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 March 1; 65(Pt 3): o507.
Published online 2009 February 11. doi:  10.1107/S1600536809004127
PMCID: PMC2968644

3-(1H-Benzotriazol-1-yl)-1-(3-methoxy­phen­yl)propan-1-one

Abstract

In the title mol­ecule, C16H15N3O2, the benzotriazole fragment and the benzene ring form a dihedral angle of 75.02 (1)°. In the crystal structure, mol­ecules related by translation along the a axis are linked into chains via weak C—H(...)π inter­actions.

Related literature

For the pharmacological activity of 1H-benzotriazole derivatives, see: Chen & Wu (2005 [triangle]). Some details of the synthesis have been described by Zhu et al. (2007 [triangle]). For reference values of geometric parameters in organic mol­ecules, see: Allen et al. (1987 [triangle]).

An external file that holds a picture, illustration, etc.
Object name is e-65-0o507-scheme1.jpg

Experimental

Crystal data

  • C16H15N3O2
  • M r = 281.31
  • Monoclinic, An external file that holds a picture, illustration, etc.
Object name is e-65-0o507-efi1.jpg
  • a = 5.3583 (14) Å
  • b = 12.976 (4) Å
  • c = 19.688 (5) Å
  • β = 91.146 (4)°
  • V = 1368.6 (6) Å3
  • Z = 4
  • Mo Kα radiation
  • μ = 0.09 mm−1
  • T = 293 (2) K
  • 0.21 × 0.15 × 0.07 mm

Data collection

  • Siemens SMART 1000 CCD area-detector diffractometer
  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996 [triangle]) T min = 0.981, T max = 0.994
  • 7461 measured reflections
  • 2693 independent reflections
  • 2279 reflections with I > 2σ(I)
  • R int = 0.018

Refinement

  • R[F 2 > 2σ(F 2)] = 0.041
  • wR(F 2) = 0.112
  • S = 1.04
  • 2693 reflections
  • 190 parameters
  • H-atom parameters constrained
  • Δρmax = 0.14 e Å−3
  • Δρmin = −0.23 e Å−3

Data collection: SMART (Siemens, 1996 [triangle]); cell refinement: SAINT (Siemens, 1996 [triangle]); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 [triangle]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 [triangle]); molecular graphics: SHELXTL (Sheldrick, 2008 [triangle]); software used to prepare material for publication: SHELXTL, PARST (Nardelli, 1995 [triangle]) and PLATON (Spek, 2003 [triangle]).

Table 1
Hydrogen-bond geometry (Å, °)

Supplementary Material

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809004127/cv2510sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536809004127/cv2510Isup2.hkl

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

Acknowledgments

This project was supported by the Natural Science Foundation of Shandong Province (grant Nos. Y2008B02 and Y2008B32).

supplementary crystallographic information

Comment

1H-Benzotriazole and its derivatives exhibit a broad spectrum of pharmacological activities, such as antifungal, antitumor and antineoplastic (Chen & Wu, 2005). In order to search for new benzotriazole derivatives with higher bioactivity, the title compound, (I), was synthesized and its structure is shown here.

In the title molecule (Fig. 1), all bond lengths and angles are within normal ranges (Allen et al., 1987). The benzotriazole system is almost planar with a dihedral angle of 1.45 (1)° between the triazole (N1–N3/C10/C11) and benzene (C10—C15) rings. The whole molecular is non-planar with a dihedral angle of 75.02 (1)° between the benzotriazole fragment and benzene C1–C6 ring. In the crystal, the molecules related by translation along axis a are linked into chains via the weak C—H···π interactions (Table 1).

Experimental

The title compound was prepared according to the literature method of Zhu et al.(2007). Single crystals suitable for X-ray diffraction were obtained by slow evaporation of an ethyl acetate solution at room temperature over a period of one week.

Refinement

All H atoms were located in difference Fourier maps and constrained to ride on their parent atoms, with C—H distances in the range 0.93–0.97 Å, and with Uiso(H) = 1.2 Ueq(C) and 1.5 Ueq(methyl C).

Figures

Fig. 1.
The molecular structure of (I) showing 50% probability displacement ellipsoids and the atom numbering scheme.

Crystal data

C16H15N3O2F(000) = 592
Mr = 281.31Dx = 1.365 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
a = 5.3583 (14) ÅCell parameters from 3062 reflections
b = 12.976 (4) Åθ = 2.6–25.9°
c = 19.688 (5) ŵ = 0.09 mm1
β = 91.146 (4)°T = 293 K
V = 1368.6 (6) Å3Block, colourless
Z = 40.21 × 0.15 × 0.07 mm

Data collection

Siemens SMART 1000 CCD area-detector diffractometer2693 independent reflections
Radiation source: fine-focus sealed tube2279 reflections with I > 2σ(I)
graphiteRint = 0.018
Detector resolution: 8.33 pixels mm-1θmax = 26.0°, θmin = 1.9°
ω scansh = −6→6
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)k = −16→16
Tmin = 0.981, Tmax = 0.994l = −24→17
7461 measured reflections

Refinement

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: inferred from neighbouring sites
wR(F2) = 0.112H-atom parameters constrained
S = 1.04w = 1/[σ2(Fo2) + (0.0577P)2 + 0.249P] where P = (Fo2 + 2Fc2)/3
2693 reflections(Δ/σ)max < 0.001
190 parametersΔρmax = 0.14 e Å3
0 restraintsΔρmin = −0.23 e Å3

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
O10.2340 (2)0.48618 (9)0.09618 (6)0.0607 (3)
O2−0.2250 (2)0.87656 (8)−0.00231 (6)0.0570 (3)
N10.0340 (2)0.44726 (9)0.23515 (6)0.0427 (3)
C60.1036 (2)0.64278 (10)0.04534 (6)0.0396 (3)
C2−0.0452 (3)0.80221 (11)−0.00439 (7)0.0444 (3)
C1−0.0680 (3)0.72307 (11)0.04300 (7)0.0428 (3)
H1A−0.19900.72400.07330.051*
C100.2033 (2)0.37083 (10)0.24527 (7)0.0390 (3)
C70.0797 (2)0.55465 (11)0.09372 (7)0.0415 (3)
C50.3012 (3)0.64292 (12)0.00019 (7)0.0462 (3)
H5A0.41760.58980.00120.055*
C8−0.1429 (3)0.55249 (11)0.13963 (7)0.0458 (3)
H8A−0.29380.55860.11190.055*
H8B−0.13480.61200.16940.055*
N20.0569 (3)0.51863 (10)0.28486 (7)0.0573 (4)
C120.5305 (3)0.33871 (12)0.32934 (8)0.0541 (4)
H12A0.61890.35650.36870.065*
C130.5867 (3)0.25211 (13)0.29353 (8)0.0579 (4)
H13A0.71780.21060.30870.070*
N30.2374 (3)0.49148 (10)0.32671 (7)0.0589 (4)
C30.1519 (3)0.80179 (12)−0.04920 (7)0.0498 (4)
H3B0.16840.8543−0.08100.060*
C110.3340 (3)0.39961 (11)0.30415 (7)0.0440 (3)
C150.2589 (3)0.28109 (11)0.20939 (8)0.0505 (4)
H15A0.16860.26170.17060.061*
C40.3230 (3)0.72214 (13)−0.04583 (7)0.0518 (4)
H4A0.45620.7221−0.07540.062*
C9−0.1613 (3)0.45603 (12)0.18278 (8)0.0516 (4)
H9A−0.32240.45530.20440.062*
H9B−0.15360.39620.15330.062*
C140.4524 (3)0.22363 (12)0.23434 (9)0.0590 (4)
H14A0.49720.16380.21160.071*
C16−0.2412 (4)0.94720 (13)−0.05808 (9)0.0621 (4)
H16A−0.37430.9952−0.05070.093*
H16B−0.27380.9098−0.09940.093*
H16C−0.08650.9839−0.06160.093*

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
O10.0544 (6)0.0619 (7)0.0661 (7)0.0170 (5)0.0131 (5)0.0130 (5)
O20.0617 (7)0.0522 (6)0.0572 (7)0.0079 (5)0.0049 (5)0.0124 (5)
N10.0441 (6)0.0438 (6)0.0404 (6)−0.0021 (5)0.0016 (5)0.0031 (5)
C60.0367 (7)0.0471 (7)0.0348 (7)−0.0026 (6)−0.0028 (5)−0.0029 (5)
C20.0446 (8)0.0454 (8)0.0430 (8)−0.0040 (6)−0.0049 (6)0.0004 (6)
C10.0406 (7)0.0493 (8)0.0386 (7)−0.0021 (6)0.0024 (6)0.0005 (6)
C100.0389 (7)0.0402 (7)0.0381 (7)−0.0062 (5)0.0051 (5)0.0047 (5)
C70.0368 (7)0.0471 (8)0.0405 (7)0.0005 (6)−0.0024 (5)−0.0024 (6)
C50.0394 (7)0.0570 (8)0.0423 (8)0.0010 (6)0.0016 (6)−0.0028 (6)
C80.0358 (7)0.0545 (8)0.0471 (8)0.0020 (6)0.0005 (6)0.0077 (6)
N20.0683 (9)0.0498 (7)0.0537 (8)0.0062 (6)0.0001 (7)−0.0052 (6)
C120.0559 (9)0.0585 (9)0.0476 (9)−0.0050 (7)−0.0089 (7)0.0084 (7)
C130.0536 (9)0.0557 (9)0.0644 (10)0.0074 (7)−0.0007 (8)0.0161 (8)
N30.0747 (9)0.0522 (8)0.0493 (8)0.0034 (7)−0.0080 (7)−0.0087 (6)
C30.0522 (9)0.0562 (9)0.0409 (8)−0.0107 (7)−0.0002 (6)0.0070 (6)
C110.0497 (8)0.0437 (7)0.0387 (7)−0.0074 (6)0.0006 (6)0.0021 (6)
C150.0588 (9)0.0473 (8)0.0453 (8)−0.0034 (7)−0.0015 (7)−0.0053 (6)
C40.0453 (8)0.0683 (10)0.0420 (8)−0.0070 (7)0.0079 (6)0.0004 (7)
C90.0385 (8)0.0610 (9)0.0552 (9)−0.0070 (7)−0.0021 (6)0.0119 (7)
C140.0703 (11)0.0457 (8)0.0613 (10)0.0074 (8)0.0072 (8)−0.0018 (7)
C160.0732 (11)0.0537 (9)0.0591 (10)0.0047 (8)−0.0062 (8)0.0119 (8)

Geometric parameters (Å, °)

O1—C71.2137 (17)C8—H8B0.9700
O2—C21.3649 (18)N2—N31.3063 (19)
O2—C161.4316 (18)C12—C131.363 (2)
N1—N21.3511 (17)C12—C111.399 (2)
N1—C101.3563 (17)C12—H12A0.9300
N1—C91.4586 (18)C13—C141.407 (2)
C6—C11.3896 (19)C13—H13A0.9300
C6—C51.3961 (19)N3—C111.3769 (19)
C6—C71.4954 (19)C3—C41.382 (2)
C2—C31.389 (2)C3—H3B0.9300
C2—C11.394 (2)C15—C141.361 (2)
C1—H1A0.9300C15—H15A0.9300
C10—C111.3933 (19)C4—H4A0.9300
C10—C151.397 (2)C9—H9A0.9700
C7—C81.511 (2)C9—H9B0.9700
C5—C41.377 (2)C14—H14A0.9300
C5—H5A0.9300C16—H16A0.9600
C8—C91.517 (2)C16—H16B0.9600
C8—H8A0.9700C16—H16C0.9600
C2—O2—C16117.48 (12)C12—C13—C14122.05 (15)
N2—N1—C10110.12 (12)C12—C13—H13A119.0
N2—N1—C9120.80 (12)C14—C13—H13A119.0
C10—N1—C9128.99 (12)N2—N3—C11107.97 (12)
C1—C6—C5119.18 (13)C4—C3—C2118.97 (13)
C1—C6—C7121.97 (12)C4—C3—H3B120.5
C5—C6—C7118.83 (12)C2—C3—H3B120.5
O2—C2—C3124.61 (13)N3—C11—C10108.32 (13)
O2—C2—C1115.41 (13)N3—C11—C12131.29 (14)
C3—C2—C1119.98 (14)C10—C11—C12120.37 (14)
C6—C1—C2120.50 (13)C14—C15—C10116.26 (14)
C6—C1—H1A119.7C14—C15—H15A121.9
C2—C1—H1A119.7C10—C15—H15A121.9
N1—C10—C11104.48 (12)C5—C4—C3121.66 (14)
N1—C10—C15133.14 (13)C5—C4—H4A119.2
C11—C10—C15122.38 (13)C3—C4—H4A119.2
O1—C7—C6121.22 (12)N1—C9—C8113.99 (12)
O1—C7—C8120.51 (13)N1—C9—H9A108.8
C6—C7—C8118.28 (12)C8—C9—H9A108.8
C4—C5—C6119.69 (14)N1—C9—H9B108.8
C4—C5—H5A120.2C8—C9—H9B108.8
C6—C5—H5A120.2H9A—C9—H9B107.7
C7—C8—C9114.27 (12)C15—C14—C13121.90 (15)
C7—C8—H8A108.7C15—C14—H14A119.0
C9—C8—H8A108.7C13—C14—H14A119.0
C7—C8—H8B108.7O2—C16—H16A109.5
C9—C8—H8B108.7O2—C16—H16B109.5
H8A—C8—H8B107.6H16A—C16—H16B109.5
N3—N2—N1109.11 (12)O2—C16—H16C109.5
C13—C12—C11117.02 (15)H16A—C16—H16C109.5
C13—C12—H12A121.5H16B—C16—H16C109.5
C11—C12—H12A121.5
C16—O2—C2—C313.0 (2)N1—N2—N3—C11−0.44 (17)
C16—O2—C2—C1−167.35 (13)O2—C2—C3—C4179.60 (13)
C5—C6—C1—C20.8 (2)C1—C2—C3—C40.0 (2)
C7—C6—C1—C2−177.70 (12)N2—N3—C11—C100.20 (17)
O2—C2—C1—C6179.60 (12)N2—N3—C11—C12178.69 (15)
C3—C2—C1—C6−0.8 (2)N1—C10—C11—N30.12 (15)
N2—N1—C10—C11−0.40 (14)C15—C10—C11—N3179.28 (13)
C9—N1—C10—C11−176.92 (12)N1—C10—C11—C12−178.56 (12)
N2—N1—C10—C15−179.42 (15)C15—C10—C11—C120.6 (2)
C9—N1—C10—C154.1 (2)C13—C12—C11—N3−177.86 (15)
C1—C6—C7—O1−178.41 (13)C13—C12—C11—C100.5 (2)
C5—C6—C7—O13.1 (2)N1—C10—C15—C14177.59 (14)
C1—C6—C7—C81.83 (19)C11—C10—C15—C14−1.3 (2)
C5—C6—C7—C8−176.67 (12)C6—C5—C4—C3−0.7 (2)
C1—C6—C5—C4−0.1 (2)C2—C3—C4—C50.7 (2)
C7—C6—C5—C4178.46 (13)N2—N1—C9—C861.53 (17)
O1—C7—C8—C9−4.4 (2)C10—N1—C9—C8−122.27 (15)
C6—C7—C8—C9175.40 (12)C7—C8—C9—N168.40 (17)
C10—N1—N2—N30.54 (16)C10—C15—C14—C131.0 (2)
C9—N1—N2—N3177.39 (12)C12—C13—C14—C150.1 (3)
C11—C12—C13—C14−0.8 (2)

Hydrogen-bond geometry (Å, °)

D—H···AD—HH···AD···AD—H···A
C9—H9A···Cg1i0.972.743.504136

Symmetry codes: (i) x−1, y, z.

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: CV2510).

References

  • Allen, F. H., Kennard, O., Watson, D. G., Brammer, L., Orpen, A. G. & Taylor, R. (1987). J. Chem. Soc. Perkin Trans. 2, pp. S1–19.
  • Chen, Z.-Y. & Wu, M.-T. (2005). Org. Lett.7, 475–477. [PubMed]
  • Nardelli, M. (1995). J. Appl. Cryst.28, 659.
  • Sheldrick, G. M. (1996). SADABS University of Göttingen, Germany.
  • Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [PubMed]
  • Siemens (1996). SMART and SAINT Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA.
  • Spek, A. L. (2003). J. Appl. Cryst.36, 7–13.
  • Zhu, Y.-J., Wang, M., Bi, J.-L. & Li, F. (2007). Acta Cryst. E63, o4548.

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