PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of actaeInternational Union of Crystallographysearchopen accessarticle submissionjournal home pagethis article
 
Acta Crystallogr Sect E Struct Rep Online. 2009 October 1; 65(Pt 10): o2424.
Published online 2009 September 9. doi:  10.1107/S1600536809035727
PMCID: PMC2970186

(E)-4-Chloro-N-[(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methyl­ene]aniline

Abstract

In the title compound, C17H13Cl2N3, the dihedral angle between the pyrazole ring system and 4-chloro­phenyl ring is 26.1 (2)°. The C=N bond linking the two aromatic rings has an E conformation.

Related literature

For the biological properties of pyrazoles, see: Pimerova & Voronina (2001 [triangle]); Selvam et al. (2005 [triangle]). For the biological activity of Schiff bases, see: Rajavel et al. (2008 [triangle]); Yu et al. (2007 [triangle]). For a related stucture, see: Sun et al. (2007 [triangle]).

An external file that holds a picture, illustration, etc.
Object name is e-65-o2424-scheme1.jpg

Experimental

Crystal data

  • C17H13Cl2N3
  • M r = 330.20
  • Orthorhombic, An external file that holds a picture, illustration, etc.
Object name is e-65-o2424-efi1.jpg
  • a = 13.6471 (6) Å
  • b = 15.6315 (3) Å
  • c = 7.3514 (6) Å
  • V = 1568.24 (15) Å3
  • Z = 4
  • Mo Kα radiation
  • μ = 0.41 mm−1
  • T = 296 K
  • 0.39 × 0.34 × 0.10 mm

Data collection

  • Rigaku R-AXIS RAPID diffractometer
  • Absorption correction: multi-scan (ABSCOR; Higashi, 1995 [triangle]) T min = 0.839, T max = 0.960
  • 14704 measured reflections
  • 3558 independent reflections
  • 2533 reflections with F 2 > 2σ(F 2)
  • R int = 0.038

Refinement

  • R[F 2 > 2σ(F 2)] = 0.032
  • wR(F 2) = 0.099
  • S = 1.00
  • 3558 reflections
  • 201 parameters
  • H-atom parameters constrained
  • Δρmax = 0.21 e Å−3
  • Δρmin = −0.24 e Å−3
  • Absolute structure: Flack (1983 [triangle]), 1627 Friedel pairs
  • Flack parameter: −0.02 (6)

Data collection: PROCESS-AUTO (Rigaku, 2006 [triangle]); cell refinement: PROCESS-AUTO; data reduction: CrystalStructure (Rigaku/MSC, 2007 [triangle]); program(s) used to solve structure: SIR97 (Altomare et al., 1999 [triangle]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 [triangle]); molecular graphics: ORTEP-3 (Farrugia, 1997 [triangle]); software used to prepare material for publication: CrystalStructure (Rigaku/MSC, 2007 [triangle]).

Supplementary Material

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809035727/rk2165sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536809035727/rk2165Isup2.hkl

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

Acknowledgments

This work was supported by the Key Discipline Open Foundation of Zhejiang University of Technology (grant No. 20080604).

supplementary crystallographic information

Comment

Pyrazoles continue to attract a great deal of attention due to their extensive utilization in the pharmaceutical and agrochemical fields (Pimerova & Voronina, 2001; Selvam et al., 2005). Schiff base compounds have been used as fine chemicals and medical substrates and they are important ligands in coordination chemistry (Rajavel et al., 2008; Yu et al., 2007). As part of our studies on the synthesis and characterization of pyrazoles containing Schiff base group, we report here the molecular and crystal structure of the title compound (Fig. 1).

Bond lengths and angles of the title molecule agree with those observed in a related compound, such as (E)-N-[(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl) methylene]aniline (Sun et al., 2007). The dihedral angle between the pyrazole ring (N1/N2/C1–C3) and the substituted phenyl ring (C6–C11) is 26.1 (2)°. The C5═N3 bond linking the two aromatic rings has an E–conformation. The angles between the conjugated linkage and the pyrazole ring (C1/C2/C3/N1/N2), and between the linkage and the substituted phenyl ring (C6–C11) are 6.3 (3)° and 38.5 (2)°, respectively.

Experimental

A solution of 5–chloro–3–methyl–1–phenyl–4–formyl–1H–pyrazole (5 mmol) and 4–chloroaniline (5 mmol) in ethanol (20 ml) was refluxed for 2 h. After cooling, filtration and drying, the title compound was obtained (yield: 84%, m.p. 434 K). The crystal used for data collection was obtained by slow evaporation from a saturated ethanol solution at room temperature.

Refinement

The H atoms were positioned geometrically with C—H = 0.93Å for aromatic H and C—H = 0.96Å for methyl H and refined as riding with Uiso(H) = 1.2Ueq(C) and Uiso(H) = 1.5Ueq(methyl C).

Figures

Fig. 1.
The molecular structure of title compound with the atom numbering scheme. Displacement ellipsoids are drawn at 50% probability level. H atoms are presented as a small spheres of arbitrary radius.

Crystal data

C17H13Cl2N3Dx = 1.399 Mg m3
Mr = 330.20Melting point: 434 K
Orthorhombic, Pca21Mo Kα radiation, λ = 0.71075 Å
Hall symbol: P 2c -2acCell parameters from 10504 reflections
a = 13.6471 (6) Åθ = 3.0–27.4°
b = 15.6315 (3) ŵ = 0.41 mm1
c = 7.3514 (6) ÅT = 296 K
V = 1568.24 (15) Å3Plate, colourless
Z = 40.39 × 0.34 × 0.10 mm
F(000) = 680.00

Data collection

Rigaku R-AXIS RAPID diffractometer2533 reflections with F2 > 2σ(F2)
Detector resolution: 10.00 pixels mm-1Rint = 0.038
ω scansθmax = 27.4°
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)h = −17→17
Tmin = 0.839, Tmax = 0.960k = −20→20
14704 measured reflectionsl = −9→9
3558 independent reflections

Refinement

Refinement on F2H-atom parameters constrained
R[F2 > 2σ(F2)] = 0.032w = 1/[σ2(Fo2) + (0.055P)2 + 0.089P] where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.099(Δ/σ)max < 0.001
S = 1.00Δρmax = 0.21 e Å3
3558 reflectionsΔρmin = −0.24 e Å3
201 parametersExtinction correction: SHELXL97 (Sheldrick, 2008)
Primary atom site location: DirectExtinction coefficient: 0.0049 (8)
Secondary atom site location: DifmapAbsolute structure: Flack (1983), 1627 Friedel pairs
Hydrogen site location: GeomFlack parameter: −0.02 (6)

Special details

Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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)

xyzUiso*/Ueq
Cl10.42986 (4)0.48323 (3)0.33646 (10)0.04844 (15)
Cl20.32167 (6)−0.08853 (5)0.43233 (18)0.0893 (3)
N10.71398 (12)0.47004 (11)0.3343 (3)0.0478 (4)
N20.62562 (11)0.51191 (10)0.3340 (2)0.0391 (3)
N30.56891 (12)0.22175 (11)0.3631 (3)0.0480 (5)
C10.55095 (13)0.45498 (12)0.3464 (3)0.0395 (4)
C20.58944 (14)0.37384 (12)0.3577 (3)0.0411 (4)
C30.69251 (14)0.38699 (14)0.3490 (4)0.0452 (5)
C40.77319 (18)0.32253 (16)0.3538 (5)0.0629 (7)
C50.53181 (17)0.29634 (13)0.3730 (3)0.0446 (5)
C60.50557 (16)0.14994 (13)0.3773 (3)0.0436 (5)
C70.5429 (2)0.07657 (16)0.4568 (4)0.0565 (6)
C80.4858 (2)0.00375 (17)0.4763 (4)0.0624 (7)
C90.3916 (2)0.00400 (16)0.4118 (3)0.0539 (6)
C100.35333 (17)0.07546 (14)0.3280 (5)0.0548 (6)
C110.41003 (16)0.14831 (14)0.3120 (3)0.0490 (6)
C120.62388 (16)0.60273 (12)0.3108 (3)0.0393 (5)
C130.55665 (18)0.65294 (14)0.4025 (3)0.0467 (5)
C140.55583 (19)0.74051 (14)0.3718 (3)0.0539 (6)
C150.6222 (2)0.77754 (17)0.2553 (3)0.0558 (7)
C160.6905 (2)0.72688 (18)0.1672 (3)0.0550 (6)
C170.69122 (17)0.63883 (17)0.1930 (3)0.0467 (5)
H50.46460.30130.39090.054*
H70.60730.07610.49780.068*
H80.5111−0.04470.53260.075*
H100.28980.07460.28250.066*
H110.38400.19680.25690.059*
H130.51260.62840.48370.056*
H140.50980.77460.43070.065*
H150.62130.83630.23570.067*
H160.73630.75200.09010.066*
H170.73630.60470.13190.056*
H410.75780.27620.27310.076*
H420.78030.30100.47540.076*
H430.83330.34900.31600.076*

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
Cl10.0317 (2)0.0431 (2)0.0705 (3)−0.0001 (2)0.0023 (3)0.0004 (3)
Cl20.0752 (5)0.0612 (4)0.1317 (7)−0.0261 (3)0.0065 (5)0.0141 (5)
N10.0334 (8)0.0459 (10)0.0642 (12)−0.0012 (7)−0.0001 (12)0.0000 (13)
N20.0288 (8)0.0372 (8)0.0513 (9)−0.0004 (6)0.0006 (11)0.0029 (10)
N30.0417 (9)0.0363 (9)0.0659 (14)−0.0003 (7)−0.0003 (10)0.0005 (10)
C10.0321 (9)0.0388 (9)0.0476 (11)−0.0005 (8)0.0036 (12)−0.0007 (12)
C20.0373 (10)0.0387 (10)0.0473 (12)−0.0003 (8)0.0025 (11)0.0031 (11)
C30.0367 (10)0.0467 (11)0.0522 (12)0.0019 (8)−0.0021 (12)0.0010 (12)
C40.0469 (13)0.0501 (13)0.092 (2)0.0085 (11)−0.0008 (16)0.0068 (17)
C50.0400 (11)0.0424 (10)0.0515 (15)−0.0033 (9)0.0034 (10)0.0036 (11)
C60.0409 (11)0.0384 (10)0.0515 (14)0.0015 (8)0.0012 (10)0.0010 (10)
C70.0449 (13)0.0452 (13)0.0795 (18)−0.0018 (10)−0.0114 (14)0.0083 (13)
C80.0650 (19)0.0426 (13)0.0795 (18)−0.0026 (11)−0.0083 (15)0.0170 (13)
C90.0514 (14)0.0456 (12)0.0647 (15)−0.0067 (11)0.0055 (13)0.0008 (12)
C100.0360 (10)0.0501 (12)0.0782 (16)0.0023 (10)−0.0013 (15)−0.0023 (14)
C110.0445 (13)0.0371 (11)0.0656 (16)0.0045 (8)−0.0004 (13)0.0010 (12)
C120.0353 (11)0.0362 (10)0.0463 (13)−0.0054 (8)−0.0049 (10)−0.0002 (10)
C130.0462 (13)0.0439 (11)0.0501 (13)−0.0043 (10)0.0019 (11)−0.0011 (10)
C140.0535 (14)0.0424 (11)0.0658 (18)0.0032 (10)−0.0061 (13)−0.0073 (13)
C150.0620 (18)0.0413 (13)0.0642 (15)−0.0111 (12)−0.0165 (14)0.0050 (12)
C160.0493 (14)0.0580 (16)0.0578 (14)−0.0171 (12)−0.0065 (12)0.0147 (13)
C170.0377 (12)0.0513 (13)0.0510 (13)−0.0063 (10)−0.0009 (10)0.0039 (11)

Geometric parameters (Å, °)

Cl1—C11.7121 (19)C12—C171.383 (3)
Cl2—C91.740 (2)C13—C141.387 (3)
N1—N21.372 (2)C14—C151.375 (3)
N1—C31.335 (2)C15—C161.384 (3)
N2—C11.356 (2)C16—C171.389 (3)
N2—C121.430 (2)C4—H410.960
N3—C51.273 (2)C4—H420.960
N3—C61.421 (2)C4—H430.960
C1—C21.375 (2)C5—H50.930
C2—C31.423 (2)C7—H70.930
C2—C51.449 (3)C8—H80.930
C3—C41.493 (3)C10—H100.930
C6—C71.384 (3)C11—H110.930
C6—C111.390 (3)C13—H130.930
C7—C81.387 (3)C14—H140.930
C8—C91.370 (4)C15—H150.930
C9—C101.379 (3)C16—H160.930
C10—C111.382 (3)C17—H170.930
C12—C131.383 (3)
N2—N1—C3105.73 (16)C14—C15—C16119.6 (2)
N1—N2—C1110.32 (15)C15—C16—C17120.5 (2)
N1—N2—C12119.23 (15)C12—C17—C16119.0 (2)
C1—N2—C12130.32 (16)C3—C4—H41109.5
C5—N3—C6118.52 (18)C3—C4—H42109.5
Cl1—C1—N2123.59 (15)C3—C4—H43109.5
Cl1—C1—C2127.52 (15)H41—C4—H42109.5
N2—C1—C2108.80 (16)H41—C4—H43109.5
C1—C2—C3103.98 (18)H42—C4—H43109.5
C1—C2—C5124.65 (19)N3—C5—H5118.5
C3—C2—C5131.37 (19)C2—C5—H5118.5
N1—C3—C2111.16 (18)C6—C7—H7119.4
N1—C3—C4119.75 (19)C8—C7—H7119.4
C2—C3—C4129.1 (2)C7—C8—H8120.4
N3—C5—C2123.1 (2)C9—C8—H8120.4
N3—C6—C7117.5 (2)C9—C10—H10120.2
N3—C6—C11124.1 (2)C11—C10—H10120.2
C7—C6—C11118.4 (2)C6—C11—H11119.6
C6—C7—C8121.1 (2)C10—C11—H11119.6
C7—C8—C9119.3 (2)C12—C13—H13120.5
Cl2—C9—C8118.8 (2)C14—C13—H13120.5
Cl2—C9—C10120.3 (2)C13—C14—H14119.6
C8—C9—C10120.8 (2)C15—C14—H14119.6
C9—C10—C11119.6 (2)C14—C15—H15120.2
C6—C11—C10120.7 (2)C16—C15—H15120.2
N2—C12—C13121.07 (19)C15—C16—H16119.7
N2—C12—C17117.95 (19)C17—C16—H16119.7
C13—C12—C17121.0 (2)C12—C17—H17120.5
C12—C13—C14119.1 (2)C16—C17—H17120.5
C13—C14—C15120.8 (2)
N2—N1—C3—C20.2 (3)C3—C2—C5—N3−7.3 (4)
N2—N1—C3—C4−179.9 (2)C5—C2—C3—N1179.7 (2)
C3—N1—N2—C1−0.7 (3)C5—C2—C3—C4−0.2 (4)
C3—N1—N2—C12−177.0 (2)N3—C6—C7—C8179.8 (2)
N1—N2—C1—Cl1−176.0 (2)N3—C6—C11—C10178.9 (2)
N1—N2—C1—C20.8 (3)C7—C6—C11—C100.7 (4)
N1—N2—C12—C13−143.5 (2)C11—C6—C7—C8−1.9 (4)
N1—N2—C12—C1736.8 (3)C6—C7—C8—C91.6 (4)
C1—N2—C12—C1341.0 (3)C7—C8—C9—Cl2178.5 (2)
C1—N2—C12—C17−138.7 (2)C7—C8—C9—C100.1 (3)
C12—N2—C1—Cl1−0.2 (3)Cl2—C9—C10—C11−179.7 (2)
C12—N2—C1—C2176.6 (2)C8—C9—C10—C11−1.3 (4)
C5—N3—C6—C7−147.9 (2)C9—C10—C11—C60.9 (4)
C5—N3—C6—C1133.9 (3)N2—C12—C13—C14−178.2 (2)
C6—N3—C5—C2−179.1 (2)N2—C12—C17—C16179.6 (2)
Cl1—C1—C2—C3176.1 (2)C13—C12—C17—C16−0.1 (3)
Cl1—C1—C2—C5−3.4 (4)C17—C12—C13—C141.5 (3)
N2—C1—C2—C3−0.6 (3)C12—C13—C14—C15−1.6 (3)
N2—C1—C2—C5179.87 (19)C13—C14—C15—C160.2 (4)
C1—C2—C3—N10.2 (3)C14—C15—C16—C171.2 (4)
C1—C2—C3—C4−179.6 (3)C15—C16—C17—C12−1.3 (3)
C1—C2—C5—N3172.0 (2)

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: RK2165).

References

  • Altomare, A., Burla, M. C., Camalli, M., Cascarano, G. L., Giacovazzo, C., Guagliardi, A., Moliterni, A. G. G., Polidori, G. & Spagna, R. (1999). J. Appl. Cryst.32, 115–119.
  • Farrugia, L. J. (1997). J. Appl. Cryst.30, 565.
  • Flack, H. D. (1983). Acta Cryst. A39, 876–881.
  • Higashi, T. (1995). ABSCOR Rigaku Corporation, Tokyo, Japan.
  • Pimerova, E. V. & Voronina, E. V. (2001). J. Pharm. Chem.35, 18–21.
  • Rajavel, R., Vadivu, M. S. & Anitha, C. (2008). Eur. J. Chem.5, 620–626.
  • Rigaku (2006). PROCESS-AUTO Rigaku Corporation, Tokyo, Japan.
  • Rigaku/MSC (2007). CrystalStructure Rigaku/MSC, The Woodlands, Texas, USA.
  • Selvam, C., Jachak, S. M., Thilagavathi, R. & Chakraborti, A. K. (2005). Bioorg. Med. Chem. Lett.15, 1793–1797. [PubMed]
  • Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [PubMed]
  • Sun, F.-M., Yang, L., Chen, X.-B. & Lian, Z.-X. (2007). Acta Cryst. E63, o4620.
  • Yu, H., Shao, L. & Fang, J. (2007). J. Organomet. Chem.692, 991–996.

Articles from Acta Crystallographica Section E: Structure Reports Online are provided here courtesy of International Union of Crystallography