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

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890

(E)-1-(1-Benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-(4-fluoro­phen­yl)prop-2-en-1-one

aX-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia, bDepartment of Organic Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625 021, Tamil Nadu, India, and cDepartment of Chemistry, Thanthai Hans Roever College, Perambalur 621 212, Tamil Nadu, India
*Correspondence e-mail: hkfun@usm.my

(Received 13 September 2011; accepted 22 September 2011; online 30 September 2011)

The asymmetric unit of the title compound, C19H16FN3O, contains two crystallographically independent mol­ecules. The triazole rings in both mol­ecules are essentially planar with maximum deviations of 0.002 (1) and 0.001 (1) Å. The dihedral angles between the benzene and fluorophenyl rings are 79.36 (9) and 89.40 (10)° in the two molecules. In the crystal, the two independent mol­ecules are linked by C—H⋯N hydrogen bonds, forming dimers. Furthermore, the crystal structure is stabilized by C—H⋯π inter­actions.

Related literature

For applications of 1,2,3-triazole, see: Banerjee et al. (1966[Banerjee, A., Nayak, P. L. & Rout, M. K. (1966). J. Indian Chem. Soc. 43, 578-82.]); Laliberte et al. (1967[Laliberte, R., Campbell, D. J. & Bruderlein, F. (1967). Can. J. Pharm. Sci. 2, 37-43.]); Suwa et al. (1984[Suwa, T., Fukushima, K. & Kyogoku, K. (1984). Jpn J. Pharmacol. 34, 89-94.]). For applications of chalcones, see: Ballesteros et al. (1995[Ballesteros, J. F., Sanz, M. J., Ubeda, A., Miranda, M. A., Iborra, S., Paya, M. & Alcaraz, M. J. (1995). J. Med. Chem. 38, 2794-2797.]); Kothari et al. (1999[Kothari, S., Vyas, R. & Verma, B. L. (1999). Indian J. Heterocycl. Chem. 8, 285-288.]); Nagaraj & Reddy (2007[Nagaraj, A. & Reddy, C. S. J. (2007). J. Heterocycl. Chem. 44, 1181-1185.]). The crystal structure is isomorphous with that of (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-phenyl­prop-2-en-1-one, see: Fun et al. (2011[Fun, H.-K., Hemamalini, M., Shanmugavelan, P., Ponnuswamy, A. & Jagatheesan, R. (2011). Acta Cryst. E67, o2707.]).

[Scheme 1]

Experimental

Crystal data
  • C19H16FN3O

  • Mr = 321.35

  • Monoclinic, P 21 /c

  • a = 12.458 (1) Å

  • b = 13.7528 (11) Å

  • c = 19.3128 (15) Å

  • β = 100.183 (2)°

  • V = 3256.8 (4) Å3

  • Z = 8

  • Mo Kα radiation

  • μ = 0.09 mm−1

  • T = 296 K

  • 0.26 × 0.22 × 0.16 mm

Data collection
  • Bruker APEXII DUO CCD area-detector diffractometer

  • Absorption correction: multi-scan (SADABS; Bruker, 2009[Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.977, Tmax = 0.986

  • 37230 measured reflections

  • 9500 independent reflections

  • 4782 reflections with I > 2σ(I)

  • Rint = 0.048

Refinement
  • R[F2 > 2σ(F2)] = 0.049

  • wR(F2) = 0.158

  • S = 0.99

  • 9500 reflections

  • 435 parameters

  • H-atom parameters constrained

  • Δρmax = 0.16 e Å−3

  • Δρmin = −0.19 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

Cg3 and Cg6 are the centroids of the of the C13A–C18A and C13B–C18B rings, respectively.

D—H⋯A D—H H⋯A DA D—H⋯A
C12B—H12C⋯N1Ai 0.97 2.46 3.422 (2) 172
C5A—H5AACg6ii 0.93 2.91 3.842 (2) 178
C12A—H12ACg3iii 0.97 2.62 3.551 (2) 161
Symmetry codes: (i) -x, -y+1, -z; (ii) [-x, y+{\script{1\over 2}}, -z+{\script{1\over 2}}]; (iii) -x+1, -y+2, -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: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.]).

Supporting information


Comment top

Organic compounds having the 1,2,3-triazole nucleus have the potential to induce antiviral, agonistic, antibacterial, antimicrobial, anti-HIV, anticonvulsant and anti-allergic activities. In addition, compounds having 1,2,3-triazole group have found industrial application such as dyes, corrosion inhibitors, sensors and photo-stabilizers (Banerjee et al., 1966; Laliberte et al., 1967; Suwa et al., 1984). The chalcone skeleton is a unique template for synthesizing various heterocyclic compounds. The compounds with the backbone of chalcones are associated with different biological activities like cardiovascular, antispasmodic, anthelmintics, antiulcer, anti-inflammatory, antiviral, antiallergic, fungicidal, bactericidal, insecticidal, antitumor, herbicidal, anticancer, antitubercular and anti-HIV (Ballesteros et al., 1995; Kothari et al., 1999; Nagaraj & Reddy, 2007). Chalcones, considered as the precursors of flavonoids and isoflavonoids, are abundant in edible plants, and have also been shown to display a diverse array of pharmacological activities. The presence of a reactive α, β-unsaturated keto function in chalcones is found to be responsible for their activities.

The asymmetric unit of the title compound, contains two crystallographically independent (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-(4-fluorophenyl)prop-2-en-1-one molecules (A & B) as shown in Fig. 1. In both molecules, the triazole (N1A–N3A/C10A,C11A and N1B–N3B/C10B,C11B) units are essentially planar, with maximum deviations of 0.002 (1) Å for atom C11A and 0.001 (1) Å for atom N3B. The dihedral angles between the phenyl ring and the flurophenyl ring in the molecules A and B are 79.36 (9)° and 89.40 (10)° respectively.

In the crystal, (Fig. 2), the two independent molecules are connected via intermolecular C—H···N hydrogen bonds, (Table 1), to form dimers. Furthermore, the crystal structure is stabilized by C—H···π interactions involving the centroids of the C13A–C18A (Cg3) and C13B–C18B (Cg6) rings. This crystal structure is isomorphous with that of (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-phenylprop-2-en-1-one (Fun et al., 2011).

Related literature top

For applications of 1,2,3-triazole, see: Banerjee et al. (1966); Laliberte et al. (1967); Suwa et al. (1984). For applications of chalcones, see: Ballesteros et al. (1995); Kothari et al. (1999); Nagaraj & Reddy (2007). The crystal structure is isomorphous with that of (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-phenylprop-2-en-1-one, see: Fun et al. (2011).

Experimental top

A mixture of 4-acetyl-1-benzyl-5-methyl-1,2,3-triazole (0.20 g, 0.01 mol) and p-fluorobenzaldehyde (0.01 mol) was stirred in ethanol (2–3 ml) and then a 50% sodium hydroxide solution (0.5 ml) was added. The mixture was stirred for 2 minutes at room temperature and poured onto excess of crushed ice and neutralized with dilute hydrochloric acid. (E)-1-(1- Benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-(4-fluorophenyl)prop-2-en-1-one, which precipitated out as a solid, was filtered and recrystallized from ethanol. Yield: 0.29 g (98%), Mp.169–170°C.

Refinement top

All hydrogen atoms were positioned geometrically [C–H = 0.93–0.97 Å] and were refined using a riding model, with Uiso(H) = 1.2 or 1.5 Ueq(C). A rotating group model was applied to the methyl groups.

Structure description top

Organic compounds having the 1,2,3-triazole nucleus have the potential to induce antiviral, agonistic, antibacterial, antimicrobial, anti-HIV, anticonvulsant and anti-allergic activities. In addition, compounds having 1,2,3-triazole group have found industrial application such as dyes, corrosion inhibitors, sensors and photo-stabilizers (Banerjee et al., 1966; Laliberte et al., 1967; Suwa et al., 1984). The chalcone skeleton is a unique template for synthesizing various heterocyclic compounds. The compounds with the backbone of chalcones are associated with different biological activities like cardiovascular, antispasmodic, anthelmintics, antiulcer, anti-inflammatory, antiviral, antiallergic, fungicidal, bactericidal, insecticidal, antitumor, herbicidal, anticancer, antitubercular and anti-HIV (Ballesteros et al., 1995; Kothari et al., 1999; Nagaraj & Reddy, 2007). Chalcones, considered as the precursors of flavonoids and isoflavonoids, are abundant in edible plants, and have also been shown to display a diverse array of pharmacological activities. The presence of a reactive α, β-unsaturated keto function in chalcones is found to be responsible for their activities.

The asymmetric unit of the title compound, contains two crystallographically independent (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-(4-fluorophenyl)prop-2-en-1-one molecules (A & B) as shown in Fig. 1. In both molecules, the triazole (N1A–N3A/C10A,C11A and N1B–N3B/C10B,C11B) units are essentially planar, with maximum deviations of 0.002 (1) Å for atom C11A and 0.001 (1) Å for atom N3B. The dihedral angles between the phenyl ring and the flurophenyl ring in the molecules A and B are 79.36 (9)° and 89.40 (10)° respectively.

In the crystal, (Fig. 2), the two independent molecules are connected via intermolecular C—H···N hydrogen bonds, (Table 1), to form dimers. Furthermore, the crystal structure is stabilized by C—H···π interactions involving the centroids of the C13A–C18A (Cg3) and C13B–C18B (Cg6) rings. This crystal structure is isomorphous with that of (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-phenylprop-2-en-1-one (Fun et al., 2011).

For applications of 1,2,3-triazole, see: Banerjee et al. (1966); Laliberte et al. (1967); Suwa et al. (1984). For applications of chalcones, see: Ballesteros et al. (1995); Kothari et al. (1999); Nagaraj & Reddy (2007). The crystal structure is isomorphous with that of (E)-1-(1-benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-phenylprop-2-en-1-one, see: Fun et al. (2011).

Computing details top

Data collection: APEX2 (Bruker, 2009); cell refinement: SAINT (Bruker, 2009); data reduction: SAINT (Bruker, 2009); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).

Figures top
[Figure 1] Fig. 1. An ORTEP view of the title compound, showing 50% probability displacement ellipsoids.
[Figure 2] Fig. 2. The crystal packing of the title compound. H atoms not involved in hydrogen bonding are omitted.
(E)-1-(1-Benzyl-5-methyl-1H-1,2,3-triazol-4-yl)-3-(4-fluorophenyl)prop-2-en-1-one top
Crystal data top
C19H16FN3OF(000) = 1344
Mr = 321.35Dx = 1.311 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 5012 reflections
a = 12.458 (1) Åθ = 2.5–28.8°
b = 13.7528 (11) ŵ = 0.09 mm1
c = 19.3128 (15) ÅT = 296 K
β = 100.183 (2)°Block, colourless
V = 3256.8 (4) Å30.26 × 0.22 × 0.16 mm
Z = 8
Data collection top
Bruker APEXII DUO CCD area-detector
diffractometer
9500 independent reflections
Radiation source: fine-focus sealed tube4782 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.048
φ and ω scansθmax = 30.1°, θmin = 1.8°
Absorption correction: multi-scan
(SADABS; Bruker, 2009)
h = 1117
Tmin = 0.977, Tmax = 0.986k = 1619
37230 measured reflectionsl = 2727
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)] = 0.049Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.158H-atom parameters constrained
S = 0.99 w = 1/[σ2(Fo2) + (0.0702P)2 + 0.2551P]
where P = (Fo2 + 2Fc2)/3
9500 reflections(Δ/σ)max = 0.001
435 parametersΔρmax = 0.16 e Å3
0 restraintsΔρmin = 0.19 e Å3
Crystal data top
C19H16FN3OV = 3256.8 (4) Å3
Mr = 321.35Z = 8
Monoclinic, P21/cMo Kα radiation
a = 12.458 (1) ŵ = 0.09 mm1
b = 13.7528 (11) ÅT = 296 K
c = 19.3128 (15) Å0.26 × 0.22 × 0.16 mm
β = 100.183 (2)°
Data collection top
Bruker APEXII DUO CCD area-detector
diffractometer
9500 independent reflections
Absorption correction: multi-scan
(SADABS; Bruker, 2009)
4782 reflections with I > 2σ(I)
Tmin = 0.977, Tmax = 0.986Rint = 0.048
37230 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0490 restraints
wR(F2) = 0.158H-atom parameters constrained
S = 0.99Δρmax = 0.16 e Å3
9500 reflectionsΔρmin = 0.19 e Å3
435 parameters
Special details top

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 > 2σ(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
F1A0.32640 (10)0.37115 (10)0.09739 (9)0.1059 (5)
O1A0.23331 (11)0.69816 (10)0.24388 (6)0.0639 (4)
N1A0.24431 (12)0.74029 (11)0.06245 (7)0.0589 (4)
N2A0.31516 (13)0.79113 (12)0.03501 (8)0.0630 (4)
N3A0.38780 (11)0.82740 (9)0.08961 (7)0.0468 (3)
C1A0.08988 (15)0.51783 (14)0.08771 (10)0.0588 (5)
H1AA0.05720.54840.05380.071*
C2A0.18483 (17)0.46491 (15)0.06714 (12)0.0710 (6)
H2AA0.21560.45890.01980.085*
C3A0.23210 (15)0.42178 (13)0.11782 (13)0.0669 (5)
C4A0.18837 (16)0.42645 (14)0.18714 (12)0.0693 (6)
H4AA0.22130.39480.22040.083*
C5A0.09391 (15)0.47917 (13)0.20721 (10)0.0576 (4)
H5AA0.06370.48360.25470.069*
C6A0.04287 (13)0.52584 (11)0.15815 (9)0.0443 (4)
C7A0.05598 (13)0.58185 (11)0.18279 (9)0.0458 (4)
H7AA0.08320.57870.23080.055*
C8A0.11174 (13)0.63664 (12)0.14531 (9)0.0474 (4)
H8AA0.09030.63990.09670.057*
C9A0.20747 (13)0.69246 (11)0.17970 (9)0.0456 (4)
C10A0.27110 (13)0.74407 (11)0.13399 (8)0.0427 (4)
C11A0.36359 (12)0.80044 (10)0.15187 (8)0.0408 (3)
C12A0.47819 (14)0.88739 (12)0.07504 (10)0.0529 (4)
H12A0.48640.87760.02650.063*
H12B0.54500.86590.10480.063*
C13A0.46318 (13)0.99394 (12)0.08708 (8)0.0449 (4)
C14A0.55168 (15)1.04882 (13)0.11866 (9)0.0538 (4)
H14A0.61801.01830.13480.065*
C15A0.54284 (19)1.14811 (15)0.12649 (10)0.0689 (5)
H15A0.60341.18430.14660.083*
C16A0.4451 (2)1.19308 (15)0.10462 (11)0.0729 (6)
H16A0.43861.25960.11140.087*
C17A0.35653 (19)1.14075 (16)0.07276 (12)0.0755 (6)
H17A0.29051.17200.05730.091*
C18A0.36500 (15)1.04084 (14)0.06344 (10)0.0618 (5)
H18A0.30491.00560.04140.074*
C19A0.42936 (15)0.83060 (14)0.22006 (9)0.0578 (5)
H19A0.50550.82450.21800.087*
H19B0.41200.78980.25690.087*
H19C0.41320.89700.22950.087*
F1B0.73003 (13)0.72639 (11)0.08097 (11)0.1253 (6)
O1B0.27643 (11)0.39555 (10)0.25084 (6)0.0671 (4)
N1B0.15078 (13)0.35495 (11)0.07189 (8)0.0592 (4)
N2B0.06363 (14)0.30509 (12)0.04708 (8)0.0655 (4)
N3B0.02495 (11)0.26840 (10)0.10339 (7)0.0519 (4)
C1OB0.16882 (13)0.35062 (11)0.14372 (8)0.0457 (4)
C1B0.49013 (17)0.58159 (14)0.08252 (11)0.0667 (5)
H1BA0.43310.55470.05070.080*
C2B0.5694 (2)0.63425 (16)0.05776 (13)0.0829 (7)
H2BA0.56670.64280.00970.099*
C3B0.65206 (19)0.67376 (15)0.10544 (16)0.0807 (7)
C4B0.65816 (18)0.66406 (16)0.17544 (16)0.0833 (7)
H4BA0.71460.69280.20670.100*
C5B0.57889 (15)0.61067 (14)0.19975 (12)0.0674 (5)
H5BA0.58250.60310.24800.081*
C6B0.49368 (13)0.56785 (11)0.15370 (9)0.0493 (4)
C7B0.41315 (13)0.51127 (12)0.18278 (9)0.0496 (4)
H7BA0.41920.51300.23150.060*
C8B0.33261 (14)0.45779 (12)0.14874 (9)0.0511 (4)
H8BA0.32110.45580.09980.061*
C9B0.26054 (13)0.40125 (12)0.18655 (9)0.0475 (4)
C11B0.08781 (13)0.29476 (11)0.16430 (8)0.0445 (4)
C12B0.07283 (14)0.20804 (13)0.09197 (11)0.0602 (5)
H12C0.11470.22250.04590.072*
H12D0.11730.22510.12660.072*
C13B0.04989 (14)0.10044 (12)0.09659 (8)0.0485 (4)
C14B0.13479 (17)0.03893 (15)0.10314 (11)0.0703 (6)
H14B0.20230.06480.10730.084*
C15B0.1208 (2)0.06059 (16)0.10362 (13)0.0865 (7)
H15B0.17900.10120.10810.104*
C16B0.0227 (2)0.09977 (16)0.09764 (11)0.0815 (7)
H16B0.01400.16690.09720.098*
C17B0.0622 (2)0.04041 (16)0.09231 (12)0.0795 (6)
H17B0.12960.06700.08880.095*
C18B0.04912 (17)0.05965 (15)0.09199 (11)0.0672 (5)
H18B0.10820.09960.08860.081*
C19B0.06490 (15)0.26518 (14)0.23379 (10)0.0615 (5)
H19D0.01150.27290.23450.092*
H19E0.10620.30510.26970.092*
H19F0.08500.19830.24230.092*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
F1A0.0656 (8)0.0858 (9)0.1618 (14)0.0349 (7)0.0079 (8)0.0050 (9)
O1A0.0682 (8)0.0721 (9)0.0517 (7)0.0202 (7)0.0112 (6)0.0022 (6)
N1A0.0605 (9)0.0638 (10)0.0503 (8)0.0176 (8)0.0043 (7)0.0003 (7)
N2A0.0675 (10)0.0705 (10)0.0498 (8)0.0217 (8)0.0067 (7)0.0012 (7)
N3A0.0483 (8)0.0418 (7)0.0513 (8)0.0087 (6)0.0116 (6)0.0008 (6)
C1A0.0569 (11)0.0603 (11)0.0593 (11)0.0115 (9)0.0107 (9)0.0058 (9)
C2A0.0655 (13)0.0687 (13)0.0746 (13)0.0138 (10)0.0008 (10)0.0025 (10)
C3A0.0474 (10)0.0463 (10)0.1058 (17)0.0100 (8)0.0106 (11)0.0024 (10)
C4A0.0607 (12)0.0569 (12)0.0966 (16)0.0093 (10)0.0309 (11)0.0143 (11)
C5A0.0572 (11)0.0540 (10)0.0639 (11)0.0057 (9)0.0171 (9)0.0092 (8)
C6A0.0436 (9)0.0342 (8)0.0565 (10)0.0009 (7)0.0125 (7)0.0026 (7)
C7A0.0446 (9)0.0414 (8)0.0528 (9)0.0008 (7)0.0128 (7)0.0001 (7)
C8A0.0470 (9)0.0438 (9)0.0521 (9)0.0061 (7)0.0105 (7)0.0017 (7)
C9A0.0459 (9)0.0391 (8)0.0524 (10)0.0018 (7)0.0102 (7)0.0015 (7)
C10A0.0420 (8)0.0382 (8)0.0469 (9)0.0019 (7)0.0047 (7)0.0008 (7)
C11A0.0419 (8)0.0337 (7)0.0471 (8)0.0003 (6)0.0089 (7)0.0002 (6)
C12A0.0509 (10)0.0477 (10)0.0643 (11)0.0064 (8)0.0217 (8)0.0028 (8)
C13A0.0448 (9)0.0461 (9)0.0463 (8)0.0051 (7)0.0146 (7)0.0049 (7)
C14A0.0514 (10)0.0583 (11)0.0512 (9)0.0069 (8)0.0083 (8)0.0000 (8)
C15A0.0820 (15)0.0608 (12)0.0643 (12)0.0183 (11)0.0141 (11)0.0139 (10)
C16A0.1014 (18)0.0482 (11)0.0758 (13)0.0028 (12)0.0340 (13)0.0037 (10)
C17A0.0717 (14)0.0663 (14)0.0938 (16)0.0204 (11)0.0288 (12)0.0190 (11)
C18A0.0478 (10)0.0605 (12)0.0775 (13)0.0021 (9)0.0121 (9)0.0093 (10)
C19A0.0532 (10)0.0644 (11)0.0545 (10)0.0138 (9)0.0058 (8)0.0048 (8)
F1B0.1008 (11)0.0844 (10)0.2067 (18)0.0360 (8)0.0705 (11)0.0100 (10)
O1B0.0653 (8)0.0783 (9)0.0552 (8)0.0194 (7)0.0037 (6)0.0041 (6)
N1B0.0631 (10)0.0599 (9)0.0537 (9)0.0172 (8)0.0082 (7)0.0033 (7)
N2B0.0758 (11)0.0642 (10)0.0533 (9)0.0206 (9)0.0028 (8)0.0022 (7)
N3B0.0494 (8)0.0445 (8)0.0583 (9)0.0085 (6)0.0002 (7)0.0061 (6)
C1OB0.0474 (9)0.0397 (8)0.0495 (9)0.0019 (7)0.0072 (7)0.0037 (7)
C1B0.0662 (12)0.0567 (11)0.0759 (13)0.0138 (10)0.0093 (10)0.0042 (10)
C2B0.0942 (17)0.0646 (13)0.0970 (17)0.0146 (12)0.0364 (14)0.0121 (12)
C3B0.0668 (14)0.0445 (11)0.140 (2)0.0101 (10)0.0443 (15)0.0029 (13)
C4B0.0537 (12)0.0662 (14)0.129 (2)0.0188 (10)0.0142 (13)0.0144 (14)
C5B0.0550 (11)0.0601 (12)0.0848 (14)0.0092 (9)0.0065 (10)0.0102 (10)
C6B0.0433 (9)0.0367 (8)0.0676 (11)0.0015 (7)0.0089 (8)0.0003 (7)
C7B0.0450 (9)0.0429 (9)0.0600 (10)0.0007 (7)0.0066 (8)0.0016 (7)
C8B0.0483 (9)0.0468 (9)0.0571 (10)0.0054 (7)0.0067 (8)0.0021 (8)
C9B0.0441 (9)0.0417 (9)0.0557 (10)0.0016 (7)0.0060 (7)0.0022 (7)
C11B0.0417 (8)0.0365 (8)0.0535 (9)0.0010 (7)0.0037 (7)0.0045 (7)
C12B0.0439 (10)0.0523 (10)0.0793 (13)0.0100 (8)0.0035 (9)0.0028 (9)
C13B0.0480 (9)0.0485 (9)0.0474 (9)0.0076 (8)0.0044 (7)0.0003 (7)
C14B0.0580 (12)0.0629 (13)0.0883 (14)0.0164 (10)0.0080 (10)0.0067 (11)
C15B0.0947 (18)0.0572 (13)0.1027 (18)0.0305 (13)0.0042 (14)0.0116 (12)
C16B0.128 (2)0.0461 (11)0.0689 (13)0.0041 (14)0.0131 (13)0.0026 (10)
C17B0.1003 (18)0.0624 (14)0.0829 (15)0.0143 (13)0.0352 (13)0.0006 (11)
C18B0.0647 (12)0.0610 (12)0.0810 (13)0.0063 (10)0.0270 (10)0.0033 (10)
C19B0.0524 (11)0.0676 (12)0.0647 (11)0.0037 (9)0.0113 (9)0.0163 (9)
Geometric parameters (Å, º) top
F1A—C3A1.363 (2)F1B—C3B1.361 (2)
O1A—C9A1.2267 (19)O1B—C9B1.2248 (19)
N1A—N2A1.309 (2)N1B—N2B1.302 (2)
N1A—C10A1.364 (2)N1B—C1OB1.367 (2)
N2A—N3A1.3573 (19)N2B—N3B1.362 (2)
N3A—C11A1.343 (2)N3B—C11B1.342 (2)
N3A—C12A1.463 (2)N3B—C12B1.458 (2)
C1A—C2A1.386 (3)C1OB—C11B1.381 (2)
C1A—C6A1.387 (2)C1OB—C9B1.463 (2)
C1A—H1AA0.9300C1B—C2B1.376 (3)
C2A—C3A1.364 (3)C1B—C6B1.381 (3)
C2A—H2AA0.9300C1B—H1BA0.9300
C3A—C4A1.355 (3)C2B—C3B1.367 (3)
C4A—C5A1.378 (3)C2B—H2BA0.9300
C4A—H4AA0.9300C3B—C4B1.347 (3)
C5A—C6A1.388 (2)C4B—C5B1.378 (3)
C5A—H5AA0.9300C4B—H4BA0.9300
C6A—C7A1.459 (2)C5B—C6B1.389 (2)
C7A—C8A1.324 (2)C5B—H5BA0.9300
C7A—H7AA0.9300C6B—C7B1.458 (2)
C8A—C9A1.474 (2)C7B—C8B1.322 (2)
C8A—H8AA0.9300C7B—H7BA0.9300
C9A—C10A1.469 (2)C8B—C9B1.475 (2)
C10A—C11A1.381 (2)C8B—H8BA0.9300
C11A—C19A1.482 (2)C11B—C19B1.478 (2)
C12A—C13A1.501 (2)C12B—C13B1.507 (2)
C12A—H12A0.9700C12B—H12C0.9700
C12A—H12B0.9700C12B—H12D0.9700
C13A—C14A1.385 (2)C13B—C18B1.372 (3)
C13A—C18A1.387 (2)C13B—C14B1.378 (2)
C14A—C15A1.380 (3)C14B—C15B1.379 (3)
C14A—H14A0.9300C14B—H14B0.9300
C15A—C16A1.365 (3)C15B—C16B1.359 (3)
C15A—H15A0.9300C15B—H15B0.9300
C16A—C17A1.369 (3)C16B—C17B1.354 (3)
C16A—H16A0.9300C16B—H16B0.9300
C17A—C18A1.392 (3)C17B—C18B1.385 (3)
C17A—H17A0.9300C17B—H17B0.9300
C18A—H18A0.9300C18B—H18B0.9300
C19A—H19A0.9600C19B—H19D0.9600
C19A—H19B0.9600C19B—H19E0.9600
C19A—H19C0.9600C19B—H19F0.9600
N2A—N1A—C10A109.14 (14)N2B—N1B—C1OB109.11 (14)
N1A—N2A—N3A106.65 (13)N1B—N2B—N3B106.92 (13)
C11A—N3A—N2A111.71 (13)C11B—N3B—N2B111.45 (13)
C11A—N3A—C12A129.08 (14)C11B—N3B—C12B128.94 (15)
N2A—N3A—C12A119.21 (13)N2B—N3B—C12B119.60 (14)
C2A—C1A—C6A120.92 (17)N1B—C1OB—C11B108.59 (14)
C2A—C1A—H1AA119.5N1B—C1OB—C9B121.66 (15)
C6A—C1A—H1AA119.5C11B—C1OB—C9B129.74 (15)
C3A—C2A—C1A118.53 (19)C2B—C1B—C6B121.3 (2)
C3A—C2A—H2AA120.7C2B—C1B—H1BA119.4
C1A—C2A—H2AA120.7C6B—C1B—H1BA119.4
C4A—C3A—F1A119.1 (2)C3B—C2B—C1B118.4 (2)
C4A—C3A—C2A122.63 (18)C3B—C2B—H2BA120.8
F1A—C3A—C2A118.3 (2)C1B—C2B—H2BA120.8
C3A—C4A—C5A118.48 (18)C4B—C3B—F1B118.9 (2)
C3A—C4A—H4AA120.8C4B—C3B—C2B122.6 (2)
C5A—C4A—H4AA120.8F1B—C3B—C2B118.5 (3)
C4A—C5A—C6A121.52 (18)C3B—C4B—C5B118.6 (2)
C4A—C5A—H5AA119.2C3B—C4B—H4BA120.7
C6A—C5A—H5AA119.2C5B—C4B—H4BA120.7
C1A—C6A—C5A117.89 (16)C4B—C5B—C6B121.3 (2)
C1A—C6A—C7A123.19 (15)C4B—C5B—H5BA119.3
C5A—C6A—C7A118.92 (15)C6B—C5B—H5BA119.3
C8A—C7A—C6A128.06 (16)C1B—C6B—C5B117.75 (17)
C8A—C7A—H7AA116.0C1B—C6B—C7B123.60 (16)
C6A—C7A—H7AA116.0C5B—C6B—C7B118.65 (17)
C7A—C8A—C9A120.73 (15)C8B—C7B—C6B128.24 (17)
C7A—C8A—H8AA119.6C8B—C7B—H7BA115.9
C9A—C8A—H8AA119.6C6B—C7B—H7BA115.9
O1A—C9A—C10A120.21 (14)C7B—C8B—C9B121.48 (16)
O1A—C9A—C8A122.37 (15)C7B—C8B—H8BA119.3
C10A—C9A—C8A117.41 (14)C9B—C8B—H8BA119.3
N1A—C10A—C11A108.58 (14)O1B—C9B—C1OB120.85 (15)
N1A—C10A—C9A121.93 (14)O1B—C9B—C8B122.15 (15)
C11A—C10A—C9A129.48 (14)C1OB—C9B—C8B116.99 (15)
N3A—C11A—C10A103.93 (13)N3B—C11B—C1OB103.93 (14)
N3A—C11A—C19A122.83 (14)N3B—C11B—C19B123.02 (15)
C10A—C11A—C19A133.24 (15)C1OB—C11B—C19B133.05 (15)
N3A—C12A—C13A113.56 (14)N3B—C12B—C13B113.92 (14)
N3A—C12A—H12A108.9N3B—C12B—H12C108.8
C13A—C12A—H12A108.9C13B—C12B—H12C108.8
N3A—C12A—H12B108.9N3B—C12B—H12D108.8
C13A—C12A—H12B108.9C13B—C12B—H12D108.8
H12A—C12A—H12B107.7H12C—C12B—H12D107.7
C14A—C13A—C18A118.58 (16)C18B—C13B—C14B117.94 (18)
C14A—C13A—C12A119.27 (15)C18B—C13B—C12B124.12 (16)
C18A—C13A—C12A122.01 (16)C14B—C13B—C12B117.90 (17)
C15A—C14A—C13A120.96 (18)C13B—C14B—C15B120.8 (2)
C15A—C14A—H14A119.5C13B—C14B—H14B119.6
C13A—C14A—H14A119.5C15B—C14B—H14B119.6
C16A—C15A—C14A119.90 (19)C16B—C15B—C14B120.5 (2)
C16A—C15A—H15A120.0C16B—C15B—H15B119.8
C14A—C15A—H15A120.0C14B—C15B—H15B119.8
C15A—C16A—C17A120.33 (19)C17B—C16B—C15B119.6 (2)
C15A—C16A—H16A119.8C17B—C16B—H16B120.2
C17A—C16A—H16A119.8C15B—C16B—H16B120.2
C16A—C17A—C18A120.2 (2)C16B—C17B—C18B120.4 (2)
C16A—C17A—H17A119.9C16B—C17B—H17B119.8
C18A—C17A—H17A119.9C18B—C17B—H17B119.8
C13A—C18A—C17A119.94 (19)C13B—C18B—C17B120.8 (2)
C13A—C18A—H18A120.0C13B—C18B—H18B119.6
C17A—C18A—H18A120.0C17B—C18B—H18B119.6
C11A—C19A—H19A109.5C11B—C19B—H19D109.5
C11A—C19A—H19B109.5C11B—C19B—H19E109.5
H19A—C19A—H19B109.5H19D—C19B—H19E109.5
C11A—C19A—H19C109.5C11B—C19B—H19F109.5
H19A—C19A—H19C109.5H19D—C19B—H19F109.5
H19B—C19A—H19C109.5H19E—C19B—H19F109.5
C10A—N1A—N2A—N3A0.1 (2)C1OB—N1B—N2B—N3B0.1 (2)
N1A—N2A—N3A—C11A0.28 (19)N1B—N2B—N3B—C11B0.2 (2)
N1A—N2A—N3A—C12A179.52 (14)N1B—N2B—N3B—C12B179.56 (15)
C6A—C1A—C2A—C3A0.9 (3)N2B—N1B—C1OB—C11B0.0 (2)
C1A—C2A—C3A—C4A1.8 (3)N2B—N1B—C1OB—C9B179.05 (15)
C1A—C2A—C3A—F1A178.96 (18)C6B—C1B—C2B—C3B0.5 (3)
F1A—C3A—C4A—C5A178.99 (17)C1B—C2B—C3B—C4B0.8 (4)
C2A—C3A—C4A—C5A1.8 (3)C1B—C2B—C3B—F1B179.57 (19)
C3A—C4A—C5A—C6A0.8 (3)F1B—C3B—C4B—C5B180.00 (19)
C2A—C1A—C6A—C5A0.0 (3)C2B—C3B—C4B—C5B1.2 (4)
C2A—C1A—C6A—C7A178.99 (17)C3B—C4B—C5B—C6B0.4 (3)
C4A—C5A—C6A—C1A0.1 (3)C2B—C1B—C6B—C5B1.3 (3)
C4A—C5A—C6A—C7A179.01 (17)C2B—C1B—C6B—C7B178.81 (18)
C1A—C6A—C7A—C8A4.2 (3)C4B—C5B—C6B—C1B0.8 (3)
C5A—C6A—C7A—C8A174.79 (17)C4B—C5B—C6B—C7B179.25 (18)
C6A—C7A—C8A—C9A176.88 (15)C1B—C6B—C7B—C8B6.9 (3)
C7A—C8A—C9A—O1A7.1 (3)C5B—C6B—C7B—C8B173.16 (18)
C7A—C8A—C9A—C10A174.33 (15)C6B—C7B—C8B—C9B177.35 (16)
N2A—N1A—C10A—C11A0.1 (2)N1B—C1OB—C9B—O1B179.00 (16)
N2A—N1A—C10A—C9A178.98 (15)C11B—C1OB—C9B—O1B2.2 (3)
O1A—C9A—C10A—N1A179.34 (16)N1B—C1OB—C9B—C8B0.3 (2)
C8A—C9A—C10A—N1A0.7 (2)C11B—C1OB—C9B—C8B178.47 (16)
O1A—C9A—C10A—C11A1.8 (3)C7B—C8B—C9B—O1B5.3 (3)
C8A—C9A—C10A—C11A179.51 (15)C7B—C8B—C9B—C1OB175.37 (15)
N2A—N3A—C11A—C10A0.31 (18)N2B—N3B—C11B—C1OB0.14 (18)
C12A—N3A—C11A—C10A179.47 (15)C12B—N3B—C11B—C1OB179.46 (16)
N2A—N3A—C11A—C19A179.59 (15)N2B—N3B—C11B—C19B179.98 (16)
C12A—N3A—C11A—C19A0.6 (3)C12B—N3B—C11B—C19B0.7 (3)
N1A—C10A—C11A—N3A0.22 (18)N1B—C1OB—C11B—N3B0.06 (18)
C9A—C10A—C11A—N3A178.72 (16)C9B—C1OB—C11B—N3B178.85 (16)
N1A—C10A—C11A—C19A179.66 (17)N1B—C1OB—C11B—C19B179.88 (18)
C9A—C10A—C11A—C19A1.4 (3)C9B—C1OB—C11B—C19B1.0 (3)
C11A—N3A—C12A—C13A75.8 (2)C11B—N3B—C12B—C13B80.5 (2)
N2A—N3A—C12A—C13A104.47 (17)N2B—N3B—C12B—C13B98.73 (19)
N3A—C12A—C13A—C14A139.38 (16)N3B—C12B—C13B—C18B17.6 (3)
N3A—C12A—C13A—C18A44.9 (2)N3B—C12B—C13B—C14B165.00 (16)
C18A—C13A—C14A—C15A0.1 (3)C18B—C13B—C14B—C15B1.2 (3)
C12A—C13A—C14A—C15A175.76 (16)C12B—C13B—C14B—C15B176.30 (19)
C13A—C14A—C15A—C16A1.7 (3)C13B—C14B—C15B—C16B0.0 (3)
C14A—C15A—C16A—C17A2.2 (3)C14B—C15B—C16B—C17B1.1 (4)
C15A—C16A—C17A—C18A1.1 (3)C15B—C16B—C17B—C18B0.8 (3)
C14A—C13A—C18A—C17A1.1 (3)C14B—C13B—C18B—C17B1.5 (3)
C12A—C13A—C18A—C17A176.80 (17)C12B—C13B—C18B—C17B175.93 (18)
C16A—C17A—C18A—C13A0.6 (3)C16B—C17B—C18B—C13B0.4 (3)
Hydrogen-bond geometry (Å, º) top
Cg3 and Cg6 are the centroids of the of the C13A–C18A and C13B–C18B rings, respectively.
D—H···AD—HH···AD···AD—H···A
C12B—H12C···N1Ai0.972.463.422 (2)172
C5A—H5AA···Cg6ii0.932.913.842 (2)178
C12A—H12A···Cg3iii0.972.623.551 (2)161
Symmetry codes: (i) x, y+1, z; (ii) x, y+1/2, z+1/2; (iii) x+1, y+2, z.

Experimental details

Crystal data
Chemical formulaC19H16FN3O
Mr321.35
Crystal system, space groupMonoclinic, P21/c
Temperature (K)296
a, b, c (Å)12.458 (1), 13.7528 (11), 19.3128 (15)
β (°) 100.183 (2)
V3)3256.8 (4)
Z8
Radiation typeMo Kα
µ (mm1)0.09
Crystal size (mm)0.26 × 0.22 × 0.16
Data collection
DiffractometerBruker APEXII DUO CCD area-detector
diffractometer
Absorption correctionMulti-scan
(SADABS; Bruker, 2009)
Tmin, Tmax0.977, 0.986
No. of measured, independent and
observed [I > 2σ(I)] reflections
37230, 9500, 4782
Rint0.048
(sin θ/λ)max1)0.706
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.049, 0.158, 0.99
No. of reflections9500
No. of parameters435
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.16, 0.19

Computer programs: APEX2 (Bruker, 2009), SAINT (Bruker, 2009), SHELXTL (Sheldrick, 2008), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).

Hydrogen-bond geometry (Å, º) top
Cg3 and Cg6 are the centroids of the of the C13A–C18A and C13B–C18B rings, respectively.
D—H···AD—HH···AD···AD—H···A
C12B—H12C···N1Ai0.972.463.422 (2)172
C5A—H5AA···Cg6ii0.932.913.842 (2)178
C12A—H12A···Cg3iii0.972.623.551 (2)161
Symmetry codes: (i) x, y+1, z; (ii) x, y+1/2, z+1/2; (iii) x+1, y+2, z.
 

Footnotes

Thomson Reuters ResearcherID: A-3561-2009.

Acknowledgements

HKF and MH thank the Malaysian Government and Universiti Sains Malaysia for the Research University Grant No. 1001/PFIZIK/811160. MH also thanks Universiti Sains Malaysia for a post-doctoral research fellowship.

References

First citationBallesteros, J. F., Sanz, M. J., Ubeda, A., Miranda, M. A., Iborra, S., Paya, M. & Alcaraz, M. J. (1995). J. Med. Chem. 38, 2794–2797.  CrossRef CAS PubMed Web of Science Google Scholar
First citationBanerjee, A., Nayak, P. L. & Rout, M. K. (1966). J. Indian Chem. Soc. 43, 578–82.  CAS Google Scholar
First citationBruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.  Google Scholar
First citationFun, H.-K., Hemamalini, M., Shanmugavelan, P., Ponnuswamy, A. & Jagatheesan, R. (2011). Acta Cryst. E67, o2707.  Web of Science CSD CrossRef IUCr Journals Google Scholar
First citationKothari, S., Vyas, R. & Verma, B. L. (1999). Indian J. Heterocycl. Chem. 8, 285–288.  CAS Google Scholar
First citationLaliberte, R., Campbell, D. J. & Bruderlein, F. (1967). Can. J. Pharm. Sci. 2, 37–43.  CAS Google Scholar
First citationNagaraj, A. & Reddy, C. S. J. (2007). J. Heterocycl. Chem. 44, 1181–1185.  CrossRef CAS Google Scholar
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationSpek, A. L. (2009). Acta Cryst. D65, 148–155.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationSuwa, T., Fukushima, K. & Kyogoku, K. (1984). Jpn J. Pharmacol. 34, 89–94.  CrossRef CAS PubMed Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Follow Acta Cryst. E
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds