Home Crystal structure of 2-amino-4-(4-bromophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile, C16H13BrN2O2
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Crystal structure of 2-amino-4-(4-bromophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile, C16H13BrN2O2

  • Yuanyuan Yu EMAIL logo
Published/Copyright: July 27, 2017

Abstract

C16H13BrN2O2, monoclinic, C2/c (no. 15), a = 13.9109(14) Å, b = 11.1819(6) Å, c = 19.533(3) Å, β = 109.162(14)°, V = 2870.0(5) Å3, Z = 8, Rgt(F) = 0.0413, wRref(F2) = 0.0957, T = 293(2) K.

CCDC no.: 1561268

The crystal structure is shown in the figure. Table 1 contains details on crystal structure and measurement conditions. Table 2 lists the atoms with their coordinates and displacement parameters.

Table 1

Data collection and handling.

Crystal:Colourless block
Size:0.20 × 0.18 × 0.17 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:29 cm−1
Diffractometer, scan mode:Xcalibur, φ and ω
2θmax, completeness:50°, >99%
N(hkl)measured, N(hkl)unique, Rint:5247, 2537, 0.031
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 1802
N(param)refined:190
Programs:CrysAlis programs [1], CrysAlisPro [2], SHELX [3]
Table 2

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

AtomxyzUiso*/Ueq
C10.2808(3)1.1609(3)0.42823(18)0.0261(8)
C20.2678(2)1.0452(3)0.44229(18)0.0252(8)
C30.1642(2)0.9879(3)0.42818(18)0.0240(8)
H3A0.16140.95630.47430.029*
C40.0838(2)1.0817(3)0.40268(18)0.0237(8)
C50.1029(3)1.1944(3)0.38832(18)0.0266(8)
C60.0270(3)1.2903(3)0.3602(2)0.0387(10)
H6A0.04461.33630.32400.046*
H6B0.02741.34380.39940.046*
C7−0.0785(3)1.2371(3)0.3268(3)0.0567(13)
H7A−0.12901.30020.31790.068*
H7B−0.08381.20050.28070.068*
C8−0.0999(3)1.1443(3)0.3762(3)0.0522(12)
H8A−0.10461.18360.41930.063*
H8B−0.16511.10710.35160.063*
C9−0.0200(3)1.0495(3)0.39848(19)0.0309(8)
C100.3537(3)0.9710(3)0.4690(2)0.0315(9)
C110.1488(2)0.8837(3)0.37521(18)0.0235(8)
C120.1430(3)0.7690(3)0.3987(2)0.0329(9)
H12A0.14450.75600.44610.040*
C130.1348(3)0.6725(3)0.3530(2)0.0389(10)
H13A0.13100.59510.36920.047*
C140.1325(3)0.6926(3)0.2837(2)0.0321(9)
C150.1358(3)0.8055(3)0.2579(2)0.0390(10)
H15A0.13250.81800.21010.047*
C160.1442(3)0.9006(3)0.3047(2)0.0347(9)
H16A0.14680.97800.28790.042*
O10.20010(17)1.23635(18)0.39944(13)0.0310(6)
O2−0.03949(18)0.9499(2)0.41529(15)0.0429(7)
N10.3692(2)1.2193(2)0.44002(17)0.0390(8)
H1A0.42601.18210.45860.047*
H1B0.36901.29380.42900.047*
N20.4207(2)0.9057(3)0.4896(2)0.0496(9)
Br10.12798(3)0.55869(4)0.22300(3)0.0586(2)

Source of materials

The title compound was synthesized according to a reported procedure [4]. A mixture of 3,5-cyclohexanedione (10 mmol), 4-bromo-benzaldehyde (10 mmol), malononitrile (10 mmol) and 4-(dimethylamino)pyridine (DMAP) (1 mmol) in ethanol (100 mL) was refluxed for 2–3 h and then cooled to room temperature. After filtering, the precipitates were sequentially washed with ice-cooled water and ethanol and then dried under vacuum.

Experimental details

All H atoms were modelled at their calculated positions and refined via the riding model. The Uiso of H-atoms were constrained to 1.2 times Ueq of their bonding atoms.

Comment

The chemistry and diverse applications of organic heterocyclic derivatives have received much attention due to their pronounced biological activity [5], [6], [7], [8]. For example, pyrans are well known to exhibit anti-HIV PR inhibitors, anti breast cancer, anti-inflammatory, anti-protozoal, antitumor, antitubercular with antimycobacterial activity.

In the crystal structure of the title compound, the newly formed pyran ring is essentially planar and perpendicular to the bromophenyl ring.

The amino group donates two hydrogen bonds, to the cyano and oxo groups, repespectively, with the following parameters: D⋯A 3.122(4) Å and D—H⋯A 176.76° for N1…N2 and D⋯A 2.983(4) Å and D—H⋯A 146.52° for N1…O2; the former is involved in the formation of a centrosymmetric H-bonded dimer.

Acknowledgement

This work was supported by the Shaanxi Provincial Scientific Technology Research and Development Program (2016JM5027) and Scientific Research Foundation Program of Shaanxi Xueqian Normal University (2015YBKJ061).

References

Agilent. CrysAlis CCD and CrysAlis RED. Agilent Technologies, Yarnton, Oxfordshire, England (2012).Search in Google Scholar

Agilent. CrysAlisPRO. Agilent Technologies, Yarnton, Oxfordshire, England (2014).Search in Google Scholar

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Received: 2017-3-3
Accepted: 2017-7-10
Published Online: 2017-7-27
Published in Print: 2017-9-26

©2017 Yuanyuan Yu, published by De Gruyter, Berlin/Boston

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

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