Literature DB >> 22904878

5-(Adamantan-1-yl)-3-(benzyl-sulfan-yl)-4-methyl-4H-1,2,4-triazole.

Ebtehal S Al-Abdullah, Ali A El-Emam, Hazem A Ghabbour, Suchada Chantrapromma, Hoong-Kun Fun.   

Abstract

In the asymmetric unit of the title adamantyl derivative, C(20)H(25)N(3)S, there are two crystallographic independent mol-ecules with slightly different conformations. In one mol-ecule, the whole benzyl group is disordered over two orientations with the refined site-occupancy ratio of 0.63 (2):0.37 (2). The dihedral angles between the 1,2,4-triazole and phenyl rings are 24.3 (8) (major component) and 25.8 (13)° (minor component) in the disordered mol-ecule, whereas the corresponding angle is 51.53 (16)° in the other mol-ecule. In the crystal, mol-ecules are linked into a chain along the a axis by a weak C-H⋯N inter-action. Weak C-H⋯π inter-actions are also observed.

Entities:  

Year:  2012        PMID: 22904878      PMCID: PMC3414345          DOI: 10.1107/S1600536812030784

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For bond-length data, see: Allen et al. (1987 ▶). For the synthesis and biological activity of adamantyl-1,2-4-triazole derivatives, see: El-Emam & Ibrahim (1991 ▶); El-Emam et al. (2004 ▶); Kadi et al. (2007 ▶, 2010 ▶); Togo et al. (1968 ▶). For related adamantyl-1,2,4-triazole structures, see: Al-Abdullah et al. (2012 ▶); El-Emam et al. (2012 ▶). For a substituted sulfanyl-1,2,4-triazole structure, see: Fun et al. (2011 ▶).

Experimental

Crystal data

C20H25N3S M = 339.49 Triclinic, a = 6.4554 (3) Å b = 14.0258 (6) Å c = 20.2264 (9) Å α = 94.610 (2)° β = 95.568 (3)° γ = 98.317 (3)° V = 1795.23 (14) Å3 Z = 4 Cu Kα radiation μ = 1.63 mm−1 T = 296 K 0.94 × 0.12 × 0.07 mm

Data collection

Bruker SMART APEXII CCD area-detector diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2009 ▶) T min = 0.310, T max = 0.900 22288 measured reflections 6505 independent reflections 4522 reflections with I > 2σ(I) R int = 0.081

Refinement

R[F 2 > 2σ(F 2)] = 0.052 wR(F 2) = 0.143 S = 1.03 6505 reflections 500 parameters 15 restraints H-atom parameters constrained Δρmax = 0.30 e Å−3 Δρmin = −0.26 e Å−3 Data collection: APEX2 (Bruker, 2009 ▶); cell refinement: SAINT (Bruker, 2009 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009 ▶). Crystal structure: contains datablock(s) global, I. DOI: 10.1107/S1600536812030784/is5162sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536812030784/is5162Isup2.hkl Supplementary material file. DOI: 10.1107/S1600536812030784/is5162Isup3.cml Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C20H25N3SZ = 4
Mr = 339.49F(000) = 728
Triclinic, P1Dx = 1.256 Mg m3
Hall symbol: -P 1Melting point = 456–458 K
a = 6.4554 (3) ÅCu Kα radiation, λ = 1.54178 Å
b = 14.0258 (6) ÅCell parameters from 6505 reflections
c = 20.2264 (9) Åθ = 3.7–69.9°
α = 94.610 (2)°µ = 1.63 mm1
β = 95.568 (3)°T = 296 K
γ = 98.317 (3)°Needle, colorless
V = 1795.23 (14) Å30.94 × 0.12 × 0.07 mm
Bruker SMART APEXII CCD area-detector diffractometer6505 independent reflections
Radiation source: fine-focus sealed tube4522 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.081
φ and ω scansθmax = 69.9°, θmin = 3.7°
Absorption correction: multi-scan (SADABS; Bruker, 2009)h = −6→7
Tmin = 0.310, Tmax = 0.900k = −17→16
22288 measured reflectionsl = −24→24
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.052H-atom parameters constrained
wR(F2) = 0.143w = 1/[σ2(Fo2) + (0.0644P)2 + 0.2321P] where P = (Fo2 + 2Fc2)/3
S = 1.03(Δ/σ)max = 0.001
6505 reflectionsΔρmax = 0.30 e Å3
500 parametersΔρmin = −0.26 e Å3
15 restraintsExtinction correction: SHELXTL (Sheldrick, 2008), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methodsExtinction coefficient: 0.0058 (5)
Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds 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 > 2sigma(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.
xyzUiso*/UeqOcc. (<1)
S1A0.13227 (11)0.28428 (5)0.53379 (3)0.0554 (2)
N1A0.1834 (3)0.32730 (13)0.67079 (9)0.0416 (4)
N2A−0.1139 (3)0.35694 (18)0.62025 (10)0.0612 (6)
N3A−0.1062 (3)0.38366 (18)0.68787 (10)0.0584 (6)
C1A0.0606 (4)0.32387 (17)0.61131 (11)0.0464 (5)
C2A0.0710 (3)0.36590 (16)0.71751 (11)0.0416 (5)
C3A0.1320 (3)0.38416 (16)0.79177 (11)0.0409 (5)
C4A0.1193 (5)0.28829 (18)0.82376 (12)0.0578 (6)
H4AA0.21810.24990.80580.069*
H4AB−0.02130.25190.81330.069*
C5A0.1715 (6)0.3083 (2)0.89991 (13)0.0725 (8)
H5AA0.16440.24680.92010.087*
C6A0.0141 (5)0.3672 (3)0.92805 (14)0.0784 (9)
H6AA−0.12730.33150.91800.094*
H6AB0.04510.37900.97620.094*
C7A0.0272 (4)0.4624 (2)0.89753 (13)0.0651 (8)
H7AA−0.07440.50000.91580.078*
C8A−0.0260 (4)0.4434 (2)0.82172 (12)0.0585 (7)
H8AA−0.02050.50450.80220.070*
H8AB−0.16770.40820.81140.070*
C9A0.3527 (4)0.4420 (2)0.81002 (12)0.0556 (6)
H9AA0.36080.50340.79070.067*
H9AB0.45570.40650.79180.067*
C10A0.4030 (4)0.4602 (2)0.88590 (14)0.0639 (7)
H10A0.54550.49650.89660.077*
C11A0.2465 (5)0.5188 (2)0.91453 (14)0.0677 (7)
H11A0.27900.53090.96260.081*
H11B0.25510.58060.89590.081*
C12A0.3925 (5)0.3650 (2)0.91542 (15)0.0770 (9)
H12A0.42890.37610.96340.092*
H12B0.49300.32800.89700.092*
C13A0.266 (3)0.4010 (6)0.5146 (6)0.072 (3)0.63 (2)
H13A0.16270.44370.50640.087*0.63 (2)
H13B0.36350.43010.55280.087*0.63 (2)
C14A0.385 (4)0.391 (3)0.4541 (7)0.055 (4)0.63 (2)
C15A0.311 (3)0.4217 (18)0.3953 (9)0.053 (2)0.63 (2)
H15A0.18370.44590.39250.064*0.63 (2)
C16A0.419 (3)0.4175 (13)0.3401 (5)0.057 (3)0.63 (2)
H16A0.36560.43900.30050.068*0.63 (2)
C17A0.607 (3)0.3810 (15)0.3441 (7)0.068 (4)0.63 (2)
H17A0.68360.37930.30740.081*0.63 (2)
C18A0.680 (2)0.3474 (14)0.4020 (10)0.067 (3)0.63 (2)
H18A0.80120.31890.40400.080*0.63 (2)
C19A0.573 (3)0.3556 (15)0.4580 (7)0.063 (4)0.63 (2)
H19A0.62890.33690.49820.075*0.63 (2)
C13X0.354 (3)0.3819 (13)0.5293 (7)0.058 (3)0.37 (2)
H13E0.31370.44430.54200.070*0.37 (2)
H13F0.47440.37320.55940.070*0.37 (2)
C14X0.407 (7)0.377 (4)0.4585 (13)0.052 (6)0.37 (2)
C15X0.293 (5)0.417 (3)0.4106 (14)0.071 (7)0.37 (2)
H15C0.16980.43990.42020.086*0.37 (2)
C16X0.359 (5)0.423 (3)0.3479 (13)0.073 (7)0.37 (2)
H16C0.28390.45170.31550.088*0.37 (2)
C17X0.540 (5)0.386 (2)0.3339 (11)0.061 (6)0.37 (2)
H17C0.58200.38740.29130.073*0.37 (2)
C18X0.657 (4)0.348 (3)0.3823 (14)0.074 (8)0.37 (2)
H18C0.78380.32840.37380.088*0.37 (2)
C19X0.585 (4)0.340 (2)0.4441 (11)0.053 (5)0.37 (2)
H19C0.65600.30850.47590.063*0.37 (2)
C20A0.3876 (4)0.2937 (2)0.67924 (14)0.0648 (7)
H20A0.40630.25490.63960.097*
H20B0.39280.25560.71660.097*
H20C0.49780.34850.68710.097*
S1B0.81154 (13)1.08284 (6)0.97495 (3)0.0710 (2)
N1B0.8218 (3)1.04770 (14)0.84119 (9)0.0455 (4)
N2B0.5528 (4)1.11795 (19)0.86704 (10)0.0656 (6)
N3B0.5424 (3)1.10162 (18)0.79771 (10)0.0613 (6)
C1B0.7201 (4)1.08489 (19)0.89102 (12)0.0526 (6)
C2B0.7028 (3)1.05931 (17)0.78341 (11)0.0447 (5)
C3B0.7402 (3)1.02536 (16)0.71346 (11)0.0410 (5)
C4B0.7354 (4)0.91500 (17)0.70604 (13)0.0534 (6)
H4BA0.84800.89810.73610.064*
H4BB0.60260.88320.71810.064*
C5B0.7617 (4)0.88001 (18)0.63401 (12)0.0558 (6)
H5BA0.76020.80980.63010.067*
C6B0.5816 (4)0.90431 (19)0.58710 (13)0.0568 (6)
H6BA0.59670.88160.54150.068*
H6BB0.44830.87230.59860.068*
C7B0.5847 (4)1.01282 (19)0.59299 (12)0.0526 (6)
H7BA0.46831.02840.56300.063*
C8B0.5606 (4)1.04849 (19)0.66446 (12)0.0521 (6)
H8BA0.42661.01800.67650.063*
H8BB0.56071.11790.66770.063*
C9B0.9480 (4)1.07541 (19)0.69275 (12)0.0509 (6)
H9BA0.94921.14490.69590.061*
H9BB1.06491.06230.72270.061*
C10B0.9735 (4)1.0386 (2)0.62118 (12)0.0581 (7)
H10B1.10791.07040.60890.070*
C11B0.7932 (5)1.0625 (2)0.57351 (13)0.0609 (7)
H11C0.79501.13200.57610.073*
H11D0.80981.04000.52800.073*
C12B0.9713 (4)0.9301 (2)0.61595 (13)0.0620 (7)
H12C1.08570.91470.64600.074*
H12D0.99120.90720.57080.074*
C13B0.6621 (5)1.1680 (2)1.01339 (13)0.0710 (8)
H13C0.66131.22370.98790.085*
H13D0.51761.13761.01410.085*
C14B0.7628 (5)1.1996 (2)1.08349 (13)0.0596 (7)
C15B0.6541 (6)1.1854 (3)1.13763 (16)0.0800 (9)
H15B0.51551.15401.13150.096*
C16B0.7500 (7)1.2179 (3)1.20200 (16)0.0967 (12)
H16B0.67371.20801.23820.116*
C17B0.9476 (7)1.2627 (3)1.21254 (16)0.0865 (10)
H17B1.00831.28441.25570.104*
C18B1.0613 (6)1.2770 (2)1.15988 (17)0.0795 (9)
H18B1.20011.30801.16700.095*
C19B0.9699 (5)1.2450 (2)1.09574 (15)0.0700 (8)
H19B1.04911.25431.06010.084*
C20B1.0230 (4)1.0113 (2)0.85207 (13)0.0618 (7)
H20D1.12671.06130.87610.093*
H20E1.06850.99260.80980.093*
H20F1.00560.95630.87750.093*
U11U22U33U12U13U23
S1A0.0688 (4)0.0476 (4)0.0462 (3)−0.0050 (3)0.0160 (3)−0.0043 (2)
N1A0.0366 (10)0.0452 (11)0.0438 (10)0.0068 (7)0.0087 (7)0.0024 (8)
N2A0.0521 (13)0.0891 (17)0.0431 (12)0.0203 (11)−0.0010 (9)−0.0001 (10)
N3A0.0450 (12)0.0905 (17)0.0419 (11)0.0249 (10)−0.0005 (8)−0.0002 (10)
C1A0.0489 (14)0.0468 (14)0.0423 (12)0.0023 (10)0.0068 (10)0.0034 (10)
C2A0.0342 (12)0.0474 (13)0.0443 (12)0.0091 (9)0.0078 (9)0.0029 (9)
C3A0.0326 (11)0.0478 (13)0.0428 (12)0.0090 (9)0.0045 (8)0.0011 (9)
C4A0.0772 (18)0.0483 (15)0.0455 (14)0.0044 (12)0.0030 (12)0.0038 (11)
C5A0.112 (3)0.0550 (17)0.0461 (15)0.0053 (16)−0.0020 (15)0.0065 (12)
C6A0.082 (2)0.100 (3)0.0439 (15)−0.0140 (17)0.0146 (13)−0.0037 (15)
C7A0.0567 (16)0.089 (2)0.0497 (15)0.0243 (14)0.0064 (11)−0.0146 (14)
C8A0.0467 (14)0.0789 (19)0.0519 (14)0.0261 (12)0.0029 (10)−0.0086 (12)
C9A0.0371 (13)0.0664 (17)0.0594 (15)−0.0004 (11)0.0043 (10)−0.0016 (12)
C10A0.0424 (15)0.078 (2)0.0634 (16)−0.0011 (12)−0.0078 (11)−0.0091 (14)
C11A0.0755 (19)0.0649 (18)0.0576 (16)0.0122 (14)−0.0035 (13)−0.0149 (13)
C12A0.085 (2)0.091 (2)0.0551 (17)0.0361 (17)−0.0184 (14)−0.0039 (15)
C13A0.113 (8)0.039 (4)0.066 (5)−0.005 (4)0.044 (5)0.002 (3)
C14A0.072 (7)0.041 (11)0.049 (8)−0.003 (4)0.019 (6)−0.006 (5)
C15A0.052 (4)0.051 (4)0.060 (6)0.003 (3)0.023 (4)0.012 (5)
C16A0.062 (9)0.066 (5)0.044 (3)0.011 (6)0.007 (4)0.008 (3)
C17A0.069 (8)0.079 (6)0.060 (8)0.017 (5)0.024 (6)0.007 (5)
C18A0.059 (4)0.057 (5)0.086 (9)0.005 (3)0.012 (5)0.014 (6)
C19A0.090 (7)0.046 (8)0.045 (4)−0.006 (4)−0.004 (4)−0.001 (5)
C13X0.073 (8)0.039 (7)0.058 (6)−0.005 (4)0.018 (5)−0.007 (4)
C14X0.076 (16)0.028 (11)0.049 (10)−0.007 (7)0.005 (7)0.011 (6)
C15X0.065 (9)0.069 (13)0.076 (17)−0.008 (8)0.028 (10)−0.009 (12)
C16X0.066 (14)0.069 (8)0.090 (14)0.021 (9)0.012 (9)0.017 (9)
C17X0.080 (18)0.059 (8)0.048 (6)0.010 (10)0.015 (10)0.022 (5)
C18X0.076 (12)0.079 (10)0.072 (15)0.021 (8)0.022 (12)0.009 (10)
C19X0.069 (9)0.030 (8)0.052 (11)−0.004 (4)0.000 (8)−0.005 (8)
C20A0.0534 (16)0.085 (2)0.0619 (16)0.0331 (14)0.0120 (12)−0.0026 (14)
S1B0.0964 (6)0.0817 (5)0.0435 (4)0.0429 (4)0.0078 (3)0.0052 (3)
N1B0.0460 (11)0.0507 (12)0.0414 (10)0.0135 (8)0.0042 (8)0.0032 (8)
N2B0.0616 (14)0.0924 (18)0.0467 (12)0.0291 (12)0.0085 (10)−0.0038 (11)
N3B0.0516 (13)0.0874 (17)0.0479 (12)0.0280 (11)0.0031 (9)−0.0050 (11)
C1B0.0553 (15)0.0584 (16)0.0462 (13)0.0163 (11)0.0074 (10)0.0012 (11)
C2B0.0399 (12)0.0504 (14)0.0441 (12)0.0103 (9)0.0024 (9)0.0024 (10)
C3B0.0362 (12)0.0432 (13)0.0428 (12)0.0068 (9)0.0022 (8)0.0003 (9)
C4B0.0592 (15)0.0433 (14)0.0568 (14)0.0067 (11)0.0062 (11)0.0028 (11)
C5B0.0675 (16)0.0426 (14)0.0556 (15)0.0101 (11)0.0053 (12)−0.0065 (11)
C6B0.0486 (15)0.0590 (16)0.0555 (15)−0.0034 (11)−0.0008 (11)−0.0094 (12)
C7B0.0501 (14)0.0594 (16)0.0458 (13)0.0122 (11)−0.0066 (10)−0.0027 (11)
C8B0.0475 (14)0.0574 (15)0.0506 (14)0.0158 (11)−0.0035 (10)−0.0039 (11)
C9B0.0431 (13)0.0530 (15)0.0509 (14)−0.0035 (10)0.0006 (10)−0.0043 (11)
C10B0.0463 (14)0.0742 (19)0.0476 (14)−0.0099 (11)0.0088 (10)−0.0023 (12)
C11B0.0711 (18)0.0626 (17)0.0440 (14)−0.0038 (13)0.0035 (12)0.0037 (11)
C12B0.0495 (15)0.080 (2)0.0560 (15)0.0184 (13)0.0066 (11)−0.0137 (13)
C13B0.079 (2)0.086 (2)0.0532 (16)0.0326 (16)0.0101 (13)0.0007 (14)
C14B0.080 (2)0.0537 (16)0.0516 (15)0.0260 (13)0.0173 (13)0.0057 (11)
C15B0.089 (2)0.084 (2)0.0680 (19)0.0085 (17)0.0321 (17)−0.0047 (16)
C16B0.130 (3)0.105 (3)0.0550 (19)0.006 (2)0.038 (2)−0.0045 (18)
C17B0.129 (3)0.073 (2)0.0564 (19)0.021 (2)0.0066 (19)−0.0063 (15)
C18B0.088 (2)0.064 (2)0.083 (2)0.0131 (16)−0.0019 (17)0.0020 (16)
C19B0.085 (2)0.073 (2)0.0595 (17)0.0221 (16)0.0185 (15)0.0159 (14)
C20B0.0616 (17)0.0743 (19)0.0538 (15)0.0314 (13)−0.0012 (11)0.0030 (13)
S1A—C1A1.748 (2)C17X—H17C0.9300
S1A—C13A1.826 (8)C18X—C19X1.384 (14)
S1A—C13X1.845 (15)C18X—H18C0.9300
N1A—C1A1.368 (3)C19X—H19C0.9300
N1A—C2A1.370 (3)C20A—H20A0.9600
N1A—C20A1.462 (3)C20A—H20B0.9600
N2A—C1A1.301 (3)C20A—H20C0.9600
N2A—N3A1.383 (3)S1B—C1B1.746 (2)
N3A—C2A1.305 (3)S1B—C13B1.814 (3)
C2A—C3A1.507 (3)N1B—C1B1.364 (3)
C3A—C9A1.530 (3)N1B—C2B1.369 (3)
C3A—C4A1.534 (3)N1B—C20B1.466 (3)
C3A—C8A1.543 (3)N2B—C1B1.303 (3)
C4A—C5A1.539 (3)N2B—N3B1.396 (3)
C4A—H4AA0.9700N3B—C2B1.310 (3)
C4A—H4AB0.9700C2B—C3B1.509 (3)
C5A—C12A1.520 (5)C3B—C9B1.534 (3)
C5A—C6A1.523 (5)C3B—C4B1.539 (3)
C5A—H5AA0.9800C3B—C8B1.539 (3)
C6A—C7A1.511 (5)C4B—C5B1.533 (3)
C6A—H6AA0.9700C4B—H4BA0.9700
C6A—H6AB0.9700C4B—H4BB0.9700
C7A—C11A1.512 (4)C5B—C12B1.523 (4)
C7A—C8A1.531 (3)C5B—C6B1.523 (4)
C7A—H7AA0.9800C5B—H5BA0.9800
C8A—H8AA0.9700C6B—C7B1.514 (4)
C8A—H8AB0.9700C6B—H6BA0.9700
C9A—C10A1.531 (4)C6B—H6BB0.9700
C9A—H9AA0.9700C7B—C8B1.521 (3)
C9A—H9AB0.9700C7B—C11B1.526 (4)
C10A—C12A1.502 (5)C7B—H7BA0.9800
C10A—C11A1.519 (4)C8B—H8BA0.9700
C10A—H10A0.9800C8B—H8BB0.9700
C11A—H11A0.9700C9B—C10B1.529 (3)
C11A—H11B0.9700C9B—H9BA0.9700
C12A—H12A0.9700C9B—H9BB0.9700
C12A—H12B0.9700C10B—C12B1.516 (4)
C13A—C14A1.516 (8)C10B—C11B1.531 (4)
C13A—H13A0.9700C10B—H10B0.9800
C13A—H13B0.9700C11B—H11C0.9700
C14A—C15A1.362 (10)C11B—H11D0.9700
C14A—C19A1.376 (11)C12B—H12C0.9700
C15A—C16A1.373 (10)C12B—H12D0.9700
C15A—H15A0.9300C13B—C14B1.505 (4)
C16A—C17A1.384 (10)C13B—H13C0.9700
C16A—H16A0.9300C13B—H13D0.9700
C17A—C18A1.365 (11)C14B—C15B1.369 (4)
C17A—H17A0.9300C14B—C19B1.385 (4)
C18A—C19A1.385 (10)C15B—C16B1.397 (5)
C18A—H18A0.9300C15B—H15B0.9300
C19A—H19A0.9300C16B—C17B1.327 (5)
C13X—C14X1.504 (14)C16B—H16B0.9300
C13X—H13E0.9700C17B—C18B1.363 (5)
C13X—H13F0.9700C17B—H17B0.9300
C14X—C15X1.362 (15)C18B—C19B1.383 (4)
C14X—C19X1.374 (14)C18B—H18B0.9300
C15X—C16X1.384 (14)C19B—H19B0.9300
C15X—H15C0.9300C20B—H20D0.9600
C16X—C17X1.385 (14)C20B—H20E0.9600
C16X—H16C0.9300C20B—H20F0.9600
C17X—C18X1.367 (15)
C1A—S1A—C13A97.2 (2)C17X—C18X—C19X119.4 (15)
C1A—S1A—C13X98.2 (4)C17X—C18X—H18C120.3
C1A—N1A—C2A105.04 (18)C19X—C18X—H18C120.3
C1A—N1A—C20A125.09 (19)C14X—C19X—C18X120.1 (15)
C2A—N1A—C20A129.9 (2)C14X—C19X—H19C120.0
C1A—N2A—N3A106.63 (19)C18X—C19X—H19C120.0
C2A—N3A—N2A108.67 (18)N1A—C20A—H20A109.5
N2A—C1A—N1A110.59 (19)N1A—C20A—H20B109.5
N2A—C1A—S1A124.74 (19)H20A—C20A—H20B109.5
N1A—C1A—S1A124.64 (17)N1A—C20A—H20C109.5
N3A—C2A—N1A109.07 (19)H20A—C20A—H20C109.5
N3A—C2A—C3A123.56 (18)H20B—C20A—H20C109.5
N1A—C2A—C3A127.36 (19)C1B—S1B—C13B100.25 (12)
C2A—C3A—C9A112.91 (18)C1B—N1B—C2B104.86 (18)
C2A—C3A—C4A110.55 (19)C1B—N1B—C20B124.2 (2)
C9A—C3A—C4A109.2 (2)C2B—N1B—C20B130.82 (19)
C2A—C3A—C8A108.14 (18)C1B—N2B—N3B106.24 (19)
C9A—C3A—C8A107.7 (2)C2B—N3B—N2B108.07 (19)
C4A—C3A—C8A108.2 (2)N2B—C1B—N1B111.3 (2)
C3A—C4A—C5A109.9 (2)N2B—C1B—S1B127.25 (18)
C3A—C4A—H4AA109.7N1B—C1B—S1B121.46 (18)
C5A—C4A—H4AA109.7N3B—C2B—N1B109.56 (19)
C3A—C4A—H4AB109.7N3B—C2B—C3B124.0 (2)
C5A—C4A—H4AB109.7N1B—C2B—C3B126.43 (19)
H4AA—C4A—H4AB108.2C2B—C3B—C9B113.09 (18)
C12A—C5A—C6A109.5 (2)C2B—C3B—C4B110.45 (19)
C12A—C5A—C4A109.0 (3)C9B—C3B—C4B109.48 (19)
C6A—C5A—C4A109.6 (3)C2B—C3B—C8B108.56 (17)
C12A—C5A—H5AA109.6C9B—C3B—C8B107.48 (19)
C6A—C5A—H5AA109.6C4B—C3B—C8B107.58 (19)
C4A—C5A—H5AA109.6C5B—C4B—C3B110.3 (2)
C7A—C6A—C5A109.5 (2)C5B—C4B—H4BA109.6
C7A—C6A—H6AA109.8C3B—C4B—H4BA109.6
C5A—C6A—H6AA109.8C5B—C4B—H4BB109.6
C7A—C6A—H6AB109.8C3B—C4B—H4BB109.6
C5A—C6A—H6AB109.8H4BA—C4B—H4BB108.1
H6AA—C6A—H6AB108.2C12B—C5B—C6B109.9 (2)
C6A—C7A—C11A109.5 (3)C12B—C5B—C4B109.0 (2)
C6A—C7A—C8A109.6 (2)C6B—C5B—C4B109.5 (2)
C11A—C7A—C8A110.3 (2)C12B—C5B—H5BA109.5
C6A—C7A—H7AA109.1C6B—C5B—H5BA109.5
C11A—C7A—H7AA109.1C4B—C5B—H5BA109.5
C8A—C7A—H7AA109.1C7B—C6B—C5B109.38 (19)
C7A—C8A—C3A110.15 (19)C7B—C6B—H6BA109.8
C7A—C8A—H8AA109.6C5B—C6B—H6BA109.8
C3A—C8A—H8AA109.6C7B—C6B—H6BB109.8
C7A—C8A—H8AB109.6C5B—C6B—H6BB109.8
C3A—C8A—H8AB109.6H6BA—C6B—H6BB108.2
H8AA—C8A—H8AB108.1C6B—C7B—C8B109.8 (2)
C3A—C9A—C10A110.3 (2)C6B—C7B—C11B109.4 (2)
C3A—C9A—H9AA109.6C8B—C7B—C11B109.4 (2)
C10A—C9A—H9AA109.6C6B—C7B—H7BA109.4
C3A—C9A—H9AB109.6C8B—C7B—H7BA109.4
C10A—C9A—H9AB109.6C11B—C7B—H7BA109.4
H9AA—C9A—H9AB108.1C7B—C8B—C3B111.25 (19)
C12A—C10A—C11A110.1 (3)C7B—C8B—H8BA109.4
C12A—C10A—C9A109.4 (2)C3B—C8B—H8BA109.4
C11A—C10A—C9A109.8 (2)C7B—C8B—H8BB109.4
C12A—C10A—H10A109.2C3B—C8B—H8BB109.4
C11A—C10A—H10A109.2H8BA—C8B—H8BB108.0
C9A—C10A—H10A109.2C10B—C9B—C3B110.14 (19)
C7A—C11A—C10A108.8 (2)C10B—C9B—H9BA109.6
C7A—C11A—H11A109.9C3B—C9B—H9BA109.6
C10A—C11A—H11A109.9C10B—C9B—H9BB109.6
C7A—C11A—H11B109.9C3B—C9B—H9BB109.6
C10A—C11A—H11B109.9H9BA—C9B—H9BB108.1
H11A—C11A—H11B108.3C12B—C10B—C9B109.9 (2)
C10A—C12A—C5A109.8 (2)C12B—C10B—C11B109.5 (2)
C10A—C12A—H12A109.7C9B—C10B—C11B109.7 (2)
C5A—C12A—H12A109.7C12B—C10B—H10B109.2
C10A—C12A—H12B109.7C9B—C10B—H10B109.2
C5A—C12A—H12B109.7C11B—C10B—H10B109.2
H12A—C12A—H12B108.2C7B—C11B—C10B108.9 (2)
C14A—C13A—S1A112.2 (15)C7B—C11B—H11C109.9
C14A—C13A—H13A109.2C10B—C11B—H11C109.9
S1A—C13A—H13A109.2C7B—C11B—H11D109.9
C14A—C13A—H13B109.2C10B—C11B—H11D109.9
S1A—C13A—H13B109.2H11C—C11B—H11D108.3
H13A—C13A—H13B107.9C10B—C12B—C5B109.7 (2)
C15A—C14A—C19A119.0 (8)C10B—C12B—H12C109.7
C15A—C14A—C13A119.9 (11)C5B—C12B—H12C109.7
C19A—C14A—C13A121.0 (11)C10B—C12B—H12D109.7
C14A—C15A—C16A121.5 (8)C5B—C12B—H12D109.7
C14A—C15A—H15A119.2H12C—C12B—H12D108.2
C16A—C15A—H15A119.2C14B—C13B—S1B108.66 (19)
C15A—C16A—C17A119.4 (9)C14B—C13B—H13C110.0
C15A—C16A—H16A120.3S1B—C13B—H13C110.0
C17A—C16A—H16A120.3C14B—C13B—H13D110.0
C18A—C17A—C16A119.5 (10)S1B—C13B—H13D110.0
C18A—C17A—H17A120.2H13C—C13B—H13D108.3
C16A—C17A—H17A120.2C15B—C14B—C19B117.2 (3)
C17A—C18A—C19A120.4 (11)C15B—C14B—C13B121.7 (3)
C17A—C18A—H18A119.8C19B—C14B—C13B121.1 (3)
C19A—C18A—H18A119.8C14B—C15B—C16B120.4 (3)
C14A—C19A—C18A120.0 (10)C14B—C15B—H15B119.8
C14A—C19A—H19A120.0C16B—C15B—H15B119.8
C18A—C19A—H19A120.0C17B—C16B—C15B121.4 (3)
C14X—C13X—S1A108 (3)C17B—C16B—H16B119.3
C14X—C13X—H13E110.2C15B—C16B—H16B119.3
S1A—C13X—H13E110.2C16B—C17B—C18B119.8 (3)
C14X—C13X—H13F110.2C16B—C17B—H17B120.1
S1A—C13X—H13F110.2C18B—C17B—H17B120.1
H13E—C13X—H13F108.5C17B—C18B—C19B119.8 (4)
C15X—C14X—C19X120.4 (14)C17B—C18B—H18B120.1
C15X—C14X—C13X120.8 (18)C19B—C18B—H18B120.1
C19X—C14X—C13X118.6 (17)C18B—C19B—C14B121.4 (3)
C14X—C15X—C16X120.1 (17)C18B—C19B—H19B119.3
C14X—C15X—H15C119.9C14B—C19B—H19B119.3
C16X—C15X—H15C119.9N1B—C20B—H20D109.5
C15X—C16X—C17X119.2 (17)N1B—C20B—H20E109.5
C15X—C16X—H16C120.4H20D—C20B—H20E109.5
C17X—C16X—H16C120.4N1B—C20B—H20F109.5
C18X—C17X—C16X120.6 (15)H20D—C20B—H20F109.5
C18X—C17X—H17C119.7H20E—C20B—H20F109.5
C16X—C17X—H17C119.7
C1A—N2A—N3A—C2A−0.1 (3)C13X—C14X—C15X—C16X172 (4)
N3A—N2A—C1A—N1A0.3 (3)C14X—C15X—C16X—C17X2 (7)
N3A—N2A—C1A—S1A−177.74 (18)C15X—C16X—C17X—C18X−3 (6)
C2A—N1A—C1A—N2A−0.4 (3)C16X—C17X—C18X—C19X5 (6)
C20A—N1A—C1A—N2A178.5 (2)C15X—C14X—C19X—C18X5 (8)
C2A—N1A—C1A—S1A177.69 (17)C13X—C14X—C19X—C18X−170 (4)
C20A—N1A—C1A—S1A−3.5 (3)C17X—C18X—C19X—C14X−6 (6)
C13A—S1A—C1A—N2A89.2 (6)C1B—N2B—N3B—C2B0.3 (3)
C13X—S1A—C1A—N2A111.7 (7)N3B—N2B—C1B—N1B0.2 (3)
C13A—S1A—C1A—N1A−88.6 (6)N3B—N2B—C1B—S1B−178.5 (2)
C13X—S1A—C1A—N1A−66.1 (7)C2B—N1B—C1B—N2B−0.5 (3)
N2A—N3A—C2A—N1A−0.1 (3)C20B—N1B—C1B—N2B175.5 (3)
N2A—N3A—C2A—C3A−178.8 (2)C2B—N1B—C1B—S1B178.19 (18)
C1A—N1A—C2A—N3A0.3 (3)C20B—N1B—C1B—S1B−5.8 (4)
C20A—N1A—C2A—N3A−178.5 (3)C13B—S1B—C1B—N2B−16.1 (3)
C1A—N1A—C2A—C3A178.9 (2)C13B—S1B—C1B—N1B165.4 (2)
C20A—N1A—C2A—C3A0.1 (4)N2B—N3B—C2B—N1B−0.6 (3)
N3A—C2A—C3A—C9A−129.8 (2)N2B—N3B—C2B—C3B176.8 (2)
N1A—C2A—C3A—C9A51.8 (3)C1B—N1B—C2B—N3B0.7 (3)
N3A—C2A—C3A—C4A107.6 (3)C20B—N1B—C2B—N3B−174.9 (3)
N1A—C2A—C3A—C4A−70.9 (3)C1B—N1B—C2B—C3B−176.6 (2)
N3A—C2A—C3A—C8A−10.7 (3)C20B—N1B—C2B—C3B7.7 (4)
N1A—C2A—C3A—C8A170.8 (2)N3B—C2B—C3B—C9B118.8 (3)
C2A—C3A—C4A—C5A−177.3 (2)N1B—C2B—C3B—C9B−64.2 (3)
C9A—C3A—C4A—C5A58.0 (3)N3B—C2B—C3B—C4B−118.1 (3)
C8A—C3A—C4A—C5A−59.0 (3)N1B—C2B—C3B—C4B58.9 (3)
C3A—C4A—C5A—C12A−59.6 (3)N3B—C2B—C3B—C8B−0.3 (3)
C3A—C4A—C5A—C6A60.2 (3)N1B—C2B—C3B—C8B176.7 (2)
C12A—C5A—C6A—C7A59.1 (3)C2B—C3B—C4B—C5B177.00 (19)
C4A—C5A—C6A—C7A−60.4 (3)C9B—C3B—C4B—C5B−57.8 (3)
C5A—C6A—C7A—C11A−60.6 (3)C8B—C3B—C4B—C5B58.7 (3)
C5A—C6A—C7A—C8A60.5 (3)C3B—C4B—C5B—C12B59.6 (3)
C6A—C7A—C8A—C3A−60.5 (3)C3B—C4B—C5B—C6B−60.7 (3)
C11A—C7A—C8A—C3A60.2 (3)C12B—C5B—C6B—C7B−59.6 (3)
C2A—C3A—C8A—C7A179.0 (2)C4B—C5B—C6B—C7B60.2 (3)
C9A—C3A—C8A—C7A−58.7 (3)C5B—C6B—C7B—C8B−59.6 (3)
C4A—C3A—C8A—C7A59.2 (3)C5B—C6B—C7B—C11B60.6 (3)
C2A—C3A—C9A—C10A178.6 (2)C6B—C7B—C8B—C3B59.8 (3)
C4A—C3A—C9A—C10A−58.0 (3)C11B—C7B—C8B—C3B−60.3 (3)
C8A—C3A—C9A—C10A59.3 (3)C2B—C3B—C8B—C7B−178.0 (2)
C3A—C9A—C10A—C12A59.8 (3)C9B—C3B—C8B—C7B59.3 (3)
C3A—C9A—C10A—C11A−61.1 (3)C4B—C3B—C8B—C7B−58.5 (3)
C6A—C7A—C11A—C10A60.8 (3)C2B—C3B—C9B—C10B−179.1 (2)
C8A—C7A—C11A—C10A−59.9 (3)C4B—C3B—C9B—C10B57.3 (3)
C12A—C10A—C11A—C7A−60.4 (3)C8B—C3B—C9B—C10B−59.3 (3)
C9A—C10A—C11A—C7A60.1 (3)C3B—C9B—C10B—C12B−59.2 (3)
C11A—C10A—C12A—C5A59.5 (3)C3B—C9B—C10B—C11B61.3 (3)
C9A—C10A—C12A—C5A−61.3 (3)C6B—C7B—C11B—C10B−60.9 (3)
C6A—C5A—C12A—C10A−58.6 (3)C8B—C7B—C11B—C10B59.5 (3)
C4A—C5A—C12A—C10A61.3 (3)C12B—C10B—C11B—C7B60.4 (3)
C1A—S1A—C13A—C14A170.0 (11)C9B—C10B—C11B—C7B−60.3 (3)
C13X—S1A—C13A—C14A75.9 (17)C9B—C10B—C12B—C5B60.9 (3)
S1A—C13A—C14A—C15A107 (3)C11B—C10B—C12B—C5B−59.6 (3)
S1A—C13A—C14A—C19A−75 (3)C6B—C5B—C12B—C10B59.2 (3)
C19A—C14A—C15A—C16A0 (5)C4B—C5B—C12B—C10B−60.9 (3)
C13A—C14A—C15A—C16A178 (2)C1B—S1B—C13B—C14B−163.3 (2)
C14A—C15A—C16A—C17A0 (4)S1B—C13B—C14B—C15B−121.0 (3)
C15A—C16A—C17A—C18A2 (3)S1B—C13B—C14B—C19B59.6 (3)
C16A—C17A—C18A—C19A−4 (3)C19B—C14B—C15B—C16B1.3 (5)
C15A—C14A—C19A—C18A−2 (5)C13B—C14B—C15B—C16B−178.2 (3)
C13A—C14A—C19A—C18A180 (2)C14B—C15B—C16B—C17B−0.2 (6)
C17A—C18A—C19A—C14A5 (4)C15B—C16B—C17B—C18B−0.6 (6)
C1A—S1A—C13X—C14X−165.8 (13)C16B—C17B—C18B—C19B0.3 (5)
C13A—S1A—C13X—C14X−76.9 (18)C17B—C18B—C19B—C14B0.8 (5)
S1A—C13X—C14X—C15X81 (6)C15B—C14B—C19B—C18B−1.5 (4)
S1A—C13X—C14X—C19X−104 (5)C13B—C14B—C19B—C18B177.9 (3)
C19X—C14X—C15X—C16X−3 (9)
D—H···AD—HH···AD···AD—H···A
C20A—H20C···N3Ai0.962.533.311 (3)138
C4A—H4AB···Cg2ii0.972.983.837 (3)148
C5B—H5BA···Cg1iii0.982.973.833 (11)147
C13A—H13B···Cg1iii0.972.683.418 (14)133
C20B—H20F···Cg3iv0.962.923.595 (3)128
C13X—H13E···Cg1iii0.972.653.42 (2)137
Table 1

Hydrogen-bond geometry (Å, °)

Cg1, Cg2 and Cg3 are the centroids of the C14A–C19A, N1B–N3B/C1B–C2B and C14B–C19B rings, respectively.

D—H⋯A D—HH⋯A DA D—H⋯A
C20A—H20C⋯N3A i 0.962.533.311 (3)138
C4A—H4ABCg2ii 0.972.983.837 (3)148
C5B—H5BACg1iii 0.982.973.833 (11)147
C13A—H13BCg1iii 0.972.683.418 (14)133
C20B—H20FCg3iv 0.962.923.595 (3)128
C13X—H13ECg1iii 0.972.653.42 (2)137

Symmetry codes: (i) ; (ii) ; (iii) ; (iv) .

  9 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.  Studies on induced influenza in man. I. Double-blind studies designed to assess prophylactic efficacy of amantadine hydrochloride against a2/Rockville/1/65 strain.

Authors:  Y Togo; R B Hornick; A T Dawkins
Journal:  JAMA       Date:  1968-03-25       Impact factor: 56.272

3.  Synthesis, antimicrobial and anti-inflammatory activities of novel 5-(1-adamantyl)-1,3,4-thiadiazole derivatives.

Authors:  Adnan A Kadi; Ebtehal S Al-Abdullah; Ihsan A Shehata; Elsayed E Habib; Tarek M Ibrahim; Ali A El-Emam
Journal:  Eur J Med Chem       Date:  2010-08-12       Impact factor: 6.514

4.  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

5.  Synthesis and anti-inflammatory and analgesic activity of some 3-(1-adamantyl)-4-substituted-5-mercapto-1,2,4-triazoles.

Authors:  A A el-Emam; T M Ibrahim
Journal:  Arzneimittelforschung       Date:  1991-12

6.  4-(3-Chloro-phen-yl)-3-[(2,6-difluoro-benz-yl)sulfan-yl]-5-(3,4,5-trimeth-oxy-phen-yl)-4H-1,2,4-triazole.

Authors:  Hoong-Kun Fun; Safra Izuani Jama Asik; B Chandrakantha; Arun M Isloor; Prakash Shetty
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-11-25

7.  Ethyl 4-{[3-(adamantan-1-yl)-4-phenyl-5-sulfanyl-idene-4,5-dihydro-1H-1,2,4-triazol-1-yl]meth-yl}piperazine-1-carboxyl-ate.

Authors:  Ebtehal S Al-Abdullah; Hanadi H Asiri; Ali A El-Emam; Seik Weng Ng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-31

8.  2-{[5-(Adamantan-1-yl)-4-methyl-4H-1,2,4-triazol-3-yl]sulfan-yl}-N,N-dimethyl-ethanamine.

Authors:  Ali A El-Emam; Siham Lahsasni; Hanadi H Asiri; Ching Kheng Quah; Hoong-Kun Fun
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-04-13

9.  Structure validation in chemical crystallography.

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

北京卡尤迪生物科技股份有限公司 © 2022-2023.