3-(2-Benzamido­phen­yl)-4-(4-hydroxy­phen­yl)-5-methyl-4H-1,2,4-triazol-1-ium chloride

Arfan, M.; Tahir, M.N.; Khan, R.; Iqbal, M.S.

doi:10.1107/S160053680802148X

organic compounds

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ISSN: 2056-9890

Volume 64| Part 8| August 2008| Page o1505

doi:10.1107/S160053680802148X

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3-(2-Benzamidophenyl)-4-(4-hydroxyphenyl)-5-methyl-4H-1,2,4-triazol-1-ium chloride

Mohammad Arfan,^a M. Nawaz Tahir,^b ^* Rasool Khan ^a and Mohammad S. Iqbal ^c

^aInstitute of Chemical Sciences, University of Peshawar, Peshawar, Pakistan, ^bDepartment of Physics, University of Sargodha, Sargodha, Pakistan, and ^cDepartment of Chemistry, Government College University, Lahore, Pakistan
^*Correspondence e-mail: dmntahir_uos@yahoo.com

(Received 8 July 2008; accepted 10 July 2008; online 16 July 2008)

In the molecule of the title compound, C₂₂H₁₉N₄O₂⁺·Cl⁻, the 1,2,4-triazole ring is oriented at dihedral angles of 75.57 (14), 53.23 (13) and 68.11 (13)° with respect to the benzamide, aniline and phenol atomatic rings, respectively. An intramolecular C—H⋯O hydrogen bond results in the formation of a non-planar ten-membered ring. In the crystal structure, intermolecular O—H⋯Cl and N—H⋯Cl hydrogen bonds link the molecules. There is a C—H⋯π contact between the methyl group and the phenyl ring, and a π–π contact between the hydroxyphenyl and phenyl rings [centroid–centroid distance = 4.687 (2) Å].

Related literature

For general background, see: Caira et al. (2004 ); Peeters et al. (1996 ). For related literature, see: Potts (1961 ).

Experimental

Crystal data

C₂₂H₁₉N₄O₂⁺·Cl⁻
M_r = 406.86
Orthorhombic, P c a 2₁
a = 17.1336 (15) Å
b = 9.8967 (9) Å
c = 12.1910 (10) Å
V = 2067.2 (3) Å³
Z = 4
Mo Kα radiation
μ = 0.21 mm⁻¹
T = 296 (2) K
0.25 × 0.20 × 0.18 mm

Data collection

Bruker Kappa APEXII CCD diffractometer
Absorption correction: multi-scan (SADABS; Bruker, 2005 ) T_min = 0.950, T_max = 0.960
13329 measured reflections
2809 independent reflections
2480 reflections with I > 2σ(I)
R_int = 0.022

Refinement

R[F² > 2σ(F²)] = 0.034
wR(F²) = 0.097
S = 1.02
2809 reflections
272 parameters
1 restraint
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.20 e Å⁻³
Δρ_min = −0.21 e Å⁻³
Absolute structure: Flack (1983 ), with 1677 Friedel pairs
Flack parameter: 0.06 (7)

Table 1
Hydrogen-bond geometry (Å, °)

Cg2 is the centroid of the C1–C6 phenyl ring.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1⋯Clⁱ	0.81 (3)	2.58 (3)	3.372 (2)	166 (3)
O2—H2A⋯Clⁱⁱ	0.76 (4)	2.34 (4)	3.090 (2)	171 (5)
N3—H3A⋯Clⁱⁱⁱ	0.97 (3)	2.14 (3)	3.068 (2)	158 (3)
C18—H18⋯O1	0.93	2.35	3.165 (3)	146
C16—H16A⋯Cg2^iv	0.96	2.84	3.367 (3)	115
Symmetry codes: (i) $[-x, -y+1, z+{\script{1\over 2}}]$ ; (ii) x, y+1, z; (iii) $[-x+{\script{1\over 2}}, y, z+{\script{1\over 2}}]$ ; (iv) $[-x+{\script{1\over 2}}, y, z-{\script{1\over 2}}]$ .

Data collection: APEX2 (Bruker, 2007 ); cell refinement: APEX2; data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997 ) and PLATON (Spek, 2003 ); software used to prepare material for publication: WinGX (Farrugia, 1999 ) and PLATON.

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S160053680802148X/hk2490sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S160053680802148X/hk2490Isup2.hkl

checkCIF report

Comment top

1,2,4-Triazole is a basic aromatic heterocycle. Its derivatives, such as fluconazole (Caira et al., 2004) and itraconazole (Peeters et al., 1996), find use as antifungals and can be prepared using various routes including Einhorn-Brunner and Pellizzari reactions (Potts, 1961).

In the molecule of the title compound (Fig. 1) the bond lengths and angles are generally within normal ranges. Rings A (C1-C6), B (C8-C13), C (N2-N4/C14/C15) and D (C17-C22) are, of course, planar, and the dihedral angles between them are A/B = 66.39 (14)°, A/C = 75.57 (14)°, A/D = 39.96 (13)°, B/C = 53.23 (13)°, B/D = 78.57 (14)° and C/D = 68.11 (13)°. The intramolecular C-H···O hydrogen bond (Table 1) results in the formation of a non-planar ten-membered ring E (O1/N1/N4/C7/C8/C13/C14/C17/C18/H18).

In the crystal structure, intermolecular O-H···Cl and N-H···Cl hydrogen bonds (Table 1) link the molecules (Fig. 2), in which they may be effective in the stabilization of the structure. The C—H···π contact (Table 1) between the methyl group and the phenyl ring and π—π contact between the two phenyl rings Cg2···Cg4ⁱ [symmetry code: (i) -x, 2 - y, 1/2 + z, where Cg2 and Cg4 are centroids of the rings (C1-C6) and (C17-C22), respectively] further stabilize the structure, with centroid-centroid distance of 4.687 (2) Å.

Related literature top

For general background, see: Caira et al. (2004); Peeters et al. (1996). For related literature, see: Potts (1961). Cg2 is the centroid of the C1–C6 phenyl ring.

Experimental top

For the preparation of the title compound, N-[2-(hydrazinylcarbonyl)phenyl]- benzamide (0.25 g, 0.98 mmol) and triethyl orthoacetate (1 ml) were refluxed for 2 h. The reaction mixture was cooled to room temperature and 4-aminophenol (0.11 g, 0.98 mmol) was added. Acetic acid (1 ml) was added to the mixture and the contents were refluxed for 1 h. Then, the reaction mixture was added to HCl (8 M) solution. It was crystallized by adding dioxane portion-wise. The crystals were separated by filtration and washed with dioxane (yield; 77%, m.p. 498 K).

Computing details top

Data collection: APEX2 (Bruker, 2007); cell refinement: APEX2 (Bruker, 2007); data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997) and PLATON (Spek, 2003); software used to prepare material for publication: WinGX (Farrugia, 1999) and PLATON (Spek, 2003).

Figures top

	Fig. 1. The molecular structure of the title molecule, with the atom-numbering scheme. Displacement ellipsoids are drawn at the 30% probability level. Hydrogen bond is shown as dotted line.
	Fig. 2. A partial packing diagram of the title compound. Hydrogen bonds are shown as dashed lines.

3-(2-Benzamidophenyl)-4-(4-hydroxyphenyl)-5-methyl-4H-1,2,4- triazol-1-ium chloride top

Crystal data top

C₂₂H₁₉N₄O₂⁺·Cl⁻	F(000) = 848
M_r = 406.86	D_x = 1.307 Mg m⁻³
Orthorhombic, Pca2₁	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2c -2ac	Cell parameters from 2009 reflections
a = 17.1336 (15) Å	θ = 2.1–28.8°
b = 9.8967 (9) Å	µ = 0.21 mm⁻¹
c = 12.191 (1) Å	T = 296 K
V = 2067.2 (3) Å³	Prismatic, black
Z = 4	0.25 × 0.20 × 0.18 mm

Data collection top

Bruker Kappa APEXII CCD diffractometer	2809 independent reflections
Radiation source: fine-focus sealed tube	2480 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.022
Detector resolution: 7.40 pixels mm^-1	θ_max = 28.8°, θ_min = 2.1°
ω scans	h = −23→18
Absorption correction: multi-scan (SADABS; Bruker, 2005)	k = −13→10
T_min = 0.950, T_max = 0.960	l = −16→12
13329 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)] = 0.034	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.097	w = 1/[σ²(F_o²) + (0.0606P)² + 0.2556P] where P = (F_o² + 2F_c²)/3
S = 1.02	(Δ/σ)_max = 0.001
2809 reflections	Δρ_max = 0.20 e Å⁻³
272 parameters	Δρ_min = −0.21 e Å⁻³
1 restraint	Absolute structure: Flack (1983) with no Friedel pairs
Primary atom site location: structure-invariant direct methods	Absolute structure parameter: 0.06 (7)

Crystal data top

C₂₂H₁₉N₄O₂⁺·Cl⁻	V = 2067.2 (3) Å³
M_r = 406.86	Z = 4
Orthorhombic, Pca2₁	Mo Kα radiation
a = 17.1336 (15) Å	µ = 0.21 mm⁻¹
b = 9.8967 (9) Å	T = 296 K
c = 12.191 (1) Å	0.25 × 0.20 × 0.18 mm

Data collection top

Bruker Kappa APEXII CCD diffractometer	2809 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2005)	2480 reflections with I > 2σ(I)
T_min = 0.950, T_max = 0.960	R_int = 0.022
13329 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.034	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.097	Δρ_max = 0.20 e Å⁻³
S = 1.02	Δρ_min = −0.21 e Å⁻³
2809 reflections	Absolute structure: Flack (1983) with no Friedel pairs
272 parameters	Absolute structure parameter: 0.06 (7)
1 restraint

Special details top

Geometry. Bond distances, angles etc have been calculated using the rounded fractional coordinates. All su's are estimated from the variances of the (full) variance-covariance matrix. The cell e.s.d.'s are taken into account in the estimation of distances, angles and torsion angles

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 > 2sigma(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

	x	y	z	U_iso*/U_eq
Cl	0.18901 (3)	0.41678 (5)	0.23611 (6)	0.0441 (2)
O1	0.08185 (11)	0.8416 (2)	0.61956 (15)	0.0523 (6)
O2	0.23156 (16)	1.1272 (2)	0.1626 (2)	0.0698 (9)
N1	−0.02194 (12)	0.7017 (2)	0.62595 (16)	0.0396 (6)
N2	0.12701 (11)	0.54036 (19)	0.55257 (17)	0.0394 (5)
N3	0.20680 (12)	0.5419 (2)	0.55843 (18)	0.0410 (6)
N4	0.17842 (10)	0.69261 (19)	0.44104 (16)	0.0345 (5)
C1	0.02424 (13)	0.8077 (2)	0.79409 (19)	0.0364 (6)
C2	−0.01415 (15)	0.7183 (3)	0.8629 (2)	0.0451 (8)
C3	−0.02023 (18)	0.7468 (4)	0.9741 (2)	0.0583 (10)
C4	0.0117 (2)	0.8628 (3)	1.0166 (3)	0.0640 (10)
C5	0.0506 (2)	0.9501 (3)	0.9485 (3)	0.0648 (10)
C6	0.05751 (18)	0.9231 (3)	0.8372 (2)	0.0513 (8)
C7	0.03122 (13)	0.7860 (2)	0.6732 (2)	0.0364 (6)
C8	−0.03057 (13)	0.6865 (2)	0.51128 (19)	0.0357 (6)
C9	−0.10597 (14)	0.6966 (3)	0.4680 (2)	0.0477 (8)
C10	−0.11851 (17)	0.6838 (3)	0.3569 (3)	0.0580 (9)
C11	−0.05706 (19)	0.6642 (3)	0.2866 (2)	0.0590 (10)
C12	0.01801 (16)	0.6538 (3)	0.3276 (2)	0.0476 (8)
C13	0.03172 (13)	0.6628 (2)	0.44022 (18)	0.0352 (6)
C14	0.11081 (12)	0.6336 (2)	0.48077 (18)	0.0340 (6)
C15	0.23791 (13)	0.6310 (2)	0.4926 (2)	0.0391 (6)
C16	0.32228 (14)	0.6578 (3)	0.4792 (3)	0.0637 (10)
C17	0.18724 (12)	0.8055 (2)	0.36715 (19)	0.0348 (6)
C18	0.16505 (16)	0.9329 (2)	0.3999 (2)	0.0441 (7)
C19	0.17852 (16)	1.0418 (3)	0.3320 (2)	0.0497 (8)
C20	0.21503 (14)	1.0236 (2)	0.2313 (2)	0.0456 (7)
C21	0.2375 (2)	0.8955 (3)	0.2002 (2)	0.0612 (9)
C22	0.22377 (19)	0.7867 (3)	0.2674 (2)	0.0575 (9)
H1	−0.061 (2)	0.684 (3)	0.661 (3)	0.0628*
H2	−0.03578	0.63946	0.83474	0.0541*
H2A	0.220 (2)	1.195 (4)	0.187 (4)	0.0839*
H3	−0.04612	0.68676	1.02018	0.0700*
H3A	0.2334 (17)	0.480 (3)	0.608 (3)	0.0492*
H4	0.00691	0.88200	1.09092	0.0768*
H5	0.07271	1.02826	0.97730	0.0778*
H6	0.08444	0.98261	0.79188	0.0616*
H9	−0.14797	0.71205	0.51465	0.0573*
H10	−0.16905	0.68850	0.32930	0.0696*
H11	−0.06583	0.65794	0.21149	0.0710*
H12	0.05962	0.64081	0.27972	0.0571*
H16A	0.33112	0.75352	0.47749	0.0956*
H16B	0.35037	0.61882	0.53950	0.0956*
H16C	0.34011	0.61830	0.41172	0.0956*
H18	0.14104	0.94552	0.46751	0.0529*
H19	0.16312	1.12783	0.35368	0.0596*
H21	0.26212	0.88257	0.13302	0.0734*
H22	0.23907	0.70060	0.24582	0.0689*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl	0.0360 (2)	0.0416 (3)	0.0547 (3)	−0.0066 (2)	0.0002 (3)	0.0095 (3)
O1	0.0540 (10)	0.0641 (11)	0.0389 (9)	−0.0263 (9)	0.0049 (8)	−0.0019 (9)
O2	0.104 (2)	0.0464 (10)	0.0590 (13)	0.0042 (12)	0.0244 (13)	0.0210 (11)
N1	0.0295 (9)	0.0549 (12)	0.0343 (10)	−0.0086 (8)	0.0027 (7)	−0.0004 (9)
N2	0.0373 (9)	0.0381 (9)	0.0428 (10)	−0.0018 (8)	−0.0011 (8)	0.0070 (9)
N3	0.0360 (9)	0.0375 (9)	0.0494 (11)	0.0008 (8)	−0.0005 (9)	0.0105 (9)
N4	0.0345 (9)	0.0309 (9)	0.0382 (10)	0.0006 (7)	0.0047 (7)	0.0034 (7)
C1	0.0332 (10)	0.0399 (11)	0.0362 (11)	0.0028 (8)	−0.0017 (9)	0.0000 (9)
C2	0.0452 (13)	0.0516 (14)	0.0386 (12)	−0.0102 (10)	−0.0013 (10)	0.0019 (11)
C3	0.0594 (16)	0.075 (2)	0.0406 (13)	−0.0120 (14)	0.0071 (12)	0.0054 (14)
C4	0.083 (2)	0.0655 (18)	0.0435 (14)	0.0084 (16)	0.0101 (15)	−0.0096 (14)
C5	0.094 (2)	0.0415 (13)	0.0588 (18)	−0.0032 (14)	0.0028 (17)	−0.0158 (13)
C6	0.0678 (17)	0.0380 (12)	0.0481 (14)	−0.0035 (11)	0.0037 (13)	0.0006 (10)
C7	0.0334 (11)	0.0384 (11)	0.0373 (11)	−0.0034 (8)	−0.0004 (9)	0.0022 (9)
C8	0.0325 (10)	0.0392 (11)	0.0353 (10)	−0.0063 (8)	−0.0030 (8)	0.0015 (9)
C9	0.0326 (10)	0.0598 (15)	0.0508 (14)	−0.0082 (10)	−0.0051 (10)	0.0026 (12)
C10	0.0462 (14)	0.0737 (18)	0.0540 (16)	−0.0104 (13)	−0.0210 (13)	0.0084 (14)
C11	0.0653 (18)	0.075 (2)	0.0367 (13)	−0.0117 (15)	−0.0159 (12)	0.0048 (13)
C12	0.0534 (14)	0.0549 (14)	0.0346 (12)	−0.0025 (11)	−0.0022 (10)	0.0006 (11)
C13	0.0366 (10)	0.0353 (10)	0.0337 (10)	−0.0039 (8)	−0.0027 (8)	0.0040 (9)
C14	0.0359 (10)	0.0325 (10)	0.0336 (10)	−0.0028 (8)	0.0028 (8)	0.0009 (8)
C15	0.0369 (12)	0.0323 (9)	0.0482 (12)	0.0022 (8)	0.0032 (10)	0.0050 (10)
C16	0.0338 (13)	0.0642 (18)	0.093 (2)	0.0031 (11)	0.0058 (14)	0.0277 (18)
C17	0.0365 (10)	0.0309 (10)	0.0369 (10)	0.0006 (8)	0.0046 (9)	0.0054 (9)
C18	0.0518 (13)	0.0379 (12)	0.0425 (12)	0.0099 (10)	0.0153 (11)	0.0057 (10)
C19	0.0625 (16)	0.0339 (11)	0.0527 (14)	0.0139 (10)	0.0168 (13)	0.0069 (11)
C20	0.0533 (12)	0.0394 (11)	0.0440 (12)	0.0020 (9)	0.0076 (12)	0.0113 (11)
C21	0.091 (2)	0.0481 (14)	0.0446 (14)	0.0031 (14)	0.0306 (15)	0.0036 (11)
C22	0.086 (2)	0.0351 (12)	0.0515 (16)	0.0072 (12)	0.0283 (14)	0.0009 (10)

Geometric parameters (Å, º) top

O1—C7	1.218 (3)	C8—C9	1.399 (3)
O2—C20	1.354 (3)	C8—C13	1.395 (3)
O2—H2A	0.76 (4)	C9—C10	1.377 (4)
N1—C7	1.363 (3)	C9—H9	0.9300
N1—C8	1.414 (3)	C10—C11	1.371 (4)
N1—H1	0.81 (3)	C10—H10	0.9300
N2—N3	1.369 (3)	C11—C12	1.384 (4)
N2—C14	1.302 (3)	C11—H11	0.9300
N3—C15	1.306 (3)	C12—C13	1.396 (3)
N3—H3A	0.97 (3)	C12—H12	0.9300
N4—C14	1.385 (3)	C13—C14	1.471 (3)
N4—C15	1.344 (3)	C15—C16	1.479 (3)
N4—C17	1.443 (3)	C16—H16A	0.9600
C1—C2	1.385 (3)	C16—H16B	0.9600
C1—C6	1.380 (4)	C16—H16C	0.9600
C1—C7	1.494 (3)	C17—C18	1.376 (3)
C2—C3	1.389 (4)	C17—C22	1.380 (3)
C2—H2	0.9300	C18—C19	1.378 (4)
C3—C4	1.373 (5)	C18—H18	0.9300
C3—H3	0.9300	C19—C20	1.390 (3)
C4—C5	1.371 (5)	C19—H19	0.9300
C4—H4	0.9300	C20—C21	1.378 (4)
C5—C6	1.388 (4)	C21—C22	1.373 (4)
C5—H5	0.9300	C21—H21	0.9300
C6—H6	0.9300	C22—H22	0.9300

Cl···O2ⁱ	3.090 (2)	C21···O1ⁱⁱⁱ	3.291 (4)
Cl···N1ⁱⁱ	3.372 (2)	C22···C16	3.338 (4)
Cl···C2ⁱⁱ	3.627 (3)	C2···H19^ix	2.9700
Cl···N3ⁱⁱⁱ	3.068 (2)	C2···H1	2.61 (4)
Cl···H2ⁱⁱ	2.9400	C4···H16A^v	2.9400
Cl···H9ⁱⁱ	3.0700	C5···H16A^v	2.8300
Cl···H1ⁱⁱ	2.58 (3)	C6···H16A^v	3.0600
Cl···H22	2.9400	C8···H5^vii	2.9400
Cl···H10^iv	2.8800	C9···H5^vii	2.7800
Cl···H2Aⁱ	2.34 (4)	C12···H2ⁱⁱ	2.9200
Cl···H3Aⁱⁱⁱ	2.14 (3)	C15···H21^v	3.0200
O1···N4	3.106 (3)	C15···H22	3.0900
O1···N2	3.187 (3)	C17···H16A	2.8600
O1···C18	3.165 (3)	C17···H12	2.9300
O1···C13	2.941 (3)	H1···H9	2.3400
O1···C14	2.710 (3)	H1···C2	2.61 (4)
O1···C21^v	3.291 (4)	H1···Cl^viii	2.58 (3)
O2···Cl^vi	3.090 (2)	H1···H2	2.2100
O1···H6	2.5200	H2···N1	2.6300
O1···H18	2.3500	H2···H1	2.2100
O1···H21^v	2.7100	H2···C12^viii	2.9200
O2···H9^vii	2.8000	H2···Cl^viii	2.9400
N1···Cl^viii	3.372 (2)	H2A···H19	2.3500
N1···N2	3.141 (3)	H2A···Cl^vi	2.34 (4)
N2···C7	3.281 (3)	H3···H11^x	2.3700
N2···N4	2.212 (3)	H3···N2^viii	2.6700
N2···O1	3.187 (3)	H3A···H16B	2.5700
N2···N1	3.141 (3)	H3A···Cl^v	2.14 (3)
N3···Cl^v	3.068 (2)	H5···C9^ix	2.7800
N3···N4	2.124 (3)	H5···C8^ix	2.9400
N4···N3	2.124 (3)	H6···O1	2.5200
N4···O1	3.106 (3)	H9···Cl^viii	3.0700
N1···H2	2.6300	H9···O2^ix	2.8000
N2···H3ⁱⁱ	2.6700	H9···H1	2.3400
N3···H22^v	2.9200	H10···Cl^xi	2.8800
N4···H12	2.8800	H11···H3^xii	2.3700
C2···Cl^viii	3.627 (3)	H12···N4	2.8800
C3···C16^v	3.505 (4)	H12···C17	2.9300
C4···C16^v	3.524 (4)	H16A···C4ⁱⁱⁱ	2.9400
C7···N2	3.281 (3)	H16A···C17	2.8600
C7···C14	3.105 (3)	H16A···C5ⁱⁱⁱ	2.8300
C12···C17	3.301 (3)	H16A···C6ⁱⁱⁱ	3.0600
C13···O1	2.941 (3)	H16B···H3A	2.5700
C13···C18	3.550 (3)	H18···O1	2.3500
C14···O1	2.710 (3)	H19···C2^vii	2.9700
C14···C7	3.105 (3)	H19···H2A	2.3500
C16···C22	3.338 (4)	H21···C15ⁱⁱⁱ	3.0200
C16···C4ⁱⁱⁱ	3.524 (4)	H21···O1ⁱⁱⁱ	2.7100
C16···C3ⁱⁱⁱ	3.505 (4)	H22···C15	3.0900
C17···C12	3.301 (3)	H22···N3ⁱⁱⁱ	2.9200
C18···C13	3.550 (3)	H22···Cl	2.9400
C18···O1	3.165 (3)

C20—O2—H2A	112 (3)	N4—C17—C18	120.0 (2)
C7—N1—C8	123.6 (2)	C17—C18—C19	119.7 (2)
N3—N2—C14	103.89 (18)	C18—C19—C20	120.3 (2)
N2—N3—C15	112.5 (2)	O2—C20—C19	122.9 (2)
C14—N4—C15	106.23 (18)	C19—C20—C21	119.2 (2)
C14—N4—C17	129.23 (18)	O2—C20—C21	117.9 (2)
C15—N4—C17	124.32 (18)	C20—C21—C22	120.6 (2)
C8—N1—H1	114 (3)	C17—C22—C21	119.8 (3)
C7—N1—H1	117 (2)	C1—C2—H2	120.00
N2—N3—H3A	119.5 (18)	C3—C2—H2	120.00
C15—N3—H3A	128.0 (18)	C2—C3—H3	120.00
C2—C1—C6	119.6 (2)	C4—C3—H3	120.00
C2—C1—C7	122.9 (2)	C3—C4—H4	120.00
C6—C1—C7	117.5 (2)	C5—C4—H4	120.00
C1—C2—C3	119.8 (3)	C4—C5—H5	120.00
C2—C3—C4	120.6 (3)	C6—C5—H5	120.00
C3—C4—C5	119.5 (3)	C1—C6—H6	120.00
C4—C5—C6	120.8 (3)	C5—C6—H6	120.00
C1—C6—C5	119.8 (3)	C8—C9—H9	120.00
N1—C7—C1	116.83 (19)	C10—C9—H9	120.00
O1—C7—N1	121.7 (2)	C9—C10—H10	120.00
O1—C7—C1	121.5 (2)	C11—C10—H10	120.00
C9—C8—C13	119.0 (2)	C10—C11—H11	120.00
N1—C8—C13	123.5 (2)	C12—C11—H11	120.00
N1—C8—C9	117.5 (2)	C11—C12—H12	120.00
C8—C9—C10	120.6 (2)	C13—C12—H12	120.00
C9—C10—C11	120.5 (3)	C15—C16—H16A	109.00
C10—C11—C12	119.9 (2)	C15—C16—H16B	109.00
C11—C12—C13	120.5 (2)	C15—C16—H16C	109.00
C12—C13—C14	118.2 (2)	H16A—C16—H16B	110.00
C8—C13—C12	119.5 (2)	H16A—C16—H16C	109.00
C8—C13—C14	122.0 (2)	H16B—C16—H16C	109.00
N2—C14—N4	110.84 (18)	C17—C18—H18	120.00
N2—C14—C13	124.17 (19)	C19—C18—H18	120.00
N4—C14—C13	124.76 (19)	C18—C19—H19	120.00
N3—C15—N4	106.5 (2)	C20—C19—H19	120.00
N4—C15—C16	127.5 (2)	C20—C21—H21	120.00
N3—C15—C16	126.0 (2)	C22—C21—H21	120.00
N4—C17—C22	119.5 (2)	C17—C22—H22	120.00
C18—C17—C22	120.3 (2)	C21—C22—H22	120.00

C8—N1—C7—O1	−9.5 (3)	C1—C2—C3—C4	−0.2 (4)
C8—N1—C7—C1	170.21 (19)	C2—C3—C4—C5	−0.7 (5)
C7—N1—C8—C9	−130.2 (2)	C3—C4—C5—C6	0.5 (5)
C7—N1—C8—C13	49.5 (3)	C4—C5—C6—C1	0.6 (5)
C14—N2—N3—C15	−0.6 (3)	N1—C8—C9—C10	179.5 (2)
N3—N2—C14—N4	0.5 (2)	C13—C8—C9—C10	−0.2 (4)
N3—N2—C14—C13	175.2 (2)	N1—C8—C13—C12	−177.8 (2)
N2—N3—C15—N4	0.4 (3)	N1—C8—C13—C14	8.3 (3)
N2—N3—C15—C16	−179.9 (2)	C9—C8—C13—C12	1.9 (3)
C15—N4—C14—N2	−0.2 (2)	C9—C8—C13—C14	−172.0 (2)
C15—N4—C14—C13	−174.9 (2)	C8—C9—C10—C11	−1.6 (4)
C17—N4—C14—N2	−175.0 (2)	C9—C10—C11—C12	1.6 (5)
C17—N4—C14—C13	10.4 (3)	C10—C11—C12—C13	0.2 (4)
C14—N4—C15—N3	−0.1 (2)	C11—C12—C13—C8	−1.9 (4)
C14—N4—C15—C16	−179.8 (2)	C11—C12—C13—C14	172.2 (2)
C17—N4—C15—N3	175.0 (2)	C8—C13—C14—N2	52.0 (3)
C17—N4—C15—C16	−4.7 (4)	C8—C13—C14—N4	−134.1 (2)
C14—N4—C17—C18	67.0 (3)	C12—C13—C14—N2	−122.0 (3)
C14—N4—C17—C22	−118.2 (3)	C12—C13—C14—N4	52.0 (3)
C15—N4—C17—C18	−106.9 (3)	N4—C17—C18—C19	175.6 (2)
C15—N4—C17—C22	67.8 (3)	C22—C17—C18—C19	0.9 (4)
C6—C1—C2—C3	1.3 (4)	N4—C17—C22—C21	−175.2 (3)
C7—C1—C2—C3	−178.2 (2)	C18—C17—C22—C21	−0.5 (4)
C2—C1—C6—C5	−1.5 (4)	C17—C18—C19—C20	−0.6 (4)
C7—C1—C6—C5	178.0 (3)	C18—C19—C20—O2	−178.2 (3)
C2—C1—C7—O1	−159.0 (2)	C18—C19—C20—C21	0.1 (4)
C2—C1—C7—N1	21.3 (3)	O2—C20—C21—C22	178.7 (3)
C6—C1—C7—O1	21.5 (3)	C19—C20—C21—C22	0.3 (4)
C6—C1—C7—N1	−158.2 (2)	C20—C21—C22—C17	−0.1 (5)

Symmetry codes: (i) x, y−1, z; (ii) −x, −y+1, z−1/2; (iii) −x+1/2, y, z−1/2; (iv) x+1/2, −y+1, z; (v) −x+1/2, y, z+1/2; (vi) x, y+1, z; (vii) −x, −y+2, z−1/2; (viii) −x, −y+1, z+1/2; (ix) −x, −y+2, z+1/2; (x) x, y, z+1; (xi) x−1/2, −y+1, z; (xii) x, y, z−1.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···Cl^viii	0.81 (3)	2.58 (3)	3.372 (2)	166 (3)
O2—H2A···Cl^vi	0.76 (4)	2.34 (4)	3.090 (2)	171 (5)
N3—H3A···Cl^v	0.97 (3)	2.14 (3)	3.068 (2)	158 (3)
C18—H18···O1	0.9300	2.3500	3.165 (3)	146.00
C16—H16A···Cg2ⁱⁱⁱ	0.9600	2.8400	3.367 (3)	115.00

Symmetry codes: (iii) −x+1/2, y, z−1/2; (v) −x+1/2, y, z+1/2; (vi) x, y+1, z; (viii) −x, −y+1, z+1/2.

Experimental details

Crystal data
Chemical formula	C₂₂H₁₉N₄O₂⁺·Cl⁻
M_r	406.86
Crystal system, space group	Orthorhombic, Pca2₁
Temperature (K)	296
a, b, c (Å)	17.1336 (15), 9.8967 (9), 12.191 (1)
V (Å³)	2067.2 (3)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.21
Crystal size (mm)	0.25 × 0.20 × 0.18

Data collection
Diffractometer	Bruker Kappa APEXII CCD diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2005)
T_min, T_max	0.950, 0.960
No. of measured, independent and observed [I > 2σ(I)] reflections	13329, 2809, 2480
R_int	0.022
(sin θ/λ)_max (Å⁻¹)	0.678

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.034, 0.097, 1.02
No. of reflections	2809
No. of parameters	272
No. of restraints	1
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.20, −0.21
Absolute structure	Flack (1983) with no Friedel pairs
Absolute structure parameter	0.06 (7)

Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997) and PLATON (Spek, 2003), WinGX (Farrugia, 1999) and PLATON (Spek, 2003).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···Clⁱ	0.81 (3)	2.58 (3)	3.372 (2)	166 (3)
O2—H2A···Clⁱⁱ	0.76 (4)	2.34 (4)	3.090 (2)	171 (5)
N3—H3A···Clⁱⁱⁱ	0.97 (3)	2.14 (3)	3.068 (2)	158 (3)
C18—H18···O1	0.9300	2.3500	3.165 (3)	146.00
C16—H16A···Cg2^iv	0.9600	2.8400	3.367 (3)	115.00

Symmetry codes: (i) −x, −y+1, z+1/2; (ii) x, y+1, z; (iii) −x+1/2, y, z+1/2; (iv) −x+1/2, y, z−1/2.

Acknowledgements

The authors acknowledge the Higher Education Commission, Islamabad, Pakistan, for funding the purchase of the diffractometer at GCU, Lahore.

References

Bruker (2005). SADABS. Bruker AXS Inc. Madison, Wisconsin, USA. Google Scholar
Bruker (2007). APEX2 and SAINT. Bruker AXS Inc. Madison, Wisconsin, USA. Google Scholar
Caira, M. R., Alkhamis, K. A. & Obaidat, R. M. (2004). J. Pharm. Sci. 93, 601–611. Web of Science CSD CrossRef PubMed CAS Google Scholar
Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565. CrossRef IUCr Journals Google Scholar
Farrugia, L. J. (1999). J. Appl. Cryst. 32, 837–838. CrossRef CAS IUCr Journals Google Scholar
Flack, H. D. (1983). Acta Cryst. A39, 876–881. CrossRef CAS Web of Science IUCr Journals Google Scholar
Peeters, O. M., Blaton, N. M. & De Ranter, C. J. (1996). Acta Cryst. C52, 2225–2229. CSD CrossRef CAS Web of Science IUCr Journals Google Scholar
Potts, K. T. (1961). Chem. Rev. 61, 87–127. CrossRef CAS Web of Science Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Spek, A. L. (2003). J. Appl. Cryst. 36, 7–13. Web of Science CrossRef CAS IUCr Journals Google Scholar

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Volume 64| Part 8| August 2008| Page o1505

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

3-(2-Benzamido­phen­yl)-4-(4-hy­droxy­phen­yl)-5-methyl-4H-1,2,4-triazol-1-ium chloride

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Experimental

Crystal data

Data collection

Refinement

Supporting information

Acknowledgements

References

organic compounds

3-(2-Benzamidophenyl)-4-(4-hydroxyphenyl)-5-methyl-4H-1,2,4-triazol-1-ium chloride