3-[5-Methyl-1-(4-methyl­phen­yl)-1H-1,2,3-triazol-4-yl]-N-phenyl-5-[4-(piperidin-1-yl)phen­yl]-4,5-dihydro-1H-pyrazole-1-carbothio­amide dimethyl­formamide hemisolvate

Abdel-Wahab, B.F.; Mohamed, H.A.; Ng, S.W.; Tiekink, E.R.T.

doi:10.1107/S1600536812024488

organic compounds

CRYSTALLOGRAPHIC
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ISSN: 2056-9890

Volume 68| Part 7| July 2012| Page o1985

https://doi.org/10.1107/S1600536812024488

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3-[5-Methyl-1-(4-methylphenyl)-1H-1,2,3-triazol-4-yl]-N-phenyl-5-[4-(piperidin-1-yl)phenyl]-4,5-dihydro-1H-pyrazole-1-carbothioamide dimethylformamide hemisolvate

Bakr F. Abdel-Wahab,^a ‡ Hanan A. Mohamed,^a Seik Weng Ng ^b,^c and Edward R. T. Tiekink ^b ^*

^aApplied Organic Chemistry Department, National Research Centre, Dokki, 12622 Giza, Egypt, ^bDepartment of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia, and ^cChemistry Department, Faculty of Science, King Abdulaziz University, PO Box 80203 Jeddah, Saudi Arabia
^*Correspondence e-mail: edward.tiekink@gmail.com

(Received 29 May 2012; accepted 29 May 2012; online 2 June 2012)

The essentially planar pyrazole ring (r.m.s. deviation = 0.013 Å) in the title hemisolvate, C₃₁H₃₃N₇S·0.5C₃H₇NO, is almost coplanar with the pendant thiourea residue [N—N—C—S torsion angle = −173.2 (4)°] and slightly twisted with respect to the triazole ring [dihedral angle = 7.7 (3)°]. An intramolecular thiourea–pyrazole N—H⋯N hydrogen bond, via an S(5) loop, is formed. Supramolecular chains along the c axis are formed in the crystal via piperidine–triazole C—H⋯N interactions. These are bridged into loosely associated double chains via C—H⋯O interactions involving the disordered (over two positions) dimethylformamide solvent molecules. The thiourea-bound phenyl ring is also disordered over two positions of equal occupancy.

Related literature

For the biological activity of related compounds, see: Abdel-Wahab et al. (2009 , 2012a ). For a related pyrazolyl-1,2,3-triazole structure, see: Abdel-Wahab et al. (2012b ).

Experimental

Crystal data

C₃₁H₃₃N₇S·0.5C₃H₇NO
M_r = 522.26
Monoclinic, C 2
a = 42.077 (4) Å
b = 5.9274 (5) Å
c = 12.0737 (11) Å
β = 105.665 (9)°
V = 2899.5 (4) Å³
Z = 4
Cu Kα radiation
μ = 1.29 mm⁻¹
T = 100 K
0.35 × 0.15 × 0.05 mm

Data collection

Agilent SuperNova Dual diffractometer with an Atlas detector
Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2012 ) T_min = 0.661, T_max = 0.938
10437 measured reflections
3317 independent reflections
3229 reflections with I > 2σ(I)
R_int = 0.037

Refinement

R[F² > 2σ(F²)] = 0.091
wR(F²) = 0.214
S = 1.11
3317 reflections
396 parameters
41 restraints
H-atom parameters constrained
Δρ_max = 0.71 e Å⁻³
Δρ_min = −1.06 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1⋯N3	0.88	2.13	2.597 (8)	112
C13—H13A⋯O1	0.98	2.56	3.466 (14)	154
C28—H28B⋯N5ⁱ	0.99	2.57	3.355 (10)	137
Symmetry code: (i) x, y, z-1.

Data collection: CrysAlis PRO (Agilent, 2012); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997 ) and DIAMOND (Brandenburg, 2006 ); software used to prepare material for publication: publCIF (Westrip, 2010 ).

Supporting information

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S1600536812024488/xu5554sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536812024488/xu5554Isup2.hkl

Supporting information file. DOI: https://doi.org/10.1107/S1600536812024488/xu5554Isup3.cml

checkCIF report

Comment top

The synthesis and crystallographic characterization of the title compound was motivated by the established biological activities exhibited by related 3-(benzofuran-2-yl)-4,5-dihydro-5-phenyl-1-(4-phenylthiazol-2-yl)-1H-pyrazole and 1,2,3-triazol-4-yl-pyrazolylthiazoles (Abdel-Wahab et al. 2012a; Abdel-Wahab et al. 2009) and accompanying structural studies (Abdel-Wahab et al., 2012b).

In (I), Fig. 1, the pyrazole ring is planar with a r.m.s. deviation = 0.013 Å; the maximum deviation is 0.005 (6) Å for the N2 atom. The thiourea group is close to co-planar with the ring [the N3—N2—C7—S1 torsion angle = -173.2 (4)°] and the connected triazole ring is slightly twisted out of the plane [dihedral angle = 7.7 (3)°]. There is a significant twist between the triazole and attached benzene rings with the dihedral angle being 49.4 (3)°. The conformation of the piperidinyl ring is close to a chair. The thiourea-N—H atom is orientated towards the pyrazole-N3 atom and forms a hydrogen bond via an S(5) loop, Table 1.

In the crystal packing, connections between molecules are of the type piperidinyl-C—H···N(triazole), Table 1, leading to the formation of a supramolecular chain along the c axis. Two chains are connected by the (disordered) dimethylformamide molecules via methyl-C13—H···O1 interactions into a loosely associated double chain, Fig. 2 and Table 1.

Related literature top

For the biological activity of related compounds, see: Abdel-Wahab et al. (2009, 2012a). For a related pyrazolyl-1,2,3-triazole structure, see: Abdel-Wahab et al. (2012b).

Experimental top

The title compound was prepared according to the reported method (Abdel-Wahab et al., 2012a). Crystals were obtained from its DMF solution by slow evaporation at room temperature.

Structure description top

For the biological activity of related compounds, see: Abdel-Wahab et al. (2009, 2012a). For a related pyrazolyl-1,2,3-triazole structure, see: Abdel-Wahab et al. (2012b).

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: ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 2006); software used to prepare material for publication: publCIF (Westrip, 2010).

Figures top

	Fig. 1. The molecular structure of (I) showing the atom-labelling scheme and displacement ellipsoids at the 50% probability level.
	Fig. 2. A view of a supramolecular chain along the c axis in (I). The dimethylformamide molecule is disordered over two positions. The C—H···O and C—H···N interactions are shown as orange and blue dashed lines, respectively.

3-[5-Methyl-1-(4-methylphenyl)-1H-1,2,3-triazol-4-yl]-N-phenyl- 5-[4-(piperidin-1-yl)phenyl]-4,5-dihydro-1H-pyrazole-1-carbothioamide dimethylformamide hemisolvate top

Crystal data top

C₃₁H₃₃N₇S·0.5C₃H₇NO	F(000) = 1216
M_r = 522.26	D_x = 1.311 Mg m⁻³
Monoclinic, C2	Cu Kα radiation, λ = 1.54184 Å
Hall symbol: C 2y	Cell parameters from 6358 reflections
a = 42.077 (4) Å	θ = 3.8–76.9°
b = 5.9274 (5) Å	µ = 1.29 mm⁻¹
c = 12.0737 (11) Å	T = 100 K
β = 105.665 (9)°	Prism, light-brown
V = 2899.5 (4) Å³	0.35 × 0.15 × 0.05 mm
Z = 4

Data collection top

Agilent SuperNova Dual diffractometer with an Atlas detector	3317 independent reflections
Radiation source: SuperNova (Cu) X-ray Source	3229 reflections with I > 2σ(I)
Mirror monochromator	R_int = 0.037
Detector resolution: 10.4041 pixels mm^-1	θ_max = 77.1°, θ_min = 3.8°
ω scan	h = −52→49
Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2012)	k = −5→7
T_min = 0.661, T_max = 0.938	l = −14→15
10437 measured reflections

Refinement top

Refinement on F²	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F² > 2σ(F²)] = 0.091	H-atom parameters constrained
wR(F²) = 0.214	w = 1/[σ²(F_o²) + (0.0422P)² + 29.4613P] where P = (F_o² + 2F_c²)/3
S = 1.11	(Δ/σ)_max = 0.001
3317 reflections	Δρ_max = 0.71 e Å⁻³
396 parameters	Δρ_min = −1.06 e Å⁻³
41 restraints	Extinction correction: SHELXL97 (Sheldrick, 2008), Fc^*=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4
Primary atom site location: structure-invariant direct methods	Extinction coefficient: 0.00150 (17)

Crystal data top

C₃₁H₃₃N₇S·0.5C₃H₇NO	V = 2899.5 (4) Å³
M_r = 522.26	Z = 4
Monoclinic, C2	Cu Kα radiation
a = 42.077 (4) Å	µ = 1.29 mm⁻¹
b = 5.9274 (5) Å	T = 100 K
c = 12.0737 (11) Å	0.35 × 0.15 × 0.05 mm
β = 105.665 (9)°

Data collection top

Agilent SuperNova Dual diffractometer with an Atlas detector	3317 independent reflections
Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2012)	3229 reflections with I > 2σ(I)
T_min = 0.661, T_max = 0.938	R_int = 0.037
10437 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.091	41 restraints
wR(F²) = 0.214	H-atom parameters constrained
S = 1.11	w = 1/[σ²(F_o²) + (0.0422P)² + 29.4613P] where P = (F_o² + 2F_c²)/3
3317 reflections	Δρ_max = 0.71 e Å⁻³
396 parameters	Δρ_min = −1.06 e Å⁻³

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq	Occ. (<1)
S1	0.59659 (4)	0.0014 (4)	0.47105 (16)	0.0329 (5)
N1	0.56945 (14)	0.4011 (13)	0.5037 (5)	0.0306 (14)
H1	0.5726	0.5285	0.5426	0.037*
N2	0.61985 (13)	0.3203 (11)	0.6223 (5)	0.0250 (13)
N3	0.61644 (13)	0.5210 (12)	0.6819 (5)	0.0251 (12)
N4	0.67600 (14)	0.7524 (12)	0.9292 (5)	0.0282 (13)
N5	0.67224 (14)	0.9126 (13)	1.0004 (5)	0.0304 (14)
N6	0.64025 (13)	0.9852 (13)	0.9628 (5)	0.0267 (13)
N7	0.72517 (13)	0.4072 (12)	0.3176 (5)	0.0261 (13)
C1	0.53887 (17)	0.3838 (17)	0.4206 (10)	0.0259 (16)	0.50
C2	0.5261 (2)	0.2040 (15)	0.3484 (10)	0.029 (2)	0.50
H2	0.5391	0.0727	0.3489	0.035*	0.50
C3	0.4944 (2)	0.2165 (17)	0.2753 (9)	0.036 (3)	0.50
H3	0.4856	0.0936	0.2259	0.043*	0.50
C4	0.47537 (19)	0.409 (2)	0.2745 (10)	0.032 (3)	0.50
H4	0.4537	0.4172	0.2245	0.038*	0.50
C5	0.4881 (2)	0.5885 (16)	0.3467 (10)	0.034 (3)	0.50
H5	0.4752	0.7199	0.3462	0.041*	0.50
C6	0.5199 (2)	0.5761 (14)	0.4198 (9)	0.029 (2)	0.50
H6	0.5286	0.6989	0.4692	0.035*	0.50
C1'	0.53743 (17)	0.3832 (17)	0.4284 (9)	0.0259 (16)	0.50
C2'	0.5190 (2)	0.1876 (15)	0.4256 (9)	0.029 (2)	0.50
H2'	0.5279	0.0650	0.4749	0.035*	0.50
C3'	0.4875 (2)	0.1716 (15)	0.3507 (10)	0.036 (3)	0.50
H3'	0.4749	0.0380	0.3489	0.043*	0.50
C4'	0.4745 (2)	0.3511 (19)	0.2787 (10)	0.032 (3)	0.50
H4'	0.4530	0.3401	0.2275	0.038*	0.50
C5'	0.4929 (2)	0.5466 (16)	0.2814 (9)	0.034 (3)	0.50
H5'	0.4840	0.6693	0.2322	0.041*	0.50
C6'	0.5244 (2)	0.5627 (14)	0.3563 (10)	0.029 (2)	0.50
H6'	0.5370	0.6963	0.3582	0.035*	0.50
C7	0.59446 (16)	0.2551 (14)	0.5330 (6)	0.0261 (15)
C8	0.65420 (15)	0.2319 (14)	0.6552 (6)	0.0252 (15)
H8	0.6543	0.0662	0.6708	0.030*
C9	0.66858 (15)	0.3640 (15)	0.7684 (6)	0.0281 (16)
H9A	0.6707	0.2663	0.8366	0.034*
H9B	0.6904	0.4294	0.7710	0.034*
C10	0.64330 (16)	0.5443 (13)	0.7621 (5)	0.0240 (15)
C11	0.64669 (17)	0.7263 (13)	0.8469 (6)	0.0246 (14)
C12	0.62375 (16)	0.8719 (14)	0.8666 (6)	0.0263 (15)
C13	0.58794 (16)	0.9065 (15)	0.8053 (6)	0.0305 (16)
H13A	0.5758	0.9465	0.8612	0.046*
H13B	0.5788	0.7670	0.7656	0.046*
H13C	0.5858	1.0285	0.7490	0.046*
C14	0.62887 (16)	1.1423 (14)	1.0318 (6)	0.0276 (16)
C15	0.61095 (18)	1.3329 (15)	0.9829 (7)	0.0327 (17)
H15	0.6065	1.3611	0.9027	0.039*
C16	0.59990 (19)	1.4774 (16)	1.0516 (7)	0.0354 (17)
H16	0.5872	1.6041	1.0173	0.043*
C17	0.6065 (2)	1.4476 (13)	1.1719 (8)	0.0363 (19)
C18	0.6245 (2)	1.2523 (16)	1.2175 (7)	0.0360 (18)
H18	0.6292	1.2239	1.2977	0.043*
C19	0.63557 (19)	1.1015 (16)	1.1493 (6)	0.0343 (17)
H19	0.6476	0.9712	1.1822	0.041*
C20	0.5944 (2)	1.6067 (17)	1.2460 (8)	0.047 (2)
H20A	0.5827	1.5227	1.2929	0.071*
H20B	0.5793	1.7156	1.1977	0.071*
H20C	0.6131	1.6871	1.2964	0.071*
C21	0.67202 (16)	0.2810 (14)	0.5649 (6)	0.0269 (16)
C22	0.67004 (19)	0.4876 (16)	0.5091 (7)	0.0350 (17)
H22	0.6565	0.6026	0.5273	0.042*
C23	0.68695 (17)	0.5317 (14)	0.4285 (6)	0.0305 (16)
H23	0.6848	0.6751	0.3921	0.037*
C24	0.70737 (16)	0.3670 (14)	0.3994 (6)	0.0258 (15)
C25	0.70995 (18)	0.1619 (14)	0.4574 (6)	0.0291 (16)
H25	0.7240	0.0480	0.4417	0.035*
C26	0.69243 (17)	0.1197 (13)	0.5380 (6)	0.0280 (15)
H26	0.6946	−0.0229	0.5751	0.034*
C27	0.71379 (18)	0.5951 (15)	0.2389 (7)	0.0318 (17)
H27A	0.7099	0.7279	0.2832	0.038*
H27B	0.6925	0.5540	0.1838	0.038*
C28	0.73850 (18)	0.6574 (14)	0.1727 (6)	0.0293 (16)
H28A	0.7592	0.7105	0.2270	0.035*
H28B	0.7295	0.7818	0.1187	0.035*
C29	0.74577 (18)	0.4548 (15)	0.1060 (6)	0.0333 (19)
H29A	0.7254	0.4055	0.0486	0.040*
H29B	0.7624	0.4954	0.0650	0.040*
C30	0.75863 (18)	0.2688 (15)	0.1902 (6)	0.0307 (17)
H30A	0.7801	0.3149	0.2423	0.037*
H30B	0.7624	0.1328	0.1479	0.037*
C31	0.73474 (18)	0.2102 (14)	0.2620 (7)	0.0313 (17)
H31A	0.7147	0.1397	0.2115	0.038*
H31B	0.7453	0.0985	0.3215	0.038*
O1	0.5327 (3)	0.8817 (18)	0.9722 (10)	0.051 (3)	0.50
N8	0.4987 (3)	1.1815 (15)	0.9647 (8)	0.039 (4)	0.50
C32	0.5278 (3)	1.0766 (18)	1.0017 (9)	0.041 (4)	0.50
H32	0.5455	1.1547	1.0528	0.049*	0.50
C33	0.4703 (3)	1.078 (3)	0.8870 (13)	0.051 (5)	0.50
H33A	0.4768	0.9346	0.8593	0.077*	0.50
H33B	0.4615	1.1789	0.8215	0.077*	0.50
H33C	0.4534	1.0509	0.9274	0.077*	0.50
C34	0.4944 (4)	1.4106 (18)	1.002 (2)	0.043 (5)	0.50
H34A	0.5155	1.4673	1.0499	0.064*	0.50
H34B	0.4780	1.4107	1.0460	0.064*	0.50
H34C	0.4867	1.5079	0.9341	0.064*	0.50

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1	0.0282 (8)	0.0365 (10)	0.0366 (9)	−0.0056 (9)	0.0133 (7)	−0.0043 (9)
N1	0.025 (3)	0.035 (4)	0.035 (3)	−0.002 (3)	0.013 (2)	−0.005 (3)
N2	0.020 (3)	0.028 (3)	0.029 (3)	0.000 (3)	0.012 (2)	−0.006 (3)
N3	0.024 (3)	0.026 (3)	0.029 (3)	−0.003 (3)	0.012 (2)	−0.002 (3)
N4	0.026 (3)	0.027 (3)	0.035 (3)	0.002 (3)	0.013 (2)	−0.004 (3)
N5	0.024 (3)	0.033 (4)	0.036 (3)	0.001 (3)	0.012 (2)	−0.004 (3)
N6	0.023 (3)	0.031 (3)	0.029 (3)	0.001 (3)	0.012 (2)	0.004 (3)
N7	0.025 (3)	0.026 (3)	0.031 (3)	0.003 (3)	0.013 (2)	0.004 (3)
C1	0.023 (3)	0.028 (4)	0.030 (4)	0.005 (3)	0.014 (3)	0.000 (3)
C2	0.029 (5)	0.025 (5)	0.032 (5)	0.000 (4)	0.009 (4)	−0.001 (5)
C3	0.030 (6)	0.033 (6)	0.043 (6)	0.003 (5)	0.006 (5)	−0.002 (6)
C4	0.026 (4)	0.031 (8)	0.036 (4)	0.001 (5)	0.005 (3)	−0.002 (5)
C5	0.030 (5)	0.030 (6)	0.047 (7)	0.000 (5)	0.019 (5)	0.003 (6)
C6	0.032 (5)	0.022 (5)	0.039 (7)	−0.006 (4)	0.017 (5)	−0.001 (5)
C1'	0.023 (3)	0.028 (4)	0.030 (4)	0.005 (3)	0.014 (3)	0.000 (3)
C2'	0.029 (5)	0.025 (5)	0.032 (5)	0.000 (4)	0.009 (4)	−0.001 (5)
C3'	0.030 (6)	0.033 (6)	0.043 (6)	0.003 (5)	0.006 (5)	−0.002 (6)
C4'	0.026 (4)	0.031 (8)	0.036 (4)	0.001 (5)	0.005 (3)	−0.002 (5)
C5'	0.030 (5)	0.030 (6)	0.047 (7)	0.000 (5)	0.019 (5)	0.003 (6)
C6'	0.032 (5)	0.022 (5)	0.039 (7)	−0.006 (4)	0.017 (5)	−0.001 (5)
C7	0.024 (3)	0.032 (4)	0.030 (3)	−0.003 (3)	0.019 (3)	0.000 (3)
C8	0.016 (3)	0.031 (4)	0.030 (3)	0.001 (3)	0.010 (3)	0.002 (3)
C9	0.016 (3)	0.040 (5)	0.030 (3)	−0.001 (3)	0.008 (2)	−0.001 (3)
C10	0.023 (3)	0.029 (4)	0.024 (3)	0.000 (3)	0.012 (2)	−0.001 (3)
C11	0.026 (3)	0.024 (4)	0.027 (3)	0.004 (3)	0.011 (3)	0.001 (3)
C12	0.022 (3)	0.034 (4)	0.024 (3)	−0.006 (3)	0.009 (3)	0.006 (3)
C13	0.024 (3)	0.033 (4)	0.038 (4)	−0.001 (3)	0.014 (3)	−0.006 (4)
C14	0.021 (3)	0.027 (4)	0.039 (4)	−0.003 (3)	0.014 (3)	−0.005 (3)
C15	0.028 (4)	0.031 (4)	0.044 (4)	0.004 (3)	0.019 (3)	0.004 (4)
C16	0.037 (4)	0.028 (4)	0.048 (4)	0.001 (4)	0.023 (3)	0.002 (4)
C17	0.048 (4)	0.014 (4)	0.057 (5)	−0.002 (3)	0.032 (4)	−0.009 (3)
C18	0.045 (4)	0.034 (4)	0.035 (4)	−0.005 (4)	0.020 (3)	−0.002 (4)
C19	0.037 (4)	0.034 (4)	0.034 (4)	0.001 (4)	0.012 (3)	−0.001 (4)
C20	0.065 (6)	0.034 (5)	0.058 (5)	0.000 (5)	0.044 (5)	−0.001 (5)
C21	0.020 (3)	0.029 (4)	0.032 (4)	−0.003 (3)	0.007 (3)	0.000 (3)
C22	0.036 (4)	0.026 (4)	0.050 (4)	0.003 (4)	0.025 (3)	−0.002 (4)
C23	0.031 (3)	0.025 (4)	0.041 (4)	0.000 (3)	0.019 (3)	0.001 (3)
C24	0.019 (3)	0.027 (4)	0.033 (3)	0.000 (3)	0.012 (3)	0.004 (3)
C25	0.029 (4)	0.024 (4)	0.040 (4)	0.004 (3)	0.019 (3)	−0.002 (3)
C26	0.029 (3)	0.021 (4)	0.040 (4)	0.004 (3)	0.018 (3)	0.005 (3)
C27	0.031 (4)	0.030 (4)	0.038 (4)	−0.001 (3)	0.017 (3)	0.006 (4)
C28	0.026 (3)	0.032 (4)	0.033 (4)	0.002 (3)	0.014 (3)	0.005 (3)
C29	0.029 (3)	0.041 (5)	0.032 (3)	0.003 (3)	0.011 (3)	0.005 (4)
C30	0.027 (3)	0.032 (4)	0.037 (4)	0.001 (3)	0.015 (3)	0.004 (4)
C31	0.030 (4)	0.027 (4)	0.043 (4)	−0.001 (3)	0.020 (3)	0.000 (3)
O1	0.046 (6)	0.048 (7)	0.059 (6)	0.003 (6)	0.017 (5)	−0.019 (6)
N8	0.038 (6)	0.033 (6)	0.050 (7)	−0.003 (6)	0.017 (6)	−0.012 (5)
C32	0.038 (7)	0.041 (8)	0.043 (7)	−0.012 (6)	0.010 (6)	−0.009 (6)
C33	0.048 (8)	0.052 (9)	0.056 (8)	0.000 (7)	0.019 (7)	−0.006 (7)
C34	0.045 (11)	0.039 (7)	0.055 (7)	0.005 (6)	0.032 (7)	−0.003 (8)

Geometric parameters (Å, º) top

S1—C7	1.693 (8)	C13—H13C	0.9800
N1—C7	1.334 (10)	C14—C19	1.391 (10)
N1—C1	1.405 (8)	C14—C15	1.398 (11)
N1—C1'	1.411 (8)	C15—C16	1.359 (11)
N1—H1	0.8800	C15—H15	0.9500
N2—C7	1.354 (9)	C16—C17	1.414 (11)
N2—N3	1.417 (8)	C16—H16	0.9500
N2—C8	1.487 (8)	C17—C18	1.412 (12)
N3—C10	1.282 (8)	C17—C20	1.482 (11)
N4—N5	1.318 (9)	C18—C19	1.378 (11)
N4—C11	1.368 (9)	C18—H18	0.9500
N5—N6	1.369 (8)	C19—H19	0.9500
N6—C12	1.359 (9)	C20—H20A	0.9800
N6—C14	1.416 (10)	C20—H20B	0.9800
N7—C24	1.411 (8)	C20—H20C	0.9800
N7—C31	1.458 (10)	C21—C26	1.382 (10)
N7—C27	1.458 (10)	C21—C22	1.389 (12)
C1—C2	1.3900	C22—C23	1.378 (10)
C1—C6	1.3900	C22—H22	0.9500
C2—C3	1.3900	C23—C24	1.406 (10)
C2—H2	0.9500	C23—H23	0.9500
C3—C4	1.3900	C24—C25	1.393 (11)
C3—H3	0.9500	C25—C26	1.392 (9)
C4—C5	1.3900	C25—H25	0.9500
C4—H4	0.9500	C26—H26	0.9500
C5—C6	1.3900	C27—C28	1.518 (9)
C5—H5	0.9500	C27—H27A	0.9900
C6—H6	0.9500	C27—H27B	0.9900
C1'—C2'	1.3900	C28—C29	1.522 (11)
C1'—C6'	1.3900	C28—H28A	0.9900
C2'—C3'	1.3900	C28—H28B	0.9900
C2'—H2'	0.9500	C29—C30	1.498 (11)
C3'—C4'	1.3900	C29—H29A	0.9900
C3'—H3'	0.9500	C29—H29B	0.9900
C4'—C5'	1.3900	C30—C31	1.534 (9)
C4'—H4'	0.9500	C30—H30A	0.9900
C5'—C6'	1.3900	C30—H30B	0.9900
C5'—H5'	0.9500	C31—H31A	0.9900
C6'—H6'	0.9500	C31—H31B	0.9900
C8—C21	1.509 (9)	O1—C32	1.242 (9)
C8—C9	1.550 (10)	N8—C32	1.338 (8)
C8—H8	1.0000	N8—C33	1.442 (9)
C9—C10	1.495 (10)	N8—C34	1.456 (9)
C9—H9A	0.9900	C32—H32	0.9500
C9—H9B	0.9900	C33—H33A	0.9800
C10—C11	1.467 (10)	C33—H33B	0.9800
C11—C12	1.363 (10)	C33—H33C	0.9800
C12—C13	1.503 (9)	C34—H34A	0.9800
C13—H13A	0.9800	C34—H34B	0.9800
C13—H13B	0.9800	C34—H34C	0.9800

C7—N1—C1	130.3 (8)	C12—C13—H13C	109.5
C7—N1—C1'	132.0 (8)	H13A—C13—H13C	109.5
C1—N1—C1'	5.1 (9)	H13B—C13—H13C	109.5
C7—N1—H1	114.9	C19—C14—C15	120.6 (7)
C1—N1—H1	114.9	C19—C14—N6	118.5 (7)
C1'—N1—H1	112.9	C15—C14—N6	120.8 (7)
C7—N2—N3	118.5 (6)	C16—C15—C14	119.1 (7)
C7—N2—C8	127.8 (6)	C16—C15—H15	120.5
N3—N2—C8	112.6 (5)	C14—C15—H15	120.5
C10—N3—N2	106.5 (6)	C15—C16—C17	123.0 (8)
N5—N4—C11	108.2 (6)	C15—C16—H16	118.5
N4—N5—N6	106.9 (6)	C17—C16—H16	118.5
C12—N6—N5	111.0 (6)	C18—C17—C16	116.0 (7)
C12—N6—C14	130.6 (6)	C18—C17—C20	121.5 (8)
N5—N6—C14	118.1 (6)	C16—C17—C20	122.5 (8)
C24—N7—C31	116.9 (6)	C19—C18—C17	122.1 (7)
C24—N7—C27	116.2 (6)	C19—C18—H18	119.0
C31—N7—C27	113.2 (6)	C17—C18—H18	119.0
C2—C1—C6	120.0	C18—C19—C14	119.2 (8)
C2—C1—N1	128.9 (7)	C18—C19—H19	120.4
C6—C1—N1	111.0 (7)	C14—C19—H19	120.4
C1—C2—C3	120.0	C17—C20—H20A	109.5
C1—C2—H2	120.0	C17—C20—H20B	109.5
C3—C2—H2	120.0	H20A—C20—H20B	109.5
C4—C3—C2	120.0	C17—C20—H20C	109.5
C4—C3—H3	120.0	H20A—C20—H20C	109.5
C2—C3—H3	120.0	H20B—C20—H20C	109.5
C5—C4—C3	120.0	C26—C21—C22	117.1 (6)
C5—C4—H4	120.0	C26—C21—C8	119.9 (7)
C3—C4—H4	120.0	C22—C21—C8	122.9 (7)
C4—C5—C6	120.0	C23—C22—C21	122.3 (8)
C4—C5—H5	120.0	C23—C22—H22	118.8
C6—C5—H5	120.0	C21—C22—H22	118.8
C5—C6—C1	120.0	C22—C23—C24	120.8 (8)
C5—C6—H6	120.0	C22—C23—H23	119.6
C1—C6—H6	120.0	C24—C23—H23	119.6
C2'—C1'—C6'	120.0	C25—C24—C23	116.7 (6)
C2'—C1'—N1	120.5 (7)	C25—C24—N7	121.0 (6)
C6'—C1'—N1	119.5 (7)	C23—C24—N7	122.2 (7)
C3'—C2'—C1'	120.0	C24—C25—C26	121.6 (7)
C3'—C2'—H2'	120.0	C24—C25—H25	119.2
C1'—C2'—H2'	120.0	C26—C25—H25	119.2
C4'—C3'—C2'	120.0	C21—C26—C25	121.3 (7)
C4'—C3'—H3'	120.0	C21—C26—H26	119.3
C2'—C3'—H3'	120.0	C25—C26—H26	119.3
C5'—C4'—C3'	120.0	N7—C27—C28	112.2 (6)
C5'—C4'—H4'	120.0	N7—C27—H27A	109.2
C3'—C4'—H4'	120.0	C28—C27—H27A	109.2
C4'—C5'—C6'	120.0	N7—C27—H27B	109.2
C4'—C5'—H5'	120.0	C28—C27—H27B	109.2
C6'—C5'—H5'	120.0	H27A—C27—H27B	107.9
C5'—C6'—C1'	120.0	C27—C28—C29	110.5 (7)
C5'—C6'—H6'	120.0	C27—C28—H28A	109.5
C1'—C6'—H6'	120.0	C29—C28—H28A	109.5
N2—C7—N1	115.0 (7)	C27—C28—H28B	109.5
N2—C7—S1	118.8 (6)	C29—C28—H28B	109.5
N1—C7—S1	126.2 (6)	H28A—C28—H28B	108.1
N2—C8—C21	112.1 (6)	C30—C29—C28	108.0 (6)
N2—C8—C9	100.2 (5)	C30—C29—H29A	110.1
C21—C8—C9	112.9 (6)	C28—C29—H29A	110.1
N2—C8—H8	110.4	C30—C29—H29B	110.1
C21—C8—H8	110.4	C28—C29—H29B	110.1
C9—C8—H8	110.4	H29A—C29—H29B	108.4
C10—C9—C8	102.3 (5)	C29—C30—C31	112.2 (6)
C10—C9—H9A	111.3	C29—C30—H30A	109.2
C8—C9—H9A	111.3	C31—C30—H30A	109.2
C10—C9—H9B	111.3	C29—C30—H30B	109.2
C8—C9—H9B	111.3	C31—C30—H30B	109.2
H9A—C9—H9B	109.2	H30A—C30—H30B	107.9
N3—C10—C11	120.4 (6)	N7—C31—C30	112.6 (7)
N3—C10—C9	115.6 (6)	N7—C31—H31A	109.1
C11—C10—C9	123.8 (6)	C30—C31—H31A	109.1
C12—C11—N4	110.1 (6)	N7—C31—H31B	109.1
C12—C11—C10	130.3 (6)	C30—C31—H31B	109.1
N4—C11—C10	119.3 (6)	H31A—C31—H31B	107.8
N6—C12—C11	103.9 (6)	C32—N8—C33	122.9 (9)
N6—C12—C13	124.6 (7)	C32—N8—C34	120.7 (10)
C11—C12—C13	131.6 (7)	C33—N8—C34	116.4 (12)
C12—C13—H13A	109.5	O1—C32—N8	123.0 (10)
C12—C13—H13B	109.5	O1—C32—H32	118.5
H13A—C13—H13B	109.5	N8—C32—H32	118.5

C7—N2—N3—C10	179.4 (6)	C9—C10—C11—N4	8.2 (10)
C8—N2—N3—C10	−11.2 (7)	N5—N6—C12—C11	0.3 (8)
C11—N4—N5—N6	0.6 (8)	C14—N6—C12—C11	−173.0 (8)
N4—N5—N6—C12	−0.6 (8)	N5—N6—C12—C13	178.3 (7)
N4—N5—N6—C14	173.7 (6)	C14—N6—C12—C13	5.0 (12)
C7—N1—C1—C2	2.2 (15)	N4—C11—C12—N6	0.1 (8)
C1'—N1—C1—C2	−110 (7)	C10—C11—C12—N6	173.6 (7)
C7—N1—C1—C6	179.2 (7)	N4—C11—C12—C13	−177.7 (7)
C1'—N1—C1—C6	67 (7)	C10—C11—C12—C13	−4.2 (13)
C6—C1—C2—C3	0.0	C12—N6—C14—C19	125.9 (8)
N1—C1—C2—C3	176.8 (13)	N5—N6—C14—C19	−47.1 (10)
C1—C2—C3—C4	0.0	C12—N6—C14—C15	−53.4 (11)
C2—C3—C4—C5	0.0	N5—N6—C14—C15	133.7 (7)
C3—C4—C5—C6	0.0	C19—C14—C15—C16	−0.5 (11)
C4—C5—C6—C1	0.0	N6—C14—C15—C16	178.7 (7)
C2—C1—C6—C5	0.0	C14—C15—C16—C17	1.8 (12)
N1—C1—C6—C5	−177.4 (11)	C15—C16—C17—C18	−2.1 (12)
C7—N1—C1'—C2'	41.5 (13)	C15—C16—C17—C20	179.8 (8)
C1—N1—C1'—C2'	114 (7)	C16—C17—C18—C19	1.1 (12)
C7—N1—C1'—C6'	−138.2 (8)	C20—C17—C18—C19	179.2 (8)
C1—N1—C1'—C6'	−66 (7)	C17—C18—C19—C14	0.1 (12)
C6'—C1'—C2'—C3'	0.0	C15—C14—C19—C18	−0.5 (11)
N1—C1'—C2'—C3'	−179.8 (11)	N6—C14—C19—C18	−179.7 (7)
C1'—C2'—C3'—C4'	0.0	N2—C8—C21—C26	−139.9 (7)
C2'—C3'—C4'—C5'	0.0	C9—C8—C21—C26	107.8 (8)
C3'—C4'—C5'—C6'	0.0	N2—C8—C21—C22	42.8 (10)
C4'—C5'—C6'—C1'	0.0	C9—C8—C21—C22	−69.5 (9)
C2'—C1'—C6'—C5'	0.0	C26—C21—C22—C23	1.3 (12)
N1—C1'—C6'—C5'	179.8 (11)	C8—C21—C22—C23	178.7 (7)
N3—N2—C7—N1	5.7 (9)	C21—C22—C23—C24	−0.4 (12)
C8—N2—C7—N1	−161.8 (6)	C22—C23—C24—C25	−1.2 (11)
N3—N2—C7—S1	−173.2 (4)	C22—C23—C24—N7	−179.6 (7)
C8—N2—C7—S1	19.2 (9)	C31—N7—C24—C25	24.7 (10)
C1—N1—C7—N2	−176.3 (9)	C27—N7—C24—C25	162.7 (7)
C1'—N1—C7—N2	−169.9 (9)	C31—N7—C24—C23	−156.9 (7)
C1—N1—C7—S1	2.6 (12)	C27—N7—C24—C23	−18.9 (10)
C1'—N1—C7—S1	8.9 (12)	C23—C24—C25—C26	1.8 (11)
C7—N2—C8—C21	64.7 (10)	N7—C24—C25—C26	−179.7 (7)
N3—N2—C8—C21	−103.4 (7)	C22—C21—C26—C25	−0.7 (11)
C7—N2—C8—C9	−175.3 (7)	C8—C21—C26—C25	−178.2 (7)
N3—N2—C8—C9	16.5 (7)	C24—C25—C26—C21	−0.9 (12)
N2—C8—C9—C10	−14.7 (7)	C24—N7—C27—C28	167.4 (6)
C21—C8—C9—C10	104.7 (7)	C31—N7—C27—C28	−53.1 (8)
N2—N3—C10—C11	−174.5 (6)	N7—C27—C28—C29	57.4 (8)
N2—N3—C10—C9	0.0 (8)	C27—C28—C29—C30	−58.0 (8)
C8—C9—C10—N3	10.2 (8)	C28—C29—C30—C31	55.9 (9)
C8—C9—C10—C11	−175.6 (6)	C24—N7—C31—C30	−170.6 (6)
N5—N4—C11—C12	−0.5 (8)	C27—N7—C31—C30	50.2 (8)
N5—N4—C11—C10	−174.8 (6)	C29—C30—C31—N7	−52.8 (9)
N3—C10—C11—C12	9.2 (11)	C33—N8—C32—O1	−0.1 (4)
C9—C10—C11—C12	−164.8 (7)	C34—N8—C32—O1	−179.8 (3)
N3—C10—C11—N4	−177.8 (7)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···N3	0.88	2.13	2.597 (8)	112
C13—H13A···O1	0.98	2.56	3.466 (14)	154
C28—H28B···N5ⁱ	0.99	2.57	3.355 (10)	137

Symmetry code: (i) x, y, z−1.

Experimental details

Crystal data
Chemical formula	C₃₁H₃₃N₇S·0.5C₃H₇NO
M_r	522.26
Crystal system, space group	Monoclinic, C2
Temperature (K)	100
a, b, c (Å)	42.077 (4), 5.9274 (5), 12.0737 (11)
β (°)	105.665 (9)
V (Å³)	2899.5 (4)
Z	4
Radiation type	Cu Kα
µ (mm⁻¹)	1.29
Crystal size (mm)	0.35 × 0.15 × 0.05

Data collection
Diffractometer	Agilent SuperNova Dual diffractometer with an Atlas detector
Absorption correction	Multi-scan (CrysAlis PRO; Agilent, 2012)
T_min, T_max	0.661, 0.938
No. of measured, independent and observed [I > 2σ(I)] reflections	10437, 3317, 3229
R_int	0.037
(sin θ/λ)_max (Å⁻¹)	0.632

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.091, 0.214, 1.11
No. of reflections	3317
No. of parameters	396
No. of restraints	41
H-atom treatment	H-atom parameters constrained
	w = 1/[σ²(F_o²) + (0.0422P)² + 29.4613P] where P = (F_o² + 2F_c²)/3
Δρ_max, Δρ_min (e Å⁻³)	0.71, −1.06

Computer programs: CrysAlis PRO (Agilent, 2012), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 2006), publCIF (Westrip, 2010).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···N3	0.88	2.13	2.597 (8)	112
C13—H13A···O1	0.98	2.56	3.466 (14)	154
C28—H28B···N5ⁱ	0.99	2.57	3.355 (10)	137

Symmetry code: (i) x, y, z−1.

Footnotes

‡Additional correspondence author, e-mail: bakrfatehy@yahoo.com.

Acknowledgements

We thank the Ministry of Higher Education (Malaysia) for funding structural studies through the High-Impact Research scheme (UM.C/HIR/MOHE/SC/12).

References

Abdel-Wahab, B. F., Abdel-Aziz, H. A. & Ahmed, E. M. (2009). Eur. J. Med. Chem. 44, 2632–2635. Web of Science PubMed CAS Google Scholar
Abdel-Wahab, B. F., Abdel-Latif, E., Mohamed, H. A. & Awad, G. E. A. (2012a). Eur. J. Med. Chem. 52, 263–268. Web of Science CAS PubMed Google Scholar
Abdel-Wahab, B. F., Abdel-Latif, E., Ng, S. W. & Tiekink, E. R. T. (2012b). Acta Cryst. E68, o1954-o1955. CSD CrossRef IUCr Journals Google Scholar
Agilent (2012). CrysAlis PRO. Agilent Technologies, Yarnton, England. Google Scholar
Brandenburg, K. (2006). DIAMOND. Crystal Impact GbR, Bonn, Germany. Google Scholar
Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565. CrossRef IUCr Journals Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Westrip, S. P. (2010). J. Appl. Cryst. 43, 920–925. Web of Science CrossRef CAS IUCr Journals Google Scholar

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3-[5-Methyl-1-(4-methyl­phen­yl)-1H-1,2,3-triazol-4-yl]-N-phenyl-5-[4-(piperidin-1-yl)phen­yl]-4,5-di­hydro-1H-pyrazole-1-carbo­thio­amide di­methyl­formamide hemisolvate

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Experimental

Crystal data

Data collection

Refinement

Supporting information

Footnotes

Acknowledgements

References

organic compounds

3-[5-Methyl-1-(4-methylphenyl)-1H-1,2,3-triazol-4-yl]-N-phenyl-5-[4-(piperidin-1-yl)phenyl]-4,5-dihydro-1H-pyrazole-1-carbothioamide dimethylformamide hemisolvate