Home Crystal structure of methyl 2,7,7-trimethyl-4-(3-methylthiophen-2-yl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate, C19H23NO3S
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Crystal structure of methyl 2,7,7-trimethyl-4-(3-methylthiophen-2-yl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate, C19H23NO3S

  • Xiao-Qing Lu , Huan-Hu Zhang , Rui Yang , Si-Yuan Zhu and Fu-Sheng Wang EMAIL logo
Published/Copyright: January 29, 2019

Abstract

C19H23NO3S, monoclinic, P21/n (no. 14), a = 9.0403(15) Å, b = 18.213(3) Å, c = 11.1889(19) Å, β = 107.964(2)°, V = 1752.4(5) Å3, Z = 4, Rgt(F) = 0.0498, wRref(F2) = 0.1536, T = 296(2) K.

CCDC no.: 1880950

The crystal structure is shown in the figure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Yellow block
Size:0.26 × 0.21 × 0.18 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.20 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω-scans
θmax, completeness:27.5°, >99%
N(hkl)measured, N(hkl)unique, Rint:10596, 3991, 0.033
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3051
N(param)refined:218
Programs:Bruker programs [1], SHELX [2], OLEX2 [3]
Table 2:

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

AtomxyzUiso*/Ueq
N10.32341(19)0.30614(8)1.07671(14)0.0338(4)
H10.3882210.3151301.1495400.041*
S10.28177(6)0.17542(3)0.64855(5)0.0460(2)
O10.2427(2)0.45008(8)0.77028(14)0.0470(4)
O20.1718(2)0.35403(9)0.64426(14)0.0539(4)
O3−0.02911(17)0.13850(8)0.82432(13)0.0432(4)
C10.2210(3)0.49559(12)0.6610(2)0.0551(6)
H1A0.2428720.5457710.6866370.083*
H1B0.2900880.4798380.6159680.083*
H1C0.1153830.4915170.6076400.083*
C20.2162(2)0.37880(10)0.74868(18)0.0328(4)
C30.2425(2)0.33292(9)0.86082(17)0.0294(4)
C40.3149(2)0.35428(10)0.97952(17)0.0313(4)
C50.3927(3)0.42595(11)1.02341(19)0.0418(5)
H5A0.4343740.4256731.1133920.063*
H5B0.4753560.4333070.9876480.063*
H5C0.3182760.4649930.9974430.063*
C60.2330(2)0.24497(10)1.06150(17)0.0309(4)
C70.1565(2)0.22066(9)0.94458(16)0.0296(4)
C80.1911(2)0.25359(9)0.83230(16)0.0288(4)
H80.0952890.2530680.7609760.035*
C90.0476(2)0.16142(10)0.92871(17)0.0321(4)
C100.0236(2)0.12802(12)1.04415(18)0.0408(5)
H10A−0.0070650.0771361.0264630.049*
H10B−0.0615100.1533681.0621050.049*
C110.1658(2)0.13083(11)1.16093(17)0.0351(4)
C120.2935(3)0.08097(13)1.1446(2)0.0522(6)
H12A0.3214650.0963361.0723990.078*
H12B0.3828730.0839121.2180630.078*
H12C0.2565460.0312501.1331430.078*
C130.1213(3)0.10645(15)1.2756(2)0.0550(6)
H13A0.0408210.1378751.2858940.083*
H13B0.0843650.0567251.2641530.083*
H13C0.2106910.1093871.3490730.083*
C140.2210(2)0.21038(11)1.17921(17)0.0369(4)
H14A0.1491860.2386821.2097580.044*
H14B0.3220450.2121401.2428170.044*
C150.3126(2)0.20888(10)0.79773(16)0.0315(4)
C160.4540(2)0.18702(12)0.8728(2)0.0419(5)
H160.4933440.1998260.9571140.050*
C170.5355(3)0.14309(12)0.8109(2)0.0467(5)
H170.6341550.1243620.8504170.056*
C180.4577(3)0.13066(12)0.6894(2)0.0439(5)
C190.5052(3)0.08490(16)0.5967(3)0.0699(8)
H19A0.4253400.0865160.5169550.105*
H19B0.6004450.1036710.5877630.105*
H19C0.5204310.0350680.6259510.105*

Source of material

A mixture of 5,5-dimethyl-cyclohexane-1,3-dione (10 mmol), 3-methylthiophene-2-carboxaldehyde (10 mmol), 3-amino-2-butenoic acid methyl ester (10 mmol) in ethanol (100 mL) was refluxed for 2–3 h and then cooled to room temperature. After filtering of the precipitates, they were sequentially washed with ice-cooled water and ethanol and then dried under a vacuum.

Experimental details

H atoms bonded to C and N atoms were positioned geometrically and refined using a riding model, with C—H = 0.93/0.96/0.97 Å and N—H = 0.86 Å with Uiso(H) = 1.2 times Ueq(C) and 1.2 times Ueq(N).

Discussion

4-Arylpolyhydroquinoline derivatives possess several types of pharmacological properties such as anticancer, anti-HIV, anticoagulant, spasmolytic, and antibacterial activity [4]. Recent research has also indicated that these heterocycles are an effective treatment to shrink cancer and control symptoms [5].

In the crystal structure of the title compound (cf. the figure), the six-membered ring containing nitrogen atom and the adjacent ring form the core of this compound. The angle between the five membered ring constructed by C15—C18 and S1 and the adjacent ring built by C3, C4, C6—C8 and N1 is 84.8°. Similar structures have also been reported. The bond lengths of this compound are in agreement with those in previously reported structure compound [6], [7]. There are also some structures that are directly related [8], [9].

References

1. Bruker: APEX3, SAINT-Plus, XPREP. Bruker AXS Inc., Madison, WI, USA (2016).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. 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

4. Laia, G. H.; Huang, Y. L.; Zhang, B. Y.: Synthesis of N-methylpiperidin-4-one derivatives and evaluation of their anti-endometrial cancer activity. Russ. J. Gener. Chem. 87 (2017) 1053–1056.10.1134/S1070363217050267Search in Google Scholar

5. Liang, L.; Wang, F.; Shi, J.; Hu, Q.; Zhang, L.; Ni, H.: One-Pot synthesis of 4-arylpolyhydroquinoline derivatives and evaluation of their anti-gastric cancer activity. Lat. Am. J. Pharm. 37 (2018) 80–84.Search in Google Scholar

6. Ozturk Yildirim, S.; Butcher, R. J.; Gunduz, M. G.; El-Khouly, A.; Simsek, R.; Safak, C.: Ethyl 2,7,7-trimethyl-4-(1-methyl-1H-indol-3-yl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate. Acta Crystallogr. E69 (2013) o40–o41.10.1107/S1600536812047976Search in Google Scholar PubMed PubMed Central

7. Scott, A.; Steiger, C. L.; Campana, C. F.; Natale, N. R.: Lanthanide and asymmetric catalyzed syntheses of sterically hindered 4-isoxazolyl-1,4-dihydropyridines and 4-isoxazolyl-quinolones. Tetrahed. Lett. 57 (2016) 423–425.10.1016/j.tetlet.2015.12.038Search in Google Scholar PubMed PubMed Central

8. Linden, A.; Safak, C.; Aydin, F.: Methyl 4-(2-chloro-5-nitrophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate. Acta Crystallogr. C60 (2004) o711–o713.10.1107/S0108270104019468Search in Google Scholar PubMed

9. Steiger, S. A.; Li, C.; Natale, N. R.: Crystal structure of ethyl 4-[4-(dimethylamino)phenyl]-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate. Acta Crystallogr. E74 (2018) 1417–1420.10.1107/S2056989018011982Search in Google Scholar PubMed PubMed Central

Received: 2018-07-20
Accepted: 2018-11-23
Published Online: 2019-01-29
Published in Print: 2019-03-26

©2019 Xiao-Qing Lu et al., published by De Gruyter, Berlin/Boston

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

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  68. The crystal structure of 2-(4-chloro-2,6-dinitrophenyl)-1-(4-chloro)diazene oxide, C12H6Cl2N4O5
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  72. Crystal structure of N-methylanilinium 5,7-dihydroxy-4-oxo-2-phenyl-4H-chromene-8-sulfonate monohydrate, C22H21NO8S
  73. Crystal structure of methyl 4-acetoxybenzoate, C10H10O4
  74. Crystal structure of catena-poly[(bis(μ-1,1′-[(5-methoxy-2,4,6-trimethyl-1,3-phenylene)bis(methylene)]bis(1H-1,2,4-triazole)-κ2N:N′)-bis(isothiocyanato-κN)manganese(II)], C34H40MnN14O2S2
  75. Crystal structure of N-(2-methylphenyl)(propan-2-yloxy)carbothioamide, C11H15NOS
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