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 5| May 2013| Page o728
https://doi.org/10.1107/S1600536813009859

4-Amino-3-(3-meth­­oxy­benz­yl)-1H-1,2,4-triazole-5(4H)-thione

B. K. Sarojini,a P. S. Manjula,a Gurumurthy Hegde,b Dalbir Kour,c Sumati Anthal,c Vivek K. Guptac and Rajni Kantc*

aDepartment of Chemistry, P A College of Engineering, Nadupadavu 574 153, D.K. Mangalore, India, bFaculty of Industrial Science and Technology, University Malaysia Pahang, LebuhrayaTunRazak, 26300 Gambang, Kuantan, Pahang Darul Makmur, Malaysia, and cX-ray Crystallography Laboratory, Post-Graduate Department of Physics & Electronics, University of Jammu, Jammu Tawi 180 006, India
*Correspondence e-mail: rkvk.paper11@gmail.com

(Received 4 April 2013; accepted 10 April 2013; online 13 April 2013)

In the title mol­ecule, C10H12N4SO, the triazole ring forms a dihedral angle of 73.0 (5)° with the benzene ring. The meth­oxy group is approximtely coplanar with the benzene ring with a C C—O—Cmeth­yl torsion angle of 4.7 (3)°. In the crystal, N—H⋯S hydrogen bonds connect pairs of inversion-related mol­ecules, which are in turn connected by N—H⋯N hydrogen bonds into chains of rings along [010]. Weak C—H⋯O hydrogen bonds connect these chains into a two-dimensional network parallel to (-102).

Related literature

For background to the chemistry of triazoles, see: Holla et al. (2001[Holla, B. S., Sarojini, B. K., Rao, B. S., Akberali, P. M. & Suchetha Kumari, N. (2001). Il Farmaco, 56, 565-570.], 2006[Holla, B. S., Rao, B. S., Sarojini, B. K., Akberali, P. M. & Suchetha Kumari, N. (2006). Euro. J. Med. Chem. 41, 657-663.]). For the biological activity of 1,2,4-triazole derivatives, see: Cansiz et al. (2001[Cansiz, A., Servi, S., Koparir, M., Altintas, M. & Digrak, M. (2001). J. Chem. Soc. Pak. 23, 237-239.]); Jones et al. (1965[Jones, D. H., Slack, R., Squires, S. & Wooldridge, K. R. H. (1965). J. Med. Chem. 8, 676-680.]); Kane et al. (1988[Kane, J. M., Dudley, M. W., Sorensen, S. M. & Miller, F. P. (1988). J. Med. Chem. 31, 1253-1258.]); Mullican et al. (1993[Mullican, M. D., Wilson, M. W., Connor, D. T., Kostlan, C. R., Schrier, D. J. & Dyer, R. D. (1993). J. Med. Chem. 36, 1090-1099.]). For related structures, see: Chen et al. (2007[Chen, X.-A., Huang, X.-B. & Wu, H.-Y. (2007). Acta Cryst. E63, o3191.]); Gao et al. (2011[Gao, Y., Zhang, L. & Wang, H. (2011). Acta Cryst. E67, o1794.]); Karczmarzyk et al. (2012[Karczmarzyk, Z., Pitucha, M., Wysocki, W., Fruziński, A. & Olender, E. (2012). Acta Cryst. E68, o3264-o3265.]). For standard bond-length data, see: Allen et al. (1987[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.]).

[Scheme 1]

Experimental

Crystal data

  • C10H12N4OS

  • Mr = 236.30

  • Monoclinic, P 21 /n

  • a = 7.4580 (3) Å

  • b = 5.8006 (2) Å

  • c = 25.2817 (10) Å

  • β = 94.513 (4)°

  • V = 1090.32 (7) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 0.28 mm−1

  • T = 293 K

  • 0.3 × 0.2 × 0.1 mm
Data collection

  • Oxford Diffraction Xcalibur Sapphire3 diffractometer

  • Absorption correction: multi-scan (CrysAlis PRO; Oxford Diffraction, 2010[Oxford Diffraction (2010). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, England.]) Tmin = 0.946, Tmax = 1.000

  • 15190 measured reflections

  • 2130 independent reflections

  • 1748 reflections with I > 2σ(I)

  • Rint = 0.042
Refinement

  • R[F2 > 2σ(F2)] = 0.036

  • wR(F2) = 0.088

  • S = 1.03

  • 2130 reflections

  • 154 parameters

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

  • Δρmax = 0.19 e Å−3

  • Δρmin = −0.24 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
C7—H7A⋯O1i 0.97 2.46 3.308 (2) 146
N6—H62⋯N1ii 0.90 (2) 2.30 (2) 3.190 (2) 174
N2—H2⋯S1iii 0.86 2.60 3.377 (1) 151
Symmetry codes: (i) [-x+{\script{1\over 2}}, y+{\script{1\over 2}}, -z+{\script{3\over 2}}]; (ii) x, y+1, z; (iii) -x+2, -y+2, -z+2.

Data collection: CrysAlis PRO (Oxford Diffraction, 2010[Oxford Diffraction (2010). CrysAlis PRO. Oxford Diffraction Ltd, 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: PLATON (Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.]); software used to prepare material for publication: PLATON.

Supporting information

Crystal structure: contains datablocks I, global. DOI: https://doi.org/10.1107/S1600536813009859/lh5605sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536813009859/lh5605Isup2.hkl

Supporting information file. DOI: https://doi.org/10.1107/S1600536813009859/lh5605Isup3.cml

checkCIF report


Comment top

The chemistry of triazoles has received considerable attention in recent years because of their versatility in the synthesis of many other heterocyclic compounds. 1,2,4-Triazole derivatives are well known for their different biological activities, therefore various 1,2,4-triazole derivatives and their N-bridged heterocyclic analogs have been extensively studied (Holla et al., 2001; 2006). The derivatives of 1,2,4-triazole are known to exhibit anti-inflammatory (Mullican et al., 1993), antiviral (Jones et al., 1965), antimicrobial (Cansiz et al., 2001), and antidepressant activity (Kane et al., 1988). Hence, synthesis of the corresponding heterocyclic compounds could be of interest from the viewpoint of chemical reactivity and biological activity. In the title compound (Fig. 1), the bond lengths and angles have normal values (Allen et al., 1987) and are comparable with closely related structures (Chen et al., 2007; Karczmarzyk et al., 2012; Gao et al., 2011). The angles around atom C3 in the triazole ring deviate from the normal angles based on Csp2 hybridization, giving bond angles of 102.72 (14)° and 130.12 (13)° for N2—C3—N4 and N2—C3—S1, respectively. The dihedral angle between the triazole ring (N1/N2/C3/N4/C5) and the benzene ring (C8—C13) is 73.0 (5)°. In the crystal, N—H···S hydrogen bonds connect pairs of inversion related molecules, which are in turn connected by N—H···N hydrogen bonds into chains of rings along [010]. In addition, weak C—H···O hydrogen bonds connect these chains into a two-dimensional network parallel to (102) (Fig. 2).

Related literature top

For background to the chemistry of triazoles, see: Holla et al. (2001, 2006). For the biological activity of 1,2,4-triazole derivatives, see: Cansiz et al. (2001); Jones et al. (1965); Kane et al. (1988); Mullican et al. (1993). For related structures, see: Chen et al. (2007); Gao et al. (2011); Karczmarzyk et al. (2012). For standard bond-length data, see: Allen et al. (1987).

Experimental top

A well triturated mixture of 3-methoxyphenylacetic acid (0.83 g.0.05 mol) and thiocarbohydrazide (0.53 g. 0.05 mol) was fused in a round bottom flask for one hour on a oil bath at 413 K. It was cooled to room temperature and washed with sodium bicarbonate (5%) solution to remove unreacted acid and again washed with water. The dried compound was recrystallized from methanol to yield single crystals (mp. 417–419 K).

Refinement top

Atoms H61 and H62 attached to N6 were located in a difference map and refined isotropically. The remaining H atoms were positioned geometrically and were treated as riding on their parent C/N atoms, with C—H distances of 0.93–0.96 Å and N—H distance of 0.86 Å with Uiso(H) = 1.2Ueq(C/N) or Uiso(H) = 1.5Ueq(Cmethyl).

Structure description top

The chemistry of triazoles has received considerable attention in recent years because of their versatility in the synthesis of many other heterocyclic compounds. 1,2,4-Triazole derivatives are well known for their different biological activities, therefore various 1,2,4-triazole derivatives and their N-bridged heterocyclic analogs have been extensively studied (Holla et al., 2001; 2006). The derivatives of 1,2,4-triazole are known to exhibit anti-inflammatory (Mullican et al., 1993), antiviral (Jones et al., 1965), antimicrobial (Cansiz et al., 2001), and antidepressant activity (Kane et al., 1988). Hence, synthesis of the corresponding heterocyclic compounds could be of interest from the viewpoint of chemical reactivity and biological activity. In the title compound (Fig. 1), the bond lengths and angles have normal values (Allen et al., 1987) and are comparable with closely related structures (Chen et al., 2007; Karczmarzyk et al., 2012; Gao et al., 2011). The angles around atom C3 in the triazole ring deviate from the normal angles based on Csp2 hybridization, giving bond angles of 102.72 (14)° and 130.12 (13)° for N2—C3—N4 and N2—C3—S1, respectively. The dihedral angle between the triazole ring (N1/N2/C3/N4/C5) and the benzene ring (C8—C13) is 73.0 (5)°. In the crystal, N—H···S hydrogen bonds connect pairs of inversion related molecules, which are in turn connected by N—H···N hydrogen bonds into chains of rings along [010]. In addition, weak C—H···O hydrogen bonds connect these chains into a two-dimensional network parallel to (102) (Fig. 2).

For background to the chemistry of triazoles, see: Holla et al. (2001, 2006). For the biological activity of 1,2,4-triazole derivatives, see: Cansiz et al. (2001); Jones et al. (1965); Kane et al. (1988); Mullican et al. (1993). For related structures, see: Chen et al. (2007); Gao et al. (2011); Karczmarzyk et al. (2012). For standard bond-length data, see: Allen et al. (1987).

Computing details top

Data collection: CrysAlis PRO (Oxford Diffraction, 2010); cell refinement: CrysAlis PRO (Oxford Diffraction, 2010); data reduction: CrysAlis PRO (Oxford Diffraction, 2010); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: PLATON (Spek, 2009); software used to prepare material for publication: PLATON (Spek, 2009).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title compound with ellipsoids drawn at the 40% probability level. H atoms are shown as small spheres of arbitrary radii.
[Figure 2] Fig. 2. Part of the crystal structure with hydrogen bonds shown as dashed lines.
4-Amino-3-(3-methoxybenzyl)-1H-1,2,4-triazole-5(4H)-thione top
Crystal data top
C10H12N4OSF(000) = 496
Mr = 236.30Dx = 1.440 Mg m−3
Monoclinic, P21/nMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ynCell parameters from 7374 reflections
a = 7.4580 (3) Åθ = 3.5–29.0°
b = 5.8006 (2) ŵ = 0.28 mm−1
c = 25.2817 (10) ÅT = 293 K
β = 94.513 (4)°Plate, white
V = 1090.32 (7) Å30.3 × 0.2 × 0.1 mm
Z = 4
Data collection top
Oxford Diffraction Xcalibur Sapphire3
diffractometer		2130 independent reflections
Radiation source: fine-focus sealed tube1748 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.042
Detector resolution: 16.1049 pixels mm-1θmax = 26.0°, θmin = 3.5°
ω scansh = −9→9
Absorption correction: multi-scan
(CrysAlis PRO; Oxford Diffraction, 2010)		k = −7→7
Tmin = 0.946, Tmax = 1.000l = −31→31
15190 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)] = 0.036Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.088H atoms treated by a mixture of independent and constrained refinement
S = 1.03 w = 1/[σ2(Fo2) + (0.0408P)2 + 0.3289P]
where P = (Fo2 + 2Fc2)/3
2130 reflections(Δ/σ)max = 0.002
154 parametersΔρmax = 0.19 e Å−3
0 restraintsΔρmin = −0.24 e Å−3
Crystal data top
C10H12N4OSV = 1090.32 (7) Å3
Mr = 236.30Z = 4
Monoclinic, P21/nMo Kα radiation
a = 7.4580 (3) ŵ = 0.28 mm−1
b = 5.8006 (2) ÅT = 293 K
c = 25.2817 (10) Å0.3 × 0.2 × 0.1 mm
β = 94.513 (4)°
Data collection top
Oxford Diffraction Xcalibur Sapphire3
diffractometer		2130 independent reflections
Absorption correction: multi-scan
(CrysAlis PRO; Oxford Diffraction, 2010)		1748 reflections with I > 2σ(I)
Tmin = 0.946, Tmax = 1.000Rint = 0.042
15190 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0360 restraints
wR(F2) = 0.088H atoms treated by a mixture of independent and constrained refinement
S = 1.03Δρmax = 0.19 e Å−3
2130 reflectionsΔρmin = −0.24 e Å−3
154 parameters
Special details top

Experimental. CrysAlis PRO, Oxford Diffraction Ltd., Version 1.171.34.40 (release 27–08-2010 CrysAlis171. NET) (compiled Aug 27 2010,11:50:40) Empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm.

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
S10.79363 (6)1.26508 (8)1.014843 (19)0.03712 (16)
O10.4364 (2)0.7659 (2)0.66746 (5)0.0467 (4)
N10.6715 (2)0.7764 (2)0.91172 (6)0.0323 (4)
N20.77124 (19)0.8746 (2)0.95420 (6)0.0319 (4)
H20.86210.80770.97070.038*
C30.7134 (2)1.0833 (3)0.96726 (6)0.0254 (4)
N40.56824 (17)1.1164 (2)0.93177 (5)0.0239 (3)
C50.5471 (2)0.9287 (3)0.89877 (6)0.0246 (4)
N60.4558 (2)1.3106 (3)0.92853 (8)0.0360 (4)
C70.4041 (2)0.9044 (3)0.85492 (6)0.0284 (4)
H7A0.29940.99080.86390.034*
H7B0.36960.74340.85190.034*
C80.4584 (2)0.9870 (3)0.80138 (6)0.0249 (4)
C90.5382 (2)1.2018 (3)0.79529 (7)0.0322 (4)
H90.56171.29720.82460.039*
C100.5823 (2)1.2730 (3)0.74597 (8)0.0339 (4)
H100.63471.41700.74230.041*
C110.5501 (2)1.1344 (3)0.70177 (7)0.0328 (4)
H110.58051.18380.66860.039*
C120.4717 (2)0.9206 (3)0.70779 (7)0.0290 (4)
C130.4246 (2)0.8490 (3)0.75726 (7)0.0271 (4)
H130.36960.70640.76070.032*
C140.4954 (3)0.8208 (4)0.61719 (8)0.0492 (5)
H14A0.43480.95720.60370.074*
H14B0.46860.69500.59320.074*
H14C0.62280.84750.62050.074*
H620.524 (3)1.436 (4)0.9246 (8)0.049 (6)*
H610.403 (3)1.324 (4)0.9573 (10)0.065 (8)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
S10.0330 (3)0.0444 (3)0.0325 (3)0.0079 (2)−0.00694 (19)−0.0124 (2)
O10.0607 (9)0.0517 (8)0.0284 (7)−0.0206 (7)0.0078 (6)−0.0085 (6)
N10.0352 (8)0.0312 (8)0.0297 (9)0.0065 (6)−0.0034 (7)−0.0030 (6)
N20.0317 (8)0.0324 (8)0.0303 (8)0.0109 (6)−0.0064 (7)−0.0018 (6)
C30.0232 (8)0.0305 (9)0.0227 (9)0.0032 (7)0.0025 (7)0.0025 (7)
N40.0223 (7)0.0239 (7)0.0250 (7)0.0044 (5)−0.0015 (6)−0.0009 (6)
C50.0267 (8)0.0244 (8)0.0228 (9)−0.0007 (7)0.0033 (7)0.0004 (6)
N60.0353 (9)0.0290 (9)0.0422 (11)0.0141 (7)−0.0073 (8)−0.0061 (7)
C70.0264 (9)0.0310 (9)0.0273 (9)−0.0015 (7)−0.0010 (7)−0.0032 (7)
C80.0204 (8)0.0265 (8)0.0272 (9)0.0033 (6)−0.0028 (7)0.0003 (7)
C90.0355 (10)0.0263 (9)0.0341 (10)−0.0017 (7)−0.0023 (8)−0.0043 (7)
C100.0326 (10)0.0238 (9)0.0450 (11)−0.0031 (7)0.0003 (8)0.0055 (8)
C110.0311 (9)0.0363 (10)0.0310 (10)−0.0006 (8)0.0016 (8)0.0079 (8)
C120.0261 (9)0.0335 (9)0.0267 (9)−0.0010 (7)−0.0012 (7)−0.0008 (7)
C130.0256 (9)0.0248 (8)0.0304 (10)−0.0024 (7)−0.0004 (7)0.0008 (7)
C140.0469 (13)0.0726 (15)0.0287 (11)−0.0096 (11)0.0073 (9)−0.0059 (10)
Geometric parameters (Å, º) top
S1—C31.6745 (17)C7—H7B0.9700
O1—C121.368 (2)C8—C131.380 (2)
O1—C141.414 (2)C8—C91.395 (2)
N1—C51.304 (2)C9—C101.377 (3)
N1—N21.381 (2)C9—H90.9300
N2—C31.335 (2)C10—C111.382 (3)
N2—H20.8600C10—H100.9300
C3—N41.364 (2)C11—C121.384 (2)
N4—C51.373 (2)C11—H110.9300
N4—N61.4029 (19)C12—C131.389 (2)
C5—C71.483 (2)C13—H130.9300
N6—H620.90 (2)C14—H14A0.9600
N6—H610.86 (3)C14—H14B0.9600
C7—C81.521 (2)C14—H14C0.9600
C7—H7A0.9700
C12—O1—C14117.84 (15)C13—C8—C7119.48 (15)
C5—N1—N2104.16 (13)C9—C8—C7121.71 (15)
C3—N2—N1113.69 (14)C10—C9—C8120.12 (16)
C3—N2—H2123.2C10—C9—H9119.9
N1—N2—H2123.2C8—C9—H9119.9
N2—C3—N4102.72 (14)C9—C10—C11121.26 (16)
N2—C3—S1130.12 (13)C9—C10—H10119.4
N4—C3—S1127.17 (12)C11—C10—H10119.4
C3—N4—C5109.59 (13)C10—C11—C12118.69 (17)
C3—N4—N6126.24 (14)C10—C11—H11120.7
C5—N4—N6124.17 (14)C12—C11—H11120.7
N1—C5—N4109.83 (15)O1—C12—C11124.32 (16)
N1—C5—C7125.34 (15)O1—C12—C13115.29 (15)
N4—C5—C7124.83 (14)C11—C12—C13120.39 (16)
N4—N6—H62108.4 (14)C8—C13—C12120.74 (15)
N4—N6—H61109.5 (17)C8—C13—H13119.6
H62—N6—H61109 (2)C12—C13—H13119.6
C5—C7—C8114.15 (14)O1—C14—H14A109.5
C5—C7—H7A108.7O1—C14—H14B109.5
C8—C7—H7A108.7H14A—C14—H14B109.5
C5—C7—H7B108.7O1—C14—H14C109.5
C8—C7—H7B108.7H14A—C14—H14C109.5
H7A—C7—H7B107.6H14B—C14—H14C109.5
C13—C8—C9118.79 (16)
C5—N1—N2—C3−0.81 (19)C5—C7—C8—C13132.14 (16)
N1—N2—C3—N41.00 (18)C5—C7—C8—C9−49.4 (2)
N1—N2—C3—S1−179.11 (13)C13—C8—C9—C10−0.1 (3)
N2—C3—N4—C5−0.80 (17)C7—C8—C9—C10−178.66 (16)
S1—C3—N4—C5179.30 (13)C8—C9—C10—C11−0.4 (3)
N2—C3—N4—N6179.29 (16)C9—C10—C11—C120.1 (3)
S1—C3—N4—N6−0.6 (3)C14—O1—C12—C114.7 (3)
N2—N1—C5—N40.25 (18)C14—O1—C12—C13−174.70 (17)
N2—N1—C5—C7−179.94 (15)C10—C11—C12—O1−178.59 (17)
C3—N4—C5—N10.36 (19)C10—C11—C12—C130.8 (3)
N6—N4—C5—N1−179.74 (16)C9—C8—C13—C121.0 (2)
C3—N4—C5—C7−179.46 (15)C7—C8—C13—C12179.59 (15)
N6—N4—C5—C70.4 (3)O1—C12—C13—C8178.05 (15)
N1—C5—C7—C8−87.4 (2)C11—C12—C13—C8−1.4 (3)
N4—C5—C7—C892.39 (19)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C7—H7A···O1i0.972.463.308 (2)146
N6—H62···N1ii0.90 (2)2.30 (2)3.190 (2)174
N2—H2···S1iii0.862.603.377 (1)151
Symmetry codes: (i) −x+1/2, y+1/2, −z+3/2; (ii) x, y+1, z; (iii) −x+2, −y+2, −z+2.

Experimental details

Crystal data
Chemical formulaC10H12N4OS
Mr236.30
Crystal system, space groupMonoclinic, P21/n
Temperature (K)293
a, b, c (Å)7.4580 (3), 5.8006 (2), 25.2817 (10)
β (°) 94.513 (4)
V (Å3)1090.32 (7)
Z4
Radiation typeMo Kα
µ (mm−1)0.28
Crystal size (mm)0.3 × 0.2 × 0.1
Data collection
DiffractometerOxford Diffraction Xcalibur Sapphire3
Absorption correctionMulti-scan
(CrysAlis PRO; Oxford Diffraction, 2010)
Tmin, Tmax0.946, 1.000
No. of measured, independent and
observed [I > 2σ(I)] reflections		15190, 2130, 1748
Rint0.042
(sin θ/λ)max (Å−1)0.617
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.036, 0.088, 1.03
No. of reflections2130
No. of parameters154
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å−3)0.19, −0.24

Computer programs: CrysAlis PRO (Oxford Diffraction, 2010), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), PLATON (Spek, 2009).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C7—H7A···O1i0.972.4593.308 (2)146
N6—H62···N1ii0.90 (2)2.30 (2)3.190 (2)174
N2—H2···S1iii0.862.5993.377 (1)151
Symmetry codes: (i) −x+1/2, y+1/2, −z+3/2; (ii) x, y+1, z; (iii) −x+2, −y+2, −z+2.
 

Acknowledgements

RK acknowledges the Department of Science & Technology for the sanction of the single-crystal X-ray diffractometer as a National Facility under a mega research project No. SR/S2/ CMP-47/2003.

References

First citationAllen, F. H., Kennard, O., Watson, D. G., Brammer, L., Orpen, A. G. & Taylor, R. (1987). J. Chem. Soc. Perkin Trans. 2, pp. S1–19.  CSD CrossRef Web of Science Google Scholar
 First citationCansiz, A., Servi, S., Koparir, M., Altintas, M. & Digrak, M. (2001). J. Chem. Soc. Pak. 23, 237–239.  CAS Google Scholar
 First citationChen, X.-A., Huang, X.-B. & Wu, H.-Y. (2007). Acta Cryst. E63, o3191.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationGao, Y., Zhang, L. & Wang, H. (2011). Acta Cryst. E67, o1794.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationHolla, B. S., Rao, B. S., Sarojini, B. K., Akberali, P. M. & Suchetha Kumari, N. (2006). Euro. J. Med. Chem. 41, 657–663.  CAS Google Scholar
 First citationHolla, B. S., Sarojini, B. K., Rao, B. S., Akberali, P. M. & Suchetha Kumari, N. (2001). Il Farmaco, 56, 565–570.  Web of Science CrossRef PubMed CAS Google Scholar
 First citationJones, D. H., Slack, R., Squires, S. & Wooldridge, K. R. H. (1965). J. Med. Chem. 8, 676–680.  CrossRef CAS Web of Science Google Scholar
 First citationKane, J. M., Dudley, M. W., Sorensen, S. M. & Miller, F. P. (1988). J. Med. Chem. 31, 1253–1258.  CrossRef CAS PubMed Web of Science Google Scholar
 First citationKarczmarzyk, Z., Pitucha, M., Wysocki, W., Fruziński, A. & Olender, E. (2012). Acta Cryst. E68, o3264–o3265.  CSD CrossRef CAS IUCr Journals Google Scholar
 First citationMullican, M. D., Wilson, M. W., Connor, D. T., Kostlan, C. R., Schrier, D. J. & Dyer, R. D. (1993). J. Med. Chem. 36, 1090–1099.  CrossRef CAS PubMed Web of Science Google Scholar
 First citationOxford Diffraction (2010). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, England.  Google Scholar
 First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationSpek, 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.

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 69| Part 5| May 2013| Page o728
https://doi.org/10.1107/S1600536813009859
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