Literature DB >> 25844234

Crystal structure of 3-[(4-benzyl-piperazin-1-yl)meth-yl]-5-(thio-phen-2-yl)-2,3-di-hydro-1,3,4-oxa-diazole-2-thione.

Fatmah A M Al-Omary1, Ali A El-Emam2, Hazem A Ghabbour3, C S Chidan Kumar4, Ching Kheng Quah5, Hoong-Kun Fun6.   

Abstract

The title 1,3,4-oxa-diazole-2-thione derivative, C18H20N4OS2, crystallized with two independent mol-ecules (A and B) in the asymmetric unit. The 2-thienyl rings in both mol-ecules are rotationally disordered over two orientations by approximately 180° about the single C-C bond that connects it to the oxa-diazole thione ring; the ratios of site occupancies for the major and minor components were fixed in the structure refinement at 0.8:0.2 and 0.9:0.1 in mol-ecules A and B, respectively. The 1,3,4-oxa-diazole-2-thione ring forms dihedral angles of 7.71 (16), 10.0 (11) and 77.50 (12)° (mol-ecule A), and 6.5 (3), 6.0 (9) and 55.30 (12)° (mol-ecule B) with the major and minor parts of the disordered thio-phene ring and the mean plane of the adjacent piperazine ring, respectively, resulting in approximately V-shaped conformations for the mol-ecules. The piperazine ring in both mol-ecules adopts a chair conformation. The terminal benzene ring is inclined towards the mean plane of the piperazine ring with N-C-C-C torsion angles of -58.2 (3) and -66.2 (3)° in mol-ecules A and B, respectively. In the crystal, no inter-molecular hydrogen bonds are observed. The crystal packing features short S⋯S contacts [3.4792 (9) Å] and π-π inter-actions [3.661 (3), 3.664 (11) and 3.5727 (10) Å], producing a three-dimensional network.

Entities:  

Keywords:  1,3,4-oxa­diazole; S⋯S contacts; crystal structure; disorder; piperazin-1-yl; π–π inter­actions

Year:  2015        PMID: 25844234      PMCID: PMC4350721          DOI: 10.1107/S2056989015002273

Source DB:  PubMed          Journal:  Acta Crystallogr E Crystallogr Commun


Related literature

For the biological activity of 1,3,4-oxa­diazole derivatives, see: Al-Deeb et al. (2006 ▸); El-Emam et al. (2004 ▸); Kadi et al. (2007 ▸); Padmavathi et al. (2009 ▸). For the synthesis of the title compound, see: Al-Omar (2010 ▸). For related 1,3,4-oxa­diazole structures, see: El-Emam et al. (2012 ▸, 2013 ▸).

Experimental

Crystal data

C18H20N4OS2 M = 372.50 Monoclinic, a = 10.6909 (5) Å b = 29.3658 (13) Å c = 15.6179 (6) Å β = 130.283 (2)° V = 3740.4 (3) Å3 Z = 8 Mo Kα radiation μ = 0.30 mm−1 T = 273 K 0.41 × 0.36 × 0.14 mm

Data collection

Bruker APEXII CCD diffractometer 88935 measured reflections 11407 independent reflections 10339 reflections with I > 2σ(I) R int = 0.034

Refinement

R[F 2 > 2σ(F 2)] = 0.059 wR(F 2) = 0.122 S = 1.19 11407 reflections 485 parameters 18 restraints H-atom parameters constrained Δρmax = 0.38 e Å−3 Δρmin = −0.42 e Å−3

Data collection: APEX2 (Bruker, 2009 ▸); cell refinement: SAINT (Bruker, 2009 ▸); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick 2008 ▸); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2015 ▸); molecular graphics: SHELXTL (Sheldrick, 2008 ▸); software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009 ▸). Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S2056989015002273/sj5443sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989015002273/sj5443Isup2.hkl Click here for additional data file. Supporting information file. DOI: 10.1107/S2056989015002273/sj5443Isup3.cml Click here for additional data file. X Y A B . DOI: 10.1107/S2056989015002273/sj5443fig1.tif The mol­ecular structure of the title compound with atom labels and 50% probability displacement ellipsoids (atoms of the minor part are labelled with the suffix X and Y for mol­ecules A and B, respectively) Click here for additional data file. . DOI: 10.1107/S2056989015002273/sj5443fig2.tif Crystal packing of the title compound, showing the S⋯S short contacts and π–π inter­actions as dashed lines. Only the major components of the thio­phene rings are shown. All the H atoms are omitted for clarity. CCDC reference: 1047059 Additional supporting information: crystallographic information; 3D view; checkCIF report
C18H20N4OS2F(000) = 1568
Mr = 372.50Dx = 1.323 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
a = 10.6909 (5) ÅCell parameters from 9237 reflections
b = 29.3658 (13) Åθ = 2.4–30.5°
c = 15.6179 (6) ŵ = 0.30 mm1
β = 130.283 (2)°T = 273 K
V = 3740.4 (3) Å3Plate, colourless
Z = 80.41 × 0.36 × 0.14 mm
Bruker APEXII CCD diffractometerRint = 0.034
φ and ω scansθmax = 30.6°, θmin = 2.2°
88935 measured reflectionsh = −15→15
11407 independent reflectionsk = −42→41
10339 reflections with I > 2σ(I)l = −22→22
Refinement on F218 restraints
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.059H-atom parameters constrained
wR(F2) = 0.122w = 1/[σ2(Fo2) + (0.0207P)2 + 3.9136P] where P = (Fo2 + 2Fc2)/3
S = 1.19(Δ/σ)max = 0.001
11407 reflectionsΔρmax = 0.38 e Å3
485 parametersΔρmin = −0.42 e Å3
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.
xyzUiso*/UeqOcc. (<1)
S1B0.86597 (6)0.54555 (2)0.95382 (4)0.03328 (11)
O1B0.56261 (15)0.54910 (4)0.88376 (10)0.0241 (2)
N1B0.40511 (17)0.56647 (5)0.70234 (13)0.0242 (3)
N2B0.56914 (17)0.56405 (5)0.75134 (13)0.0240 (3)
N3B0.64150 (18)0.61694 (6)0.66687 (13)0.0260 (3)
N4B0.64546 (19)0.71415 (6)0.67316 (13)0.0310 (3)
C1B0.6665 (2)0.55360 (6)0.86079 (15)0.0241 (3)
C2B0.4084 (2)0.55740 (6)0.78476 (14)0.0219 (3)
C3B0.2721 (2)0.55573 (6)0.78285 (15)0.0225 (3)
C4B0.2698 (4)0.54323 (10)0.8668 (3)0.0270 (6)0.8
H4BA0.36220.53380.93770.032*0.8
C5B0.1129 (8)0.5463 (4)0.8336 (6)0.0365 (16)0.8
H5BA0.08860.53860.87930.044*0.8
C6B0.0010 (6)0.5619 (3)0.7273 (5)0.0358 (13)0.8
H6BA−0.10880.56660.69220.043*0.8
S2B0.08174 (8)0.57204 (3)0.66379 (7)0.03174 (14)0.8
C4Y0.122 (2)0.5646 (6)0.7033 (14)0.055 (5)*0.2
H4YA0.08480.57220.63240.066*0.2
C5Y0.015 (3)0.5625 (12)0.725 (2)0.039 (6)*0.2
H5YA−0.09660.56940.67470.046*0.2
C6Y0.103 (2)0.5484 (12)0.835 (2)0.023 (4)*0.2
H6YA0.05730.54490.86910.028*0.2
S2Y0.3049 (4)0.53795 (12)0.9013 (3)0.0243 (7)*0.2
C7B0.6198 (2)0.57087 (7)0.68367 (16)0.0270 (4)
H7BA0.72220.55480.71990.032*
H7BB0.53810.55700.61070.032*
C8B0.7695 (2)0.64187 (6)0.77012 (14)0.0256 (3)
H8BA0.87060.62450.81430.031*
H8BB0.73640.64610.81460.031*
C9B0.7969 (2)0.68769 (7)0.74051 (16)0.0302 (4)
H9BA0.88110.70420.80870.036*
H9BB0.83450.68330.69880.036*
C10B0.5211 (3)0.68905 (8)0.56929 (17)0.0386 (5)
H10C0.55860.68480.52750.046*
H10D0.42010.70650.52300.046*
C11B0.4893 (2)0.64320 (7)0.59601 (16)0.0317 (4)
H11C0.44670.64740.63460.038*
H11D0.40790.62670.52690.038*
C12B0.6695 (3)0.75944 (8)0.64694 (19)0.0439 (6)
H12C0.56430.77470.59630.053*
H12D0.71300.75630.60870.053*
C13B0.7846 (2)0.78830 (7)0.75006 (19)0.0365 (5)
C14B0.9356 (3)0.80127 (8)0.7843 (2)0.0442 (5)
H14B0.96560.79200.74280.053*
C15B1.0420 (3)0.82762 (8)0.8787 (2)0.0504 (7)
H15B1.14260.83610.90020.061*
C16B1.0000 (3)0.84134 (8)0.9410 (2)0.0536 (7)
H16B1.07200.85911.00480.064*
C17B0.8495 (3)0.82871 (8)0.9084 (3)0.0533 (6)
H17B0.82050.83790.95050.064*
C18B0.7424 (3)0.80236 (8)0.8128 (2)0.0458 (6)
H18B0.64130.79410.79090.055*
S1A0.40017 (6)0.46380 (2)0.54540 (4)0.02973 (11)
O1A0.22909 (14)0.45426 (4)0.61460 (10)0.0228 (2)
N1A0.41622 (17)0.43676 (5)0.79594 (12)0.0224 (3)
N2A0.48826 (17)0.44323 (5)0.74796 (12)0.0212 (3)
N3A0.71546 (17)0.38885 (5)0.83070 (12)0.0216 (3)
N4A0.7102 (2)0.29173 (5)0.83187 (13)0.0288 (3)
C1A0.3773 (2)0.45354 (6)0.63837 (14)0.0218 (3)
C2A0.2620 (2)0.44351 (6)0.71288 (14)0.0207 (3)
C3A0.1288 (2)0.44023 (6)0.71368 (14)0.0218 (3)
C4A−0.0338 (3)0.45153 (8)0.6297 (2)0.0265 (5)0.9
H4AA−0.07610.46300.56010.032*0.9
C5A−0.1282 (5)0.4435 (2)0.6622 (4)0.0308 (11)0.9
H5AA−0.24000.44940.61630.037*0.9
C6A−0.0374 (5)0.4264 (2)0.7679 (4)0.0303 (9)0.9
H6AA−0.08080.41870.80180.036*0.9
S2A0.16500 (7)0.42031 (2)0.83162 (5)0.02979 (12)0.9
C4X0.125 (2)0.4241 (7)0.7841 (18)0.030 (4)*0.1
H4XA0.21940.41200.85060.036*0.1
C5X−0.025 (4)0.424 (2)0.762 (3)0.022 (6)*0.1
H5XA−0.04110.41550.81180.027*0.1
C6X−0.145 (4)0.4397 (16)0.654 (3)0.010 (5)*0.1
H6XA−0.25630.44070.61820.012*0.1
S2X−0.0673 (7)0.45671 (18)0.5915 (4)0.0191 (11)*0.1
C7A0.6656 (2)0.43542 (6)0.81358 (15)0.0229 (3)
H7AA0.69850.45060.77570.028*
H7AB0.72440.44970.88640.028*
C8A0.7067 (3)0.36412 (7)0.90800 (16)0.0296 (4)
H8AA0.59300.35990.87410.035*
H8AB0.76090.38150.97660.035*
C9A0.7893 (3)0.31819 (7)0.93468 (16)0.0351 (4)
H9AA0.90420.32250.97170.042*
H9AB0.78280.30160.98540.042*
C10A0.7223 (2)0.31688 (6)0.75678 (15)0.0267 (4)
H10A0.67140.29940.68870.032*
H10B0.83680.32130.79290.032*
C11A0.6385 (2)0.36268 (6)0.72752 (14)0.0218 (3)
H11A0.64800.37920.67820.026*
H11B0.52300.35840.68870.026*
C12A0.7871 (3)0.24680 (7)0.85974 (18)0.0402 (5)
H12A0.78550.23250.91500.048*
H12B0.90080.25060.89330.048*
C13A0.7034 (3)0.21574 (6)0.75928 (17)0.0330 (4)
C14A0.5388 (3)0.20464 (8)0.6944 (2)0.0407 (5)
H14A0.47740.21690.71170.049*
C15A0.4650 (3)0.17530 (8)0.6036 (2)0.0450 (5)
H15A0.35450.16810.56050.054*
C16A0.5548 (3)0.15663 (7)0.5769 (2)0.0433 (5)
H16A0.50490.13720.51570.052*
C17A0.7186 (3)0.16709 (7)0.6416 (2)0.0433 (5)
H17A0.78000.15430.62480.052*
C18A0.7922 (3)0.19659 (7)0.7316 (2)0.0382 (5)
H18A0.90270.20370.77420.046*
U11U22U33U12U13U23
S1B0.0208 (2)0.0416 (3)0.0332 (2)0.00472 (18)0.01552 (19)0.0035 (2)
O1B0.0221 (6)0.0267 (6)0.0252 (6)−0.0003 (5)0.0160 (5)−0.0005 (5)
N1B0.0194 (6)0.0317 (8)0.0249 (7)−0.0051 (6)0.0159 (6)−0.0065 (6)
N2B0.0185 (6)0.0310 (8)0.0250 (7)−0.0034 (5)0.0152 (6)−0.0047 (6)
N3B0.0204 (7)0.0353 (8)0.0221 (7)−0.0060 (6)0.0137 (6)−0.0054 (6)
N4B0.0224 (7)0.0316 (8)0.0254 (8)−0.0034 (6)0.0094 (6)0.0073 (6)
C1B0.0237 (8)0.0220 (8)0.0295 (8)−0.0013 (6)0.0186 (7)−0.0034 (6)
C2B0.0206 (7)0.0219 (8)0.0246 (8)−0.0025 (6)0.0153 (7)−0.0045 (6)
C3B0.0225 (7)0.0228 (8)0.0261 (8)−0.0037 (6)0.0174 (7)−0.0054 (6)
C4B0.0241 (13)0.0294 (13)0.0281 (15)−0.0001 (10)0.0171 (13)−0.0019 (12)
C5B0.041 (2)0.042 (3)0.046 (2)−0.0133 (15)0.0372 (19)−0.0147 (13)
C6B0.0233 (15)0.056 (2)0.0382 (18)−0.0136 (13)0.0243 (15)−0.0155 (13)
S2B0.0208 (3)0.0468 (4)0.0288 (3)−0.0045 (3)0.0166 (3)−0.0058 (3)
C7B0.0259 (8)0.0342 (9)0.0297 (9)−0.0057 (7)0.0219 (7)−0.0085 (7)
C8B0.0182 (7)0.0303 (9)0.0216 (8)−0.0015 (6)0.0099 (7)−0.0016 (7)
C9B0.0192 (8)0.0359 (10)0.0273 (9)−0.0051 (7)0.0113 (7)0.0011 (7)
C10B0.0272 (9)0.0465 (12)0.0224 (9)−0.0055 (8)0.0072 (8)0.0069 (8)
C11B0.0198 (8)0.0413 (11)0.0220 (8)−0.0054 (7)0.0081 (7)−0.0003 (7)
C12B0.0359 (11)0.0420 (12)0.0372 (11)−0.0041 (9)0.0163 (10)0.0159 (9)
C13B0.0266 (9)0.0269 (9)0.0408 (11)0.0001 (7)0.0150 (9)0.0139 (8)
C14B0.0326 (10)0.0374 (11)0.0535 (14)−0.0034 (9)0.0238 (10)0.0112 (10)
C15B0.0289 (10)0.0337 (11)0.0622 (16)−0.0023 (9)0.0175 (11)0.0104 (11)
C16B0.0430 (13)0.0246 (10)0.0505 (14)0.0019 (9)0.0110 (11)0.0058 (10)
C17B0.0570 (15)0.0327 (12)0.0638 (17)0.0086 (11)0.0363 (14)0.0064 (11)
C18B0.0333 (11)0.0344 (11)0.0604 (15)0.0036 (9)0.0261 (11)0.0099 (10)
S1A0.0307 (2)0.0384 (3)0.0258 (2)0.00467 (19)0.02082 (19)0.00510 (18)
O1A0.0198 (5)0.0271 (6)0.0211 (6)0.0010 (5)0.0130 (5)0.0004 (5)
N1A0.0204 (6)0.0269 (7)0.0221 (7)−0.0001 (5)0.0147 (6)−0.0013 (5)
N2A0.0195 (6)0.0243 (7)0.0216 (6)0.0011 (5)0.0141 (6)−0.0001 (5)
N3A0.0192 (6)0.0242 (7)0.0200 (6)0.0013 (5)0.0120 (6)−0.0014 (5)
N4A0.0396 (9)0.0247 (7)0.0245 (7)0.0114 (6)0.0218 (7)0.0063 (6)
C1A0.0209 (7)0.0202 (7)0.0245 (8)0.0012 (6)0.0148 (7)−0.0002 (6)
C2A0.0217 (7)0.0200 (7)0.0217 (7)−0.0002 (6)0.0146 (6)−0.0020 (6)
C3A0.0194 (7)0.0225 (8)0.0230 (8)−0.0011 (6)0.0135 (6)−0.0024 (6)
C4A0.0231 (10)0.0308 (11)0.0251 (12)−0.0005 (8)0.0154 (10)−0.0001 (10)
C5A0.0218 (14)0.033 (2)0.0358 (17)−0.0034 (13)0.0179 (13)−0.0032 (13)
C6A0.0215 (12)0.0390 (17)0.0345 (14)−0.0028 (10)0.0200 (11)−0.0025 (11)
S2A0.0218 (2)0.0423 (3)0.0259 (3)−0.0006 (2)0.0158 (2)0.0029 (2)
C7A0.0170 (7)0.0260 (8)0.0239 (8)−0.0023 (6)0.0123 (6)−0.0037 (6)
C8A0.0387 (10)0.0305 (9)0.0233 (8)0.0077 (8)0.0218 (8)0.0032 (7)
C9A0.0461 (12)0.0333 (10)0.0218 (8)0.0142 (9)0.0201 (9)0.0061 (7)
C10A0.0304 (9)0.0285 (9)0.0244 (8)0.0067 (7)0.0191 (7)0.0019 (7)
C11A0.0228 (7)0.0235 (8)0.0185 (7)0.0012 (6)0.0130 (6)0.0006 (6)
C12A0.0545 (13)0.0310 (10)0.0327 (10)0.0205 (9)0.0272 (10)0.0101 (8)
C13A0.0525 (12)0.0221 (8)0.0351 (10)0.0144 (8)0.0331 (10)0.0109 (7)
C14A0.0559 (14)0.0341 (11)0.0505 (13)0.0101 (10)0.0427 (12)0.0072 (9)
C15A0.0579 (15)0.0338 (11)0.0504 (14)0.0004 (10)0.0382 (13)0.0051 (10)
C16A0.0722 (17)0.0240 (9)0.0413 (12)0.0055 (10)0.0402 (12)0.0065 (8)
C17A0.0719 (16)0.0300 (10)0.0500 (13)0.0129 (10)0.0493 (13)0.0064 (9)
C18A0.0518 (13)0.0305 (10)0.0456 (12)0.0117 (9)0.0374 (11)0.0063 (9)
S1B—C1B1.6452 (18)S1A—C1A1.6484 (18)
O1B—C2B1.368 (2)O1A—C2A1.372 (2)
O1B—C1B1.377 (2)O1A—C1A1.374 (2)
N1B—C2B1.293 (2)N1A—C2A1.294 (2)
N1B—N2B1.3894 (19)N1A—N2A1.3917 (19)
N2B—C1B1.341 (2)N2A—C1A1.343 (2)
N2B—C7B1.481 (2)N2A—C7A1.478 (2)
N3B—C7B1.425 (2)N3A—C7A1.429 (2)
N3B—C11B1.463 (2)N3A—C8A1.463 (2)
N3B—C8B1.468 (2)N3A—C11A1.466 (2)
N4B—C9B1.459 (2)N4A—C10A1.461 (2)
N4B—C12B1.463 (3)N4A—C9A1.463 (2)
N4B—C10B1.467 (3)N4A—C12A1.464 (2)
C2B—C3B1.439 (2)C2A—C3A1.436 (2)
C3B—C4Y1.267 (17)C3A—C4X1.22 (2)
C3B—C4B1.377 (4)C3A—C4A1.380 (3)
C3B—S2B1.7132 (19)C3A—S2A1.7213 (18)
C3B—S2Y1.726 (4)C3A—S2X1.759 (6)
C4B—C5B1.403 (6)C4A—C5A1.411 (4)
C4B—H4BA0.9300C4A—H4AA0.9300
C5B—C6B1.353 (5)C5A—C6A1.360 (4)
C5B—H5BA0.9300C5A—H5AA0.9300
C6B—S2B1.710 (5)C6A—S2A1.709 (4)
C6B—H6BA0.9300C6A—H6AA0.9300
C4Y—C5Y1.395 (18)C4X—C5X1.413 (19)
C4Y—H4YA0.9300C4X—H4XA0.9300
C5Y—C6Y1.384 (15)C5X—C6X1.383 (17)
C5Y—H5YA0.9300C5X—H5XA0.9300
C6Y—S2Y1.716 (18)C6X—S2X1.712 (19)
C6Y—H6YA0.9300C6X—H6XA0.9300
C7B—H7BA0.9700C7A—H7AA0.9700
C7B—H7BB0.9700C7A—H7AB0.9700
C8B—C9B1.512 (3)C8A—C9A1.515 (3)
C8B—H8BA0.9700C8A—H8AA0.9700
C8B—H8BB0.9700C8A—H8AB0.9700
C9B—H9BA0.9700C9A—H9AA0.9700
C9B—H9BB0.9700C9A—H9AB0.9700
C10B—C11B1.512 (3)C10A—C11A1.513 (2)
C10B—H10C0.9700C10A—H10A0.9700
C10B—H10D0.9700C10A—H10B0.9700
C11B—H11C0.9700C11A—H11A0.9700
C11B—H11D0.9700C11A—H11B0.9700
C12B—C13B1.504 (3)C12A—C13A1.510 (3)
C12B—H12C0.9700C12A—H12A0.9700
C12B—H12D0.9700C12A—H12B0.9700
C13B—C18B1.381 (4)C13A—C14A1.387 (3)
C13B—C14B1.386 (3)C13A—C18A1.391 (3)
C14B—C15B1.378 (4)C14A—C15A1.388 (3)
C14B—H14B0.9300C14A—H14A0.9300
C15B—C16B1.369 (4)C15A—C16A1.384 (3)
C15B—H15B0.9300C15A—H15A0.9300
C16B—C17B1.389 (4)C16A—C17A1.375 (4)
C16B—H16B0.9300C16A—H16A0.9300
C17B—C18B1.388 (4)C17A—C18A1.384 (3)
C17B—H17B0.9300C17A—H17A0.9300
C18B—H18B0.9300C18A—H18A0.9300
C2B—O1B—C1B105.92 (13)C2A—O1A—C1A106.11 (13)
C2B—N1B—N2B103.24 (14)C2A—N1A—N2A103.26 (13)
C1B—N2B—N1B112.16 (14)C1A—N2A—N1A112.15 (13)
C1B—N2B—C7B126.86 (15)C1A—N2A—C7A126.78 (14)
N1B—N2B—C7B120.94 (14)N1A—N2A—C7A120.91 (14)
C7B—N3B—C11B113.95 (15)C7A—N3A—C8A114.47 (14)
C7B—N3B—C8B114.72 (15)C7A—N3A—C11A114.82 (14)
C11B—N3B—C8B111.03 (15)C8A—N3A—C11A110.91 (14)
C9B—N4B—C12B111.82 (16)C10A—N4A—C9A108.92 (16)
C9B—N4B—C10B108.63 (17)C10A—N4A—C12A111.72 (16)
C12B—N4B—C10B110.18 (16)C9A—N4A—C12A109.72 (15)
N2B—C1B—O1B105.16 (14)N2A—C1A—O1A105.17 (14)
N2B—C1B—S1B130.80 (14)N2A—C1A—S1A130.72 (13)
O1B—C1B—S1B124.01 (14)O1A—C1A—S1A124.11 (13)
N1B—C2B—O1B113.52 (14)N1A—C2A—O1A113.30 (14)
N1B—C2B—C3B127.69 (16)N1A—C2A—C3A127.53 (16)
O1B—C2B—C3B118.79 (15)O1A—C2A—C3A119.16 (15)
C4Y—C3B—C2B129.5 (7)C4X—C3A—C2A130.0 (9)
C4B—C3B—C2B129.1 (2)C4A—C3A—C2A128.50 (18)
C4B—C3B—S2B111.59 (17)C4A—C3A—S2A111.88 (15)
C2B—C3B—S2B119.30 (13)C2A—C3A—S2A119.61 (13)
C4Y—C3B—S2Y111.4 (7)C4X—C3A—S2X112.0 (10)
C2B—C3B—S2Y119.13 (17)C2A—C3A—S2X117.7 (2)
C3B—C4B—C5B112.6 (4)C3A—C4A—C5A111.8 (3)
C3B—C4B—H4BA123.7C3A—C4A—H4AA124.1
C5B—C4B—H4BA123.7C5A—C4A—H4AA124.1
C6B—C5B—C4B111.8 (5)C6A—C5A—C4A112.5 (4)
C6B—C5B—H5BA124.1C6A—C5A—H5AA123.7
C4B—C5B—H5BA124.1C4A—C5A—H5AA123.7
C5B—C6B—S2B113.2 (4)C5A—C6A—S2A112.7 (3)
C5B—C6B—H6BA123.4C5A—C6A—H6AA123.6
S2B—C6B—H6BA123.4S2A—C6A—H6AA123.6
C6B—S2B—C3B90.74 (19)C6A—S2A—C3A90.99 (14)
C3B—C4Y—C5Y118.1 (15)C3A—C4X—C5X118.3 (18)
C3B—C4Y—H4YA120.9C3A—C4X—H4XA120.8
C5Y—C4Y—H4YA120.9C5X—C4X—H4XA120.8
C6Y—C5Y—C4Y108.0 (19)C6X—C5X—C4X108 (2)
C6Y—C5Y—H5YA126.0C6X—C5X—H5XA126.1
C4Y—C5Y—H5YA126.0C4X—C5X—H5XA126.1
C5Y—C6Y—S2Y112.5 (17)C5X—C6X—S2X112.6 (19)
C5Y—C6Y—H6YA123.7C5X—C6X—H6XA123.7
S2Y—C6Y—H6YA123.7S2X—C6X—H6XA123.7
C6Y—S2Y—C3B89.7 (8)C6X—S2X—C3A88.9 (10)
N3B—C7B—N2B115.96 (15)N3A—C7A—N2A115.75 (14)
N3B—C7B—H7BA108.3N3A—C7A—H7AA108.3
N2B—C7B—H7BA108.3N2A—C7A—H7AA108.3
N3B—C7B—H7BB108.3N3A—C7A—H7AB108.3
N2B—C7B—H7BB108.3N2A—C7A—H7AB108.3
H7BA—C7B—H7BB107.4H7AA—C7A—H7AB107.4
N3B—C8B—C9B109.59 (15)N3A—C8A—C9A109.39 (15)
N3B—C8B—H8BA109.8N3A—C8A—H8AA109.8
C9B—C8B—H8BA109.8C9A—C8A—H8AA109.8
N3B—C8B—H8BB109.8N3A—C8A—H8AB109.8
C9B—C8B—H8BB109.8C9A—C8A—H8AB109.8
H8BA—C8B—H8BB108.2H8AA—C8A—H8AB108.2
N4B—C9B—C8B110.47 (15)N4A—C9A—C8A110.51 (15)
N4B—C9B—H9BA109.6N4A—C9A—H9AA109.5
C8B—C9B—H9BA109.6C8A—C9A—H9AA109.5
N4B—C9B—H9BB109.6N4A—C9A—H9AB109.5
C8B—C9B—H9BB109.6C8A—C9A—H9AB109.5
H9BA—C9B—H9BB108.1H9AA—C9A—H9AB108.1
N4B—C10B—C11B110.30 (16)N4A—C10A—C11A110.44 (14)
N4B—C10B—H10C109.6N4A—C10A—H10A109.6
C11B—C10B—H10C109.6C11A—C10A—H10A109.6
N4B—C10B—H10D109.6N4A—C10A—H10B109.6
C11B—C10B—H10D109.6C11A—C10A—H10B109.6
H10C—C10B—H10D108.1H10A—C10A—H10B108.1
N3B—C11B—C10B109.84 (16)N3A—C11A—C10A109.39 (14)
N3B—C11B—H11C109.7N3A—C11A—H11A109.8
C10B—C11B—H11C109.7C10A—C11A—H11A109.8
N3B—C11B—H11D109.7N3A—C11A—H11B109.8
C10B—C11B—H11D109.7C10A—C11A—H11B109.8
H11C—C11B—H11D108.2H11A—C11A—H11B108.2
N4B—C12B—C13B112.51 (17)N4A—C12A—C13A113.20 (17)
N4B—C12B—H12C109.1N4A—C12A—H12A108.9
C13B—C12B—H12C109.1C13A—C12A—H12A108.9
N4B—C12B—H12D109.1N4A—C12A—H12B108.9
C13B—C12B—H12D109.1C13A—C12A—H12B108.9
H12C—C12B—H12D107.8H12A—C12A—H12B107.8
C18B—C13B—C14B118.5 (2)C14A—C13A—C18A118.5 (2)
C18B—C13B—C12B120.8 (2)C14A—C13A—C12A121.40 (19)
C14B—C13B—C12B120.7 (2)C18A—C13A—C12A120.1 (2)
C15B—C14B—C13B121.2 (3)C13A—C14A—C15A120.5 (2)
C15B—C14B—H14B119.4C13A—C14A—H14A119.8
C13B—C14B—H14B119.4C15A—C14A—H14A119.8
C16B—C15B—C14B120.1 (2)C16A—C15A—C14A120.4 (3)
C16B—C15B—H15B119.9C16A—C15A—H15A119.8
C14B—C15B—H15B119.9C14A—C15A—H15A119.8
C15B—C16B—C17B119.7 (3)C17A—C16A—C15A119.4 (2)
C15B—C16B—H16B120.1C17A—C16A—H16A120.3
C17B—C16B—H16B120.1C15A—C16A—H16A120.3
C18B—C17B—C16B119.8 (3)C16A—C17A—C18A120.3 (2)
C18B—C17B—H17B120.1C16A—C17A—H17A119.8
C16B—C17B—H17B120.1C18A—C17A—H17A119.8
C13B—C18B—C17B120.6 (2)C17A—C18A—C13A120.9 (2)
C13B—C18B—H18B119.7C17A—C18A—H18A119.5
C17B—C18B—H18B119.7C13A—C18A—H18A119.5
C2B—N1B—N2B—C1B0.15 (19)C2A—N1A—N2A—C1A−0.09 (19)
C2B—N1B—N2B—C7B177.93 (16)C2A—N1A—N2A—C7A−175.66 (15)
N1B—N2B—C1B—O1B−0.04 (19)N1A—N2A—C1A—O1A0.61 (18)
C7B—N2B—C1B—O1B−177.65 (16)C7A—N2A—C1A—O1A175.86 (15)
N1B—N2B—C1B—S1B178.23 (14)N1A—N2A—C1A—S1A−179.50 (13)
C7B—N2B—C1B—S1B0.6 (3)C7A—N2A—C1A—S1A−4.2 (3)
C2B—O1B—C1B—N2B−0.08 (18)C2A—O1A—C1A—N2A−0.86 (17)
C2B—O1B—C1B—S1B−178.50 (13)C2A—O1A—C1A—S1A179.24 (13)
N2B—N1B—C2B—O1B−0.21 (19)N2A—N1A—C2A—O1A−0.50 (18)
N2B—N1B—C2B—C3B179.12 (17)N2A—N1A—C2A—C3A178.47 (16)
C1B—O1B—C2B—N1B0.19 (19)C1A—O1A—C2A—N1A0.88 (19)
C1B—O1B—C2B—C3B−179.20 (15)C1A—O1A—C2A—C3A−178.17 (15)
N1B—C2B—C3B—C4Y−3.6 (11)N1A—C2A—C3A—C4X−12.6 (14)
O1B—C2B—C3B—C4Y175.7 (11)O1A—C2A—C3A—C4X166.3 (14)
N1B—C2B—C3B—C4B175.1 (2)N1A—C2A—C3A—C4A173.0 (2)
O1B—C2B—C3B—C4B−5.6 (3)O1A—C2A—C3A—C4A−8.1 (3)
N1B—C2B—C3B—S2B−6.3 (3)N1A—C2A—C3A—S2A−6.5 (3)
O1B—C2B—C3B—S2B172.95 (12)O1A—C2A—C3A—S2A172.39 (12)
N1B—C2B—C3B—S2Y174.4 (2)N1A—C2A—C3A—S2X173.9 (2)
O1B—C2B—C3B—S2Y−6.3 (3)O1A—C2A—C3A—S2X−7.2 (3)
C4Y—C3B—C4B—C5B−1.6 (10)C4X—C3A—C4A—C5A4.5 (11)
C2B—C3B—C4B—C5B179.5 (5)C2A—C3A—C4A—C5A−179.9 (3)
S2B—C3B—C4B—C5B0.9 (5)S2A—C3A—C4A—C5A−0.4 (4)
S2Y—C3B—C4B—C5B−176.9 (15)S2X—C3A—C4A—C5A175.8 (14)
C3B—C4B—C5B—C6B−1.4 (10)C3A—C4A—C5A—C6A−0.4 (6)
C4B—C5B—C6B—S2B1.3 (10)C4A—C5A—C6A—S2A1.0 (7)
C5B—C6B—S2B—C3B−0.7 (7)C5A—C6A—S2A—C3A−1.0 (5)
C4Y—C3B—S2B—C6B13 (5)C4X—C3A—S2A—C6A−24 (5)
C4B—C3B—S2B—C6B−0.1 (3)C4A—C3A—S2A—C6A0.8 (3)
C2B—C3B—S2B—C6B−178.9 (3)C2A—C3A—S2A—C6A−179.6 (3)
S2Y—C3B—S2B—C6B0.3 (3)S2X—C3A—S2A—C6A−0.1 (3)
C4B—C3B—C4Y—C5Y4 (2)C4A—C3A—C4X—C5X−3 (3)
C2B—C3B—C4Y—C5Y−176.7 (18)C2A—C3A—C4X—C5X−178 (3)
S2B—C3B—C4Y—C5Y−163 (6)S2A—C3A—C4X—C5X154 (7)
S2Y—C3B—C4Y—C5Y5 (2)S2X—C3A—C4X—C5X−5 (4)
C3B—C4Y—C5Y—C6Y−3 (4)C3A—C4X—C5X—C6X6 (6)
C4Y—C5Y—C6Y—S2Y−1 (4)C4X—C5X—C6X—S2X−5 (6)
C5Y—C6Y—S2Y—C3B3 (3)C5X—C6X—S2X—C3A2 (4)
C4Y—C3B—S2Y—C6Y−4.6 (16)C4X—C3A—S2X—C6X1 (2)
C4B—C3B—S2Y—C6Y0.3 (17)C4A—C3A—S2X—C6X−8 (2)
C2B—C3B—S2Y—C6Y177.1 (13)C2A—C3A—S2X—C6X175.9 (17)
S2B—C3B—S2Y—C6Y−2.1 (13)S2A—C3A—S2X—C6X−3.6 (17)
C11B—N3B—C7B—N2B−68.0 (2)C8A—N3A—C7A—N2A−70.88 (19)
C8B—N3B—C7B—N2B61.6 (2)C11A—N3A—C7A—N2A59.11 (19)
C1B—N2B—C7B—N3B−98.4 (2)C1A—N2A—C7A—N3A−98.7 (2)
N1B—N2B—C7B—N3B84.2 (2)N1A—N2A—C7A—N3A76.1 (2)
C7B—N3B—C8B—C9B172.08 (15)C7A—N3A—C8A—C9A−170.33 (16)
C11B—N3B—C8B—C9B−56.94 (19)C11A—N3A—C8A—C9A57.8 (2)
C12B—N4B—C9B—C8B177.67 (18)C10A—N4A—C9A—C8A59.8 (2)
C10B—N4B—C9B—C8B−60.5 (2)C12A—N4A—C9A—C8A−177.65 (19)
N3B—C8B—C9B—N4B59.0 (2)N3A—C8A—C9A—N4A−58.7 (2)
C9B—N4B—C10B—C11B60.3 (2)C9A—N4A—C10A—C11A−59.9 (2)
C12B—N4B—C10B—C11B−176.93 (19)C12A—N4A—C10A—C11A178.73 (17)
C7B—N3B—C11B—C10B−171.68 (16)C7A—N3A—C11A—C10A170.34 (14)
C8B—N3B—C11B—C10B56.9 (2)C8A—N3A—C11A—C10A−57.95 (18)
N4B—C10B—C11B—N3B−58.7 (2)N4A—C10A—C11A—N3A59.00 (19)
C9B—N4B—C12B—C13B−64.3 (3)C10A—N4A—C12A—C13A−64.0 (2)
C10B—N4B—C12B—C13B174.8 (2)C9A—N4A—C12A—C13A175.08 (19)
N4B—C12B—C13B—C18B−66.2 (3)N4A—C12A—C13A—C14A−58.2 (3)
N4B—C12B—C13B—C14B113.6 (2)N4A—C12A—C13A—C18A123.5 (2)
C18B—C13B—C14B—C15B0.0 (3)C18A—C13A—C14A—C15A−0.4 (3)
C12B—C13B—C14B—C15B−179.9 (2)C12A—C13A—C14A—C15A−178.7 (2)
C13B—C14B—C15B—C16B0.3 (4)C13A—C14A—C15A—C16A0.2 (3)
C14B—C15B—C16B—C17B−0.2 (4)C14A—C15A—C16A—C17A0.5 (3)
C15B—C16B—C17B—C18B−0.2 (4)C15A—C16A—C17A—C18A−1.0 (3)
C14B—C13B—C18B—C17B−0.3 (3)C16A—C17A—C18A—C13A0.8 (3)
C12B—C13B—C18B—C17B179.5 (2)C14A—C13A—C18A—C17A−0.1 (3)
C16B—C17B—C18B—C13B0.4 (4)C12A—C13A—C18A—C17A178.27 (19)
  8 in total

1.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

2.  Synthesis, antimicrobial and cytotoxic activities of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles.

Authors:  V Padmavathi; G Sudhakar Reddy; A Padmaja; P Kondaiah
Journal:  Eur J Med Chem       Date:  2008-11-01       Impact factor: 6.514

3.  Synthesis, antimicrobial, and anti-HIV-1 activity of certain 5-(1-adamantyl)-2-substituted thio-1,3,4-oxadiazoles and 5-(1-adamantyl)-3-substituted aminomethyl-1,3,4-oxadiazoline-2-thiones.

Authors:  Ali A El-Emam; Omar A Al-Deeb; Mohamed Al-Omar; Jochen Lehmann
Journal:  Bioorg Med Chem       Date:  2004-10-01       Impact factor: 3.641

4.  3-[(N-Methyl-anilino)meth-yl]-5-(thio-phen-2-yl)-1,3,4-oxadiazole-2(3H)-thione.

Authors:  Ali A El-Emam; Mohamed A Al-Omar; Hazem A Ghabbour; Hoong-Kun Fun; Tze Shyang Chia
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-04-13

5.  Crystal structure refinement with SHELXL.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr C Struct Chem       Date:  2015-01-01       Impact factor: 1.172

6.  Synthesis and antimicrobial activity of new 5-(2-thienyl)-1,2,4-triazoles and 5-(2-thienyl)-1,3,4-oxadiazoles and related derivatives.

Authors:  Mohamed A Al-Omar
Journal:  Molecules       Date:  2010-01-22       Impact factor: 4.411

7.  3-[(4-Phenyl-piperazin-1-yl)meth-yl]-5-(thio-phen-2-yl)-2,3-di-hydro-1,3,4-oxa-diazole-2-thione.

Authors:  Ali A El-Emam; Mohamed A Al-Omar; Abdul-Rahman M Al-Obaid; Seik Weng Ng; Edward R T Tiekink
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-04-10

8.  Structure validation in chemical crystallography.

Authors:  Anthony L Spek
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
  8 in total
  1 in total

1.  Crystal structure of 3-{[4-(2-meth-oxy-phen-yl)piperazin-1-yl]meth-yl}-5-(thio-phen-2-yl)-1,3,4-oxa-diazole-2(3H)-thione.

Authors:  Monirah A Al-Alshaikh; Hatem A Abuelizz; Ali A El-Emam; Mohammed S M Abdelbaky; Santiago Garcia-Granda
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2016-01-30
  1 in total

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