Home Physical Sciences Crystal structure of 3-((3-nitrophenyl)sulfonamido)propanoic acid — 4,4′-bipyridine (1/1), C19H18N4O6S
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Crystal structure of 3-((3-nitrophenyl)sulfonamido)propanoic acid — 4,4′-bipyridine (1/1), C19H18N4O6S

  • Xiao-Miao Chen ORCID logo EMAIL logo , Zheng-Jun Liu , Jing-Song Cheng , Rong-Fei Zhao and Lan Qin
Published/Copyright: May 21, 2020

Abstract

C19H18N4O6S, monoclinic, P21/n (no. 14), a = 8.343(4) Å, b = 7.367(3) Å, c = 31.532(14) Å, β = 97.398(8)°, V = 1921.8(14) Å3, Z = 4, Rgt(F) = 0.0420, wRref(F2) = 0.1158, T = 296.15 K.

CCDC no.: 1509570

The molecular structure is shown in the figure. Table 1 contains crystallographic data and Table 2 contains the list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Yellow block
Size:0.32 × 0.21 × 0.17 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.22 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω
θmax, completeness:25.0°, >99%
N(hkl)measured, N(hkl)unique, Rint:9298, 3372, 0.029
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 2569
N(param)refined:279
Programs:Bruker [1], SHELX [2], [3], Olex2 [4]
Table 2:

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

AtomxyzUiso*/Ueq
S10.77366(6)0.04750(8)0.66439(2)0.04207(19)
O11.1862(2)0.4214(3)0.60436(5)0.0626(5)
O20.9970(2)0.4060(3)0.54952(6)0.0787(6)
O30.63382(18)0.1455(2)0.67080(5)0.0594(5)
O40.75810(18)−0.1214(2)0.64291(5)0.0525(4)
O51.0997(3)−0.4700(3)0.74676(7)0.0811(6)
O61.2458(2)−0.3503(3)0.79975(6)0.0699(5)
N10.8796(2)0.0477(3)0.39833(6)0.0563(5)
N20.3723(2)0.3264(3)0.54736(6)0.0507(5)
N31.1397(2)−0.3428(3)0.76985(6)0.0535(5)
N40.8818(2)0.1731(3)0.63859(5)0.0434(5)
C10.9365(3)0.1019(4)0.43682(8)0.0568(7)
H1A1.0478670.0981110.4445390.068*
C20.8439(3)0.1636(3)0.46652(7)0.0505(6)
H20.8919980.2008240.4933500.061*
C30.6797(2)0.1698(3)0.45631(6)0.0389(5)
C40.6202(3)0.1195(3)0.41567(7)0.0529(6)
H4A0.5096970.1259840.4066760.063*
C50.7221(3)0.0600(4)0.38829(8)0.0625(7)
H50.6777730.0259840.3608690.075*
C60.5732(2)0.2249(3)0.48772(7)0.0392(5)
C70.6236(3)0.2233(3)0.53093(7)0.0478(6)
H70.7285970.1876180.5409710.057*
C80.5221(3)0.2731(3)0.55904(8)0.0525(6)
H80.5601290.2694340.5880750.063*
C90.3216(3)0.3299(3)0.50611(8)0.0502(6)
H90.2165150.3684570.4971900.060*
C100.4160(3)0.2795(3)0.47563(7)0.0472(6)
H100.3740360.2821880.4468490.057*
C111.0373(3)0.4323(3)0.58653(8)0.0489(6)
C120.9215(3)0.4835(3)0.61636(8)0.0544(6)
H12A0.8136580.4874890.6006510.065*
H12B0.9476530.6045830.6271770.065*
C130.9209(3)0.3576(3)0.65322(7)0.0534(6)
H13A1.0263710.3587280.6702470.064*
H13B0.8419800.3985110.6711700.064*
C140.8822(2)0.0093(3)0.71510(6)0.0387(5)
C150.8844(3)0.1381(3)0.74662(7)0.0536(6)
H150.8244760.2441770.7416190.064*
C160.9748(3)0.1101(4)0.78531(8)0.0622(7)
H160.9770050.1982830.8064720.075*
C171.0619(3)−0.0459(4)0.79335(7)0.0538(6)
H171.124269−0.0653020.8196010.065*
C181.0544(2)−0.1722(3)0.76157(7)0.0414(5)
C190.9670(2)−0.1482(3)0.72244(6)0.0397(5)
H190.965133−0.2366980.7013490.048*
H11.259(4)0.382(4)0.5824(11)0.107(11)*
H40.957(3)0.109(3)0.6299(7)0.050(7)*

Source of material

To a 18 mL mixed solution of N,N-dimethylformamide and water (1:1.5) was added Mn(CH3COO)2 ⋅ 4H2O (122.5 mg, 0.5 mmol), 3-((3-nitrophenyl)sulfonamido)propanoic acid (274.3 mg, 1.0 mmol) and 4,4′-bipyridine (156.2 mg, 1.0 mmol). Then the pH of the mixture was adjusted to 7 and added to a 20 mL Teflon-lined reaction vessel. After heating at 80 degrees for 24 h, it was filtrated and naturally evaporated for one week to give slightly yellow block crystals as an unexpected product.

Experimental details

Hydrogen atoms were positioned geometrically. Their Uiso values were set to 1.2Ueq of the parent atoms. The structure was solved with the ShelXT [3] structure solution program using Intrinsic Phasing and refined with the ShelXL [4] refinement package.

Comment

Sulfonamide and its derivatives have attracted wide attention due to their various biological activities, such as antibacterial [5], [6], antiviral [7], [8], antimalarial [9], [10] and anticancer [8], [11]. In addition, N and O atoms in the structure can be used as electron donors for coordination bonds, which may result in different coordination modes [12], [13], which facilitates the construction of metal-organic coordination polymers. In recent years, sulfonamide and its derivatives have been widely used to construct metal-organic coordination polymers [14], [15]. A new crystal structure of a sulfonamide compound was unexpectedly obtained when we were trying to construct metal-organic coordination polymers.

The asymmetric unit of the title complex contains two independent molecules, 3-((3-nitrophenyl)sulfonamido)propanoic acid and 4,4′-bipyridine, respectively. The extended 3D network is formed through π⋯π stacking interactions between 4,4′-bipyridine molecules (centroid-centroid separations: 3.535 Å) and hydrogen bonds (O1⋯N2#1: 2.617(3) Å, O1-H1⋯N2#1 angle 178.3°; N4⋯N1#2: 2.926(3) Å, N4-H4⋯N1#2 angle 173.2°; symmetry code: #1 = 1 + x, +y, +z; #2 = 2 − x, −y, 1 − z) through carboxylic oxygen atoms, amino nitrogen atoms and pyridine nitrogen atoms. All bond lengths and angles are within the expectations.

Acknowledgements

This work was financially supported by the Youth Growth S&T Personnel Foundation of Guizhou Education Department (KY[2018]329).

References

1. Bruker. SAINT, APEX2 and SADABS. Bruker AXS Inc., Madison, WI, USA (2009).Search in Google Scholar

2. Sheldrick, G. M.: SHELXT-integrated space-group and crystal-structure determination. Acta Crystallogr. A71 (2015) 3–8.10.1107/S2053273314026370Search in Google Scholar PubMed PubMed Central

3. Sheldrick, G. M.: Crystal structure refinement with SHELXL. Acta Crystallogr. C71 (2015) 3–8.10.1107/S2053229614024218Search in Google Scholar PubMed PubMed Central

4. Dolomanov, O. V.; Bourhis, L. J.; Gildea, R. J.; Howard, J. A. K.; Puschmann, H.: OLEX2: a complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 42 (2009) 339–341.10.1107/S0021889808042726Search in Google Scholar

5. Si, Y.; Basak, S.; Li, Y.; Merino, J.; Iuliano, J. N.; Walker, S. G.; Tonge, P. J.: Antibacterial activity and mode of action of a sulfonamide-based class of oxaborole leucyl-tRNA-synthetase inhibitors. ACS Infect. Dis. 5 (2019) 1231–1238.10.1021/acsinfecdis.9b00071Search in Google Scholar PubMed PubMed Central

6. Naaz, F.; Srivastava, R.; Singh, A.; Verma, R.; Singh, V. K.; Singh, R. K.: Molecular modeling, synthesis, antibacterial and cytotoxicity evaluation of sulfonamide derivatives of benzimidazole, indazole, benzothiazole and thiazole. Bioorg. Med. Chem. 26 (2018) 3414–3428.10.1016/j.bmc.2018.05.015Search in Google Scholar PubMed

7. He, F. C.; Shi, J.; Wang, Y. J.; Wang, S.; Chen, J.; Gan, X.; Song, B.; Hu, D.: Synthesis, antiviral activity, and mechanisms of purine nucleoside derivatives containing a sulfonamide moiety. J. Agric. Food Chem. 67 (2019) 8459–8467.10.1021/acs.jafc.9b02681Search in Google Scholar PubMed

8. Andrea, S.; Takashi, O.; Antonio, M. A. C. T.: Anticancer and antiviral sulfonamides. Curr. Med. Chem. 10 (2003) 925–953.10.2174/0929867033457647Search in Google Scholar PubMed

9. Andrews, K. T.; Fisher, G. M.; Sumanadasa, S. D. M.; Skinner-Adams, T.; Moeker, J.; Lopez, M.; Poulsen, S.-A.: Antimalarial activity of compounds comprising a primary benzene sulfonamide fragment. Bioorg. Med. Chem. Lett. 23 (2013) 6114–6117.10.1016/j.bmcl.2013.09.015Search in Google Scholar PubMed

10. Kumar Parai, M.; Panda, G.; Srivastava, K.; Kumar Puri, S.: Design, synthesis and antimalarial activity of benzene and isoquinoline sulfonamide derivatives. Bioorg. Med. Chem. Lett. 18 (2008) 776–781.10.1016/j.bmcl.2007.11.038Search in Google Scholar PubMed

11. Ghorab, M. M.; Ragab, F. A.; Heiba, H. I.; El-Gazzar, M. G.; Zahran, S. S.: Synthesis, anticancer and radiosensitizing evaluation of some novel sulfonamide derivatives. Eur. J. Med. Chem. 92 (2015) 682–692.10.1016/j.ejmech.2015.01.036Search in Google Scholar PubMed

12. Cheng, M. Q.; Chen, X. M.; Liu, Z. J.; Li, Y. J.: Crystal structure of ((4-acetamidophenyl)sulfonyl)(carboxylatomethyl) amide-κ2N,O)bis(1,10-phenantroline-κ2N,N′)nickel(II) heptahydrate, [Ni(abgly)(phen)2]⋅7H2O, C34H40N6NiO12S. Z. Kristallogr. NCS 228 (2013) 491–493.10.1515/ncrs.2013.0228Search in Google Scholar

13. Cheng, M. Q.; Chen, X. M.; Liu, Z. J.; Feng, C. Q.: Syntheses, structures, and thermal properties of two new Mn(II) and Ni(II) complexes of 3-nitrobenzenesulfonyl- glycine acid and 4-chlorobenzenesulfonyl-glycine acid ligands. Synth. React. Inorg. Met.-Org. Nano-Met. Chem. 44 (2013) 27–32.10.1080/15533174.2013.763278Search in Google Scholar

14. Liu, Z. J.; Chen, X. M.; Cheng, J. S.; Deng, T. L.; Qin, L.: Crystal structure of poly[(μ2-(carboxylatomethyl)((3-nitrophenyl)sulfonyl)amido-κ3N:O: O′)(μ2-4,4′-bipyridine-κ2N:N′) nickel(II)], C18H14NiN4O6S. Z. Kristallogr. NCS 234 (2019) 549–550.10.1515/ncrs-2018-0551Search in Google Scholar

15. Chen, X. M.; Liu, Z. J.; Deng, T. L.: Crystal structure of poly-{diaqua-bis[(μ2-3-nitrobenzenesulfonylglycine-κ3N:O:O′)(4,4′-bipyridine)manganese(II)]}-dimethylformamide (1/1), C39H35Mn2N9O15S2. Z. Kristallogr. NCS 233 (2018) 893–895.10.1515/ncrs-2018-0082Search in Google Scholar

Received: 2020-04-19
Accepted: 2020-05-11
Published Online: 2020-05-21
Published in Print: 2020-08-26

©2020 Xiao-Miao Chen et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

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  64. Crystal structure of poly[diaqua-bis(μ2-4-(3-(pyridin-3-yl)-1H-1,2,4-triazol-5-yl)benzoato-κ2N:O)nickel(II)], C28H22O6N8Ni
  65. Crystal structure of 4,4′-bis(pyridin-1-ium-4-yl)biphenyl poly[bis(μ2-4,4′-bis(pyrid-4-yl)biphenyl-K2N:N′)-tetrakis(μ4-4′-methyl-[1,1′-biphenyl]-3,5-dicarboxylato-K4O,O′:O′′:O′′′)-bis[[μ2-1,1′-biphenyl]-3-carboxyl-5-carboxylato-K2O:O′]tetracobalt(II)]— [1,1′-biphenyl]-3,5-dicarboxylic acid (1/2), C93H68N3O16Co2
  66. The crystal structure of 4a-formyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydro-1-2-6a,6b,9,9,12a-heptamethylpicen-10-yl acetate, C32H50O3
  67. Crystal structure of 3,3′-(1,2-phenylenebis(methylene))bis(1-methyl-1H-imidazol-3-ium) bis(hexafluoridophosphate), C16H20F12N4P2
  68. Crystal structure of catena-poly[diaqua-(μ2-tartrato-κ4O,O′:O′′,O′′′)zinc(II)], C4H8O8Zn
  69. The crystal structure of (6aR,6bS,8aS,8bR,9S,11aS,12aS,12bS)-10-(4-acetoxy-3-methylbutyl)-6a,8a,9-trimethyl-3,4,5,6,6a,6b,7,8,8a,8b,9,10,11a,12,12a,12b-hexadecahydro-1H-naphtho[2′,1′:4,5]indeno[2,1-b]furan-4-yl acetate, C31H48O5
  70. Crystal structure of 4,4′-(oxybis(methylene))bis(bromobenzene), C14H12Br2O
  71. Crystal structure of (N,N-dimethylsulphoxide)-[N-(3-ethoxy-2-(oxide)benzylidene)-3-methoxybenzenecarbohydrazonato-κ3N,O,O′]-dioxo-molybdenum(VI), C19H22MoN2O7S
  72. Crystal structure of dichlorido-bis(dimethyl sulphoxide-κO)-bis(4-methylbenzyl-κC1)tin(IV), C20H30Cl2O2S2Sn
  73. Crystal structure of (E)-2-amino-N′-(2-hydroxy-4-(2-(piperidin-1-yl)ethoxy)benzylidene)benzohydrazide monohydrate, C21H26N4O3 ⋅ H2O
  74. Crystal structure of chloridotris(4-chlorophenyl)(dimethyl sulfoxide-κO)tin(IV), C20H18Cl4OSSn
  75. Crystal structure of catena{di-aqua-sodium-[N-(hydroxyethyl), N-isopropyl-dithiocarbamato]}n, [C6H16NNaO2S2]n
  76. Crystal structure of 2,2,4,4,6,6-hexakis(4-chlorophenyl)-1,3,5,2,4,6-trithiatristanninane, C36H24Cl6S3Sn3
  77. Crystal structure of 6-methoxy-3-(5-(3-methoxyphenyl)-1,3,4-oxadiazol-2-yl)-4H-chromen-4-one-methanol (1/1), C20H18N2O6
  78. Crystal structure of hexanedihydrazide, C6H14N4O2
  79. Crystal structure of tert-butyl 2-(hydroxymethyl)-5-{4-[(methoxycarbonyl)amino]phenyl}-2,5-dihydro-1H-pyrrole-1-carboxylate, C18H24N2O5
  80. Crystal structure of [(Z)-O-isopropyl N-(4-nitrophenyl)thiocarbamato-κS]-(triphenylphosphine-κP)-gold(I), C28H26AuN2O3PS
  81. Crystal structure of [O-ethyl N-(4-nitrophenyl)thiocarbamato-κS](tri-4-tolylphosphine-κP)gold(I) tetrahydrofuran solvate, C30H30AuN2O3PS, C4H8O
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