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

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 66| Part 8| August 2010| Pages o2023-o2024
https://doi.org/10.1107/S1600536810027273

Benzyl N-{(1S)-2-hy­dr­oxy-1-[N′-(2-nitro­benzyl­­idene)hydrazinylcarbon­yl]eth­yl}carbamate

Marcus V. N. de Souza,a Alessandra C. Pinheiro,a Edward R. T. Tiekink,b* Solange M. S. V. Wardellc and James L. Wardelld‡

aFundação Oswaldo Cruz, Instituto de Tecnologia em Fármacos – Farmanguinhos, R. Sizenando Nabuco, 100, Manguinhos, 21041-250 Rio de Janeiro, RJ, Brazil, bDepartment of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia, cCHEMSOL, 1 Harcourt Road, Aberdeen AB15 5NY, Scotland, and dCentro de Desenvolvimento Tecnológico em Saúde (CDTS), Fundação Oswaldo Cruz (FIOCRUZ), Casa Amarela, Campus de Manguinhos, Av. Brasil 4365, 21040-900 Rio de Janeiro, RJ, Brazil
*Correspondence e-mail: edward.tiekink@gmail.com

(Received 1 July 2010; accepted 9 July 2010; online 14 July 2010)

The carbamate and hydrazone groups in the title compound, C18H18N4O6, are approximately orthogonal [dihedral angle = 83.3 (4)°], and the carbonyl groups are effectively anti [O=C⋯C=O torsion angle = −116.2 (7)°]. The conformation about the imine bond [1.295 (11) Å] is E. The crystal packing is dominated by O—H⋯O and N—H⋯O hydrogen bonding, which leads to two-dimensional arrays in the ab plane.

Related literature

For background to the anti-tumour potential of L-serine derivatives, see: Jiao et al. (2009[Jiao, X., Wang, L., Xiao, Q., Xie, P. & Liang, X. (2009). J. Asian Nat. Prod. Res. 11, 274-280.]); Yakura et al. (2007[Yakura, T., Yoshimoto, Y., Ishida, C. & Mabuchi, S. (2007). Tetrahedron, 63, 4429-4438.]); Takahashi et al. (1988[Takahashi, A., Nakamura, H., Ikeda, D., Naganawa, H., Kameyama, T., Kurasawa, S., Okami, Y., Takeuchi, T. & Iitaka, Y. (1988). J. Antibiot. 41, 1568-1574.]); Sin et al. (1998[Sin, N., Meng, L., Auth, H. & Crews, C. M. (1998). Bioorg. Med. Chem. 6, 1209-1217.]). For background of the anti-tumour potential of N-acyl­hydrazone L-serine derivatives, see: Rollas & Küçükgüzel (2007[Rollas, S. & Küçükgüzel, S. G. (2007). Molecules, 12, 1910-1939.]); Terzioğlu & Gürsoy (2003[Terzioğlu, N. & Gürsoy, A. (2003). Eur. J. Med. Chem. 38, 633-643.]).

[Scheme 1]

Experimental

Crystal data

  • C18H18N4O6

  • Mr = 386.36

  • Triclinic, P 1

  • a = 4.6675 (7) Å

  • b = 5.7001 (7) Å

  • c = 16.645 (3) Å

  • α = 90.457 (9)°

  • β = 92.087 (7)°

  • γ = 97.319 (9)°

  • V = 438.90 (11) Å3

  • Z = 1

  • Mo Kα radiation

  • μ = 0.11 mm−1

  • T = 120 K

  • 0.20 × 0.07 × 0.01 mm
Data collection

  • Nonius KappaCCD area-detector diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 2007[Sheldrick, G. M. (2007). SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.624, Tmax = 1.000

  • 7083 measured reflections

  • 1791 independent reflections

  • 1243 reflections with I > 2σ(I)

  • Rint = 0.093
Refinement

  • R[F2 > 2σ(F2)] = 0.089

  • wR(F2) = 0.190

  • S = 1.14

  • 1791 reflections

  • 262 parameters

  • 6 restraints

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.39 e Å−3

  • Δρmin = −0.32 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
O3—H3o⋯O2i 0.84 (8) 1.97 (9) 2.712 (9) 147 (8)
N1—H1n⋯O3ii 0.88 (7) 2.12 (7) 2.974 (10) 167 (8)
N2—H2n⋯O4iii 0.88 (4) 1.95 (5) 2.775 (10) 155 (9)
Symmetry codes: (i) x, y+1, z; (ii) x+1, y, z; (iii) x-1, y, z.

Data collection: COLLECT (Hooft, 1998[Hooft, R. W. W. (1998). COLLECT. Nonius BV, Delft, The Netherlands.]); cell refinement: DENZO (Otwinowski & Minor, 1997[Otwinowski, Z. & Minor, W. (1997). Methods in Enzymology, Vol. 276, Macromolecular Crystallography, Part A, edited by C. W. Carter Jr & R. M. Sweet, pp. 307-326. New York: Academic Press.]) and COLLECT; data reduction: DENZO and COLLECT; 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 (Farrugia, 1997[Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565.]) and DIAMOND (Brandenburg, 2006[Brandenburg, K. (2006). DIAMOND. Crystal Impact GbR, Bonn, Germany.]); software used to prepare material for publication: publCIF (Westrip, 2010[Westrip, S. P. (2010). J. Appl. Cryst. 43, 920-925.]).

Supporting information

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S1600536810027273/zs2049sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810027273/zs2049Isup2.hkl

checkCIF report


Comment top

Several L-serine derivatives have been found to have potential in anti-cancer therapy, for example, conagenin, a naturally occurring serine derivative, was shown to improve the anti-tumour efficacy of adriamycin and mitomycin C against murine leukemias (Jiao et al., 2009; Yakura et al., 2007). Other L-serine derivatives reported as potential new anti-tumour agents include the antibiotic thrazarine, which sensitizes tumour cells to macrophage-mediated cytolysis (Takahashi et al., 1988), and eponemycin, an immunomodulator, which plays a crucial role in tumour progression and metastases by supplying essential nutrients to B16 melanoma cells (Sin et al., 1998).

Following on from such reports, we have synthesized some N-acylhydrazone L-serine derivatives from L-serine to screen for anti-tumour activity. The choice of N-acylhydrazonyl derivatives was suggested by publications indicating that compounds with such groups can aid anti-tumour activities (Rollas & Küçükgüzel, 2007; Terzioğlu & Gürsoy, 2003). We now report the structure of the title compound (I). While the solid, isolated by recrystallization from methanol, was purely in the E-form, NMR spectra in DMSO-d6 solution indicated that both E and Z forms are produced.

Significant twists are evident in the molecular structure of (I) (Fig. 1). The twisting is most pronounced about the central methine link with the dihedral angle formed between the least-squares planes through the carbamate group (N1,C1,O1,O2; r.m.s. = 0.0028 Å) and the hydrazone group (N2,N2,C4,O4; r.m.s. = 0.0202 Å) being 83.3 (4)°. The dihedral angle O2–C2···C4–O4 is -116.2 (7)° indicating an anti disposition for the carbonyl-O2 and O4 atoms. While the benzyl-benzene ring is approximately co-planar with the carbamate group [the O1–C1–C12–C13 torsion angle is -171.3 (8)°], the benzene ring adjacent to the hydrazone residue is not [N3–C5–C6–C7 = -137.9 (9) °]; the dihedral angle formed between the terminal benzene rings is 67.8 (4) °. The conformation about the imine C5═N3 bond [1.295 (11) Å] is E.

The crystal packing is dominated by O–H···O and N–H···O hydrogen bonding (Table 1). The hydroxyl group hydrogen bonds with the carbonyl-O2 to form a chain along the b axis. Each N–H hydrogen-bonds to an O atom, N1–H to the hydroxy-O3 atom to form a chain along the a axis, and N3–H to a carbonyl-O4 atom to form an amide-type tape along the a axis. The net result of the hydrogen bonding is the formation of two-dimensional arrays in the ab plane (Fig. 2), that stack along the c axis (Fig. 3).

Related literature top

For background to the anti-tumour potential of L-serine derivatives, see: Jiao et al. (2009); Yakura et al. (2007); Takahashi et al. (1988); Sin et al. (1998). For background of the anti-tumour potential of N-acylhydrazone L-serine derivatives, see: Rollas & Küçükgüzel (2007); Terzioğlu & Gürsoy (2003).

Experimental top

An ethanolic solution of 2-nitrobenzaldehyde (1.05 mmol) and PhCH2O(CO)NHCH(CH2OH)CONHNH2, prepared from L-serine and hydrazine hydrate, (1.0 mmol) was refluxed for 4 h. After rotary evaporation, the residue was washed with cold ethanol (3 x 10 ml), and recrystallized from methanol. The crystals used in the structure determination were grown from methanol solution, m.p. 428–429 K.

1H NMR (500 MHz, DMSO-d6) δ (p.p.m.): 11.88 and 11.71 (1H, s, NHN, (E/Z)-diastereomer), 8.66 and 8.39 (1H, s, N═CH, (E/Z)-diastereomer), 8.07 (2H, m, H3 and H6), 7.80 (1H, m, H5), 7.67 (1H, m, H4), 7.44 (d, J = 7.8) and 7.34 (m), (1H, NHCH, (E/Z)-diastereomer), 7.38–7.30 (5H, m, Ph), 5.05 and 5.04 (2H, s, CH2Ph, (E/Z)-diastereomer), 5.03 (m) and 4.89 (t, J = 5.9), (1H, OH, (E/Z)-diastereomer), 5.03 and 4.15 (1H, m, CH, (E/Z)-diastereomer), 3.80–3.60 (2H, m, CH2OH). 13C NMR (125 MHz, DMSO-d6) δ (p.p.m.): 171.7, 167.4, 156.0, 148.2, 148.1, 142.4, 138.8, 137.0, 136.9, 133.8, 133.6, 130.6, 130.5, 128.7, 128.4, 128.0, 127.8, 127.7, 124.7, 124.6, 65.6, 65.4, 61.4, 61.1, 56.5, 54.4. IR (cm-1; KBr): 3392 (O—H), 1694 (COCH), 1672 (COO), 1555 and 1342 (NO2). EM/ESI: [M—H]: 385.3.

Refinement top

The C-bound H atoms were geometrically placed (C–H = 0.95–1.00 Å) and refined as riding with Uiso(H) = 1.2Ueq(C). The O– and N-bound H atoms were located from a difference map and refined with the distance restraints O–H = 0.84±0.01 and N–H = 0.88±0.01 Å, and with Uiso(H) = 1.2Ueq(N) or 1.5Ueq(O). In the absence of significant anomalous scattering effects, 1489 Friedel pairs were averaged in the final refinement. However, the absolute configuration was assigned on the basis of the chiralty of the L-serine starting material.

Structure description top

Several L-serine derivatives have been found to have potential in anti-cancer therapy, for example, conagenin, a naturally occurring serine derivative, was shown to improve the anti-tumour efficacy of adriamycin and mitomycin C against murine leukemias (Jiao et al., 2009; Yakura et al., 2007). Other L-serine derivatives reported as potential new anti-tumour agents include the antibiotic thrazarine, which sensitizes tumour cells to macrophage-mediated cytolysis (Takahashi et al., 1988), and eponemycin, an immunomodulator, which plays a crucial role in tumour progression and metastases by supplying essential nutrients to B16 melanoma cells (Sin et al., 1998).

Following on from such reports, we have synthesized some N-acylhydrazone L-serine derivatives from L-serine to screen for anti-tumour activity. The choice of N-acylhydrazonyl derivatives was suggested by publications indicating that compounds with such groups can aid anti-tumour activities (Rollas & Küçükgüzel, 2007; Terzioğlu & Gürsoy, 2003). We now report the structure of the title compound (I). While the solid, isolated by recrystallization from methanol, was purely in the E-form, NMR spectra in DMSO-d6 solution indicated that both E and Z forms are produced.

Significant twists are evident in the molecular structure of (I) (Fig. 1). The twisting is most pronounced about the central methine link with the dihedral angle formed between the least-squares planes through the carbamate group (N1,C1,O1,O2; r.m.s. = 0.0028 Å) and the hydrazone group (N2,N2,C4,O4; r.m.s. = 0.0202 Å) being 83.3 (4)°. The dihedral angle O2–C2···C4–O4 is -116.2 (7)° indicating an anti disposition for the carbonyl-O2 and O4 atoms. While the benzyl-benzene ring is approximately co-planar with the carbamate group [the O1–C1–C12–C13 torsion angle is -171.3 (8)°], the benzene ring adjacent to the hydrazone residue is not [N3–C5–C6–C7 = -137.9 (9) °]; the dihedral angle formed between the terminal benzene rings is 67.8 (4) °. The conformation about the imine C5═N3 bond [1.295 (11) Å] is E.

The crystal packing is dominated by O–H···O and N–H···O hydrogen bonding (Table 1). The hydroxyl group hydrogen bonds with the carbonyl-O2 to form a chain along the b axis. Each N–H hydrogen-bonds to an O atom, N1–H to the hydroxy-O3 atom to form a chain along the a axis, and N3–H to a carbonyl-O4 atom to form an amide-type tape along the a axis. The net result of the hydrogen bonding is the formation of two-dimensional arrays in the ab plane (Fig. 2), that stack along the c axis (Fig. 3).

For background to the anti-tumour potential of L-serine derivatives, see: Jiao et al. (2009); Yakura et al. (2007); Takahashi et al. (1988); Sin et al. (1998). For background of the anti-tumour potential of N-acylhydrazone L-serine derivatives, see: Rollas & Küçükgüzel (2007); Terzioğlu & Gürsoy (2003).

Computing details top

Data collection: COLLECT (Hooft, 1998); cell refinement: DENZO (Otwinowski & Minor, 1997) and COLLECT (Hooft, 1998); data reduction: DENZO (Otwinowski & Minor, 1997) and COLLECT (Hooft, 1998); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 2006); software used to prepare material for publication: publCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. The molecular structure of (I) showing the atom-labelling scheme and displacement ellipsoids at the 50% probability level.
[Figure 2] Fig. 2. A view of the two-dimensional supramolecular array in the ab plane in (I) with the O–H···O and N–H···O hydrogen bonding shown as orange and blue dashed lines, respectively.
[Figure 3] Fig. 3. A view in projection down the a axis of (I) showing the stacking of the two-dimensional arrays along the c axis.
Benzyl N-{(1S)-2-hydroxy-1-[N'-(2- nitrobenzylidene)hydrazinylcarbonyl]ethyl}carbamate top
Crystal data top
C18H18N4O6Z = 1
Mr = 386.36F(000) = 202
Triclinic, P1Dx = 1.462 Mg m−3
Hall symbol: P 1Melting point = 428–429 K
a = 4.6675 (7) ÅMo Kα radiation, λ = 0.71073 Å
b = 5.7001 (7) ÅCell parameters from 18416 reflections
c = 16.645 (3) Åθ = 2.9–27.5°
α = 90.457 (9)°µ = 0.11 mm−1
β = 92.087 (7)°T = 120 K
γ = 97.319 (9)°Plate, colourless
V = 438.90 (11) Å30.20 × 0.07 × 0.01 mm
Data collection top
Nonius KappaCCD area-detector
diffractometer		1791 independent reflections
Radiation source: Enraf Nonius FR591 rotating anode1243 reflections with I > 2σ(I)
10 cm confocal mirrors monochromatorRint = 0.093
Detector resolution: 9.091 pixels mm-1θmax = 26.5°, θmin = 3.6°
φ and ω scansh = −5→5
Absorption correction: multi-scan
(SADABS; Sheldrick, 2007)		k = −6→7
Tmin = 0.624, Tmax = 1.000l = −20→20
7083 measured reflections
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)] = 0.089Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.190H atoms treated by a mixture of independent and constrained refinement
S = 1.14 w = 1/[σ2(Fo2) + (0.037P)2 + 1.2849P]
where P = (Fo2 + 2Fc2)/3
1791 reflections(Δ/σ)max < 0.001
262 parametersΔρmax = 0.39 e Å−3
6 restraintsΔρmin = −0.32 e Å−3
Crystal data top
C18H18N4O6γ = 97.319 (9)°
Mr = 386.36V = 438.90 (11) Å3
Triclinic, P1Z = 1
a = 4.6675 (7) ÅMo Kα radiation
b = 5.7001 (7) ŵ = 0.11 mm−1
c = 16.645 (3) ÅT = 120 K
α = 90.457 (9)°0.20 × 0.07 × 0.01 mm
β = 92.087 (7)°
Data collection top
Nonius KappaCCD area-detector
diffractometer		1791 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 2007)		1243 reflections with I > 2σ(I)
Tmin = 0.624, Tmax = 1.000Rint = 0.093
7083 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0896 restraints
wR(F2) = 0.190H atoms treated by a mixture of independent and constrained refinement
S = 1.14Δρmax = 0.39 e Å−3
1791 reflectionsΔρmin = −0.32 e Å−3
262 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
O10.2947 (12)0.8892 (10)0.3007 (4)0.0270 (14)
O2−0.0905 (13)0.6386 (10)0.2534 (4)0.0294 (15)
O3−0.4518 (12)1.3215 (11)0.1633 (4)0.0297 (15)
H3O−0.350 (19)1.374 (18)0.204 (4)0.045*
O40.1745 (14)0.8327 (12)0.0625 (4)0.0395 (17)
O5−0.6765 (15)0.6119 (12)−0.2286 (4)0.0427 (19)
O6−0.6271 (16)0.4575 (13)−0.3452 (4)0.0450 (19)
N10.0112 (16)1.0119 (13)0.2030 (5)0.0267 (17)
H1N0.156 (13)1.122 (12)0.195 (6)0.032*
N2−0.2884 (15)0.7320 (14)0.0165 (5)0.0285 (18)
H2N−0.469 (7)0.718 (17)0.031 (5)0.034*
N3−0.1965 (16)0.5952 (12)−0.0441 (5)0.0272 (18)
N4−0.5754 (16)0.4722 (12)−0.2727 (5)0.0291 (18)
C10.0588 (17)0.8301 (16)0.2530 (5)0.024 (2)
C2−0.2011 (19)0.9716 (15)0.1386 (5)0.025 (2)
H2−0.37850.87600.15850.030*
C3−0.278 (2)1.2117 (16)0.1085 (5)0.029 (2)
H3A−0.09781.31880.10040.035*
H3B−0.38421.18770.05590.035*
C4−0.0811 (19)0.8361 (14)0.0693 (5)0.0221 (19)
C5−0.398 (2)0.4987 (15)−0.0938 (5)0.026 (2)
H5−0.59280.5308−0.09210.031*
C6−0.3011 (19)0.3339 (14)−0.1536 (6)0.026 (2)
C7−0.3789 (19)0.3147 (14)−0.2349 (6)0.026 (2)
C8−0.2776 (19)0.1553 (16)−0.2870 (6)0.029 (2)
H8−0.33470.1492−0.34240.035*
C9−0.092 (2)0.0061 (16)−0.2560 (6)0.032 (2)
H9−0.0215−0.1062−0.29020.039*
C10−0.006 (2)0.0190 (16)−0.1754 (6)0.031 (2)
H100.1263−0.0809−0.15480.038*
C11−0.1140 (18)0.1766 (14)−0.1252 (5)0.026 (2)
H11−0.06000.1790−0.06960.031*
C120.347 (2)0.7141 (16)0.3589 (6)0.030 (2)
H12A0.40090.57240.33130.036*
H12B0.16910.66620.38840.036*
C130.5886 (19)0.8140 (16)0.4173 (6)0.026 (2)
C140.737 (2)1.0378 (16)0.4112 (6)0.030 (2)
H140.68571.13800.36910.035*
C150.958 (2)1.1178 (18)0.4651 (6)0.038 (2)
H151.06091.27140.45960.045*
C161.031 (2)0.9758 (18)0.5270 (6)0.038 (3)
H161.18471.03110.56420.045*
C170.881 (2)0.7527 (18)0.5351 (6)0.037 (3)
H170.92940.65460.57810.045*
C180.659 (2)0.6729 (16)0.4798 (6)0.031 (2)
H180.55430.51990.48530.037*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
O10.024 (3)0.030 (3)0.027 (4)0.003 (3)0.002 (3)0.012 (3)
O20.021 (3)0.029 (3)0.036 (4)−0.002 (3)−0.002 (3)0.000 (3)
O30.023 (4)0.035 (4)0.032 (4)0.003 (3)0.003 (3)−0.006 (3)
O40.022 (4)0.049 (4)0.047 (4)0.003 (3)−0.001 (3)−0.015 (3)
O50.048 (5)0.043 (4)0.041 (4)0.024 (4)−0.002 (4)−0.006 (3)
O60.053 (5)0.057 (5)0.027 (4)0.018 (4)−0.008 (3)−0.001 (3)
N10.022 (4)0.032 (5)0.025 (4)0.001 (3)−0.002 (3)−0.006 (3)
N20.016 (4)0.038 (4)0.032 (4)0.003 (3)0.003 (3)−0.013 (4)
N30.026 (4)0.024 (4)0.033 (4)0.003 (3)0.003 (4)0.000 (3)
N40.030 (5)0.022 (4)0.035 (5)0.004 (3)−0.004 (4)0.005 (3)
C10.010 (4)0.037 (5)0.023 (5)0.000 (4)−0.005 (4)−0.008 (4)
C20.018 (5)0.028 (5)0.028 (5)−0.003 (4)0.003 (4)−0.001 (4)
C30.039 (6)0.026 (5)0.022 (5)0.003 (4)−0.005 (4)−0.004 (4)
C40.026 (5)0.020 (4)0.021 (5)0.002 (3)0.013 (4)0.005 (3)
C50.028 (5)0.028 (5)0.022 (5)0.005 (4)0.004 (4)−0.006 (4)
C60.026 (5)0.016 (4)0.037 (6)0.000 (4)−0.004 (4)−0.007 (4)
C70.020 (5)0.016 (4)0.041 (6)−0.004 (3)0.005 (4)−0.001 (4)
C80.032 (5)0.034 (5)0.019 (5)0.000 (4)0.000 (4)−0.011 (4)
C90.037 (6)0.027 (5)0.036 (6)0.012 (4)0.006 (5)−0.013 (4)
C100.032 (5)0.028 (5)0.034 (6)0.000 (4)0.007 (5)−0.010 (4)
C110.028 (5)0.023 (5)0.023 (5)−0.005 (4)−0.001 (4)0.003 (4)
C120.031 (5)0.025 (5)0.033 (6)0.005 (4)−0.005 (4)0.002 (4)
C130.023 (5)0.030 (5)0.025 (5)0.005 (4)0.011 (4)0.000 (4)
C140.030 (5)0.030 (5)0.028 (5)0.003 (4)−0.005 (4)−0.002 (4)
C150.039 (6)0.036 (6)0.036 (6)−0.001 (5)−0.010 (5)0.000 (5)
C160.026 (5)0.046 (6)0.040 (6)0.004 (5)−0.007 (5)−0.021 (5)
C170.036 (6)0.043 (6)0.034 (6)0.010 (5)−0.009 (5)−0.004 (5)
C180.034 (6)0.026 (5)0.031 (6)0.000 (4)−0.001 (4)0.000 (4)
Geometric parameters (Å, º) top
O1—C11.340 (10)C6—C111.402 (12)
O1—C121.433 (10)C7—C81.388 (12)
O2—C11.218 (11)C8—C91.381 (13)
O3—C31.433 (11)C8—H80.9500
O3—H3O0.84 (8)C9—C101.384 (13)
O4—C41.205 (10)C9—H90.9500
O5—N41.228 (10)C10—C111.375 (12)
O6—N41.223 (10)C10—H100.9500
N1—C11.369 (12)C11—H110.9500
N1—C21.430 (11)C12—C131.513 (13)
N1—H1N0.88 (7)C12—H12A0.9900
N2—C41.358 (11)C12—H12B0.9900
N2—N31.383 (10)C13—C141.379 (12)
N2—H2N0.88 (4)C13—C181.376 (13)
N3—C51.295 (11)C14—C151.372 (13)
N4—C71.490 (11)C14—H140.9500
C2—C41.544 (12)C15—C161.376 (15)
C2—C31.541 (12)C15—H150.9500
C2—H21.0000C16—C171.381 (14)
C3—H3A0.9900C16—H160.9500
C3—H3B0.9900C17—C181.391 (13)
C5—C61.485 (12)C17—H170.9500
C5—H50.9500C18—H180.9500
C6—C71.387 (13)
C1—O1—C12114.3 (7)C8—C7—N4115.2 (8)
C3—O3—H3O110 (7)C9—C8—C7118.1 (8)
C1—N1—C2119.6 (7)C9—C8—H8120.9
C1—N1—H1N118 (6)C7—C8—H8120.9
C2—N1—H1N116 (6)C10—C9—C8120.5 (8)
C4—N2—N3116.5 (7)C10—C9—H9119.8
C4—N2—H2N118 (6)C8—C9—H9119.8
N3—N2—H2N123 (6)C9—C10—C11119.9 (9)
C5—N3—N2115.3 (7)C9—C10—H10120.1
O6—N4—O5123.4 (8)C11—C10—H10120.1
O6—N4—C7119.1 (7)C10—C11—C6122.0 (8)
O5—N4—C7117.5 (7)C10—C11—H11119.0
O2—C1—O1124.3 (8)C6—C11—H11119.0
O2—C1—N1124.7 (8)O1—C12—C13109.6 (7)
O1—C1—N1111.0 (7)O1—C12—H12A109.7
N1—C2—C4109.8 (7)C13—C12—H12A109.7
N1—C2—C3109.1 (7)O1—C12—H12B109.7
C4—C2—C3109.9 (7)C13—C12—H12B109.7
N1—C2—H2109.3H12A—C12—H12B108.2
C4—C2—H2109.3C14—C13—C18119.1 (8)
C3—C2—H2109.3C14—C13—C12123.3 (8)
O3—C3—C2112.7 (7)C18—C13—C12117.5 (8)
O3—C3—H3A109.1C13—C14—C15120.9 (9)
C2—C3—H3A109.1C13—C14—H14119.6
O3—C3—H3B109.1C15—C14—H14119.6
C2—C3—H3B109.1C16—C15—C14120.1 (10)
H3A—C3—H3B107.8C16—C15—H15120.0
O4—C4—N2124.3 (8)C14—C15—H15120.0
O4—C4—C2121.9 (8)C15—C16—C17120.0 (9)
N2—C4—C2113.7 (7)C15—C16—H16120.0
N3—C5—C6114.6 (8)C17—C16—H16120.0
N3—C5—H5122.7C16—C17—C18119.4 (10)
C6—C5—H5122.7C16—C17—H17120.3
C7—C6—C11115.8 (8)C18—C17—H17120.3
C7—C6—C5127.2 (8)C13—C18—C17120.5 (9)
C11—C6—C5117.0 (8)C13—C18—H18119.7
C6—C7—C8123.6 (8)C17—C18—H18119.7
C6—C7—N4121.2 (7)
C4—N2—N3—C5−179.8 (9)O6—N4—C7—C6176.4 (9)
C12—O1—C1—O2−5.2 (12)O5—N4—C7—C6−3.3 (12)
C12—O1—C1—N1175.7 (7)O6—N4—C7—C8−2.2 (11)
C2—N1—C1—O2−9.2 (13)O5—N4—C7—C8178.1 (8)
C2—N1—C1—O1169.9 (7)C6—C7—C8—C90.7 (13)
C1—N1—C2—C4−76.5 (9)N4—C7—C8—C9179.2 (8)
C1—N1—C2—C3163.0 (8)C7—C8—C9—C10−1.0 (14)
N1—C2—C3—O3−73.3 (9)C8—C9—C10—C111.9 (14)
C4—C2—C3—O3166.2 (7)C9—C10—C11—C6−2.6 (14)
N3—N2—C4—O46.5 (13)C7—C6—C11—C102.2 (12)
N3—N2—C4—C2−176.0 (7)C5—C6—C11—C10−178.9 (8)
N1—C2—C4—O4−20.2 (11)C1—O1—C12—C13−171.3 (8)
C3—C2—C4—O499.8 (10)O1—C12—C13—C14−2.3 (12)
N1—C2—C4—N2162.3 (8)O1—C12—C13—C18177.0 (8)
C3—C2—C4—N2−77.7 (9)C18—C13—C14—C152.0 (14)
N2—N3—C5—C6−174.3 (7)C12—C13—C14—C15−178.8 (9)
N3—C5—C6—C7−137.9 (9)C13—C14—C15—C16−1.1 (15)
N3—C5—C6—C1143.3 (12)C14—C15—C16—C17−0.2 (15)
C11—C6—C7—C8−1.3 (12)C15—C16—C17—C180.6 (15)
C5—C6—C7—C8179.9 (9)C14—C13—C18—C17−1.6 (14)
C11—C6—C7—N4−179.7 (8)C12—C13—C18—C17179.2 (9)
C5—C6—C7—N41.5 (13)C16—C17—C18—C130.3 (15)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O3—H3o···O2i0.84 (8)1.97 (9)2.712 (9)147 (8)
N1—H1n···O3ii0.88 (7)2.12 (7)2.974 (10)167 (8)
N2—H2n···O4iii0.88 (4)1.95 (5)2.775 (10)155 (9)
Symmetry codes: (i) x, y+1, z; (ii) x+1, y, z; (iii) x−1, y, z.

Experimental details

Crystal data
Chemical formulaC18H18N4O6
Mr386.36
Crystal system, space groupTriclinic, P1
Temperature (K)120
a, b, c (Å)4.6675 (7), 5.7001 (7), 16.645 (3)
α, β, γ (°)90.457 (9), 92.087 (7), 97.319 (9)
V (Å3)438.90 (11)
Z1
Radiation typeMo Kα
µ (mm−1)0.11
Crystal size (mm)0.20 × 0.07 × 0.01
Data collection
DiffractometerNonius KappaCCD area-detector
Absorption correctionMulti-scan
(SADABS; Sheldrick, 2007)
Tmin, Tmax0.624, 1.000
No. of measured, independent and
observed [I > 2σ(I)] reflections		7083, 1791, 1243
Rint0.093
(sin θ/λ)max (Å−1)0.628
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.089, 0.190, 1.14
No. of reflections1791
No. of parameters262
No. of restraints6
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å−3)0.39, −0.32

Computer programs: DENZO (Otwinowski & Minor, 1997) and COLLECT (Hooft, 1998), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 2006), publCIF (Westrip, 2010).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O3—H3o···O2i0.84 (8)1.97 (9)2.712 (9)147 (8)
N1—H1n···O3ii0.88 (7)2.12 (7)2.974 (10)167 (8)
N2—H2n···O4iii0.88 (4)1.95 (5)2.775 (10)155 (9)
Symmetry codes: (i) x, y+1, z; (ii) x+1, y, z; (iii) x−1, y, z.
 

Footnotes

‡Additional correspondence author, e-mail: j.wardell@abdn.ac.uk.

Acknowledgements

The use of the EPSRC X-ray crystallographic service at the University of Southampton, England, and the valuable assistance of the staff there is gratefully acknowledged. JLW acknowledges support from CAPES (Brazil).

References

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ISSN: 2056-9890
Volume 66| Part 8| August 2010| Pages o2023-o2024
https://doi.org/10.1107/S1600536810027273
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