Home Synthesis and crystal structure of 2-(2-oxo-2-(thiophen-2-yl)ethyl)-4H-chromen-4-one, C15H10O3S
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Synthesis and crystal structure of 2-(2-oxo-2-(thiophen-2-yl)ethyl)-4H-chromen-4-one, C15H10O3S

  • Yang Chen , Tao Xiao ORCID logo EMAIL logo , Feng Liu and Xiaolong Yan
Published/Copyright: September 12, 2022
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Zeitschrift für Kristallographie - New Crystal Structures
From the journal Zeitschrift für Kristallographie - New Crystal Structures Volume 237 Issue 6

Abstract

C15H10O3S, monoclinic, P21/c (no. 14), a = 12.391(5) Å, b = 21.034(8) Å, c = 10.777(4) Å, β = 113.589(7)°, V = 2574.1(16) Å3, Z = 8, R gt (F) = 0.0704, wR ref (F 2) = 0.1988, T = 296(2) K.

CCDC no.: 2190717

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: Colorless block
Size: 0.30 × 0.20 × 0.10 mm
Wavelength: Mo Kα radiation (0.71073 Å)
μ: 0.25 mm−1
Diffractometer, scan mode: Bruker APEX-II, φ and ω
θ max, completeness: 27.6°, >99%
N(hkl)measured, N(hkl)unique, R int: 22478, 5933, 0.082
Criterion for I obs, N(hkl)gt: I obs > 2 σ(I obs), 3359
N(param)refined: 343
Programs: Bruker [1], SHELX [2, 3]
Table 2:

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

Atom x y z U iso*/U eq
S1 −0.02165 (9) 0.58715 (6) 0.34984 (12) 0.0787 (4)
O1 0.38585 (18) 0.45925 (10) 0.7059 (2) 0.0451 (5)
O2 0.7018 (2) 0.55179 (12) 0.8538 (3) 0.0627 (7)
O3 0.1955 (2) 0.56075 (17) 0.5979 (3) 0.0834 (10)
C1 0.4113 (3) 0.50569 (15) 0.6340 (3) 0.0428 (7)
C2 0.5125 (3) 0.53832 (16) 0.6811 (3) 0.0456 (8)
H2A 0.5231 0.5709 0.6287 0.055*
C3 0.6054 (3) 0.52437 (15) 0.8108 (3) 0.0445 (8)
C4 0.5795 (3) 0.47294 (14) 0.8868 (3) 0.0388 (7)
C5 0.6593 (3) 0.45248 (17) 1.0130 (3) 0.0512 (8)
H5A 0.7325 0.4721 1.0527 0.061*
C6 0.6314 (4) 0.40386 (18) 1.0794 (4) 0.0615 (10)
H6A 0.6856 0.3905 1.1636 0.074*
C7 0.5221 (4) 0.37463 (18) 1.0210 (4) 0.0619 (10)
H7A 0.5039 0.3416 1.0666 0.074*
C8 0.4408 (3) 0.39345 (16) 0.8975 (4) 0.0508 (8)
H8A 0.3677 0.3736 0.8588 0.061*
C9 0.4702 (3) 0.44313 (14) 0.8312 (3) 0.0383 (7)
C10 0.3155 (3) 0.51322 (18) 0.4964 (3) 0.0520 (9)
H10A 0.2954 0.4716 0.4547 0.062*
H10B 0.3453 0.5385 0.4415 0.062*
C11 0.2042 (3) 0.54443 (17) 0.4945 (4) 0.0513 (8)
C12 0.1096 (3) 0.55526 (16) 0.3611 (3) 0.0481 (8)
C13 0.1066 (3) 0.54333 (17) 0.2350 (4) 0.0556 (9)
H13A 0.1694 0.5262 0.2197 0.067*
C14 −0.0023 (4) 0.5599 (2) 0.1304 (4) 0.0715 (12)
H14A −0.0196 0.5548 0.0387 0.086*
C15 −0.0779 (4) 0.5840 (2) 0.1791 (5) 0.0773 (13)
H15A −0.1535 0.5976 0.1243 0.093*
S2 0.02856 (8) 0.27082 (5) 0.32347 (12) 0.0654 (3)
O4 0.47417 (19) 0.28071 (11) 0.2899 (2) 0.0490 (6)
O5 0.5275 (3) 0.12748 (12) 0.0881 (3) 0.0671 (7)
O6 0.2282 (2) 0.21088 (13) 0.2878 (4) 0.0851 (10)
C16 0.3850 (3) 0.25461 (16) 0.1814 (3) 0.0448 (7)
C17 0.4002 (3) 0.20556 (16) 0.1126 (4) 0.0495 (8)
H17A 0.3360 0.1909 0.0378 0.059*
C18 0.5116 (3) 0.17412 (16) 0.1489 (4) 0.0494 (8)
C19 0.6080 (3) 0.20308 (16) 0.2661 (3) 0.0463 (8)
C20 0.7238 (3) 0.18005 (19) 0.3170 (4) 0.0640 (11)
H20A 0.7423 0.1453 0.2758 0.077*
C21 0.8102 (4) 0.2081 (2) 0.4268 (5) 0.0743 (12)
H21A 0.8865 0.1921 0.4608 0.089*
C22 0.7832 (4) 0.2602 (2) 0.4867 (5) 0.0729 (12)
H22A 0.8425 0.2793 0.5604 0.088*
C23 0.6720 (3) 0.2845 (2) 0.4406 (4) 0.0610 (10)
H23A 0.6548 0.3196 0.4817 0.073*
C24 0.5851 (3) 0.25505 (16) 0.3302 (3) 0.0462 (8)
C25 0.2731 (3) 0.28920 (17) 0.1552 (4) 0.0521 (9)
H25A 0.2221 0.2858 0.0599 0.063*
H25B 0.2904 0.3339 0.1761 0.063*
C26 0.2088 (3) 0.26337 (16) 0.2388 (4) 0.0500 (8)
C27 0.1198 (3) 0.30401 (16) 0.2549 (3) 0.0458 (8)
C28 0.0966 (3) 0.36809 (17) 0.2296 (4) 0.0548 (9)
H28A 0.1376 0.3948 0.1950 0.066*
C29 0.0033 (4) 0.3876 (2) 0.2626 (5) 0.0726 (12)
H29A −0.0256 0.4290 0.2505 0.087*
C30 −0.0404 (3) 0.3405 (2) 0.3138 (4) 0.0690 (11)
H30B −0.1023 0.3461 0.3408 0.083*

Source of material

In a 50 ml flask, a mixture of o-hydroxyacetophenone, carbon disulfide, potassium carbonate and bromoethane were stirred in DMSO at 40 °C. The reaction was monitored by silica gel thin layer chromatography (TLC, 254 nm). After completion of the reaction, the mixture was poured into ice water, stirred for 20 min and the yellow intermediate 2-(ethylthio)-4H-chromen-4-one was obtained by filtration. A solution of this intermediate, 2-acetylthiophene and t–BuOK in DMSO (10 ml) was stirred at room temperature for 2–3 h and then separated by chromatographic column (PE:EA = 5:1) to obtain the title product. A share of 20 mg of the obtained white title compound was dissolved in 2 ml of methanol to obtain colorless crystals after two days by slow evaporation.

Experimental details

Hydrogen atoms were placed in their geometrically idealized positions and constrained to ride on their parent atoms, with constrained isotropic displacement parameters.

Comment

Chromone, has been proved to be related to biological activity [4–7]. Most research on chromone so far mainly focuses on 2-mono, 3-mono and substituted compounds to show different effects on biological activity.

The asymmetric unit contains two crystallographically independent molecules, and one of these molecules is shown in the figure. In the molecule, the benzene ring (C4/C5/C6/C7/C8/C9) and the pyran ring (C1/C2/C3/C4/C9/O1) are approximately in the same plane and their dihedral angle is only 1.3°, while the thiophene ring (C12/C13/C14/C15/S1) and the 4H-chromen-4-one ring (C1/C2/C3/C4/C5/C6/C7/C8/C9/O1) present a dihedral angle of about 68.6°. This structure may increase its likelihood of interactions with bioactive molecules. The bond lengths and angles of the title compound are similar to those given in the references [8–11].

Corresponding author: Tao Xiao, Department of Chemistry and Molecular Engineering, Nanjing Tech University, 30 South Puzhu Road, Nanjing, 211816, China, E-mail:

Funding source: Nanjing Senega Medical Technology Co. Ltd.

Acknowledgments

This work was supported by Nanjing Senega Medical Technology Co. Ltd., also, we appreciate Wang huaqin in Nanjing University and Wu wenyuan in Nanjing Tech University for some data analysis.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by Nanjing Senega Medical Technology Co. Ltd.

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

References

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Received: 2022-07-22
Accepted: 2022-08-26
Published Online: 2022-09-12
Published in Print: 2022-12-16

© 2022 the author(s), published by De Gruyter, Berlin/Boston

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

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https://doi.org/10.1515/ncrs-2022-0371
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Articles in the same Issue

  1. Frontmatter
  2. New Crystal Structures
  3. The crystal structure of 1,5-bis(4-chlorophenyl)-3-(3-methylphenyl)pentane- 1,5-dione, C48H40Cl4O4
  4. Crystal structure of (bis(1,10-phenanthroline-κ 2 N,N′))-(3,5-dinitrosalicylato-κ 2 O,O′)nickel(II), C31H18N6NiO7
  5. Crystal structure of {N,N′-bis(4-fluoro-salicylaldehyde)-3,6-dioxa-1,8-diaminooctane-κ4 O,N,N′,O′}zinc(II), C20H20F2N2O4Zn
  6. [5-Bromo-2-(2-(dimethylamino)ethyliminomethyl)phenolato-κ3 N,N′,O]-isothiocyanato-nickel(II), C12H14BrN3NiOS
  7. Crystal structure of 9-bromo-4-(6-methoxypyridin-2-yl)-5,6-dihydrobenzo[h]quinazolin- 2-amine, C18H15BrN4O
  8. The crystal structure of imidazolium nitrate, C3H5O3N3
  9. Crystal structure of diiodido-bis(6,6′-dimethoxy-2,2′-(ethane-1,2-diylbis(nitrilomethanylylidene)) diphenolato)tricadmium(II), C36H36Cd3I2N4O8
  10. Crystal structure of [diaqua-bis(2-((1H-tetrazol-1-yl)methyl)-5-carboxy-1H-imidazole-4-carboxylato-κ2 N,O) manganese(II)] dihydrate, C14H18MnN12O12
  11. Crystal structure of Diaqua[5,5′-dicarboxy-2,2′-(propane-1,3-diyl)bis(1H-imidazole-4-carboxylato-k4 O,O′,N,N′)]iron(II), C13H14FeN4O10
  12. Crystal structure of poly[dimethanol-κ1O-(µ2-(E)-2-((2-oxidobenzylidene)amino)acetato)-(µ3-(E)-2-((2-oxidobenzylidene)amino)acetato)dicadmium(II)], C20H22Cd2N2O8
  13. Crystal structure of N 2,N 6-bis(2-(((E)-quinolin-8-ylmethylene)amino)phenyl)pyridine-2,6-dicarboxamide, C39H27N7O2
  14. An I 6 2 − anion in the crystal structure of theophyllinium triiodide monohydrate, C7H11I3N4O3
  15. The crystal structure of poly[6,6′-oxybis(4-(pyridin-1-ium-1-yl)-1,3,5,2,4,6-trioxatriborinan-2-olate)], [B6O9](C5H5N)2
  16. The crystal structure of (carbonato κ2 O,O′)(2-oxopyridin-1(2H)-olato-κN)tris(trimethylphosphine)rhodium(III) water solvate, C15H33NO5P3Rh
  17. The crystal structure of dibromido-bis((RS)-2-(4-chlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)hexanenitrile-κ1 N)zinc(II), C30H34Br2Cl2N8Zn
  18. Synthesis and crystal structure of 3-(((7-hydroxy-3-(4-hydroxy-3,5-dinitrophenyl)-4-oxo-4H-chromen-8-yl)methyl)(nitroso)amino)propanoic acid, C19H14N4O11
  19. The crystal structure of 3-((4-chloro-N-(2-methoxyethyl)benzamido)methyl)phenyl methanesulfonate, C18H20ClNO5S
  20. Crystal structure of di([1,1′:3′,1″-terphenyl]-2′-yl)tellane, C36H26Te
  21. The crystal structure of diaqua-bis(pyrazolo[1,5-a]-pyrimidine-3-carboxylato-κ2 N,O)zinc(II), C14H12N6O6Zn
  22. Crystal structure of N′,N‴-((1E,2E)-1,2-diphenylethane-1,2-diylidene)bis(4-methylbenzohydrazide) – water – methanol (1/1/1), C31H32N4O4
  23. Crystal structure of 3-((2,4-dichlorobenzyl)thio)-5-methyl-7-(trifluoromethyl)-[1,2,4]triazolo [4,3-c]pyrimidine, C14H9Cl2F3N4S
  24. Crystal structure of 3,5,6,7-tetramethoxy-3′,4′-methylenedioxy-flavone, C20H18O8
  25. Crystal structure of catena-poly[(5,5′-dimethyl-2,2′-bipyridine-κ 2 N,N′)-(μ 3-hydrogen-1,1′,1″-(1,3,5-triazine-2,4,6-triyl)tris(piperidine-4-carboxylato)- κ 5 O:O,O′:O″,O‴)-cadmium(II)], C33H40CdN8O6
  26. The crystal structure of 3,5-bis(propan-2-yl)-1H-pyrazol-4-amine, C9H17N3
  27. Crystal structure of [(1,4,7,10-tetraoxacyclododecane-κ 4 O,O′,O″, O‴)-tris(nitrato-κ 2 O,O′)gadolinium(III)], C8H16N3O13Gd
  28. The crystal structure of 2,2′-((pyridine-2,6-diylbis(methylene))bis(sulfanediyl))-bis(4,5-dihydro-1H-imidazol-3-ium) bromide, C13H19Br2N5S2
  29. Crystal structure of E-2-chloro-N′-(1-(5-chloro-2-hydroxyphenyl)propylidene)benzohydrazide, C16H14Cl2N2O2
  30. Crystal structure of 3-(adamantan-1-yl)-4-methyl-5-{[(4-nitrophenyl)methyl]sulfanyl}-4H-1,2,4-triazole, C20H24N4O2S
  31. The crystal structure of dimethanol-κ1O-(5,10,15,20-tetrakis(4-nitrophenyl)porphyrin-21,23-diido-κ4 O,O′,O″,O′″)manganese(III) trans-dicyanido-κ1C-bis(acetylacetonato-κ2 O,O′)ruthenium(III), C58H46N10O14RuMn
  32. The crystal structure of nitroxyl-κ N-{hydridotris(3-trifluoromethyl-5-methylpyrazolyl-1-yl-κN 3)borato}nickel(II), C15H13BF9N7NiO
  33. The crystal structure of [(2,2′-bipyridine-κ2 N,N)-bis(6-phenylpyridine-2-carboxylato- κ2 N,O)nickel(II)] monohydrate, C34H26N4O5Ni
  34. The crystal structure of 5-(2-fluoro-3-methoxyphenyl)-1-(2-fluoro-6-(trifluoromethyl)benzyl)-6-methylpyrimidine-2,4(1H,3H)-dione, C20H15F5N2O3
  35. The crystal structure of ethyl 2,3,5-trifluoro-4-(4-oxo-3,4-dihydropyridin-1(2H)-yl)benzoate, C14H12F3NO3
  36. [2,2′-{Ethane-1,2-diylbis[(azanylylidene)methanylylidene]}bis(3-bromo-2-hydroxyphenyl)]iron(III) nitrate, C20H12Br2CuN2O2
  37. The crystal structure of 1-(2-iodophenyl)-4-phenyl-1H-1,2,3-triazole, C14H10IN3
  38. Synthesis and crystal structure of 2-(2-oxo-2-(thiophen-2-yl)ethyl)-4H-chromen-4-one, C15H10O3S
  39. {6,6′-((1E,1′E)-((2,2-dimethylpropane-1,3-diyl)bis(azaneylylidene))bis(methaneylylidene))bis(2-bromo-4-chlorophenolate)-κ4N,N′,O,O′}copper(II), C19H16Br2Cl2CuN2O2
  40. The crystal structure of N′-[bis(2-hydroxyphenyl)methylidene]pyridine-4-carbohydrazide, C19H15N3O3
  41. Crystal structure of 2-chloro-6-formylphenolato-κ2O,O′-(6,6′-(((2,2-dimethylpropane-1,3-diyl)bis(azaneylylidene))bis(methaneylylidene))bis(2-chlorophenolato)κ4 N,N,O,O′)cobalt(III), C26H22Cl3CoN2O4
  42. The crystal structure of tetrakis(6-phenylpyridine-2-carboxylate-κ 2 N,O)-bis(μ2-6-phenylpyridine-2-carboxylate-κ 2 O:O′)-bis(μ2-6-phenylpyridine-2-carboxylate-κ 3N,O:O)tetralead(II) C48H32N4O8Pb2
  43. The crystal structure of 3,7-dihydroxy-9-methoxy-4a-methyl-4aH-benzo[c] chromene-2,6-dione —dichloromethane (1/1), C16H14Cl2O6
  44. The crystal structure of (Z)-6-(((5-chloro-2-hydroxyphenyl)amino)methylene)- 4-nitrocyclohexa, C13H9ClN2O4
  45. Crystal structure of dichlorido-tetra((E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pent-1-en-3-ol-κ1 N)zinc(II), C60H68O4N12Cl10Zn
  46. The crystal structure of 4-(2-bromoethoxy)-2-hydroxybenzaldehyde, C9H9BrO3
  47. The crystal structure of 5-azido-1-methyl-4-nitroimidazole, C4H4O2N6
  48. Crystal structure of dibromido-tetra((E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pent-1-en-3-ol-κ 1 N)zinc(II), C60H68O4N12Br2Cl8Zn
  49. Crystal structure of tetrasodium-bis(μ 2-oxido)-hexafluoro-didioxo-molybdenum(V), Na2(Mo2O4F6)
  50. Crystal structure of (E)-N′-(2-chloro-6-hydroxybenzylidene)-4- hydroxybenzohydrazide-water (1/1), C14H13Cl1N2O4
  51. Crystal structure of (E)-N-(4-morpholinophenyl)-1-(quinolin-2-yl)methanimine, C20H19N3O
  52. The crystal structure of catena-poly[(1,10-phenanthroline-κ2 N,N′)-(μ3-2-hydroxybenzene-1,3-dicarboxylato-κ5 O,O′:O″,O‴:O‴)cadmium(II)], C20H12CdN2O5
  53. The crystal structure of 2,6-di-tert-butyl-4-(4-(methylthio)benzylidene)cyclohexa-2,5-dien-1-one, C22H28OS
  54. La3.65Mg30Sb1.07 as a disordered derivative of Th2Ni17-type structure
  55. Crystal structure of (E)-N-(4-morpholinophenyl)-1-(quinoxalin-2-yl)methanimine, C19H18N4O
  56. The crystal structure of 2,2′-(1,2-phenylenebis(methylene))bis(1,3-dimethylisothiouronium) bromide, C14H24Br2N4S2
  57. Crystal structure of tetraaqua-bis[4-(1H-1,2,4-triazol-1-yl)benzoato-κ1 N]zinc(II), C18H20ZnN6O8
  58. Crystal structure of bis(tricarbonyl)-{(S)-(tert-butoxycarbonyl)(1-methoxy-1-oxo-3-sulfido-k2 S:S′-propan-2-yl)amido-k2N:N′}diiron(I) (Fe—Fe), C15H15Fe2NO10S
  59. Crystal structure of (E)-3-((4-chlorophenyl)thio)-4-hydroxypent-3-en-2-one, C11H11ClO2S
  60. The crystal structure of (E)-3′,6′-bis(diethylamino)-2-((5-(diethylamino)-2-hydroxybenzylidene)amino)spiro[isoindoline-1,9′-xanthen]-3-one, C39H45N5O3
  61. The crystal structure of 2-(4-methoxynaphthalen-1-yl)-4H-chromen-4-one, C20H14O3
  62. The crystal structure of trans-dichlorido-(ethylenediamine-κ 2 N,N′)-bis(triphenylphosphine-κ 1 P)ruthenium(II), C38H38Cl2N2P2Ru
  63. The double polymeric chain of catena-poly[(μ2-6-bromopyridine-3-carboxylato-κ2 O,O′) (6-bromopyridine-3-carboxylato-κ2 O,O′) (μ2-1,2-bis(4-pyridyl)ethylene-κ2 N:N′)cobalt(II)], C24H16CoBr2N4O4
  64. The crystal structure of tert-butyl 2-(4-(12-bromo [2.2]paracyclophanyl)carbamoyl)pyrrolidine-1-carboxylate, C26H31BrN2O3
  65. The crystal structure of (Z)-2-(2,3-dimethoxybenzylidene)naphtho[1,2-b]furan-3(2H)-one, C21H16O4
  66. Crystal structure of 2-hydroxy-1-tosylindolin-3-yl- 2-naphthoate, C26H21N1S1O5
  67. The crystal structure of 1-methyl-N-(1-methyl-1H-imidazole-2-carbonyl)-1H-imidazole-2-carboxamide, C10H11N5O2
  68. The crystal structure of (E)-2-((5-bromo-2-hydroxybenzylidene)amino)-3′,6′-bis(ethylamino)-2′, 7′-dimethylspiro[isoindoline-1,9′-xanthen]-3-one, C33H31BrN4O3
  69. The crystal structure of dimethanol-5,15-diphenylporphyrin-21,23-diido-κ4 N,Nʹ,Nʺ,Nʹʺ-manganese(III) trans-dicyanido-bis(acetylacetonato-κ2O,Oʹ)ruthenium(III), C46H42N6O6RuMn
  70. Crystal structure of 1,4,8,11-tetraazacyclotetradecane-1,8-diium bis(3,5-dicarboxybenzoate), C28H36N4O12
  71. Bifurcated halogen bonds in the crystal structure of 2,2′-bi(1,8-naphthyridine)—1,4-diiodotetrafluorobenzene (1/1), C22H10F4I2N4
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