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

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890

N-(2-Bromo-4-methyl­phen­yl)-2-(5-methyl-2-phenyl­pyrazolo­[1,5-a]pyrimidin-7-yl)acetamide

aLaboratoire de Chimie Organique Hétérocyclique URAC21, Pôle de Compétences Pharmacochimie, Université Mohammed V-Agdal, Avenue Ibn Battouta, BP 1014, Rabat, Morocco, bInstitut de Chimie Organique et Analytique, Université d'Orléans, UMR CNRS 6005, BP 6759, 45067 Orléans Cedex 2, France, cInstitute of Nanmaterials and Nanotechnology, MASCIR, Rabat, Morocco, and dLaboratoire de Chimie du Solide Appliquée, Université Mohammed V-Agdal, Faculté des Sciences, Avenue Ibn Battouta, BP 1014, Rabat, Morocco
*Correspondence e-mail: i_bassoude@yahoo.fr

(Received 23 April 2013; accepted 30 April 2013; online 4 May 2013)

The fused pyrazole and pyrimidine rings in the title compound, C22H19BrN4O, are almost coplanar, their planes being inclined to one another by 2.08 (13)°. The dihedral angles formed by the mean plane of the fused ring system and the phenyl and benzene rings are 16.21 (4) and 82.84 (4)°, respectively. An intra­molecular N—H⋯N hydrogen bond is observed. In the crystal, mol­ecules form inversion dimers via pairs of C—H⋯O hydrogen bonds. ππ inter­actions, with centroid–centroid distances of 3.4916 (9) Å, connect the dimers into a three-dimensional network.

Related literature

For pharmacological and biochemical properties of pyrazolo­[1,5-a]pyrimidine derivatives, see: Selleri et al. (2005[Selleri, S., Gratteri, P., Costagli, C., Bonaccini, C., Costanzo, A., Melani, F., Guerrini, G., Ciciani, G., Costa, B., Spinetti, F., Martini, C. & Bruni, F. (2005). Bioorg. Med. Chem. 13, 4821-4834.]); Almansa et al. (2001[Almansa, C. A., Alberto, F., Cavalcanti, F. L., Gomez, L. A., Miralles, A., Merlos, M., Garcia-Rafanell, J. & Forn, J. (2001). J. Med. Chem. 44, 350-361.]); Suzuki et al. (2001[Suzuki, M., Iwasaki, H., Fujikawa, Y., Sakashita, M., Kitahara, M. & Sakoda, R. (2001). Bioorg. Med. Chem. Lett. 11, 1285-1288.]); Chen et al. (2004[Chen, C., Wilcoxen, K. M., Huang, C. Q., Xie, Y.-F., McCarthy, J. R., Webb, T. R., Zhu, Y.-F., Saunders, J., Liu, X.-J., Chen, T.-K., Bozigian, H. & Grigoriadis, D. E. (2004). J. Med. Chem. 47, 4787-4798.]). For related structures, see: Bassoude et al. (2013a[Bassoude, I., Berteina-Raboin, S., Essassi, E. M., Guillaumet, G. & El Ammari, L. (2013a). Acta Cryst. E69, o740.],b[Bassoude, I., Berteina-Raboin, S., Essassi, E. M., Guillaumet, G. & El Ammari, L. (2013b). Acta Cryst. E69, o749.]).

[Scheme 1]

Experimental

Crystal data
  • C22H19BrN4O

  • Mr = 435.32

  • Monoclinic, P 21 /c

  • a = 9.8102 (6) Å

  • b = 7.2915 (4) Å

  • c = 27.0162 (14) Å

  • β = 92.942 (3)°

  • V = 1929.95 (19) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 2.15 mm−1

  • T = 296 K

  • 0.42 × 0.33 × 0.25 mm

Data collection
  • Bruker X8 APEXII area-detector diffractometer

  • Absorption correction: multi-scan (SADABS; Bruker, 2009[Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.739, Tmax = 0.867

  • 29996 measured reflections

  • 6371 independent reflections

  • 3830 reflections with I > 2σ(I)

  • Rint = 0.044

Refinement
  • R[F2 > 2σ(F2)] = 0.041

  • wR(F2) = 0.107

  • S = 1.02

  • 6371 reflections

  • 253 parameters

  • H-atom parameters constrained

  • Δρmax = 0.41 e Å−3

  • Δρmin = −0.62 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
N4—H4A⋯N2 0.86 2.17 2.927 (2) 147
C14—H14⋯O1i 0.93 2.43 3.189 (2) 139
Symmetry code: (i) -x+2, -y+1, -z.

Data collection: APEX2 (Bruker, 2009[Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Bruker, 2009[Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; 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: ORTEP-3 for Windows (Farrugia, 2012[Farrugia, L. J. (2012). J. Appl. Cryst. 45, 849-854.]); software used to prepare material for publication: PLATON (Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.]) and publCIF (Westrip, 2010[Westrip, S. P. (2010). J. Appl. Cryst. 43, 920-925.]).

Supporting information


Comment top

Pyrazolo[1,5-a]pyrimidines have attracted considerable interest because of their biological activity. For instance, they are known for their potent utility as selective peripheral benzodiazepine receptor ligands (Selleri et al., 2005), COX-2 selective inhibitors (Almansa et al., 2001), HMG-CoA reductase inhibitors (Suzuki et al., 2001) and CRF1 antagonists (Chen et al., 2004). Our research group targeted at the development of heterocycles with a bridgehead nitrogen atom such the title compound and related compounds recently published (Bassoude et al. 2013a, 2013b).

The crystal structure of the title compound is built up from two fused five (N2/N3/C3–C5) and six-membered (N1/N3/C1–C3/C6) rings linked to one phenyl ring (C17–C22) and to a 2-bromo-4-methylphenyl ring (Br1/C9–C14) through an acetamide group as shown in Fig. 1. The pyrazole and pyrimidine rings are essentially planar with the maximum deviation of 0.0039 (15) and 0.0076 (15) Å for atom C3. The plane through the fused ring system makes a dihedral angles of 16.21 (4)° and 82.84 (4)° with the phenyl ring and with the 2-bromo-4-methylphenyl ring, respectively.

In the crystal (Fig. 2) molecules form inversion dimers via pairs of C14—H14···O1 hydrogen bonds. In addition, ππ interactions connect the dimers into a three-dimensional network, with centroid–centroid distances of 3.4916 (9) Å. An intramolecular N4—H4A···N2 hydrogen bond my help to define the conformation of the molecule.

Related literature top

For pharmacological and biochemical properties of pyrazolo[1,5-a]pyrimidine derivatives, see: Selleri et al. (2005); Almansa et al. (2001); Suzuki et al. (2001); Chen et al. (2004). For related structures, see: Bassoude et al. (2013a,b).

Experimental top

To a solution of 2-bromo-4-methylaniline (0.1 ml, 0.78 mmol) in 4 ml dichloromethane, under argon and at 273 K, were added 0.8 ml of trimethylaluminium in toluene (2M, 1.6 mmol), then the mixture was stirred for 15 min followed by addition of 0.2 g (0.68 mmol) of 7-ethoxycarbonyl-methyl-5-methylpyrazolo[1,5-a]pyrimidine. The reaction mixture was stirred to room temperature for 30 min then heated to reflux for 5 h. After evaporation of solvent under reduced pressure, the residue was extracted with CH2Cl2 and washed with a saturated NaCl solution. The combined organic layers were dried with MgSO4 and concentrated under vacuum. The residue was purified on silica gel by column chromatography using mixture of petroleum ether and ethyl acetate (9:1 v/v) as eluent. The compound was recrystallized from a mixture of cyclohexane/ diethyl ether (1:1 v/v) to give colourless crystals.

Refinement top

All H atoms could be located in a difference Fourier map and were treated as riding, with C—H = 0.93–0.97 Å, N–H = 0.86 Å, and with Uiso(H) = 1.2 Ueq(C, N) or 1.5 Ueq(C) for methyl H atoms. Two outliers (1 0 0; 0 0 2) were omitted from the last refinement cycles

Computing details top

Data collection: APEX2 (Bruker, 2009); cell refinement: SAINT (Bruker, 2009); data reduction: SAINT (Bruker, 2009); 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, 2012); software used to prepare material for publication: PLATON (Spek, 2009) and publCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title compound with displacement ellipsoids drawn at the 50% probability level. H atoms are represented as small circles of arbitrary radii.
[Figure 2] Fig. 2. Partial crystal packing of the title compound showing C14–H14A···O1 and N4–H4···N2 hydrogen bonds as blue dashed lines and a π···π contact as green line. The red spheres represent the centroids of the pyrimidine rings.
N-(2-Bromo-4-methylphenyl)-2-(5-methyl-2-phenylpyrazolo[1,5-a]pyrimidin-7-yl)acetamide top
Crystal data top
C22H19BrN4OF(000) = 888
Mr = 435.32Dx = 1.498 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 6371 reflections
a = 9.8102 (6) Åθ = 2.5–31.4°
b = 7.2915 (4) ŵ = 2.15 mm1
c = 27.0162 (14) ÅT = 296 K
β = 92.942 (3)°Block, colourless
V = 1929.95 (19) Å30.42 × 0.33 × 0.25 mm
Z = 4
Data collection top
Bruker X8 APEXII area-detector
diffractometer
6371 independent reflections
Radiation source: fine-focus sealed tube3830 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.044
ϕ and ω scansθmax = 31.4°, θmin = 2.5°
Absorption correction: multi-scan
(SADABS; Bruker, 2009)
h = 1414
Tmin = 0.739, Tmax = 0.867k = 1010
29996 measured reflectionsl = 3939
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)] = 0.041Hydrogen site location: difference Fourier map
wR(F2) = 0.107H-atom parameters constrained
S = 1.02 w = 1/[σ2(Fo2) + (0.0467P)2 + 0.2795P]
where P = (Fo2 + 2Fc2)/3
6371 reflections(Δ/σ)max = 0.001
253 parametersΔρmax = 0.41 e Å3
0 restraintsΔρmin = 0.62 e Å3
Crystal data top
C22H19BrN4OV = 1929.95 (19) Å3
Mr = 435.32Z = 4
Monoclinic, P21/cMo Kα radiation
a = 9.8102 (6) ŵ = 2.15 mm1
b = 7.2915 (4) ÅT = 296 K
c = 27.0162 (14) Å0.42 × 0.33 × 0.25 mm
β = 92.942 (3)°
Data collection top
Bruker X8 APEXII area-detector
diffractometer
6371 independent reflections
Absorption correction: multi-scan
(SADABS; Bruker, 2009)
3830 reflections with I > 2σ(I)
Tmin = 0.739, Tmax = 0.867Rint = 0.044
29996 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0410 restraints
wR(F2) = 0.107H-atom parameters constrained
S = 1.02Δρmax = 0.41 e Å3
6371 reflectionsΔρmin = 0.62 e Å3
253 parameters
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.

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
C10.6173 (2)0.8274 (2)0.03898 (7)0.0377 (4)
H10.68360.86880.05970.045*
C20.4907 (2)0.7594 (2)0.05997 (7)0.0389 (4)
C30.41574 (19)0.7044 (2)0.01713 (7)0.0363 (4)
C40.3365 (2)0.6608 (2)0.05592 (7)0.0389 (4)
H40.24780.61550.05390.047*
C50.41646 (19)0.6987 (2)0.09908 (7)0.0345 (4)
C60.64217 (19)0.8324 (2)0.01096 (7)0.0329 (4)
C70.76984 (19)0.9055 (2)0.03730 (7)0.0366 (4)
H7A0.74460.97450.06610.044*
H7B0.81410.98940.01540.044*
C80.87117 (19)0.7571 (2)0.05392 (7)0.0330 (4)
C90.89437 (18)0.4831 (2)0.10641 (7)0.0332 (4)
C100.89659 (19)0.4341 (2)0.15591 (7)0.0361 (4)
C110.9568 (2)0.2718 (3)0.17291 (8)0.0422 (5)
H110.95570.24160.20630.051*
C121.0184 (2)0.1551 (3)0.14043 (8)0.0436 (5)
C131.0160 (2)0.2037 (3)0.09087 (8)0.0432 (5)
H131.05670.12650.06850.052*
C140.9547 (2)0.3641 (3)0.07366 (8)0.0397 (4)
H140.95380.39250.04010.048*
C151.0869 (3)0.0203 (3)0.15829 (10)0.0691 (7)
H15A1.17060.00850.17660.104*
H15B1.10600.09550.13030.104*
H15C1.02740.08540.17930.104*
C160.4645 (2)0.7598 (3)0.11515 (8)0.0512 (5)
H16C0.49950.87090.12870.077*
H16A0.36800.75230.12290.077*
H16B0.50910.65630.12920.077*
C170.38277 (19)0.6745 (2)0.15115 (7)0.0361 (4)
C180.2742 (2)0.5647 (3)0.16391 (9)0.0470 (5)
H180.22090.50640.13920.056*
C190.2447 (2)0.5415 (3)0.21290 (9)0.0541 (6)
H190.17210.46700.22090.065*
C200.3217 (2)0.6275 (3)0.25011 (9)0.0533 (6)
H200.30130.61160.28310.064*
C210.4294 (2)0.7376 (3)0.23797 (9)0.0518 (5)
H210.48180.79660.26280.062*
C220.4595 (2)0.7604 (3)0.18897 (8)0.0452 (5)
H220.53260.83450.18120.054*
N10.39309 (17)0.6994 (2)0.03282 (6)0.0405 (4)
N20.54163 (15)0.7640 (2)0.08894 (6)0.0338 (3)
N30.53930 (15)0.76798 (18)0.03862 (6)0.0317 (3)
N40.82608 (16)0.6428 (2)0.08896 (6)0.0370 (4)
H4A0.74990.66950.10160.044*
O10.98349 (14)0.74725 (19)0.03713 (5)0.0453 (3)
Br10.81300 (3)0.58958 (3)0.201758 (8)0.05961 (10)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.0391 (11)0.0356 (9)0.0378 (10)0.0071 (8)0.0030 (9)0.0039 (8)
C20.0459 (12)0.0288 (8)0.0409 (11)0.0120 (8)0.0089 (9)0.0027 (7)
C30.0315 (10)0.0304 (8)0.0458 (12)0.0060 (7)0.0103 (9)0.0036 (7)
C40.0268 (10)0.0370 (9)0.0523 (12)0.0007 (8)0.0044 (9)0.0031 (8)
C50.0282 (10)0.0278 (8)0.0473 (11)0.0048 (7)0.0008 (8)0.0028 (7)
C60.0303 (10)0.0275 (8)0.0405 (10)0.0056 (7)0.0035 (8)0.0011 (7)
C70.0330 (10)0.0341 (9)0.0420 (11)0.0014 (8)0.0036 (8)0.0021 (7)
C80.0294 (10)0.0381 (9)0.0309 (9)0.0008 (7)0.0032 (8)0.0041 (7)
C90.0223 (9)0.0400 (9)0.0371 (10)0.0042 (7)0.0009 (8)0.0022 (7)
C100.0291 (10)0.0442 (10)0.0350 (10)0.0004 (8)0.0005 (8)0.0002 (8)
C110.0409 (12)0.0462 (10)0.0387 (11)0.0011 (9)0.0055 (9)0.0086 (8)
C120.0366 (11)0.0381 (9)0.0549 (13)0.0032 (8)0.0102 (10)0.0024 (9)
C130.0359 (11)0.0409 (10)0.0522 (13)0.0050 (8)0.0026 (9)0.0077 (9)
C140.0345 (11)0.0466 (10)0.0377 (11)0.0048 (8)0.0027 (9)0.0010 (8)
C150.0758 (19)0.0495 (12)0.0796 (18)0.0205 (13)0.0183 (15)0.0084 (12)
C160.0619 (15)0.0482 (11)0.0422 (12)0.0110 (10)0.0118 (11)0.0065 (9)
C170.0277 (10)0.0335 (9)0.0470 (12)0.0077 (7)0.0010 (8)0.0020 (8)
C180.0373 (12)0.0483 (11)0.0551 (13)0.0024 (9)0.0001 (10)0.0032 (9)
C190.0418 (13)0.0624 (13)0.0588 (15)0.0058 (11)0.0085 (11)0.0066 (11)
C200.0467 (14)0.0681 (14)0.0455 (13)0.0084 (11)0.0074 (11)0.0030 (10)
C210.0453 (13)0.0632 (13)0.0466 (13)0.0024 (11)0.0013 (10)0.0085 (10)
C220.0366 (11)0.0490 (11)0.0501 (13)0.0034 (9)0.0015 (10)0.0048 (9)
N10.0393 (10)0.0358 (8)0.0451 (10)0.0055 (7)0.0107 (8)0.0041 (7)
N20.0292 (8)0.0355 (7)0.0362 (9)0.0033 (6)0.0027 (7)0.0015 (6)
N30.0276 (8)0.0296 (7)0.0371 (9)0.0048 (6)0.0056 (7)0.0012 (6)
N40.0279 (9)0.0454 (8)0.0379 (9)0.0098 (7)0.0046 (7)0.0059 (7)
O10.0352 (8)0.0541 (8)0.0474 (8)0.0065 (6)0.0094 (7)0.0049 (6)
Br10.0728 (2)0.06541 (16)0.04192 (14)0.01753 (12)0.01561 (12)0.00091 (10)
Geometric parameters (Å, º) top
C1—C61.359 (3)C11—H110.9300
C1—C21.428 (3)C12—C131.384 (3)
C1—H10.9300C12—C151.512 (3)
C2—N11.311 (3)C13—C141.385 (3)
C2—C161.500 (3)C13—H130.9300
C3—N11.357 (2)C14—H140.9300
C3—C41.374 (3)C15—H15A0.9600
C3—N31.396 (2)C15—H15B0.9600
C4—C51.399 (3)C15—H15C0.9600
C4—H40.9300C16—H16C0.9600
C5—N21.358 (2)C16—H16A0.9600
C5—C171.472 (3)C16—H16B0.9600
C6—N31.369 (2)C17—C221.387 (3)
C6—C71.506 (3)C17—C181.390 (3)
C7—C81.521 (2)C18—C191.380 (3)
C7—H7A0.9700C18—H180.9300
C7—H7B0.9700C19—C201.377 (3)
C8—O11.215 (2)C19—H190.9300
C8—N41.353 (2)C20—C211.380 (3)
C9—C101.383 (3)C20—H200.9300
C9—C141.393 (3)C21—C221.381 (3)
C9—N41.412 (2)C21—H210.9300
C10—C111.390 (3)C22—H220.9300
C10—Br11.8962 (19)N2—N31.359 (2)
C11—C121.384 (3)N4—H4A0.8600
C6—C1—C2120.76 (19)C13—C14—C9120.30 (19)
C6—C1—H1119.6C13—C14—H14119.8
C2—C1—H1119.6C9—C14—H14119.8
N1—C2—C1122.65 (18)C12—C15—H15A109.5
N1—C2—C16117.63 (19)C12—C15—H15B109.5
C1—C2—C16119.7 (2)H15A—C15—H15B109.5
N1—C3—C4133.01 (18)C12—C15—H15C109.5
N1—C3—N3121.12 (18)H15A—C15—H15C109.5
C4—C3—N3105.85 (16)H15B—C15—H15C109.5
C3—C4—C5105.95 (17)C2—C16—H16C109.5
C3—C4—H4127.0C2—C16—H16A109.5
C5—C4—H4127.0H16C—C16—H16A109.5
N2—C5—C4112.04 (17)C2—C16—H16B109.5
N2—C5—C17118.99 (17)H16C—C16—H16B109.5
C4—C5—C17128.97 (18)H16A—C16—H16B109.5
C1—C6—N3115.66 (17)C22—C17—C18118.12 (19)
C1—C6—C7125.52 (18)C22—C17—C5120.65 (18)
N3—C6—C7118.81 (16)C18—C17—C5121.24 (18)
C6—C7—C8113.78 (14)C19—C18—C17120.7 (2)
C6—C7—H7A108.8C19—C18—H18119.7
C8—C7—H7A108.8C17—C18—H18119.7
C6—C7—H7B108.8C20—C19—C18120.7 (2)
C8—C7—H7B108.8C20—C19—H19119.7
H7A—C7—H7B107.7C18—C19—H19119.7
O1—C8—N4124.06 (17)C19—C20—C21119.3 (2)
O1—C8—C7121.57 (17)C19—C20—H20120.4
N4—C8—C7114.36 (16)C21—C20—H20120.4
C10—C9—C14117.85 (17)C20—C21—C22120.1 (2)
C10—C9—N4121.28 (16)C20—C21—H21119.9
C14—C9—N4120.76 (17)C22—C21—H21119.9
C9—C10—C11121.64 (18)C21—C22—C17121.1 (2)
C9—C10—Br1119.42 (14)C21—C22—H22119.4
C11—C10—Br1118.93 (15)C17—C22—H22119.4
C12—C11—C10120.42 (19)C2—N1—C3117.42 (17)
C12—C11—H11119.8C5—N2—N3103.92 (14)
C10—C11—H11119.8N2—N3—C6125.34 (15)
C11—C12—C13118.01 (18)N2—N3—C3112.24 (15)
C11—C12—C15121.3 (2)C6—N3—C3122.38 (16)
C13—C12—C15120.7 (2)C8—N4—C9125.11 (15)
C12—C13—C14121.77 (19)C8—N4—H4A117.4
C12—C13—H13119.1C9—N4—H4A117.4
C14—C13—H13119.1
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N4—H4A···N20.862.172.927 (2)147
C14—H14···O1i0.932.433.189 (2)139
Symmetry code: (i) x+2, y+1, z.

Experimental details

Crystal data
Chemical formulaC22H19BrN4O
Mr435.32
Crystal system, space groupMonoclinic, P21/c
Temperature (K)296
a, b, c (Å)9.8102 (6), 7.2915 (4), 27.0162 (14)
β (°) 92.942 (3)
V3)1929.95 (19)
Z4
Radiation typeMo Kα
µ (mm1)2.15
Crystal size (mm)0.42 × 0.33 × 0.25
Data collection
DiffractometerBruker X8 APEXII area-detector
diffractometer
Absorption correctionMulti-scan
(SADABS; Bruker, 2009)
Tmin, Tmax0.739, 0.867
No. of measured, independent and
observed [I > 2σ(I)] reflections
29996, 6371, 3830
Rint0.044
(sin θ/λ)max1)0.733
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.041, 0.107, 1.02
No. of reflections6371
No. of parameters253
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.41, 0.62

Computer programs: APEX2 (Bruker, 2009), SAINT (Bruker, 2009), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 2012), PLATON (Spek, 2009) and publCIF (Westrip, 2010).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N4—H4A···N20.862.172.927 (2)147.2
C14—H14···O1i0.932.433.189 (2)138.9
Symmetry code: (i) x+2, y+1, z.
 

Acknowledgements

The authors thank the Unit of Support for Technical and Scientific Research (UATRS, CNRST) for the X-ray diffraction measurements.

References

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