Issue contents
Download PDF of article
Download CIF
3D view
Navigation
Highlighting
Dictionary of Crystallography reference
IUPAC Gold Book reference
more ...
Download citation
FormatBIBTeX
EndNote
RefMan
Refer
Medline
CIF
SGML
Plain Text
share
Previous article
Next article
Previous article
Issue contents
Download PDF of article
Download CIF
3D view
Navigation
Highlighting
Dictionary of Crystallography reference
IUPAC Gold Book reference
more ...
Download citation
FormatBIBTeX
EndNote
RefMan
Refer
Medline
CIF
SGML
Plain Text
share
Next article

organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 69| Part 6| June 2013| Pages o972-o973
doi:10.1107/S1600536813013950

6-[3-(p-Tolyl­sulfonyl­amino)­prop­yl]diquino­thia­zine†

Małgorzata Jeleń,a Aleksander Shkurenko,b Kinga Suwińska,b,c Krystian Plutaa* and Beata Morak-Młodawskaa

aDepartment of Organic Chemistry, The Medical University of Silesia, ul. Jagiellońska 4, PL–41 200 Sosnowiec, Poland, bInstitute of Physical Chemistry, Polish Academy of Sciences, ul. Kasprzaka 44/52, PL–01 224 Warsaw, Poland, and cFaculty of Biology and Environmental Sciences, Cardinal Stefan Wyszynski University, ul. Wóycickiego 1/3, PL–01 938, Warszawa, Poland
*Correspondence e-mail: pluta@sum.edu.pl

(Received 18 March 2013; accepted 20 May 2013; online 25 May 2013)

In the title mol­ecule {systematic name: N-[3-(diquino[3,2-b;2′,3′-e][1,4]thia­zin-6-yl)prop­yl]-4-methyl­benzene­sulfon­amide}, C28H24N4O2S2, the penta­cyclic system is relatively planar [maximum deviation from the mean plane = 0.242 (1) Å]. The dihedral angle between two quinoline ring systems is 8.23 (2)° and that between the two halves of the 1,4-thia­zine ring is 5.68 (3)°. The conformation adopted by the 3-(p-tolyl­sulfonyl­amino)­propyl substituent allows for the formation of an intra­molecular N—H⋯N hydrogen bond and places the benzene ring of this substituent above one of the quinoline fragments of the penta­cyclic system. In the crystal, mol­ecules are arranged via π–π stacking inter­actions into (0-11) layers [centroid–centroid distances = 3.981 (1)–4.320 (1) Å for the rings in the penta­cyclic system and 3.645 (1) Å for the tolyl benzene rings]. In addition, mol­ecules are involved in weak C—H⋯O, which connect the layers, and C—H⋯S hydrogen bonds. The title compound shows promising anti­cancer activity against renal cancer cell line UO-31.

Related literature

For the structures of hetero­penta­cenes, see: Anthony (2006[Anthony, J. E. (2006). Chem. Rev. 106, 5028-5048.]); Isaia et al. (2009[Isaia, F., Aragoni, M. C., Arca, M., Demartin, F., Devillanova, F. A., Ennas, G., Garau, A., Lippolis, V., Mancini, A. & Verani, G. (2009). Eur. J. Inorg. Chem. pp. 3667-3672.]); Yoshida et al. (1994[Yoshida, S., Kozawa, K., Sato, N. & Uchida, T. (1994). Bull. Chem. Soc. Jpn, 67, 2017-2023.]). For recent literature on the biological activity of pheno­thia­zines, see: Aaron et al. (2009[Aaron, J. J., Gaye Seye, M. D., Trajkovska, S. & Motohashi, N. (2009). Top. Heterocycl. Chem. 16, 153-231.]); Pluta et al. (2011[Pluta, K., Morak-Młodawska, B. & Jeleń, M. (2011). Eur. J. Med. Chem. 46, 3179-3189.]). For the synthesis and biological activity of 6-substituted diquino­thia­zines, see: Nowak et al. (2007[Nowak, M., Pluta, K., Suwińska, K. & Straver, L. (2007). J. Heterocycl. Chem. 44, 543-550.]); Jeleń & Pluta (2009[Jeleń, M. & Pluta, K. (2009). Heterocycles, 78, 2325-2336.]); Pluta et al. (2010[Pluta, K., Jeleń, M., Morak-Młodawska, B., Zimecki, M., Artym, J. & Kocięba, M. (2010). Pharmacol. Rep. 62, 319-332.]). For crystal structures of pheno­thia­zines, see: Chu (1988[Chu, S. S. C. (1988). Phenothiazines and 1,4-Benzothiazines - Chemical and Biological Aspects, edited by R. R. Gupta, pp. 475-526. Amsterdam: Elsevier.]). For information on aza­pheno­thia­zines, their nomenclature and synthesis, see: Pluta et al. (2009[Pluta, K., Morak-Młodawska, B. & Jeleń, M. (2009). J. Heterocycl. Chem. 46, 355-391.]). For hetero­penta­cenes with quinoline moieties containing nitro­gen, sulfur, oxygen and selenium, see: Nowak et al. (2002[Nowak, M., Pluta, K. & Suwińska, K. (2002). New J. Chem. 26, 1216-1220.]); Pluta et al. (2000[Pluta, K., Nowak, M. & Suwińska, K. (2000). J. Chem. Crystallogr. 30, 479-482.]).

[Scheme 1]

Experimental

Crystal data

  • C28H24N4O2S2

  • Mr = 512.63

  • Triclinic, [P \overline 1]

  • a = 9.3986 (3) Å

  • b = 10.3793 (3) Å

  • c = 12.6207 (3) Å

  • α = 80.735 (2)°

  • β = 81.959 (2)°

  • γ = 77.999 (2)°

  • V = 1181.30 (6) Å3

  • Z = 2

  • Mo Kα radiation

  • μ = 0.26 mm−1

  • T = 100 K

  • 0.39 × 0.34 × 0.23 mm
Data collection

  • Agilent SuperNova Dual (Cu at zero, Eos) diffractometer

  • Absorption correction: analytical [CrysAlis PRO (Agilent, 2012[Agilent (2012). CrysAlis PRO. Agilent Technologies, Yarnton, England.]) and Clark & Reid (1995[Clark, R. C. & Reid, J. S. (1995). Acta Cryst. A51, 887-897.])] Tmin = 0.937, Tmax = 0.965

  • 24091 measured reflections

  • 7396 independent reflections

  • 6770 reflections with I > 2σ(I)

  • Rint = 0.015
Refinement

  • R[F2 > 2σ(F2)] = 0.033

  • wR(F2) = 0.093

  • S = 1.04

  • 7396 reflections

  • 329 parameters

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.42 e Å−3

  • Δρmin = −0.40 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
N18—H18⋯N5 0.876 (14) 2.243 (15) 2.9973 (12) 144.1 (12)
C15—H15A⋯O20i 0.99 2.33 3.1641 (12) 141
C11—H11⋯O21ii 0.95 2.55 3.3933 (13) 149
C15—H15B⋯S13iii 0.99 2.86 3.6912 (11) 142
C17—H17B⋯O21iv 0.99 2.47 3.3013 (13) 141
Symmetry codes: (i) -x+1, -y+1, -z+2; (ii) x, y, z-1; (iii) -x+1, -y+1, -z+1; (iv) -x, -y+1, -z+2.

Data collection: CrysAlis PRO (Agilent, 2012[Agilent (2012). CrysAlis PRO. Agilent Technologies, Yarnton, England.]); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: ORTEPIII (Burnett & Johnson, 1996[Burnett, M. N. & Johnson, C. K. (1996). ORTEPIII. Report ORNL-6895. Oak Ridge National Laboratory, Tennessee, USA.]) and Mercury (Macrae et al., 2008[Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466-470.]); software used to prepare material for publication: publCIF (Westrip, 2010[Westrip, S. P. (2010). J. Appl. Cryst. 43, 920-925.]).

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536813013950/gk2566sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536813013950/gk2566Isup2.hkl

Supporting information file. DOI: 10.1107/S1600536813013950/gk2566Isup3.cml

checkCIF report


Comment top

Heteropentacenes, mainly aza-, thia- and azathiapentacenes, are considered as polyheterocyclic donor molecules to form organic semiconductors (Anthony, 2006). We obtained heteropentacenes containing nitrogen, sulfur, oxygen and selenium via the annulation reactions (Nowak et al., 2002). One of this type was 6H-5,6,7-triaza-13-thiapentacene (II, Figure 2) which can be regarded as a new modified phenothiazine system, pentacyclic diquinothiazine, where two quinoline rings were incorporated in the ring system instead of benzene rings. This compound was further transformed by introduction of 6-alkyl, aryl, heteroaryl and aminoalkyl substituents at the thiazine nitrogen atoms. It is well known that neuroleptic phenothiazines have tricyclic dibenzothiazine ring system and the aminoalkyl substituent at the thiazine nitrogen atom in position 10. All these compounds are folded and have the central thiazine ring in a boat conformation with the aminoalkyl group in the equatorial position. 6-Substituted diquinothiazines with the aminoalkyl groups and their acyl and sulfonyl derivatives exhibit promising anticancer activities against the cell lines of 9 types of human cancer: leukemia, melanoma, non-small cell lung cancer, colon cancer, CNS cancer, ovarian cancer, renal cancer, prostate cancer and breast cancer (Pluta et al., 2010). None of phenothiazines or azaphenothiazine with the p-tolylsulfonylaminopropyl substituent have been examined by X-ray crystallography so far. The title compound (I) was obtained in a few step synthesis starting from the reactions of heteropentacenes, 6H-5,6,7-triaza-13-thiapentacene (II) and 5,7-diaza-6,13-dithiapentacene (III), with appropriate reagents (see Experimental). The structure of the title compound was assigned by spectroscopic (1H NMR and MS) analysis. The diquinothiazine structure of C2v symmetry shows a lack of the Smiles rearrangement during thiazine ring closure (Jeleń & Pluta, 2009). X-ray analysis fully confirmed this structure as 6-[3(p-tolylsulfonylamino)propyl]diquino[3,2 - b;2',3'-e][1,4]thiazine. All the classical neuroleptic phenothiazines are folded along the N–S axis with the dihedral angle of 134.0–153.6° and with the aminoalkyl group in equatorial positions (Chu, 1988). The title molecule is close to planar with the dihedral angle between the quinoline rings of 171.77 (2)° and the angle between two halves of the thiazine ring of 174.32 (3)°. The S13···N6–C15 angle is 176.70 (6)°. The endocyclic bond angles at heteroatoms in the central ring (C12A–S13–C13A and C5A–N6–C6A) are quite large, 102.56 (4)° and 125.04 (8)° in accord with the thiazine ring flat conformation. It is interesting that the planarity of the triazathiapentacene system is dependent on the substituent nature at the thiazine nitrogen atom. When the substituent was an electron-donating group (phenyl in compound IV; Pluta et al., 2000), the ring system was folded, when electron-deficient ( p-nitrophenyl group in compound V; Nowak et al., 2007) the system was almost planar. The bonds around the sulfur atom S19 of the sulfonamide group show a distortion from tetrahedral geometry. Whereas the O22—S19—O21 bond angle is 119.98 (5)°, three other O–S19–X (N18 or C22) bond angles are 106.68 (4)–107.48 (5)°. The bonds around thiazine N6 and sulfonamide N18 atoms show planar and pyramidal arrangement, respectively, as shown by the sum bond angles (359.97 (8)° and 340.25 (9)°, repectively). The p-tolylsulfonylaminopropyl substituent is not coplanar with pentacyclic ring system and shows unexpectedly U-conformation with the benzene ring placed over the pentacene system, with the dihedral angle between the C22–C26 and N6/C5A/C6A/C12A/C13A/S13 planes of 30.15 (3)°. The torsion angles including the propyl group (C15–C16–C17) show the synclinal/synclinal arrangement of the carbon chain. The torsion angles involving the sulfonamide group (C17–N18–S19–C22) show antiperiplanar/synclinal/synclinal arrangement. There is intramolecular N18–H18···N5 hydrogen bond which stabilizes the U shape of the p-tolylsulfonylaminopropyl substituent. Three intermolecular C–H···O hydrogen bonds involving the sulfonamide group and one C–H···S hydrogen bond involving the thiazine sulfur atom exist in the crystal. The molecules which are related via centers of symmetry at 0,1/2,1/2 and 1/2,1/2,1/2 stack in ribbons along the a direction via π–π interactions of the pentacyclic systems. The ribbons are further arranged into (0 -1 1) layers via another π–π interactions between benzene rings of toluene substituents (Figure 3). Layers are glued together by the mentioned above C–H···O hydrogen bonds between aromatic carbon atoms of pentacyclic systems of one layer and sulfonamide oxygen atoms of the neighbouring layer.

The title compound shows promising anticancer activity against renal cancer cell line UO-31.

Related literature top

For the structures of heteropentacenes, see: Anthony (2006); Isaia et al. (2009); Yoshida et al. (1994). For recent literature on the biological activity of phenothiazines, see: Aaron et al. (2009); Pluta et al. (2011). For the synthesis and biological activity of 6-substituted diquinothiazines, see: Nowak et al. (2007); Jeleń & Pluta (2009); Pluta et al. (2010). For crystal structures of phenothiazines, see: Chu (1988). For information on azaphenothiazines, their nomenclature and synthesis, see: Pluta et al. (2009). For heteropentacenes with quinoline moieties containing nitrogen, sulfur, oxygen and selenium, see: Nowak et al. (2002); Pluta et al. (2000).

Experimental top

The title compound was obtained in a few step synthesis as described by Jeleń et al. (2009) starting from the reactions of 6H-5,6,7-triaza-13-thiapentacene (II) with phthalimidopropyl bromide (followed by hydrolysis) or 5,7-diaza-6,13-dithiapentacene (III) with 1,3-diaminopropane to obtain aminopropyldiquinothiazine (IV). Compound (IV) was sulfonylated with p-toluenesulfonyl chloride. The title compound has melting point 439–440 K. X-ray quality crystals were grown from chloroform-ethanol mixture by slow evaporation.

Refinement top

All H atoms were treated as riding atoms in geometrically calculated positions, with d(C–H) = 0.95, 0.99 and 0.98 Å for aromatic, methylene and methyl hydrogens, respectively, except of the H atom in the N–H group of which positional parameters were refined freely, Uiso(H) = kUeq(C,N), where k = 1.5 for the methyl group and k = 1.2 otherwise.

Computing details top

Data collection: CrysAlis PRO (Agilent, 2012); cell refinement: CrysAlis PRO (Agilent, 2012); data reduction: CrysAlis PRO (Agilent, 2012); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEPIII (Burnett & Johnson, 1996) and Mercury (Macrae et al., 2008); software used to prepare material for publication: publCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. Molecular structure with displacement ellipsoids shown at the 50% probability level.
[Figure 2] Fig. 2. Related compounds.
[Figure 3] Fig. 3. Structure of the (0 -1 1) layer: the π–π stacking interactions between pentacyclic systems are 3.589 (1) and 3.841 (1) Å [distance measured between r.m.s. planes of fully eclipsed and partially eclipsed benzene rings of pentacyclic systems, respectively] and 3.453 (1) Å between r.m.s. planes of benzene rings of toluene substituents.
N-[3-(Diquino[3,2-b;2',3'-e][1,4]thiazin-6-yl)propyl]-4-methylbenzenesulfonamide top
Crystal data top
C28H24N4O2S2Z = 2
Mr = 512.63F(000) = 536
Triclinic, P1Dx = 1.441 Mg m−3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 9.3986 (3) ÅCell parameters from 16661 reflections
b = 10.3793 (3) Åθ = 3.3–32.2°
c = 12.6207 (3) ŵ = 0.26 mm−1
α = 80.735 (2)°T = 100 K
β = 81.959 (2)°Block, yellow
γ = 77.999 (2)°0.39 × 0.34 × 0.23 mm
V = 1181.30 (6) Å3
Data collection top
Agilent SuperNova Dual (Cu at zero, Eos)
diffractometer		7396 independent reflections
Radiation source: SuperNova (Mo) X-ray Source6770 reflections with I > 2σ(I)
Mirror monochromatorRint = 0.015
Detector resolution: 16.2974 pixels mm-1θmax = 31.0°, θmin = 3.3°
ω scansh = −13→13
Absorption correction: analytical
[CrysAlis PRO (Agilent, 2012) and Clark & Reid (1995)]		k = −15→15
Tmin = 0.937, Tmax = 0.965l = −18→18
24091 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.033Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.093H atoms treated by a mixture of independent and constrained refinement
S = 1.04 w = 1/[σ2(Fo2) + (0.0463P)2 + 0.437P]
where P = (Fo2 + 2Fc2)/3
7396 reflections(Δ/σ)max = 0.002
329 parametersΔρmax = 0.42 e Å−3
0 restraintsΔρmin = −0.40 e Å−3
Crystal data top
C28H24N4O2S2γ = 77.999 (2)°
Mr = 512.63V = 1181.30 (6) Å3
Triclinic, P1Z = 2
a = 9.3986 (3) ÅMo Kα radiation
b = 10.3793 (3) ŵ = 0.26 mm−1
c = 12.6207 (3) ÅT = 100 K
α = 80.735 (2)°0.39 × 0.34 × 0.23 mm
β = 81.959 (2)°
Data collection top
Agilent SuperNova Dual (Cu at zero, Eos)
diffractometer		7396 independent reflections
Absorption correction: analytical
[CrysAlis PRO (Agilent, 2012) and Clark & Reid (1995)]		6770 reflections with I > 2σ(I)
Tmin = 0.937, Tmax = 0.965Rint = 0.015
24091 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0330 restraints
wR(F2) = 0.093H atoms treated by a mixture of independent and constrained refinement
S = 1.04Δρmax = 0.42 e Å−3
7396 reflectionsΔρmin = −0.40 e Å−3
329 parameters
Special details top

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
C10.49893 (13)1.01160 (10)0.71760 (9)0.0272 (2)
H10.47591.09110.66910.033*
C20.55824 (14)1.01426 (11)0.81047 (10)0.0316 (2)
H20.57501.09580.82660.038*
C30.59430 (13)0.89597 (11)0.88211 (10)0.0284 (2)
H30.63540.89870.94620.034*
C40.57070 (11)0.77664 (10)0.86036 (8)0.02243 (18)
H40.59720.69750.90850.027*
C4A0.50694 (10)0.77236 (9)0.76632 (8)0.01797 (16)
N50.47657 (8)0.65388 (8)0.75030 (6)0.01707 (14)
C5A0.41609 (9)0.64626 (9)0.66422 (7)0.01604 (16)
N60.38838 (9)0.52185 (8)0.65386 (7)0.01928 (15)
C6A0.31384 (10)0.49652 (9)0.57300 (8)0.01871 (17)
N70.28831 (10)0.37503 (8)0.58262 (7)0.02115 (16)
C7A0.21392 (11)0.34230 (10)0.50797 (8)0.02097 (18)
C80.18288 (13)0.21269 (10)0.52247 (9)0.0270 (2)
H80.21610.15000.58160.032*
C90.10458 (14)0.17702 (11)0.45114 (10)0.0307 (2)
H90.08410.08970.46130.037*
C100.05463 (14)0.26913 (12)0.36322 (9)0.0301 (2)
H10−0.00110.24400.31540.036*
C110.08566 (12)0.39472 (11)0.34607 (9)0.0264 (2)
H110.05360.45550.28560.032*
C11A0.16556 (11)0.43355 (10)0.41872 (8)0.02102 (18)
C120.19770 (11)0.56268 (10)0.40906 (8)0.02207 (18)
H120.16970.62670.34920.026*
C12A0.26858 (11)0.59588 (9)0.48515 (8)0.01975 (17)
S130.30095 (3)0.75808 (3)0.46855 (2)0.02831 (7)
C13A0.37960 (10)0.76078 (9)0.58521 (7)0.01722 (16)
C140.40755 (10)0.87994 (9)0.60157 (8)0.01950 (17)
H140.38340.95650.55030.023*
C14A0.47201 (11)0.89058 (9)0.69388 (8)0.01988 (17)
C150.43639 (12)0.40812 (9)0.73615 (8)0.02281 (19)
H15A0.51340.42940.77280.027*
H15B0.48030.32950.69940.027*
C160.31325 (14)0.37268 (10)0.82111 (9)0.0278 (2)
H16A0.24560.33600.78590.033*
H16B0.35610.30150.87610.033*
C170.22489 (12)0.48651 (11)0.87824 (8)0.02409 (19)
H17A0.18970.56230.82390.029*
H17B0.13830.45780.92220.029*
S190.22842 (3)0.62938 (3)1.034198 (18)0.02204 (6)
O200.33837 (9)0.65975 (8)1.08936 (6)0.02723 (16)
O210.11287 (9)0.56819 (11)1.09446 (7)0.0372 (2)
C220.14699 (11)0.77850 (11)0.95968 (8)0.02354 (19)
C230.01915 (12)0.78269 (14)0.91344 (9)0.0304 (2)
H23−0.02680.70750.92450.036*
C24−0.03909 (13)0.89937 (15)0.85096 (9)0.0369 (3)
H24−0.12540.90300.81850.044*
C250.02520 (14)1.01107 (14)0.83459 (9)0.0362 (3)
C260.15136 (14)1.00516 (13)0.88263 (9)0.0333 (3)
H260.19591.08110.87300.040*
C270.21278 (12)0.88873 (11)0.94467 (9)0.0267 (2)
H270.29950.88490.97660.032*
C28−0.04257 (19)1.13661 (16)0.76733 (10)0.0514 (4)
H28A−0.03951.11990.69270.077*
H28B0.01221.20690.76870.077*
H28C−0.14451.16460.79690.077*
N180.31353 (9)0.52970 (8)0.94864 (7)0.01995 (15)
H180.3886 (16)0.5609 (14)0.9126 (12)0.024*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.0354 (5)0.0178 (4)0.0308 (5)−0.0121 (4)−0.0060 (4)0.0007 (4)
C20.0432 (6)0.0208 (5)0.0365 (6)−0.0153 (4)−0.0099 (5)−0.0036 (4)
C30.0364 (6)0.0247 (5)0.0287 (5)−0.0130 (4)−0.0091 (4)−0.0036 (4)
C40.0260 (4)0.0203 (4)0.0232 (4)−0.0087 (4)−0.0054 (4)−0.0016 (3)
C4A0.0181 (4)0.0161 (4)0.0200 (4)−0.0056 (3)−0.0007 (3)−0.0017 (3)
N50.0176 (3)0.0150 (3)0.0190 (3)−0.0036 (3)−0.0033 (3)−0.0016 (3)
C5A0.0156 (4)0.0133 (4)0.0186 (4)−0.0022 (3)−0.0027 (3)−0.0006 (3)
N60.0259 (4)0.0122 (3)0.0209 (4)−0.0029 (3)−0.0114 (3)0.0011 (3)
C6A0.0212 (4)0.0156 (4)0.0197 (4)−0.0018 (3)−0.0078 (3)−0.0010 (3)
N70.0264 (4)0.0150 (3)0.0237 (4)−0.0026 (3)−0.0111 (3)−0.0019 (3)
C7A0.0241 (4)0.0182 (4)0.0219 (4)−0.0021 (3)−0.0083 (3)−0.0040 (3)
C80.0350 (5)0.0179 (4)0.0307 (5)−0.0035 (4)−0.0140 (4)−0.0039 (4)
C90.0391 (6)0.0228 (5)0.0351 (6)−0.0074 (4)−0.0132 (5)−0.0083 (4)
C100.0360 (6)0.0325 (6)0.0268 (5)−0.0084 (5)−0.0110 (4)−0.0098 (4)
C110.0310 (5)0.0312 (5)0.0197 (4)−0.0075 (4)−0.0088 (4)−0.0040 (4)
C11A0.0230 (4)0.0231 (4)0.0180 (4)−0.0041 (3)−0.0055 (3)−0.0032 (3)
C120.0249 (4)0.0227 (4)0.0187 (4)−0.0048 (4)−0.0076 (3)0.0018 (3)
C12A0.0226 (4)0.0168 (4)0.0195 (4)−0.0034 (3)−0.0065 (3)0.0017 (3)
S130.04278 (16)0.01844 (12)0.02660 (13)−0.01033 (10)−0.01874 (11)0.00722 (9)
C13A0.0170 (4)0.0157 (4)0.0179 (4)−0.0031 (3)−0.0020 (3)0.0011 (3)
C140.0209 (4)0.0157 (4)0.0208 (4)−0.0053 (3)−0.0008 (3)0.0020 (3)
C14A0.0217 (4)0.0166 (4)0.0217 (4)−0.0074 (3)−0.0005 (3)−0.0005 (3)
C150.0339 (5)0.0117 (4)0.0240 (4)−0.0009 (3)−0.0167 (4)0.0013 (3)
C160.0453 (6)0.0167 (4)0.0254 (5)−0.0128 (4)−0.0162 (4)0.0049 (4)
C170.0271 (5)0.0251 (5)0.0229 (4)−0.0127 (4)−0.0096 (4)0.0044 (4)
S190.01835 (11)0.03176 (13)0.01380 (10)−0.00181 (9)−0.00435 (8)0.00184 (8)
O200.0256 (4)0.0342 (4)0.0215 (3)0.0027 (3)−0.0122 (3)−0.0053 (3)
O210.0277 (4)0.0619 (6)0.0180 (3)−0.0125 (4)−0.0001 (3)0.0093 (4)
C220.0180 (4)0.0338 (5)0.0146 (4)0.0056 (4)−0.0031 (3)−0.0036 (4)
C230.0186 (4)0.0486 (7)0.0199 (4)0.0054 (4)−0.0045 (4)−0.0059 (4)
C240.0257 (5)0.0564 (8)0.0206 (5)0.0174 (5)−0.0085 (4)−0.0093 (5)
C250.0381 (6)0.0426 (7)0.0156 (4)0.0209 (5)−0.0028 (4)−0.0052 (4)
C260.0376 (6)0.0310 (6)0.0231 (5)0.0113 (5)−0.0010 (4)−0.0044 (4)
C270.0252 (5)0.0290 (5)0.0222 (4)0.0066 (4)−0.0048 (4)−0.0055 (4)
C280.0593 (9)0.0539 (9)0.0213 (5)0.0314 (7)−0.0067 (5)−0.0004 (5)
N180.0201 (4)0.0214 (4)0.0187 (4)−0.0059 (3)−0.0051 (3)0.0011 (3)
Geometric parameters (Å, º) top
C1—C21.3730 (16)S13—C13A1.7440 (10)
C1—C14A1.4163 (13)C13A—C141.3689 (13)
C1—H10.9500C14—C14A1.4152 (14)
C2—C31.4124 (16)C14—H140.9500
C2—H20.9500C15—C161.5256 (17)
C3—C41.3782 (14)C15—H15A0.9900
C3—H30.9500C15—H15B0.9900
C4—C4A1.4130 (13)C16—C171.5179 (16)
C4—H40.9500C16—H16A0.9900
C4A—N51.3699 (11)C16—H16B0.9900
C4A—C14A1.4158 (13)C17—N181.4748 (13)
N5—C5A1.3149 (12)C17—H17A0.9900
C5A—N61.3986 (11)C17—H17B0.9900
C5A—C13A1.4384 (12)S19—O201.4351 (8)
N6—C6A1.4016 (12)S19—O211.4357 (9)
N6—C151.4800 (12)S19—N181.6279 (9)
C6A—N71.3156 (12)S19—C221.7623 (11)
C6A—C12A1.4335 (13)C22—C271.3852 (17)
N7—C7A1.3704 (12)C22—C231.3974 (14)
C7A—C11A1.4118 (14)C23—C241.3877 (17)
C7A—C81.4133 (14)C23—H230.9500
C8—C91.3765 (15)C24—C251.390 (2)
C8—H80.9500C24—H240.9500
C9—C101.4082 (17)C25—C261.3914 (19)
C9—H90.9500C25—C281.5080 (17)
C10—C111.3714 (16)C26—C271.3923 (15)
C10—H100.9500C26—H260.9500
C11—C11A1.4158 (13)C27—H270.9500
C11—H110.9500C28—H28A0.9800
C11A—C121.4170 (14)C28—H28B0.9800
C12—C12A1.3660 (13)C28—H28C0.9800
C12—H120.9500N18—H180.876 (15)
C12A—S131.7471 (10)
C2—C1—C14A120.16 (10)C14A—C14—H14119.6
C2—C1—H1119.9C14—C14A—C4A116.65 (8)
C14A—C1—H1119.9C14—C14A—C1123.70 (9)
C1—C2—C3120.11 (10)C4A—C14A—C1119.63 (9)
C1—C2—H2119.9N6—C15—C16113.75 (9)
C3—C2—H2119.9N6—C15—H15A108.8
C4—C3—C2120.90 (10)C16—C15—H15A108.8
C4—C3—H3119.6N6—C15—H15B108.8
C2—C3—H3119.6C16—C15—H15B108.8
C3—C4—C4A119.82 (10)H15A—C15—H15B107.7
C3—C4—H4120.1C17—C16—C15115.55 (8)
C4A—C4—H4120.1C17—C16—H16A108.4
N5—C4A—C4118.46 (8)C15—C16—H16A108.4
N5—C4A—C14A122.16 (9)C17—C16—H16B108.4
C4—C4A—C14A119.35 (8)C15—C16—H16B108.4
C5A—N5—C4A120.21 (8)H16A—C16—H16B107.5
N5—C5A—N6116.71 (8)N18—C17—C16111.15 (9)
N5—C5A—C13A121.40 (8)N18—C17—H17A109.4
N6—C5A—C13A121.88 (8)C16—C17—H17A109.4
C5A—N6—C6A125.03 (8)N18—C17—H17B109.4
C5A—N6—C15118.16 (8)C16—C17—H17B109.4
C6A—N6—C15116.78 (7)H17A—C17—H17B108.0
N7—C6A—N6115.61 (8)O20—S19—O21119.96 (5)
N7—C6A—C12A121.93 (8)O20—S19—N18106.67 (5)
N6—C6A—C12A122.46 (8)O21—S19—N18106.71 (6)
C6A—N7—C7A119.45 (8)O20—S19—C22107.48 (5)
N7—C7A—C11A122.50 (9)O21—S19—C22107.68 (5)
N7—C7A—C8118.34 (9)N18—S19—C22107.82 (4)
C11A—C7A—C8119.15 (9)C27—C22—C23120.77 (10)
C9—C8—C7A120.19 (10)C27—C22—S19119.75 (8)
C9—C8—H8119.9C23—C22—S19119.44 (9)
C7A—C8—H8119.9C24—C23—C22118.36 (13)
C8—C9—C10120.41 (10)C24—C23—H23120.8
C8—C9—H9119.8C22—C23—H23120.8
C10—C9—H9119.8C23—C24—C25121.87 (11)
C11—C10—C9120.59 (10)C23—C24—H24119.1
C11—C10—H10119.7C25—C24—H24119.1
C9—C10—H10119.7C24—C25—C26118.76 (11)
C10—C11—C11A119.87 (10)C24—C25—C28120.26 (13)
C10—C11—H11120.1C26—C25—C28120.97 (15)
C11A—C11—H11120.1C25—C26—C27120.43 (13)
C7A—C11A—C11119.76 (9)C25—C26—H26119.8
C7A—C11A—C12116.77 (9)C27—C26—H26119.8
C11—C11A—C12123.45 (9)C22—C27—C26119.80 (11)
C12A—C12—C11A120.52 (9)C22—C27—H27120.1
C12A—C12—H12119.7C26—C27—H27120.1
C11A—C12—H12119.7C25—C28—H28A109.5
C12—C12A—C6A118.79 (9)C25—C28—H28B109.5
C12—C12A—S13117.62 (7)H28A—C28—H28B109.5
C6A—C12A—S13123.58 (7)C25—C28—H28C109.5
C13A—S13—C12A102.57 (4)H28A—C28—H28C109.5
C14—C13A—C5A118.69 (8)H28B—C28—H28C109.5
C14—C13A—S13117.28 (7)C17—N18—S19117.64 (7)
C5A—C13A—S13124.04 (7)C17—N18—H18112.7 (9)
C13A—C14—C14A120.87 (9)S19—N18—H18109.9 (9)
C13A—C14—H14119.6
C14A—C1—C2—C30.77 (19)C6A—C12A—S13—C13A−4.78 (10)
C1—C2—C3—C4−0.06 (19)N5—C5A—C13A—C14−0.73 (14)
C2—C3—C4—C4A−1.26 (17)N6—C5A—C13A—C14178.87 (8)
C3—C4—C4A—N5−176.04 (10)N5—C5A—C13A—S13179.35 (7)
C3—C4—C4A—C14A1.85 (15)N6—C5A—C13A—S13−1.05 (13)
C4—C4A—N5—C5A179.42 (9)C12A—S13—C13A—C14−174.70 (8)
C14A—C4A—N5—C5A1.59 (14)C12A—S13—C13A—C5A5.22 (9)
C4A—N5—C5A—N6−179.91 (8)C5A—C13A—C14—C14A0.45 (14)
C4A—N5—C5A—C13A−0.29 (13)S13—C13A—C14—C14A−179.63 (7)
N5—C5A—N6—C6A174.38 (9)C13A—C14—C14A—C4A0.75 (14)
C13A—C5A—N6—C6A−5.24 (15)C13A—C14—C14A—C1−177.64 (10)
N5—C5A—N6—C15−3.43 (13)N5—C4A—C14A—C14−1.80 (14)
C13A—C5A—N6—C15176.96 (9)C4—C4A—C14A—C14−179.61 (9)
C5A—N6—C6A—N7−174.51 (9)N5—C4A—C14A—C1176.66 (9)
C15—N6—C6A—N73.32 (13)C4—C4A—C14A—C1−1.14 (14)
C5A—N6—C6A—C12A5.71 (15)C2—C1—C14A—C14178.19 (11)
C15—N6—C6A—C12A−176.46 (9)C2—C1—C14A—C4A−0.16 (16)
N6—C6A—N7—C7A178.97 (9)C5A—N6—C15—C16100.99 (10)
C12A—C6A—N7—C7A−1.25 (15)C6A—N6—C15—C16−76.99 (11)
C6A—N7—C7A—C11A1.42 (15)N6—C15—C16—C17−53.22 (11)
C6A—N7—C7A—C8−177.56 (10)C15—C16—C17—N18−68.56 (11)
N7—C7A—C8—C9178.05 (11)O20—S19—C22—C2713.31 (10)
C11A—C7A—C8—C9−0.96 (17)O21—S19—C22—C27143.85 (9)
C7A—C8—C9—C10−0.04 (19)N18—S19—C22—C27−101.35 (9)
C8—C9—C10—C111.32 (19)O20—S19—C22—C23−168.77 (8)
C9—C10—C11—C11A−1.55 (18)O21—S19—C22—C23−38.23 (10)
N7—C7A—C11A—C11−178.25 (10)N18—S19—C22—C2376.58 (9)
C8—C7A—C11A—C110.72 (15)C27—C22—C23—C240.85 (15)
N7—C7A—C11A—C120.08 (15)S19—C22—C23—C24−177.05 (8)
C8—C7A—C11A—C12179.05 (10)C22—C23—C24—C25−0.71 (16)
C10—C11—C11A—C7A0.53 (16)C23—C24—C25—C26−0.14 (17)
C10—C11—C11A—C12−177.68 (11)C23—C24—C25—C28−179.19 (10)
C7A—C11A—C12—C12A−1.76 (15)C24—C25—C26—C270.86 (16)
C11—C11A—C12—C12A176.50 (10)C28—C25—C26—C27179.91 (10)
C11A—C12—C12A—C6A1.94 (15)C23—C22—C27—C26−0.16 (16)
C11A—C12—C12A—S13−178.82 (8)S19—C22—C27—C26177.74 (8)
N7—C6A—C12A—C12−0.41 (15)C25—C26—C27—C22−0.72 (16)
N6—C6A—C12A—C12179.35 (9)C16—C17—N18—S19−167.83 (7)
N7—C6A—C12A—S13−179.61 (8)O20—S19—N18—C17−177.97 (7)
N6—C6A—C12A—S130.16 (14)O21—S19—N18—C1752.66 (8)
C12—C12A—S13—C13A176.02 (8)C22—S19—N18—C17−62.78 (8)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N18—H18···N50.876 (14)2.243 (15)2.9973 (12)144.1 (12)
C15—H15A···O20i0.992.333.1641 (12)141
C11—H11···O21ii0.952.553.3933 (13)149
C15—H15B···S13iii0.992.863.6912 (11)142
C17—H17B···O21iv0.992.473.3013 (13)141
Symmetry codes: (i) −x+1, −y+1, −z+2; (ii) x, y, z−1; (iii) −x+1, −y+1, −z+1; (iv) −x, −y+1, −z+2.

Experimental details

Crystal data
Chemical formulaC28H24N4O2S2
Mr512.63
Crystal system, space groupTriclinic, P1
Temperature (K)100
a, b, c (Å)9.3986 (3), 10.3793 (3), 12.6207 (3)
α, β, γ (°)80.735 (2), 81.959 (2), 77.999 (2)
V (Å3)1181.30 (6)
Z2
Radiation typeMo Kα
µ (mm−1)0.26
Crystal size (mm)0.39 × 0.34 × 0.23
Data collection
DiffractometerAgilent SuperNova Dual (Cu at zero, Eos)
diffractometer
Absorption correctionAnalytical
[CrysAlis PRO (Agilent, 2012) and Clark & Reid (1995)]
Tmin, Tmax0.937, 0.965
No. of measured, independent and
observed [I > 2σ(I)] reflections		24091, 7396, 6770
Rint0.015
(sin θ/λ)max (Å−1)0.725
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.033, 0.093, 1.04
No. of reflections7396
No. of parameters329
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å−3)0.42, −0.40

Computer programs: CrysAlis PRO (Agilent, 2012), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEPIII (Burnett & Johnson, 1996) and Mercury (Macrae et al., 2008), publCIF (Westrip, 2010).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N18—H18···N50.876 (14)2.243 (15)2.9973 (12)144.1 (12)
C15—H15A···O20i0.992.333.1641 (12)141
C11—H11···O21ii0.952.553.3933 (13)149
C15—H15B···S13iii0.992.863.6912 (11)142
C17—H17B···O21iv0.992.473.3013 (13)141
Symmetry codes: (i) −x+1, −y+1, −z+2; (ii) x, y, z−1; (iii) −x+1, −y+1, −z+1; (iv) −x, −y+1, −z+2.
 

Footnotes

†Part CXXXVII in the series of `Azinyl Sulfides'.

Acknowledgements

The work was supported by the Medical University of Silesia (grant KNW-1–006/P/2/0).

References

First citationAaron, J. J., Gaye Seye, M. D., Trajkovska, S. & Motohashi, N. (2009). Top. Heterocycl. Chem. 16, 153–231.  CrossRef CAS Google Scholar
 First citationAgilent (2012). CrysAlis PRO. Agilent Technologies, Yarnton, England.  Google Scholar
 First citationAnthony, J. E. (2006). Chem. Rev. 106, 5028–5048.  Web of Science CrossRef PubMed CAS Google Scholar
 First citationBurnett, M. N. & Johnson, C. K. (1996). ORTEPIII. Report ORNL-6895. Oak Ridge National Laboratory, Tennessee, USA.  Google Scholar
 First citationChu, S. S. C. (1988). Phenothiazines and 1,4-Benzothiazines – Chemical and Biological Aspects, edited by R. R. Gupta, pp. 475–526. Amsterdam: Elsevier.  Google Scholar
 First citationClark, R. C. & Reid, J. S. (1995). Acta Cryst. A51, 887–897.  CrossRef CAS Web of Science IUCr Journals Google Scholar
 First citationIsaia, F., Aragoni, M. C., Arca, M., Demartin, F., Devillanova, F. A., Ennas, G., Garau, A., Lippolis, V., Mancini, A. & Verani, G. (2009). Eur. J. Inorg. Chem. pp. 3667–3672.  Web of Science CSD CrossRef Google Scholar
 First citationJeleń, M. & Pluta, K. (2009). Heterocycles, 78, 2325–2336.  Google Scholar
 First citationMacrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466–470.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationNowak, M., Pluta, K. & Suwińska, K. (2002). New J. Chem. 26, 1216–1220.  Web of Science CSD CrossRef CAS Google Scholar
 First citationNowak, M., Pluta, K., Suwińska, K. & Straver, L. (2007). J. Heterocycl. Chem. 44, 543–550.  CrossRef CAS Google Scholar
 First citationPluta, K., Jeleń, M., Morak-Młodawska, B., Zimecki, M., Artym, J. & Kocięba, M. (2010). Pharmacol. Rep. 62, 319–332.  Web of Science CrossRef CAS PubMed Google Scholar
 First citationPluta, K., Morak-Młodawska, B. & Jeleń, M. (2009). J. Heterocycl. Chem. 46, 355–391.  Web of Science CrossRef CAS Google Scholar
 First citationPluta, K., Morak-Młodawska, B. & Jeleń, M. (2011). Eur. J. Med. Chem. 46, 3179–3189.  Web of Science CrossRef CAS PubMed Google Scholar
 First citationPluta, K., Nowak, M. & Suwińska, K. (2000). J. Chem. Crystallogr. 30, 479–482.  Web of Science CSD CrossRef CAS Google Scholar
 First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationWestrip, S. P. (2010). J. Appl. Cryst. 43, 920–925.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationYoshida, S., Kozawa, K., Sato, N. & Uchida, T. (1994). Bull. Chem. Soc. Jpn, 67, 2017–2023.  CrossRef CAS Web of Science Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 69| Part 6| June 2013| Pages o972-o973
doi:10.1107/S1600536813013950
Follow Acta Cryst. E
Sign up for e-alerts
E-alerts
Follow Acta Cryst. on Twitter
Twitter
Follow us on facebook
Facebook
Sign up for RSS feeds
RSS