Home Structure of the mixed crystal (S)-(6-(bromo/chloro)-2-methoxy-2,6-dihydroquinolin-3-yl)(phenyl)methanol, C17H14Br0.5Cl0.5NO2
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Structure of the mixed crystal (S)-(6-(bromo/chloro)-2-methoxy-2,6-dihydroquinolin-3-yl)(phenyl)methanol, C17H14Br0.5Cl0.5NO2

  • Yi-Ding Geng ORCID logo EMAIL logo and Yi-Xia Gong ORCID logo EMAIL logo
Published/Copyright: October 28, 2020

Abstract

C17H14Br0.5Cl0.5NO2, monoclinic, P21/n (no. 14), a = 11.7324(5) Å, b = 7.4663(3) Å, c = 17.2211(8) Å, β = 104.890(1)°, V = 1457.87(11) Å3, Z = 4, Rgt(F) = 0.0334, wRref(F2) = 0.0693, T = 296(2) K.

CCDC no.: 2023467

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

Table 1:

Data collection and handling.

Crystal:Colorless block
Size:0.22 × 0.20 × 0.18 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:1.54 mm−1
Diffractometer, scan mode:φ and ω
θmax, completeness:25.4°, >99%
N(hkl)measured, N(hkl)unique, Rint:9234, 2657, 0.025
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 2002
N(param)refined:200
Programs:CrysAlisPRO [1], SHELX [2], [3], Olex2 [4]
Table 2:

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

AtomxyzUiso*/Ueq
Br1a1.41206 (3)1.04035 (6)0.18054 (3)0.07752 (18)
Cl1a1.41206 (3)1.04035 (6)0.18054 (3)0.07752 (18)
O10.84304 (15)0.4759 (2)0.01229 (11)0.0548 (4)
H10.843 (3)0.379 (4)0.0451 (18)0.107 (11)*
N20.88432 (14)1.1003 (2)0.08544 (10)0.0356 (4)
O20.70300 (11)0.96332 (17)0.04293 (9)0.0414 (4)
C11.24940 (18)1.0518 (3)0.15357 (13)0.0493 (6)
C21.19650 (19)1.2169 (3)0.15795 (13)0.0513 (6)
H21.24261.31730.17610.062*
C31.07620 (19)1.2308 (3)0.13540 (13)0.0467 (6)
H31.04081.34140.13790.056*
C41.00544 (17)1.0799 (2)0.10843 (11)0.0340 (4)
C51.06005 (17)0.9130 (3)0.10586 (12)0.0354 (5)
C61.18443 (18)0.9014 (3)0.12836 (13)0.0461 (5)
H61.22160.79230.12600.055*
C70.98660 (17)0.7620 (3)0.07995 (12)0.0377 (5)
H71.02040.65070.07630.045*
C80.86783 (16)0.7786 (2)0.06057 (11)0.0317 (4)
C90.82178 (16)0.9555 (2)0.06403 (11)0.0319 (4)
C100.64854 (19)1.1335 (3)0.04726 (16)0.0568 (7)
H10A0.68241.18720.09870.085*
H10B0.56541.11720.04040.085*
H10C0.66141.21030.00560.085*
C110.78257 (17)0.6236 (2)0.03587 (12)0.0350 (5)
H110.7160 (15)0.651 (2)−0.0170 (10)0.025 (5)*
C120.72397 (16)0.5738 (2)0.10156 (11)0.0321 (4)
C130.60314 (18)0.5884 (3)0.08942 (14)0.0456 (5)
H130.55770.63580.04150.055*
C140.5494 (2)0.5329 (3)0.14807 (17)0.0605 (7)
H140.46810.54310.13920.073*
C150.6149 (2)0.4633 (3)0.21893 (16)0.0603 (7)
H150.57820.42470.25780.072*
C160.7352 (2)0.4507 (3)0.23245 (14)0.0546 (6)
H160.78010.40450.28080.065*
C170.78936 (19)0.5066 (3)0.17443 (12)0.0418 (5)
H170.87100.49900.18440.050*
  1. aOccupancy: 0.5.

Source of material

All chemicals, reagents and solvents are of analytical grade and are commercially available. Preparation of the title compund: 6-bromo-3-(chloro(phenyl)methyl)-2-methoxyquinoline (5 g, 14.63 mmol) was dissolved in acetonitrile (100 mL) at room temperature, followed by addition of H2O (0.30 g, 16.10 mmol), (2S,3R)-2-amino-3-hydroxy-N-((S)-1-(naphthalen-1-yl) ethyl)-N-(4-nitrobenzyl)butanamide (0.56 g, 1.463 mmol), potassium carbonate (5.72 g, 43.89 mmol) and tetrabutylammonium iodide (0.51 g, 1.463 mmol) in order. Then the mixture reacted under stirring at 82 °C for 2 h. Subsequently, the reaction mixture was poured into water and extracted with dichloromethane. The organic phase was dehydrated with anhydrous sodium sulfate and concentrated at reduced pressure to afford a deep yellow liquid. The crude mixture was purified by silica gel column chromatography, eluted with petroleum ether and ethyl acetate (8:1) to give a white solid (3.71 g, yield 78.2%). Crystals were grown in n-hexane and ethyl acetate (3:1) at room temperature.

Experimental details

Hydrogen atoms were placed in their geometrically idealized positions and constrained to ride on their parent atoms.

Discussion

The title compound is an important intermediate for the synthesis of quinoline compounds and can be used in the fields of medicine and organic synthesis [5], [6]. It can participate in the synthesis of alkaloids like Bedaquiline for the preparation of anti-tuberculosis drugs [7]. The structure of the title compound was elucidated by X-ray diffraction and the derived parameters are as expected.


Corresponding authors: Yi-Ding Geng and Yi-Xia Gong, College of pharmacy, Jiamusi University, Jiamusi, 154007, P. R. China, (Y.-D. Geng); and (Y.-X. Gong)

Funding source: Provincial Basic Scientific Research Operating Expenses Project of HeiLongJiang Province

Award Identifier / Grant number: 2018-KYYWF-0951

  1. Author contribution: 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 the Provincial Basic Scientific Research Operating Expenses Project of HeiLongJiang Province (2018-KYYWF-0951).

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

References

1. Oxford Diffraction: CrysAlisPRO; Oxford Diffraction Ltd.: Abingdon, Oxfordshire, England, 2006.Search in Google Scholar

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3. Sheldrick, G. M. Crystal structure refinement with SHELXL. Acta Crystallogr. 2015, C71, 3–8; https://doi.org/10.1107/s2053229614024218.Search in Google Scholar

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. 2009, 42, 339–341; https://doi.org/10.1107/s0021889808042726.Search in Google Scholar

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7. Muscia, G. C., Carnevale, J. P., Luczywo, A., Pelaez, M. V., Toole, A. R., Buldain, G. Y., Casal, J. J., Asis, S. E. Synthesis, anti-tuberculosis activity and QSAR study of 2,4-diarylquinolines and analogous polycyclic derivatives. Arab. J. Chem. 2019, 12, 932–945; https://doi.org/10.1016/j.arabjc.2018.10.003.Search in Google Scholar

Received: 2020-08-18
Accepted: 2020-10-09
Published Online: 2020-10-28
Published in Print: 2021-01-26

© 2020 Yi-Ding Geng and Yi-Xia Gong, published by De Gruyter, Berlin/Boston

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

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