1-[3-(4-Chloro­phen­yl)-5-(4-meth­oxy­phen­yl)-4,5-dihydro-1H-pyrazol-1-yl]butan-1-one

Fun, H.-K.; Quah, C.K.; Samshuddin, S.; Narayana, B.; Sarojini, B.K.

doi:10.1107/S1600536812009105

organic compounds

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ISSN: 2056-9890

Volume 68| Part 4| April 2012| Page o975

doi:10.1107/S1600536812009105

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1-[3-(4-Chlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl]butan-1-one

Hoong-Kun Fun,^a ^*‡ Ching Kheng Quah,^a § S. Samshuddin,^b B. Narayana ^b and B. K. Sarojini ^c

^aX-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia, ^bDepartment of Studies in Chemistry, Mangalore University, Mangalagangotri 574 199, India, and ^cDepartment of Chemistry, P. A. College of Engineering, Nadupadavu, Mangalore 574 153, India
^*Correspondence e-mail: hkfun@usm.my

(Received 27 February 2012; accepted 29 February 2012; online 7 March 2012)

In the title compound, C₂₀H₂₁ClN₂O₂, the benzene rings form dihedral angles of 6.35 (5) and 81.82 (5)° with the mean plane of the 4,5-dihydro-1H-pyrazole ring (r.m.s. deviation = 0.145 Å). This latter ring adopts an envelope conformation with the CH grouping as the flap. The dihedral angle between the benzene rings is 75.63 (4)°. In the crystal, molecules are linked by C—H⋯Cl and C—H⋯O hydrogen bonds into chains along [-201]. The crystal structure also features C—H⋯π interactions.

Related literature

For a related structure, see: Fun et al. (2010 ). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986 ). For standard bond lengths, see: Allen et al. (1987 ).

Experimental

Crystal data

C₂₀H₂₁ClN₂O₂
M_r = 356.84
Triclinic, $[P \overline 1]$
a = 6.7918 (3) Å
b = 10.8822 (4) Å
c = 13.2576 (5) Å
α = 109.202 (1)°
β = 91.396 (1)°
γ = 105.087 (1)°
V = 886.93 (6) Å³
Z = 2
Mo Kα radiation
μ = 0.23 mm⁻¹
T = 100 K
0.43 × 0.17 × 0.14 mm

Data collection

Bruker SMART APEXII DUO CCD diffractometer
Absorption correction: multi-scan (SADABS; Bruker, 2009 ) T_min = 0.908, T_max = 0.968
17324 measured reflections
6403 independent reflections
5492 reflections with I > 2σ(I)
R_int = 0.021

Refinement

R[F² > 2σ(F²)] = 0.035
wR(F²) = 0.104
S = 1.04
6403 reflections
228 parameters
H-atom parameters constrained
Δρ_max = 0.43 e Å⁻³
Δρ_min = −0.30 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

Cg1 is the centroid of the C1–C6 benzene ring.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C11—H11A⋯Cl1ⁱ	0.93	2.73	3.4539 (10)	135
C14—H14A⋯O2ⁱⁱ	0.93	2.51	3.3253 (12)	147
C18—H18A⋯Cg1ⁱⁱⁱ	0.97	2.62	3.4514 (9)	144
Symmetry codes: (i) -x+1, -y+1, -z+1; (ii) -x-1, -y+1, -z+2; (iii) x-1, y, z.

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

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536812009105/hb6658sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536812009105/hb6658Isup2.hkl

Supporting information file. DOI: 10.1107/S1600536812009105/hb6658Isup3.cml

checkCIF report

Comment top

In continuation of our work on the synthesis and sturctures of pyrazoline derivatives (Fun et al., 2010), the title compound (I) is prepared and its crystal structure is reported.

In the title molecule (Fig. 1), the two benzene rings (C1-C6 and C10-C15) form dihedral angles of 6.35 (5) and 81.82 (5)°, respectively, with the mean plane of 4,5-dihydro-1H-pyrazole ring (N1/N2/C7-C9, r.m.s. deviation = 0.145 Å). The dihedral angle between the two benzene rings is 75.63 (4)°. Bond lengths are comparable with a related structure (Fun et al., 2010).

In the crystal structure, Fig. 2, molecules are linked via C11–H11A···Cl1 and C14–H14A···O2 hydrogen bonds (Table 1) into chains along [-201]. The crystal structure is further consolidated by C18–H18A···Cg1ⁱⁱⁱ (Table 1) interactions, where Cg1 is the centroid of C1-C6 benzene ring.

Related literature top

For a related structure, see: Fun et al. (2010). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986). For standard bond lengths, see: Allen et al. (1987).

Experimental top

A mixture of (2E)-1-(4-chlorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one (2.72 g, 0.01 mol) and hydrazine hydrate (0.5 ml, 0.01 mol) in 25 ml butyric acid was refluxed for 8 h. The reaction mixture was cooled and poured into 50 ml ice-cold water. The precipitate was collected by filtration and purified by recrystallization from ethanol. Colourless blocks of (I) were grown from a DMF solution by slow evaporation and yield of the compound was 76% (m.p. : 369 K).

Structure description top

In continuation of our work on the synthesis and sturctures of pyrazoline derivatives (Fun et al., 2010), the title compound (I) is prepared and its crystal structure is reported.

For a related structure, see: Fun et al. (2010). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986). For standard bond lengths, see: Allen et al. (1987).

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 molecular structure of the title compound showing 50% probability displacement ellipsoids for non-H atoms.
	Fig. 2. The crystal structure of the title compound, viewed along the b axis. H atoms not involved in hydrogen bonds (dashed lines) have been omitted for clarity.

1-[3-(4-Chlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol- 1-yl]butan-1-one top

Crystal data top

C₂₀H₂₁ClN₂O₂	Z = 2
M_r = 356.84	F(000) = 376
Triclinic, P1	D_x = 1.336 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 6.7918 (3) Å	Cell parameters from 8526 reflections
b = 10.8822 (4) Å	θ = 3.1–32.7°
c = 13.2576 (5) Å	µ = 0.23 mm⁻¹
α = 109.202 (1)°	T = 100 K
β = 91.396 (1)°	Block, colourless
γ = 105.087 (1)°	0.43 × 0.17 × 0.14 mm
V = 886.93 (6) Å³

Data collection top

Bruker SMART APEXII DUO CCD diffractometer	6403 independent reflections
Radiation source: fine-focus sealed tube	5492 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.021
φ and ω scans	θ_max = 32.7°, θ_min = 1.6°
Absorption correction: multi-scan (SADABS; Bruker, 2009)	h = −10→9
T_min = 0.908, T_max = 0.968	k = −16→16
17324 measured reflections	l = −20→20

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)] = 0.035	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.104	H-atom parameters constrained
S = 1.04	w = 1/[σ²(F_o²) + (0.0556P)² + 0.2279P] where P = (F_o² + 2F_c²)/3
6403 reflections	(Δ/σ)_max = 0.001
228 parameters	Δρ_max = 0.43 e Å⁻³
0 restraints	Δρ_min = −0.30 e Å⁻³

Crystal data top

C₂₀H₂₁ClN₂O₂	γ = 105.087 (1)°
M_r = 356.84	V = 886.93 (6) Å³
Triclinic, P1	Z = 2
a = 6.7918 (3) Å	Mo Kα radiation
b = 10.8822 (4) Å	µ = 0.23 mm⁻¹
c = 13.2576 (5) Å	T = 100 K
α = 109.202 (1)°	0.43 × 0.17 × 0.14 mm
β = 91.396 (1)°

Data collection top

Bruker SMART APEXII DUO CCD diffractometer	6403 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2009)	5492 reflections with I > 2σ(I)
T_min = 0.908, T_max = 0.968	R_int = 0.021
17324 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.035	0 restraints
wR(F²) = 0.104	H-atom parameters constrained
S = 1.04	Δρ_max = 0.43 e Å⁻³
6403 reflections	Δρ_min = −0.30 e Å⁻³
228 parameters

Special details top

Experimental. The crystal was placed in the cold stream of an Oxford Cryosystems Cobra open-flow nitrogen cryostat (Cosier & Glazer, 1986) operating at 100.0 (1) K.

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds 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 > 2sigma(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
Cl1	0.89607 (4)	0.72819 (3)	0.48730 (2)	0.02770 (7)
O1	−0.64280 (11)	0.12922 (7)	0.66911 (6)	0.02244 (14)
O2	−0.24411 (10)	0.75836 (7)	0.97896 (5)	0.01753 (13)
N1	0.11361 (11)	0.74489 (7)	0.79068 (6)	0.01296 (12)
N2	−0.00821 (11)	0.71541 (7)	0.86691 (6)	0.01292 (12)
C1	0.42153 (13)	0.77985 (9)	0.65141 (7)	0.01642 (15)
H1A	0.3354	0.8358	0.6629	0.020*
C2	0.57466 (14)	0.79372 (10)	0.58516 (7)	0.01864 (16)
H2A	0.5930	0.8594	0.5530	0.022*
C3	0.70038 (13)	0.70779 (10)	0.56759 (7)	0.01822 (16)
C4	0.67516 (13)	0.60834 (9)	0.61348 (7)	0.01807 (16)
H4A	0.7585	0.5505	0.5995	0.022*
C5	0.52253 (13)	0.59623 (9)	0.68109 (7)	0.01569 (15)
H5A	0.5051	0.5304	0.7130	0.019*
C6	0.39554 (12)	0.68211 (8)	0.70129 (6)	0.01347 (14)
C7	0.24252 (12)	0.67322 (8)	0.77666 (6)	0.01296 (14)
C8	0.22791 (12)	0.59223 (8)	0.85087 (7)	0.01436 (14)
H8A	0.3390	0.6342	0.9095	0.017*
H8B	0.2293	0.4998	0.8123	0.017*
C9	0.01915 (12)	0.59689 (8)	0.89181 (6)	0.01294 (14)
H9A	0.0297	0.6161	0.9696	0.016*
C10	−0.15764 (12)	0.47169 (8)	0.83447 (6)	0.01292 (14)
C11	−0.15456 (14)	0.38856 (9)	0.72900 (7)	0.01689 (15)
H11A	−0.0403	0.4090	0.6939	0.020*
C12	−0.31873 (14)	0.27611 (9)	0.67577 (7)	0.01846 (16)
H12A	−0.3135	0.2218	0.6057	0.022*
C13	−0.49209 (13)	0.24412 (9)	0.72721 (7)	0.01629 (15)
C14	−0.49940 (13)	0.32638 (9)	0.83207 (7)	0.01572 (15)
H14A	−0.6146	0.3067	0.8668	0.019*
C15	−0.33179 (13)	0.43875 (8)	0.88443 (7)	0.01423 (14)
H15A	−0.3366	0.4930	0.9546	0.017*
C16	−0.82621 (16)	0.09749 (11)	0.71737 (10)	0.0288 (2)
H16A	−0.9211	0.0160	0.6690	0.043*
H16B	−0.8873	0.1709	0.7324	0.043*
H16C	−0.7935	0.0843	0.7832	0.043*
C17	−0.14102 (12)	0.78735 (8)	0.91064 (6)	0.01265 (14)
C18	−0.14900 (12)	0.90227 (8)	0.87211 (6)	0.01306 (14)
H18A	−0.1800	0.8672	0.7944	0.016*
H18B	−0.0151	0.9688	0.8905	0.016*
C19	−0.30931 (13)	0.97135 (8)	0.92125 (7)	0.01505 (14)
H19A	−0.2782	1.0069	0.9990	0.018*
H19B	−0.4434	0.9050	0.9030	0.018*
C20	−0.31538 (16)	1.08654 (9)	0.88125 (8)	0.02108 (17)
H20A	−0.4138	1.1302	0.9160	0.032*
H20B	−0.3541	1.0508	0.8048	0.032*
H20C	−0.1820	1.1513	0.8977	0.032*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.02295 (12)	0.03579 (14)	0.02385 (12)	0.00841 (9)	0.01502 (9)	0.00879 (9)
O1	0.0177 (3)	0.0192 (3)	0.0253 (3)	−0.0002 (2)	0.0032 (2)	0.0053 (3)
O2	0.0185 (3)	0.0192 (3)	0.0194 (3)	0.0091 (2)	0.0097 (2)	0.0092 (2)
N1	0.0110 (3)	0.0152 (3)	0.0140 (3)	0.0049 (2)	0.0047 (2)	0.0057 (2)
N2	0.0127 (3)	0.0142 (3)	0.0155 (3)	0.0067 (2)	0.0061 (2)	0.0074 (2)
C1	0.0142 (3)	0.0208 (4)	0.0165 (3)	0.0072 (3)	0.0039 (3)	0.0075 (3)
C2	0.0175 (4)	0.0238 (4)	0.0162 (4)	0.0058 (3)	0.0050 (3)	0.0088 (3)
C3	0.0136 (3)	0.0243 (4)	0.0136 (3)	0.0046 (3)	0.0052 (3)	0.0030 (3)
C4	0.0143 (4)	0.0214 (4)	0.0175 (4)	0.0078 (3)	0.0053 (3)	0.0031 (3)
C5	0.0133 (3)	0.0176 (3)	0.0163 (3)	0.0064 (3)	0.0041 (3)	0.0043 (3)
C6	0.0105 (3)	0.0168 (3)	0.0130 (3)	0.0049 (3)	0.0027 (2)	0.0042 (3)
C7	0.0103 (3)	0.0150 (3)	0.0140 (3)	0.0044 (3)	0.0025 (2)	0.0050 (3)
C8	0.0120 (3)	0.0169 (3)	0.0178 (3)	0.0069 (3)	0.0042 (3)	0.0083 (3)
C9	0.0130 (3)	0.0143 (3)	0.0144 (3)	0.0065 (3)	0.0041 (3)	0.0065 (3)
C10	0.0130 (3)	0.0142 (3)	0.0144 (3)	0.0062 (3)	0.0047 (3)	0.0066 (3)
C11	0.0159 (4)	0.0189 (4)	0.0159 (3)	0.0053 (3)	0.0071 (3)	0.0055 (3)
C12	0.0185 (4)	0.0191 (4)	0.0160 (3)	0.0048 (3)	0.0054 (3)	0.0038 (3)
C13	0.0151 (3)	0.0153 (3)	0.0192 (4)	0.0039 (3)	0.0028 (3)	0.0071 (3)
C14	0.0144 (3)	0.0170 (3)	0.0197 (4)	0.0060 (3)	0.0070 (3)	0.0098 (3)
C15	0.0157 (3)	0.0156 (3)	0.0150 (3)	0.0074 (3)	0.0061 (3)	0.0074 (3)
C16	0.0190 (4)	0.0264 (5)	0.0360 (5)	−0.0015 (4)	0.0059 (4)	0.0101 (4)
C17	0.0113 (3)	0.0130 (3)	0.0137 (3)	0.0050 (2)	0.0024 (2)	0.0035 (3)
C18	0.0122 (3)	0.0136 (3)	0.0150 (3)	0.0056 (3)	0.0033 (3)	0.0054 (3)
C19	0.0141 (3)	0.0148 (3)	0.0174 (3)	0.0073 (3)	0.0025 (3)	0.0045 (3)
C20	0.0252 (4)	0.0186 (4)	0.0230 (4)	0.0121 (3)	0.0016 (3)	0.0073 (3)

Geometric parameters (Å, º) top

Cl1—C3	1.7377 (9)	C9—H9A	0.9800
O1—C13	1.3661 (11)	C10—C15	1.3928 (11)
O1—C16	1.4285 (13)	C10—C11	1.3976 (11)
O2—C17	1.2305 (10)	C11—C12	1.3864 (12)
N1—C7	1.2952 (10)	C11—H11A	0.9300
N1—N2	1.3874 (9)	C12—C13	1.3981 (12)
N2—C17	1.3628 (10)	C12—H12A	0.9300
N2—C9	1.4862 (10)	C13—C14	1.3944 (12)
C1—C2	1.3878 (12)	C14—C15	1.3970 (12)
C1—C6	1.4036 (12)	C14—H14A	0.9300
C1—H1A	0.9300	C15—H15A	0.9300
C2—C3	1.3928 (13)	C16—H16A	0.9600
C2—H2A	0.9300	C16—H16B	0.9600
C3—C4	1.3829 (13)	C16—H16C	0.9600
C4—C5	1.3955 (12)	C17—C18	1.5106 (11)
C4—H4A	0.9300	C18—C19	1.5210 (11)
C5—C6	1.3983 (11)	C18—H18A	0.9700
C5—H5A	0.9300	C18—H18B	0.9700
C6—C7	1.4662 (11)	C19—C20	1.5222 (12)
C7—C8	1.5114 (11)	C19—H19A	0.9700
C8—C9	1.5376 (11)	C19—H19B	0.9700
C8—H8A	0.9700	C20—H20A	0.9600
C8—H8B	0.9700	C20—H20B	0.9600
C9—C10	1.5161 (11)	C20—H20C	0.9600

C13—O1—C16	116.96 (8)	C12—C11—H11A	119.4
C7—N1—N2	107.57 (7)	C10—C11—H11A	119.4
C17—N2—N1	122.26 (7)	C11—C12—C13	120.15 (8)
C17—N2—C9	124.98 (7)	C11—C12—H12A	119.9
N1—N2—C9	112.74 (6)	C13—C12—H12A	119.9
C2—C1—C6	120.57 (8)	O1—C13—C14	124.71 (8)
C2—C1—H1A	119.7	O1—C13—C12	115.63 (8)
C6—C1—H1A	119.7	C14—C13—C12	119.63 (8)
C1—C2—C3	118.99 (8)	C13—C14—C15	119.28 (8)
C1—C2—H2A	120.5	C13—C14—H14A	120.4
C3—C2—H2A	120.5	C15—C14—H14A	120.4
C4—C3—C2	121.74 (8)	C10—C15—C14	121.80 (8)
C4—C3—Cl1	119.37 (7)	C10—C15—H15A	119.1
C2—C3—Cl1	118.87 (7)	C14—C15—H15A	119.1
C3—C4—C5	118.89 (8)	O1—C16—H16A	109.5
C3—C4—H4A	120.6	O1—C16—H16B	109.5
C5—C4—H4A	120.6	H16A—C16—H16B	109.5
C4—C5—C6	120.66 (8)	O1—C16—H16C	109.5
C4—C5—H5A	119.7	H16A—C16—H16C	109.5
C6—C5—H5A	119.7	H16B—C16—H16C	109.5
C5—C6—C1	119.12 (8)	O2—C17—N2	119.86 (7)
C5—C6—C7	120.28 (7)	O2—C17—C18	123.61 (7)
C1—C6—C7	120.57 (7)	N2—C17—C18	116.52 (7)
N1—C7—C6	121.23 (7)	C17—C18—C19	112.44 (7)
N1—C7—C8	113.34 (7)	C17—C18—H18A	109.1
C6—C7—C8	125.25 (7)	C19—C18—H18A	109.1
C7—C8—C9	101.98 (6)	C17—C18—H18B	109.1
C7—C8—H8A	111.4	C19—C18—H18B	109.1
C9—C8—H8A	111.4	H18A—C18—H18B	107.8
C7—C8—H8B	111.4	C18—C19—C20	111.65 (7)
C9—C8—H8B	111.4	C18—C19—H19A	109.3
H8A—C8—H8B	109.2	C20—C19—H19A	109.3
N2—C9—C10	110.38 (6)	C18—C19—H19B	109.3
N2—C9—C8	99.94 (6)	C20—C19—H19B	109.3
C10—C9—C8	114.84 (7)	H19A—C19—H19B	108.0
N2—C9—H9A	110.4	C19—C20—H20A	109.5
C10—C9—H9A	110.4	C19—C20—H20B	109.5
C8—C9—H9A	110.4	H20A—C20—H20B	109.5
C15—C10—C11	117.92 (8)	C19—C20—H20C	109.5
C15—C10—C9	120.71 (7)	H20A—C20—H20C	109.5
C11—C10—C9	121.33 (7)	H20B—C20—H20C	109.5
C12—C11—C10	121.22 (8)

C7—N1—N2—C17	170.91 (8)	C7—C8—C9—C10	98.74 (7)
C7—N1—N2—C9	−10.65 (9)	N2—C9—C10—C15	−91.37 (9)
C6—C1—C2—C3	0.94 (13)	C8—C9—C10—C15	156.62 (7)
C1—C2—C3—C4	0.68 (14)	N2—C9—C10—C11	86.38 (9)
C1—C2—C3—Cl1	−178.41 (7)	C8—C9—C10—C11	−25.64 (11)
C2—C3—C4—C5	−1.50 (14)	C15—C10—C11—C12	−0.50 (13)
Cl1—C3—C4—C5	177.60 (7)	C9—C10—C11—C12	−178.30 (8)
C3—C4—C5—C6	0.70 (13)	C10—C11—C12—C13	0.25 (14)
C4—C5—C6—C1	0.87 (13)	C16—O1—C13—C14	4.58 (13)
C4—C5—C6—C7	−176.92 (8)	C16—O1—C13—C12	−176.96 (8)
C2—C1—C6—C5	−1.70 (13)	C11—C12—C13—O1	−178.16 (8)
C2—C1—C6—C7	176.08 (8)	C11—C12—C13—C14	0.38 (13)
N2—N1—C7—C6	−179.36 (7)	O1—C13—C14—C15	177.66 (8)
N2—N1—C7—C8	−4.00 (9)	C12—C13—C14—C15	−0.74 (13)
C5—C6—C7—N1	−174.99 (8)	C11—C10—C15—C14	0.12 (12)
C1—C6—C7—N1	7.25 (12)	C9—C10—C15—C14	177.94 (7)
C5—C6—C7—C8	10.22 (12)	C13—C14—C15—C10	0.49 (12)
C1—C6—C7—C8	−167.54 (8)	N1—N2—C17—O2	−179.14 (7)
N1—C7—C8—C9	15.87 (9)	C9—N2—C17—O2	2.62 (12)
C6—C7—C8—C9	−168.98 (7)	N1—N2—C17—C18	−0.20 (11)
C17—N2—C9—C10	76.57 (10)	C9—N2—C17—C18	−178.45 (7)
N1—N2—C9—C10	−101.82 (8)	O2—C17—C18—C19	−4.07 (11)
C17—N2—C9—C8	−162.10 (8)	N2—C17—C18—C19	177.04 (7)
N1—N2—C9—C8	19.52 (8)	C17—C18—C19—C20	−179.85 (7)
C7—C8—C9—N2	−19.34 (8)

Hydrogen-bond geometry (Å, º) top

Cg1 is the centroid of the C1–C6 benzene ring.

D—H···A	D—H	H···A	D···A	D—H···A
C11—H11A···Cl1ⁱ	0.93	2.73	3.4539 (10)	135
C14—H14A···O2ⁱⁱ	0.93	2.51	3.3253 (12)	147
C18—H18A···Cg1ⁱⁱⁱ	0.97	2.62	3.4514 (9)	144

Symmetry codes: (i) −x+1, −y+1, −z+1; (ii) −x−1, −y+1, −z+2; (iii) x−1, y, z.

Experimental details

Crystal data
Chemical formula	C₂₀H₂₁ClN₂O₂
M_r	356.84
Crystal system, space group	Triclinic, P1
Temperature (K)	100
a, b, c (Å)	6.7918 (3), 10.8822 (4), 13.2576 (5)
α, β, γ (°)	109.202 (1), 91.396 (1), 105.087 (1)
V (Å³)	886.93 (6)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.23
Crystal size (mm)	0.43 × 0.17 × 0.14

Data collection
Diffractometer	Bruker SMART APEXII DUO CCD
Absorption correction	Multi-scan (SADABS; Bruker, 2009)
T_min, T_max	0.908, 0.968
No. of measured, independent and observed [I > 2σ(I)] reflections	17324, 6403, 5492
R_int	0.021
(sin θ/λ)_max (Å⁻¹)	0.760

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.035, 0.104, 1.04
No. of reflections	6403
No. of parameters	228
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.43, −0.30

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

Hydrogen-bond geometry (Å, º) top

Cg1 is the centroid of the C1–C6 benzene ring.

D—H···A	D—H	H···A	D···A	D—H···A
C11—H11A···Cl1ⁱ	0.93	2.73	3.4539 (10)	135
C14—H14A···O2ⁱⁱ	0.93	2.51	3.3253 (12)	147
C18—H18A···Cg1ⁱⁱⁱ	0.97	2.62	3.4514 (9)	144

Symmetry codes: (i) −x+1, −y+1, −z+1; (ii) −x−1, −y+1, −z+2; (iii) x−1, y, z.

Footnotes

‡Thomson Reuters ResearcherID: A-3561-2009.

§Thomson Reuters ResearcherID: A-5525-2009.

Acknowledgements

The authors thank Universiti Sains Malaysia (USM) for the Research University Grant (No. 1001/PFIZIK/811160). BN thanks the UGC for financial assistance through an SAP and BSR one-time grant for the purchase of chemicals. SS thanks Mangalore University for the research facilities.

References

Allen, F. H., Kennard, O., Watson, D. G., Brammer, L., Orpen, A. G. & Taylor, R. (1987). J. Chem. Soc. Perkin Trans. 2, pp. S1–19. CSD CrossRef Web of Science Google Scholar
Bruker (2009). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
Cosier, J. & Glazer, A. M. (1986). J. Appl. Cryst. 19, 105–107. CrossRef CAS Web of Science IUCr Journals Google Scholar
Fun, H.-K., Hemamalini, M., Samshuddin, S., Narayana, B. & Yathirajan, H. S. (2010). Acta Cryst. E66, o582–o583. Web of Science CSD CrossRef CAS IUCr Journals Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Spek, A. L. (2009). Acta Cryst. D65, 148–155. Web of Science CrossRef CAS IUCr Journals Google Scholar

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Volume 68| Part 4| April 2012| Page o975

doi:10.1107/S1600536812009105

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

1-[3-(4-Chloro­phen­yl)-5-(4-meth­­oxy­phen­yl)-4,5-di­hydro-1H-pyrazol-1-yl]butan-1-one

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Experimental

Crystal data

Data collection

Refinement

Supporting information

Footnotes

Acknowledgements

References

organic compounds

1-[3-(4-Chlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl]butan-1-one