organic compounds
4-[(E)-4-Methoxybenzylideneamino]-3-{1-[4-(2-methylpropyl)phenyl]ethyl}-1H-1,2,4-triazole-5(4H)-thione
aX-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia, and bDepartment of Studies in Chemistry, Mangalore University, Mangalagangotri, Mangalore 574 199, India
*Correspondence e-mail: hkfun@usm.my
In the title compound, C22H26N4OS, the benzene rings of the (2-methylpropyl)phenyl and 4-methoxyphenyl units form dihedral angles of 66.85 (3) and 25.96 (3)°, respectively, with the triazole ring. The dihedral angle between the two benzene rings is 87.42 (2)°. The –CH(CH3) linkage is disordered over two orientations with occupancies of 0.907 (3) and 0.093 (3). An intramolecular C—H⋯S hydrogen bond generates an S(6) ring motif. Intermolecular N—H⋯S hydrogen bonds and C—H⋯π interactions are observed.
Related literature
For the pharmaceutical applications of triazole compounds, see: Amir & Kumar (2007); Clemons et al. (2004); Demirbas & Ugurluoglu (2004); Demirbas et al. (2002); Johnston (2002); Shujuan et al. (2004). For bond-length data, see: Allen et al. (1987). For hydrogen-bond motifs, see: Bernstein et al. (1995). For the stability of the temperature controller used for the data collection, see: Cosier & Glazer (1986).
Experimental
Crystal data
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Refinement
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Data collection: APEX2 (Bruker, 2005); cell SAINT (Bruker, 2005); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009).
Supporting information
10.1107/S1600536809014949/ci2785sup1.cif
contains datablocks global, I. DOI:Structure factors: contains datablock I. DOI: 10.1107/S1600536809014949/ci2785Isup2.hkl
The title compound, a Schiff base, was obtained by refluxing a mixture of 4-amino-5-[1-(4-isobutylphenyl)ethyl]-4H-1,2,4-triazole-3-thiol (0.01 mol), 4-methylbenzaldehyde (0.01 mol) in ethanol (50 ml) and 3 drops of concentrated Sulfuric acid for 3 h. The solid product obtained was collected by filtration, washed with ethanol and dried. It was then recrystallized using ethanol. Single crystals suitable for X-ray analysis were obtained by slow evaporation of an ethanol-N,N-dimethyl formamide (DMF) (3:1) solution.
The CH(CH3) unit is disordered over two orientations with occupancies of 0.907 (3) and 0.093 (3). N-bound H atoms were located in a difference Fourier map and were refined freely. C-bound H atoms were positioned geometrically [C-H = 0.93–0.97 Å] and refined using a riding model, with Uiso(H) = 1.2Ueq(C) and 1.5Ueq(methyl C). A rotating-group model was used for methyl groups.
Data collection: APEX2 (Bruker, 2005); cell
SAINT (Bruker, 2005); data reduction: SAINT (Bruker, 2005); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).Fig. 1. The molecular structure of the title compound, showing 50% probability displacement ellipsoids and the atom-numbering scheme. Both disorder components are shown. The dashed line indicates a hydrogen bond. | |
Fig. 2. Part of the crystal packing of the title compound, viewed along the a axis. Hydrogen bonds are shown as dashed lines. Only the major disorder component is shown. |
C22H26N4OS | Z = 2 |
Mr = 394.53 | F(000) = 420 |
Triclinic, P1 | Dx = 1.259 Mg m−3 |
Hall symbol: -P 1 | Mo Kα radiation, λ = 0.71073 Å |
a = 7.9446 (1) Å | Cell parameters from 9938 reflections |
b = 11.1392 (2) Å | θ = 2.8–36.8° |
c = 12.3797 (2) Å | µ = 0.18 mm−1 |
α = 77.769 (1)° | T = 100 K |
β = 79.025 (1)° | Block, colourless |
γ = 80.063 (1)° | 0.50 × 0.27 × 0.13 mm |
V = 1041.08 (3) Å3 |
Bruker SMART APEXII CCD area-detector diffractometer | 9105 independent reflections |
Radiation source: fine-focus sealed tube | 7573 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.029 |
ϕ and ω scans | θmax = 35.0°, θmin = 1.9° |
Absorption correction: multi-scan (SADABS; Bruker, 2005) | h = −12→12 |
Tmin = 0.918, Tmax = 0.977 | k = −17→17 |
38166 measured reflections | l = −19→19 |
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.040 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.111 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.03 | w = 1/[σ2(Fo2) + (0.0555P)2 + 0.2526P] where P = (Fo2 + 2Fc2)/3 |
9105 reflections | (Δ/σ)max = 0.001 |
281 parameters | Δρmax = 0.65 e Å−3 |
0 restraints | Δρmin = −0.29 e Å−3 |
C22H26N4OS | γ = 80.063 (1)° |
Mr = 394.53 | V = 1041.08 (3) Å3 |
Triclinic, P1 | Z = 2 |
a = 7.9446 (1) Å | Mo Kα radiation |
b = 11.1392 (2) Å | µ = 0.18 mm−1 |
c = 12.3797 (2) Å | T = 100 K |
α = 77.769 (1)° | 0.50 × 0.27 × 0.13 mm |
β = 79.025 (1)° |
Bruker SMART APEXII CCD area-detector diffractometer | 9105 independent reflections |
Absorption correction: multi-scan (SADABS; Bruker, 2005) | 7573 reflections with I > 2σ(I) |
Tmin = 0.918, Tmax = 0.977 | Rint = 0.029 |
38166 measured reflections |
R[F2 > 2σ(F2)] = 0.040 | 0 restraints |
wR(F2) = 0.111 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.03 | Δρmax = 0.65 e Å−3 |
9105 reflections | Δρmin = −0.29 e Å−3 |
281 parameters |
Experimental. The crystal was placed in the cold stream of an Oxford Cyrosystems Cobra open-flow nitrogen cryostat (Cosier & Glazer, 1986) operating at 100.0 (1) K. |
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 | Occ. (<1) | |
S1 | 0.28546 (3) | 0.91565 (2) | 0.481988 (17) | 0.01833 (5) | |
O1 | 1.15746 (9) | 0.44217 (7) | 0.65279 (6) | 0.02374 (14) | |
N1 | 0.01719 (10) | 0.92699 (7) | 0.65460 (6) | 0.01744 (13) | |
N2 | −0.04031 (10) | 0.86893 (8) | 0.76193 (6) | 0.01929 (14) | |
N3 | 0.23009 (9) | 0.79552 (7) | 0.70327 (6) | 0.01442 (12) | |
N4 | 0.38158 (9) | 0.71119 (7) | 0.70940 (6) | 0.01542 (12) | |
C1 | 0.17881 (10) | 0.88191 (8) | 0.61363 (7) | 0.01473 (13) | |
C2 | 0.09098 (11) | 0.78783 (8) | 0.78932 (7) | 0.01672 (14) | |
C3 | 0.09472 (18) | 0.69214 (14) | 0.89541 (11) | 0.0151 (2) | 0.907 (3) |
H3A | 0.1528 | 0.6133 | 0.8746 | 0.018* | 0.907 (3) |
C14 | −0.09117 (14) | 0.67381 (11) | 0.95160 (9) | 0.0238 (3) | 0.907 (3) |
H14A | −0.1459 | 0.6413 | 0.9034 | 0.036* | 0.907 (3) |
H14B | −0.1551 | 0.7520 | 0.9651 | 0.036* | 0.907 (3) |
H14C | −0.0886 | 0.6167 | 1.0214 | 0.036* | 0.907 (3) |
C3A | 0.061 (2) | 0.7326 (14) | 0.9050 (13) | 0.021 (2) | 0.093 (3) |
H3AA | −0.0491 | 0.7717 | 0.9410 | 0.025* | 0.093 (3) |
C14A | 0.0488 (19) | 0.6028 (14) | 0.9039 (10) | 0.037 (4) | 0.093 (3) |
H14D | −0.0359 | 0.6001 | 0.8588 | 0.056* | 0.093 (3) |
H14E | 0.0149 | 0.5605 | 0.9790 | 0.056* | 0.093 (3) |
H14F | 0.1593 | 0.5630 | 0.8731 | 0.056* | 0.093 (3) |
C13 | 0.73078 (13) | 0.89352 (10) | 1.25067 (9) | 0.02513 (18) | |
H13A | 0.8040 | 0.9571 | 1.2222 | 0.038* | |
H13B | 0.8007 | 0.8137 | 1.2582 | 0.038* | |
H13C | 0.6668 | 0.9055 | 1.3225 | 0.038* | |
C4 | 0.19848 (11) | 0.72643 (8) | 0.97397 (7) | 0.01640 (14) | |
C5 | 0.13401 (11) | 0.81940 (9) | 1.03721 (7) | 0.01883 (15) | |
H5A | 0.0272 | 0.8665 | 1.0283 | 0.023* | |
C6 | 0.22794 (12) | 0.84237 (9) | 1.11351 (7) | 0.01903 (15) | |
H6A | 0.1821 | 0.9037 | 1.1556 | 0.023* | |
C7 | 0.39036 (11) | 0.77416 (8) | 1.12736 (7) | 0.01561 (14) | |
C8 | 0.45494 (11) | 0.68414 (8) | 1.06158 (7) | 0.01569 (14) | |
H8A | 0.5638 | 0.6392 | 1.0679 | 0.019* | |
C9 | 0.36033 (11) | 0.65989 (8) | 0.98659 (7) | 0.01643 (14) | |
H9A | 0.4061 | 0.5984 | 0.9445 | 0.020* | |
C10 | 0.49455 (13) | 0.79371 (8) | 1.21069 (7) | 0.01946 (16) | |
H10A | 0.5707 | 0.7175 | 1.2312 | 0.023* | |
H10B | 0.4157 | 0.8096 | 1.2778 | 0.023* | |
C11 | 0.60476 (11) | 0.90032 (8) | 1.16960 (7) | 0.01771 (15) | |
H11A | 0.6727 | 0.8897 | 1.0966 | 0.021* | |
C12 | 0.49358 (13) | 1.02704 (9) | 1.15505 (8) | 0.02153 (16) | |
H12A | 0.5671 | 1.0909 | 1.1330 | 0.032* | |
H12B | 0.4201 | 1.0371 | 1.2246 | 0.032* | |
H12C | 0.4236 | 1.0329 | 1.0984 | 0.032* | |
C15 | 0.52183 (11) | 0.75344 (8) | 0.65702 (7) | 0.01516 (14) | |
H15A | 0.5176 | 0.8354 | 0.6196 | 0.018* | |
C16 | 0.68701 (10) | 0.67289 (8) | 0.65650 (7) | 0.01452 (13) | |
C17 | 0.70399 (11) | 0.55401 (8) | 0.72377 (7) | 0.01873 (15) | |
H17A | 0.6074 | 0.5249 | 0.7704 | 0.022* | |
C18 | 0.86260 (12) | 0.48024 (9) | 0.72112 (8) | 0.02101 (16) | |
H18A | 0.8731 | 0.4024 | 0.7669 | 0.025* | |
C19 | 1.00817 (11) | 0.52267 (8) | 0.64930 (7) | 0.01772 (15) | |
C20 | 0.99354 (11) | 0.63973 (8) | 0.58088 (7) | 0.01699 (14) | |
H20A | 1.0895 | 0.6678 | 0.5327 | 0.020* | |
C21 | 0.83293 (11) | 0.71389 (8) | 0.58586 (7) | 0.01655 (14) | |
H21A | 0.8229 | 0.7924 | 0.5411 | 0.020* | |
C22 | 1.30675 (12) | 0.47650 (9) | 0.57506 (8) | 0.02174 (16) | |
H22A | 1.3986 | 0.4081 | 0.5787 | 0.033* | |
H22B | 1.3432 | 0.5464 | 0.5936 | 0.033* | |
H22C | 1.2787 | 0.4981 | 0.5007 | 0.033* | |
H1N1 | −0.0570 (19) | 0.9791 (14) | 0.6181 (12) | 0.032 (4)* |
U11 | U22 | U33 | U12 | U13 | U23 | |
S1 | 0.01509 (9) | 0.02322 (11) | 0.01447 (9) | 0.00021 (7) | −0.00279 (6) | −0.00051 (7) |
O1 | 0.0149 (3) | 0.0231 (3) | 0.0274 (3) | 0.0035 (2) | −0.0003 (2) | 0.0004 (3) |
N1 | 0.0139 (3) | 0.0221 (3) | 0.0159 (3) | 0.0014 (3) | −0.0040 (2) | −0.0045 (2) |
N2 | 0.0143 (3) | 0.0277 (4) | 0.0161 (3) | −0.0012 (3) | −0.0027 (2) | −0.0057 (3) |
N3 | 0.0122 (3) | 0.0167 (3) | 0.0142 (3) | −0.0006 (2) | −0.0029 (2) | −0.0028 (2) |
N4 | 0.0137 (3) | 0.0163 (3) | 0.0160 (3) | 0.0004 (2) | −0.0041 (2) | −0.0028 (2) |
C1 | 0.0137 (3) | 0.0164 (3) | 0.0148 (3) | −0.0007 (3) | −0.0043 (2) | −0.0037 (3) |
C2 | 0.0133 (3) | 0.0229 (4) | 0.0148 (3) | −0.0038 (3) | −0.0024 (2) | −0.0041 (3) |
C3 | 0.0142 (5) | 0.0172 (6) | 0.0143 (4) | −0.0034 (4) | −0.0019 (3) | −0.0028 (4) |
C14 | 0.0181 (4) | 0.0339 (6) | 0.0210 (4) | −0.0111 (4) | −0.0002 (3) | −0.0054 (4) |
C3A | 0.018 (6) | 0.017 (6) | 0.026 (6) | −0.002 (5) | −0.008 (4) | 0.002 (5) |
C14A | 0.044 (8) | 0.047 (8) | 0.025 (5) | −0.025 (6) | −0.012 (5) | 0.003 (5) |
C13 | 0.0234 (4) | 0.0274 (5) | 0.0288 (4) | −0.0026 (4) | −0.0101 (4) | −0.0098 (4) |
C4 | 0.0156 (3) | 0.0199 (4) | 0.0137 (3) | −0.0054 (3) | −0.0023 (3) | −0.0007 (3) |
C5 | 0.0148 (3) | 0.0208 (4) | 0.0198 (4) | −0.0007 (3) | −0.0028 (3) | −0.0029 (3) |
C6 | 0.0184 (4) | 0.0192 (4) | 0.0192 (3) | −0.0010 (3) | −0.0015 (3) | −0.0056 (3) |
C7 | 0.0182 (3) | 0.0152 (3) | 0.0134 (3) | −0.0034 (3) | −0.0030 (3) | −0.0012 (2) |
C8 | 0.0152 (3) | 0.0154 (3) | 0.0163 (3) | −0.0019 (3) | −0.0035 (3) | −0.0020 (3) |
C9 | 0.0173 (3) | 0.0169 (3) | 0.0155 (3) | −0.0033 (3) | −0.0018 (3) | −0.0038 (3) |
C10 | 0.0255 (4) | 0.0182 (4) | 0.0164 (3) | −0.0046 (3) | −0.0076 (3) | −0.0019 (3) |
C11 | 0.0176 (4) | 0.0198 (4) | 0.0170 (3) | −0.0031 (3) | −0.0031 (3) | −0.0057 (3) |
C12 | 0.0224 (4) | 0.0187 (4) | 0.0234 (4) | −0.0041 (3) | −0.0035 (3) | −0.0028 (3) |
C15 | 0.0154 (3) | 0.0146 (3) | 0.0162 (3) | −0.0009 (3) | −0.0050 (3) | −0.0032 (3) |
C16 | 0.0137 (3) | 0.0147 (3) | 0.0153 (3) | −0.0011 (3) | −0.0032 (2) | −0.0027 (2) |
C17 | 0.0154 (3) | 0.0185 (4) | 0.0188 (3) | −0.0009 (3) | −0.0010 (3) | 0.0015 (3) |
C18 | 0.0173 (4) | 0.0188 (4) | 0.0220 (4) | 0.0000 (3) | −0.0008 (3) | 0.0031 (3) |
C19 | 0.0148 (3) | 0.0176 (4) | 0.0194 (3) | 0.0000 (3) | −0.0025 (3) | −0.0025 (3) |
C20 | 0.0146 (3) | 0.0163 (3) | 0.0196 (3) | −0.0032 (3) | −0.0013 (3) | −0.0027 (3) |
C21 | 0.0164 (3) | 0.0142 (3) | 0.0187 (3) | −0.0027 (3) | −0.0030 (3) | −0.0018 (3) |
C22 | 0.0152 (4) | 0.0257 (4) | 0.0237 (4) | 0.0000 (3) | −0.0010 (3) | −0.0072 (3) |
S1—C1 | 1.6852 (8) | C5—H5A | 0.93 |
O1—C19 | 1.3597 (11) | C6—C7 | 1.4009 (12) |
O1—C22 | 1.4300 (11) | C6—H6A | 0.93 |
N1—C1 | 1.3399 (11) | C7—C8 | 1.3932 (12) |
N1—N2 | 1.3781 (11) | C7—C10 | 1.5098 (12) |
N1—H1N1 | 0.872 (15) | C8—C9 | 1.3935 (11) |
N2—C2 | 1.3033 (12) | C8—H8A | 0.93 |
N3—C1 | 1.3813 (10) | C9—H9A | 0.93 |
N3—C2 | 1.3818 (11) | C10—C11 | 1.5392 (12) |
N3—N4 | 1.3968 (10) | C10—H10A | 0.97 |
N4—C15 | 1.2885 (11) | C10—H10B | 0.97 |
C2—C3A | 1.425 (15) | C11—C12 | 1.5257 (13) |
C2—C3 | 1.5075 (16) | C11—H11A | 0.98 |
C3—C4 | 1.5307 (15) | C12—H12A | 0.96 |
C3—C14 | 1.5360 (17) | C12—H12B | 0.96 |
C3—H3A | 0.98 | C12—H12C | 0.96 |
C14—H14A | 0.96 | C15—C16 | 1.4561 (12) |
C14—H14B | 0.96 | C15—H15A | 0.93 |
C14—H14C | 0.96 | C16—C21 | 1.3945 (11) |
C3A—C14A | 1.47 (2) | C16—C17 | 1.4068 (12) |
C3A—C4 | 1.492 (14) | C17—C18 | 1.3793 (12) |
C3A—H3AA | 0.98 | C17—H17A | 0.93 |
C14A—H14D | 0.96 | C18—C19 | 1.4038 (12) |
C14A—H14E | 0.96 | C18—H18A | 0.93 |
C14A—H14F | 0.96 | C19—C20 | 1.3958 (12) |
C13—C11 | 1.5295 (13) | C20—C21 | 1.3935 (12) |
C13—H13A | 0.96 | C20—H20A | 0.930 |
C13—H13B | 0.96 | C21—H21A | 0.93 |
C13—H13C | 0.96 | C22—H22A | 0.96 |
C4—C9 | 1.3876 (12) | C22—H22B | 0.96 |
C4—C5 | 1.3983 (13) | C22—H22C | 0.96 |
C5—C6 | 1.3968 (12) | ||
C19—O1—C22 | 117.43 (7) | C8—C7—C10 | 119.69 (8) |
C1—N1—N2 | 113.71 (7) | C6—C7—C10 | 122.67 (8) |
C1—N1—H1N1 | 127.2 (10) | C7—C8—C9 | 121.59 (8) |
N2—N1—H1N1 | 118.4 (10) | C7—C8—H8A | 119.2 |
C2—N2—N1 | 104.40 (7) | C9—C8—H8A | 119.2 |
C1—N3—C2 | 108.44 (7) | C4—C9—C8 | 120.72 (8) |
C1—N3—N4 | 129.86 (7) | C4—C9—H9A | 119.6 |
C2—N3—N4 | 120.95 (7) | C8—C9—H9A | 119.6 |
C15—N4—N3 | 115.36 (7) | C7—C10—C11 | 115.19 (7) |
N1—C1—N3 | 102.87 (7) | C7—C10—H10A | 108.5 |
N1—C1—S1 | 127.94 (7) | C11—C10—H10A | 108.5 |
N3—C1—S1 | 129.04 (6) | C7—C10—H10B | 108.5 |
N2—C2—N3 | 110.38 (7) | C11—C10—H10B | 108.5 |
N2—C2—C3A | 111.2 (7) | H10A—C10—H10B | 107.5 |
N3—C2—C3A | 137.2 (6) | C12—C11—C13 | 110.49 (7) |
N2—C2—C3 | 126.82 (9) | C12—C11—C10 | 112.14 (7) |
N3—C2—C3 | 122.71 (9) | C13—C11—C10 | 109.89 (7) |
C2—C3—C4 | 111.44 (10) | C12—C11—H11A | 108.1 |
C2—C3—C14 | 109.65 (11) | C13—C11—H11A | 108.1 |
C4—C3—C14 | 112.38 (9) | C10—C11—H11A | 108.1 |
C2—C3—H3A | 107.7 | C11—C12—H12A | 109.5 |
C4—C3—H3A | 107.7 | C11—C12—H12B | 109.5 |
C14—C3—H3A | 107.7 | H12A—C12—H12B | 109.5 |
C2—C3A—C14A | 103.8 (12) | C11—C12—H12C | 109.5 |
C2—C3A—C4 | 118.7 (10) | H12A—C12—H12C | 109.5 |
C14A—C3A—C4 | 105.1 (10) | H12B—C12—H12C | 109.5 |
C2—C3A—H3AA | 109.6 | N4—C15—C16 | 119.97 (7) |
C14A—C3A—H3AA | 109.6 | N4—C15—H15A | 120.0 |
C4—C3A—H3AA | 109.6 | C16—C15—H15A | 120.0 |
C3A—C14A—H14D | 109.5 | C21—C16—C17 | 118.75 (8) |
C3A—C14A—H14E | 109.5 | C21—C16—C15 | 119.08 (7) |
H14D—C14A—H14E | 109.5 | C17—C16—C15 | 122.16 (7) |
C3A—C14A—H14F | 109.5 | C18—C17—C16 | 120.57 (8) |
H14D—C14A—H14F | 109.5 | C18—C17—H17A | 119.7 |
H14E—C14A—H14F | 109.5 | C16—C17—H17A | 119.7 |
C11—C13—H13A | 109.5 | C17—C18—C19 | 119.99 (8) |
C11—C13—H13B | 109.5 | C17—C18—H18A | 120.0 |
H13A—C13—H13B | 109.5 | C19—C18—H18A | 120.0 |
C11—C13—H13C | 109.5 | O1—C19—C20 | 124.62 (8) |
H13A—C13—H13C | 109.5 | O1—C19—C18 | 115.08 (8) |
H13B—C13—H13C | 109.5 | C20—C19—C18 | 120.30 (8) |
C9—C4—C5 | 118.33 (8) | C21—C20—C19 | 118.99 (8) |
C9—C4—C3A | 137.9 (7) | C21—C20—H20A | 120.5 |
C5—C4—C3A | 103.8 (7) | C19—C20—H20A | 120.5 |
C9—C4—C3 | 119.03 (9) | C20—C21—C16 | 121.39 (8) |
C5—C4—C3 | 122.60 (9) | C20—C21—H21A | 119.3 |
C6—C5—C4 | 120.85 (8) | C16—C21—H21A | 119.3 |
C6—C5—H5A | 119.6 | O1—C22—H22A | 109.5 |
C4—C5—H5A | 119.6 | O1—C22—H22B | 109.5 |
C5—C6—C7 | 120.84 (8) | H22A—C22—H22B | 109.5 |
C5—C6—H6A | 119.6 | O1—C22—H22C | 109.5 |
C7—C6—H6A | 119.6 | H22A—C22—H22C | 109.5 |
C8—C7—C6 | 117.63 (8) | H22B—C22—H22C | 109.5 |
C1—N1—N2—C2 | 1.66 (10) | C14—C3—C4—C9 | 129.28 (11) |
C1—N3—N4—C15 | 41.04 (12) | C2—C3—C4—C5 | 75.33 (12) |
C2—N3—N4—C15 | −150.12 (8) | C14—C3—C4—C5 | −48.21 (15) |
N2—N1—C1—N3 | −3.89 (9) | C2—C3—C4—C3A | 62.7 (18) |
N2—N1—C1—S1 | 171.98 (6) | C14—C3—C4—C3A | −60.8 (18) |
C2—N3—C1—N1 | 4.54 (9) | C9—C4—C5—C6 | −1.79 (13) |
N4—N3—C1—N1 | 174.46 (8) | C3A—C4—C5—C6 | 179.9 (6) |
C2—N3—C1—S1 | −171.28 (7) | C3—C4—C5—C6 | 175.71 (9) |
N4—N3—C1—S1 | −1.35 (13) | C4—C5—C6—C7 | 1.00 (13) |
N1—N2—C2—N3 | 1.41 (9) | C5—C6—C7—C8 | 0.72 (12) |
N1—N2—C2—C3A | 171.1 (7) | C5—C6—C7—C10 | −178.53 (8) |
N1—N2—C2—C3 | −175.19 (9) | C6—C7—C8—C9 | −1.67 (12) |
C1—N3—C2—N2 | −3.89 (10) | C10—C7—C8—C9 | 177.61 (8) |
N4—N3—C2—N2 | −174.88 (7) | C5—C4—C9—C8 | 0.86 (12) |
C1—N3—C2—C3A | −169.6 (10) | C3A—C4—C9—C8 | 178.3 (8) |
N4—N3—C2—C3A | 19.4 (10) | C3—C4—C9—C8 | −176.73 (9) |
C1—N3—C2—C3 | 172.88 (9) | C7—C8—C9—C4 | 0.89 (12) |
N4—N3—C2—C3 | 1.89 (13) | C8—C7—C10—C11 | 96.95 (10) |
N2—C2—C3—C4 | −107.03 (11) | C6—C7—C10—C11 | −83.81 (11) |
N3—C2—C3—C4 | 76.76 (13) | C7—C10—C11—C12 | 68.35 (10) |
C3A—C2—C3—C4 | −65.9 (18) | C7—C10—C11—C13 | −168.35 (8) |
N2—C2—C3—C14 | 18.05 (15) | N3—N4—C15—C16 | −179.10 (7) |
N3—C2—C3—C14 | −158.17 (9) | N4—C15—C16—C21 | 170.31 (8) |
C3A—C2—C3—C14 | 59.2 (18) | N4—C15—C16—C17 | −8.71 (12) |
N2—C2—C3A—C14A | 113.0 (10) | C21—C16—C17—C18 | 0.99 (13) |
N3—C2—C3A—C14A | −81.3 (12) | C15—C16—C17—C18 | −179.99 (8) |
C3—C2—C3A—C14A | −32.6 (14) | C16—C17—C18—C19 | −1.21 (14) |
N2—C2—C3A—C4 | −130.8 (10) | C22—O1—C19—C20 | −4.71 (13) |
N3—C2—C3A—C4 | 34.9 (18) | C22—O1—C19—C18 | 175.19 (8) |
C3—C2—C3A—C4 | 83.6 (19) | C17—C18—C19—O1 | −179.50 (8) |
C2—C3A—C4—C9 | −73.2 (14) | C17—C18—C19—C20 | 0.41 (14) |
C14A—C3A—C4—C9 | 42.3 (15) | O1—C19—C20—C21 | −179.51 (8) |
C2—C3A—C4—C5 | 104.5 (11) | C18—C19—C20—C21 | 0.59 (13) |
C14A—C3A—C4—C5 | −140.0 (10) | C19—C20—C21—C16 | −0.81 (13) |
C2—C3A—C4—C3 | −86 (2) | C17—C16—C21—C20 | 0.03 (13) |
C14A—C3A—C4—C3 | 29.1 (12) | C15—C16—C21—C20 | −179.02 (8) |
C2—C3—C4—C9 | −107.18 (11) |
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1N1···S1i | 0.87 (2) | 2.39 (2) | 3.2482 (8) | 168 (1) |
C15—H15A···S1 | 0.93 | 2.66 | 3.1947 (9) | 117 |
C13—H13A···Cg1ii | 0.96 | 2.77 | 3.5416 (12) | 138 |
C12—H12A···Cg2ii | 0.96 | 2.73 | 3.5417 (11) | 142 |
C18—H18A···Cg2iii | 0.93 | 2.80 | 3.5903 (10) | 144 |
C22—H22C···Cg3iv | 0.96 | 2.78 | 3.5783 (10) | 142 |
C14A—H14D···Cg3v | 0.96 | 2.88 | 3.769 (13) | 155 |
Symmetry codes: (i) −x, −y+2, −z+1; (ii) −x+1, −y+2, −z+2; (iii) −x+1, −y+1, −z+2; (iv) −x+2, −y+1, −z+1; (v) x−1, y, z. |
Experimental details
Crystal data | |
Chemical formula | C22H26N4OS |
Mr | 394.53 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 100 |
a, b, c (Å) | 7.9446 (1), 11.1392 (2), 12.3797 (2) |
α, β, γ (°) | 77.769 (1), 79.025 (1), 80.063 (1) |
V (Å3) | 1041.08 (3) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.18 |
Crystal size (mm) | 0.50 × 0.27 × 0.13 |
Data collection | |
Diffractometer | Bruker SMART APEXII CCD area-detector diffractometer |
Absorption correction | Multi-scan (SADABS; Bruker, 2005) |
Tmin, Tmax | 0.918, 0.977 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 38166, 9105, 7573 |
Rint | 0.029 |
(sin θ/λ)max (Å−1) | 0.807 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.040, 0.111, 1.03 |
No. of reflections | 9105 |
No. of parameters | 281 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.65, −0.29 |
Computer programs: APEX2 (Bruker, 2005), SAINT (Bruker, 2005), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1N1···S1i | 0.87 (2) | 2.39 (2) | 3.2482 (8) | 168 (1) |
C15—H15A···S1 | 0.93 | 2.66 | 3.1947 (9) | 117 |
C13—H13A···Cg1ii | 0.96 | 2.77 | 3.5416 (12) | 138 |
C12—H12A···Cg2ii | 0.96 | 2.73 | 3.5417 (11) | 142 |
C18—H18A···Cg2iii | 0.93 | 2.80 | 3.5903 (10) | 144 |
C22—H22C···Cg3iv | 0.96 | 2.78 | 3.5783 (10) | 142 |
C14A—H14D···Cg3v | 0.96 | 2.88 | 3.769 (13) | 155 |
Symmetry codes: (i) −x, −y+2, −z+1; (ii) −x+1, −y+2, −z+2; (iii) −x+1, −y+1, −z+2; (iv) −x+2, −y+1, −z+1; (v) x−1, y, z. |
Acknowledgements
HKF and SRJ thank the Malaysian Government and Universiti Sains Malaysia for the Science Fund grant No. 305/PFIZIK/613312. SRJ thanks Universiti Sains Malaysia for a post-doctoral research fellowship. HKF also thanks Universiti Sains Malaysia for the Research University Golden Goose grant No.1001/PFIZIK/811012.
References
Allen, F. H., Kennard, O., Watson, D. G., Brammer, L., Orpen, A. G. & Taylor, R. (1987). J. Chem. Soc. Perkin Trans. 2, pp. S1–19. CrossRef Web of Science Google Scholar
Amir, M. & Kumar, S. (2007). Acta Pharm. 57, 31–45. CrossRef PubMed CAS Google Scholar
Bernstein, J., Davis, R. E., Shimoni, L. & Chang, N.-L. (1995). Angew. Chem. Int. Ed. Engl. 34, 1555–1573. CrossRef CAS Web of Science Google Scholar
Bruker (2005). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
Clemons, M., Coleman, R. E. & Verma, S. (2004). Cancer Treat. Rev. 30, 325–332. Web of Science CrossRef PubMed CAS Google Scholar
Cosier, J. & Glazer, A. M. (1986). J. Appl. Cryst. 19, 105–107. CrossRef CAS Web of Science IUCr Journals Google Scholar
Demirbas, N. & Ugurluoglu, R. (2004). Turk. J. Chem. 28, 679–690. CAS Google Scholar
Demirbas, N., Ugurluoglu, R. & Demirbasx, A. (2002). Bioorg. Med. Chem. 10, 3717–3723. Web of Science CrossRef PubMed CAS Google Scholar
Johnston, G. A. R. (2002). Curr. Top. Med. Chem. 2, 903–913. CrossRef PubMed CAS Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Shujuan, S., Hongxiang, L., Gao, Y., Fan, P., Ma, B., Ge, W. & Wang, X. (2004). J. Pharm. Biomed. Anal. 34, 1117–1124. Web of Science PubMed Google Scholar
Spek, A. L. (2009). Acta Cryst. D65, 148–155. Web of Science CrossRef CAS IUCr Journals 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.
Several compounds containing 1,2,4-triazole rings are well known as drugs. For example, fluconazole is used as an antimicrobial drug (Shujuan et al., 2004), while vorozole, letrozole and anastrozole are non-steroidal drugs used for the treatment of cancer (Clemons et al., 2004) and loreclezole is used as an anticonvulsant (Johnston 2002) agent. 1,2,4-Triazoles and their derivatives represent an overwhelming and rapidly developing field in modern heterocyclic chemistry. Similarly, ibuprofen belongs to the class of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) with antipyretic, anti-inflammatory and analgesic properties (Amir & Kumar, 2007). Schiff base derivatives of acetic acid hydrazides containing 1,2,4-triazol-5-one ring have displayed antitumor activity against breast cancer, while 2-phenyl ethylidenamino and 2-phenyl ethylamino derivatives of 4-amino-1,2,4-triazol-5-ones have been found to be effective towards non-small cell lung cancer, CNC and breast cancer (Demirbas et al., 2002, 2004). Due to the progress that occurs in dealing with the chemistry of substituted 4-amino-1,2,4-triazole-3-thiones and their derivatives as well as their biological activities, we synthesized the title compound and herein report its crystal structure.
Bond lengths in the title molecule (Fig. 1) are found to have normal values (Allen et al., 1987). The triazole ring is planar to within ±0.024 (1) Å. The dihedral angle formed by the triazole (N1/N2/C2/N3/C1) ring with the C4-C9 and C16-C21 benzene rings are 66.85 (3)° and 25.96 (3)°, respectively. The dihedral angle between the two benzene rings of 87.42 (2)°, indicates that these rings are oriented almost perpendicular to each other. An intramolecular C—H···S hydrogen bond generates an S(6) ring motif (Bernstein et al., 1995).
The crystal packing is stabilized by intermolecular N—H···S hydrogen bonding together with weak C—H···π interactions (Table 1) (Fig 2).