5-tert-Butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)-2-thien­yl]-1,3-benzoxazole

Li, Y.-F.; Wang, L.-T.; Jian, F.-F.

doi:10.1107/S1600536808037665

organic compounds

CRYSTALLOGRAPHIC
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ISSN: 2056-9890

Volume 64| Part 12| December 2008| Page o2410

doi:10.1107/S1600536808037665

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5-tert-Butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)-2-thienyl]-1,3-benzoxazole

Yu-Feng Li,^a Lin-Tong Wang ^a and Fang-Fang Jian ^b ^*

^aMicroscale Science Institute, Department of Chemistry and Chemical Engineering, Weifang University, Weifang 261061, People's Republic of China, and ^bMicroscale Science Institute, Weifang University, Weifang 261061, People's Republic of China
^*Correspondence e-mail: ffjian2008@163.com

(Received 10 October 2008; accepted 13 November 2008; online 22 November 2008)

The title compound, C₂₆H₂₆N₂O₂S, was prepared by the reaction of thiophene-2,5-dicarboxylic acid and 2-amino-4-tert-butylphenol. One of the tert-butyl groups is disordered over two conformations, with occupancies of 0.539 (1) and 0.461 (2). The two 1,3-benzoxazole rings are almost planar, with dihedral angles of 0.83 (18) and 1.64 (17)° between the five- and six-membered rings. The thiophene ring makes dihedral angles of 21.54 (19) and 4.49 (18)° with the planes of the five-membered oxazole rings. The crystal packing is controlled by π–π stacking interactions involving the thiophene and benzene rings, with a centroid–centroid distance of 3.748 (2) Å.

Related literature

For background on fluorescent whitening agents, see: Chen et al. (2008 ). For a related structure, see: Cowley et al. (2002 ).

Experimental

Crystal data

C₂₆H₂₆N₂O₂S
M_r = 430.56
Triclinic, $[P \overline 1]$
a = 6.0852 (12) Å
b = 11.520 (2) Å
c = 16.986 (3) Å
α = 72.79 (3)°
β = 88.88 (3)°
γ = 79.32 (3)°
V = 1116.9 (4) Å³
Z = 2
Mo Kα radiation
μ = 0.17 mm⁻¹
T = 293 (2) K
0.25 × 0.20 × 0.18 mm

Data collection

Bruker SMART CCD area-detector diffractometer
Absorption correction: none
6826 measured reflections
4783 independent reflections
2940 reflections with I > 2σ(I)
R_int = 0.031

Refinement

R[F² > 2σ(F²)] = 0.061
wR(F²) = 0.187
S = 1.04
4783 reflections
309 parameters
57 restraints
H-atom parameters constrained
Δρ_max = 0.48 e Å⁻³
Δρ_min = −0.32 e Å⁻³

Data collection: SMART (Bruker, 1997 ); cell refinement: SAINT (Bruker, 1997); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL.

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808037665/at2649sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808037665/at2649Isup2.hkl

checkCIF report

Comment top

Fluorescent whitening agents have received considerable attention in the literature. They are attractive from several points of view in application (Chen et al., 2008). As part of our search for new fluorescent whitening agent compounds we synthesized the title compound (I), and describe its structure here.

In (I) (Fig. 1), the C12—S1 bond length of 1.715 (3)Å is comparable with C—S bond [1.688 (2) Å] reported (Cowley et al., 2002). The two 1,3-benzoxazole rings (N1/O1/C5-C11) and (N2/O2/C16-C22) are almost planar, with dihedral angles of 0.83 (18)° and 1.64 (17)°, respectively, between the five- and six-membered rings. The thiophene ring (S1/C12-C15) makes dihedral angles of 21.54 (19)° and 4.49 (18)°, respectively, with the five membered rings (O1/N1/C7/C8/C11) and (O2/N2/C16-C18).

In the crystal structure, there is no classical hydrogen bonds. The crystal packing is controlled by π-π stacking interactions involving the thiophene (Cg1: S1/C12-C15) and benzene (Cg2ⁱ: C17-C22) [ (i) 2 - x, 1 - y, - z] rings, with a centroid-centroid distance of 3.748 (2)Å.

Related literature top

For related literature, see: Chen et al. (2008); Cowley et al. (2002).

Experimental top

A mixture of the thiophene-2,5-dicarboxylic acid (0.05 mol), and 4-tert-butyl-2-aminophenol (0.1 mol) was stirred in refluxing toluene (20 mL) for 4 h to afford the title compound (0.086 mol, yield 86%). Single crystals suitable for X-ray measurements were obtained by recrystallization from ethanol at room temperature.

Computing details top

Data collection: SMART (Bruker, 1997); cell refinement: SAINT (Bruker, 1997); data reduction: SAINT (Bruker, 1997); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top

Fig. 1. The structure of the title compound showing 30% probability displacement ellipsoids and the atom-numbering scheme.

5-tert-Butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)-2-thienyl]-1,3-benzoxazole top

Crystal data top

C₂₆H₂₆N₂O₂S	Z = 2
M_r = 430.56	F(000) = 456
Triclinic, P1	D_x = 1.280 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 6.0852 (12) Å	Cell parameters from 1520 reflections
b = 11.520 (2) Å	θ = 2.5–23.6°
c = 16.986 (3) Å	µ = 0.17 mm⁻¹
α = 72.79 (3)°	T = 293 K
β = 88.88 (3)°	Block, yellow
γ = 79.32 (3)°	0.25 × 0.20 × 0.18 mm
V = 1116.9 (4) Å³

Data collection top

Bruker SMART CCD area-detector diffractometer	2940 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.031
Graphite monochromator	θ_max = 27.0°, θ_min = 1.9°
ϕ and ω scans	h = −7→7
6826 measured reflections	k = −14→14
4783 independent reflections	l = −21→17

Refinement top

Refinement on F²	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F² > 2σ(F²)] = 0.061	H-atom parameters constrained
wR(F²) = 0.187	w = 1/[σ²(F_o²) + (0.083P)² + 0.378P] where P = (F_o² + 2F_c²)/3
S = 1.04	(Δ/σ)_max < 0.001
4783 reflections	Δρ_max = 0.48 e Å⁻³
309 parameters	Δρ_min = −0.32 e Å⁻³
57 restraints	Extinction correction: SHELXL97 (Sheldrick, 2008), Fc^*=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4
Primary atom site location: structure-invariant direct methods	Extinction coefficient: 0.026 (4)

Crystal data top

C₂₆H₂₆N₂O₂S	γ = 79.32 (3)°
M_r = 430.56	V = 1116.9 (4) Å³
Triclinic, P1	Z = 2
a = 6.0852 (12) Å	Mo Kα radiation
b = 11.520 (2) Å	µ = 0.17 mm⁻¹
c = 16.986 (3) Å	T = 293 K
α = 72.79 (3)°	0.25 × 0.20 × 0.18 mm
β = 88.88 (3)°

Data collection top

Bruker SMART CCD area-detector diffractometer	2940 reflections with I > 2σ(I)
6826 measured reflections	R_int = 0.031
4783 independent reflections

Refinement top

R[F² > 2σ(F²)] = 0.061	57 restraints
wR(F²) = 0.187	H-atom parameters constrained
S = 1.04	Δρ_max = 0.48 e Å⁻³
4783 reflections	Δρ_min = −0.32 e Å⁻³
309 parameters

Special details top

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

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

	x	y	z	U_iso*/U_eq	Occ. (<1)
S1	0.58719 (14)	0.77701 (8)	0.00117 (5)	0.0601 (3)
O1	0.2519 (4)	1.00117 (19)	−0.08466 (12)	0.0567 (7)
O2	1.1731 (3)	0.55542 (18)	0.07064 (12)	0.0517 (7)
N1	0.3847 (5)	1.0267 (3)	−0.21200 (16)	0.0621 (9)
N2	0.8447 (4)	0.5523 (2)	0.13353 (16)	0.0568 (9)
C1	−0.1548 (7)	1.4283 (4)	−0.4007 (3)	0.0955 (17)
C2	−0.3823 (7)	1.2682 (4)	−0.3939 (2)	0.0812 (14)
C3	−0.4984 (8)	1.4230 (4)	−0.3198 (3)	0.0971 (17)
C4	−0.2957 (6)	1.3431 (3)	−0.34509 (19)	0.0553 (10)
C5	−0.1536 (5)	1.2540 (3)	−0.27123 (18)	0.0509 (10)
C6	0.0494 (5)	1.1872 (3)	−0.28414 (18)	0.0563 (10)
C7	0.1771 (5)	1.1053 (3)	−0.21673 (18)	0.0513 (10)
C8	0.0973 (5)	1.0894 (3)	−0.13912 (17)	0.0502 (10)
C9	−0.1032 (6)	1.1522 (3)	−0.1232 (2)	0.0639 (11)
C10	−0.2260 (6)	1.2345 (3)	−0.19051 (19)	0.0589 (11)
C11	0.4174 (5)	0.9704 (3)	−0.13440 (18)	0.0522 (10)
C12	0.6087 (5)	0.8788 (3)	−0.09425 (18)	0.0520 (10)
C13	0.8153 (6)	0.8580 (3)	−0.12375 (19)	0.0567 (11)
C14	0.9600 (6)	0.7598 (3)	−0.06945 (19)	0.0549 (11)
C15	0.8597 (5)	0.7069 (3)	0.00045 (18)	0.0506 (10)
C16	0.9503 (5)	0.6044 (3)	0.07071 (19)	0.0501 (10)
C17	1.2069 (5)	0.4605 (3)	0.14351 (17)	0.0472 (9)
C18	1.0079 (5)	0.4580 (3)	0.18216 (18)	0.0482 (10)
C19	0.9930 (5)	0.3697 (3)	0.25628 (18)	0.0545 (10)
C20	1.1818 (5)	0.2826 (3)	0.29081 (18)	0.0506 (10)
C21	1.3811 (5)	0.2891 (3)	0.24862 (19)	0.0562 (11)
C22	1.4005 (5)	0.3778 (3)	0.17496 (19)	0.0543 (10)
C23	1.1718 (5)	0.1827 (3)	0.37112 (19)	0.0642 (11)
C24	1.3987 (10)	0.1150 (10)	0.4102 (6)	0.163 (4)	0.539 (8)
C25	1.0524 (16)	0.0853 (6)	0.3523 (4)	0.098 (3)	0.539 (8)
C26	1.0314 (17)	0.2331 (7)	0.4322 (4)	0.112 (4)	0.539 (8)
C26'	0.9370 (10)	0.1644 (12)	0.3948 (8)	0.160 (5)	0.461 (8)
C24'	1.273 (2)	0.2224 (8)	0.4398 (5)	0.104 (4)	0.461 (8)
C25'	1.3145 (18)	0.0592 (6)	0.3717 (6)	0.111 (4)	0.461 (8)
H1A	−0.24570	1.48400	−0.44690	0.1440*
H1B	−0.03250	1.37960	−0.42020	0.1440*
H1C	−0.09720	1.47480	−0.37020	0.1440*
H2A	−0.47220	1.32330	−0.44060	0.1220*
H3B	−0.44820	1.47120	−0.28870	0.1450*
H3C	−0.59200	1.37060	−0.28640	0.1450*
H6A	0.10010	1.19690	−0.33730	0.0680*
H9A	−0.15400	1.14010	−0.06990	0.0760*
H2B	−0.47120	1.21410	−0.35930	0.1220*
H2C	−0.25800	1.21990	−0.41260	0.1220*
H3A	−0.58200	1.47730	−0.36820	0.1450*
H19A	0.85790	0.36850	0.28280	0.0650*
H21A	1.50760	0.23040	0.27150	0.0680*
H22A	1.53530	0.38140	0.14850	0.0650*
H24A	1.44840	0.04530	0.39010	0.2450*	0.539 (8)
H24B	1.38780	0.08690	0.46900	0.2450*	0.539 (8)
H24C	1.50390	0.17000	0.39630	0.2450*	0.539 (8)
H25A	0.99670	0.11480	0.29600	0.1460*	0.539 (8)
H25B	0.93010	0.07220	0.38830	0.1460*	0.539 (8)
H25C	1.15680	0.00880	0.36080	0.1460*	0.539 (8)
H26A	0.87580	0.23900	0.41970	0.1680*	0.539 (8)
H26B	1.05960	0.31370	0.42880	0.1680*	0.539 (8)
H26C	1.06940	0.17870	0.48700	0.1680*	0.539 (8)
H10A	−0.36330	1.27920	−0.18190	0.0710*
H13A	0.85680	0.90420	−0.17470	0.0680*
H14A	1.10850	0.73370	−0.08010	0.0660*
H24D	1.33780	0.29410	0.41540	0.1560*	0.461 (8)
H24E	1.38710	0.15600	0.47090	0.1560*	0.461 (8)
H24F	1.15780	0.24140	0.47580	0.1560*	0.461 (8)
H25D	1.24530	0.02460	0.33590	0.1670*	0.461 (8)
H25E	1.32770	0.00360	0.42680	0.1670*	0.461 (8)
H25F	1.46060	0.07150	0.35280	0.1670*	0.461 (8)
H26D	0.86350	0.14870	0.35050	0.2400*	0.461 (8)
H26E	0.85490	0.23750	0.40530	0.2400*	0.461 (8)
H26F	0.94360	0.09520	0.44350	0.2400*	0.461 (8)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1	0.0560 (5)	0.0611 (5)	0.0504 (5)	−0.0031 (4)	−0.0010 (4)	−0.0020 (4)
O2	0.0479 (12)	0.0515 (11)	0.0502 (12)	−0.0087 (9)	−0.0014 (9)	−0.0071 (9)
O1	0.0662 (14)	0.0563 (12)	0.0404 (11)	−0.0022 (11)	−0.0055 (10)	−0.0086 (9)
N1	0.0601 (17)	0.0672 (17)	0.0474 (15)	0.0009 (14)	−0.0021 (12)	−0.0072 (13)
N2	0.0476 (15)	0.0606 (15)	0.0517 (15)	−0.0058 (12)	−0.0029 (12)	−0.0030 (12)
C1	0.096 (3)	0.072 (3)	0.093 (3)	−0.018 (2)	−0.024 (2)	0.017 (2)
C2	0.091 (3)	0.079 (2)	0.073 (2)	−0.004 (2)	−0.028 (2)	−0.027 (2)
C3	0.101 (3)	0.095 (3)	0.081 (3)	0.036 (3)	−0.025 (2)	−0.036 (2)
C4	0.062 (2)	0.0510 (17)	0.0498 (17)	−0.0043 (15)	−0.0088 (15)	−0.0136 (14)
C5	0.060 (2)	0.0474 (16)	0.0457 (17)	−0.0102 (14)	−0.0036 (14)	−0.0142 (13)
C6	0.063 (2)	0.0590 (18)	0.0402 (16)	−0.0035 (16)	0.0005 (14)	−0.0094 (13)
C7	0.0578 (19)	0.0460 (16)	0.0454 (17)	−0.0063 (14)	0.0001 (14)	−0.0087 (13)
C8	0.063 (2)	0.0462 (16)	0.0393 (16)	−0.0076 (14)	−0.0022 (14)	−0.0107 (12)
C9	0.073 (2)	0.071 (2)	0.0438 (17)	−0.0045 (18)	0.0058 (16)	−0.0170 (15)
C10	0.061 (2)	0.0587 (19)	0.0548 (19)	−0.0007 (16)	−0.0010 (15)	−0.0200 (15)
C11	0.0556 (19)	0.0516 (17)	0.0470 (17)	−0.0095 (14)	−0.0017 (14)	−0.0110 (14)
C12	0.058 (2)	0.0505 (17)	0.0451 (16)	−0.0104 (14)	−0.0066 (14)	−0.0098 (13)
C13	0.062 (2)	0.0580 (18)	0.0468 (17)	−0.0165 (16)	−0.0009 (15)	−0.0071 (14)
C14	0.0524 (19)	0.0587 (18)	0.0517 (18)	−0.0119 (15)	0.0000 (14)	−0.0126 (14)
C15	0.0501 (18)	0.0497 (16)	0.0481 (17)	−0.0081 (14)	−0.0054 (14)	−0.0089 (13)
C16	0.0460 (17)	0.0499 (16)	0.0522 (18)	−0.0063 (14)	−0.0045 (14)	−0.0130 (14)
C17	0.0506 (18)	0.0442 (15)	0.0450 (16)	−0.0111 (13)	−0.0034 (13)	−0.0089 (12)
C18	0.0430 (17)	0.0492 (16)	0.0488 (17)	−0.0039 (13)	−0.0017 (13)	−0.0117 (13)
C19	0.0480 (18)	0.0606 (18)	0.0500 (17)	−0.0110 (15)	0.0031 (14)	−0.0086 (14)
C20	0.0497 (18)	0.0504 (16)	0.0494 (17)	−0.0081 (14)	−0.0056 (14)	−0.0119 (13)
C21	0.0496 (18)	0.0532 (18)	0.0602 (19)	−0.0018 (14)	−0.0120 (15)	−0.0121 (15)
C22	0.0417 (17)	0.0567 (18)	0.0612 (19)	−0.0060 (14)	0.0003 (14)	−0.0143 (15)
C23	0.063 (2)	0.062 (2)	0.0541 (19)	−0.0060 (17)	−0.0094 (16)	0.0005 (15)
C24	0.120 (7)	0.187 (9)	0.111 (7)	−0.025 (7)	−0.024 (6)	0.062 (6)
C25	0.149 (8)	0.065 (4)	0.072 (5)	−0.040 (5)	0.013 (5)	0.002 (3)
C26	0.182 (9)	0.084 (5)	0.059 (4)	−0.017 (6)	0.040 (5)	−0.013 (4)
C24'	0.168 (9)	0.087 (6)	0.051 (4)	−0.022 (6)	−0.015 (5)	−0.010 (4)
C25'	0.178 (10)	0.046 (4)	0.091 (6)	0.001 (5)	0.022 (6)	−0.007 (4)
C26'	0.105 (7)	0.175 (10)	0.143 (9)	−0.048 (7)	0.010 (7)	0.053 (7)

Geometric parameters (Å, º) top

S1—C15	1.706 (3)	C14—H14A	0.9300
S1—C12	1.715 (3)	C15—C16	1.440 (4)
O2—C16	1.369 (3)	C17—C18	1.367 (4)
O2—C17	1.377 (3)	C17—C22	1.374 (4)
O1—C11	1.366 (4)	C18—C19	1.379 (4)
O1—C8	1.377 (3)	C19—C20	1.386 (4)
N1—C11	1.286 (4)	C19—H19A	0.9300
N1—C7	1.400 (4)	C20—C21	1.399 (4)
N2—C16	1.284 (4)	C20—C23	1.511 (4)
N2—C18	1.397 (4)	C21—C22	1.380 (4)
C1—C4	1.524 (5)	C21—H21A	0.9300
C1—H1A	0.9600	C22—H22A	0.9300
C1—H1B	0.9600	C23—C26	1.511 (4)
C1—H1C	0.9600	C23—C26'	1.512 (5)
C2—C4	1.523 (5)	C23—C24	1.512 (5)
C2—H2A	0.9600	C23—C25'	1.521 (5)
C2—H2B	0.9600	C23—C24'	1.550 (5)
C2—H2C	0.9600	C23—C25	1.553 (4)
C3—C4	1.531 (5)	C24—H24A	0.9600
C3—H3A	0.9600	C24—H24B	0.9600
C3—H3B	0.9600	C24—H24C	0.9600
C3—H3C	0.9600	C25—H25A	0.9600
C4—C5	1.526 (4)	C25—H25B	0.9600
C5—C6	1.379 (4)	C25—H25C	0.9600
C5—C10	1.398 (4)	C26—H26A	0.9600
C6—C7	1.389 (4)	C26—H26B	0.9600
C6—H6A	0.9300	C26—H26C	0.9600
C7—C8	1.368 (4)	C24'—H24D	0.9600
C8—C9	1.365 (5)	C24'—H24E	0.9600
C9—C10	1.376 (4)	C24'—H24F	0.9600
C9—H9A	0.9300	C25'—H25D	0.9600
C10—H10A	0.9300	C25'—H25E	0.9600
C11—C12	1.444 (4)	C25'—H25F	0.9600
C12—C13	1.350 (4)	C26'—H26D	0.9600
C13—C14	1.397 (4)	C26'—H26E	0.9600
C13—H13A	0.9300	C26'—H26F	0.9600
C14—C15	1.355 (4)

C15—S1—C12	90.76 (15)	C19—C18—N2	130.7 (3)
C16—O2—C17	103.0 (2)	C18—C19—C20	119.2 (3)
C11—O1—C8	103.4 (2)	C18—C19—H19A	120.4
C11—N1—C7	103.6 (3)	C20—C19—H19A	120.4
C16—N2—C18	104.0 (3)	C19—C20—C21	118.0 (3)
C4—C1—H1A	109.5	C19—C20—C23	120.9 (3)
C4—C1—H1B	109.5	C21—C20—C23	121.1 (3)
H1A—C1—H1B	109.5	C22—C21—C20	123.7 (3)
C4—C1—H1C	109.5	C22—C21—H21A	118.1
H1A—C1—H1C	109.5	C20—C21—H21A	118.1
H1B—C1—H1C	109.5	C17—C22—C21	115.4 (3)
C4—C2—H2A	109.5	C17—C22—H22A	122.3
C4—C2—H2B	109.5	C21—C22—H22A	122.3
H2A—C2—H2B	109.5	C26—C23—C20	111.4 (4)
C4—C2—H2C	109.5	C26—C23—C26'	53.4 (5)
H2A—C2—H2C	109.5	C20—C23—C26'	113.9 (5)
H2B—C2—H2C	109.5	C26—C23—C24	110.0 (3)
C4—C3—H3A	109.5	C20—C23—C24	114.0 (5)
C4—C3—H3B	109.5	C26'—C23—C24	132.0 (6)
H3A—C3—H3B	109.5	C26—C23—C25'	136.2 (5)
C4—C3—H3C	109.5	C20—C23—C25'	112.4 (4)
H3A—C3—H3C	109.5	C26'—C23—C25'	109.2 (4)
H3B—C3—H3C	109.5	C24—C23—C25'	47.4 (4)
C2—C4—C1	108.9 (3)	C26—C23—C24'	56.9 (4)
C2—C4—C5	108.7 (3)	C20—C23—C24'	107.2 (4)
C1—C4—C5	110.1 (3)	C26'—C23—C24'	107.4 (4)
C2—C4—C3	107.8 (3)	C24—C23—C24'	60.3 (4)
C1—C4—C3	108.6 (3)	C25'—C23—C24'	106.3 (4)
C5—C4—C3	112.7 (3)	C26—C23—C25	106.7 (3)
C6—C5—C10	118.6 (3)	C20—C23—C25	107.4 (3)
C6—C5—C4	119.4 (3)	C26'—C23—C25	54.6 (5)
C10—C5—C4	122.0 (3)	C24—C23—C25	107.0 (3)
C5—C6—C7	119.1 (3)	C25'—C23—C25	62.3 (4)
C5—C6—H6A	120.4	C24'—C23—C25	145.2 (5)
C7—C6—H6A	120.4	C23—C24—H24A	109.5
C8—C7—C6	119.8 (3)	C23—C24—H24B	109.5
C8—C7—N1	109.2 (3)	H24A—C24—H24B	109.5
C6—C7—N1	131.1 (3)	C23—C24—H24C	109.5
C9—C8—C7	123.4 (3)	H24A—C24—H24C	109.5
C9—C8—O1	128.8 (3)	H24B—C24—H24C	109.5
C7—C8—O1	107.9 (3)	C23—C25—H25A	109.5
C8—C9—C10	116.1 (3)	C23—C25—H25B	109.5
C8—C9—H9A	121.9	H25A—C25—H25B	109.5
C10—C9—H9A	121.9	C23—C25—H25C	109.5
C9—C10—C5	123.0 (3)	H25A—C25—H25C	109.5
C9—C10—H10A	118.5	H25B—C25—H25C	109.5
C5—C10—H10A	118.5	C23—C26—H26A	109.5
N1—C11—O1	116.0 (3)	C23—C26—H26B	109.5
N1—C11—C12	127.4 (3)	H26A—C26—H26B	109.5
O1—C11—C12	116.6 (3)	C23—C26—H26C	109.5
C13—C12—C11	127.6 (3)	H26A—C26—H26C	109.5
C13—C12—S1	111.9 (2)	H26B—C26—H26C	109.5
C11—C12—S1	120.4 (3)	C23—C24'—H24D	109.5
C12—C13—C14	112.7 (3)	C23—C24'—H24E	109.5
C12—C13—H13A	123.6	H24D—C24'—H24E	109.5
C14—C13—H13A	123.6	C23—C24'—H24F	109.5
C15—C14—C13	112.4 (3)	H24D—C24'—H24F	109.5
C15—C14—H14A	123.8	H24E—C24'—H24F	109.5
C13—C14—H14A	123.8	C23—C25'—H25D	109.5
C14—C15—C16	129.5 (3)	C23—C25'—H25E	109.5
C14—C15—S1	112.2 (2)	H25D—C25'—H25E	109.5
C16—C15—S1	118.3 (2)	C23—C25'—H25F	109.5
N2—C16—O2	115.9 (3)	H25D—C25'—H25F	109.5
N2—C16—C15	127.2 (3)	H25E—C25'—H25F	109.5
O2—C16—C15	116.9 (3)	C23—C26'—H26D	109.5
C18—C17—C22	123.2 (3)	C23—C26'—H26E	109.5
C18—C17—O2	108.3 (2)	H26D—C26'—H26E	109.5
C22—C17—O2	128.5 (3)	C23—C26'—H26F	109.5
C17—C18—C19	120.5 (3)	H26D—C26'—H26F	109.5
C17—C18—N2	108.8 (3)	H26E—C26'—H26F	109.5

C2—C4—C5—C6	68.7 (4)	C12—S1—C15—C16	179.9 (2)
C1—C4—C5—C6	−50.5 (4)	C18—N2—C16—O2	−0.1 (4)
C3—C4—C5—C6	−171.8 (3)	C18—N2—C16—C15	179.1 (3)
C2—C4—C5—C10	−109.1 (4)	C17—O2—C16—N2	0.1 (3)
C1—C4—C5—C10	131.7 (4)	C17—O2—C16—C15	−179.2 (2)
C3—C4—C5—C10	10.4 (5)	C14—C15—C16—N2	−175.3 (3)
C10—C5—C6—C7	−1.5 (5)	S1—C15—C16—N2	5.0 (4)
C4—C5—C6—C7	−179.4 (3)	C14—C15—C16—O2	3.9 (5)
C5—C6—C7—C8	1.9 (5)	S1—C15—C16—O2	−175.8 (2)
C5—C6—C7—N1	179.6 (3)	C16—O2—C17—C18	0.0 (3)
C11—N1—C7—C8	−0.3 (4)	C16—O2—C17—C22	178.8 (3)
C11—N1—C7—C6	−178.1 (3)	C22—C17—C18—C19	−0.2 (5)
C6—C7—C8—C9	−1.2 (5)	O2—C17—C18—C19	178.7 (3)
N1—C7—C8—C9	−179.4 (3)	C22—C17—C18—N2	−178.9 (3)
C6—C7—C8—O1	178.0 (3)	O2—C17—C18—N2	0.0 (3)
N1—C7—C8—O1	−0.1 (3)	C16—N2—C18—C17	0.0 (3)
C11—O1—C8—C9	179.6 (3)	C16—N2—C18—C19	−178.5 (3)
C11—O1—C8—C7	0.4 (3)	C17—C18—C19—C20	−0.6 (5)
C7—C8—C9—C10	0.2 (5)	N2—C18—C19—C20	177.8 (3)
O1—C8—C9—C10	−179.0 (3)	C18—C19—C20—C21	0.4 (4)
C8—C9—C10—C5	0.2 (5)	C18—C19—C20—C23	−178.8 (3)
C6—C5—C10—C9	0.4 (5)	C19—C20—C21—C22	0.5 (5)
C4—C5—C10—C9	178.3 (3)	C23—C20—C21—C22	179.8 (3)
C7—N1—C11—O1	0.6 (4)	C18—C17—C22—C21	1.0 (4)
C7—N1—C11—C12	−179.3 (3)	O2—C17—C22—C21	−177.6 (3)
C8—O1—C11—N1	−0.6 (4)	C20—C21—C22—C17	−1.2 (5)
C8—O1—C11—C12	179.3 (3)	C19—C20—C23—C26	−41.2 (5)
N1—C11—C12—C13	20.3 (6)	C21—C20—C23—C26	139.6 (5)
O1—C11—C12—C13	−159.6 (3)	C19—C20—C23—C26'	17.0 (7)
N1—C11—C12—S1	−157.8 (3)	C21—C20—C23—C26'	−162.3 (6)
O1—C11—C12—S1	22.3 (4)	C19—C20—C23—C24	−166.3 (5)
C15—S1—C12—C13	0.1 (3)	C21—C20—C23—C24	14.5 (6)
C15—S1—C12—C11	178.5 (3)	C19—C20—C23—C25'	141.8 (5)
C11—C12—C13—C14	−178.5 (3)	C21—C20—C23—C25'	−37.4 (6)
S1—C12—C13—C14	−0.3 (4)	C19—C20—C23—C24'	−101.7 (5)
C12—C13—C14—C15	0.4 (4)	C21—C20—C23—C24'	79.0 (6)
C13—C14—C15—C16	179.9 (3)	C19—C20—C23—C25	75.3 (5)
C13—C14—C15—S1	−0.4 (4)	C21—C20—C23—C25	−104.0 (5)
C12—S1—C15—C14	0.2 (3)

Experimental details

Crystal data
Chemical formula	C₂₆H₂₆N₂O₂S
M_r	430.56
Crystal system, space group	Triclinic, P1
Temperature (K)	293
a, b, c (Å)	6.0852 (12), 11.520 (2), 16.986 (3)
α, β, γ (°)	72.79 (3), 88.88 (3), 79.32 (3)
V (Å³)	1116.9 (4)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.17
Crystal size (mm)	0.25 × 0.20 × 0.18

Data collection
Diffractometer	Bruker SMART CCD area-detector diffractometer
Absorption correction	–
No. of measured, independent and observed [I > 2σ(I)] reflections	6826, 4783, 2940
R_int	0.031
(sin θ/λ)_max (Å⁻¹)	0.639

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.061, 0.187, 1.04
No. of reflections	4783
No. of parameters	309
No. of restraints	57
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.48, −0.32

Computer programs: SMART (Bruker, 1997), SAINT (Bruker, 1997), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

References

Bruker (1997). SMART and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
Chen, B., Wen, J. & Chen, J.-H. (2008). J. Taiyuan Univ. Technol. 39, 241–244. CAS Google Scholar
Cowley, A. R., Dilworth, J. R. & Dorinelly, P. S. (2002). J. Am. Chem. Soc. 124, 5270–5271. Web of Science CSD CrossRef PubMed CAS Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar

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