0.0019 (5) |
C10A | 0.0187 (6) | 0.0171 (6) | 0.0131 (6) | −0.0043 (5) | 0.0072 (5) | 0.0013 (5) |
C11 | 0.0202 (6) | 0.0146 (6) | 0.0159 (6) | −0.0028 (5) | 0.0102 (5) | −0.0017 (5) |
C12 | 0.0218 (7) | 0.0111 (6) | 0.0192 (6) | −0.0015 (5) | 0.0119 (5) | −0.0014 (5) |
C12A | 0.0153 (6) | 0.0119 (6) | 0.0110 (5) | 0.0008 (4) | 0.0046 (5) | 0.0017 (4) |
C51 | 0.0138 (6) | 0.0125 (6) | 0.0092 (5) | 0.0018 (4) | 0.0034 (4) | −0.0022 (4) |
O51 | 0.0134 (4) | 0.0178 (5) | 0.0177 (5) | −0.0026 (4) | 0.0008 (4) | −0.0008 (4) |
C52 | 0.0222 (7) | 0.0187 (7) | 0.0159 (6) | 0.0018 (5) | 0.0026 (5) | 0.0047 (5) |
C111 | 0.0372 (8) | 0.0185 (7) | 0.0268 (7) | −0.0051 (6) | 0.0229 (7) | −0.0056 (6) |
C1—C2 | 1.3855 (19) | C8—H8 | 0.9500 |
C1—C12A | 1.3977 (19) | C9—C10 | 1.391 (2) |
C1—H1 | 0.9500 | C9—H9 | 0.9500 |
C2—C3 | 1.384 (2) | C10—C10A | 1.397 (2) |
C2—Cl2 | 1.7453 (15) | C10—H10 | 0.9500 |
C3—C4 | 1.3896 (19) | C10A—C11 | 1.518 (2) |
C3—H3 | 0.9500 | C11—C111 | 1.532 (2) |
C4—C4A | 1.3923 (18) | C11—C12 | 1.5505 (19) |
C4—H4 | 0.9500 | C11—H11 | 1.0000 |
C4A—C12A | 1.4022 (18) | C12—C12A | 1.5115 (18) |
C4A—N5 | 1.4365 (17) | C12—H12A | 0.9900 |
N5—C51 | 1.3622 (17) | C12—H12B | 0.9900 |
N5—C6 | 1.4751 (17) | C51—O51 | 1.2264 (17) |
C6—C6A | 1.5152 (19) | C51—C52 | 1.5052 (19) |
C6—H6A | 0.9900 | C52—H52C | 0.9800 |
C6—H6B | 0.9900 | C52—H52A | 0.9800 |
C6A—C7 | 1.3884 (19) | C52—H52B | 0.9800 |
C6A—C10A | 1.398 (2) | C111—H11A | 0.9800 |
C7—C8 | 1.392 (2) | C111—H11B | 0.9800 |
C7—H7 | 0.9500 | C111—H11C | 0.9800 |
C8—C9 | 1.380 (2) | ||
C2—C1—C12A | 120.37 (12) | C9—C10—C10A | 121.58 (14) |
C2—C1—H1 | 119.8 | C9—C10—H10 | 119.2 |
C12A—C1—H1 | 119.8 | C10A—C10—H10 | 119.2 |
C3—C2—C1 | 122.25 (12) | C10—C10A—C6A | 118.40 (13) |
C3—C2—Cl2 | 118.89 (10) | C10—C10A—C11 | 121.93 (13) |
C1—C2—Cl2 | 118.86 (11) | C6A—C10A—C11 | 119.66 (12) |
C2—C3—C4 | 117.74 (12) | C10A—C11—C111 | 113.42 (12) |
C2—C3—H3 | 121.1 | C10A—C11—C12 | 111.47 (12) |
C4—C3—H3 | 121.1 | C111—C11—C12 | 108.62 (12) |
C3—C4—C4A | 120.84 (12) | C10A—C11—H11 | 107.7 |
C3—C4—H4 | 119.6 | C111—C11—H11 | 107.7 |
C4A—C4—H4 | 119.6 | C12—C11—H11 | 107.7 |
C4—C4A—C12A | 121.19 (12) | C12A—C12—C11 | 117.97 (11) |
C4—C4A—N5 | 118.87 (11) | C12A—C12—H12A | 107.8 |
C12A—C4A—N5 | 119.94 (11) | C11—C12—H12A | 107.8 |
C51—N5—C4A | 122.11 (11) | C12A—C12—H12B | 107.8 |
C51—N5—C6 | 118.05 (11) | C11—C12—H12B | 107.8 |
C4A—N5—C6 | 119.52 (10) | H12A—C12—H12B | 107.2 |
N5—C6—C6A | 113.90 (11) | C1—C12A—C4A | 117.57 (12) |
N5—C6—H6A | 108.8 | C1—C12A—C12 | 118.81 (12) |
C6A—C6—H6A | 108.8 | C4A—C12A—C12 | 123.59 (12) |
N5—C6—H6B | 108.8 | O51—C51—N5 | 121.65 (12) |
C6A—C6—H6B | 108.8 | O51—C51—C52 | 121.13 (12) |
H6A—C6—H6B | 107.7 | N5—C51—C52 | 117.21 (11) |
C7—C6A—C10A | 119.69 (13) | C51—C52—H52C | 109.5 |
C7—C6A—C6 | 117.71 (12) | C51—C52—H52A | 109.5 |
C10A—C6A—C6 | 122.51 (12) | H52C—C52—H52A | 109.5 |
C6A—C7—C8 | 121.24 (14) | C51—C52—H52B | 109.5 |
C6A—C7—H7 | 119.4 | H52C—C52—H52B | 109.5 |
C8—C7—H7 | 119.4 | H52A—C52—H52B | 109.5 |
C9—C8—C7 | 119.48 (14) | C11—C111—H11A | 109.5 |
C9—C8—H8 | 120.3 | C11—C111—H11B | 109.5 |
C7—C8—H8 | 120.3 | H11A—C111—H11B | 109.5 |
C8—C9—C10 | 119.54 (14) | C11—C111—H11C | 109.5 |
C8—C9—H9 | 120.2 | H11A—C111—H11C | 109.5 |
C10—C9—H9 | 120.2 | H11B—C111—H11C | 109.5 |
C12A—C1—C2—C3 | 1.6 (2) | C7—C6A—C10A—C10 | −1.80 (19) |
C12A—C1—C2—Cl2 | −178.50 (10) | C6—C6A—C10A—C10 | −178.39 (12) |
C1—C2—C3—C4 | −1.19 (19) | C7—C6A—C10A—C11 | 179.29 (12) |
Cl2—C2—C3—C4 | 178.94 (10) | C6—C6A—C10A—C11 | 2.70 (18) |
C2—C3—C4—C4A | −0.56 (19) | C10—C10A—C11—C111 | 34.86 (18) |
C3—C4—C4A—C12A | 1.90 (19) | C6A—C10A—C11—C111 | −146.27 (12) |
C3—C4—C4A—N5 | −177.81 (11) | C10—C10A—C11—C12 | −88.11 (16) |
C4—C4A—N5—C51 | 84.18 (16) | C6A—C10A—C11—C12 | 90.76 (15) |
C12A—C4A—N5—C51 | −95.53 (15) | C10A—C11—C12—C12A | −39.95 (16) |
C4—C4A—N5—C6 | −89.12 (15) | C111—C11—C12—C12A | −165.63 (12) |
C12A—C4A—N5—C6 | 91.16 (15) | C2—C1—C12A—C4A | −0.27 (19) |
C51—N5—C6—C6A | 151.63 (11) | C2—C1—C12A—C12 | 178.12 (12) |
C4A—N5—C6—C6A | −34.80 (16) | C4—C4A—C12A—C1 | −1.45 (18) |
N5—C6—C6A—C7 | 131.79 (13) | N5—C4A—C12A—C1 | 178.26 (11) |
N5—C6—C6A—C10A | −51.56 (17) | C4—C4A—C12A—C12 | −179.75 (12) |
C10A—C6A—C7—C8 | −0.2 (2) | N5—C4A—C12A—C12 | −0.05 (18) |
C6—C6A—C7—C8 | 176.60 (12) | C11—C12—C12A—C1 | 140.65 (13) |
C6A—C7—C8—C9 | 1.7 (2) | C11—C12—C12A—C4A | −41.07 (18) |
C7—C8—C9—C10 | −1.2 (2) | C4A—N5—C51—O51 | −174.78 (11) |
C8—C9—C10—C10A | −0.8 (2) | C6—N5—C51—O51 | −1.39 (18) |
C9—C10—C10A—C6A | 2.3 (2) | C4A—N5—C51—C52 | 6.19 (17) |
C9—C10—C10A—C11 | −178.83 (13) | C6—N5—C51—C52 | 179.59 (11) |
D—H···A | D—H | H···A | D···A | D—H···A |
C3—H3···O51i | 0.95 | 2.56 | 3.361 (3) | 142 |
C4—H4···O51ii | 0.95 | 2.43 | 3.303 (3) | 152 |
C6—H6A···Cg3iii | 0.99 | 2.70 | 3.673 (3) | 149 |
C8—H8···Cg2iv | 0.95 | 2.86 | 3.802 (3) | 169 |
Symmetry codes: (i) x−1, y, z; (ii) −x+1, −y+1, −z+1; (iii) −x+1, −y+1, −z; (iv) −x, −y+1, −z. |
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