Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536805030308/is6124sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536805030308/is6124Isup2.hkl |
CCDC reference: 287611
The title compound was prepared according to the method described by Zhang et al. (2004).
All H atoms were positioned geometrically and treated as riding, with C—H = 0.93–0.98 Å, N—H = 0.86 Å and Uiso(H) = 1.2Ueq(C,N), or Uiso(H) = 1.5Ueq(C) for the methyl H atoms.
Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997a); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997a); molecular graphics: SHELXTL (Sheldrick, 1997b); software used to prepare material for publication: SHELXTL, PARST (Nardelli, 1995) and PLATON (Spek, 2003).
C22H27N3O9S | F(000) = 536 |
Mr = 509.53 | Dx = 1.283 Mg m−3 |
Monoclinic, P21 | Mo Kα radiation, λ = 0.71073 Å |
a = 11.547 (5) Å | Cell parameters from 1389 reflections |
b = 9.113 (4) Å | θ = 2.6–19.0° |
c = 12.801 (5) Å | µ = 0.18 mm−1 |
β = 101.651 (8)° | T = 293 K |
V = 1319.3 (9) Å3 | Needle, colorless |
Z = 2 | 0.55 × 0.08 × 0.08 mm |
Siemens SMART CCD area detector diffractometer | 5040 independent reflections |
Radiation source: fine-focus sealed tube | 3120 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.030 |
Detector resolution: 8.33 pixels mm-1 | θmax = 26.2°, θmin = 1.6° |
ω scans | h = −7→14 |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | k = −11→11 |
Tmin = 0.910, Tmax = 0.986 | l = −15→15 |
7435 measured reflections |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.063 | H-atom parameters constrained |
wR(F2) = 0.132 | w = 1/[σ2(Fo2) + (0.0433P)2] where P = (Fo2 + 2Fc2)/3 |
S = 1.06 | (Δ/σ)max < 0.001 |
5040 reflections | Δρmax = 0.19 e Å−3 |
316 parameters | Δρmin = −0.18 e Å−3 |
1 restraint | Absolute structure: Flack (1983), 2229 Friedel paris |
Primary atom site location: structure-invariant direct methods | Absolute structure parameter: 0.06 (11) |
C22H27N3O9S | V = 1319.3 (9) Å3 |
Mr = 509.53 | Z = 2 |
Monoclinic, P21 | Mo Kα radiation |
a = 11.547 (5) Å | µ = 0.18 mm−1 |
b = 9.113 (4) Å | T = 293 K |
c = 12.801 (5) Å | 0.55 × 0.08 × 0.08 mm |
β = 101.651 (8)° |
Siemens SMART CCD area detector diffractometer | 5040 independent reflections |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | 3120 reflections with I > 2σ(I) |
Tmin = 0.910, Tmax = 0.986 | Rint = 0.030 |
7435 measured reflections |
R[F2 > 2σ(F2)] = 0.063 | H-atom parameters constrained |
wR(F2) = 0.132 | Δρmax = 0.19 e Å−3 |
S = 1.06 | Δρmin = −0.18 e Å−3 |
5040 reflections | Absolute structure: Flack (1983), 2229 Friedel paris |
316 parameters | Absolute structure parameter: 0.06 (11) |
1 restraint |
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. |
x | y | z | Uiso*/Ueq | ||
S1 | 0.16605 (9) | 0.20227 (13) | 0.96169 (10) | 0.0779 (4) | |
O1 | −0.1073 (2) | 0.4398 (3) | 0.8421 (2) | 0.0672 (8) | |
O2 | −0.1962 (2) | 0.1678 (3) | 1.0197 (3) | 0.0726 (8) | |
O3 | −0.2033 (3) | 0.3103 (4) | 1.1606 (3) | 0.1023 (11) | |
O4 | −0.4102 (2) | 0.2211 (3) | 0.8765 (2) | 0.0818 (9) | |
O5 | −0.4155 (3) | −0.0010 (4) | 0.8045 (3) | 0.1005 (12) | |
O6 | −0.3602 (2) | 0.4916 (3) | 0.7979 (2) | 0.0755 (9) | |
O7 | −0.5309 (3) | 0.4461 (5) | 0.6862 (4) | 0.1372 (16) | |
O8 | −0.2651 (4) | 0.5056 (5) | 0.5745 (3) | 0.1051 (11) | |
O9 | −0.3481 (5) | 0.7213 (6) | 0.5820 (5) | 0.181 (3) | |
N1 | −0.0077 (3) | 0.3666 (4) | 1.0105 (3) | 0.0660 (9) | |
H1A | −0.0283 | 0.4318 | 1.0518 | 0.079* | |
N2 | 0.1599 (3) | 0.3509 (4) | 1.1353 (3) | 0.0703 (10) | |
H2A | 0.2315 | 0.3218 | 1.1575 | 0.084* | |
N3 | 0.1065 (3) | 0.4364 (4) | 1.2002 (3) | 0.0648 (9) | |
C1 | −0.0924 (3) | 0.3242 (5) | 0.9180 (3) | 0.0649 (11) | |
H1B | −0.0643 | 0.2362 | 0.8867 | 0.078* | |
C2 | −0.2108 (3) | 0.2914 (5) | 0.9484 (3) | 0.0608 (10) | |
H2B | −0.2395 | 0.3771 | 0.9818 | 0.073* | |
C3 | −0.2967 (3) | 0.2486 (5) | 0.8494 (4) | 0.0688 (12) | |
H3B | −0.2690 | 0.1573 | 0.8222 | 0.083* | |
C4 | −0.3076 (3) | 0.3640 (5) | 0.7632 (4) | 0.0702 (12) | |
H4A | −0.3566 | 0.3271 | 0.6968 | 0.084* | |
C5 | −0.1852 (4) | 0.4024 (5) | 0.7455 (4) | 0.0699 (12) | |
H5A | −0.1530 | 0.3173 | 0.7143 | 0.084* | |
C6 | −0.1919 (3) | 0.1919 (6) | 1.1244 (4) | 0.0732 (12) | |
C7 | −0.1730 (5) | 0.0513 (6) | 1.1853 (4) | 0.0987 (17) | |
H7A | −0.1698 | 0.0704 | 1.2596 | 0.148* | |
H7B | −0.1000 | 0.0076 | 1.1765 | 0.148* | |
H7C | −0.2372 | −0.0146 | 1.1591 | 0.148* | |
C8 | −0.4606 (4) | 0.0908 (6) | 0.8489 (4) | 0.0735 (13) | |
C9 | −0.5771 (4) | 0.0786 (8) | 0.8817 (5) | 0.132 (2) | |
H9A | −0.6114 | −0.0155 | 0.8609 | 0.198* | |
H9B | −0.6289 | 0.1546 | 0.8477 | 0.198* | |
H9C | −0.5659 | 0.0890 | 0.9578 | 0.198* | |
C10 | −0.4737 (4) | 0.5219 (6) | 0.7531 (5) | 0.0897 (15) | |
C11 | −0.5124 (4) | 0.6577 (6) | 0.7956 (5) | 0.121 (2) | |
H11A | −0.5931 | 0.6770 | 0.7622 | 0.182* | |
H11B | −0.4634 | 0.7372 | 0.7814 | 0.182* | |
H11C | −0.5062 | 0.6481 | 0.8712 | 0.182* | |
C12 | −0.1845 (4) | 0.5328 (6) | 0.6723 (4) | 0.0876 (15) | |
H12A | −0.2077 | 0.6207 | 0.7056 | 0.105* | |
H12B | −0.1056 | 0.5476 | 0.6590 | 0.105* | |
C13 | −0.3421 (7) | 0.6100 (10) | 0.5379 (5) | 0.123 (2) | |
C14 | −0.4214 (7) | 0.5605 (10) | 0.4359 (5) | 0.197 (4) | |
H14A | −0.4768 | 0.6370 | 0.4095 | 0.295* | |
H14B | −0.4635 | 0.4739 | 0.4492 | 0.295* | |
H14C | −0.3745 | 0.5391 | 0.3838 | 0.295* | |
C15 | 0.1012 (3) | 0.3117 (4) | 1.0369 (3) | 0.0598 (11) | |
C16 | 0.1638 (4) | 0.4628 (5) | 1.2942 (4) | 0.0744 (13) | |
H16A | 0.2388 | 0.4226 | 1.3160 | 0.089* | |
C17 | 0.1161 (5) | 0.5526 (5) | 1.3678 (4) | 0.0795 (14) | |
C18 | 0.0034 (5) | 0.6037 (6) | 1.3424 (4) | 0.0968 (16) | |
H18A | −0.0453 | 0.5753 | 1.2786 | 0.116* | |
C19 | −0.0394 (7) | 0.6966 (9) | 1.4097 (6) | 0.138 (2) | |
H19A | −0.1170 | 0.7299 | 1.3919 | 0.166* | |
C20 | 0.0325 (11) | 0.7408 (10) | 1.5040 (8) | 0.161 (4) | |
H20A | 0.0043 | 0.8047 | 1.5497 | 0.193* | |
C21 | 0.1428 (10) | 0.6907 (10) | 1.5286 (6) | 0.159 (3) | |
H21A | 0.1908 | 0.7210 | 1.5922 | 0.191* | |
C22 | 0.1891 (6) | 0.5952 (8) | 1.4634 (5) | 0.113 (2) | |
H22A | 0.2663 | 0.5607 | 1.4828 | 0.136* |
U11 | U22 | U33 | U12 | U13 | U23 | |
S1 | 0.0625 (6) | 0.0779 (9) | 0.1007 (8) | 0.0222 (6) | 0.0344 (6) | 0.0112 (7) |
O1 | 0.0507 (15) | 0.0650 (19) | 0.083 (2) | −0.0069 (14) | 0.0073 (14) | −0.0107 (17) |
O2 | 0.0694 (19) | 0.058 (2) | 0.093 (2) | 0.0059 (14) | 0.0239 (16) | −0.0122 (18) |
O3 | 0.121 (3) | 0.086 (3) | 0.110 (3) | 0.010 (2) | 0.047 (2) | −0.024 (2) |
O4 | 0.0499 (15) | 0.078 (2) | 0.123 (2) | −0.0088 (15) | 0.0291 (15) | −0.0333 (19) |
O5 | 0.079 (2) | 0.080 (2) | 0.150 (3) | −0.0252 (18) | 0.042 (2) | −0.045 (2) |
O6 | 0.0497 (16) | 0.0609 (19) | 0.109 (2) | 0.0032 (14) | 0.0003 (15) | −0.0298 (17) |
O7 | 0.066 (2) | 0.134 (4) | 0.190 (4) | 0.005 (2) | −0.025 (2) | −0.052 (3) |
O8 | 0.120 (3) | 0.099 (3) | 0.084 (2) | −0.005 (2) | −0.008 (2) | −0.016 (2) |
O9 | 0.205 (5) | 0.103 (4) | 0.191 (5) | 0.013 (4) | −0.067 (4) | −0.007 (3) |
N1 | 0.0445 (18) | 0.067 (2) | 0.088 (2) | 0.0072 (16) | 0.0161 (17) | −0.0135 (19) |
N2 | 0.0465 (19) | 0.078 (3) | 0.087 (3) | 0.0061 (18) | 0.015 (2) | 0.016 (2) |
N3 | 0.059 (2) | 0.060 (2) | 0.077 (3) | −0.0045 (18) | 0.019 (2) | 0.019 (2) |
C1 | 0.048 (2) | 0.054 (3) | 0.092 (3) | 0.0017 (19) | 0.014 (2) | −0.013 (2) |
C2 | 0.049 (2) | 0.051 (3) | 0.085 (3) | 0.0000 (19) | 0.019 (2) | −0.012 (2) |
C3 | 0.048 (2) | 0.058 (3) | 0.106 (3) | −0.0021 (19) | 0.028 (2) | −0.025 (3) |
C4 | 0.056 (3) | 0.064 (3) | 0.089 (3) | −0.002 (2) | 0.009 (2) | −0.028 (3) |
C5 | 0.062 (3) | 0.067 (3) | 0.082 (3) | −0.002 (2) | 0.017 (2) | −0.025 (3) |
C6 | 0.059 (2) | 0.077 (4) | 0.090 (3) | 0.005 (3) | 0.032 (2) | −0.018 (3) |
C7 | 0.102 (4) | 0.091 (4) | 0.107 (4) | 0.028 (3) | 0.030 (3) | 0.003 (3) |
C8 | 0.055 (3) | 0.080 (4) | 0.085 (3) | −0.016 (2) | 0.014 (2) | −0.017 (3) |
C9 | 0.071 (3) | 0.160 (6) | 0.180 (6) | −0.048 (3) | 0.062 (4) | −0.048 (5) |
C10 | 0.050 (3) | 0.082 (4) | 0.132 (4) | −0.003 (3) | 0.007 (3) | −0.020 (3) |
C11 | 0.085 (3) | 0.083 (4) | 0.195 (6) | 0.025 (3) | 0.024 (4) | −0.012 (4) |
C12 | 0.080 (3) | 0.090 (4) | 0.089 (3) | −0.003 (3) | 0.007 (3) | −0.003 (3) |
C13 | 0.135 (6) | 0.105 (6) | 0.108 (5) | −0.019 (5) | −0.028 (4) | 0.010 (5) |
C14 | 0.207 (8) | 0.202 (9) | 0.135 (5) | −0.016 (7) | −0.074 (6) | −0.008 (6) |
C15 | 0.043 (2) | 0.057 (3) | 0.081 (3) | 0.0014 (19) | 0.019 (2) | 0.016 (2) |
C16 | 0.069 (3) | 0.079 (4) | 0.071 (3) | −0.007 (3) | 0.005 (3) | 0.023 (3) |
C17 | 0.104 (4) | 0.068 (3) | 0.069 (3) | −0.017 (3) | 0.024 (3) | 0.017 (3) |
C18 | 0.120 (5) | 0.095 (4) | 0.090 (4) | 0.009 (3) | 0.056 (4) | 0.009 (3) |
C19 | 0.183 (7) | 0.129 (6) | 0.125 (5) | 0.007 (6) | 0.081 (5) | 0.014 (5) |
C20 | 0.275 (13) | 0.103 (6) | 0.134 (8) | −0.001 (7) | 0.110 (9) | −0.009 (5) |
C21 | 0.280 (11) | 0.121 (7) | 0.078 (4) | −0.043 (8) | 0.043 (7) | −0.006 (5) |
C22 | 0.154 (6) | 0.116 (5) | 0.068 (4) | −0.024 (4) | 0.019 (4) | 0.013 (4) |
S1—C15 | 1.665 (4) | C6—C7 | 1.493 (6) |
O1—C5 | 1.417 (5) | C7—H7A | 0.9600 |
O1—C1 | 1.420 (5) | C7—H7B | 0.9600 |
O2—C6 | 1.350 (5) | C7—H7C | 0.9600 |
O2—C2 | 1.438 (5) | C8—C9 | 1.493 (6) |
O3—C6 | 1.192 (5) | C9—H9A | 0.9600 |
O4—C8 | 1.338 (5) | C9—H9B | 0.9600 |
O4—C3 | 1.444 (4) | C9—H9C | 0.9600 |
O5—C8 | 1.189 (5) | C10—C11 | 1.457 (7) |
O6—C10 | 1.348 (5) | C11—H11A | 0.9600 |
O6—C4 | 1.424 (5) | C11—H11B | 0.9600 |
O7—C10 | 1.191 (5) | C11—H11C | 0.9600 |
O8—C13 | 1.322 (8) | C12—H12A | 0.9700 |
O8—C12 | 1.423 (5) | C12—H12B | 0.9700 |
O9—C13 | 1.170 (8) | C13—C14 | 1.504 (8) |
N1—C15 | 1.332 (5) | C14—H14A | 0.9600 |
N1—C1 | 1.429 (5) | C14—H14B | 0.9600 |
N1—H1A | 0.8600 | C14—H14C | 0.9600 |
N2—C15 | 1.352 (5) | C16—C17 | 1.439 (7) |
N2—N3 | 1.373 (5) | C16—H16A | 0.9300 |
N2—H2A | 0.8600 | C17—C18 | 1.359 (7) |
N3—C16 | 1.274 (5) | C17—C22 | 1.394 (7) |
C1—C2 | 1.525 (5) | C18—C19 | 1.369 (8) |
C1—H1B | 0.9800 | C18—H18A | 0.9300 |
C2—C3 | 1.494 (5) | C19—C20 | 1.380 (10) |
C2—H2B | 0.9800 | C19—H19A | 0.9300 |
C3—C4 | 1.512 (6) | C20—C21 | 1.329 (10) |
C3—H3B | 0.9800 | C20—H20A | 0.9300 |
C4—C5 | 1.516 (5) | C21—C22 | 1.386 (10) |
C4—H4A | 0.9800 | C21—H21A | 0.9300 |
C5—C12 | 1.514 (6) | C22—H22A | 0.9300 |
C5—H5A | 0.9800 | ||
C5—O1—C1 | 112.7 (3) | C8—C9—H9A | 109.5 |
C6—O2—C2 | 118.6 (3) | C8—C9—H9B | 109.5 |
C8—O4—C3 | 117.2 (3) | H9A—C9—H9B | 109.5 |
C10—O6—C4 | 118.3 (3) | C8—C9—H9C | 109.5 |
C13—O8—C12 | 117.4 (5) | H9A—C9—H9C | 109.5 |
C15—N1—C1 | 124.2 (4) | H9B—C9—H9C | 109.5 |
C15—N1—H1A | 117.9 | O7—C10—O6 | 122.5 (5) |
C1—N1—H1A | 117.9 | O7—C10—C11 | 126.4 (5) |
C15—N2—N3 | 120.8 (3) | O6—C10—C11 | 111.2 (4) |
C15—N2—H2A | 119.6 | C10—C11—H11A | 109.5 |
N3—N2—H2A | 119.6 | C10—C11—H11B | 109.5 |
C16—N3—N2 | 117.9 (4) | H11A—C11—H11B | 109.5 |
O1—C1—N1 | 109.5 (3) | C10—C11—H11C | 109.5 |
O1—C1—C2 | 109.2 (3) | H11A—C11—H11C | 109.5 |
N1—C1—C2 | 109.9 (3) | H11B—C11—H11C | 109.5 |
O1—C1—H1B | 109.4 | O8—C12—C5 | 108.9 (4) |
N1—C1—H1B | 109.4 | O8—C12—H12A | 109.9 |
C2—C1—H1B | 109.4 | C5—C12—H12A | 109.9 |
O2—C2—C3 | 107.8 (3) | O8—C12—H12B | 109.9 |
O2—C2—C1 | 108.6 (3) | C5—C12—H12B | 109.9 |
C3—C2—C1 | 108.1 (3) | H12A—C12—H12B | 108.3 |
O2—C2—H2B | 110.7 | O9—C13—O8 | 123.6 (6) |
C3—C2—H2B | 110.7 | O9—C13—C14 | 126.5 (8) |
C1—C2—H2B | 110.7 | O8—C13—C14 | 109.9 (8) |
O4—C3—C2 | 108.7 (3) | C13—C14—H14A | 109.5 |
O4—C3—C4 | 110.5 (3) | C13—C14—H14B | 109.5 |
C2—C3—C4 | 112.4 (3) | H14A—C14—H14B | 109.5 |
O4—C3—H3B | 108.4 | C13—C14—H14C | 109.5 |
C2—C3—H3B | 108.4 | H14A—C14—H14C | 109.5 |
C4—C3—H3B | 108.4 | H14B—C14—H14C | 109.5 |
O6—C4—C3 | 108.6 (3) | N1—C15—N2 | 114.0 (4) |
O6—C4—C5 | 109.1 (3) | N1—C15—S1 | 126.2 (3) |
C3—C4—C5 | 109.1 (3) | N2—C15—S1 | 119.8 (3) |
O6—C4—H4A | 110.0 | N3—C16—C17 | 122.1 (5) |
C3—C4—H4A | 110.0 | N3—C16—H16A | 119.0 |
C5—C4—H4A | 110.0 | C17—C16—H16A | 119.0 |
O1—C5—C12 | 105.7 (3) | C18—C17—C22 | 119.7 (6) |
O1—C5—C4 | 111.8 (3) | C18—C17—C16 | 120.9 (5) |
C12—C5—C4 | 113.3 (4) | C22—C17—C16 | 119.3 (6) |
O1—C5—H5A | 108.6 | C17—C18—C19 | 120.8 (6) |
C12—C5—H5A | 108.6 | C17—C18—H18A | 119.6 |
C4—C5—H5A | 108.6 | C19—C18—H18A | 119.6 |
O3—C6—O2 | 123.3 (5) | C18—C19—C20 | 120.1 (8) |
O3—C6—C7 | 126.2 (5) | C18—C19—H19A | 119.9 |
O2—C6—C7 | 110.6 (4) | C20—C19—H19A | 119.9 |
C6—C7—H7A | 109.5 | C21—C20—C19 | 119.0 (10) |
C6—C7—H7B | 109.5 | C21—C20—H20A | 120.5 |
H7A—C7—H7B | 109.5 | C19—C20—H20A | 120.5 |
C6—C7—H7C | 109.5 | C20—C21—C22 | 122.8 (9) |
H7A—C7—H7C | 109.5 | C20—C21—H21A | 118.6 |
H7B—C7—H7C | 109.5 | C22—C21—H21A | 118.6 |
O5—C8—O4 | 122.8 (4) | C21—C22—C17 | 117.7 (7) |
O5—C8—C9 | 126.0 (5) | C21—C22—H22A | 121.1 |
O4—C8—C9 | 111.1 (5) | C17—C22—H22A | 121.1 |
C15—N2—N3—C16 | 176.1 (4) | C3—C4—C5—C12 | −171.5 (4) |
C5—O1—C1—N1 | 176.6 (3) | C2—O2—C6—O3 | 2.5 (6) |
C5—O1—C1—C2 | −63.0 (4) | C2—O2—C6—C7 | −178.4 (3) |
C15—N1—C1—O1 | −108.2 (4) | C3—O4—C8—O5 | 0.5 (7) |
C15—N1—C1—C2 | 131.9 (4) | C3—O4—C8—C9 | −179.9 (4) |
C6—O2—C2—C3 | −138.3 (3) | C4—O6—C10—O7 | 0.1 (8) |
C6—O2—C2—C1 | 104.9 (4) | C4—O6—C10—C11 | −178.5 (5) |
O1—C1—C2—O2 | 176.2 (3) | C13—O8—C12—C5 | 130.7 (5) |
N1—C1—C2—O2 | −63.7 (4) | O1—C5—C12—O8 | −177.6 (3) |
O1—C1—C2—C3 | 59.5 (4) | C4—C5—C12—O8 | −54.9 (5) |
N1—C1—C2—C3 | 179.6 (3) | C12—O8—C13—O9 | −0.9 (11) |
C8—O4—C3—C2 | −125.4 (4) | C12—O8—C13—C14 | −178.6 (6) |
C8—O4—C3—C4 | 110.9 (4) | C1—N1—C15—N2 | −170.6 (4) |
O2—C2—C3—O4 | 64.4 (4) | C1—N1—C15—S1 | 8.7 (6) |
C1—C2—C3—O4 | −178.4 (3) | N3—N2—C15—N1 | 1.8 (5) |
O2—C2—C3—C4 | −173.0 (3) | N3—N2—C15—S1 | −177.5 (3) |
C1—C2—C3—C4 | −55.8 (4) | N2—N3—C16—C17 | 179.2 (4) |
C10—O6—C4—C3 | −106.2 (4) | N3—C16—C17—C18 | 5.3 (7) |
C10—O6—C4—C5 | 135.1 (4) | N3—C16—C17—C22 | −170.6 (4) |
O4—C3—C4—O6 | 54.9 (4) | C22—C17—C18—C19 | 0.0 (8) |
C2—C3—C4—O6 | −66.7 (4) | C16—C17—C18—C19 | −175.9 (5) |
O4—C3—C4—C5 | 173.7 (3) | C17—C18—C19—C20 | 0.8 (10) |
C2—C3—C4—C5 | 52.1 (4) | C18—C19—C20—C21 | −0.7 (12) |
C1—O1—C5—C12 | −176.4 (3) | C19—C20—C21—C22 | −0.1 (14) |
C1—O1—C5—C4 | 59.9 (4) | C20—C21—C22—C17 | 0.8 (12) |
O6—C4—C5—O1 | 66.2 (5) | C18—C17—C22—C21 | −0.7 (8) |
C3—C4—C5—O1 | −52.3 (4) | C16—C17—C22—C21 | 175.2 (5) |
O6—C4—C5—C12 | −53.1 (5) |
D—H···A | D—H | H···A | D···A | D—H···A |
C7—H7B···O1i | 0.96 | 2.53 | 3.477 (6) | 169 |
C11—H11B···O5ii | 0.96 | 2.45 | 3.300 (7) | 147 |
C16—H16A···O9i | 0.93 | 2.45 | 3.244 (8) | 143 |
Symmetry codes: (i) −x, y−1/2, −z+2; (ii) x, y+1, z. |
Experimental details
Crystal data | |
Chemical formula | C22H27N3O9S |
Mr | 509.53 |
Crystal system, space group | Monoclinic, P21 |
Temperature (K) | 293 |
a, b, c (Å) | 11.547 (5), 9.113 (4), 12.801 (5) |
β (°) | 101.651 (8) |
V (Å3) | 1319.3 (9) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.18 |
Crystal size (mm) | 0.55 × 0.08 × 0.08 |
Data collection | |
Diffractometer | Siemens SMART CCD area detector diffractometer |
Absorption correction | Multi-scan (SADABS; Sheldrick, 1996) |
Tmin, Tmax | 0.910, 0.986 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 7435, 5040, 3120 |
Rint | 0.030 |
(sin θ/λ)max (Å−1) | 0.620 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.063, 0.132, 1.06 |
No. of reflections | 5040 |
No. of parameters | 316 |
No. of restraints | 1 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.19, −0.18 |
Absolute structure | Flack (1983), 2229 Friedel paris |
Absolute structure parameter | 0.06 (11) |
Computer programs: SMART (Siemens, 1996), SAINT (Siemens, 1996), SAINT, SHELXS97 (Sheldrick, 1997a), SHELXL97 (Sheldrick, 1997a), SHELXTL (Sheldrick, 1997b), SHELXTL, PARST (Nardelli, 1995) and PLATON (Spek, 2003).
S1—C15 | 1.665 (4) | N1—C1 | 1.429 (5) |
O1—C5 | 1.417 (5) | N2—C15 | 1.352 (5) |
O1—C1 | 1.420 (5) | N2—N3 | 1.373 (5) |
N1—C15 | 1.332 (5) | N3—C16 | 1.274 (5) |
C1—N1—C15—N2 | −170.6 (4) | C1—N1—C15—S1 | 8.7 (6) |
D—H···A | D—H | H···A | D···A | D—H···A |
C7—H7B···O1i | 0.96 | 2.53 | 3.477 (6) | 169 |
C11—H11B···O5ii | 0.96 | 2.45 | 3.300 (7) | 147 |
C16—H16A···O9i | 0.93 | 2.45 | 3.244 (8) | 143 |
Symmetry codes: (i) −x, y−1/2, −z+2; (ii) x, y+1, z. |
In the title compound, (I), the bond lengths and angles of the xylopyranosyl ring are comparable to those in the related compounds 4-methoxybenzaldehyde 4-(2,3,4,6-tetra-O-acetyl-β-D– glucopyranosyl)thiosemicarbazone (Zhang et al., 2004) and benzaldehyde 1-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)thiosemicarbazone (Yang et al., 2004). The acetyl group at atom C4 occupies an axial position, while all other substituents are in equatorial positions. The pyranosyl ring adopts a chair conformation, and atom S1 is in a synperiplanar position with respect to atom C1, the C1—N1—C15—S1 torsion angle being 8.7 (6)°.
In the crystal structure of (I), the molecules are linked by C11—H11B···O5ii hydrogen bonds (Table 2) into chains parallel to the b axis (Fig. 2). The packing is further stabilized by two additional C7—H7B···O10Bi and C16—H16A···O9i interactions (Table 2), giving a three-dimensional framework.