Dimethyl 3-acetyl-3-(1,3-benzothia­zol-2-yl)penta­nedioate

Baryala, Y.; Salem, M.; Essassi, E.M.; Reuter, H.; Izaaryene, M.

doi:10.1107/S1600536808035782

organic compounds

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ISSN: 2056-9890

Volume 64| Part 12| December 2008| Page o2290

doi:10.1107/S1600536808035782

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Dimethyl 3-acetyl-3-(1,3-benzothiazol-2-yl)pentanedioate

Yamna Baryala,^a Moussa Salem,^a El Mokhtar Essassi,^b Hans Reuter ^c ^* and Maher Izaaryene ^c

^aLaboratoire de Chimie Organique et Études Physicochimiques, ENS Rabat, Morocco, ^bLaboratoire de Chimie Organique Hétérocyclique, Université Mohammed V Rabat, Morocco, and ^cInstitute of Chemistry, University of Osnabrück, Barbarastrasse 7, D-49069 Osnabrück, Germany
^*Correspondence e-mail: hreuter@uos.de

(Received 19 September 2008; accepted 31 October 2008; online 8 November 2008)

The title compound, C₁₆H₁₇NO₅S, was one of two condensation products from the reaction of 1-(1,3-benzothiazol-2-yl)propan-2-one with methyl chloroacetate. The non-H atoms in each of the four substituent groups on the central quaternary C atom are virtually coplanar. The maximum deviations from the least-squares planes are 0.015 (2) and 0.020 (2) Å for the methyl C atoms in the methyl acetate substituents and 0.033 (1) Å for the linked C atom of the benzothiazole substituent. The S, C and N atoms in the thiazole ring of the benzothiazole substituent lie −0.037 (2), 0.046 (2) and −0.028 (2) Å, respectively, from the mean plane defined by the benzene ring atoms.

Related literature

For general background, see: Palmer et al. (1971 ); Bénéteau et al., 1999 ; El-Sherbeny (2000 ); Abayeh et al. (1994 ); Ivanov & Yuritsyn (1971 ); Monsanto (1968 ); Lee et al. (2001 ). For related structures, see: Chen (1994 ); Chu et al. (2003 ).

Experimental

Crystal data

C₁₆H₁₇NO₅S
M_r = 335.37
Monoclinic, P 2₁ /c
a = 14.4075 (3) Å
b = 8.8089 (2) Å
c = 13.8968 (3) Å
β = 118.011 (1)°
V = 1557.10 (6) Å³
Z = 4
Mo Kα radiation
μ = 0.23 mm⁻¹
T = 100 (2) K
0.54 × 0.47 × 0.25 mm

Data collection

Bruker APEXII CCD area-detector diffractometer
Absorption correction: multi-scan (SADABS; Bruker, 2004 ) T_min = 0.883, T_max = 0.945
94263 measured reflections
3766 independent reflections
3396 reflections with I > 2σ(I)
R_int = 0.030

Refinement

R[F² > 2σ(F²)] = 0.030
wR(F²) = 0.083
S = 1.02
3766 reflections
211 parameters
H-atom parameters constrained
Δρ_max = 0.40 e Å⁻³
Δρ_min = −0.23 e Å⁻³

Data collection: SMART (Bruker, 2004); 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: DIAMOND (Brandenburg, 1999 ); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808035782/fj2155sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808035782/fj2155Isup2.hkl

checkCIF report

Comment top

Benzothiazole compounds show interesting biological and pharmacological properties (see, e.g., Palmer et al., 1971; Bénéteau et al., 1999; El-Sherbeny, 2000; Abayeh et al., 1994). Besides some few papers with industrial background (see, e.g., Ivanov & Yuritsyn, 1971; Monsanto, 1968) many papers discuss the synthesis, structure-property relationship and complexation behaviour of these compounds. An important group among the different derivatives of benzothiazole are those substituted at C2 (see, e.g., Lee et al., 2001).

In the following we describe the synthesis and structural characterization of such a kind of benzothiazole derivative. This compound, dimethyl 3-acetyl-3-(1,3-benzothiazol-2-yl)pentanedioate, 3, was synthesized according to reaction scheme 1 through alkylation of 1-(1,3-benzothiazol-2-yl)propan-2-one, 1, with methyl chloroacetate under classical condensation conditions, giving methyl 2-(2-(2-oxopropylidene)1,3-benzothiazol-3(2H)-yl)acetate, 2, as second reaction product. The starting material 1 was obtained by condensing 2-aminothiophenol with ethyl acetoacetate in xylene at 160° C for 1 h 30 min.

The structure of the title compound can be best described in relation to the central quaternary carbon atom [C1] surrounded by a benzothiazole moiety, two methyl acetate residues and an acetyl group (Fig. 1). The corresponding bond lengths at C1 of 1.537 (2) Å [C30], 1.538 (2) Å [C20], 1.561 (2) Å [C10] and 1.521 (2) Å are in good agreement with carbon-carbon single bonds, as well as are the angles of 110.9 (1)° - 108.5 (1)° in the range for a tetrahedral coordination. Within the benzothiazole rest bond lengths and angles are very similar to those in comparable compounds like the 2-methyl benzothiazole molecule (Chen, 1994; Chu et al., 2003), which was found as non complexing agent in some crystal structures. Especially the bond angle at the sulfur [88.99 (6)°] and nitrogen [110.5 (1)°] atoms as well as the lengths of the sulfur carbon bonds [1.734 (1)/1.755 (1) A] and the carbon nitrogen double bond between C2 and N3 [129.2 (2) A] are very similar. In relation to the benzenic part [C4 - C9] of the benzothiazole rest which is almost planar [maximal deviation from the least squares plain: -0.0031 (8) Å] the remaining atoms [S1, C2, N3] of the thiazole ring lie -0.037 (2), 0.046 (2) and -0.028 (2) Å above/below this point of reference. This conformation is somewhat different to the 2-methyl benzothiazole molecule where the corresponding values are -0.028 (1), -0.004 (5), 0.017 (4) Å (Chen, 1994) and -0.024 (1), -0.030 (3), -0.017 (3) Å (Chu et al., 2003), respectively, indicating a conformational flexibility of the thiazole moitie. Bond angles and lengths of the two methyl acetate rests as well as those of the acetyl moietie are in the expected ranges [f.e. d(C=O) = 1.201 (2) - 1.206 (2) Å, d(C_carbonyl—O_methoxy) = 1.341 (2)/1.332 (2) Å, d(C_methyl—O) = 1.450 (2)/1.450 (2) Å].

Intermolecular forces are restricted mainly to van der Waals ones. No π-π interactions as well as classical hydrogen bonds are found although there are two short intramolecular contacts between the oxygen atoms of two carbonyl groups and adjacent hydrogen atoms [d(O21 - H301) = 2.49 Å, d(O31—H202) = 2.54 Å] and one short intermolecular contact between the sulfur atom of the benzothiazole group and the hydrogen atom of a methylene group [d(Sn1—H301) = 2.86 Å] of a neigbhouring molecule.

Related literature top

For general background, see: Palmer et al. (1971); Bénéteau et al., 1999; El-Sherbeny (2000); Abayeh et al. (1994); Ivanov & Yuritsyn (1971); Monsanto (1968); Lee et al. (2001). For related structures, see: Chen (1994); Chu et al. (2003).

Experimental top

All solvents and reagents were used as received from Aldrich and Fluka. IR data were recorded using a Bruker VERTEX 70 FTIR spectrometer with ATR device. Wavelengths (ν) are reported in cm^{-1. 1}H and ¹³C NMR were obtained at ambient temperature using a Bruker AVANCE 300 A spectrometer. Chemical shifts (δ) are reported in parts per million (p.p.m.) relative to internal standards. Mass spectra were carried out using a LCQ Advantage MAX spectrometer employing Electro Spray Ionization (ESI).

2.84 g (2.61 mmol) methyl chloroacetate were added in one portion to a stirred solution of 100 ml acetone containing 1 g (5.23 mmol) 1-(benzothiazol-2-yl)propan-2-one, 1, and 7.22 g (52.3 mmol) K₂CO₃. The reaction mixture was refluxed for 12 h, filtered off and the solvent evaporated. After cooling a pale white precipitate of 2 appeared. These crystals were collected by filtration and recrystallized from ethanol (yield 0.5 g, 36.5%). The filtrate was leaved overnight at room temperature. Thereafter a second crystalline product was obtained which on recrystallization from ethanol gave white single crystals of 3 (yield 0.8 g, 45.6%).

Methyl 2-(2-(2-oxopropylidene)1,3-benzothiazol-3(2H)-yl)acetate, 2: mp. 208–210° C; IR (ATR), ν[cm^-1]): 1608; 1739; ¹H-NMR (300 MHz; CDCl₃), δ (p.p.m.): 3.78 (s, 2H), 5.75 (s,1H), 6.9–7.6 (m, 4H); ¹³C-NMR (75 MHZ; CDCl₃), δ (p.p.m.): 29.3; 46,9, 53,1; 90.9; 109.5; 122.7; 123.3; 127.2; 139.4; 160.5; 167.2, 191.5.

Dimethyl 3-acetyl-3-(1,3-benzothiazol-2-yl)pentandioate, 3: mp: 166–168° C; IR (ATR), ν[cm^-1): 1617; 1718; ¹H-NMR (30 MHz; CDCl₃), δ (p.p.m.): 2.24 (s, 3H), 3.54–371 (m, 10H) 7.4–8.0 (m, 4H);¹³C-NMR (75 MHz; CDCl₃), δ (p.p.m.): 25.7; 38.9; 51.9, 57.5, 121.6, 123.4, 125.5, 126.2, 135.4, 152.4, 152.6 169.8, 171.0, 203.6; MS(ESI): m/z 336 [M+1]⁺, 639 [2M+23]⁺.

A suitable single-crystal of 3 was selected under a polarization microsope and mounted on a 50 µm MicroMesh MiTeGen Micromount^TMusing FROMBLIN Y perfluoropolyether (LVAC 16/6, Aldrich).

Computing details top

Data collection: SMART (Bruker, 2004); cell refinement: SMART (Bruker, 2004); data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: DIAMOND (Brandenburg, 1999); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top

	Fig. 1. Thermal ellipsoid plot of the title compound with the atomic numbering scheme used. With exception of the hydrogen atoms, which are represented as spheres of arbitrary radius, all other atoms are shown as thermal displacement ellipsoids (oxygen = white, one octant; carbon = grey; nitrogen = white; sulfur = grey, one octant) representing the 50% probability level.
	Fig. 2. The formation of the title compound.

Dimethyl 3-acetyl-3-(1,3-benzothiazol-2-yl)pentanedioate top

Crystal data top

C₁₆H₁₇NO₅S	F(000) = 704
M_r = 335.37	D_x = 1.431 Mg m⁻³
Monoclinic, P2₁/c	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybc	Cell parameters from 9633 reflections
a = 14.4075 (3) Å	θ = 2.8–32.7°
b = 8.8089 (2) Å	µ = 0.23 mm⁻¹
c = 13.8968 (3) Å	T = 100 K
β = 118.011 (1)°	Irregular, colourless
V = 1557.10 (6) Å³	0.54 × 0.47 × 0.25 mm
Z = 4

Data collection top

Bruker APEXII CCD area-detector diffractometer	3766 independent reflections
Radiation source: fine-focus sealed tube	3396 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.030
ϕ and ω scans	θ_max = 28.0°, θ_min = 1.6°
Absorption correction: multi-scan (SADABS; Bruker, 2004)	h = −16→19
T_min = 0.884, T_max = 0.945	k = −11→11
94263 measured reflections	l = −18→17

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)] = 0.031	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.083	H-atom parameters constrained
S = 1.02	w = 1/[σ²(F_o²) + (0.0379P)² + 0.9909P] where P = (F_o² + 2F_c²)/3
3766 reflections	(Δ/σ)_max = 0.001
211 parameters	Δρ_max = 0.40 e Å⁻³
0 restraints	Δρ_min = −0.23 e Å⁻³

Crystal data top

C₁₆H₁₇NO₅S	V = 1557.10 (6) Å³
M_r = 335.37	Z = 4
Monoclinic, P2₁/c	Mo Kα radiation
a = 14.4075 (3) Å	µ = 0.23 mm⁻¹
b = 8.8089 (2) Å	T = 100 K
c = 13.8968 (3) Å	0.54 × 0.47 × 0.25 mm
β = 118.011 (1)°

Data collection top

Bruker APEXII CCD area-detector diffractometer	3766 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2004)	3396 reflections with I > 2σ(I)
T_min = 0.884, T_max = 0.945	R_int = 0.030
94263 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.031	0 restraints
wR(F²) = 0.083	H-atom parameters constrained
S = 1.02	Δρ_max = 0.40 e Å⁻³
3766 reflections	Δρ_min = −0.23 e Å⁻³
211 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
S1	0.07547 (2)	0.86573 (3)	0.43919 (2)	0.01676 (8)
C2	0.19378 (9)	0.80630 (13)	0.54977 (9)	0.0140 (2)
N3	0.20635 (8)	0.66132 (11)	0.56438 (8)	0.01443 (19)
C4	0.11159 (9)	0.42603 (14)	0.47444 (10)	0.0170 (2)
H4	0.1637	0.3622	0.5273	0.024 (2)*
C5	0.02392 (10)	0.36495 (14)	0.38745 (10)	0.0190 (2)
H5	0.0163	0.2578	0.3802	0.024 (2)*
C6	−0.05382 (10)	0.45859 (15)	0.30984 (10)	0.0193 (2)
H6	−0.1132	0.4135	0.2508	0.024 (2)*
C7	−0.04607 (9)	0.61526 (15)	0.31719 (9)	0.0179 (2)
H7	−0.0991	0.6784	0.2646	0.024 (2)*
C8	0.04263 (9)	0.67687 (14)	0.40475 (9)	0.0149 (2)
C9	0.12163 (9)	0.58417 (13)	0.48265 (9)	0.0141 (2)
C1	0.27346 (9)	0.92387 (13)	0.62176 (9)	0.0145 (2)
C10	0.22105 (9)	1.00619 (14)	0.68333 (9)	0.0160 (2)
O10	0.18549 (8)	1.13226 (10)	0.65710 (8)	0.0249 (2)
C11	0.20998 (10)	0.91849 (15)	0.77027 (10)	0.0219 (3)
H111	0.2794	0.9052	0.8335	0.0431 (14)*
H112	0.1792	0.8188	0.7417	0.0431 (14)*
H113	0.1641	0.9743	0.7922	0.0431 (14)*
C20	0.37450 (9)	0.84101 (13)	0.70162 (10)	0.0173 (2)
H201	0.3553	0.7532	0.7331	0.0431 (14)*
H202	0.4102	0.8014	0.6608	0.0431 (14)*
C21	0.45015 (9)	0.94072 (14)	0.79307 (10)	0.0170 (2)
O21	0.43873 (8)	1.07423 (11)	0.80278 (8)	0.0304 (2)
O22	0.53173 (7)	0.86031 (10)	0.86465 (8)	0.0229 (2)
C22	0.60859 (10)	0.94308 (15)	0.95845 (11)	0.0232 (3)
H221	0.6652	0.8742	1.0055	0.0431 (14)*
H222	0.5747	0.9852	0.9993	0.0431 (14)*
H223	0.6379	1.0258	0.9339	0.0431 (14)*
C30	0.29294 (10)	1.04297 (13)	0.55238 (10)	0.0168 (2)
H301	0.2280	1.1038	0.5129	0.0431 (14)*
H302	0.3489	1.1126	0.6021	0.0431 (14)*
C31	0.32428 (9)	0.98185 (14)	0.47030 (10)	0.0177 (2)
O31	0.34329 (8)	0.85225 (11)	0.45908 (8)	0.0272 (2)
O32	0.32806 (9)	1.09691 (11)	0.40907 (8)	0.0281 (2)
C32	0.36038 (13)	1.05932 (17)	0.32765 (12)	0.0309 (3)
H321	0.3587	1.1509	0.2869	0.0431 (14)*
H322	0.3123	0.9833	0.2774	0.0431 (14)*
H323	0.4320	1.0183	0.3636	0.0431 (14)*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1	0.01835 (15)	0.01332 (14)	0.01468 (14)	0.00202 (10)	0.00450 (11)	0.00100 (10)
C2	0.0143 (5)	0.0144 (5)	0.0137 (5)	0.0014 (4)	0.0071 (4)	0.0008 (4)
N3	0.0153 (4)	0.0135 (5)	0.0152 (5)	−0.0003 (4)	0.0078 (4)	−0.0001 (4)
C4	0.0197 (6)	0.0144 (5)	0.0205 (6)	0.0007 (4)	0.0124 (5)	0.0000 (4)
C5	0.0231 (6)	0.0159 (6)	0.0229 (6)	−0.0043 (5)	0.0150 (5)	−0.0047 (5)
C6	0.0201 (6)	0.0236 (6)	0.0165 (5)	−0.0058 (5)	0.0105 (5)	−0.0067 (5)
C7	0.0184 (5)	0.0222 (6)	0.0134 (5)	0.0001 (5)	0.0077 (5)	−0.0014 (4)
C8	0.0178 (5)	0.0144 (5)	0.0153 (5)	0.0001 (4)	0.0100 (5)	−0.0011 (4)
C9	0.0155 (5)	0.0150 (5)	0.0146 (5)	−0.0009 (4)	0.0094 (4)	−0.0010 (4)
C1	0.0161 (5)	0.0113 (5)	0.0160 (5)	0.0002 (4)	0.0074 (4)	0.0002 (4)
C10	0.0153 (5)	0.0164 (6)	0.0149 (5)	−0.0015 (4)	0.0059 (4)	−0.0022 (4)
O10	0.0319 (5)	0.0192 (5)	0.0284 (5)	0.0088 (4)	0.0181 (4)	0.0030 (4)
C11	0.0260 (6)	0.0235 (6)	0.0189 (6)	−0.0034 (5)	0.0127 (5)	−0.0007 (5)
C20	0.0157 (5)	0.0131 (5)	0.0193 (6)	0.0001 (4)	0.0050 (5)	−0.0006 (4)
C21	0.0146 (5)	0.0172 (6)	0.0189 (6)	−0.0013 (4)	0.0077 (5)	−0.0003 (4)
O21	0.0262 (5)	0.0173 (5)	0.0323 (5)	0.0016 (4)	0.0011 (4)	−0.0066 (4)
O22	0.0195 (4)	0.0179 (4)	0.0214 (4)	−0.0004 (3)	0.0013 (4)	−0.0009 (4)
C22	0.0160 (5)	0.0240 (6)	0.0220 (6)	−0.0038 (5)	0.0026 (5)	−0.0027 (5)
C30	0.0211 (6)	0.0121 (5)	0.0191 (6)	−0.0011 (4)	0.0110 (5)	−0.0004 (4)
C31	0.0172 (5)	0.0173 (6)	0.0187 (6)	−0.0036 (4)	0.0086 (5)	−0.0019 (5)
O31	0.0409 (6)	0.0178 (5)	0.0324 (5)	0.0027 (4)	0.0250 (5)	−0.0007 (4)
O32	0.0501 (6)	0.0179 (5)	0.0291 (5)	−0.0045 (4)	0.0290 (5)	−0.0020 (4)
C32	0.0486 (9)	0.0270 (7)	0.0308 (7)	−0.0086 (6)	0.0300 (7)	−0.0046 (6)

Geometric parameters (Å, º) top

S1—C8	1.7343 (12)	C11—H112	0.9800
S1—C2	1.7552 (12)	C11—H113	0.9800
C2—N3	1.2924 (15)	C20—C21	1.5078 (16)
C2—C1	1.5207 (16)	C20—H201	0.9900
N3—C9	1.3926 (15)	C20—H202	0.9900
C4—C5	1.3827 (18)	C21—O21	1.2038 (16)
C4—C9	1.3997 (16)	C21—O22	1.3320 (15)
C4—H4	0.9500	O22—C22	1.4496 (15)
C5—C6	1.4012 (18)	C22—H221	0.9800
C5—H5	0.9500	C22—H222	0.9800
C6—C7	1.3845 (18)	C22—H223	0.9800
C6—H6	0.9500	C30—C31	1.5095 (16)
C7—C8	1.3957 (17)	C30—H301	0.9900
C7—H7	0.9500	C30—H302	0.9900
C8—C9	1.4060 (16)	C31—O31	1.2012 (15)
C1—C30	1.5373 (16)	C31—O32	1.3409 (15)
C1—C20	1.5383 (16)	O32—C32	1.4497 (16)
C1—C10	1.5605 (16)	C32—H321	0.9800
C10—O10	1.2055 (15)	C32—H322	0.9800
C10—C11	1.5043 (17)	C32—H323	0.9800
C11—H111	0.9800

C8—S1—C2	88.99 (6)	C10—C11—H113	109.5
N3—C2—C1	124.25 (10)	H111—C11—H113	109.5
N3—C2—S1	116.04 (9)	H112—C11—H113	109.5
C1—C2—S1	119.70 (8)	C21—C20—C1	113.34 (10)
C2—N3—C9	110.46 (10)	C21—C20—H201	108.9
C5—C4—C9	118.40 (11)	C1—C20—H201	108.9
C5—C4—H4	120.8	C21—C20—H202	108.9
C9—C4—H4	120.8	C1—C20—H202	108.9
C4—C5—C6	121.04 (11)	H201—C20—H202	107.7
C4—C5—H5	119.5	O21—C21—O22	123.70 (11)
C6—C5—H5	119.5	O21—C21—C20	125.51 (11)
C7—C6—C5	121.49 (11)	O22—C21—C20	110.77 (10)
C7—C6—H6	119.3	C21—O22—C22	115.95 (10)
C5—C6—H6	119.3	O22—C22—H221	109.5
C6—C7—C8	117.45 (11)	O22—C22—H222	109.5
C6—C7—H7	121.3	H221—C22—H222	109.5
C8—C7—H7	121.3	O22—C22—H223	109.5
C7—C8—C9	121.61 (11)	H221—C22—H223	109.5
C7—C8—S1	129.28 (10)	H222—C22—H223	109.5
C9—C8—S1	109.11 (9)	C31—C30—C1	115.97 (10)
N3—C9—C4	124.73 (11)	C31—C30—H301	108.3
N3—C9—C8	115.28 (10)	C1—C30—H301	108.3
C4—C9—C8	120.00 (11)	C31—C30—H302	108.3
C2—C1—C30	110.85 (9)	C1—C30—H302	108.3
C2—C1—C20	108.53 (9)	H301—C30—H302	107.4
C30—C1—C20	112.75 (10)	O31—C31—O32	123.80 (11)
C2—C1—C10	105.49 (9)	O31—C31—C30	127.20 (11)
C30—C1—C10	107.74 (9)	O32—C31—C30	109.00 (10)
C20—C1—C10	111.26 (9)	C31—O32—C32	116.51 (11)
O10—C10—C11	121.71 (11)	O32—C32—H321	109.5
O10—C10—C1	120.57 (11)	O32—C32—H322	109.5
C11—C10—C1	117.58 (10)	H321—C32—H322	109.5
C10—C11—H111	109.5	O32—C32—H323	109.5
C10—C11—H112	109.5	H321—C32—H323	109.5
H111—C11—H112	109.5	H322—C32—H323	109.5

C8—S1—C2—N3	−3.31 (9)	N3—C2—C1—C10	−111.43 (12)
C8—S1—C2—C1	177.11 (9)	S1—C2—C1—C10	68.12 (11)
C1—C2—N3—C9	−177.68 (10)	C2—C1—C10—O10	−104.69 (13)
S1—C2—N3—C9	2.75 (12)	C30—C1—C10—O10	13.77 (15)
C9—C4—C5—C6	−0.72 (17)	C20—C1—C10—O10	137.83 (12)
C4—C5—C6—C7	−0.08 (18)	C2—C1—C10—C11	71.08 (12)
C5—C6—C7—C8	0.34 (17)	C30—C1—C10—C11	−170.47 (10)
C6—C7—C8—C9	0.21 (17)	C20—C1—C10—C11	−46.41 (14)
C6—C7—C8—S1	−178.77 (9)	C2—C1—C20—C21	−167.17 (9)
C2—S1—C8—C7	−178.22 (11)	C30—C1—C20—C21	69.63 (13)
C2—S1—C8—C9	2.70 (8)	C10—C1—C20—C21	−51.54 (13)
C2—N3—C9—C4	179.46 (11)	C1—C20—C21—O21	−3.89 (18)
C2—N3—C9—C8	−0.50 (14)	C1—C20—C21—O22	174.63 (10)
C5—C4—C9—N3	−178.70 (10)	O21—C21—O22—C22	0.40 (18)
C5—C4—C9—C8	1.25 (17)	C20—C21—O22—C22	−178.16 (10)
C7—C8—C9—N3	178.94 (10)	C2—C1—C30—C31	−53.93 (13)
S1—C8—C9—N3	−1.90 (12)	C20—C1—C30—C31	67.97 (13)
C7—C8—C9—C4	−1.02 (17)	C10—C1—C30—C31	−168.88 (10)
S1—C8—C9—C4	178.15 (9)	C1—C30—C31—O31	−6.12 (19)
N3—C2—C1—C30	132.23 (12)	C1—C30—C31—O32	173.84 (10)
S1—C2—C1—C30	−48.22 (12)	O31—C31—O32—C32	−1.96 (19)
N3—C2—C1—C20	7.89 (15)	C30—C31—O32—C32	178.08 (11)
S1—C2—C1—C20	−172.56 (8)

Experimental details

Crystal data
Chemical formula	C₁₆H₁₇NO₅S
M_r	335.37
Crystal system, space group	Monoclinic, P2₁/c
Temperature (K)	100
a, b, c (Å)	14.4075 (3), 8.8089 (2), 13.8968 (3)
β (°)	118.011 (1)
V (Å³)	1557.10 (6)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.23
Crystal size (mm)	0.54 × 0.47 × 0.25

Data collection
Diffractometer	Bruker APEXII CCD area-detector diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2004)
T_min, T_max	0.884, 0.945
No. of measured, independent and observed [I > 2σ(I)] reflections	94263, 3766, 3396
R_int	0.030
(sin θ/λ)_max (Å⁻¹)	0.661

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.031, 0.083, 1.02
No. of reflections	3766
No. of parameters	211
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.40, −0.23

Computer programs: SMART (Bruker, 2004), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), DIAMOND (Brandenburg, 1999), SHELXTL (Sheldrick, 2008).

References

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