N-Cyclo-hexyl-4-meth-yl-N-propyl-benzene-sulfonamide.

The title compound, C(16)H(25)NO(2)S, is a sulfonamide derivative with the substitution of propyl and cyclo-hexyl groups at the N atom. The least-squares plane through all six C atoms of the cyclo-hexyl ring forms a dihedral angle of 58.88 (12)° with the toluene ring. No hydrogen-bonding inter-actions are present in the crystal structure.

Related literature

For the synthesis and related structures, see: Haider et al. (2009 ▶, 2010 ▶).

Experimental

Crystal data

C16H25NO2S

M = 295.43

Monoclinic,

a = 7.8207 (5) Å

b = 25.2915 (16) Å

c = 8.3135 (6) Å

β = 102.411 (3)°

V = 1605.96 (19) Å3

Z = 4

Mo Kα radiation

μ = 0.20 mm−1

T = 296 K

0.16 × 0.08 × 0.06 mm

Data collection

Bruker Kappa APEXII CCD diffractometer

Absorption correction: multi-scan (SADABS; Bruker, 2007 ▶) T min = 0.980, T max = 0.988

12946 measured reflections

3004 independent reflections

1271 reflections with I > 2σ(I)

R int = 0.124

Refinement

R[F 2 > 2σ(F 2)] = 0.062

wR(F 2) = 0.128

S = 0.90

3003 reflections

183 parameters

H-atom parameters constrained

Δρmax = 0.17 e Å−3

Δρmin = −0.23 e Å−3

Data collection: APEX2 (Bruker, 2007 ▶); cell refinement: SAINT (Bruker, 2007 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997 ▶) and PLATON (Spek, 2009 ▶); software used to prepare material for publication: WinGX (Farrugia, 1999 ▶) and PLATON.

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536810006756/om2321sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536810006756/om2321Isup2.hkl

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

C16H25NO2S	F(000) = 640
Mr = 295.43	Dx = 1.222 Mg m−3
Monoclinic, P21/n	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2yn	Cell parameters from 856 reflections
a = 7.8207 (5) Å	θ = 2.6–17.1°
b = 25.2915 (16) Å	µ = 0.20 mm−1
c = 8.3135 (6) Å	T = 296 K
β = 102.411 (3)°	Needle, colorless
V = 1605.96 (19) Å3	0.16 × 0.08 × 0.06 mm
Z = 4

Bruker Kappa APEXII CCD diffractometer	3004 independent reflections
Radiation source: fine-focus sealed tube	1271 reflections with I > 2σ(I)
graphite	Rint = 0.124
φ and ω scans	θmax = 25.6°, θmin = 1.6°
Absorption correction: multi-scan (SADABS; Bruker, 2007)	h = −9→9
Tmin = 0.980, Tmax = 0.988	k = −30→30
12946 measured reflections	l = −8→10

Refinement on F2	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.062	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.128	H-atom parameters constrained
S = 0.90	w = 1/[σ2(Fo2) + (0.0333P)2 + 0.8827P] where P = (Fo2 + 2Fc2)/3
3003 reflections	(Δ/σ)max < 0.001
183 parameters	Δρmax = 0.17 e Å−3
0 restraints	Δρmin = −0.23 e Å−3

Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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 > 2σ(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.

	x	y	z	Uiso*/Ueq	Occ. (<1)
S1	−0.12769 (14)	0.12574 (4)	0.82665 (13)	0.0507 (3)
O1	−0.1615 (4)	0.15917 (11)	0.9551 (3)	0.0687 (9)
O2	−0.2485 (3)	0.08478 (11)	0.7610 (3)	0.0626 (8)
N1	0.0618 (4)	0.09828 (12)	0.8964 (4)	0.0444 (8)
C1	−0.1095 (5)	0.16743 (15)	0.6605 (5)	0.0410 (10)
C2	−0.0304 (5)	0.21596 (16)	0.6879 (5)	0.0570 (12)
H2	0.0079	0.2283	0.7950	0.068*
C3	−0.0076 (5)	0.24655 (16)	0.5559 (6)	0.0583 (12)
H3	0.0477	0.2792	0.5761	0.070*
C4	−0.0647 (5)	0.22991 (16)	0.3951 (5)	0.0475 (11)
C5	−0.1461 (5)	0.18147 (16)	0.3710 (5)	0.0510 (11)
H5	−0.1880	0.1695	0.2639	0.061*
C6	−0.1676 (5)	0.14986 (15)	0.5021 (5)	0.0464 (11)
H6	−0.2211	0.1170	0.4824	0.056*
C7	0.1201 (5)	0.05534 (15)	0.7993 (5)	0.0479 (11)
H7	0.0146	0.0388	0.7337	0.058*
C8	0.2179 (5)	0.01308 (14)	0.9125 (5)	0.0559 (12)
H8A	0.1448	0.0002	0.9847	0.067*
H8B	0.3230	0.0282	0.9804	0.067*
C9	0.2676 (6)	−0.03285 (16)	0.8126 (6)	0.0709 (14)
H9A	0.3344	−0.0587	0.8867	0.085*
H9B	0.1620	−0.0500	0.7525	0.085*
C10	0.3749 (6)	−0.01397 (16)	0.6925 (5)	0.0611 (13)
H10A	0.3995	−0.0436	0.6269	0.073*
H10B	0.4857	0.0000	0.7531	0.073*
C11	0.2786 (6)	0.02856 (18)	0.5800 (5)	0.0739 (14)
H11A	0.1737	0.0137	0.5110	0.089*
H11B	0.3526	0.0416	0.5089	0.089*
C12	0.2289 (6)	0.07402 (16)	0.6810 (5)	0.0654 (13)
H12A	0.3346	0.0908	0.7423	0.078*
H12B	0.1635	0.1002	0.6073	0.078*
C13	−0.0380 (6)	0.26366 (17)	0.2532 (5)	0.0729 (14)
H13A	0.0274	0.2947	0.2949	0.109*	0.50
H13B	−0.1497	0.2739	0.1878	0.109*	0.50
H13C	0.0254	0.2439	0.1865	0.109*	0.50
H13D	−0.0920	0.2470	0.1512	0.109*	0.50
H13E	0.0851	0.2678	0.2583	0.109*	0.50
H13F	−0.0900	0.2978	0.2597	0.109*	0.50
C14	0.1931 (5)	0.12873 (15)	1.0130 (4)	0.0508 (11)
H14A	0.1650	0.1660	0.9987	0.061*
H14B	0.3067	0.1233	0.9866	0.061*
C15	0.2050 (5)	0.11426 (15)	1.1910 (5)	0.0560 (12)
H15A	0.2365	0.0772	1.2070	0.067*
H15B	0.0913	0.1191	1.2179	0.067*
C16	0.3390 (6)	0.14751 (16)	1.3061 (5)	0.0729 (14)
H16A	0.4510	0.1438	1.2774	0.109*
H16B	0.3473	0.1359	1.4174	0.109*
H16C	0.3038	0.1839	1.2965	0.109*

	U11	U22	U33	U12	U13	U23
S1	0.0461 (7)	0.0630 (7)	0.0445 (7)	0.0111 (7)	0.0127 (5)	0.0063 (6)
O1	0.076 (2)	0.086 (2)	0.050 (2)	0.0307 (17)	0.0248 (16)	−0.0003 (16)
O2	0.0441 (18)	0.072 (2)	0.071 (2)	−0.0052 (16)	0.0099 (15)	0.0123 (16)
N1	0.042 (2)	0.053 (2)	0.036 (2)	0.0063 (17)	0.0035 (16)	0.0006 (16)
C1	0.041 (3)	0.044 (2)	0.038 (3)	0.005 (2)	0.006 (2)	−0.004 (2)
C2	0.067 (3)	0.054 (3)	0.044 (3)	0.002 (2)	−0.002 (2)	−0.013 (2)
C3	0.066 (3)	0.042 (3)	0.061 (3)	−0.007 (2)	0.002 (3)	−0.002 (2)
C4	0.042 (3)	0.051 (3)	0.048 (3)	0.006 (2)	0.007 (2)	0.007 (2)
C5	0.059 (3)	0.054 (3)	0.036 (3)	0.003 (2)	0.002 (2)	−0.001 (2)
C6	0.047 (3)	0.044 (2)	0.045 (3)	−0.005 (2)	0.004 (2)	−0.004 (2)
C7	0.044 (3)	0.060 (3)	0.041 (3)	0.004 (2)	0.010 (2)	0.000 (2)
C8	0.063 (3)	0.053 (3)	0.058 (3)	0.004 (2)	0.027 (2)	0.013 (2)
C9	0.073 (4)	0.052 (3)	0.097 (4)	0.005 (3)	0.040 (3)	0.000 (3)
C10	0.056 (3)	0.058 (3)	0.073 (3)	0.002 (2)	0.024 (3)	−0.009 (2)
C11	0.070 (4)	0.100 (4)	0.057 (3)	0.019 (3)	0.026 (3)	0.002 (3)
C12	0.072 (3)	0.073 (3)	0.058 (3)	0.026 (3)	0.028 (3)	0.023 (2)
C13	0.074 (3)	0.075 (3)	0.070 (3)	−0.007 (3)	0.016 (3)	0.016 (3)
C14	0.052 (3)	0.054 (3)	0.046 (3)	0.006 (2)	0.007 (2)	0.004 (2)
C15	0.060 (3)	0.064 (3)	0.043 (3)	−0.003 (2)	0.008 (2)	0.002 (2)
C16	0.089 (4)	0.075 (3)	0.048 (3)	−0.011 (3)	−0.001 (3)	0.004 (2)

S1—O2	1.429 (3)	C9—H9B	0.9700
S1—O1	1.430 (3)	C10—C11	1.516 (5)
S1—N1	1.627 (3)	C10—H10A	0.9700
S1—C1	1.767 (4)	C10—H10B	0.9700
N1—C14	1.469 (4)	C11—C12	1.522 (5)
N1—C7	1.482 (4)	C11—H11A	0.9700
C1—C2	1.371 (5)	C11—H11B	0.9700
C1—C6	1.372 (5)	C12—H12A	0.9700
C2—C3	1.385 (5)	C12—H12B	0.9700
C2—H2	0.9300	C13—H13A	0.9600
C3—C4	1.381 (5)	C13—H13B	0.9600
C3—H3	0.9300	C13—H13C	0.9600
C4—C5	1.375 (5)	C13—H13D	0.9600
C4—C13	1.507 (5)	C13—H13E	0.9600
C5—C6	1.391 (5)	C13—H13F	0.9600
C5—H5	0.9300	C14—C15	1.507 (5)
C6—H6	0.9300	C14—H14A	0.9700
C7—C12	1.508 (5)	C14—H14B	0.9700
C7—C8	1.518 (5)	C15—C16	1.513 (5)
C7—H7	0.9800	C15—H15A	0.9700
C8—C9	1.526 (5)	C15—H15B	0.9700
C8—H8A	0.9700	C16—H16A	0.9600
C8—H8B	0.9700	C16—H16B	0.9600
C9—C10	1.513 (5)	C16—H16C	0.9600
C9—H9A	0.9700
O2—S1—O1	120.02 (18)	C10—C11—C12	110.3 (4)
O2—S1—N1	107.69 (17)	C10—C11—H11A	109.6
O1—S1—N1	106.65 (17)	C12—C11—H11A	109.6
O2—S1—C1	106.95 (18)	C10—C11—H11B	109.6
O1—S1—C1	106.83 (18)	C12—C11—H11B	109.6
N1—S1—C1	108.25 (16)	H11A—C11—H11B	108.1
C14—N1—C7	119.4 (3)	C7—C12—C11	111.7 (4)
C14—N1—S1	117.7 (2)	C7—C12—H12A	109.3
C7—N1—S1	118.8 (3)	C11—C12—H12A	109.3
C2—C1—C6	119.6 (4)	C7—C12—H12B	109.3
C2—C1—S1	120.9 (3)	C11—C12—H12B	109.3
C6—C1—S1	119.4 (3)	H12A—C12—H12B	107.9
C1—C2—C3	119.9 (4)	C4—C13—H13A	109.5
C1—C2—H2	120.0	C4—C13—H13B	109.5
C3—C2—H2	120.0	H13A—C13—H13B	109.5
C4—C3—C2	121.8 (4)	C4—C13—H13C	109.5
C4—C3—H3	119.1	H13A—C13—H13C	109.5
C2—C3—H3	119.1	H13B—C13—H13C	109.5
C5—C4—C3	117.1 (4)	C4—C13—H13D	109.5
C5—C4—C13	121.9 (4)	H13A—C13—H13D	141.1
C3—C4—C13	121.0 (4)	H13B—C13—H13D	56.3
C4—C5—C6	121.8 (4)	H13C—C13—H13D	56.3
C4—C5—H5	119.1	C4—C13—H13E	109.5
C6—C5—H5	119.1	H13A—C13—H13E	56.3
C1—C6—C5	119.7 (4)	H13B—C13—H13E	141.1
C1—C6—H6	120.1	H13C—C13—H13E	56.3
C5—C6—H6	120.1	H13D—C13—H13E	109.5
N1—C7—C12	114.1 (3)	C4—C13—H13F	109.5
N1—C7—C8	110.6 (3)	H13A—C13—H13F	56.3
C12—C7—C8	110.2 (3)	H13B—C13—H13F	56.3
N1—C7—H7	107.2	H13C—C13—H13F	141.1
C12—C7—H7	107.2	H13D—C13—H13F	109.5
C8—C7—H7	107.2	H13E—C13—H13F	109.5
C7—C8—C9	110.6 (3)	N1—C14—C15	114.1 (3)
C7—C8—H8A	109.5	N1—C14—H14A	108.7
C9—C8—H8A	109.5	C15—C14—H14A	108.7
C7—C8—H8B	109.5	N1—C14—H14B	108.7
C9—C8—H8B	109.5	C15—C14—H14B	108.7
H8A—C8—H8B	108.1	H14A—C14—H14B	107.6
C10—C9—C8	111.2 (3)	C14—C15—C16	112.0 (3)
C10—C9—H9A	109.4	C14—C15—H15A	109.2
C8—C9—H9A	109.4	C16—C15—H15A	109.2
C10—C9—H9B	109.4	C14—C15—H15B	109.2
C8—C9—H9B	109.4	C16—C15—H15B	109.2
H9A—C9—H9B	108.0	H15A—C15—H15B	107.9
C9—C10—C11	111.0 (3)	C15—C16—H16A	109.5
C9—C10—H10A	109.4	C15—C16—H16B	109.5
C11—C10—H10A	109.4	H16A—C16—H16B	109.5
C9—C10—H10B	109.4	C15—C16—H16C	109.5
C11—C10—H10B	109.4	H16A—C16—H16C	109.5
H10A—C10—H10B	108.0	H16B—C16—H16C	109.5
O2—S1—N1—C14	−161.9 (3)	C2—C1—C6—C5	−0.2 (6)
O1—S1—N1—C14	−31.8 (3)	S1—C1—C6—C5	−177.0 (3)
C1—S1—N1—C14	82.8 (3)	C4—C5—C6—C1	1.2 (6)
O2—S1—N1—C7	41.0 (3)	C14—N1—C7—C12	−64.2 (5)
O1—S1—N1—C7	171.1 (3)	S1—N1—C7—C12	92.5 (4)
C1—S1—N1—C7	−74.3 (3)	C14—N1—C7—C8	60.7 (4)
O2—S1—C1—C2	167.1 (3)	S1—N1—C7—C8	−142.6 (3)
O1—S1—C1—C2	37.4 (4)	N1—C7—C8—C9	176.3 (3)
N1—S1—C1—C2	−77.1 (3)	C12—C7—C8—C9	−56.6 (5)
O2—S1—C1—C6	−16.1 (3)	C7—C8—C9—C10	56.6 (5)
O1—S1—C1—C6	−145.8 (3)	C8—C9—C10—C11	−56.2 (5)
N1—S1—C1—C6	99.7 (3)	C9—C10—C11—C12	55.7 (5)
C6—C1—C2—C3	−0.9 (6)	N1—C7—C12—C11	−177.7 (3)
S1—C1—C2—C3	175.9 (3)	C8—C7—C12—C11	57.2 (5)
C1—C2—C3—C4	0.9 (6)	C10—C11—C12—C7	−56.7 (5)
C2—C3—C4—C5	0.1 (6)	C7—N1—C14—C15	−104.2 (4)
C2—C3—C4—C13	−179.7 (4)	S1—N1—C14—C15	98.8 (3)
C3—C4—C5—C6	−1.2 (6)	N1—C14—C15—C16	−178.8 (3)
C13—C4—C5—C6	178.7 (4)