Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S010827010100097X/na1496sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S010827010100097X/na1496Isup2.hkl |
CCDC reference: 164648
For related literature, see: Allen et al. (1987); Beddoes et al. (1986); El-Sayed, Barnhart, Ammon & Wassel (1986); Gadaginamath & Patil (1999); Govindasamy et al. (1999); Nigović et al. (2000); Okabe & Adachi (1998); Papenstasion & Newmeyer (1972); Polletto et al. (1974); Rajeswaran et al. (1999); Rodriguez et al. (1985); Sankaranarayanan et al. (2000); Schollmeyer et al. (1995); Sivaraman et al. (1994a, 1994b, 1996); Yokum & Fronczek (1997); Zhang & Liebeskind (1996).
3-Bromo-(1-phenylsulfonylindol-2-yl-methyl)-N-methylaniline was treated with tetrakis(triphenylphosphine)palladium(0) in DMF at 353 K and gave the corresponding debrominated product of the title compound in 70% yield.
All the hydrogen atoms were included in calculated positions and allowed to ride on their corresponding parent atoms.
Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ZORTEP (Zsolnai, 1997); software used to prepare material for publication: SHELXL97 and PARST (Nardelli, 1995).
Fig. 1. Molecular structure showing 50% probability displacement ellipsoids with the atom-numbering scheme. | |
Fig. 2. Packing of the molecule viewed down the a axis showing C—H···π interaction. |
C22H20N2O2S | Dx = 1.311 Mg m−3 |
Mr = 376.46 | Mo Kα radiation, λ = 0.71073 Å |
Orthorhombic, P212121 | Cell parameters from 4762 reflections |
a = 8.3162 (2) Å | θ = 1.6–28.3° |
b = 11.2384 (3) Å | µ = 0.19 mm−1 |
c = 20.4080 (5) Å | T = 293 K |
V = 1907.35 (8) Å3 | Block, yellow |
Z = 4 | 0.44 × 0.42 × 0.24 mm |
F(000) = 792 |
Siemens SMART CCD area detector diffractometer | 3474 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.035 |
Graphite monochromator | θmax = 28.3°, θmin = 2.0° |
ω scans | h = −10→11 |
13206 measured reflections | k = −14→10 |
4707 independent reflections | l = −22→27 |
Refinement on F2 | Hydrogen site location: inferred from neighbouring sites |
Least-squares matrix: full | H-atom parameters constrained |
R[F2 > 2σ(F2)] = 0.041 | Calculated w = 1/[σ2(Fo2) + (0.0673P)2 + 0.2417P] where P = (Fo2 + 2Fc2)/3 |
wR(F2) = 0.119 | (Δ/σ)max < 0.001 |
S = 0.91 | Δρmax = 0.17 e Å−3 |
4707 reflections | Δρmin = −0.19 e Å−3 |
245 parameters | Extinction correction: SHELXL97 (Sheldrick, 1997), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4 |
0 restraints | Extinction coefficient: 0.0070 (12) |
Primary atom site location: structure-invariant direct methods | Absolute structure: Flack (1983) |
Secondary atom site location: difference Fourier map | Absolute structure parameter: 0.06 (8) |
C22H20N2O2S | V = 1907.35 (8) Å3 |
Mr = 376.46 | Z = 4 |
Orthorhombic, P212121 | Mo Kα radiation |
a = 8.3162 (2) Å | µ = 0.19 mm−1 |
b = 11.2384 (3) Å | T = 293 K |
c = 20.4080 (5) Å | 0.44 × 0.42 × 0.24 mm |
Siemens SMART CCD area detector diffractometer | 3474 reflections with I > 2σ(I) |
13206 measured reflections | Rint = 0.035 |
4707 independent reflections |
R[F2 > 2σ(F2)] = 0.041 | H-atom parameters constrained |
wR(F2) = 0.119 | Δρmax = 0.17 e Å−3 |
S = 0.91 | Δρmin = −0.19 e Å−3 |
4707 reflections | Absolute structure: Flack (1983) |
245 parameters | Absolute structure parameter: 0.06 (8) |
0 restraints |
Experimental. Data were collected over a hemisphere of reciprocal space, by a combination of three sets of exposures; each set had a different ϕ angle (0, 88 and 180°) for the crystal and each exposure of 30 s covered 0.3° in ω. The crystal-to-detector distance was 4 cm and the detector swing angle was -35°. Coverage of the unique set was over 99% complete. Crystal decay was monitored by repeating 30 initial frames at the end of data collection and analysing the duplicate reflections; it was found negligible. |
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes. |
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 > σ(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. |
x | y | z | Uiso*/Ueq | ||
S1 | −0.53831 (7) | −0.59191 (6) | −0.18734 (3) | 0.06009 (17) | |
O1 | −0.4736 (2) | −0.68787 (18) | −0.22452 (8) | 0.0782 (5) | |
O2 | −0.5188 (2) | −0.47274 (17) | −0.20896 (9) | 0.0864 (6) | |
N1 | −0.7355 (2) | −0.61532 (16) | −0.18227 (8) | 0.0537 (4) | |
C1 | −0.8477 (3) | −0.53331 (19) | −0.15495 (10) | 0.0538 (5) | |
C2 | −0.9893 (3) | −0.58827 (19) | −0.14875 (11) | 0.0583 (5) | |
H2 | −1.0828 | −0.5537 | −0.1326 | 0.070* | |
C3 | −0.9748 (3) | −0.70952 (19) | −0.17101 (10) | 0.0534 (5) | |
C4 | −0.8141 (3) | −0.72642 (19) | −0.18967 (10) | 0.0507 (5) | |
C5 | −1.0820 (3) | −0.8044 (2) | −0.17505 (12) | 0.0680 (6) | |
H5 | −1.1897 | −0.7940 | −0.1641 | 0.082* | |
C6 | −1.0267 (3) | −0.9140 (2) | −0.19547 (12) | 0.0738 (6) | |
H6 | −1.0970 | −0.9782 | −0.1978 | 0.089* | |
C7 | −0.8671 (4) | −0.9286 (2) | −0.21244 (13) | 0.0749 (7) | |
H7 | −0.8320 | −1.0034 | −0.2256 | 0.090* | |
C8 | −0.7583 (3) | −0.8365 (2) | −0.21058 (11) | 0.0652 (6) | |
H8 | −0.6516 | −0.8475 | −0.2228 | 0.078* | |
C9 | −0.4707 (2) | −0.60162 (19) | −0.10583 (10) | 0.0538 (5) | |
C10 | −0.4021 (3) | −0.5042 (2) | −0.07598 (14) | 0.0736 (7) | |
H10 | −0.3902 | −0.4328 | −0.0986 | 0.088* | |
C11 | −0.3511 (4) | −0.5146 (3) | −0.01152 (15) | 0.0891 (9) | |
H11 | −0.3016 | −0.4505 | 0.0091 | 0.107* | |
C12 | −0.3731 (4) | −0.6189 (3) | 0.02193 (15) | 0.0929 (10) | |
H12 | −0.3413 | −0.6242 | 0.0655 | 0.111* | |
C13 | −0.4408 (4) | −0.7148 (3) | −0.00770 (15) | 0.0892 (9) | |
H13 | −0.4551 | −0.7851 | 0.0156 | 0.107* | |
C14 | −0.4885 (4) | −0.7080 (2) | −0.07251 (12) | 0.0698 (6) | |
H14 | −0.5320 | −0.7742 | −0.0934 | 0.084* | |
C15 | −0.8045 (3) | −0.4069 (2) | −0.13825 (13) | 0.0698 (6) | |
H15A | −0.7016 | −0.4058 | −0.1159 | 0.084* | |
H15B | −0.7937 | −0.3613 | −0.1784 | 0.084* | |
N16 | −0.9251 (3) | −0.35120 (17) | −0.09670 (12) | 0.0776 (6) | |
C17 | −1.0245 (5) | −0.2598 (3) | −0.12489 (19) | 0.1061 (11) | |
H17A | −1.0101 | −0.2589 | −0.1716 | 0.159* | |
H17B | −0.9945 | −0.1840 | −0.1071 | 0.159* | |
H17C | −1.1352 | −0.2757 | −0.1148 | 0.159* | |
C18 | −0.9234 (3) | −0.37291 (19) | −0.02964 (14) | 0.0637 (6) | |
C19 | −0.8243 (3) | −0.4597 (2) | −0.00238 (13) | 0.0690 (6) | |
H19 | −0.7569 | −0.5035 | −0.0296 | 0.083* | |
C20 | −0.8236 (4) | −0.4822 (3) | 0.06377 (13) | 0.0828 (8) | |
H20 | −0.7548 | −0.5398 | 0.0807 | 0.099* | |
C21 | −0.9236 (5) | −0.4206 (3) | 0.10500 (17) | 0.1034 (11) | |
H21 | −0.9251 | −0.4373 | 0.1496 | 0.124* | |
C22 | −1.0197 (5) | −0.3354 (3) | 0.0797 (2) | 0.1087 (12) | |
H22 | −1.0868 | −0.2927 | 0.1076 | 0.130* | |
C23 | −1.0209 (4) | −0.3100 (2) | 0.01354 (18) | 0.0863 (9) | |
H23 | −1.0876 | −0.2502 | −0.0023 | 0.104* |
U11 | U22 | U33 | U12 | U13 | U23 | |
S1 | 0.0502 (3) | 0.0798 (4) | 0.0502 (3) | −0.0021 (3) | 0.0122 (2) | 0.0113 (3) |
O1 | 0.0586 (9) | 0.1168 (14) | 0.0592 (9) | 0.0102 (10) | 0.0194 (8) | −0.0119 (9) |
O2 | 0.0836 (13) | 0.0927 (12) | 0.0830 (12) | −0.0124 (11) | 0.0190 (10) | 0.0367 (10) |
N1 | 0.0491 (9) | 0.0669 (11) | 0.0451 (8) | 0.0071 (8) | 0.0044 (7) | 0.0003 (8) |
C1 | 0.0574 (12) | 0.0523 (12) | 0.0517 (11) | 0.0128 (10) | 0.0015 (9) | 0.0084 (9) |
C2 | 0.0531 (13) | 0.0592 (12) | 0.0626 (12) | 0.0161 (10) | 0.0083 (9) | 0.0072 (10) |
C3 | 0.0506 (10) | 0.0628 (12) | 0.0467 (10) | 0.0080 (10) | 0.0026 (9) | 0.0030 (9) |
C4 | 0.0513 (11) | 0.0622 (12) | 0.0386 (9) | 0.0034 (9) | 0.0027 (9) | −0.0013 (9) |
C5 | 0.0534 (13) | 0.0840 (17) | 0.0664 (14) | −0.0033 (12) | 0.0053 (11) | 0.0013 (13) |
C6 | 0.0763 (15) | 0.0758 (15) | 0.0692 (15) | −0.0113 (14) | −0.0004 (13) | −0.0112 (13) |
C7 | 0.0831 (18) | 0.0711 (16) | 0.0705 (15) | 0.0047 (14) | −0.0014 (14) | −0.0225 (12) |
C8 | 0.0596 (14) | 0.0791 (16) | 0.0569 (12) | 0.0120 (12) | 0.0050 (10) | −0.0179 (11) |
C9 | 0.0407 (9) | 0.0643 (12) | 0.0565 (11) | 0.0018 (10) | 0.0059 (9) | 0.0000 (10) |
C10 | 0.0617 (14) | 0.0726 (16) | 0.0864 (18) | −0.0103 (12) | 0.0060 (13) | −0.0047 (13) |
C11 | 0.0685 (17) | 0.113 (2) | 0.0856 (19) | −0.0088 (16) | −0.0093 (15) | −0.0324 (18) |
C12 | 0.085 (2) | 0.129 (3) | 0.0649 (16) | 0.018 (2) | −0.0157 (15) | −0.0065 (18) |
C13 | 0.108 (2) | 0.0901 (19) | 0.0698 (16) | 0.0154 (19) | −0.0091 (17) | 0.0151 (15) |
C14 | 0.0824 (18) | 0.0636 (13) | 0.0634 (13) | 0.0044 (12) | −0.0062 (12) | 0.0064 (11) |
C15 | 0.0774 (16) | 0.0571 (14) | 0.0748 (15) | 0.0051 (12) | −0.0002 (13) | 0.0112 (12) |
N16 | 0.0884 (16) | 0.0535 (11) | 0.0909 (16) | 0.0262 (11) | −0.0047 (12) | 0.0021 (10) |
C17 | 0.117 (3) | 0.0704 (17) | 0.131 (3) | 0.0382 (18) | −0.035 (2) | 0.0006 (18) |
C18 | 0.0622 (14) | 0.0440 (11) | 0.0851 (16) | −0.0007 (10) | 0.0026 (11) | −0.0121 (10) |
C19 | 0.0747 (16) | 0.0616 (13) | 0.0706 (14) | 0.0103 (12) | 0.0030 (13) | −0.0064 (12) |
C20 | 0.100 (2) | 0.0768 (17) | 0.0712 (16) | −0.0009 (16) | −0.0046 (16) | −0.0026 (14) |
C21 | 0.134 (3) | 0.097 (2) | 0.0794 (19) | −0.014 (2) | 0.023 (2) | −0.0246 (18) |
C22 | 0.120 (3) | 0.089 (2) | 0.117 (3) | 0.000 (2) | 0.045 (2) | −0.040 (2) |
C23 | 0.0768 (17) | 0.0580 (14) | 0.124 (3) | 0.0031 (13) | 0.0109 (18) | −0.0210 (15) |
S1—O1 | 1.424 (2) | C11—H11 | 0.9300 |
S1—O2 | 1.419 (2) | C12—C13 | 1.358 (5) |
S1—N1 | 1.664 (2) | C12—H12 | 0.9300 |
S1—C9 | 1.759 (2) | C13—C14 | 1.383 (4) |
N1—C4 | 1.417 (3) | C13—H13 | 0.9300 |
N1—C1 | 1.425 (3) | C14—H14 | 0.9300 |
C1—C2 | 1.335 (3) | C15—N16 | 1.454 (3) |
C1—C15 | 1.505 (3) | C15—H15A | 0.9700 |
C2—C3 | 1.441 (3) | C15—H15B | 0.9700 |
C2—H2 | 0.9300 | N16—C18 | 1.390 (4) |
C3—C5 | 1.393 (3) | N16—C17 | 1.438 (3) |
C3—C4 | 1.402 (3) | C17—H17A | 0.9600 |
C4—C8 | 1.389 (3) | C17—H17B | 0.9600 |
C5—C6 | 1.379 (3) | C17—H17C | 0.9600 |
C5—H5 | 0.9300 | C18—C23 | 1.390 (4) |
C6—C7 | 1.381 (4) | C18—C19 | 1.393 (4) |
C6—H6 | 0.9300 | C19—C20 | 1.374 (4) |
C7—C8 | 1.375 (4) | C19—H19 | 0.9300 |
C7—H7 | 0.9300 | C20—C21 | 1.370 (4) |
C8—H8 | 0.9300 | C20—H20 | 0.9300 |
C9—C10 | 1.377 (3) | C21—C22 | 1.350 (5) |
C9—C14 | 1.384 (3) | C21—H21 | 0.9300 |
C10—C11 | 1.387 (4) | C22—C23 | 1.380 (5) |
C10—H10 | 0.9300 | C22—H22 | 0.9300 |
C11—C12 | 1.369 (4) | C23—H23 | 0.9300 |
O1—S1—O2 | 120.4 (1) | C13—C12—C11 | 120.9 (3) |
O1—S1—N1 | 106.6 (1) | C13—C12—H12 | 119.6 |
O2—S1—N1 | 106.3 (1) | C11—C12—H12 | 119.6 |
O1—S1—C9 | 109.6 (1) | C12—C13—C14 | 120.1 (3) |
O2—S1—C9 | 108.4 (1) | C12—C13—H13 | 119.9 |
N1—S1—C9 | 104.3 (1) | C14—C13—H13 | 119.9 |
C4—N1—C1 | 108.0 (2) | C13—C14—C9 | 119.1 (3) |
C4—N1—S1 | 125.9 (1) | C13—C14—H14 | 120.4 |
C1—N1—S1 | 124.6 (2) | C9—C14—H14 | 120.4 |
C2—C1—N1 | 108.4 (2) | N16—C15—C1 | 112.0 (2) |
C2—C1—C15 | 128.7 (2) | N16—C15—H15A | 109.2 |
N1—C1—C15 | 122.9 (2) | C1—C15—H15A | 109.2 |
C1—C2—C3 | 109.5 (2) | N16—C15—H15B | 109.2 |
C1—C2—H2 | 125.3 | C1—C15—H15B | 109.2 |
C3—C2—H2 | 125.3 | H15A—C15—H15B | 107.9 |
C5—C3—C4 | 119.4 (2) | C18—N16—C17 | 121.7 (2) |
C5—C3—C2 | 133.6 (2) | C18—N16—C15 | 119.4 (2) |
C4—C3—C2 | 107.1 (2) | C17—N16—C15 | 118.0 (3) |
C8—C4—C3 | 121.5 (2) | N16—C17—H17A | 109.5 |
C8—C4—N1 | 131.6 (2) | N16—C17—H17B | 109.5 |
C3—C4—N1 | 106.9 (2) | H17A—C17—H17B | 109.5 |
C6—C5—C3 | 119.2 (2) | N16—C17—H17C | 109.5 |
C6—C5—H5 | 120.4 | H17A—C17—H17C | 109.5 |
C3—C5—H5 | 120.4 | H17B—C17—H17C | 109.5 |
C5—C6—C7 | 120.2 (2) | N16—C18—C23 | 121.9 (3) |
C5—C6—H6 | 119.9 | N16—C18—C19 | 121.5 (2) |
C7—C6—H6 | 119.9 | C23—C18—C19 | 116.6 (3) |
C8—C7—C6 | 122.4 (2) | C20—C19—C18 | 121.6 (3) |
C8—C7—H7 | 118.8 | C20—C19—H19 | 119.2 |
C6—C7—H7 | 118.8 | C18—C19—H19 | 119.2 |
C7—C8—C4 | 117.3 (2) | C19—C20—C21 | 120.5 (3) |
C7—C8—H8 | 121.4 | C19—C20—H20 | 119.7 |
C4—C8—H8 | 121.4 | C21—C20—H20 | 119.7 |
C10—C9—C14 | 121.0 (2) | C22—C21—C20 | 118.9 (3) |
C10—C9—S1 | 120.1 (2) | C22—C21—H21 | 120.6 |
C14—C9—S1 | 119.0 (2) | C20—C21—H21 | 120.6 |
C9—C10—C11 | 118.6 (3) | C21—C22—C23 | 121.7 (3) |
C9—C10—H10 | 120.7 | C21—C22—H22 | 119.2 |
C11—C10—H10 | 120.7 | C23—C22—H22 | 119.2 |
C12—C11—C10 | 120.3 (3) | C22—C23—C18 | 120.7 (3) |
C12—C11—H11 | 119.9 | C22—C23—H23 | 119.6 |
C10—C11—H11 | 119.9 | C18—C23—H23 | 119.6 |
O1—S1—N1—C4 | 22.4 (2) | O2—S1—C9—C10 | −4.2 (2) |
O2—S1—N1—C4 | 152.0 (2) | N1—S1—C9—C10 | −117.2 (2) |
C9—S1—N1—C4 | −93.6 (2) | O1—S1—C9—C14 | −51.3 (2) |
O1—S1—N1—C1 | −173.1 (2) | O2—S1—C9—C14 | 175.5 (2) |
O2—S1—N1—C1 | −43.5 (2) | N1—S1—C9—C14 | 62.5 (2) |
C9—S1—N1—C1 | 71.0 (2) | C14—C9—C10—C11 | −0.1 (4) |
C4—N1—C1—C2 | −2.8 (2) | S1—C9—C10—C11 | 179.6 (2) |
S1—N1—C1—C2 | −169.7 (2) | C9—C10—C11—C12 | −1.8 (4) |
C4—N1—C1—C15 | 178.0 (2) | C10—C11—C12—C13 | 1.9 (5) |
S1—N1—C1—C15 | 11.1 (3) | C11—C12—C13—C14 | 0.0 (5) |
N1—C1—C2—C3 | 0.8 (2) | C12—C13—C14—C9 | −1.9 (5) |
C15—C1—C2—C3 | 179.9 (2) | C10—C9—C14—C13 | 2.0 (4) |
C1—C2—C3—C5 | 179.6 (2) | S1—C9—C14—C13 | −177.7 (2) |
C1—C2—C3—C4 | 1.5 (2) | C2—C1—C15—N16 | 15.4 (3) |
C5—C3—C4—C8 | −1.6 (3) | N1—C1—C15—N16 | −165.7 (2) |
C2—C3—C4—C8 | 176.8 (2) | C1—C15—N16—C18 | 81.2 (3) |
C5—C3—C4—N1 | 178.4 (2) | C1—C15—N16—C17 | −109.3 (3) |
C2—C3—C4—N1 | −3.2 (2) | C17—N16—C18—C23 | 1.9 (4) |
C1—N1—C4—C8 | −176.3 (2) | C15—N16—C18—C23 | 171.0 (2) |
S1—N1—C4—C8 | −9.6 (3) | C17—N16—C18—C19 | −178.6 (3) |
C1—N1—C4—C3 | 3.7 (2) | C15—N16—C18—C19 | −9.4 (4) |
S1—N1—C4—C3 | 170.4 (2) | N16—C18—C19—C20 | −179.3 (3) |
C4—C3—C5—C6 | 1.9 (3) | C23—C18—C19—C20 | 0.3 (4) |
C2—C3—C5—C6 | −176.0 (2) | C18—C19—C20—C21 | 1.1 (5) |
C3—C5—C6—C7 | −0.8 (4) | C19—C20—C21—C22 | −1.6 (5) |
C5—C6—C7—C8 | −0.7 (4) | C20—C21—C22—C23 | 0.8 (6) |
C6—C7—C8—C4 | 1.0 (4) | C21—C22—C23—C18 | 0.7 (5) |
C3—C4—C8—C7 | 0.2 (3) | N16—C18—C23—C22 | 178.4 (3) |
N1—C4—C8—C7 | −179.8 (2) | C19—C18—C23—C22 | −1.2 (4) |
O1—S1—C9—C10 | 129.0 (2) |
D—H···A | D—H | H···A | D···A | D—H···A |
C8—H8···O1 | 0.93 | 2.33 | 2.911 (3) | 121 |
C10—H10···O2 | 0.93 | 2.53 | 2.904 (3) | 104 |
C8—H8···O2i | 0.93 | 2.43 | 3.217 (3) | 142 |
C12—H12···Cg1ii | 0.93 | 2.75 | 3.568 (5) | 148 |
Symmetry codes: (i) −x−1, y−1/2, −z−1/2; (ii) x+1/2, −y−3/2, −z. |
Experimental details
Crystal data | |
Chemical formula | C22H20N2O2S |
Mr | 376.46 |
Crystal system, space group | Orthorhombic, P212121 |
Temperature (K) | 293 |
a, b, c (Å) | 8.3162 (2), 11.2384 (3), 20.4080 (5) |
V (Å3) | 1907.35 (8) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.19 |
Crystal size (mm) | 0.44 × 0.42 × 0.24 |
Data collection | |
Diffractometer | Siemens SMART CCD area detector diffractometer |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 13206, 4707, 3474 |
Rint | 0.035 |
(sin θ/λ)max (Å−1) | 0.667 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.041, 0.119, 0.91 |
No. of reflections | 4707 |
No. of parameters | 245 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.17, −0.19 |
Absolute structure | Flack (1983) |
Absolute structure parameter | 0.06 (8) |
Computer programs: SMART (Siemens, 1996), SAINT (Siemens, 1996), SAINT, SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), ZORTEP (Zsolnai, 1997), SHELXL97 and PARST (Nardelli, 1995).
S1—O1 | 1.424 (2) | S1—C9 | 1.759 (2) |
S1—O2 | 1.419 (2) | N1—C4 | 1.417 (3) |
S1—N1 | 1.664 (2) | N1—C1 | 1.425 (3) |
O1—S1—O2 | 120.4 (1) | C4—N1—C1 | 108.0 (2) |
O1—S1—N1 | 106.6 (1) | C4—N1—S1 | 125.9 (1) |
O2—S1—N1 | 106.3 (1) | C1—N1—S1 | 124.6 (2) |
O1—S1—C9 | 109.6 (1) | C18—N16—C17 | 121.7 (2) |
O2—S1—C9 | 108.4 (1) | C18—N16—C15 | 119.4 (2) |
N1—S1—C9 | 104.3 (1) | C17—N16—C15 | 118.0 (3) |
C1—C15—N16—C18 | 81.2 (3) | C1—C15—N16—C17 | −109.3 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
C8—H8···O1 | 0.93 | 2.33 | 2.911 (3) | 121 |
C10—H10···O2 | 0.93 | 2.53 | 2.904 (3) | 104 |
C8—H8···O2i | 0.93 | 2.43 | 3.217 (3) | 142 |
C12—H12···Cg1ii | 0.93 | 2.75 | 3.568 (5) | 148 |
Symmetry codes: (i) −x−1, y−1/2, −z−1/2; (ii) x+1/2, −y−3/2, −z. |
Subscribe to Acta Crystallographica Section C: Structural Chemistry
The full text of this article is available to subscribers to the journal.
- Information on subscribing
- Sample issue
- Purchase subscription
- Reduced-price subscriptions
- If you have already subscribed, you may need to register
The biological activities of indoles and their derivatives have been known for a long time. The indole unit occurs naturally in a wide variety of structures. The indole ring system occurs in plants (Nigović et al., 2000). Indolines and their oxidized counter parts are important pharmacophores that appear in numerous biologically active compounds most notably those affecting central nervous system (Zhang & Liebeskind, 1996). Certain indole derivatives possess antidepressive (Papenstasion & Newmeyer, 1972), anti-inflammatory (Rodriguez et al., 1985; Polletto et al., 1974), antimicrobial (El-Sayed et al., 1986; Gadaginamath, 1999), antitumor (Schollmeyer et al., 1995) and antibacterial (Okabe & Adachi, 1998) activities. They have been proven to display high aldose reductase inhibitory activity (Rajeswaran et al., 1999). Because of the wide range of biological activities of indole derivatives, we have undertaken the X-ray studies on an indole derivative, (I), in order to study its conformations in the solid state. \sch
The indole system is not strictly planar and the dihedral angle formed by the pyrrole and benzo planes is 2.7 (1)°. Atom N1 deviates by -0.104 (2) Å from the mean plane passing through S1, C1 and C4. This slight pyramidalization behaviour is also observed in related indoles (Yokum & Fronczek, 1997; Beddoes et al., 1986). The torsion angles O2—S1—N1—C4 = 152.0 (2)° and O2—S1—C9—C14 = 175.5 (2)° describe the conformation of the phenylsulfonyl group with respect to the indole system which cause the best planes of the indole and phenyl rings to form a dihedral angle of 89.6 (1)° as observed in similar structures (Yokum & Fronczek, 1997).
In the benzene ring of the indole system, endocyclic angles at C8 and C5 are contracted to 117.3 (2) and 119.2 (2)° while those at C7 and C4 are expanded to 122.4 (2) and 121.5 (2)°, respectively. This would appear to be a real effect caused by the fusion of the smaller pyrrole ring to the six-membered benzene ring. A similar effect has also been observed by Sivaraman et al. (1994a,b, 1996), Govindasamy et al. (1999) and Sankaranarayanan et al. (2000).
The phenyl ring attached to N16 is inclined to an angle of 83.1 (1)° with indole mean plane and 66.0 (1)° with the phenyl ring of the sulfonyl group. The sum of the angles around N16 [359.1 (4)°] is indicative of sp2 hybridized character. The orientation of the indole substituent is influenced by a weak interaction C8—H8···O1 quantitatively defined by the torsion angles C8—C4—N1—S1 [-9.6 (3)°], C4—N1—S1—C9 [-93.6 (2)°] while the orientation of the phenyl bound to the sulfonyl group is governed by the C10—H10···O2 interaction (Table. 2) quantitatively defined by the torsion angle O2—S1—C9—C10 [-4.2 (2)°].
The angular disposition of the bonds about the S atom shows significant deviation from that of a regular tetrahedron, with the largest deviation in O—S—O angle. The widening of the angle O1—S1—O2 = 120.4 (1)° from the ideal tetrahedral value is presumably the result of the repulsive interactions between the short S═O bonds similar to that observed in related structures (Govindasamy et al., 1999; Rodriguez et al., 1985; Beddoes et al., 1986). The S—N and S—C bond distances agree well with the literature values of 1.642 (24) and 1.758 (13) Å (Allen et al., 1987), respectively.
In addition to van der Waals interactions, the molecular packing is stabilized by a C—H···O hydrogen bond and C—H···π interaction (Table 2), where Cg1 is the ring centroid of the benzene ring (C3—C8).