3-Methyl-2,6-dinitro-N-(3-pent­yl)-4-[(2,3,4-tri-O-acetyl-β-d-xylos­yl)amino­methyl]­aniline

Bai, L.; Wang, X.; Cai, B.

doi:10.1107/S1600536808023192

organic compounds

CRYSTALLOGRAPHIC
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ISSN: 2056-9890

Volume 64| Part 8| August 2008| Page o1623

doi:10.1107/S1600536808023192

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3-Methyl-2,6-dinitro-N-(3-pentyl)-4-[(2,3,4-tri-O-acetyl-β-D-xylosyl)aminomethyl]aniline

Lifei Bai,^a Xiaoming Wang ^b and Baochang Cai ^a ^*

^aJiangsu Key Laboratory of Chinese Medicine Processing, Nanjing University of Chinese Medicine, Nanjing 210029, People's Republic of China, and ^bState Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Hankou Road, Nanjing 210093, People's Republic of China
^*Correspondence e-mail: bccai@hotmail.com

(Received 2 April 2008; accepted 23 July 2008; online 31 July 2008)

In the title compound, C₂₄H₃₄N₄O₁₁, the hexopyranosyl ring adopts a chair conformation. The four substituents are in equatorial positions. The molecule shows an intramolecular N—H⋯O hydrogen bond.

Related literature

For related literature, see: Grichar & Dotray (2007 ); Kubátová et al. (2006 ); Wang et al. (2008 ); Yang et al. (2004 ).

Experimental

Crystal data

C₂₄H₃₄N₄O₁₁
M_r = 554.55
Orthorhombic, P 2₁ 2₁ 2₁
a = 7.4100 (15) Å
b = 11.044 (2) Å
c = 34.106 (7) Å
V = 2791.1 (10) Å³
Z = 4
Mo Kα radiation
μ = 0.10 mm⁻¹
T = 293 (2) K
0.30 × 0.20 × 0.10 mm

Data collection

Enraf–Nonius CAD-4 diffractometer
Absorption correction: ψ scan (XCAD4; Harms & Wocadlo, 1995 ) T_min = 0.969, T_max = 0.990
2870 measured reflections
2870 independent reflections
1662 reflections with I > 2σ(I)
3 standard reflections every 200 reflections intensity decay: none

Refinement

R[F² > 2σ(F²)] = 0.067
wR(F²) = 0.196
S = 1.04
2870 reflections
352 parameters
13 restraints
H-atom parameters constrained
Δρ_max = 0.17 e Å⁻³
Δρ_min = −0.23 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1A⋯O4	0.86	1.92	2.621 (8)	138

Data collection: CAD-4 Software (Enraf–Nonius, 1989 ); cell refinement: CAD-4 Software; data reduction: XCAD4 (Harms & Wocadlo, 1995); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL.

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808023192/er2053sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808023192/er2053Isup2.hkl

checkCIF report

Comment top

Pendimethaline(3,4-dimethyl-2,6-dinitro-N-(pentan-3-yl)benzenamine) plays an important role in controlling weeds (Grichar & Dotray, 2007). However, problems such as toxic residues and environmental pollution were protruded increasingly by using amounts of herbicides during the past decades (Kubátová et al., 2006). In the search for a new herbicide with high efficiency and low toxicity, we obtained the title compound. All bond lengths and angles in the title molecule show normal values. The hexopyranosyl ring adopts a chair conformation (Fig. 1). The three acetyl groups are individually planar and occupy equatorial positions (Yang et al., 2004; Wang et al.,2008). The torsion angle C14—N4—C13—C9 is 95.8°.

Related literature top

For related literature, see: Grichar & Dotray (2007); Kubátová et al. (2006); Wang et al. (2008); Yang et al. (2004).

Experimental top

The title compound was prepared from β-D-1-amine-2,3,4-tri-O-acetyl-xylosyl with 4-(bromomethyl)-3-methyl-2,6-dinitro-N-(pentan-3-yl)benzenamine in dimethylformamide (DMF) in the presence of sodium carbonate. Fine yellow block crystals suitable for single-crystal X-ray diffraction were obtained by slow evaporation of an acetonitrile and ethyl acetate (1:10) solution at room temperature.

Computing details top

Data collection: CAD-4 Software (Enraf–Nonius, 1989); cell refinement: CAD-4 Software (Enraf–Nonius, 1989); data reduction: XCAD4 (Harms & Wocadlo, 1995); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top

Fig. 1. The asymmetric unit of the title compound, showing the atom-labelling scheme. Displacement ellipsoids are drawn at the 50% probability level.

3-Methyl-2,6-dinitro-N-(3-pentyl)-4-[(2,3,4-tri-O- acetyl-β-D-xylosyl)aminomethyl]aniline top

Crystal data top

C₂₄H₃₄N₄O₁₁	F(000) = 1176
M_r = 554.55	D_x = 1.320 Mg m⁻³
Orthorhombic, P2₁2₁2₁	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ac 2ab	Cell parameters from 25 reflections
a = 7.4100 (15) Å	θ = 10–13°
b = 11.044 (2) Å	µ = 0.11 mm⁻¹
c = 34.106 (7) Å	T = 293 K
V = 2791.1 (10) Å³	Block, yellow
Z = 4	0.30 × 0.20 × 0.10 mm

Data collection top

Enraf–Nonius CAD-4 diffractometer	1662 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.000
Graphite monochromator	θ_max = 25.1°, θ_min = 1.2°
ω/2θ scans	h = 0→8
Absorption correction: ψ scan (XCAD4; Harms & Wocadlo, 1995)	k = 0→13
T_min = 0.969, T_max = 0.990	l = 0→40
2870 measured reflections	3 standard reflections every 200 reflections
2870 independent reflections	intensity decay: none

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.067	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.196	H-atom parameters constrained
S = 1.04	w = 1/[σ²(F_o²) + (0.1035P)²] where P = (F_o² + 2F_c²)/3
2870 reflections	(Δ/σ)_max < 0.001
352 parameters	Δρ_max = 0.18 e Å⁻³
13 restraints	Δρ_min = −0.23 e Å⁻³

Crystal data top

C₂₄H₃₄N₄O₁₁	V = 2791.1 (10) Å³
M_r = 554.55	Z = 4
Orthorhombic, P2₁2₁2₁	Mo Kα radiation
a = 7.4100 (15) Å	µ = 0.11 mm⁻¹
b = 11.044 (2) Å	T = 293 K
c = 34.106 (7) Å	0.30 × 0.20 × 0.10 mm

Data collection top

Enraf–Nonius CAD-4 diffractometer	1662 reflections with I > 2σ(I)
Absorption correction: ψ scan (XCAD4; Harms & Wocadlo, 1995)	R_int = 0.000
T_min = 0.969, T_max = 0.990	3 standard reflections every 200 reflections
2870 measured reflections	intensity decay: none
2870 independent reflections

Refinement top

R[F² > 2σ(F²)] = 0.067	13 restraints
wR(F²) = 0.196	H-atom parameters constrained
S = 1.04	Δρ_max = 0.18 e Å⁻³
2870 reflections	Δρ_min = −0.23 e Å⁻³
352 parameters

Special details top

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) top

	x	y	z	U_iso*/U_eq
N1	0.8178 (10)	0.2626 (5)	0.1700 (2)	0.095 (2)
H1A	0.9024	0.2234	0.1583	0.114*
C1	0.8949 (13)	0.0842 (12)	0.2352 (3)	0.142 (5)
H1B	0.9437	0.0066	0.2422	0.213*
H1C	0.8294	0.1169	0.2571	0.213*
H1D	0.9916	0.1381	0.2284	0.213*
O1	0.6282 (15)	0.4037 (7)	0.2480 (2)	0.166 (5)
C2	0.7702 (12)	0.0702 (7)	0.2009 (2)	0.080 (2)
H2A	0.6772	0.0123	0.2079	0.096*
H2B	0.8382	0.0362	0.1792	0.096*
N2	0.5848 (15)	0.4284 (7)	0.2134 (4)	0.124 (4)
O2	0.4388 (11)	0.4255 (7)	0.1997 (4)	0.178 (5)
N3	1.1129 (8)	0.3679 (5)	0.12461 (15)	0.0628 (15)
O3	1.2320 (8)	0.4167 (5)	0.10820 (17)	0.0993 (19)
C3	0.3754 (17)	0.0983 (10)	0.1705 (3)	0.139 (4)
H3A	0.2938	0.0809	0.1494	0.209*
H3B	0.3169	0.1501	0.1892	0.209*
H3C	0.4102	0.0241	0.1831	0.209*
N4	1.1134 (7)	0.8095 (4)	0.14687 (15)	0.0598 (14)
H4A	1.2215	0.8042	0.1559	0.072*
O4	1.0911 (9)	0.2574 (4)	0.12117 (18)	0.104 (2)
C4	0.5383 (12)	0.1598 (8)	0.1548 (3)	0.100 (3)
H4B	0.5028	0.2358	0.1428	0.120*
H4C	0.5921	0.1095	0.1347	0.120*
O5	1.0104 (14)	1.2551 (5)	0.0281 (2)	0.138 (3)
C5	0.6794 (10)	0.1850 (6)	0.1869 (2)	0.0673 (19)
H5A	0.6221	0.2262	0.2090	0.081*
O6	1.0543 (7)	1.0657 (3)	0.00833 (11)	0.0597 (11)
C6	0.8401 (10)	0.3854 (5)	0.1690 (2)	0.0645 (19)
C7	0.7377 (10)	0.4713 (6)	0.1903 (2)	0.071 (2)
O7	1.3806 (6)	0.9512 (4)	0.02752 (12)	0.0577 (11)
C8	0.7674 (9)	0.5952 (5)	0.18989 (18)	0.0544 (16)
O8	1.3595 (8)	0.8031 (5)	−0.01708 (16)	0.0878 (16)
O9	1.3373 (6)	0.7535 (3)	0.08050 (13)	0.0579 (11)
C9	0.9162 (9)	0.6406 (5)	0.16961 (17)	0.0497 (15)
O10	1.5721 (9)	0.8095 (5)	0.1159 (2)	0.128 (3)
C10	1.0208 (9)	0.5642 (5)	0.14899 (18)	0.0547 (16)
H10A	1.1179	0.5954	0.1349	0.066*
O11	0.9818 (6)	0.9650 (4)	0.10992 (12)	0.0625 (12)
C11	0.9889 (8)	0.4396 (5)	0.14790 (19)	0.0576 (16)
C12	0.6414 (11)	0.6798 (6)	0.2129 (2)	0.082 (2)
H12A	0.5486	0.6329	0.2253	0.124*
H12B	0.5873	0.7369	0.1952	0.124*
H12C	0.7095	0.7224	0.2324	0.124*
C13	0.9561 (11)	0.7768 (5)	0.1707 (2)	0.070 (2)
H13A	0.8515	0.8207	0.1612	0.084*
H13B	0.9773	0.8013	0.1976	0.084*
C14	1.0783 (9)	0.8495 (5)	0.1089 (2)	0.0573 (17)
H14A	1.0031	0.7893	0.0955	0.069*
C15	0.9289 (9)	1.0028 (6)	0.07198 (19)	0.0647 (18)
H15A	0.8525	1.0738	0.0739	0.078*
H15B	0.8606	0.9390	0.0593	0.078*
C16	1.0952 (9)	1.0320 (5)	0.04803 (17)	0.0544 (16)
H16A	1.1638	1.0968	0.0608	0.065*
C17	1.2120 (8)	0.9170 (5)	0.04514 (17)	0.0498 (15)
H17A	1.1512	0.8556	0.0292	0.060*
C18	1.2506 (9)	0.8685 (5)	0.08543 (19)	0.0559 (16)
H18A	1.3310	0.9240	0.0995	0.067*
C19	1.0118 (14)	1.2105 (7)	−0.0406 (3)	0.105 (3)
H19A	0.9922	1.2957	−0.0442	0.157*
H19B	0.9113	1.1662	−0.0511	0.157*
H19C	1.1202	1.1867	−0.0539	0.157*
C20	1.0292 (12)	1.1850 (6)	0.0003 (3)	0.080 (2)
C21	1.6071 (11)	0.9433 (6)	−0.0209 (2)	0.077 (2)
H21A	1.6419	0.8986	−0.0438	0.115*
H21B	1.7018	0.9391	−0.0017	0.115*
H21C	1.5860	1.0263	−0.0278	0.115*
C22	1.4367 (10)	0.8896 (6)	−0.00402 (19)	0.0584 (17)
C23	1.5679 (9)	0.6105 (6)	0.0884 (2)	0.079 (2)
H23A	1.6864	0.6008	0.0993	0.118*
H23B	1.5732	0.6002	0.0605	0.118*
H23C	1.4883	0.5510	0.0995	0.118*
C24	1.4995 (9)	0.7333 (7)	0.0977 (2)	0.070 (2)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
N1	0.101 (5)	0.037 (3)	0.148 (5)	−0.011 (3)	0.056 (4)	−0.014 (3)
C1	0.098 (7)	0.224 (14)	0.104 (6)	0.023 (9)	−0.032 (6)	−0.029 (8)
O1	0.280 (13)	0.079 (4)	0.140 (5)	−0.068 (6)	0.113 (8)	−0.038 (4)
C2	0.100 (6)	0.062 (5)	0.079 (5)	0.001 (5)	0.003 (4)	0.005 (4)
N2	0.115 (8)	0.045 (4)	0.212 (10)	−0.009 (5)	0.088 (8)	−0.011 (6)
O2	0.076 (5)	0.080 (5)	0.379 (16)	−0.002 (4)	0.097 (8)	−0.002 (7)
N3	0.067 (4)	0.048 (3)	0.073 (3)	0.004 (3)	0.026 (3)	0.007 (3)
O3	0.088 (4)	0.063 (3)	0.147 (5)	−0.010 (3)	0.068 (4)	−0.007 (3)
C3	0.141 (9)	0.128 (9)	0.148 (9)	−0.052 (9)	−0.028 (8)	−0.006 (7)
N4	0.058 (3)	0.050 (3)	0.071 (3)	−0.014 (3)	−0.001 (3)	0.010 (3)
O4	0.123 (5)	0.045 (3)	0.145 (5)	−0.001 (3)	0.073 (4)	−0.011 (3)
C4	0.104 (7)	0.072 (5)	0.124 (7)	−0.013 (6)	−0.006 (6)	0.009 (5)
O5	0.245 (10)	0.046 (3)	0.122 (5)	0.025 (5)	−0.041 (6)	0.004 (3)
C5	0.077 (5)	0.039 (3)	0.086 (4)	−0.008 (3)	0.026 (4)	−0.004 (3)
O6	0.078 (3)	0.039 (2)	0.062 (2)	−0.002 (2)	0.000 (2)	0.0058 (19)
C6	0.073 (5)	0.032 (3)	0.088 (5)	−0.011 (3)	0.032 (4)	−0.010 (3)
C7	0.056 (4)	0.039 (4)	0.119 (6)	−0.012 (3)	0.025 (4)	0.002 (4)
O7	0.061 (3)	0.039 (2)	0.072 (3)	−0.003 (2)	0.001 (2)	−0.004 (2)
C8	0.058 (4)	0.035 (3)	0.070 (4)	−0.006 (3)	0.018 (4)	0.000 (3)
O8	0.096 (4)	0.066 (3)	0.101 (4)	−0.001 (3)	0.007 (3)	−0.026 (3)
O9	0.050 (2)	0.037 (2)	0.087 (3)	0.000 (2)	−0.007 (2)	−0.007 (2)
C9	0.057 (4)	0.028 (3)	0.064 (4)	−0.005 (3)	0.000 (3)	0.006 (3)
O10	0.097 (5)	0.076 (4)	0.210 (7)	−0.011 (4)	−0.072 (5)	−0.023 (5)
C10	0.048 (4)	0.039 (3)	0.077 (4)	−0.006 (3)	0.003 (3)	0.006 (3)
O11	0.070 (3)	0.045 (2)	0.073 (3)	0.009 (2)	0.006 (2)	0.003 (2)
C11	0.052 (4)	0.037 (3)	0.084 (4)	0.002 (3)	0.020 (3)	−0.001 (3)
C12	0.084 (5)	0.045 (4)	0.118 (6)	0.007 (4)	0.058 (5)	−0.007 (4)
C13	0.092 (5)	0.033 (3)	0.085 (5)	−0.009 (4)	0.027 (4)	0.006 (3)
C14	0.059 (4)	0.034 (3)	0.078 (4)	−0.002 (3)	0.008 (4)	−0.002 (3)
C15	0.065 (4)	0.051 (4)	0.078 (4)	0.004 (4)	0.016 (4)	0.003 (3)
C16	0.063 (4)	0.033 (3)	0.068 (4)	0.000 (3)	0.000 (3)	−0.002 (3)
C17	0.044 (3)	0.034 (3)	0.071 (4)	−0.007 (3)	−0.008 (3)	0.009 (3)
C18	0.051 (4)	0.028 (3)	0.089 (4)	0.000 (3)	−0.001 (4)	0.001 (3)
C19	0.122 (7)	0.058 (5)	0.135 (7)	−0.013 (5)	−0.033 (7)	0.030 (5)
C20	0.104 (7)	0.038 (4)	0.100 (6)	−0.006 (4)	−0.024 (5)	0.016 (4)
C21	0.084 (5)	0.063 (4)	0.082 (5)	−0.002 (4)	0.019 (4)	−0.005 (4)
C22	0.059 (4)	0.044 (4)	0.072 (4)	0.003 (3)	−0.001 (4)	−0.004 (3)
C23	0.046 (4)	0.069 (5)	0.121 (6)	0.006 (4)	−0.002 (4)	0.012 (4)
C24	0.044 (4)	0.059 (4)	0.107 (5)	−0.005 (4)	−0.014 (4)	0.014 (4)

Geometric parameters (Å, º) top

N1—C6	1.367 (8)	O8—C22	1.199 (8)
N1—C5	1.455 (9)	O9—C24	1.355 (8)
N1—H1A	0.8600	O9—C18	1.433 (7)
C1—C2	1.500 (10)	C9—C10	1.345 (8)
C1—H1B	0.9600	C9—C13	1.533 (8)
C1—H1C	0.9600	O10—C24	1.177 (8)
C1—H1D	0.9600	C10—C11	1.396 (8)
O1—N2	1.253 (15)	C10—H10A	0.9300
C2—C5	1.512 (10)	O11—C15	1.415 (7)
C2—H2A	0.9700	O11—C14	1.463 (7)
C2—H2B	0.9700	C12—H12A	0.9600
N2—O2	1.178 (15)	C12—H12B	0.9600
N2—C7	1.458 (10)	C12—H12C	0.9600
N3—O3	1.176 (7)	C13—H13A	0.9700
N3—O4	1.238 (7)	C13—H13B	0.9700
N3—C11	1.450 (8)	C14—C18	1.522 (9)
C3—C4	1.484 (13)	C14—H14A	0.9800
C3—H3A	0.9600	C15—C16	1.513 (8)
C3—H3B	0.9600	C15—H15A	0.9700
C3—H3C	0.9600	C15—H15B	0.9700
N4—C14	1.393 (8)	C16—C17	1.540 (8)
N4—C13	1.465 (9)	C16—H16A	0.9800
N4—H4A	0.8600	C17—C18	1.503 (8)
C4—C5	1.538 (11)	C17—H17A	0.9800
C4—H4B	0.9700	C18—H18A	0.9800
C4—H4C	0.9700	C19—C20	1.427 (11)
O5—C20	1.231 (9)	C19—H19A	0.9600
C5—H5A	0.9800	C19—H19B	0.9600
O6—C20	1.359 (8)	C19—H19C	0.9600
O6—C16	1.436 (7)	C21—C22	1.509 (10)
C6—C7	1.416 (9)	C21—H21A	0.9600
C6—C11	1.446 (9)	C21—H21B	0.9600
C7—C8	1.386 (8)	C21—H21C	0.9600
O7—C22	1.339 (7)	C23—C24	1.482 (10)
O7—C17	1.437 (7)	C23—H23A	0.9600
C8—C9	1.395 (8)	C23—H23B	0.9600
C8—C12	1.536 (9)	C23—H23C	0.9600

C6—N1—C5	132.8 (6)	C8—C12—H12C	109.5
C6—N1—H1A	113.6	H12A—C12—H12C	109.5
C5—N1—H1A	113.6	H12B—C12—H12C	109.5
C2—C1—H1B	109.5	N4—C13—C9	112.4 (6)
C2—C1—H1C	109.5	N4—C13—H13A	109.1
H1B—C1—H1C	109.5	C9—C13—H13A	109.1
C2—C1—H1D	109.5	N4—C13—H13B	109.1
H1B—C1—H1D	109.5	C9—C13—H13B	109.1
H1C—C1—H1D	109.5	H13A—C13—H13B	107.9
C1—C2—C5	115.8 (8)	N4—C14—O11	110.2 (5)
C1—C2—H2A	108.3	N4—C14—C18	112.1 (6)
C5—C2—H2A	108.3	O11—C14—C18	107.6 (4)
C1—C2—H2B	108.3	N4—C14—H14A	109.0
C5—C2—H2B	108.3	O11—C14—H14A	109.0
H2A—C2—H2B	107.4	C18—C14—H14A	109.0
O2—N2—O1	127.1 (11)	O11—C15—C16	109.3 (5)
O2—N2—C7	120.6 (13)	O11—C15—H15A	109.8
O1—N2—C7	112.2 (12)	C16—C15—H15A	109.8
O3—N3—O4	120.3 (6)	O11—C15—H15B	109.8
O3—N3—C11	119.1 (5)	C16—C15—H15B	109.8
O4—N3—C11	120.5 (6)	H15A—C15—H15B	108.3
C4—C3—H3A	109.5	O6—C16—C15	113.1 (5)
C4—C3—H3B	109.5	O6—C16—C17	105.8 (4)
H3A—C3—H3B	109.5	C15—C16—C17	108.4 (5)
C4—C3—H3C	109.5	O6—C16—H16A	109.8
H3A—C3—H3C	109.5	C15—C16—H16A	109.8
H3B—C3—H3C	109.5	C17—C16—H16A	109.8
C14—N4—C13	116.4 (6)	O7—C17—C18	108.1 (5)
C14—N4—H4A	121.8	O7—C17—C16	107.4 (4)
C13—N4—H4A	121.8	C18—C17—C16	110.1 (5)
C3—C4—C5	112.4 (7)	O7—C17—H17A	110.4
C3—C4—H4B	109.1	C18—C17—H17A	110.4
C5—C4—H4B	109.1	C16—C17—H17A	110.4
C3—C4—H4C	109.1	O9—C18—C17	107.1 (5)
C5—C4—H4C	109.1	O9—C18—C14	108.4 (4)
H4B—C4—H4C	107.9	C17—C18—C14	111.7 (5)
N1—C5—C2	107.8 (6)	O9—C18—H18A	109.8
N1—C5—C4	107.8 (6)	C17—C18—H18A	109.8
C2—C5—C4	112.1 (6)	C14—C18—H18A	109.8
N1—C5—H5A	109.7	C20—C19—H19A	109.5
C2—C5—H5A	109.7	C20—C19—H19B	109.5
C4—C5—H5A	109.7	H19A—C19—H19B	109.5
C20—O6—C16	118.1 (5)	C20—C19—H19C	109.5
N1—C6—C7	125.9 (6)	H19A—C19—H19C	109.5
N1—C6—C11	121.0 (6)	H19B—C19—H19C	109.5
C7—C6—C11	112.8 (5)	O5—C20—O6	117.9 (7)
C8—C7—C6	124.8 (6)	O5—C20—C19	128.1 (7)
C8—C7—N2	116.7 (6)	O6—C20—C19	113.7 (7)
C6—C7—N2	118.5 (6)	C22—C21—H21A	109.5
C22—O7—C17	118.2 (5)	C22—C21—H21B	109.5
C7—C8—C9	119.1 (6)	H21A—C21—H21B	109.5
C7—C8—C12	119.9 (6)	C22—C21—H21C	109.5
C9—C8—C12	121.0 (5)	H21A—C21—H21C	109.5
C24—O9—C18	119.5 (5)	H21B—C21—H21C	109.5
C10—C9—C8	119.3 (5)	O8—C22—O7	123.7 (7)
C10—C9—C13	121.2 (6)	O8—C22—C21	124.8 (7)
C8—C9—C13	119.5 (6)	O7—C22—C21	111.5 (6)
C9—C10—C11	122.3 (6)	C24—C23—H23A	109.5
C9—C10—H10A	118.8	C24—C23—H23B	109.5
C11—C10—H10A	118.8	H23A—C23—H23B	109.5
C15—O11—C14	111.7 (5)	C24—C23—H23C	109.5
C10—C11—C6	121.6 (6)	H23A—C23—H23C	109.5
C10—C11—N3	116.4 (6)	H23B—C23—H23C	109.5
C6—C11—N3	122.0 (5)	O10—C24—O9	121.1 (7)
C8—C12—H12A	109.5	O10—C24—C23	127.6 (7)
C8—C12—H12B	109.5	O9—C24—C23	111.2 (7)
H12A—C12—H12B	109.5

C6—N1—C5—C2	−145.8 (9)	O4—N3—C11—C6	2.2 (10)
C6—N1—C5—C4	93.0 (11)	C14—N4—C13—C9	95.8 (7)
C1—C2—C5—N1	68.2 (9)	C10—C9—C13—N4	0.9 (9)
C1—C2—C5—C4	−173.4 (7)	C8—C9—C13—N4	−178.2 (5)
C3—C4—C5—N1	−170.6 (8)	C13—N4—C14—O11	66.0 (6)
C3—C4—C5—C2	71.0 (10)	C13—N4—C14—C18	−174.1 (5)
C5—N1—C6—C7	9.7 (15)	C15—O11—C14—N4	−174.5 (5)
C5—N1—C6—C11	−176.7 (7)	C15—O11—C14—C18	63.1 (6)
N1—C6—C7—C8	177.5 (8)	C14—O11—C15—C16	−66.7 (6)
C11—C6—C7—C8	3.4 (12)	C20—O6—C16—C15	91.4 (7)
N1—C6—C7—N2	−5.1 (14)	C20—O6—C16—C17	−150.0 (6)
C11—C6—C7—N2	−179.2 (9)	O11—C15—C16—O6	177.2 (4)
O2—N2—C7—C8	85.5 (12)	O11—C15—C16—C17	60.2 (6)
O1—N2—C7—C8	−91.0 (9)	C22—O7—C17—C18	114.5 (6)
O2—N2—C7—C6	−92.1 (11)	C22—O7—C17—C16	−126.7 (5)
O1—N2—C7—C6	91.4 (10)	O6—C16—C17—O7	66.9 (6)
C6—C7—C8—C9	−5.2 (12)	C15—C16—C17—O7	−171.5 (5)
N2—C7—C8—C9	177.4 (9)	O6—C16—C17—C18	−175.6 (5)
C6—C7—C8—C12	177.2 (8)	C15—C16—C17—C18	−54.1 (6)
N2—C7—C8—C12	−0.3 (12)	C24—O9—C18—C17	125.1 (6)
C7—C8—C9—C10	4.1 (10)	C24—O9—C18—C14	−114.2 (6)
C12—C8—C9—C10	−178.3 (6)	O7—C17—C18—O9	−70.9 (6)
C7—C8—C9—C13	−176.8 (7)	C16—C17—C18—O9	172.1 (4)
C12—C8—C9—C13	0.8 (10)	O7—C17—C18—C14	170.5 (5)
C8—C9—C10—C11	−1.7 (10)	C16—C17—C18—C14	53.5 (6)
C13—C9—C10—C11	179.2 (7)	N4—C14—C18—O9	64.8 (7)
C9—C10—C11—C6	0.2 (10)	O11—C14—C18—O9	−173.9 (5)
C9—C10—C11—N3	−179.7 (6)	N4—C14—C18—C17	−177.4 (5)
N1—C6—C11—C10	−175.3 (7)	O11—C14—C18—C17	−56.1 (6)
C7—C6—C11—C10	−0.9 (10)	C16—O6—C20—O5	−12.9 (12)
N1—C6—C11—N3	4.6 (11)	C16—O6—C20—C19	172.6 (7)
C7—C6—C11—N3	179.0 (7)	C17—O7—C22—O8	−4.5 (9)
O3—N3—C11—C10	0.2 (10)	C17—O7—C22—C21	175.2 (5)
O4—N3—C11—C10	−177.9 (7)	C18—O9—C24—O10	−1.5 (10)
O3—N3—C11—C6	−179.7 (7)	C18—O9—C24—C23	−178.9 (6)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1A···O4	0.86	1.92	2.621 (8)	138

Experimental details

Crystal data
Chemical formula	C₂₄H₃₄N₄O₁₁
M_r	554.55
Crystal system, space group	Orthorhombic, P2₁2₁2₁
Temperature (K)	293
a, b, c (Å)	7.4100 (15), 11.044 (2), 34.106 (7)
V (Å³)	2791.1 (10)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.11
Crystal size (mm)	0.30 × 0.20 × 0.10

Data collection
Diffractometer	Enraf–Nonius CAD-4 diffractometer
Absorption correction	ψ scan (XCAD4; Harms & Wocadlo, 1995)
T_min, T_max	0.969, 0.990
No. of measured, independent and observed [I > 2σ(I)] reflections	2870, 2870, 1662
R_int	0.000
(sin θ/λ)_max (Å⁻¹)	0.598

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.067, 0.196, 1.04
No. of reflections	2870
No. of parameters	352
No. of restraints	13
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.18, −0.23

Computer programs: CAD-4 Software (Enraf–Nonius, 1989), XCAD4 (Harms & Wocadlo, 1995), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1A···O4	0.86	1.92	2.621 (8)	137.5

References

Enraf–Nonius (1989). CAD-4 Software. Enraf–Nonius, Delft, The Netherlands. Google Scholar
Grichar, W. J. & Dotray, P. A. (2007). Crop Prot. 26, 1826–1830. Web of Science CrossRef CAS Google Scholar
Harms, K. & Wocadlo, S. (1995). XCAD4. University of Marburg, Germany. Google Scholar
Kubátová, A., Dronen, L. C. & Hawthorne, S. B. (2006). Environ. Toxicol. Chem. 25, 1742–1745. Web of Science PubMed Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Wang, X., Li, X., Yin, Y., Pang, Y. & Yang, Y. (2008). Acta Cryst. E64, o669. Web of Science CSD CrossRef IUCr Journals Google Scholar
Yang, B., Zhang, S.-S., Wang, Y.-F., Li, X.-M., Jiao, K., Kassim, M. & Yamin, B. M. (2004). Acta Cryst. E60, o1902–o1904. Web of Science CSD CrossRef IUCr Journals Google Scholar

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Volume 64| Part 8| August 2008| Page o1623

doi:10.1107/S1600536808023192

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

3-Methyl-2,6-di­nitro-N-(3-pent­yl)-4-[(2,3,4-tri-O-acetyl-β-D-xylos­yl)amino­methyl]­aniline

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Experimental

Crystal data

Data collection

Refinement

Supporting information

References

organic compounds

3-Methyl-2,6-dinitro-N-(3-pentyl)-4-[(2,3,4-tri-O-acetyl-β-D-xylosyl)aminomethyl]aniline