Home Crystal structure of 1-ferrocenylsulfonyl-1H-imidazo[4,5-b]pyridine, C16H13FeN3O2S
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Crystal structure of 1-ferrocenylsulfonyl-1H-imidazo[4,5-b]pyridine, C16H13FeN3O2S

  • Jing Hu , Lu-Yao Wang EMAIL logo , Xiao-Long Guo and Lu Li
Published/Copyright: March 13, 2017

Abstract

C16H13FeN3O2S, triclinic, P1̅, a = 8.1311(9) Å, b = 11.6852(13) Å, c = 17.044(2) Å, α = 102.754(6)°, β = 92.548(7)°, γ = 105.563(6)°, V = 1512.3(3) Å3, Z = 4, Rgt(F) = 0.0473, wRref(F2) = 0.1307, T = 296(2) K.

CCDC no.:: 1504597

One of two crystallographically independent complexes forming the asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details of the measurement method and a list of the atoms including atomic coordinates and displacement parameters.

Table 1

Data collection and handling.

Crystal:Yellow block
Size:0.40 × 0.30 × 0.20 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:11.5 cm−1
Diffractometer, scan mode:Bruker P4, ω scans
2θmax, completeness:53°, 98.6%
N(hkl)measured, N(hkl)unique, Rint:19703, 6091, 0.041
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 4666
N(param)refined:415
Programs:Bruker programs [1], SHELX [2]
Table 2

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2).

AtomxyzUiso*/Ueq
Fe11.19212(5)0.33355(4)0.31342(3)0.03820(14)
S10.85732(10)0.26505(7)0.41406(5)0.0435(2)
O10.9501(3)0.2775(2)0.48935(14)0.0568(6)
O20.7819(3)0.3565(2)0.40026(17)0.0612(7)
N10.6876(3)0.1392(2)0.40096(17)0.0448(6)
N20.4138(4)0.0219(3)0.3671(2)0.0569(7)
N30.8141(4)−0.0066(3)0.44394(17)0.0517(7)
C10.5207(4)0.1266(3)0.3703(2)0.0539(8)
H10.48910.18890.35340.065*
C20.6836(4)0.0263(3)0.41729(19)0.0433(7)
C30.7673(5)−0.1214(3)0.4535(2)0.0596(9)
H30.8525−0.15130.47230.072*
C40.6012(5)−0.1987(3)0.4372(2)0.0618(10)
H40.5789−0.27700.44590.074*
C50.4688(5)−0.1613(3)0.4086(2)0.0577(9)
H50.3566−0.21210.39760.069*
C60.5118(4)−0.0445(3)0.3970(2)0.0470(7)
C70.9712(4)0.2260(2)0.33508(18)0.0369(6)
C80.9489(4)0.2519(3)0.25767(19)0.0441(7)
H80.86790.29300.24090.053*
C91.0644(4)0.2047(3)0.2095(2)0.0498(8)
H91.08100.21070.15380.060*
C101.1568(4)0.1515(3)0.2568(2)0.0457(7)
H101.24830.11500.23900.055*
C111.1003(4)0.1630(2)0.33398(18)0.0383(6)
H111.14110.13350.37850.046*
C121.4413(5)0.4314(4)0.3124(3)0.0718(12)
H121.52830.39960.28430.086*
C131.4095(4)0.4305(3)0.3904(2)0.0576(9)
H131.46980.39790.42730.069*
C141.2767(5)0.4827(3)0.4085(3)0.0674(11)
H141.22880.49520.46040.081*
C151.2263(6)0.5165(3)0.3390(4)0.0885(17)
H151.13690.55720.33380.106*
C161.3287(8)0.4837(4)0.2791(3)0.0929(18)
H161.32430.49710.22440.112*
Fe20.85776(6)0.73437(4)0.19340(3)0.04590(15)
S20.75741(10)0.68109(7)−0.00391(5)0.04133(19)
O30.9231(3)0.7328(2)−0.02459(15)0.0556(6)
O40.6875(3)0.55166(19)−0.01933(14)0.0509(6)
N40.6176(3)0.7246(2)−0.05864(15)0.0422(6)
N50.3691(4)0.7106(3)−0.1282(2)0.0602(8)
N60.7571(4)0.9421(2)−0.04033(18)0.0521(7)
C170.4572(5)0.6530(3)−0.0947(2)0.0538(9)
H170.41550.5706−0.09490.065*
C180.4746(4)0.8305(3)−0.1124(2)0.0459(7)
C190.6296(4)0.8422(3)−0.06850(18)0.0398(7)
C200.7267(5)1.0416(3)−0.0581(2)0.0588(9)
H200.81091.1160−0.03970.071*
C210.5784(5)1.0408(3)−0.1020(3)0.0601(9)
H210.56671.1134−0.11220.072*
C220.4495(5)0.9348(3)−0.1303(2)0.0573(9)
H220.34970.9327−0.16010.069*
C230.7354(4)0.7501(3)0.09337(18)0.0393(6)
C240.6116(4)0.6974(3)0.14197(19)0.0446(7)
H240.52490.61750.12640.053*
C250.6383(5)0.7847(3)0.2164(2)0.0543(8)
H250.57500.77380.26310.065*
C260.7738(5)0.8874(3)0.2149(2)0.0548(9)
H260.81920.95960.26000.066*
C270.8367(4)0.8691(3)0.1389(2)0.0470(8)
H270.92980.92630.12050.056*
C281.0276(6)0.7610(5)0.2916(3)0.0795(12)
H281.04850.82970.33930.095*
C290.9091(7)0.6555(6)0.2829(4)0.0959(15)
H290.83240.63260.32320.115*
C300.9139(7)0.5808(4)0.2065(4)0.1039(18)
H300.84450.49600.18400.125*
C311.0497(8)0.6550(6)0.1685(3)0.0969(16)
H311.09100.63070.11600.116*
C321.1126(5)0.7639(4)0.2269(3)0.0721(11)
H321.20440.83430.22060.087*

Source of material

All reagents and solvents were purchased form commercial sources and used as received. The title compound is obtained from a reaction of 1H-imidazo[4,5-b]pyridine and ferrocenylsulfonyl chloride. A solution of 1H-imidazo[4,5-b]pyridine (0.32 g, 2.7 mmol) in acetonitrile (18 mL) was added to a mixture of ferrocenylsulfonylchloride (0.72 g, 2.5 mmol) and anhydrous sodium carbonate (0.26 g, 2.5 mmol) with constant stirring. The mixture was heated to reflux temperatures for 48 h. The acetonitrile was evaporated under vacuum to leave a brown solid. The crude product was purified by column chromatography (SiO2, petroleum ether) to give the title compound (0.41 g, 45% yield) in form of yellow crystals, mp: 473–474 K.

Experimental details

The crystal structure was solved by the direct method. Hydrogen atoms were positioned geometrically and allowed to ride on their respective parent atoms. C—H distances were set to 0.93 Å and their Uiso set to 1.2 times the Ueq for the atoms to which they are bonded.

Comment

Some imidazo[4,5-b]pyridines possess diverse pharmacological properties, including anticancer, antiviral, and other important biological activities [3], [4], [5]. The asymmetric unit of the title compound contains two 1-ferrocenylsulfonyl-1H-imidazo[4,5-b]pyridine complexes, which are very similar. There is an imidazo[4,5-b]pyridinyl and a ferrocenyl moiety in the structure. The imidazo[4,5-b]pyridinyl is almost planar in both independent complexes. There are small differences in bond lengths between the substituted and unsubstituted cyclopentadienyl ring [6, 7] . The five-membered rings of the ferrocenyl moieties are almost parallel to each other.

Acknowledgement

This work is financially supported by the Ministry of Education of Beijing’s University Key Teacher (2010).

References

1 Bruker. APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA, (2013).Search in Google Scholar

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3 Rajesh, P. K.; Mohammad, U. S.; Ganesh, R. J.: Eco-friendly and facile synthesis of 2-substituted-1H-imidazo[4,5-b]pyridine in aqueous medium by air oxidation. Tetrahedron Lett. 50 (2009) 1780–1782.10.1016/j.tetlet.2008.12.104Search in Google Scholar

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Received: 2016-9-16
Accepted: 2017-2-21
Published Online: 2017-3-13
Published in Print: 2017-5-24

©2017 Jing Hu et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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