Crystal structure of 4,5-bis­(3,4,5-tri­meth­oxy­phen­yl)-2H-1,2,3-triazole methanol monosolvate

Madadi, N.R.; Penthala, N.R.; Bommagani, S.; Parkin, S.; Crooks, P.A.

doi:10.1107/S1600536814020911

organic compounds

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ISSN: 2056-9890

Volume 70| Part 10| October 2014| Pages o1128-o1129

doi:10.1107/S1600536814020911

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Crystal structure of 4,5-bis(3,4,5-trimethoxyphenyl)-2H-1,2,3-triazole methanol monosolvate

Nikhil Reddy Madadi,^a Narsimha Reddy Penthala,^a Shobanbabu Bommagani,^a Sean Parkin ^b and Peter A. Crooks ^a ^*

^aDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock AR 72205, USA, and ^bDepartment of Chemistry, University of Kentucky, Lexington KY 40506, USA
^*Correspondence e-mail: pacrooks@uams.edu

Edited by J. Simpson, University of Otago, New Zealand (Received 17 September 2014; accepted 18 September 2014; online 24 September 2014)

The title compound, C₂₀H₂₃N₃O₆·CH₃OH, was synthesized by [3 + 2] cycloaddition of (Z)-2,3-bis(3,4,5-trimethoxyphenyl)acrylonitrile with sodium azide and ammonium chloride in DMF/water. The central nitrogen of the triazole ring is protonated. The dihedral angles between the triazole ring and the 3,4,5-trimethoxyphenyl ring planes are 34.31 (4) and 45.03 (5)°, while that between the 3,4,5-trimethoxyphenyl rings is 51.87 (5)°. In the crystal, the molecules, along with two methanol solvent molecules are linked into an R⁴₄(10) centrosymmetric dimer by N—H⋯O and O—H⋯N hydrogen bonds.

Keywords: crystal structure; hydrogen bonds; 1,2,3-triazole.

CCDC reference: 1025101

1. Related literature

The synthetic procedure has been described by Madadi et al. (2014 ) and by Penthala et al. (2014 ). For structure-related activity, see: Young & Chaplin (2004 ); Pettit et al. (1995 ); Hsieh et al. (2005 ); Carr et al. (2010 ); Banimustafa et al. (2013 ); Demchuk et al. (2014 ).

2. Experimental

2.1. Crystal data

C₂₀H₂₃N₃O₆·CH₄O
M_r = 433.45
Triclinic, $[P \overline 1]$
a = 10.1458 (1) Å
b = 10.6090 (1) Å
c = 11.0435 (2) Å
α = 89.5708 (6)°
β = 72.5903 (6)°
γ = 70.7146 (7)°
V = 1065.07 (2) Å³
Z = 2
Mo Kα radiation
μ = 0.10 mm⁻¹
T = 90 K
0.24 × 0.22 × 0.20 mm

2.2. Data collection

Nonius KappaCCD diffractometer
Absorption correction: multi-scan (SADABS; Sheldrick, 2008a ) T_min = 0.882, T_max = 0.970
28813 measured reflections
4887 independent reflections
3960 reflections with I > 2σ(I)
R_int = 0.037

2.3. Refinement

R[F² > 2σ(F²)] = 0.045
wR(F²) = 0.127
S = 1.05
4887 reflections
291 parameters
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.28 e Å⁻³
Δρ_min = −0.30 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N2—H2N⋯O1M	0.936 (17)	1.797 (18)	2.7303 (15)	174.2 (16)
O1M—H1M⋯N3ⁱ	0.84	1.97	2.8101 (15)	177
Symmetry code: (i) -x+2, -y+1, -z+1.

Data collection: COLLECT (Nonius, 1998 ); cell refinement: SCALEPACK (Otwinowski & Minor, 2006 ); data reduction: DENZO-SMN (Otwinowski & Minor, 2006); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008b ); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2008b); molecular graphics: XP in SHELXTL (Sheldrick, 2008b); software used to prepare material for publication: SHELX (Sheldrick, 2008b).

Supporting information

CCDC reference: 1025101

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536814020911/sj5427sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536814020911/sj5427Isup2.hkl

Supporting information file. DOI: 10.1107/S1600536814020911/sj5427Isup3.cml

checkCIF report

Comment top

Antimitotic agents are a major class of anticancer drugs that target the microtubules. There are three major binding sites on tubulin, namely the colchicine, taxane and vinca domains. Lately, anti-mitotic agents such as combretastatin A-4 that bind to the colchicine binding site are receiving much attention due to their potent anticancer and antiangiogenic properties. Combretastatin A-4 is a cis configured natural product extracted from the South African willow tree combretum caffrum (Pettit et al., 1995). Its phosphate prodrug (CA-4P) is currently in phase 3 clinical trials for anaplastic thyroid cancer, and it has successfully arrested tumor growth in a wide spectrum of tumor models (Young and Chaplin, 2004). However, recent studies have reported the chemical instability of CA-4 due to cis-trans isomerization to the more thermodynamically stable, but less potent, trans-CA-4 isomer (Hsieh et al., 2005). Recently, much research has been conducted to stabilize the cis configuration by replacing the ethylene bridge with heterocyclic ring systems, including thiazoles, tetrazoles, imidazoles, pyrazoles, oxazolones, triazoles, and furanones (Carr et al., 2010; Banimustafa et al., 2013; Demchuk et al., 2014). One approach we are exploring is the replacement of the ethylene bridge in the cis stilbene scaffold with a triazole moiety to produce geometrically stable triazole analogs of CA4 with improved water solubility.

The title compound structure determination was performed to determine unequivocally the position of the hydrogen atom on the triazole ring system, which cannot be easily determined by NMR spectroscopy, and to obtain detailed information on the structural conformation of the molecule that may be useful in structure-activity relationship (SAR) analysis. The title compound was synthesized in two steps as described by Madadi et al., 2014 and Penthala et al., 2014).

In the first step, (Z)-2,3-bis(3,4,5-trimethoxyphenyl)acrylonitrile was synthesized by reacting 2-(3,4,5-trimethoxyphenyl)acetonitrile with 3,4,5-trimethoxybenzaldehyde in 5% NaOMe in methanol to afford the product in 85% yield. In the second step 4,5-bis(3,4,5-trimethoxyphenyl)-2H-1,2,3- triazole was synthesized by refluxing a mixture of (Z)-2,3-bis(3,4,5-trimethoxyphenyl)acrylonitrile, sodium azide and ammonium chloride in a DMF/water mixture to afford the desired product in 64% yield. The crystal structure of the compound indicates the presence of a 2H nitrogen on the triazole ring, i.e. protonation of the middle N atom. The molecules, along with two methanol solvent molecules, are linked into an R⁴₄(10) centrosymmetric dimer by N—H···O and O—H···N intermolecular hydrogen bonds. The dihedral angles between the triazole ring and the two 3,4,5-trimethoxyphenyl ring planes are 34.31 (4)° and 45.03 (5)°, while that between the two 3,4,5-trimethoxyphenyl rings is 51.87 (5)°.

Related literature top

The synthetic procedure has been described by Madadi et al. (2014) and by Penthala et al. (2014). For structure-related activity, see: Young & Chaplin (2004); Pettit et al. (1995); Hsieh et al. (2005); Carr et al. (2010); Banimustafa et al. (2013); Demchuk et al. (2014).

Experimental top

A mixture of (Z)-2,3-bis(3,4,5-trimethoxyphenyl)acrylonitrile, sodium azide and ammonium chloride in a mole ratio of 1:3:3, respectively, was refluxed in 10% aqueous DMF for 5 hrs. The reaction was monitored by TLC. When the (Z)-2,3-bis(3,4,5-trimethoxyphenyl)-acrylonitrile strating material had completely disappeared, cold water was added and the mixture was stirred over 10–15 min, during which the final product precipitated out. The product was purified by flash column chromatography utilizing ethyl acetate/methanol to afford 4,5-bis(3,4,5-trimethoxyphenyl)-2H-1,2,3-triazole in 64% yield. Crystallization from methanol afforded a white crystalline product: 4,5-bis(3,4,5-trimethoxyphenyl)-2H-1,2,3-triazole methanolate, which was suitable for X-ray crystallographic analysis.

¹H NMR (400 MHz, CDCl₃-d): δ 3.93 (s, 3H, –OCH3), 6.87 (d, J = 8 Hz, 1H, ArH), 7.05 (d, J = 12 Hz, 2H, ArH),), 7.42 (s, 2H, ArH), 7.78 (s, 1H, ArH) p.p.m. ¹³C NMR (400 MHz,CDCl₃-d): δ 55.87, 55.96, 111.05, 127.31, 129.80, 129.89, 130.54, 132.60, 132.86, 149.15, 149.54 p.p.m. HRMS (ESI): m/z calcd for C₂₀H₂₃N₃O₆ [M—H] 350.0463; found 350.0480.

Computing details top

Data collection: COLLECT (Nonius, 1998); cell refinement: SCALEPACK (Otwinowski & Minor, 2006); data reduction: DENZO-SMN (Otwinowski & Minor, 2006); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008b); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2008b); molecular graphics: XP in SHELXTL (Sheldrick, 2008b); software used to prepare material for publication: SHELX (Sheldrick, 2008b).

Figures top

Fig. 1. A view of the asymmetric unit of the structure with the atom numbering scheme. Displacement ellipsoids are drawn at the 50% probability level and a hydrogen bond is drawn as a dashed line.

4,5-Bis(3,4,5-trimethoxyphenyl)-2H-1,2,3-triazole methanol monosolvate top

Crystal data top

C₂₀H₂₃N₃O₆·CH₄O	Z = 2
M_r = 433.45	F(000) = 460
Triclinic, P1	D_x = 1.352 Mg m⁻³
a = 10.1458 (1) Å	Mo Kα radiation, λ = 0.71073 Å
b = 10.6090 (1) Å	Cell parameters from 11695 reflections
c = 11.0435 (2) Å	θ = 1.0–27.5°
α = 89.5708 (6)°	µ = 0.10 mm⁻¹
β = 72.5903 (6)°	T = 90 K
γ = 70.7146 (7)°	Block, colourless
V = 1065.07 (2) Å³	0.24 × 0.22 × 0.20 mm

Data collection top

Nonius KappaCCD diffractometer	4887 independent reflections
Radiation source: fine-focus sealed-tube	3960 reflections with I > 2σ(I)
Detector resolution: 9.1 pixels mm^-1	R_int = 0.037
ϕ and ω scans at fixed χ = 55°	θ_max = 27.5°, θ_min = 1.9°
Absorption correction: multi-scan (SADABS; Sheldrick, 2008a)	h = −13→13
T_min = 0.882, T_max = 0.970	k = −13→13
28813 measured reflections	l = −14→14

Refinement top

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)] = 0.045	Hydrogen site location: difference Fourier map
wR(F²) = 0.127	H atoms treated by a mixture of independent and constrained refinement
S = 1.05	w = 1/[σ²(F_o²) + (0.0731P)² + 0.3615P] where P = (F_o² + 2F_c²)/3
4887 reflections	(Δ/σ)_max < 0.001
291 parameters	Δρ_max = 0.28 e Å⁻³
0 restraints	Δρ_min = −0.30 e Å⁻³

Crystal data top

C₂₀H₂₃N₃O₆·CH₄O	γ = 70.7146 (7)°
M_r = 433.45	V = 1065.07 (2) Å³
Triclinic, P1	Z = 2
a = 10.1458 (1) Å	Mo Kα radiation
b = 10.6090 (1) Å	µ = 0.10 mm⁻¹
c = 11.0435 (2) Å	T = 90 K
α = 89.5708 (6)°	0.24 × 0.22 × 0.20 mm
β = 72.5903 (6)°

Data collection top

Nonius KappaCCD diffractometer	4887 independent reflections
Absorption correction: multi-scan (SADABS; Sheldrick, 2008a)	3960 reflections with I > 2σ(I)
T_min = 0.882, T_max = 0.970	R_int = 0.037
28813 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.045	0 restraints
wR(F²) = 0.127	H atoms treated by a mixture of independent and constrained refinement
S = 1.05	Δρ_max = 0.28 e Å⁻³
4887 reflections	Δρ_min = −0.30 e Å⁻³
291 parameters

Special details top

Experimental. The crystal was mounted with polyisobutene oil on the tip of a fine glass fibre, fastened in a copper mounting pin with electrical solder. It was placed directly into the cold stream of a liquid nitrogen based cryostat.

Diffraction data were collected with the crystal at 90 K, which is standard practice in this laboratory for the majority of flash-cooled crystals.

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
N1	0.60782 (12)	0.74167 (11)	0.56615 (11)	0.0185 (2)
N2	0.73493 (13)	0.64285 (12)	0.54691 (11)	0.0195 (3)
H2N	0.8264 (19)	0.6486 (17)	0.5010 (16)	0.023*
N3	0.72437 (12)	0.53382 (11)	0.60414 (11)	0.0182 (2)
O1	0.10274 (10)	1.12766 (9)	0.78293 (10)	0.0199 (2)
O2	−0.09566 (10)	1.00928 (10)	0.79884 (9)	0.0203 (2)
O3	−0.01750 (10)	0.74272 (10)	0.76182 (10)	0.0212 (2)
O4	0.55195 (11)	0.11586 (9)	0.76505 (9)	0.0200 (2)
O5	0.35131 (11)	0.22077 (10)	0.98936 (9)	0.0226 (2)
O6	0.26188 (10)	0.48551 (10)	1.06686 (9)	0.0203 (2)
C1	0.34889 (14)	0.77606 (13)	0.68391 (12)	0.0156 (3)
C2	0.30637 (14)	0.91466 (13)	0.71055 (12)	0.0161 (3)
H2	0.3785	0.9560	0.7006	0.019*
C3	0.15713 (14)	0.99221 (13)	0.75193 (12)	0.0160 (3)
C4	0.05096 (14)	0.93156 (13)	0.76591 (12)	0.0162 (3)
C5	0.09440 (14)	0.79251 (14)	0.74196 (12)	0.0171 (3)
C6	0.24333 (14)	0.71422 (14)	0.69882 (13)	0.0177 (3)
H6	0.2728	0.6199	0.6798	0.021*
C7	0.50685 (14)	0.69379 (13)	0.64045 (12)	0.0162 (3)
C8	0.57985 (14)	0.56334 (13)	0.66514 (12)	0.0159 (3)
C9	0.52294 (14)	0.47110 (13)	0.74808 (13)	0.0162 (3)
C10	0.56894 (14)	0.33457 (13)	0.70935 (13)	0.0167 (3)
H10	0.6368	0.2988	0.6270	0.020*
C11	0.51433 (14)	0.25086 (13)	0.79276 (13)	0.0161 (3)
C12	0.41268 (14)	0.30331 (14)	0.91361 (13)	0.0172 (3)
C13	0.36502 (14)	0.44122 (14)	0.94987 (12)	0.0165 (3)
C14	0.42169 (14)	0.52434 (14)	0.86842 (13)	0.0170 (3)
H14	0.3916	0.6173	0.8946	0.020*
C15	0.20801 (16)	1.19411 (14)	0.76486 (15)	0.0231 (3)
H15A	0.2708	1.1587	0.8184	0.035*
H15B	0.1565	1.2907	0.7887	0.035*
H15C	0.2688	1.1785	0.6751	0.035*
C16	−0.17239 (16)	1.02141 (16)	0.93261 (14)	0.0265 (3)
H16A	−0.1634	0.9319	0.9605	0.040*
H16B	−0.2765	1.0745	0.9489	0.040*
H16C	−0.1297	1.0661	0.9799	0.040*
C17	0.02045 (17)	0.60063 (15)	0.75393 (16)	0.0279 (3)
H17A	0.0798	0.5621	0.6663	0.042*
H17B	−0.0694	0.5778	0.7781	0.042*
H17C	0.0771	0.5642	0.8119	0.042*
C18	0.64600 (16)	0.06014 (15)	0.63927 (14)	0.0242 (3)
H18A	0.6015	0.1072	0.5768	0.036*
H18B	0.6593	−0.0354	0.6287	0.036*
H18C	0.7417	0.0703	0.6259	0.036*
C19	0.38996 (17)	0.19362 (16)	1.10416 (14)	0.0247 (3)
H19A	0.4925	0.1338	1.0826	0.037*
H19B	0.3256	0.1506	1.1593	0.037*
H19C	0.3781	0.2780	1.1489	0.037*
C20	0.19984 (16)	0.62778 (14)	1.10034 (13)	0.0220 (3)
H20A	0.2772	0.6621	1.1044	0.033*
H20B	0.1235	0.6476	1.1837	0.033*
H20C	0.1564	0.6709	1.0358	0.033*
O1M	1.00187 (11)	0.66705 (10)	0.42773 (10)	0.0244 (2)
H1M	1.0849	0.6076	0.4149	0.037*
C1M	1.01117 (17)	0.79571 (15)	0.45053 (15)	0.0269 (3)
H1M1	0.9119	0.8626	0.4814	0.040*
H1M2	1.0672	0.8206	0.3710	0.040*
H1M3	1.0608	0.7922	0.5148	0.040*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
N1	0.0160 (5)	0.0170 (6)	0.0195 (6)	−0.0042 (4)	−0.0029 (4)	0.0023 (5)
N2	0.0155 (5)	0.0163 (6)	0.0228 (6)	−0.0052 (4)	−0.0011 (5)	0.0035 (5)
N3	0.0172 (5)	0.0164 (6)	0.0194 (6)	−0.0070 (4)	−0.0022 (4)	0.0033 (4)
O1	0.0167 (5)	0.0148 (5)	0.0270 (5)	−0.0046 (4)	−0.0063 (4)	0.0008 (4)
O2	0.0127 (4)	0.0229 (5)	0.0217 (5)	−0.0030 (4)	−0.0039 (4)	0.0033 (4)
O3	0.0166 (5)	0.0193 (5)	0.0281 (5)	−0.0088 (4)	−0.0047 (4)	0.0020 (4)
O4	0.0235 (5)	0.0141 (5)	0.0203 (5)	−0.0063 (4)	−0.0039 (4)	0.0011 (4)
O5	0.0322 (6)	0.0247 (5)	0.0171 (5)	−0.0179 (5)	−0.0077 (4)	0.0070 (4)
O6	0.0205 (5)	0.0186 (5)	0.0170 (5)	−0.0062 (4)	0.0003 (4)	0.0006 (4)
C1	0.0150 (6)	0.0161 (6)	0.0139 (6)	−0.0034 (5)	−0.0041 (5)	0.0031 (5)
C2	0.0161 (6)	0.0175 (7)	0.0160 (6)	−0.0074 (5)	−0.0052 (5)	0.0033 (5)
C3	0.0176 (6)	0.0147 (6)	0.0152 (6)	−0.0041 (5)	−0.0062 (5)	0.0030 (5)
C4	0.0138 (6)	0.0180 (7)	0.0156 (6)	−0.0034 (5)	−0.0053 (5)	0.0033 (5)
C5	0.0161 (6)	0.0219 (7)	0.0156 (6)	−0.0087 (5)	−0.0060 (5)	0.0042 (5)
C6	0.0188 (6)	0.0167 (7)	0.0178 (6)	−0.0069 (5)	−0.0054 (5)	0.0025 (5)
C7	0.0169 (6)	0.0164 (7)	0.0144 (6)	−0.0061 (5)	−0.0032 (5)	0.0014 (5)
C8	0.0142 (6)	0.0158 (6)	0.0154 (6)	−0.0043 (5)	−0.0022 (5)	−0.0007 (5)
C9	0.0147 (6)	0.0164 (7)	0.0179 (6)	−0.0050 (5)	−0.0061 (5)	0.0031 (5)
C10	0.0151 (6)	0.0172 (7)	0.0162 (6)	−0.0050 (5)	−0.0033 (5)	0.0012 (5)
C11	0.0167 (6)	0.0138 (6)	0.0195 (6)	−0.0055 (5)	−0.0080 (5)	0.0026 (5)
C12	0.0187 (6)	0.0196 (7)	0.0169 (6)	−0.0106 (5)	−0.0064 (5)	0.0050 (5)
C13	0.0140 (6)	0.0201 (7)	0.0151 (6)	−0.0062 (5)	−0.0040 (5)	0.0022 (5)
C14	0.0168 (6)	0.0153 (6)	0.0186 (6)	−0.0055 (5)	−0.0052 (5)	0.0015 (5)
C15	0.0216 (7)	0.0172 (7)	0.0318 (8)	−0.0079 (6)	−0.0089 (6)	0.0026 (6)
C16	0.0197 (7)	0.0293 (8)	0.0235 (7)	−0.0057 (6)	−0.0001 (6)	0.0031 (6)
C17	0.0246 (7)	0.0220 (8)	0.0373 (9)	−0.0128 (6)	−0.0047 (6)	0.0022 (6)
C18	0.0259 (7)	0.0177 (7)	0.0246 (7)	−0.0079 (6)	−0.0011 (6)	−0.0030 (6)
C19	0.0263 (7)	0.0267 (8)	0.0212 (7)	−0.0093 (6)	−0.0075 (6)	0.0089 (6)
C20	0.0215 (7)	0.0190 (7)	0.0191 (7)	−0.0030 (6)	−0.0017 (5)	−0.0013 (5)
O1M	0.0200 (5)	0.0177 (5)	0.0302 (6)	−0.0046 (4)	−0.0028 (4)	0.0040 (4)
C1M	0.0278 (7)	0.0227 (8)	0.0301 (8)	−0.0100 (6)	−0.0073 (6)	0.0020 (6)

Geometric parameters (Å, º) top

N1—N2	1.3243 (16)	C10—C11	1.3970 (18)
N1—C7	1.3473 (16)	C10—H10	0.9500
N2—N3	1.3339 (16)	C11—C12	1.4010 (19)
N2—H2N	0.936 (17)	C12—C13	1.4002 (19)
N3—C8	1.3455 (16)	C13—C14	1.3895 (18)
O1—C3	1.3628 (16)	C14—H14	0.9500
O1—C15	1.4301 (16)	C15—H15A	0.9800
O2—C4	1.3768 (15)	C15—H15B	0.9800
O2—C16	1.4330 (17)	C15—H15C	0.9800
O3—C5	1.3645 (16)	C16—H16A	0.9800
O3—C17	1.4236 (17)	C16—H16B	0.9800
O4—C11	1.3661 (16)	C16—H16C	0.9800
O4—C18	1.4268 (17)	C17—H17A	0.9800
O5—C12	1.3755 (16)	C17—H17B	0.9800
O5—C19	1.4358 (17)	C17—H17C	0.9800
O6—C13	1.3639 (16)	C18—H18A	0.9800
O6—C20	1.4326 (16)	C18—H18B	0.9800
C1—C2	1.3950 (19)	C18—H18C	0.9800
C1—C6	1.4006 (18)	C19—H19A	0.9800
C1—C7	1.4774 (18)	C19—H19B	0.9800
C2—C3	1.3954 (18)	C19—H19C	0.9800
C2—H2	0.9500	C20—H20A	0.9800
C3—C4	1.3982 (19)	C20—H20B	0.9800
C4—C5	1.3953 (19)	C20—H20C	0.9800
C5—C6	1.3950 (18)	O1M—C1M	1.4282 (18)
C6—H6	0.9500	O1M—H1M	0.8400
C7—C8	1.4057 (19)	C1M—H1M1	0.9800
C8—C9	1.4743 (18)	C1M—H1M2	0.9800
C9—C10	1.3936 (19)	C1M—H1M3	0.9800
C9—C14	1.3970 (18)

N2—N1—C7	104.56 (11)	O6—C13—C12	115.88 (11)
N1—N2—N3	114.49 (11)	C14—C13—C12	120.27 (12)
N1—N2—H2N	124.0 (10)	C13—C14—C9	119.97 (12)
N3—N2—H2N	121.4 (11)	C13—C14—H14	120.0
N2—N3—C8	105.06 (11)	C9—C14—H14	120.0
C3—O1—C15	116.70 (10)	O1—C15—H15A	109.5
C4—O2—C16	113.71 (10)	O1—C15—H15B	109.5
C5—O3—C17	117.30 (11)	H15A—C15—H15B	109.5
C11—O4—C18	116.84 (10)	O1—C15—H15C	109.5
C12—O5—C19	116.01 (11)	H15A—C15—H15C	109.5
C13—O6—C20	116.87 (10)	H15B—C15—H15C	109.5
C2—C1—C6	120.65 (12)	O2—C16—H16A	109.5
C2—C1—C7	119.59 (12)	O2—C16—H16B	109.5
C6—C1—C7	119.77 (12)	H16A—C16—H16B	109.5
C1—C2—C3	119.53 (12)	O2—C16—H16C	109.5
C1—C2—H2	120.2	H16A—C16—H16C	109.5
C3—C2—H2	120.2	H16B—C16—H16C	109.5
O1—C3—C2	124.68 (12)	O3—C17—H17A	109.5
O1—C3—C4	115.06 (11)	O3—C17—H17B	109.5
C2—C3—C4	120.25 (12)	H17A—C17—H17B	109.5
O2—C4—C5	120.10 (11)	O3—C17—H17C	109.5
O2—C4—C3	120.05 (12)	H17A—C17—H17C	109.5
C5—C4—C3	119.81 (12)	H17B—C17—H17C	109.5
O3—C5—C6	124.27 (12)	O4—C18—H18A	109.5
O3—C5—C4	115.33 (11)	O4—C18—H18B	109.5
C6—C5—C4	120.39 (12)	H18A—C18—H18B	109.5
C5—C6—C1	119.32 (12)	O4—C18—H18C	109.5
C5—C6—H6	120.3	H18A—C18—H18C	109.5
C1—C6—H6	120.3	H18B—C18—H18C	109.5
N1—C7—C8	108.49 (11)	O5—C19—H19A	109.5
N1—C7—C1	121.12 (12)	O5—C19—H19B	109.5
C8—C7—C1	130.39 (12)	H19A—C19—H19B	109.5
N3—C8—C7	107.40 (11)	O5—C19—H19C	109.5
N3—C8—C9	121.97 (12)	H19A—C19—H19C	109.5
C7—C8—C9	130.48 (12)	H19B—C19—H19C	109.5
C10—C9—C14	120.46 (12)	O6—C20—H20A	109.5
C10—C9—C8	121.60 (12)	O6—C20—H20B	109.5
C14—C9—C8	117.94 (12)	H20A—C20—H20B	109.5
C9—C10—C11	119.35 (12)	O6—C20—H20C	109.5
C9—C10—H10	120.3	H20A—C20—H20C	109.5
C11—C10—H10	120.3	H20B—C20—H20C	109.5
O4—C11—C10	124.35 (12)	C1M—O1M—H1M	109.5
O4—C11—C12	115.03 (11)	O1M—C1M—H1M1	109.5
C10—C11—C12	120.62 (12)	O1M—C1M—H1M2	109.5
O5—C12—C13	121.12 (12)	H1M1—C1M—H1M2	109.5
O5—C12—C11	119.30 (12)	O1M—C1M—H1M3	109.5
C13—C12—C11	119.29 (12)	H1M1—C1M—H1M3	109.5
O6—C13—C14	123.85 (12)	H1M2—C1M—H1M3	109.5

C7—N1—N2—N3	−0.41 (15)	N2—N3—C8—C9	−175.64 (12)
N1—N2—N3—C8	0.07 (16)	N1—C7—C8—N3	−0.54 (15)
C6—C1—C2—C3	−0.27 (19)	C1—C7—C8—N3	−179.60 (13)
C7—C1—C2—C3	−179.82 (12)	N1—C7—C8—C9	174.91 (13)
C15—O1—C3—C2	3.37 (19)	C1—C7—C8—C9	−4.1 (2)
C15—O1—C3—C4	−177.50 (12)	N3—C8—C9—C10	−47.04 (19)
C1—C2—C3—O1	178.74 (12)	C7—C8—C9—C10	138.07 (15)
C1—C2—C3—C4	−0.36 (19)	N3—C8—C9—C14	132.31 (14)
C16—O2—C4—C5	85.75 (15)	C7—C8—C9—C14	−42.6 (2)
C16—O2—C4—C3	−96.54 (15)	C14—C9—C10—C11	−0.87 (19)
O1—C3—C4—O2	4.99 (18)	C8—C9—C10—C11	178.47 (12)
C2—C3—C4—O2	−175.83 (11)	C18—O4—C11—C10	−4.16 (18)
O1—C3—C4—C5	−177.30 (11)	C18—O4—C11—C12	175.12 (12)
C2—C3—C4—C5	1.9 (2)	C9—C10—C11—O4	−179.85 (12)
C17—O3—C5—C6	8.57 (19)	C9—C10—C11—C12	0.91 (19)
C17—O3—C5—C4	−172.45 (12)	C19—O5—C12—C13	−72.53 (17)
O2—C4—C5—O3	−4.09 (18)	C19—O5—C12—C11	113.70 (14)
C3—C4—C5—O3	178.19 (12)	O4—C11—C12—O5	−4.85 (18)
O2—C4—C5—C6	174.92 (12)	C10—C11—C12—O5	174.46 (11)
C3—C4—C5—C6	−2.79 (19)	O4—C11—C12—C13	−178.74 (11)
O3—C5—C6—C1	−178.92 (12)	C10—C11—C12—C13	0.6 (2)
C4—C5—C6—C1	2.16 (19)	C20—O6—C13—C14	6.21 (18)
C2—C1—C6—C5	−0.6 (2)	C20—O6—C13—C12	−173.47 (11)
C7—C1—C6—C5	178.93 (12)	O5—C12—C13—O6	3.80 (18)
N2—N1—C7—C8	0.56 (15)	C11—C12—C13—O6	177.57 (11)
N2—N1—C7—C1	179.72 (12)	O5—C12—C13—C14	−175.89 (12)
C2—C1—C7—N1	−34.27 (18)	C11—C12—C13—C14	−2.11 (19)
C6—C1—C7—N1	146.18 (13)	O6—C13—C14—C9	−177.50 (12)
C2—C1—C7—C8	144.69 (15)	C12—C13—C14—C9	2.16 (19)
C6—C1—C7—C8	−34.9 (2)	C10—C9—C14—C13	−0.66 (19)
N2—N3—C8—C7	0.28 (15)	C8—C9—C14—C13	179.98 (12)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N2—H2N···O1M	0.936 (17)	1.797 (18)	2.7303 (15)	174.2 (16)
O1M—H1M···N3ⁱ	0.84	1.97	2.8101 (15)	177

Symmetry code: (i) −x+2, −y+1, −z+1.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N2—H2N···O1M	0.936 (17)	1.797 (18)	2.7303 (15)	174.2 (16)
O1M—H1M···N3ⁱ	0.84	1.97	2.8101 (15)	176.5

Symmetry code: (i) −x+2, −y+1, −z+1.

Acknowledgements

This investigation was supported NIH/National Cancer Institute (CA140409) United States, and we also thank the Arkansas Research Alliance for financial support.

References

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Volume 70| Part 10| October 2014| Pages o1128-o1129

doi:10.1107/S1600536814020911

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

Crystal structure of 4,5-bis­­(3,4,5-tri­meth­­oxy­phen­yl)-2H-1,2,3-triazole methanol monosolvate

1. Related literature

2. Experimental

2.1. Crystal data

2.2. Data collection

2.3. Refinement

Supporting information

Acknowledgements

References

organic compounds

Crystal structure of 4,5-bis(3,4,5-trimethoxyphenyl)-2H-1,2,3-triazole methanol monosolvate