Crystal structure and Hirshfeld surface analysis of N-(tert-but­yl)-2-(phenyl­ethyn­yl)imidazo[1,2-a]pyridin-3-amine

Tber, Z.; Kansiz, S.; El Hafi, M.; Loubidi, M.; Jouha, J.; Dege, N.; Essassi, E.M.; Mague, J.T.

doi:10.1107/S2056989019012751

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ISSN: 2056-9890

Volume 75| Part 10| October 2019| Pages 1564-1567

https://doi.org/10.1107/S2056989019012751

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Crystal structure and Hirshfeld surface analysis of N-(tert-butyl)-2-(phenylethynyl)imidazo[1,2-a]pyridin-3-amine

Zahira Tber,^a ^* Sevgi Kansiz,^b Mohamed El Hafi,^c Mohamed Loubidi,^a Jabrane Jouha,^d Necmi Dege,^e El Mokhtar Essassi ^c and Joel T. Mague ^f

^aLaboratoire de Chimie Bioorganique & Analytique, URAC 22 Université Hassan II Mohammedia-Casablanca, Faculté des Sciences et Techniques, BP 146, 28800 Mohammedia, Morocco, ^bOndokuz Mayıs University, Faculty of Arts and Sciences, Department of Physics, 55139 Samsun, Turkey, ^cLaboratoire de Chimie Organique Hétérocyclique, Centre de Recherche des Sciences des Médicaments, Pôle de Compétence Pharmacochimie, Av Ibn Battouta, BP 1014, Faculté des Sciences, Université Mohammed V, Rabat, Morocco, ^dLaboratoire de Chimie Organique et Analytique, Université Sultan Moulay Slimane, Faculté des Sciences et Techniques, BP 523, 23000 Beni-Mellal, Morocco, ^eOndokuz Mayıs University, Faculty of Arts and Sciences, Department of Physics, 55139, Samsun, Turkey, and ^fDepartment of Chemistry, Tulane University, New Orleans, LA 70118, USA
^*Correspondence e-mail: tber.zahira1@gmail.com

Edited by H. Stoeckli-Evans, University of Neuchâtel, Switzerland (Received 19 July 2019; accepted 13 September 2019; online 27 September 2019)

The bicyclic imidazo[1,2-a]pyridine core of the title compound, C₁₉H₁₉N₃, is relatively planar with an r.m.s. deviation of 0.040 Å. The phenyl ring is inclined to the mean plane of the imidazo[1,2-a]pyridine unit by 18.2 (1)°. In the crystal, molecules are linked by N—H⋯H hydrogen bonds, forming chains along the c-axis direction. The chains are linked by C—H⋯π interactions, forming slabs parallel to the ac plane. The Hirshfeld surface analysis and fingerprint plots reveal that the crystal structure is dominated by H⋯H (54%) and C⋯H/H⋯C (35.6%) contacts. The crystal studied was refined as an inversion twin

Keywords: crystal structure; alkyne; imidazo[1,2-a]pyridin; hydrogen bonding; C—H⋯π(ring) interaction; Hirshfeld surface.

CCDC reference: 1953481

1. Chemical context

Compounds containing the imidazo[1,2-a]pyridine moiety have received considerable attention because of their interesting biological activities. For instance, it is found in several commercialized drugs such as the sedative Zolpidem, the anxiolytics Alpidem, Saridipem and Necopidem, the heart-failure drug Olprinone and the antiulcer drug Zolimidine (Baviskar et al., 2011 ). As a continuation of our research on nitrogen-bridgehead heterocycles (Tber et al., 2015 ), we report herein on the molecular and crystal structures, along with the Hirshfeld surface analysis, of the title compound, N-(tert-butyl)-2-(phenylethynyl)imidazo[1,2-a]pyridin-3-amine.

2. Structural commentary

In the title compound (Fig. 1), the fused bicyclic imidazo[1,2-a]pyridine portion is slightly twisted with a dihedral angle of 3.6 (1)° between the mean planes of the five- and six-membered rings. The dihedral angle between the mean plane of the imidazo[1,2-a]pyridine moiety (r.m.s.deviation = 0.040 Å; N1/N2/C1–C7) and the phenyl ring (C10–C15) is 18.2 (1)°.

Figure 1
The molecular structure of the title compound, with atom labelling. Displacement ellipsoids are drawn at the 50% probability level.

3. Supramolecular features

In the crystal, molecules are connected into chains along the c-axis direction by N3—H3A⋯N1ⁱ hydrogen bonds (Table 1 and Fig. 2). These chains are linked by C2—H2⋯Cg4ⁱⁱ and C17—H17C⋯Cg3ⁱⁱⁱ interactions, forming slabs parallel to the ac plane (Fig. 3 and Table 1).

Table 1
Hydrogen-bond geometry (Å, °)

Cg3 and Cg4 are the centroids of the C10–C15 and N1/N2/C1–C7 rings, respectively.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N3—H3A⋯N1ⁱ	0.89	2.26	3.150 (2)	178
C2—H2⋯Cg4ⁱⁱ	0.93	2.98	3.890 (3)	167
C17—H17C⋯Cg3ⁱⁱⁱ	0.96	2.95	3.896 (3)	170
Symmetry codes: (i) $[-x+{\script{1\over 2}}, y, z-{\script{1\over 2}}]$ ; (ii) $[x-{\script{1\over 2}}, -y, z]$ ; (iii) x-1, y, z.

Figure 2
A partial view along the a axis of the crystal packing of the title compound, showing the N—H⋯N hydrogen-bonded chains (dashed lines; Table 1

). The C-bound H atoms have been omitted.

Figure 3
A view along the c axis of the crystal packing of the title compound. The C—H⋯π(ring) interactions and N—H⋯H hydrogen bonds (see Table 1

) are indicated by dashed lines. Only the H atoms (grey balls) involved in the various intermolecular interactions have been included.

4. Hirshfeld surface analysis

The Hirshfield surface analysis (Spackman & Jayatilaka, 2009 ; McKinnon et al., 2007 ) was carried out using CrystalExplorer17.5 (Turner et al., 2017 ). The Hirshfeld surfaces and their associated two-dimensional fingerprint plots were used to quantify the various intermolecular interactions in the title compound. The molecular Hirshfeld surfaces were generated using a standard (high) surface resolution with the three-dimensional d_norm surfaces mapped over a fixed colour scale of −0.379 (red) to 1.341 (blue). The red spots on the surface indicate the intermolecular contacts involved in the hydrogen bonds. Fig. 4a illustrates the intermolecular N—H⋯N hydrogen bonding of the title compound with d_norm mapped on Hirshfeld surface, and the C—H⋯π(ring) contacts are visualized in Fig. 4b. The fingerprint plots are given in Fig. 5. They reveal that the principal intermolecular interactions are H⋯H at 54.0% (Fig. 5b) and C⋯H/H⋯C at 35.6% (Fig. 5c), followed by N⋯H/H⋯N interactions at 10.2% (Fig. 5d).

Figure 4
The Hirshfeld surface of the title compound mapped over d_norm, showing (a) N—H⋯N hydrogen bonds and (b) C—H⋯π(ring) interactions.

Figure 5
(a) The full two-dimensional fingerprint plot for the title compound and fingerprint plots delineated into (b) H⋯H, (c) C⋯H/H⋯C and (d) N⋯H/H⋯N contacts.

5. Database survey

A search of the Cambridge Structural Database (Version 5.40, last update May 2019; Groom et al., 2016 ) for an imidazol[1,2-a]pyridine unit substituted with a phenylethynyl group, viz. 2-(phenylethynyl)imidazo[1,2-a]pyridine, gave zero hits. A search for N-(tert-butyl)imidazo[1,2-a]pyridin-3-amines gave six hits (see supporting information). As in the title compound, the (tert-butyl-amine group lies almost normal to the plane of the imidazol[1,2-a]pyridine unit, with the torsion angle (cf. C16—N3—C7—C6; Fig. 1) varying from ca 75.0 to 90.7°, compared to −89.0 (2)° in the title compound.

6. Synthesis and crystallization

tert-Butylisonitrile (1.63 mmol, 1.05 equiv) was added to a mixture of 2-aminopyridine (146 mg, 1.55 mmol), phenylpropargyl aldehyde (1.63 mmol, 1.05 equiv) and perchloric acid (1 M solution in methanol, 0.07 mmol, 0.05 equiv) in a 50 ml flask at room temperature. The reaction mixture was stirred for 4 h at rt. The crude product was purified by flash chromatography on silica gel (2:8 ethyl acetate/petroleum ether). Colourless crystals were isolated when the solvent was allowed to evaporate (yield: 67%; m.p. 440–442 K).

7. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2. The C-bound H atoms were placed in idealized positions and refined as riding: C—H = 0.93–0.96 Å with U_iso(H) = 1.5U_eq(C-methyl) and 1.2U_eq(C) for other C-bound H atoms. The NH H atom was located in a difference-Fourier map. Its parameters were adjusted to give N—H = 0.89 Å and it was then refined as riding with U_iso(H) = 1.2U_eq(N). The crystal studied was refined as an inversion twin, with a final BASF value of 0.3 (6).

Table 2
Experimental details

Crystal data
Chemical formula	C₁₉H₁₉N₃
M_r	289.37
Crystal system, space group	Orthorhombic, Pca2₁
Temperature (K)	298
a, b, c (Å)	9.3492 (2), 16.3716 (3), 10.8030 (2)
V (Å³)	1653.52 (6)
Z	4
Radiation type	Cu Kα
μ (mm⁻¹)	0.54
Crystal size (mm)	0.28 × 0.18 × 0.07

Data collection
Diffractometer	Bruker D8 VENTURE PHOTON 100 CMOS
Absorption correction	Multi-scan (SADABS; Krause et al., 2015 )
T_min, T_max	0.86, 0.96
No. of measured, independent and observed [I > 2σ(I)] reflections	12219, 2789, 2610
R_int	0.034
(sin θ/λ)_max (Å⁻¹)	0.618

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.035, 0.094, 1.05
No. of reflections	2789
No. of parameters	204
No. of restraints	1
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.12, −0.11
Computer programs: APEX3 and SAINT (Bruker, 2016 ), SHELXT (Sheldrick, 2015a ), Mercury (Macrae, et al., 2008 ), SHELXL2018/1 (Sheldrick, 2015b ), PLATON (Spek, 2009 ) and publCIF (Westrip, 2010 ).

Supporting information

CCDC reference: 1953481

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S2056989019012751/su5507sup1.cif

Supporting information file. DOI: https://doi.org/10.1107/S2056989019012751/su5507Isup3.cdx

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S2056989019012751/su5507Isup4.hkl

CSD search. DOI: https://doi.org/10.1107/S2056989019012751/su5507sup5.pdf

checkCIF report

Computing details top

Data collection: APEX3 (Bruker, 2016); cell refinement: SAINT (Bruker, 2016); data reduction: SAINT (Bruker, 2016); program(s) used to solve structure: SHELXT (Sheldrick, 2015a); program(s) used to refine structure: SHELXL2018/1 (Sheldrick, 2015b); molecular graphics: Mercury (Macrae, et al., 2008); software used to prepare material for publication: SHELXL2018/1 (Sheldrick, 2015b), PLATON (Spek, 2009) and publCIF (Westrip, 2010).

N-(tert-butyl)-2-(phenylethynyl)imidazo[1,2-a]pyridin-3-\ amine top

Crystal data top

C₁₉H₁₉N₃	D_x = 1.162 Mg m⁻³
M_r = 289.37	Cu Kα radiation, λ = 1.54178 Å
Orthorhombic, Pca2₁	Cell parameters from 9967 reflections
a = 9.3492 (2) Å	θ = 2.7–72.4°
b = 16.3716 (3) Å	µ = 0.54 mm⁻¹
c = 10.8030 (2) Å	T = 298 K
V = 1653.52 (6) Å³	Plate, colourless
Z = 4	0.28 × 0.18 × 0.07 mm
F(000) = 616

Data collection top

Bruker D8 VENTURE PHOTON 100 CMOS diffractometer	2789 independent reflections
Radiation source: INCOATEC IµS micro-focus source	2610 reflections with I > 2σ(I)
Mirror monochromator	R_int = 0.034
ω scans	θ_max = 72.4°, θ_min = 2.7°
Absorption correction: multi-scan (SADABS; Krause et al., 2015)	h = −11→10
T_min = 0.86, T_max = 0.96	k = −18→20
12219 measured reflections	l = −11→13

Refinement top

Refinement on F²	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: mixed
R[F² > 2σ(F²)] = 0.035	H-atom parameters constrained
wR(F²) = 0.094	w = 1/[σ²(F_o²) + (0.0557P)² + 0.0961P] where P = (F_o² + 2F_c²)/3
S = 1.05	(Δ/σ)_max < 0.001
2789 reflections	Δρ_max = 0.12 e Å⁻³
204 parameters	Δρ_min = −0.11 e Å⁻³
1 restraint	Extinction correction: (SHELXL-2018/1; Sheldrick, 2015b), Fc^*=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4
Primary atom site location: structure-invariant direct methods	Extinction coefficient: 0.0082 (9)

Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Refinement. Refinement of F² against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F², conventional R-factors R are based on F, with F set to zero for negative F². The threshold expression of F² > 2sigma(F²) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F² are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger. H-atoms attached to carbon were placed in calculated positions (C—H = 0.93 - 0.96 Å) while that attached to nitrogen was placed in a location derived from a difference map and its parameters adjusted to give N—H = 0.89 Å. All were included as riding contributions with isotropic displacement parameters 1.2 - 1.5 times those of the attached atoms. Refined as a 2-component inversion twin.

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

	x	y	z	U_iso*/U_eq
N1	0.20226 (17)	0.18945 (10)	0.67968 (18)	0.0554 (4)
N2	0.02701 (15)	0.12386 (9)	0.57937 (16)	0.0468 (4)
N3	0.04415 (16)	0.17555 (10)	0.37051 (16)	0.0502 (4)
H3A	0.116767	0.178516	0.317433	0.060*
C1	−0.0790 (2)	0.06627 (13)	0.5650 (3)	0.0660 (6)
H1	−0.121888	0.057890	0.488345	0.079*
C2	−0.1189 (3)	0.02246 (16)	0.6643 (4)	0.0865 (9)
H2	−0.188532	−0.017726	0.655677	0.104*
C3	−0.0571 (3)	0.03642 (18)	0.7815 (3)	0.0880 (9)
H3	−0.089464	0.007113	0.849685	0.106*
C4	0.0493 (3)	0.09212 (17)	0.7959 (3)	0.0750 (7)
H4	0.090129	0.101102	0.873222	0.090*
C5	0.0964 (2)	0.13603 (12)	0.6914 (2)	0.0516 (4)
C6	0.19772 (17)	0.21348 (11)	0.55737 (18)	0.0451 (4)
C7	0.08982 (17)	0.17490 (10)	0.49231 (18)	0.0428 (4)
C8	0.29559 (19)	0.27114 (12)	0.5063 (2)	0.0519 (4)
C9	0.3769 (2)	0.31813 (12)	0.4592 (2)	0.0544 (5)
C10	0.47560 (19)	0.37266 (12)	0.4002 (2)	0.0523 (5)
C11	0.4920 (3)	0.37126 (14)	0.2731 (3)	0.0645 (6)
H11	0.437975	0.335322	0.225549	0.077*
C12	0.5885 (3)	0.42310 (16)	0.2164 (3)	0.0807 (8)
H12	0.599034	0.421939	0.130835	0.097*
C13	0.6684 (3)	0.47609 (16)	0.2855 (4)	0.0835 (9)
H13	0.733481	0.510687	0.246809	0.100*
C14	0.6530 (3)	0.47829 (15)	0.4107 (4)	0.0828 (8)
H14	0.707257	0.514665	0.457238	0.099*
C15	0.5569 (2)	0.42660 (13)	0.4694 (3)	0.0660 (6)
H15	0.547037	0.428209	0.555024	0.079*
C16	−0.0652 (2)	0.23805 (15)	0.3328 (2)	0.0611 (5)
C17	−0.1897 (3)	0.2367 (2)	0.4234 (3)	0.0999 (11)
H17A	−0.154972	0.247021	0.505559	0.150*
H17B	−0.235099	0.184099	0.420959	0.150*
H17C	−0.257708	0.278058	0.400960	0.150*
C18	−0.1144 (4)	0.2142 (3)	0.2049 (3)	0.1049 (11)
H18A	−0.160262	0.161741	0.208243	0.157*
H18B	−0.033439	0.211409	0.150395	0.157*
H18C	−0.180883	0.254133	0.174553	0.157*
C19	0.0016 (3)	0.32261 (16)	0.3294 (3)	0.0822 (8)
H19A	0.032518	0.337470	0.411127	0.123*
H19B	−0.067847	0.361435	0.300697	0.123*
H19C	0.082190	0.322349	0.274433	0.123*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
N1	0.0528 (9)	0.0651 (10)	0.0483 (9)	−0.0013 (7)	−0.0038 (7)	0.0078 (8)
N2	0.0442 (7)	0.0412 (7)	0.0549 (10)	−0.0007 (6)	0.0074 (6)	0.0037 (7)
N3	0.0454 (8)	0.0635 (9)	0.0418 (9)	−0.0071 (7)	0.0053 (6)	−0.0064 (7)
C1	0.0603 (11)	0.0552 (11)	0.0826 (18)	−0.0148 (9)	0.0118 (11)	−0.0021 (11)
C2	0.0792 (16)	0.0627 (14)	0.118 (3)	−0.0184 (12)	0.0232 (16)	0.0196 (16)
C3	0.0804 (16)	0.0857 (18)	0.098 (2)	0.0008 (13)	0.0196 (16)	0.0453 (17)
C4	0.0718 (14)	0.0842 (16)	0.0690 (17)	0.0079 (12)	0.0108 (12)	0.0342 (13)
C5	0.0512 (9)	0.0544 (10)	0.0493 (11)	0.0076 (8)	0.0024 (8)	0.0110 (9)
C6	0.0438 (8)	0.0480 (8)	0.0435 (10)	−0.0012 (7)	−0.0002 (7)	0.0028 (8)
C7	0.0409 (8)	0.0443 (8)	0.0433 (10)	−0.0013 (7)	0.0053 (7)	0.0016 (7)
C8	0.0472 (9)	0.0575 (10)	0.0509 (11)	−0.0078 (8)	−0.0058 (8)	0.0028 (9)
C9	0.0471 (9)	0.0565 (10)	0.0596 (12)	−0.0067 (8)	−0.0050 (9)	0.0053 (9)
C10	0.0427 (9)	0.0475 (9)	0.0668 (14)	−0.0015 (7)	−0.0020 (8)	0.0078 (9)
C11	0.0659 (12)	0.0624 (12)	0.0653 (15)	−0.0104 (10)	−0.0010 (11)	0.0067 (11)
C12	0.0838 (16)	0.0754 (15)	0.083 (2)	−0.0081 (14)	0.0188 (14)	0.0157 (14)
C13	0.0701 (14)	0.0645 (14)	0.116 (3)	−0.0156 (11)	0.0163 (15)	0.0214 (15)
C14	0.0692 (15)	0.0616 (13)	0.118 (3)	−0.0214 (11)	−0.0035 (16)	0.0017 (15)
C15	0.0618 (12)	0.0595 (11)	0.0767 (16)	−0.0109 (10)	−0.0044 (11)	0.0020 (12)
C16	0.0461 (9)	0.0900 (14)	0.0471 (11)	−0.0011 (10)	−0.0041 (8)	0.0094 (11)
C17	0.0589 (13)	0.153 (3)	0.088 (2)	0.0322 (16)	0.0195 (12)	0.039 (2)
C18	0.0932 (19)	0.163 (3)	0.0583 (16)	−0.032 (2)	−0.0257 (15)	0.013 (2)
C19	0.0817 (15)	0.0769 (15)	0.088 (2)	0.0111 (13)	−0.0097 (15)	0.0147 (16)

Geometric parameters (Å, º) top

N1—C5	1.327 (3)	C11—C12	1.381 (3)
N1—C6	1.379 (3)	C11—H11	0.9300
N2—C1	1.377 (2)	C12—C13	1.367 (4)
N2—C5	1.388 (3)	C12—H12	0.9300
N2—C7	1.388 (2)	C13—C14	1.361 (5)
N3—C7	1.383 (3)	C13—H13	0.9300
N3—C16	1.503 (3)	C14—C15	1.388 (3)
N3—H3A	0.8900	C14—H14	0.9300
C1—C2	1.344 (4)	C15—H15	0.9300
C1—H1	0.9300	C16—C18	1.508 (4)
C2—C3	1.410 (5)	C16—C19	1.519 (4)
C2—H2	0.9300	C16—C17	1.522 (3)
C3—C4	1.358 (4)	C17—H17A	0.9600
C3—H3	0.9300	C17—H17B	0.9600
C4—C5	1.409 (3)	C17—H17C	0.9600
C4—H4	0.9300	C18—H18A	0.9600
C6—C7	1.382 (2)	C18—H18B	0.9600
C6—C8	1.426 (2)	C18—H18C	0.9600
C8—C9	1.195 (3)	C19—H19A	0.9600
C9—C10	1.434 (3)	C19—H19B	0.9600
C10—C11	1.382 (3)	C19—H19C	0.9600
C10—C15	1.384 (3)

C5—N1—C6	104.87 (17)	C13—C12—C11	120.4 (3)
C1—N2—C5	122.23 (19)	C13—C12—H12	119.8
C1—N2—C7	129.8 (2)	C11—C12—H12	119.8
C5—N2—C7	107.87 (15)	C14—C13—C12	120.1 (2)
C7—N3—C16	118.26 (16)	C14—C13—H13	120.0
C7—N3—H3A	112.2	C12—C13—H13	120.0
C16—N3—H3A	107.9	C13—C14—C15	120.4 (3)
C2—C1—N2	118.4 (3)	C13—C14—H14	119.8
C2—C1—H1	120.8	C15—C14—H14	119.8
N2—C1—H1	120.8	C10—C15—C14	119.8 (3)
C1—C2—C3	121.1 (2)	C10—C15—H15	120.1
C1—C2—H2	119.5	C14—C15—H15	120.1
C3—C2—H2	119.5	N3—C16—C18	106.2 (2)
C4—C3—C2	120.8 (2)	N3—C16—C19	110.32 (16)
C4—C3—H3	119.6	C18—C16—C19	109.9 (2)
C2—C3—H3	119.6	N3—C16—C17	109.6 (2)
C3—C4—C5	118.6 (3)	C18—C16—C17	110.6 (2)
C3—C4—H4	120.7	C19—C16—C17	110.1 (3)
C5—C4—H4	120.7	C16—C17—H17A	109.5
N1—C5—N2	111.09 (18)	C16—C17—H17B	109.5
N1—C5—C4	130.3 (2)	H17A—C17—H17B	109.5
N2—C5—C4	118.65 (19)	C16—C17—H17C	109.5
N1—C6—C7	112.28 (16)	H17A—C17—H17C	109.5
N1—C6—C8	122.66 (17)	H17B—C17—H17C	109.5
C7—C6—C8	125.06 (17)	C16—C18—H18A	109.5
C6—C7—N3	134.86 (17)	C16—C18—H18B	109.5
C6—C7—N2	103.85 (16)	H18A—C18—H18B	109.5
N3—C7—N2	121.22 (16)	C16—C18—H18C	109.5
C9—C8—C6	177.5 (2)	H18A—C18—H18C	109.5
C8—C9—C10	178.3 (2)	H18B—C18—H18C	109.5
C11—C10—C15	119.1 (2)	C16—C19—H19A	109.5
C11—C10—C9	120.2 (2)	C16—C19—H19B	109.5
C15—C10—C9	120.7 (2)	H19A—C19—H19B	109.5
C12—C11—C10	120.2 (3)	C16—C19—H19C	109.5
C12—C11—H11	119.9	H19A—C19—H19C	109.5
C10—C11—H11	119.9	H19B—C19—H19C	109.5

C5—N2—C1—C2	2.1 (3)	C8—C6—C7—N2	178.52 (17)
C7—N2—C1—C2	178.0 (2)	C16—N3—C7—C6	−89.0 (2)
N2—C1—C2—C3	1.8 (4)	C16—N3—C7—N2	94.6 (2)
C1—C2—C3—C4	−2.9 (5)	C1—N2—C7—C6	−174.58 (19)
C2—C3—C4—C5	0.2 (4)	C5—N2—C7—C6	1.78 (19)
C6—N1—C5—N2	1.5 (2)	C1—N2—C7—N3	2.8 (3)
C6—N1—C5—C4	−179.3 (2)	C5—N2—C7—N3	179.13 (16)
C1—N2—C5—N1	174.53 (18)	C15—C10—C11—C12	0.1 (4)
C7—N2—C5—N1	−2.2 (2)	C9—C10—C11—C12	−179.2 (2)
C1—N2—C5—C4	−4.8 (3)	C10—C11—C12—C13	0.0 (4)
C7—N2—C5—C4	178.52 (18)	C11—C12—C13—C14	−0.3 (4)
C3—C4—C5—N1	−175.7 (2)	C12—C13—C14—C15	0.4 (4)
C3—C4—C5—N2	3.5 (3)	C11—C10—C15—C14	0.1 (3)
C5—N1—C6—C7	−0.4 (2)	C9—C10—C15—C14	179.3 (2)
C5—N1—C6—C8	−179.81 (17)	C13—C14—C15—C10	−0.3 (4)
N1—C6—C7—N3	−177.7 (2)	C7—N3—C16—C18	−169.4 (2)
C8—C6—C7—N3	1.7 (3)	C7—N3—C16—C19	71.5 (2)
N1—C6—C7—N2	−0.9 (2)	C7—N3—C16—C17	−49.8 (3)

Hydrogen-bond geometry (Å, º) top

Cg3 and Cg4 are the centroids of the C10–C15 and N1/N2/C1–C7 rings, respectively.

D—H···A	D—H	H···A	D···A	D—H···A
N3—H3A···N1ⁱ	0.89	2.26	3.150 (2)	178
C2—H2···Cg4ⁱⁱ	0.93	2.98	3.890 (3)	167
C17—H17C···Cg3ⁱⁱⁱ	0.96	2.95	3.896 (3)	170

Symmetry codes: (i) −x+1/2, y, z−1/2; (ii) x−1/2, −y, z; (iii) x−1, y, z.

Funding information

The support of NSF–MRI grant No. 1228232 for the purchase of the diffractometer and Tulane University for support of the Tulane Crystallography Laboratory are gratefully acknowledged.

References

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Volume 75| Part 10| October 2019| Pages 1564-1567

https://doi.org/10.1107/S2056989019012751

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research communications\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Crystal structure and Hirshfeld surface analysis of N-(tert-but­yl)-2-(phenyl­ethyn­yl)imidazo[1,2-a]pyridin-3-amine

1. Chemical context

2. Structural commentary

3. Supra­molecular features

4. Hirshfeld surface analysis

5. Database survey

6. Synthesis and crystallization

7. Refinement

Supporting information

Funding information

References

research communications

Crystal structure and Hirshfeld surface analysis of N-(tert-butyl)-2-(phenylethynyl)imidazo[1,2-a]pyridin-3-amine

3. Supramolecular features