Methyl 2-{[(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-yl­idene)(thio­phen-2-yl)meth­yl]amino}-3-phenyl­propionate

Zhu, H.; Zhao, X.; Wang, Z.; Ren, J.; Zhang, M.

doi:10.1107/S1600536811029904

organic compounds

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ISSN: 2056-9890

Volume 67| Part 8| August 2011| Page o2200

doi:10.1107/S1600536811029904

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Methyl 2-{[(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-ylidene)(thiophen-2-yl)methyl]amino}-3-phenylpropionate

Hualing Zhu,^a ^* Xinxin Zhao,^a Zhan Wang,^a Junjie Ren ^a and Miao Zhang ^a

^aDepartment of Basic Science, Tianjin Agricultural College, Tianjin Jinjing Road No. 22, Tianjin 300384, People's Republic of China
^*Correspondence e-mail: zhuhualing2004@126.com

(Received 12 July 2011; accepted 24 July 2011; online 30 July 2011)

In the title compound, C₂₅H₂₃N₃O₃S, an intramolecular N—H⋯O interaction generates an S(6) ring, which stabilizes the enamine–keto form of the compound. This S(6) ring and the pyrazole ring are essentially coplanar, making a dihedral angle of 1.49 (6)°. The bond lengths within the S(6) ring of the molecule lie between classical single- and double-bond lengths, indicating extensive conjugation. The structure exhibits a thienyl-ring flip disorder, with occupancy factors in the ratio 64.7 (3):35.3 (3).

Related literature

The high biological activities of pyrazole derivatives are reported by Li et al. (2004 ) and Tan et al.(2009 ). The antibacterial and biological activities of amino acid esters are described by Xiong et al. (1993 ). Structures related to the title compound have been reported by Zhu et al. (2010 ) and Zhang et al. (2010 ).

Experimental

Crystal data

C₂₅H₂₃N₃O₃S
M_r = 445.52
Monoclinic, P 2₁
a = 6.649 (2) Å
b = 18.712 (6) Å
c = 9.349 (3) Å
β = 104.903 (5)°
V = 1124.0 (7) Å³
Z = 2
Mo Kα radiation
μ = 0.18 mm⁻¹
T = 113 K
0.20 × 0.18 × 0.12 mm

Data collection

Rigaku Saturn724 CCD diffractometer
Absorption correction: multi-scan (CrystalClear; Rigaku, 2008 ) T_min = 0.966, T_max = 0.979
11848 measured reflections
2747 independent reflections
2315 reflections with I > 2σ(I)
R_int = 0.041

Refinement

R[F² > 2σ(F²)] = 0.034
wR(F²) = 0.064
S = 0.98
2747 reflections
353 parameters
215 restraints
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.15 e Å⁻³
Δρ_min = −0.20 e Å⁻³
Absolute structure: Flack (1983 ), 2401 Friedel pairs
Flack parameter: 0.05 (8)

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N3—H1⋯O1	0.88	1.93	2.668 (2)	141

Data collection: CrystalClear (Rigaku, 2008); cell refinement: CrystalClear; data reduction: CrystalClear; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997 ); software used to prepare material for publication: SHELXL97.

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536811029904/om2448sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536811029904/om2448Isup2.hkl

Supporting information file. DOI: 10.1107/S1600536811029904/om2448Isup3.cml

checkCIF report

Comment top

Pyrazole derivatives have drawn attentionfrom agricultural chemists for their high biological activity and low toxicity. They are widely used as pesticide, miticide and weed killers, and with the positional changes of the substituent group of pyrazole ring, more and more new pyrazole agricultural chemicals are synthesized and commercialized (Tan et al.,2009), so pyrazole derivatives have become one of the focal points to the creation of new agricultural chemicals. Amino acid esters also possess good antibacterial and biological activity (Xiong et al.,1993).

In the molecule of the title compound (Fig. 1), there is an intramolecular N3—H1···O1 interaction that generates a S(6) ring, and stabilizes the enamine–keto form of the compound. The dihedral angle between this S(6) ring and the pyrazole ring is 1.49 (6)°, indicating that they are essentially coplanar, as seen in Methyl 2-{[(1Z)-(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4- ylidene)(methyl)methyl]amino}-3-phenylpropanoate(1.50 (15)°; Zhu et al., 2010). The bond lengths within this part of the molecular lie between classical single-and double-bond lengths, indicating extensive conjugation. The S(6) ring makes dihedral angles of 54.29 (6)°,82.21 (22)° and 28.53 (6)° with the benzene ring of phenylalanine methyl ester, the thiazole ring and benzene ring bonded to pyrazole ring, respectively.

Atoms N3, C16, C24 and O2 are not coplanar, the torsion angle is 37.17 (22)°, similar to some other 4-acylpyrazolone Schiff Bases (Zhang et al., 2010). The bond lengths in this part of the molecule indicate that only C24—O2 is a classical double bond, other bonds are classical single bonds.

The structure exhibits a thienyl-ring flip disorder with the occupancy factors in the ratio 67/33.

Related literature top

The high biological activities of pyrazole derivatives are reported by Li et al. (2004) and Tan et al.(2009). The antibacterial and biological activities of amino acid esters are described by Xiong et al. (1993). Structures related to the title compound have been reported by Zhu et al. (2010) and Zhang et al. (2010).

Experimental top

The title compound was synthesized by refluxing the mixture of 1-phenyl-3-methyl-4-(2-thenoyl)pyrazolone-5 (HPMTP) (10m mol) and phenylalanine methyl ester(10m mol) in ethanol (100 ml) over a steam bath for about 7 h, then the solution was cooled down to room temperature. After five days, pale yellow blocks were obtained and dried in the air. The product was recrystallized from ethanol which afforded pale yellow crystals suitable for X-ray analysis.

Computing details top

Data collection: CrystalClear (Rigaku, 2008); cell refinement: CrystalClear (Rigaku, 2008); data reduction: CrystalClear (Rigaku, 2008); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top

Fig. 1. The molecular structure of the title compound with the atom numbering scheme. Displacement ellipsoids are drawn at the 30% probability level. H atoms are presented as a small spheres of arbitrary radii.

Methyl 2-{[(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol- 4-ylidene)(thiophen-2-yl)methyl]-amino}-3-phenylpropionate top

Crystal data top

C₂₅H₂₃N₃O₃S	F(000) = 468
M_r = 445.52	D_x = 1.316 Mg m⁻³
Monoclinic, P2₁	Mo Kα radiation, λ = 0.71073 Å
a = 6.649 (2) Å	Cell parameters from 5148 reflections
b = 18.712 (6) Å	θ = 2.2–27.9°
c = 9.349 (3) Å	µ = 0.18 mm⁻¹
β = 104.903 (5)°	T = 113 K
V = 1124.0 (7) Å³	Block, pale yellow
Z = 2	0.20 × 0.18 × 0.12 mm

Data collection top

Rigaku Saturn724 CCD diffractometer	2747 independent reflections
Radiation source: rotating anode	2315 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.041
ω and ϕ scans	θ_max = 27.9°, θ_min = 2.2°
Absorption correction: multi-scan (CrystalClear; Rigaku, 2008)	h = −8→8
T_min = 0.966, T_max = 0.979	k = −24→24
11848 measured reflections	l = −12→12

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)] = 0.034	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.064	w = 1/[σ²(F_o²) + (0.0327P)²] where P = (F_o² + 2F_c²)/3
S = 0.98	(Δ/σ)_max < 0.001
2747 reflections	Δρ_max = 0.15 e Å⁻³
353 parameters	Δρ_min = −0.20 e Å⁻³
215 restraints	Absolute structure: Flack (1983), 2401 Friedel pairs
Primary atom site location: structure-invariant direct methods	Absolute structure parameter: 0.05 (8)

Crystal data top

C₂₅H₂₃N₃O₃S	V = 1124.0 (7) Å³
M_r = 445.52	Z = 2
Monoclinic, P2₁	Mo Kα radiation
a = 6.649 (2) Å	µ = 0.18 mm⁻¹
b = 18.712 (6) Å	T = 113 K
c = 9.349 (3) Å	0.20 × 0.18 × 0.12 mm
β = 104.903 (5)°

Data collection top

Rigaku Saturn724 CCD diffractometer	2747 independent reflections
Absorption correction: multi-scan (CrystalClear; Rigaku, 2008)	2315 reflections with I > 2σ(I)
T_min = 0.966, T_max = 0.979	R_int = 0.041
11848 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.034	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.064	Δρ_max = 0.15 e Å⁻³
S = 0.98	Δρ_min = −0.20 e Å⁻³
2747 reflections	Absolute structure: Flack (1983), 2401 Friedel pairs
353 parameters	Absolute structure parameter: 0.05 (8)
215 restraints

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)
O1	1.1534 (2)	0.63768 (7)	0.18356 (15)	0.0277 (3)
O2	0.5930 (2)	0.61573 (8)	−0.05979 (16)	0.0351 (4)
O3	0.3142 (2)	0.68792 (8)	−0.10026 (16)	0.0306 (4)
N1	1.3400 (2)	0.65769 (9)	0.42905 (17)	0.0222 (4)
N2	1.3238 (2)	0.70218 (10)	0.54712 (17)	0.0249 (4)
N3	0.8186 (3)	0.72194 (9)	0.11372 (18)	0.0247 (4)
H1	0.8944	0.6858	0.0974	0.028 (6)*
C1	1.5151 (3)	0.61245 (11)	0.4456 (2)	0.0226 (4)
C2	1.5855 (3)	0.59401 (13)	0.3226 (2)	0.0314 (5)
H2	1.5161	0.6115	0.2273	0.038*
C3	1.7570 (3)	0.55012 (14)	0.3403 (3)	0.0380 (6)
H3	1.8053	0.5378	0.2564	0.046*
C4	1.8595 (3)	0.52384 (13)	0.4775 (3)	0.0361 (6)
H4	1.9765	0.4933	0.4879	0.043*
C5	1.7900 (3)	0.54243 (12)	0.5997 (3)	0.0317 (5)
H5	1.8598	0.5246	0.6946	0.038*
C6	1.6182 (3)	0.58712 (11)	0.5842 (2)	0.0260 (5)
H6	1.5719	0.6002	0.6686	0.031*
C7	1.1799 (3)	0.66940 (11)	0.3045 (2)	0.0230 (4)
C8	1.0560 (3)	0.72515 (10)	0.3459 (2)	0.0209 (4)
C9	1.1586 (3)	0.74221 (11)	0.4976 (2)	0.0237 (4)
C10	1.1023 (3)	0.79648 (13)	0.5971 (2)	0.0335 (5)
H10A	1.2064	0.7961	0.6928	0.050*
H10B	0.9652	0.7851	0.6119	0.050*
H10C	1.0983	0.8439	0.5521	0.050*
C11	0.8795 (3)	0.75220 (10)	0.2467 (2)	0.0209 (4)
C12	0.7620 (11)	0.8131 (3)	0.2843 (9)	0.0201 (13)	0.647 (3)
C13	0.7922 (16)	0.8830 (4)	0.2580 (9)	0.038 (2)	0.647 (3)
C14	0.6536 (12)	0.9317 (5)	0.3156 (10)	0.0313 (13)	0.647 (3)
C15	0.5342 (14)	0.8917 (3)	0.3807 (9)	0.0291 (14)	0.647 (3)
S1	0.5747 (3)	0.80143 (13)	0.3760 (3)	0.0387 (4)	0.647 (3)
C12'	0.757 (2)	0.8125 (5)	0.2850 (18)	0.028 (2)	0.353 (3)
C13'	0.617 (2)	0.8021 (10)	0.3677 (17)	0.036 (3)	0.353 (3)
H13A	0.5751	0.7559	0.3975	0.043*	0.353 (3)
C15'	0.621 (2)	0.9239 (10)	0.3287 (18)	0.034 (2)	0.353 (3)
C14'	0.528 (3)	0.8741 (7)	0.395 (2)	0.037 (2)	0.353 (3)
S1'	0.7937 (7)	0.8971 (2)	0.2379 (5)	0.0324 (8)	0.353 (3)
C16	0.6425 (3)	0.74125 (11)	−0.0075 (2)	0.0231 (4)
H16	0.5549	0.7779	0.0258	0.028*
C17	0.7166 (3)	0.76982 (11)	−0.1407 (2)	0.0255 (5)
H17A	0.8063	0.7335	−0.1703	0.031*
H17B	0.5940	0.7775	−0.2254	0.031*
C18	0.8361 (3)	0.83898 (11)	−0.1058 (2)	0.0270 (5)
C19	1.0459 (3)	0.83866 (14)	−0.0317 (2)	0.0329 (5)
H19	1.1163	0.7946	−0.0048	0.040*
C20	1.1537 (4)	0.90311 (16)	0.0032 (3)	0.0435 (6)
H20	1.2974	0.9027	0.0535	0.052*
C21	1.0520 (5)	0.96732 (15)	−0.0351 (3)	0.0496 (7)
H21	1.1249	1.0111	−0.0100	0.060*
C22	0.8446 (5)	0.96765 (14)	−0.1097 (3)	0.0512 (7)
H22	0.7747	1.0118	−0.1372	0.061*
C23	0.7374 (4)	0.90402 (13)	−0.1449 (2)	0.0386 (6)
H23	0.5943	0.9049	−0.1966	0.046*
C24	0.5168 (3)	0.67377 (11)	−0.0565 (2)	0.0246 (5)
C25	0.1802 (3)	0.62806 (13)	−0.1612 (3)	0.0384 (6)
H25A	0.2104	0.6123	−0.2534	0.058*
H25B	0.0343	0.6429	−0.1814	0.058*
H25C	0.2055	0.5886	−0.0899	0.058*
H13	0.894 (5)	0.907 (2)	0.219 (4)	0.046*	0.647 (3)
H14	0.639 (10)	0.9824 (9)	0.298 (6)	0.046*	0.647 (3)
H15	0.416 (4)	0.904 (3)	0.416 (4)	0.046*	0.647 (3)
H15'	0.627 (19)	0.9752 (12)	0.327 (11)	0.046*	0.353 (3)
H14'	0.449 (10)	0.892 (4)	0.460 (6)	0.046*	0.353 (3)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
O1	0.0368 (8)	0.0247 (8)	0.0186 (7)	0.0067 (6)	0.0015 (6)	−0.0056 (6)
O2	0.0449 (9)	0.0197 (8)	0.0349 (9)	0.0023 (8)	−0.0003 (7)	−0.0039 (7)
O3	0.0288 (8)	0.0279 (9)	0.0349 (8)	−0.0047 (7)	0.0078 (6)	−0.0087 (7)
N1	0.0266 (9)	0.0233 (9)	0.0155 (8)	0.0027 (7)	0.0033 (7)	−0.0024 (7)
N2	0.0287 (9)	0.0279 (9)	0.0179 (9)	0.0009 (8)	0.0057 (7)	−0.0056 (7)
N3	0.0332 (10)	0.0204 (9)	0.0174 (8)	0.0069 (8)	0.0007 (7)	−0.0025 (7)
C1	0.0232 (10)	0.0190 (10)	0.0255 (11)	−0.0015 (9)	0.0061 (8)	−0.0012 (8)
C2	0.0318 (12)	0.0378 (13)	0.0256 (11)	0.0017 (10)	0.0093 (9)	0.0003 (10)
C3	0.0329 (13)	0.0452 (14)	0.0379 (13)	0.0052 (11)	0.0127 (10)	−0.0081 (11)
C4	0.0264 (12)	0.0326 (13)	0.0473 (14)	0.0058 (10)	0.0061 (11)	−0.0046 (11)
C5	0.0279 (12)	0.0279 (12)	0.0341 (12)	−0.0020 (10)	−0.0015 (10)	0.0020 (10)
C6	0.0291 (11)	0.0243 (11)	0.0232 (10)	−0.0020 (9)	0.0042 (9)	−0.0010 (9)
C7	0.0280 (11)	0.0183 (10)	0.0216 (10)	−0.0012 (9)	0.0041 (9)	−0.0004 (8)
C8	0.0230 (10)	0.0206 (10)	0.0188 (10)	−0.0010 (9)	0.0047 (8)	−0.0012 (8)
C9	0.0267 (11)	0.0244 (11)	0.0194 (10)	0.0004 (9)	0.0051 (8)	−0.0025 (8)
C10	0.0385 (13)	0.0410 (13)	0.0187 (10)	0.0095 (11)	0.0032 (9)	−0.0069 (10)
C11	0.0264 (11)	0.0173 (10)	0.0196 (10)	−0.0025 (8)	0.0069 (9)	−0.0011 (8)
C12	0.020 (2)	0.022 (2)	0.016 (2)	−0.001 (2)	0.0006 (19)	−0.003 (2)
C13	0.041 (3)	0.031 (4)	0.045 (3)	0.007 (3)	0.016 (2)	0.000 (3)
C14	0.034 (3)	0.021 (2)	0.038 (2)	−0.006 (2)	0.0089 (18)	−0.0018 (19)
C15	0.033 (2)	0.024 (3)	0.035 (2)	0.005 (2)	0.0174 (19)	−0.002 (2)
S1	0.0402 (9)	0.0331 (7)	0.0529 (8)	0.0029 (7)	0.0304 (7)	0.0005 (6)
C12'	0.029 (4)	0.025 (4)	0.031 (4)	0.001 (4)	0.009 (4)	−0.004 (4)
C13'	0.036 (4)	0.031 (4)	0.041 (4)	0.011 (4)	0.013 (4)	−0.011 (3)
C15'	0.038 (4)	0.022 (4)	0.043 (4)	0.000 (4)	0.012 (3)	−0.007 (3)
C14'	0.037 (3)	0.037 (4)	0.043 (4)	−0.002 (4)	0.018 (3)	0.001 (4)
S1'	0.0388 (13)	0.0156 (12)	0.0468 (15)	−0.0019 (10)	0.0183 (11)	−0.0063 (11)
C16	0.0286 (11)	0.0199 (10)	0.0186 (10)	0.0026 (9)	0.0020 (9)	−0.0013 (8)
C17	0.0310 (12)	0.0252 (11)	0.0169 (10)	0.0014 (9)	0.0000 (9)	−0.0017 (8)
C18	0.0330 (12)	0.0277 (12)	0.0206 (10)	−0.0031 (10)	0.0073 (9)	−0.0021 (9)
C19	0.0322 (13)	0.0415 (14)	0.0262 (11)	−0.0043 (11)	0.0095 (10)	−0.0095 (11)
C20	0.0389 (14)	0.0619 (18)	0.0340 (13)	−0.0207 (14)	0.0174 (11)	−0.0165 (13)
C21	0.078 (2)	0.0411 (16)	0.0351 (13)	−0.0313 (15)	0.0243 (14)	−0.0092 (12)
C22	0.079 (2)	0.0269 (13)	0.0446 (15)	−0.0080 (14)	0.0107 (15)	0.0088 (11)
C23	0.0482 (14)	0.0307 (12)	0.0322 (12)	−0.0045 (11)	0.0019 (11)	0.0068 (11)
C24	0.0343 (12)	0.0234 (11)	0.0156 (10)	−0.0001 (10)	0.0056 (9)	0.0001 (8)
C25	0.0351 (13)	0.0377 (14)	0.0431 (14)	−0.0114 (11)	0.0112 (11)	−0.0139 (11)

Geometric parameters (Å, º) top

O1—C7	1.249 (2)	C14—H15'	0.85 (5)
O2—C24	1.202 (2)	C15—S1	1.712 (5)
O3—C24	1.330 (2)	C15—H15	0.959 (10)
O3—C25	1.453 (2)	C15—H14'	1.04 (4)
N1—C7	1.378 (2)	S1—H13A	0.8749
N1—N2	1.409 (2)	C12'—C13'	1.368 (9)
N1—C1	1.415 (3)	C12'—S1'	1.678 (9)
N2—C9	1.311 (3)	C13'—C14'	1.518 (10)
N3—C11	1.331 (2)	C13'—H13A	0.9699
N3—C16	1.450 (3)	C15'—C14'	1.349 (9)
N3—H1	0.8800	C15'—S1'	1.674 (9)
C1—C6	1.384 (3)	C15'—H14	1.15 (3)
C1—C2	1.392 (3)	C15'—H15'	0.962 (11)
C2—C3	1.380 (3)	C14'—H15	1.00 (3)
C2—H2	0.9500	C14'—H14'	0.961 (11)
C3—C4	1.379 (3)	S1'—H13	0.76 (2)
C3—H3	0.9500	C16—C24	1.519 (3)
C4—C5	1.382 (3)	C16—C17	1.547 (3)
C4—H4	0.9500	C16—H16	1.0000
C5—C6	1.393 (3)	C17—C18	1.510 (3)
C5—H5	0.9500	C17—H17A	0.9900
C6—H6	0.9500	C17—H17B	0.9900
C7—C8	1.443 (3)	C18—C19	1.389 (3)
C8—C11	1.391 (3)	C18—C23	1.386 (3)
C8—C9	1.442 (3)	C19—C20	1.398 (4)
C9—C10	1.489 (3)	C19—H19	0.9500
C10—H10A	0.9800	C20—C21	1.380 (4)
C10—H10B	0.9800	C20—H20	0.9500
C10—H10C	0.9800	C21—C22	1.376 (4)
C11—C12	1.474 (5)	C21—H21	0.9500
C11—C12'	1.489 (9)	C22—C23	1.383 (3)
C12—C13	1.356 (7)	C22—H22	0.9500
C12—S1	1.698 (5)	C23—H23	0.9500
C13—C14	1.491 (8)	C25—H25A	0.9800
C13—H13	0.963 (10)	C25—H25B	0.9800
C14—C15	1.345 (6)	C25—H25C	0.9800
C14—H14	0.963 (10)

C24—O3—C25	115.95 (17)	H15—C15—H14'	27 (5)
C7—N1—N2	111.72 (15)	C12—S1—C15	91.5 (4)
C7—N1—C1	128.47 (17)	C12—S1—H13A	106.4
N2—N1—C1	119.63 (15)	C15—S1—H13A	161.0
C9—N2—N1	106.65 (15)	C13'—C12'—C11	121.6 (10)
C11—N3—C16	127.91 (17)	C13'—C12'—S1'	116.7 (10)
C11—N3—H1	116.0	C11—C12'—S1'	121.6 (7)
C16—N3—H1	116.0	C12'—C13'—C14'	108.5 (15)
C6—C1—C2	119.8 (2)	C12'—C13'—H13A	125.1
C6—C1—N1	120.16 (18)	C14'—C13'—H13A	126.3
C2—C1—N1	120.00 (18)	C14'—C15'—S1'	118.6 (15)
C3—C2—C1	119.4 (2)	C14'—C15'—H14	150 (3)
C3—C2—H2	120.3	S1'—C15'—H14	92 (3)
C1—C2—H2	120.3	C14'—C15'—H15'	137 (6)
C4—C3—C2	121.3 (2)	S1'—C15'—H15'	104 (7)
C4—C3—H3	119.3	H14—C15'—H15'	15 (8)
C2—C3—H3	119.3	C15'—C14'—C13'	107.1 (18)
C3—C4—C5	119.2 (2)	C15'—C14'—H15	99 (3)
C3—C4—H4	120.4	C13'—C14'—H15	151 (3)
C5—C4—H4	120.4	C15'—C14'—H14'	116 (6)
C4—C5—C6	120.3 (2)	C13'—C14'—H14'	136 (5)
C4—C5—H5	119.9	H15—C14'—H14'	28 (5)
C6—C5—H5	119.9	C15'—S1'—C12'	89.0 (8)
C1—C6—C5	119.9 (2)	C15'—S1'—H13	144 (3)
C1—C6—H6	120.1	C12'—S1'—H13	119 (3)
C5—C6—H6	120.1	N3—C16—C24	107.42 (16)
O1—C7—N1	126.01 (18)	N3—C16—C17	110.79 (17)
O1—C7—C8	129.01 (18)	C24—C16—C17	108.01 (16)
N1—C7—C8	104.97 (16)	N3—C16—H16	110.2
C11—C8—C9	132.86 (18)	C24—C16—H16	110.2
C11—C8—C7	121.75 (18)	C17—C16—H16	110.2
C9—C8—C7	105.39 (16)	C18—C17—C16	112.39 (16)
N2—C9—C8	111.26 (17)	C18—C17—H17A	109.1
N2—C9—C10	119.42 (18)	C16—C17—H17A	109.1
C8—C9—C10	129.32 (18)	C18—C17—H17B	109.1
C9—C10—H10A	109.5	C16—C17—H17B	109.1
C9—C10—H10B	109.5	H17A—C17—H17B	107.9
H10A—C10—H10B	109.5	C19—C18—C23	118.8 (2)
C9—C10—H10C	109.5	C19—C18—C17	120.6 (2)
H10A—C10—H10C	109.5	C23—C18—C17	120.54 (19)
H10B—C10—H10C	109.5	C18—C19—C20	120.1 (2)
N3—C11—C8	118.04 (17)	C18—C19—H19	119.9
N3—C11—C12	119.9 (4)	C20—C19—H19	119.9
C8—C11—C12	122.0 (4)	C21—C20—C19	120.2 (2)
N3—C11—C12'	119.5 (7)	C21—C20—H20	119.9
C8—C11—C12'	122.4 (7)	C19—C20—H20	119.9
C12—C11—C12'	1.4 (7)	C22—C21—C20	119.7 (2)
C13—C12—C11	126.2 (6)	C22—C21—H21	120.1
C13—C12—S1	112.2 (6)	C20—C21—H21	120.1
C11—C12—S1	121.5 (4)	C21—C22—C23	120.3 (3)
C12—C13—C14	112.9 (9)	C21—C22—H22	119.8
C12—C13—H13	132 (3)	C23—C22—H22	119.8
C14—C13—H13	115 (3)	C22—C23—C18	120.8 (2)
C15—C14—C13	108.4 (9)	C22—C23—H23	119.6
C15—C14—H14	125 (3)	C18—C23—H23	119.6
C13—C14—H14	126 (3)	O2—C24—O3	124.90 (19)
C15—C14—H15'	108 (7)	O2—C24—C16	123.79 (19)
C13—C14—H15'	143 (7)	O3—C24—C16	111.26 (17)
H14—C14—H15'	19 (8)	O3—C25—H25A	109.5
C14—C15—S1	115.0 (7)	O3—C25—H25B	109.5
C14—C15—H15	131 (3)	H25A—C25—H25B	109.5
S1—C15—H15	114 (3)	O3—C25—H25C	109.5
C14—C15—H14'	144 (5)	H25A—C25—H25C	109.5
S1—C15—H14'	98 (5)	H25B—C25—H25C	109.5

C7—N1—N2—C9	−1.1 (2)	C12'—C11—C12—S1	21 (39)
C1—N1—N2—C9	174.54 (17)	C11—C12—C13—C14	−177.4 (9)
C7—N1—C1—C6	−156.68 (19)	S1—C12—C13—C14	−0.2 (3)
N2—N1—C1—C6	28.5 (3)	C12—C13—C14—C15	0.4 (5)
C7—N1—C1—C2	24.1 (3)	C13—C14—C15—S1	−0.5 (6)
N2—N1—C1—C2	−150.69 (19)	C13—C12—S1—C15	−0.1 (2)
C6—C1—C2—C3	0.5 (3)	C11—C12—S1—C15	177.3 (7)
N1—C1—C2—C3	179.7 (2)	C14—C15—S1—C12	0.4 (4)
C1—C2—C3—C4	0.3 (4)	N3—C11—C12'—C13'	99.4 (8)
C2—C3—C4—C5	−0.6 (4)	C8—C11—C12'—C13'	−79.7 (9)
C3—C4—C5—C6	0.1 (3)	C12—C11—C12'—C13'	−154 (40)
C2—C1—C6—C5	−1.0 (3)	N3—C11—C12'—S1'	−84.4 (11)
N1—C1—C6—C5	179.79 (18)	C8—C11—C12'—S1'	96.5 (11)
C4—C5—C6—C1	0.7 (3)	C12—C11—C12'—S1'	22 (38)
N2—N1—C7—O1	−179.70 (19)	C11—C12'—C13'—C14'	176.6 (17)
C1—N1—C7—O1	5.2 (3)	S1'—C12'—C13'—C14'	0.2 (4)
N2—N1—C7—C8	0.5 (2)	S1'—C15'—C14'—C13'	0.8 (10)
C1—N1—C7—C8	−174.58 (18)	C12'—C13'—C14'—C15'	−0.6 (7)
O1—C7—C8—C11	−0.5 (3)	C14'—C15'—S1'—C12'	−0.6 (7)
N1—C7—C8—C11	179.22 (18)	C13'—C12'—S1'—C15'	0.2 (3)
O1—C7—C8—C9	−179.6 (2)	C11—C12'—S1'—C15'	−176.2 (16)
N1—C7—C8—C9	0.1 (2)	C11—N3—C16—C24	−128.0 (2)
N1—N2—C9—C8	1.1 (2)	C11—N3—C16—C17	114.3 (2)
N1—N2—C9—C10	−178.75 (18)	N3—C16—C17—C18	−65.0 (2)
C11—C8—C9—N2	−179.8 (2)	C24—C16—C17—C18	177.56 (17)
C7—C8—C9—N2	−0.8 (2)	C16—C17—C18—C19	82.1 (2)
C11—C8—C9—C10	0.1 (4)	C16—C17—C18—C23	−96.9 (2)
C7—C8—C9—C10	179.0 (2)	C23—C18—C19—C20	0.5 (3)
C16—N3—C11—C8	−179.25 (18)	C17—C18—C19—C20	−178.42 (19)
C16—N3—C11—C12	0.0 (4)	C18—C19—C20—C21	0.3 (3)
C16—N3—C11—C12'	1.6 (6)	C19—C20—C21—C22	−0.9 (4)
C9—C8—C11—N3	−176.8 (2)	C20—C21—C22—C23	0.7 (4)
C7—C8—C11—N3	4.4 (3)	C21—C22—C23—C18	0.1 (4)
C9—C8—C11—C12	3.9 (4)	C19—C18—C23—C22	−0.7 (3)
C7—C8—C11—C12	−174.9 (3)	C17—C18—C23—C22	178.2 (2)
C9—C8—C11—C12'	2.3 (6)	C25—O3—C24—O2	−2.4 (3)
C7—C8—C11—C12'	−176.5 (5)	C25—O3—C24—C16	175.07 (17)
N3—C11—C12—C13	−87.5 (5)	N3—C16—C24—O2	−37.1 (3)
C8—C11—C12—C13	91.7 (5)	C17—C16—C24—O2	82.4 (2)
C12'—C11—C12—C13	−162 (40)	N3—C16—C24—O3	145.40 (16)
N3—C11—C12—S1	95.4 (5)	C17—C16—C24—O3	−95.05 (19)
C8—C11—C12—S1	−85.4 (5)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N3—H1···O1	0.88	1.93	2.668 (2)	141

Experimental details

Crystal data
Chemical formula	C₂₅H₂₃N₃O₃S
M_r	445.52
Crystal system, space group	Monoclinic, P2₁
Temperature (K)	113
a, b, c (Å)	6.649 (2), 18.712 (6), 9.349 (3)
β (°)	104.903 (5)
V (Å³)	1124.0 (7)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.18
Crystal size (mm)	0.20 × 0.18 × 0.12

Data collection
Diffractometer	Rigaku Saturn724 CCD diffractometer
Absorption correction	Multi-scan (CrystalClear; Rigaku, 2008)
T_min, T_max	0.966, 0.979
No. of measured, independent and observed [I > 2σ(I)] reflections	11848, 2747, 2315
R_int	0.041
(sin θ/λ)_max (Å⁻¹)	0.658

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.034, 0.064, 0.98
No. of reflections	2747
No. of parameters	353
No. of restraints	215
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.15, −0.20
Absolute structure	Flack (1983), 2401 Friedel pairs
Absolute structure parameter	0.05 (8)

Computer programs: CrystalClear (Rigaku, 2008), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N3—H1···O1	0.88	1.93	2.668 (2)	141.0

Acknowledgements

The authors are grateful for financial support from the Spark Program, Foundation of Science and Technology Department of China (grant Nos. 09ZHXHNC07900 and 2010 GA610009).

References

Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565. CrossRef IUCr Journals Google Scholar
Flack, H. D. (1983). Acta Cryst. A39, 876–881. CrossRef CAS Web of Science IUCr Journals Google Scholar
Li, J., Jiang, L. & An, Y. (2004). Chin. J. Appl. Chem. 21, 150–153. CAS Google Scholar
Rigaku (2008). CrystalClear. Rigaku Corporation, Tokyo, Japan. Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Tan, C., Pan, L. & Fu, Y. (2009). Mod. Agrochem. 2, 6–12. Google Scholar
Xiong, G., Yang, Z. & Guo, A. (1993). Fine Chem. 6, 1–3. Google Scholar
Zhang, X., Huang, M., Du, C. & Han, J. (2010). Acta Cryst. E66, o273. Web of Science CSD CrossRef IUCr Journals Google Scholar
Zhu, H., Shi, J., Wei, Z., Dai, R. & Zhang, X. (2010). Acta Cryst. E66, o1352. Web of Science CSD CrossRef IUCr Journals Google Scholar

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Volume 67| Part 8| August 2011| Page o2200

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organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Methyl 2-{[(3-methyl-5-oxo-1-phenyl-4,5-di­hydro-1H-pyrazol-4-yl­­idene)(thio­phen-2-yl)meth­yl]amino}-3-phenyl­propionate

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Experimental

Crystal data

Data collection

Refinement

Supporting information

Acknowledgements

References

organic compounds

Methyl 2-{[(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-ylidene)(thiophen-2-yl)methyl]amino}-3-phenylpropionate