4,6-Dimeth­oxy-2-(methyl­sulfon­yl)pyrimidine

Fun, H.-K.; Yeap, C.S.; Rai, S.; Isloor, A.M.; Shetty, P.

doi:10.1107/S1600536810025067

4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine

H.-K. Fun, C. S. Yeap, S. Rai, A. M. Isloor and P. Shetty

The asymmetric unit of the title compound, C₇H₁₀N₂O₄S, comprises of two independent molecules (A and B) which differ in the orientation of the methylsulfonyl group [C—S—C—N = 157.98 (13)° in molecule A and 6.09 (18)° in molecule B]. In the crystal structure, molecules of type A are linked into chains along the a axis by intermolecular C—H

O hydrogen bonds. The B molecules are linked to these chains by C—H

O hydrogen bonds.

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Supporting information

	Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536810025067/ci5121sup1.cif Contains datablocks global, I
	Structure factor file (CIF format) https://doi.org/10.1107/S1600536810025067/ci5121Isup2.hkl Contains datablock I

CCDC reference: 788319

checkCIF report

Key indicators

Single-crystal X-ray study
T = 296 K
Mean (C-C) = 0.003 Å
R factor = 0.044
wR factor = 0.156
Data-to-parameter ratio = 27.3

checkCIF/PLATON results

No syntax errors found



Alert level C
PLAT242_ALERT_2_C Check Low       Ueq as Compared to Neighbors for        S1B
PLAT250_ALERT_2_C Large U3/U1 Ratio for Average U(i,j) Tensor ....       2.12
PLAT911_ALERT_3_C Missing # FCF Refl Between THmin & STh/L=  0.600         26
PLAT912_ALERT_4_C Missing # of FCF Reflections Above STh/L=  0.600         59

Alert level G
PLAT960_ALERT_3_G Number of Intensities with I .LT. - 2*sig(I) ..           8
PLAT154_ALERT_1_G The su's on the Cell Angles are Equal  (x 10000)        800 Deg.
PLAT720_ALERT_4_G Number of Unusual/Non-Standard Labels ..........         20

   0 ALERT level A = In general: serious problem
   0 ALERT level B = Potentially serious problem
   4 ALERT level C = Check and explain
   3 ALERT level G = General alerts; check

   1 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
   2 ALERT type 2 Indicator that the structure model may be wrong or deficient
   2 ALERT type 3 Indicator that the structure quality may be low
   2 ALERT type 4 Improvement, methodology, query or suggestion
   0 ALERT type 5 Informative message, check

Comment top

Compounds containing 4,6-dimethoxypyrimidin-2-yl moieties display excellent herbicidal activity (Xi et al., 2006). Most sulfonylurea herbicides and all pyrimidinylbenzoate herbicides (He et al., 2007), such as nicofulfuron, amidosulfuron, halopyrazosulfuron, ethoxysulfuron, pyriminobac-methyl and pyriftalid, possess 4,6-dimethoxypyrimidin-2-yl groups (Li et al., 2006), while sulfometuron-methyl, a kind of sulfonylurea, contains a 4,6-dimethylpyrimidin-2-yl group, which suggests that the two disubstituted pyrimidin- 2-yl groups possess high biological activity (Gerorge, 1983).

There are two molecules, A and B, in the asymmetric unit (Fig. 1) of the title compound. The molecules A and B differ in the orientation of the methylsulfonyl group [C7A—S1A—C1A—N1A = 157.98 (13)° and C7B—S1B—C1B—N2B = 6.09 (18)°]

In the crystal structure, the A molecules are linked into chains along a axis by intermolecular C3A—H3AA···O2A and C7A—H7AA···O4A hydrogen bonds. The B molecules are linked to these chains by intermolecular C5A—H5AC···O2B hydrogen bonds.

Related literature top

For general background and applications of 4,6-dimethoxypyrimidin-2-yl derivatives, see: Xi et al. (2006); He et al. (2007); Li et al. (2006); Gerorge (1983).

Experimental top

Periodic acid (2.63 mmol, 600 mg) was dissolved in acetonitrile (6 ml) by stirring at room temperature for 1 h. To this solution, chromium trioxide (0.125 mmol, 12.5 mg) was added and stirred for 5 min to give a clear orange solution. H₅IO₆/CrO₃ solution (1.7 ml) was added to a solution of 4,6-dimethoxy-2-methylmercaptopyrimidine (0.23 mmol) in ethyl acetate and was stirred at room temperature for 30 min. The reaction mixture was quenched with saturated sodium sulphite and was loaded on to a silica column. The column was eluted with acetone to obtain 4,6-dimethoxy-2-methylsulfonylpyrimidine. Single crystals were recrystallized from an dichloromethane solution (yield: 87%, m.p. 402–405 K).

Structure description top

For general background and applications of 4,6-dimethoxypyrimidin-2-yl derivatives, see: Xi et al. (2006); He et al. (2007); Li et al. (2006); Gerorge (1983).

Computing details top

Data collection: APEX2 (Bruker, 2009); cell refinement: SAINT (Bruker, 2009); data reduction: SAINT (Bruker, 2009); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).

Figures top

	Fig. 1. The two independent molecules of the title compound with atom labels and 30% probability displacement ellipsoids for non-H atoms.
	Fig. 2. The crystal packing of title compound, viewed down the b axis showing chains along the a axis.

4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine top

Crystal data top

C₇H₁₀N₂O₄S	Z = 4
M_r = 218.23	F(000) = 456
Triclinic, P1	D_x = 1.470 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 8.349 (2) Å	Cell parameters from 8362 reflections
b = 11.067 (3) Å	θ = 2.2–32.1°
c = 11.438 (3) Å	µ = 0.32 mm⁻¹
α = 108.457 (8)°	T = 296 K
β = 92.774 (8)°	Plate, colourless
γ = 98.504 (8)°	0.38 × 0.30 × 0.08 mm
V = 986.4 (4) Å³

Data collection top

Bruker APEXII DUO CCD area-detector diffractometer	7063 independent reflections
Radiation source: fine-focus sealed tube	4866 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.042
φ and ω scans	θ_max = 32.5°, θ_min = 1.9°
Absorption correction: multi-scan (SADABS; Bruker, 2009)	h = −12→12
T_min = 0.889, T_max = 0.974	k = −16→16
29277 measured reflections	l = −17→16

Refinement top

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)] = 0.044	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.156	H-atom parameters constrained
S = 1.08	w = 1/[σ²(F_o²) + (0.0771P)² + 0.1962P] where P = (F_o² + 2F_c²)/3
7063 reflections	(Δ/σ)_max = 0.001
259 parameters	Δρ_max = 0.50 e Å⁻³
0 restraints	Δρ_min = −0.50 e Å⁻³

Crystal data top

C₇H₁₀N₂O₄S	γ = 98.504 (8)°
M_r = 218.23	V = 986.4 (4) Å³
Triclinic, P1	Z = 4
a = 8.349 (2) Å	Mo Kα radiation
b = 11.067 (3) Å	µ = 0.32 mm⁻¹
c = 11.438 (3) Å	T = 296 K
α = 108.457 (8)°	0.38 × 0.30 × 0.08 mm
β = 92.774 (8)°

Data collection top

Bruker APEXII DUO CCD area-detector diffractometer	7063 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2009)	4866 reflections with I > 2σ(I)
T_min = 0.889, T_max = 0.974	R_int = 0.042
29277 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.044	0 restraints
wR(F²) = 0.156	H-atom parameters constrained
S = 1.08	Δρ_max = 0.50 e Å⁻³
7063 reflections	Δρ_min = −0.50 e Å⁻³
259 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
S1A	−0.01034 (4)	0.04422 (4)	0.19330 (4)	0.03856 (12)
O1A	−0.02361 (19)	0.10070 (16)	0.32304 (15)	0.0632 (4)
O2A	−0.08995 (15)	0.09457 (13)	0.10934 (15)	0.0518 (3)
O3A	0.50597 (16)	0.29863 (13)	0.14202 (15)	0.0528 (3)
O4A	0.51835 (16)	−0.11116 (13)	0.16945 (16)	0.0543 (3)
N1A	0.26662 (16)	0.17382 (13)	0.16027 (13)	0.0362 (3)
N2A	0.27464 (15)	−0.03547 (13)	0.17789 (13)	0.0364 (3)
C1A	0.20400 (17)	0.06224 (14)	0.17287 (14)	0.0334 (3)
C2A	0.43408 (19)	−0.01755 (16)	0.16718 (16)	0.0386 (3)
C3A	0.51867 (19)	0.09495 (18)	0.15559 (17)	0.0435 (4)
H3AA	0.6304	0.1068	0.1502	0.052*
C4A	0.42742 (19)	0.18858 (16)	0.15246 (15)	0.0378 (3)
C5A	0.4131 (3)	0.3951 (2)	0.1326 (3)	0.0608 (5)
H5AA	0.4838	0.4653	0.1194	0.091*
H5AB	0.3635	0.4268	0.2078	0.091*
H5AC	0.3300	0.3577	0.0642	0.091*
C6A	0.4289 (3)	−0.2300 (2)	0.1768 (3)	0.0630 (6)
H6AA	0.5032	−0.2872	0.1814	0.095*
H6AB	0.3525	−0.2704	0.1045	0.095*
H6AC	0.3714	−0.2116	0.2494	0.095*
C7A	−0.0758 (2)	−0.12239 (17)	0.1485 (2)	0.0476 (4)
H7AA	−0.1909	−0.1400	0.1536	0.071*
H7AB	−0.0197	−0.1571	0.2024	0.071*
H7AC	−0.0529	−0.1618	0.0648	0.071*
S1B	0.91824 (6)	0.54889 (4)	0.18573 (4)	0.04122 (12)
O1B	1.0732 (2)	0.63051 (15)	0.21079 (16)	0.0655 (4)
O2B	0.8041 (2)	0.56321 (17)	0.09628 (13)	0.0639 (4)
O3B	0.7212 (2)	0.42513 (15)	0.54172 (14)	0.0673 (5)
O4B	0.6688 (2)	0.83263 (14)	0.52687 (15)	0.0629 (4)
N1B	0.78624 (19)	0.69578 (14)	0.36974 (14)	0.0437 (3)
N2B	0.81160 (19)	0.48548 (14)	0.37722 (13)	0.0414 (3)
C1B	0.8263 (2)	0.57971 (16)	0.32927 (15)	0.0382 (3)
C2B	0.7173 (2)	0.71868 (18)	0.47615 (17)	0.0471 (4)
C3B	0.6896 (3)	0.6287 (2)	0.53590 (18)	0.0574 (5)
H3BA	0.6383	0.6454	0.6084	0.069*
C4B	0.7415 (3)	0.51237 (18)	0.48331 (17)	0.0479 (4)
C5B	0.7711 (4)	0.3023 (2)	0.4853 (2)	0.0658 (6)
H5BA	0.7710	0.2564	0.5438	0.099*
H5BB	0.8787	0.3163	0.4607	0.099*
H5BC	0.6967	0.2525	0.4138	0.099*
C6B	0.7263 (4)	0.9364 (2)	0.4804 (2)	0.0717 (7)
H6BA	0.7075	1.0168	0.5370	0.108*
H6BB	0.6689	0.9210	0.4009	0.108*
H6BC	0.8408	0.9406	0.4725	0.108*
C7B	0.9425 (3)	0.38667 (19)	0.1441 (2)	0.0596 (6)
H7BA	0.9860	0.3620	0.0655	0.089*
H7BB	0.8389	0.3332	0.1384	0.089*
H7BC	1.0160	0.3758	0.2058	0.089*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1A	0.02471 (18)	0.03529 (19)	0.0583 (3)	0.00757 (13)	0.01261 (15)	0.01667 (17)
O1A	0.0498 (8)	0.0687 (9)	0.0636 (9)	0.0117 (7)	0.0238 (7)	0.0079 (7)
O2A	0.0291 (6)	0.0482 (7)	0.0888 (10)	0.0116 (5)	0.0074 (6)	0.0351 (7)
O3A	0.0338 (6)	0.0503 (7)	0.0794 (10)	−0.0034 (5)	0.0040 (6)	0.0332 (7)
O4A	0.0313 (6)	0.0516 (7)	0.0890 (10)	0.0153 (5)	0.0114 (6)	0.0311 (7)
N1A	0.0264 (6)	0.0368 (6)	0.0450 (7)	0.0026 (5)	0.0036 (5)	0.0143 (5)
N2A	0.0255 (6)	0.0385 (6)	0.0472 (7)	0.0077 (5)	0.0063 (5)	0.0156 (6)
C1A	0.0226 (6)	0.0364 (7)	0.0410 (8)	0.0041 (5)	0.0052 (5)	0.0126 (6)
C2A	0.0265 (7)	0.0440 (8)	0.0473 (9)	0.0093 (6)	0.0055 (6)	0.0159 (7)
C3A	0.0235 (7)	0.0518 (9)	0.0575 (10)	0.0048 (6)	0.0060 (6)	0.0216 (8)
C4A	0.0283 (7)	0.0419 (8)	0.0433 (8)	0.0003 (6)	0.0034 (6)	0.0167 (6)
C5A	0.0500 (11)	0.0536 (11)	0.0890 (16)	0.0007 (9)	0.0077 (10)	0.0411 (11)
C6A	0.0476 (11)	0.0511 (11)	0.1001 (18)	0.0169 (9)	0.0138 (11)	0.0339 (11)
C7A	0.0319 (8)	0.0385 (8)	0.0761 (13)	0.0027 (6)	0.0102 (8)	0.0249 (8)
S1B	0.0485 (2)	0.0379 (2)	0.0431 (2)	0.01011 (16)	0.01501 (17)	0.01859 (16)
O1B	0.0583 (9)	0.0610 (9)	0.0768 (10)	−0.0036 (7)	0.0250 (8)	0.0258 (8)
O2B	0.0830 (12)	0.0751 (10)	0.0444 (7)	0.0300 (9)	0.0083 (7)	0.0269 (7)
O3B	0.1028 (14)	0.0552 (8)	0.0543 (8)	0.0157 (8)	0.0304 (8)	0.0283 (7)
O4B	0.0800 (11)	0.0481 (8)	0.0605 (9)	0.0220 (7)	0.0250 (8)	0.0102 (7)
N1B	0.0480 (8)	0.0403 (7)	0.0440 (8)	0.0111 (6)	0.0096 (6)	0.0132 (6)
N2B	0.0465 (8)	0.0401 (7)	0.0396 (7)	0.0060 (6)	0.0089 (6)	0.0160 (6)
C1B	0.0382 (8)	0.0395 (8)	0.0376 (8)	0.0067 (6)	0.0064 (6)	0.0134 (6)
C2B	0.0506 (10)	0.0433 (9)	0.0442 (9)	0.0100 (7)	0.0103 (7)	0.0084 (7)
C3B	0.0775 (15)	0.0518 (11)	0.0430 (10)	0.0119 (10)	0.0243 (9)	0.0126 (8)
C4B	0.0593 (11)	0.0450 (9)	0.0394 (9)	0.0040 (8)	0.0115 (8)	0.0151 (7)
C5B	0.0955 (19)	0.0489 (11)	0.0579 (13)	0.0094 (11)	0.0111 (12)	0.0255 (10)
C6B	0.104 (2)	0.0477 (11)	0.0687 (14)	0.0285 (12)	0.0197 (13)	0.0182 (10)
C7B	0.0803 (15)	0.0423 (10)	0.0653 (13)	0.0231 (9)	0.0347 (11)	0.0206 (9)

Geometric parameters (Å, º) top

S1A—O1A	1.4334 (16)	S1B—O1B	1.4234 (16)
S1A—O2A	1.4356 (14)	S1B—O2B	1.4260 (16)
S1A—C7A	1.7429 (18)	S1B—C7B	1.751 (2)
S1A—C1A	1.8059 (15)	S1B—C1B	1.8018 (17)
O3A—C4A	1.338 (2)	O3B—C4B	1.333 (2)
O3A—C5A	1.436 (3)	O3B—C5B	1.441 (3)
O4A—C2A	1.342 (2)	O4B—C2B	1.342 (2)
O4A—C6A	1.443 (2)	O4B—C6B	1.442 (3)
N1A—C1A	1.322 (2)	N1B—C1B	1.320 (2)
N1A—C4A	1.339 (2)	N1B—C2B	1.339 (2)
N2A—C1A	1.321 (2)	N2B—C1B	1.317 (2)
N2A—C2A	1.334 (2)	N2B—C4B	1.340 (2)
C2A—C3A	1.386 (2)	C2B—C3B	1.375 (3)
C3A—C4A	1.382 (2)	C3B—C4B	1.381 (3)
C3A—H3AA	0.93	C3B—H3BA	0.93
C5A—H5AA	0.96	C5B—H5BA	0.96
C5A—H5AB	0.96	C5B—H5BB	0.96
C5A—H5AC	0.96	C5B—H5BC	0.96
C6A—H6AA	0.96	C6B—H6BA	0.96
C6A—H6AB	0.96	C6B—H6BB	0.96
C6A—H6AC	0.96	C6B—H6BC	0.96
C7A—H7AA	0.96	C7B—H7BA	0.96
C7A—H7AB	0.96	C7B—H7BB	0.96
C7A—H7AC	0.96	C7B—H7BC	0.96

O1A—S1A—O2A	117.87 (10)	O1B—S1B—O2B	117.30 (11)
O1A—S1A—C7A	109.37 (10)	O1B—S1B—C7B	110.02 (12)
O2A—S1A—C7A	109.13 (9)	O2B—S1B—C7B	109.13 (12)
O1A—S1A—C1A	107.07 (8)	O1B—S1B—C1B	107.47 (9)
O2A—S1A—C1A	108.07 (8)	O2B—S1B—C1B	107.25 (9)
C7A—S1A—C1A	104.49 (8)	C7B—S1B—C1B	104.92 (9)
C4A—O3A—C5A	118.66 (14)	C4B—O3B—C5B	118.20 (16)
C2A—O4A—C6A	117.66 (14)	C2B—O4B—C6B	117.81 (17)
C1A—N1A—C4A	113.74 (14)	C1B—N1B—C2B	113.47 (15)
C1A—N2A—C2A	113.88 (14)	C1B—N2B—C4B	113.85 (15)
N2A—C1A—N1A	130.25 (14)	N2B—C1B—N1B	130.63 (16)
N2A—C1A—S1A	115.13 (11)	N2B—C1B—S1B	115.98 (12)
N1A—C1A—S1A	114.55 (11)	N1B—C1B—S1B	113.38 (13)
N2A—C2A—O4A	119.16 (15)	N1B—C2B—O4B	119.64 (18)
N2A—C2A—C3A	123.00 (15)	N1B—C2B—C3B	122.83 (17)
O4A—C2A—C3A	117.83 (15)	O4B—C2B—C3B	117.51 (17)
C4A—C3A—C2A	116.11 (15)	C2B—C3B—C4B	116.88 (17)
C4A—C3A—H3AA	121.9	C2B—C3B—H3BA	121.6
C2A—C3A—H3AA	121.9	C4B—C3B—H3BA	121.6
O3A—C4A—N1A	119.54 (15)	O3B—C4B—N2B	119.62 (17)
O3A—C4A—C3A	117.47 (15)	O3B—C4B—C3B	118.09 (17)
N1A—C4A—C3A	122.99 (15)	N2B—C4B—C3B	122.29 (17)
O3A—C5A—H5AA	109.5	O3B—C5B—H5BA	109.5
O3A—C5A—H5AB	109.5	O3B—C5B—H5BB	109.5
H5AA—C5A—H5AB	109.5	H5BA—C5B—H5BB	109.5
O3A—C5A—H5AC	109.5	O3B—C5B—H5BC	109.5
H5AA—C5A—H5AC	109.5	H5BA—C5B—H5BC	109.5
H5AB—C5A—H5AC	109.5	H5BB—C5B—H5BC	109.5
O4A—C6A—H6AA	109.5	O4B—C6B—H6BA	109.5
O4A—C6A—H6AB	109.5	O4B—C6B—H6BB	109.5
H6AA—C6A—H6AB	109.5	H6BA—C6B—H6BB	109.5
O4A—C6A—H6AC	109.5	O4B—C6B—H6BC	109.5
H6AA—C6A—H6AC	109.5	H6BA—C6B—H6BC	109.5
H6AB—C6A—H6AC	109.5	H6BB—C6B—H6BC	109.5
S1A—C7A—H7AA	109.5	S1B—C7B—H7BA	109.5
S1A—C7A—H7AB	109.5	S1B—C7B—H7BB	109.5
H7AA—C7A—H7AB	109.5	H7BA—C7B—H7BB	109.5
S1A—C7A—H7AC	109.5	S1B—C7B—H7BC	109.5
H7AA—C7A—H7AC	109.5	H7BA—C7B—H7BC	109.5
H7AB—C7A—H7AC	109.5	H7BB—C7B—H7BC	109.5

C2A—N2A—C1A—N1A	−0.7 (3)	C4B—N2B—C1B—N1B	1.4 (3)
C2A—N2A—C1A—S1A	−177.62 (12)	C4B—N2B—C1B—S1B	−179.50 (13)
C4A—N1A—C1A—N2A	−0.6 (3)	C2B—N1B—C1B—N2B	−1.2 (3)
C4A—N1A—C1A—S1A	176.33 (12)	C2B—N1B—C1B—S1B	179.75 (13)
O1A—S1A—C1A—N2A	91.31 (14)	O1B—S1B—C1B—N2B	−110.99 (15)
O2A—S1A—C1A—N2A	−140.77 (13)	O2B—S1B—C1B—N2B	122.06 (15)
C7A—S1A—C1A—N2A	−24.64 (15)	C7B—S1B—C1B—N2B	6.09 (18)
O1A—S1A—C1A—N1A	−86.07 (14)	O1B—S1B—C1B—N1B	68.23 (16)
O2A—S1A—C1A—N1A	41.86 (14)	O2B—S1B—C1B—N1B	−58.72 (16)
C7A—S1A—C1A—N1A	157.98 (13)	C7B—S1B—C1B—N1B	−174.69 (15)
C1A—N2A—C2A—O4A	−179.19 (16)	C1B—N1B—C2B—O4B	−179.21 (18)
C1A—N2A—C2A—C3A	1.8 (2)	C1B—N1B—C2B—C3B	−0.8 (3)
C6A—O4A—C2A—N2A	3.3 (3)	C6B—O4B—C2B—N1B	−14.0 (3)
C6A—O4A—C2A—C3A	−177.70 (18)	C6B—O4B—C2B—C3B	167.5 (2)
N2A—C2A—C3A—C4A	−1.6 (3)	N1B—C2B—C3B—C4B	2.1 (3)
O4A—C2A—C3A—C4A	179.42 (16)	O4B—C2B—C3B—C4B	−179.4 (2)
C5A—O3A—C4A—N1A	−3.4 (3)	C5B—O3B—C4B—N2B	−2.2 (3)
C5A—O3A—C4A—C3A	177.06 (19)	C5B—O3B—C4B—C3B	178.3 (2)
C1A—N1A—C4A—O3A	−178.65 (15)	C1B—N2B—C4B—O3B	−179.31 (19)
C1A—N1A—C4A—C3A	0.8 (2)	C1B—N2B—C4B—C3B	0.2 (3)
C2A—C3A—C4A—O3A	179.63 (16)	C2B—C3B—C4B—O3B	177.7 (2)
C2A—C3A—C4A—N1A	0.1 (3)	C2B—C3B—C4B—N2B	−1.8 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C3A—H3AA···O2Aⁱ	0.93	2.42	3.336 (2)	169
C5A—H5AC···O2Bⁱⁱ	0.96	2.55	3.303 (3)	135
C7A—H7AA···O4Aⁱⁱⁱ	0.96	2.50	3.426 (2)	161

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

Experimental details

Crystal data
Chemical formula	C₇H₁₀N₂O₄S
M_r	218.23
Crystal system, space group	Triclinic, P1
Temperature (K)	296
a, b, c (Å)	8.349 (2), 11.067 (3), 11.438 (3)
α, β, γ (°)	108.457 (8), 92.774 (8), 98.504 (8)
V (Å³)	986.4 (4)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.32
Crystal size (mm)	0.38 × 0.30 × 0.08

Data collection
Diffractometer	Bruker APEXII DUO CCD area-detector
Absorption correction	Multi-scan (SADABS; Bruker, 2009)
T_min, T_max	0.889, 0.974
No. of measured, independent and observed [I > 2σ(I)] reflections	29277, 7063, 4866
R_int	0.042
(sin θ/λ)_max (Å⁻¹)	0.756

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.044, 0.156, 1.08
No. of reflections	7063
No. of parameters	259
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.50, −0.50

Computer programs: APEX2 (Bruker, 2009), SAINT (Bruker, 2009), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).