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Acta Crystallogr Sect E Struct Rep Online. 2008 September 1; 64(Pt 9): o1700.
Published online 2008 August 6. doi:  10.1107/S1600536808023921
PMCID: PMC2960675

3,5-Bis[1-acetyl-5-(4-chloro­phen­yl)-4,5-dihydro-1H-pyrazol-3-yl]-2,6-dimethyl­pyridine

Abstract

The title compound, C29H27Cl2N5O2, contains a central pyridine ring and two functionalized pyrazoline rings. The pyridine ring and the two attached pyrazoline rings are nearly coplanar, whereas the terminal chloro­phenyl rings are nearly perpendicular to the attached pyrazoline rings [dihedral angles = 86.78 (1) and 77.70 (1)°]. Mol­ecules are linked by weak inter­molecular C—H(...)O hydrogen bonding.

Related literature

For general background, see: Ahn et al. (2004 [triangle]); Palaska et al. (1996 [triangle]); Yar et al. (2006 [triangle])

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Object name is e-64-o1700-scheme1.jpg

Experimental

Crystal data

  • C29H27Cl2N5O2
  • M r = 548.46
  • Monoclinic, An external file that holds a picture, illustration, etc.
Object name is e-64-o1700-efi1.jpg
  • a = 12.345 (3) Å
  • b = 9.6763 (19) Å
  • c = 13.268 (3) Å
  • β = 115.00 (3)°
  • V = 1436.4 (5) Å3
  • Z = 2
  • Mo Kα radiation
  • μ = 0.26 mm−1
  • T = 296 (2) K
  • 0.30 × 0.20 × 0.20 mm

Data collection

  • Bruker SMART CCD area-detector diffractometer
  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996 [triangle]) T min = 0.926, T max = 0.950
  • 7509 measured reflections
  • 3736 independent reflections
  • 2520 reflections with I > 2σ(I)
  • R int = 0.027

Refinement

  • R[F 2 > 2σ(F 2)] = 0.036
  • wR(F 2) = 0.077
  • S = 0.91
  • 3736 reflections
  • 344 parameters
  • 1 restraint
  • H-atom parameters constrained
  • Δρmax = 0.14 e Å−3
  • Δρmin = −0.15 e Å−3
  • Absolute structure: Flack (1983 [triangle]), 1031 Friedel pairs
  • Flack parameter: 0.06 (6)

Data collection: SMART (Bruker, 2000 [triangle]); cell refinement: SAINT (Bruker, 2000 [triangle]); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 [triangle]); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL.

Table 1
Hydrogen-bond geometry (Å, °)

Supplementary Material

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808023921/xu2444sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536808023921/xu2444Isup2.hkl

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

Acknowledgments

The authors thank the Instrument Analysis and Research Center of Shanghai University for the data collection. The project was supported by the Key Subject of Shanghai Municipal Education Commission (grant No. J50102) and the Foundation of the Education Commission of Shanghai Municipality, China (grant No. 08zz44).

supplementary crystallographic information

Comment

The pyrazoline derivatives are well known nitrogen-containing heterocyclic compounds which show various biological activities and pharmacological properties (Palaska et al., 1996). Some of them can be anti-bacterial and anti-fungal, others are anti-diabetic, anti-inflammatory and also active against many Mycobacterias (Ahn et al., 2004; Yar et al., 2006). As the stereochemistry may be an important modulator of biological activity, the crystal structure of the title compound has been determined.

The molecular structure is shown in Fig. 1. There are two chlorophenyl rings bonded with two pyrazoline rings in cis-arrangement, and these two pyrazoline rings are further bonded with the same pyridine ring. The central pyridine ring and two attached pyrazoline rings are nearly coplanar with the dihedral angles of 1.32 (2) and 4.88 (2)°, whereas the dihedral angles between each chlorophenyl plane and the attached pyrazoline planes are 86.78 (1) and 77.70 (1)°.

In the crystal structure, there are weak intermolecular C—H···O hydrogen bonding (Table 1 and Fig. 2).

Experimental

2,6-Dimethyl-3,5-di-[3-(4-chloro-phenyl)-acryloyl-pyridine (1 mmol, 0.436 g) and 85% hydrazine hydrate solution (4 mmol, 0.235 g) were dissolved in 5 ml of acetic acid solution. The solution was refluxed for 8 h, and allowed to cool to room temperature. The reaction mixture was poured into crushed ice, then neutralized with dilute sodium hydroxide solution. The solid separated was filtered off, washed with water, dried and recrystallized from ethyl acetate to give a colorless compound in a yield of of 40%. Single crystals suitable for X-ray analysis were obtained form tetrahydrofuran at room temperature.

Refinement

All H atoms were placed in calculated positions, with C—H = 0.93–0.99 Å, and included in the final cycles of refinement using a riding model, Uiso(H) = 1.5Ueq(C) (for methyl groups) or 1.2Ueq(C) (for others). There is a void of 56 Å3 in the crystal structure, but no solvent molecule could be located reasonably.

Figures

Fig. 1.
The molecular structure of the title molecule, with the atom-numbering scheme. Displacement ellipsoids are drawn at the 30% probability level.
Fig. 2.
Crystal packing diagram of compound (I), Hydrogen bonding is indicated by dashed lines.

Crystal data

C29H27Cl2N5O2F000 = 572
Mr = 548.46Dx = 1.268 Mg m3
Monoclinic, P21Melting point = 547–549 K
Hall symbol: P 2ybMo Kα radiation λ = 0.71073 Å
a = 12.345 (3) ÅCell parameters from 2029 reflections
b = 9.6763 (19) Åθ = 2.7–20.6º
c = 13.268 (3) ŵ = 0.26 mm1
β = 115.00 (3)ºT = 296 (2) K
V = 1436.4 (5) Å3Block, colorless
Z = 20.30 × 0.20 × 0.20 mm

Data collection

Bruker SMART CCD area-detector diffractometer3736 independent reflections
Radiation source: fine-focus sealed tube2520 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.027
T = 173(2) Kθmax = 25.0º
ω scansθmin = 2.7º
Absorption correction: multi-scan(SADABS; Sheldrick, 1996)h = −14→14
Tmin = 0.926, Tmax = 0.950k = −5→11
7509 measured reflectionsl = −15→15

Refinement

Refinement on F2Hydrogen site location: inferred from neighbouring sites
Least-squares matrix: fullH-atom parameters constrained
R[F2 > 2σ(F2)] = 0.036  w = 1/[σ2(Fo2) + (0.0287P)2] where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.077(Δ/σ)max < 0.001
S = 0.91Δρmax = 0.14 e Å3
3736 reflectionsΔρmin = −0.15 e Å3
344 parametersExtinction correction: none
1 restraintAbsolute structure: Flack (1983), 1031 Friedel pairs
Primary atom site location: structure-invariant direct methodsFlack parameter: 0.06 (6)
Secondary atom site location: difference Fourier map

Special details

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)

xyzUiso*/Ueq
Cl10.82566 (10)0.19017 (14)0.84787 (9)0.1067 (4)
Cl20.93108 (9)−0.23669 (14)0.26803 (10)0.1163 (4)
N40.3040 (2)0.0470 (3)−0.03488 (19)0.0535 (7)
O20.4646 (2)0.0216 (3)−0.19685 (16)0.0699 (7)
N20.2426 (2)0.4329 (3)0.4064 (2)0.0591 (7)
C30.3001 (3)0.2513 (3)0.1935 (2)0.0518 (8)
H3A0.37720.29010.21410.062*
C20.2559 (3)0.1586 (3)0.1053 (2)0.0472 (8)
N50.3995 (2)0.0474 (3)−0.06575 (19)0.0520 (7)
N10.0772 (2)0.1372 (3)0.1322 (2)0.0595 (7)
C80.2922 (3)0.3870 (3)0.3447 (2)0.0511 (8)
N30.3251 (2)0.5240 (3)0.4848 (2)0.0588 (7)
C210.5046 (3)0.1276 (3)0.0106 (2)0.0498 (8)
H21A0.52600.1990−0.03240.060*
C10.1420 (3)0.1018 (3)0.0771 (2)0.0533 (8)
C40.2348 (3)0.2885 (3)0.2519 (2)0.0501 (8)
C190.3333 (3)0.1291 (3)0.0493 (2)0.0474 (8)
C200.4534 (2)0.1978 (3)0.0844 (2)0.0503 (8)
H20A0.50480.18140.16410.060*
H20B0.44470.29860.07050.060*
C130.5391 (3)0.4494 (3)0.5838 (3)0.0547 (8)
C240.6109 (2)0.0369 (3)0.0729 (2)0.0475 (8)
O10.3715 (2)0.6813 (3)0.6201 (2)0.0844 (8)
C70.0821 (3)−0.0002 (4)−0.0160 (3)0.0701 (10)
H7A0.0072−0.0321−0.01500.105*
H7B0.1351−0.0793−0.00610.105*
H7C0.06500.0446−0.08740.105*
C290.6086 (3)−0.0608 (4)0.1481 (3)0.0580 (9)
H29A0.5379−0.07060.15930.070*
C110.2948 (4)0.6055 (4)0.5529 (3)0.0677 (10)
C90.4157 (3)0.4450 (3)0.3751 (2)0.0564 (9)
H9A0.41600.50880.31690.068*
H9B0.47430.37020.38600.068*
C180.5107 (3)0.3598 (4)0.6500 (3)0.0598 (9)
H18A0.42980.35070.63880.072*
C100.4435 (3)0.5226 (4)0.4848 (2)0.0578 (9)
H10A0.46940.61930.47970.069*
C250.7154 (3)0.0477 (4)0.0600 (3)0.0642 (10)
H25A0.72080.11430.00970.077*
C170.5992 (3)0.2823 (4)0.7333 (3)0.0667 (9)
H17A0.57870.22200.77900.080*
C220.3836 (3)0.0014 (3)−0.1681 (3)0.0563 (9)
C280.7057 (3)−0.1451 (4)0.2079 (3)0.0667 (10)
H28A0.7016−0.21120.25910.080*
C140.6579 (3)0.4611 (4)0.6040 (3)0.0742 (11)
H14A0.68010.52410.56110.089*
C270.8074 (3)−0.1310 (4)0.1916 (3)0.0684 (10)
C60.0396 (3)0.2566 (5)0.2730 (3)0.0917 (14)
H6A−0.03340.20130.23720.138*
H6B0.01870.35490.26600.138*
H6C0.08000.23180.35190.138*
C50.1217 (3)0.2283 (3)0.2175 (3)0.0572 (9)
C160.7161 (3)0.2940 (4)0.7486 (3)0.0690 (10)
C260.8133 (3)−0.0363 (5)0.1185 (3)0.0753 (11)
H26A0.8842−0.02760.10740.090*
C150.7466 (3)0.3822 (5)0.6863 (3)0.0814 (12)
H15A0.82770.39080.69800.098*
C120.1685 (3)0.5944 (5)0.5398 (3)0.0878 (12)
H12A0.15670.65700.59240.132*
H12B0.15250.49920.55480.132*
H12C0.11360.61970.46370.132*
C230.2705 (3)−0.0739 (4)−0.2390 (3)0.0778 (11)
H23A0.2731−0.1018−0.30890.117*
H23B0.2019−0.0129−0.25480.117*
H23C0.2629−0.1561−0.19940.117*

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
Cl10.0941 (8)0.1130 (9)0.1006 (8)0.0245 (7)0.0290 (6)0.0137 (7)
Cl20.0693 (7)0.1272 (11)0.1354 (10)0.0249 (7)0.0267 (6)0.0115 (8)
N40.0520 (16)0.065 (2)0.0518 (16)−0.0009 (14)0.0295 (13)−0.0093 (15)
O20.0865 (17)0.0762 (18)0.0682 (15)−0.0036 (13)0.0531 (14)−0.0109 (13)
N20.0685 (18)0.064 (2)0.0524 (16)0.0096 (16)0.0333 (15)−0.0045 (15)
C30.0518 (18)0.058 (2)0.0517 (18)−0.0006 (17)0.0278 (16)−0.0058 (17)
C20.0498 (18)0.051 (2)0.0464 (18)0.0020 (15)0.0262 (16)−0.0037 (16)
N50.0536 (16)0.0614 (19)0.0479 (15)−0.0026 (14)0.0282 (13)−0.0081 (14)
N10.0504 (16)0.070 (2)0.0659 (18)−0.0028 (14)0.0323 (15)−0.0081 (16)
C80.063 (2)0.051 (2)0.0437 (18)0.0075 (17)0.0274 (17)−0.0005 (16)
N30.0655 (18)0.062 (2)0.0556 (16)0.0036 (15)0.0319 (15)−0.0152 (15)
C210.0572 (19)0.050 (2)0.0508 (18)−0.0131 (17)0.0315 (16)−0.0076 (17)
C10.0519 (19)0.059 (2)0.0488 (19)−0.0016 (17)0.0213 (16)−0.0033 (17)
C40.060 (2)0.050 (2)0.0499 (19)0.0034 (17)0.0320 (16)0.0011 (17)
C190.0526 (19)0.047 (2)0.0435 (18)0.0018 (16)0.0214 (15)−0.0054 (16)
C200.0570 (19)0.051 (2)0.0503 (18)−0.0052 (16)0.0297 (16)−0.0076 (17)
C130.067 (2)0.051 (2)0.054 (2)−0.0064 (18)0.0341 (18)−0.0127 (17)
C240.0502 (19)0.049 (2)0.0514 (19)−0.0069 (17)0.0292 (16)−0.0083 (17)
O10.109 (2)0.0778 (19)0.0720 (17)0.0029 (17)0.0441 (16)−0.0235 (16)
C70.065 (2)0.077 (3)0.076 (2)−0.013 (2)0.037 (2)−0.018 (2)
C290.052 (2)0.063 (2)0.067 (2)−0.0037 (18)0.0330 (18)−0.006 (2)
C110.084 (3)0.066 (3)0.057 (2)0.021 (2)0.034 (2)−0.002 (2)
C90.075 (2)0.052 (2)0.052 (2)−0.0078 (18)0.0363 (18)−0.0114 (17)
C180.064 (2)0.066 (3)0.061 (2)−0.0023 (19)0.0382 (19)−0.0068 (19)
C100.071 (2)0.055 (2)0.056 (2)−0.0092 (19)0.0355 (19)−0.0090 (18)
C250.066 (2)0.070 (3)0.072 (2)−0.008 (2)0.043 (2)−0.001 (2)
C170.085 (3)0.066 (3)0.066 (2)0.004 (2)0.047 (2)0.001 (2)
C220.067 (2)0.054 (2)0.052 (2)0.0047 (18)0.0293 (19)−0.0077 (17)
C280.070 (2)0.069 (3)0.071 (2)−0.002 (2)0.039 (2)0.002 (2)
C140.079 (3)0.078 (3)0.080 (3)−0.020 (2)0.047 (2)−0.001 (2)
C270.051 (2)0.076 (3)0.073 (2)0.003 (2)0.0206 (19)−0.009 (2)
C60.075 (2)0.126 (4)0.101 (3)−0.013 (3)0.063 (2)−0.034 (3)
C50.053 (2)0.068 (3)0.059 (2)0.0039 (18)0.0314 (17)−0.0082 (19)
C160.069 (2)0.072 (3)0.062 (2)0.003 (2)0.025 (2)−0.006 (2)
C260.054 (2)0.092 (3)0.092 (3)−0.007 (2)0.042 (2)−0.010 (2)
C150.064 (3)0.090 (3)0.095 (3)−0.007 (2)0.039 (2)0.005 (3)
C120.087 (3)0.101 (3)0.082 (3)0.027 (2)0.042 (2)−0.015 (2)
C230.076 (2)0.088 (3)0.069 (2)−0.005 (2)0.030 (2)−0.032 (2)

Geometric parameters (Å, °)

Cl1—C161.752 (4)C7—H7B0.9800
Cl2—C271.760 (4)C7—H7C0.9800
N4—C191.291 (3)C29—C281.389 (4)
N4—N51.401 (3)C29—H29A0.9500
O2—C221.227 (3)C11—C121.498 (5)
N2—C81.291 (3)C9—C101.543 (4)
N2—N31.415 (3)C9—H9A0.9900
C3—C41.382 (4)C9—H9B0.9900
C3—C21.390 (4)C18—C171.399 (4)
C3—H3A0.9500C18—H18A0.9500
C2—C11.406 (4)C10—H10A1.0000
C2—C191.465 (4)C25—C261.390 (5)
N5—C221.362 (4)C25—H25A0.9500
N5—C211.484 (3)C17—C161.374 (4)
N1—C11.336 (3)C17—H17A0.9500
N1—C51.355 (4)C22—C231.502 (4)
C8—C41.480 (4)C28—C271.367 (4)
C8—C91.511 (4)C28—H28A0.9500
N3—C111.365 (4)C14—C151.400 (5)
N3—C101.460 (4)C14—H14A0.9500
C21—C241.502 (4)C27—C261.359 (5)
C21—C201.530 (4)C6—C51.509 (4)
C21—H21A1.0000C6—H6A0.9800
C1—C71.508 (4)C6—H6B0.9800
C4—C51.399 (4)C6—H6C0.9800
C19—C201.508 (4)C16—C151.348 (5)
C20—H20A0.9900C26—H26A0.9500
C20—H20B0.9900C15—H15A0.9500
C13—C181.381 (4)C12—H12A0.9800
C13—C141.380 (4)C12—H12B0.9800
C13—C101.519 (4)C12—H12C0.9800
C24—C251.376 (4)C23—H23A0.9800
C24—C291.384 (4)C23—H23B0.9800
O1—C111.231 (4)C23—H23C0.9800
C7—H7A0.9800
C19—N4—N5106.8 (2)C8—C9—H9B111.1
C8—N2—N3107.0 (3)C10—C9—H9B111.1
C4—C3—C2121.8 (3)H9A—C9—H9B109.1
C4—C3—H3A119.1C13—C18—C17121.0 (3)
C2—C3—H3A119.1C13—C18—H18A119.5
C3—C2—C1117.9 (2)C17—C18—H18A119.5
C3—C2—C19116.4 (3)N3—C10—C13114.6 (3)
C1—C2—C19125.6 (3)N3—C10—C9100.4 (2)
C22—N5—N4120.4 (3)C13—C10—C9111.7 (3)
C22—N5—C21124.5 (3)N3—C10—H10A109.9
N4—N5—C21113.8 (2)C13—C10—H10A109.9
C1—N1—C5119.9 (3)C9—C10—H10A109.9
N2—C8—C4124.1 (3)C24—C25—C26121.8 (3)
N2—C8—C9113.5 (3)C24—C25—H25A119.1
C4—C8—C9122.4 (3)C26—C25—H25A119.1
C11—N3—N2122.1 (3)C16—C17—C18119.6 (3)
C11—N3—C10124.0 (3)C16—C17—H17A120.2
N2—N3—C10113.8 (2)C18—C17—H17A120.2
N5—C21—C24112.2 (2)O2—C22—N5117.7 (3)
N5—C21—C20101.0 (2)O2—C22—C23123.1 (3)
C24—C21—C20114.1 (2)N5—C22—C23119.1 (3)
N5—C21—H21A109.7C27—C28—C29118.7 (3)
C24—C21—H21A109.7C27—C28—H28A120.7
C20—C21—H21A109.7C29—C28—H28A120.7
N1—C1—C2121.2 (3)C13—C14—C15121.6 (3)
N1—C1—C7114.6 (3)C13—C14—H14A119.2
C2—C1—C7124.2 (3)C15—C14—H14A119.2
C3—C4—C5116.5 (3)C26—C27—C28120.7 (3)
C3—C4—C8116.6 (3)C26—C27—Cl2120.5 (3)
C5—C4—C8126.9 (3)C28—C27—Cl2118.8 (3)
N4—C19—C2123.7 (3)C5—C6—H6A109.5
N4—C19—C20114.7 (2)C5—C6—H6B109.5
C2—C19—C20121.6 (3)H6A—C6—H6B109.5
C19—C20—C21103.0 (2)C5—C6—H6C109.5
C19—C20—H20A111.2H6A—C6—H6C109.5
C21—C20—H20A111.2H6B—C6—H6C109.5
C19—C20—H20B111.2N1—C5—C4122.7 (3)
C21—C20—H20B111.2N1—C5—C6114.0 (3)
H20A—C20—H20B109.1C4—C5—C6123.3 (3)
C18—C13—C14117.5 (3)C15—C16—C17120.6 (3)
C18—C13—C10121.9 (3)C15—C16—Cl1119.8 (3)
C14—C13—C10120.3 (3)C17—C16—Cl1119.5 (3)
C25—C24—C29116.6 (3)C27—C26—C25119.8 (3)
C25—C24—C21122.3 (3)C27—C26—H26A120.1
C29—C24—C21121.1 (3)C25—C26—H26A120.1
C1—C7—H7A109.5C16—C15—C14119.6 (3)
C1—C7—H7B109.5C16—C15—H15A120.2
H7A—C7—H7B109.5C14—C15—H15A120.2
C1—C7—H7C109.5C11—C12—H12A109.5
H7A—C7—H7C109.5C11—C12—H12B109.5
H7B—C7—H7C109.5H12A—C12—H12B109.5
C28—C29—C24122.5 (3)C11—C12—H12C109.5
C28—C29—H29A118.7H12A—C12—H12C109.5
C24—C29—H29A118.7H12B—C12—H12C109.5
O1—C11—N3118.8 (3)C22—C23—H23A109.5
O1—C11—C12124.8 (3)C22—C23—H23B109.5
N3—C11—C12116.4 (3)H23A—C23—H23B109.5
C8—C9—C10103.2 (2)C22—C23—H23C109.5
C8—C9—H9A111.1H23A—C23—H23C109.5
C10—C9—H9A111.1H23B—C23—H23C109.5
C4—C3—C2—C1−0.5 (5)N2—N3—C11—C12−0.4 (5)
C4—C3—C2—C19179.3 (3)C10—N3—C11—C12179.1 (3)
C19—N4—N5—C22−162.3 (3)N2—C8—C9—C108.9 (3)
C19—N4—N5—C215.3 (3)C4—C8—C9—C10−171.8 (3)
N3—N2—C8—C4−179.9 (3)C14—C13—C18—C17−1.0 (5)
N3—N2—C8—C9−0.6 (3)C10—C13—C18—C17173.1 (3)
C8—N2—N3—C11170.7 (3)C11—N3—C10—C1374.2 (4)
C8—N2—N3—C10−8.9 (3)N2—N3—C10—C13−106.2 (3)
C22—N5—C21—C24−79.9 (4)C11—N3—C10—C9−165.9 (3)
N4—N5—C21—C24113.0 (3)N2—N3—C10—C913.7 (3)
C22—N5—C21—C20158.2 (3)C18—C13—C10—N317.2 (4)
N4—N5—C21—C20−8.9 (3)C14—C13—C10—N3−168.8 (3)
C5—N1—C1—C2−0.6 (5)C18—C13—C10—C9−96.1 (3)
C5—N1—C1—C7−179.9 (3)C14—C13—C10—C977.8 (4)
C3—C2—C1—N11.0 (4)C8—C9—C10—N3−12.5 (3)
C19—C2—C1—N1−178.8 (3)C8—C9—C10—C13109.4 (3)
C3—C2—C1—C7−179.9 (3)C29—C24—C25—C260.7 (5)
C19—C2—C1—C70.4 (5)C21—C24—C25—C26179.7 (3)
C2—C3—C4—C5−0.2 (5)C13—C18—C17—C16−0.9 (5)
C2—C3—C4—C8179.4 (3)N4—N5—C22—O2170.1 (3)
N2—C8—C4—C3179.2 (3)C21—N5—C22—O23.8 (5)
C9—C8—C4—C30.0 (4)N4—N5—C22—C23−11.4 (4)
N2—C8—C4—C5−1.2 (5)C21—N5—C22—C23−177.6 (3)
C9—C8—C4—C5179.6 (3)C24—C29—C28—C27−0.1 (5)
N5—N4—C19—C2179.1 (3)C18—C13—C14—C151.9 (5)
N5—N4—C19—C201.1 (3)C10—C13—C14—C15−172.3 (3)
C3—C2—C19—N4−178.9 (3)C29—C28—C27—C260.1 (5)
C1—C2—C19—N40.9 (5)C29—C28—C27—Cl2179.5 (3)
C3—C2—C19—C20−1.1 (4)C1—N1—C5—C4−0.2 (5)
C1—C2—C19—C20178.7 (3)C1—N1—C5—C6−179.0 (3)
N4—C19—C20—C21−6.5 (3)C3—C4—C5—N10.6 (5)
C2—C19—C20—C21175.5 (3)C8—C4—C5—N1−179.0 (3)
N5—C21—C20—C198.4 (3)C3—C4—C5—C6179.3 (3)
C24—C21—C20—C19−112.2 (3)C8—C4—C5—C6−0.3 (5)
N5—C21—C24—C25116.5 (3)C18—C17—C16—C151.9 (5)
C20—C21—C24—C25−129.5 (3)C18—C17—C16—Cl1−176.6 (3)
N5—C21—C24—C29−64.7 (4)C28—C27—C26—C250.3 (6)
C20—C21—C24—C2949.4 (4)Cl2—C27—C26—C25−179.1 (3)
C25—C24—C29—C28−0.3 (5)C24—C25—C26—C27−0.8 (5)
C21—C24—C29—C28−179.3 (3)C17—C16—C15—C14−1.0 (6)
N2—N3—C11—O1179.2 (3)Cl1—C16—C15—C14177.5 (3)
C10—N3—C11—O1−1.3 (5)C13—C14—C15—C16−1.0 (6)

Hydrogen-bond geometry (Å, °)

D—H···AD—HH···AD···AD—H···A
C9—H9A···O2i0.992.593.358 (3)135
C17—H17A···O2ii0.952.503.359 (4)151

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

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: XU2444).

References

  • Ahn, J. H., Kim, H. M., Jung, S. H., Kang, S. K., Kim, K. R., Rhee, S. D., Yang, S. D., Cheon, H. G. & Kim, S. S. (2004). Bioorg. Med. Chem. Lett.14, 4461–4465. [PubMed]
  • Bruker (2000). SMART and SAINT Bruker AXS Inc., Madison, Wisconsin, USA.
  • Flack, H. D. (1983). Acta Cryst. A39, 876–881.
  • Palaska, E., Erol, D. & Demirdamar, R. (1996). Eur. J. Med. Chem.31, 43–47.
  • Sheldrick, G. M. (1996). SADABS University of Göttingen, Germany.
  • Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [PubMed]
  • Yar, M. S., Siddiqui, A. A. & Ali, M. A. (2006). Bioorg. Med. Chem. Lett.16, 4571–4574. [PubMed]

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