2,4-Dibromo-6-[(quinolin-8-yl­amino)­methyl­idene]cyclo­hexa-2,4-dien-1-one monohydrate

Kawamoto, K.; Shibahara, T.

doi:10.1107/S1600536811048793

organic compounds

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Volume 67| Part 12| December 2011| Page o3380

https://doi.org/10.1107/S1600536811048793

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2,4-Dibromo-6-[(quinolin-8-ylamino)methylidene]cyclohexa-2,4-dien-1-one monohydrate

Keisuke Kawamoto ^a and Takashi Shibahara ^a ^*

^aDepartment of Chemistry, Okayama University of Science, Ridai-cho, Okayama 700-0005, Japan
^*Correspondence e-mail: shiba@chem.ous.ac.jp

(Received 27 October 2011; accepted 16 November 2011; online 19 November 2011)

In the title compound, C₁₆H₁₀Br₂N₂O·H₂O, bifurcated intramolecular N—H⋯(N,O) hydrogen bonding defines the essential planarity of the main molecule: the dihedral angle between the quinoline and benzene rings is 7.53 (8)°. Intermolecular O—H⋯O and weak C—H⋯O hydrogen bonds consolidate the crystal packing, which exhibits π–π interactions with a distance of 3.588 (1) Å between the centroids of the aromatic rings and short Br⋯Br contacts of 3.5757 (6) Å.

Related literature

For a related structure, see: Shibahara et al. (2010 ).

Experimental

Crystal data

C₁₆H₁₀Br₂N₂O·H₂O
M_r = 424.09
Triclinic, $[P \overline 1]$
a = 7.0027 (8) Å
b = 8.2782 (11) Å
c = 12.9164 (19) Å
α = 94.953 (9)°
β = 102.010 (5)°
γ = 94.551 (6)°
V = 725.99 (17) Å³
Z = 2
Mo Kα radiation
μ = 5.61 mm⁻¹
T = 93 K
0.64 × 0.58 × 0.18 mm

Data collection

Rigaku Mercury70 diffractometer
Absorption correction: multi-scan (REQAB; Rigaku, 1998 ) T_min = 0.145, T_max = 0.364
6768 measured reflections
3281 independent reflections
3070 reflections with F² > 2σ(F²)
R_int = 0.049

Refinement

R[F² > 2σ(F²)] = 0.038
wR(F²) = 0.104
S = 1.00
3281 reflections
239 parameters
3 restraints
H-atom parameters constrained
Δρ_max = 1.13 e Å⁻³
Δρ_min = −1.49 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O2—H2a⋯O1	0.95	1.86	2.802 (4)	171
N1—H4⋯O1	0.83	1.90	2.592 (4)	140
N1—H4⋯N2	0.83	2.31	2.668 (3)	107
C7—H3⋯O2ⁱ	0.95	2.31	3.234 (4)	166
Symmetry code: (i) x, y-1, z.

Data collection: CrystalClear (Rigaku, 2007 ); 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: CrystalStructure (Rigaku, 2010 ); software used to prepare material for publication: CrystalStructure.

Supporting information

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S1600536811048793/cv5187sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536811048793/cv5187Isup2.hkl

Supporting information file. DOI: https://doi.org/10.1107/S1600536811048793/cv5187Isup3.cml

checkCIF report

Comment top

The title dibromo compound (I) was obtained by the condensation reaction of salicylaldehyde with 8-aminoquinoline. We have reported the synthesis and X-ray structure of the corresponding dichloro compound 2,4-Dichloro-6-(8-quinolylaminomethylene)cyclohexa-2,4-dien-1-one methanol solvate (II).methanol (Shibahara et al., 2010). The compounds (I) and (II) exist in the keto form and the C=O and N—H bonds are mutually cis in the crystal structure (Fig. 1). The dihedral angle between the quinoline and benzene rings in (I) [7.53 (8)°] is smaller than that in (II) [11.17 (3)°]. The crystal packing of (I) exhibits π-π interactions with the distance of 3.588 (1) Å between the centroids of aromatic rings.

In the crystal structure of (I).H₂O, H₂O molecule are linked through intermolecular O—H···O, weak C—H···O hydrogen bonds (Table 1). There are short Br···Br contacts of 3.5757 (6) Å (the sum of van der Waals radii of Br, 3.70 Å). In addition, the O···O distance (2.981 (4) Å) between two adjacent water molecules is shorter than the sum (3.04 Å) of van der Waals radii.

Related literature top

For a related structure, see: Shibahara et al. (2010).

Experimental top

Refluxing a suspension of 8-aminoquinoline (104 mg, 0.7 mmol) and 3,5-dibromo-salicylaldehyde (200 mg, 0.7 mmol) in acetonitrile (2 ml) at 65°C for three hours gave red powder, C₁₆H₁₀Br₂N₂O (I), Yield 256 mg (83%). Anal. Found: C, 47.27; H, 2.05; N, 6.69%. Calcd for C₁₆H₁₀Br₂N₂O (I): C, 47.32; H, 2.48; N, 6.90%. Orange block single crystals of (I).H₂O suitable for X-ray analysis were obtained by dissolving 10 mg of (I) in acetonitrile (10 ml) containing small amount of water (ca 0.2%) followed by the slow evaporation of the acetonitrile solution Yield 90%. Anal. Found: C, 45.51; H, 2.76; N, 6.34%. Calcd for C₁₆H₁₀Br₂N₂O (I).H₂O: C, 45.31; H, 2.85; N, 6.61%.

Structure description top

For a related structure, see: Shibahara et al. (2010).

Computing details top

Data collection: CrystalClear (Rigaku, 2007); cell refinement: CrystalClear (Rigaku, 2007); data reduction: CrystalClear (Rigaku, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: CrystalStructure (Rigaku, 2010); software used to prepare material for publication: CrystalStructure (Rigaku, 2010).

Figures top

Fig. 1. The molecular structure of (I).H₂O with the atom–labeling scheme. Displacement ellipsoids are drawn at the 50% probability level. Hydrogen bonds are shown as dashed lines.

2,4-Dibromo-6-[(quinolin-8-ylamino)methylidene]cyclohexa-2,4-dien-1-one monohydrate top

Crystal data top

C₁₆H₁₀Br₂N₂O·H₂O	Z = 2
M_r = 424.09	F(000) = 416.00
Triclinic, P1	D_x = 1.940 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71075 Å
a = 7.0027 (8) Å	Cell parameters from 2134 reflections
b = 8.2782 (11) Å	θ = 3.1–30.0°
c = 12.9164 (19) Å	µ = 5.61 mm⁻¹
α = 94.953 (9)°	T = 93 K
β = 102.010 (5)°	Block, orange
γ = 94.551 (6)°	0.64 × 0.58 × 0.18 mm
V = 725.99 (17) Å³

Data collection top

Rigaku Mercury70 diffractometer	3070 reflections with F² > 2σ(F²)
Detector resolution: 7.314 pixels mm^-1	R_int = 0.049
ω scans	θ_max = 27.5°
Absorption correction: multi-scan (REQAB; Rigaku, 1998)	h = −9→9
T_min = 0.145, T_max = 0.364	k = −10→10
6768 measured reflections	l = −16→16
3281 independent reflections

Refinement top

Refinement on F²	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.038	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.104	H-atom parameters constrained
S = 1.00	w = 1/[σ²(F_o²) + (0.0485P)² + 1.155P] where P = (F_o² + 2F_c²)/3
3281 reflections	(Δ/σ)_max < 0.001
239 parameters	Δρ_max = 1.13 e Å⁻³
3 restraints	Δρ_min = −1.49 e Å⁻³
Primary atom site location: structure-invariant direct methods

Crystal data top

C₁₆H₁₀Br₂N₂O·H₂O	γ = 94.551 (6)°
M_r = 424.09	V = 725.99 (17) Å³
Triclinic, P1	Z = 2
a = 7.0027 (8) Å	Mo Kα radiation
b = 8.2782 (11) Å	µ = 5.61 mm⁻¹
c = 12.9164 (19) Å	T = 93 K
α = 94.953 (9)°	0.64 × 0.58 × 0.18 mm
β = 102.010 (5)°

Data collection top

Rigaku Mercury70 diffractometer	3281 independent reflections
Absorption correction: multi-scan (REQAB; Rigaku, 1998)	3070 reflections with F² > 2σ(F²)
T_min = 0.145, T_max = 0.364	R_int = 0.049
6768 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.038	3 restraints
wR(F²) = 0.104	H-atom parameters constrained
S = 1.00	Δρ_max = 1.13 e Å⁻³
3281 reflections	Δρ_min = −1.49 e Å⁻³
239 parameters

Special details top

Geometry. The dihedral angle between the quinoline rings (C8~C16, N2) and the benzene rings (C1~C6) is 7.53 (8)^o: Mean derivations of the atoms from the former and latter planes are 0.004 and 0.015 Å, respectively.

Refinement. Refinement was performed using all reflections. The weighted R-factor (wR) and goodness of fit (S) are based on F². R-factor (gt) are based on F. The threshold expression of F² > 2.0 σ(F²) is used only for calculating R-factor (gt).

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
Br2	−0.34236 (4)	−0.27358 (3)	0.49272 (2)	0.01502 (11)
Br1	−0.11289 (4)	0.39307 (3)	0.60673 (2)	0.01673 (11)
O2	0.0121 (4)	0.5645 (3)	0.8971 (3)	0.0284 (6)
O1	0.1087 (3)	0.2673 (3)	0.81099 (16)	0.0151 (4)
N1	0.2083 (4)	0.0514 (3)	0.94081 (18)	0.0110 (5)
N2	0.4089 (4)	0.3076 (3)	1.06739 (19)	0.0134 (5)
C9	0.2975 (4)	−0.1272 (4)	1.0815 (3)	0.0125 (5)
C10	0.3944 (4)	−0.1428 (4)	1.1866 (3)	0.0139 (6)
C11	0.4926 (4)	−0.0104 (4)	1.2520 (2)	0.0138 (5)
C12	0.5002 (4)	0.1450 (4)	1.2159 (2)	0.0123 (5)
C16	0.4041 (4)	0.1628 (4)	1.1104 (2)	0.0109 (5)
C13	0.6009 (4)	0.2872 (4)	1.2787 (3)	0.0155 (6)
C14	0.6063 (4)	0.4315 (4)	1.2356 (3)	0.0165 (6)
C15	0.5084 (4)	0.4354 (4)	1.1284 (3)	0.0145 (6)
C8	0.3016 (4)	0.0233 (4)	1.0440 (2)	0.0103 (5)
C7	0.1134 (4)	−0.0578 (4)	0.8644 (2)	0.0112 (5)
C6	0.0197 (4)	−0.0169 (4)	0.7638 (2)	0.0112 (5)
C5	−0.0839 (4)	−0.1449 (4)	0.6883 (3)	0.0123 (5)
C4	−0.1845 (4)	−0.1088 (4)	0.5924 (2)	0.0121 (5)
C3	−0.1870 (4)	0.0531 (4)	0.5671 (3)	0.0133 (5)
C2	−0.0905 (4)	0.1771 (4)	0.6392 (2)	0.0121 (5)
C1	0.0202 (4)	0.1516 (4)	0.7428 (2)	0.0112 (5)
H1	−0.2620	0.0797	0.4991	0.0342*
H2	−0.0912	−0.2521	0.7072	0.0161*
H4	0.2139	0.1456	0.9242	0.0275*
H5	0.2367	−0.2221	1.0381	0.0106*
H6	0.3890	−0.2477	1.2091	0.0202*
H7	0.5539	−0.0174	1.3234	0.0211*
H8	0.6675	0.2841	1.3519	0.0097*
H9	0.6727	0.5322	1.2716	0.0153*
H2a	0.0342	0.4649	0.8612	0.0548*
H2b	−0.1246	0.5552	0.8955	0.1042*
H10	0.5148	0.5362	1.0986	0.0174*
H3	0.1074	−0.1692	0.8772	0.0135*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Br2	0.02026 (17)	0.01242 (17)	0.00997 (16)	0.00054 (11)	0.00004 (11)	−0.00334 (11)
Br1	0.02187 (18)	0.01128 (17)	0.01506 (17)	−0.00026 (11)	−0.00019 (12)	0.00230 (12)
O2	0.0317 (13)	0.0174 (12)	0.0381 (15)	0.0017 (9)	0.0168 (11)	−0.0071 (11)
O1	0.0196 (10)	0.0114 (9)	0.0125 (10)	−0.0009 (8)	0.0020 (8)	−0.0027 (8)
N1	0.0143 (10)	0.0124 (11)	0.0077 (11)	0.0023 (9)	0.0054 (8)	0.0003 (9)
N2	0.0162 (11)	0.0138 (11)	0.0106 (11)	0.0008 (9)	0.0049 (9)	−0.0005 (9)
C9	0.0154 (12)	0.0125 (13)	0.0103 (12)	0.0012 (10)	0.0056 (10)	−0.0013 (10)
C10	0.0170 (13)	0.0147 (13)	0.0124 (13)	0.0037 (10)	0.0080 (10)	0.0014 (11)
C11	0.0145 (12)	0.0200 (14)	0.0073 (12)	0.0034 (10)	0.0031 (10)	−0.0000 (11)
C12	0.0119 (12)	0.0176 (14)	0.0086 (12)	0.0018 (10)	0.0055 (9)	−0.0011 (10)
C16	0.0126 (12)	0.0138 (13)	0.0082 (12)	0.0024 (9)	0.0069 (9)	−0.0000 (10)
C13	0.0158 (12)	0.0220 (15)	0.0084 (12)	0.0008 (11)	0.0040 (10)	−0.0020 (11)
C14	0.0170 (13)	0.0196 (15)	0.0128 (13)	−0.0022 (11)	0.0070 (10)	−0.0050 (11)
C15	0.0179 (13)	0.0135 (13)	0.0126 (13)	0.0003 (10)	0.0067 (10)	−0.0029 (11)
C8	0.0114 (11)	0.0143 (13)	0.0060 (12)	0.0033 (10)	0.0046 (9)	−0.0021 (10)
C7	0.0133 (11)	0.0117 (12)	0.0093 (12)	0.0007 (10)	0.0048 (9)	−0.0012 (10)
C6	0.0129 (12)	0.0117 (13)	0.0102 (12)	0.0017 (9)	0.0058 (9)	−0.0003 (10)
C5	0.0145 (12)	0.0120 (13)	0.0112 (13)	0.0024 (10)	0.0050 (10)	−0.0010 (10)
C4	0.0138 (12)	0.0130 (13)	0.0093 (12)	−0.0001 (10)	0.0044 (9)	−0.0038 (10)
C3	0.0156 (12)	0.0160 (14)	0.0094 (12)	0.0024 (10)	0.0052 (10)	0.0007 (10)
C2	0.0147 (12)	0.0115 (12)	0.0105 (12)	0.0020 (10)	0.0030 (10)	0.0017 (10)
C1	0.0138 (12)	0.0129 (13)	0.0079 (12)	0.0016 (9)	0.0047 (9)	0.0001 (10)

Geometric parameters (Å, º) top

Br2—C4	1.899 (3)	C6—C1	1.444 (4)
Br1—C2	1.883 (3)	C5—C4	1.362 (4)
O1—C1	1.269 (3)	C4—C3	1.407 (4)
N1—C8	1.405 (4)	C3—C2	1.357 (4)
N1—C7	1.308 (4)	C2—C1	1.441 (4)
N2—C16	1.365 (4)	O2—H2a	0.950
N2—C15	1.318 (4)	O2—H2b	0.950
C9—C10	1.408 (4)	N1—H4	0.827
C9—C8	1.375 (4)	C9—H5	0.940
C10—C11	1.366 (4)	C10—H6	0.940
C11—C12	1.406 (5)	C11—H7	0.941
C12—C16	1.415 (4)	C13—H8	0.966
C12—C13	1.417 (4)	C14—H9	0.953
C16—C8	1.423 (4)	C15—H10	0.950
C13—C14	1.362 (5)	C7—H3	0.950
C14—C15	1.417 (4)	C5—H2	0.941
C7—C6	1.411 (4)	C3—H1	0.977
C6—C5	1.416 (4)

Br1···O1	3.079 (2)	N1···H5^v	3.5727
O1···N1	2.592 (4)	N2···H5^vi	3.1676
O1···N2	3.507 (3)	N2···H2bⁱⁱⁱ	2.4795
O1···C7	2.836 (4)	N2···H10^iv	2.7204
N1···N2	2.668 (3)	C9···H4^v	3.5576
N1···C1	2.846 (4)	C9···H4^vi	3.4525
N2···C13	2.806 (4)	C9···H10ⁱ	3.2816
C9···C12	2.810 (4)	C10···H4^vi	3.3478
C9···C7	2.957 (4)	C10···H9ⁱ	3.5628
C10···C16	2.793 (5)	C10···H10ⁱ	3.0491
C11···C8	2.789 (4)	C11···H1^xi	3.2864
C12···C15	2.746 (5)	C11···H4^vi	3.5395
C16···C14	2.738 (4)	C12···H2^v	3.3776
C15···C8	3.584 (4)	C12···H3^vi	3.2196
C6···C3	2.782 (4)	C16···H5^vi	3.4957
C5···C2	2.794 (4)	C16···H2bⁱⁱⁱ	3.1593
C4···C1	2.847 (4)	C16···H3^vi	3.3870
Br2···Br1ⁱ	3.5758 (6)	C13···H1^xi	3.4564
Br1···Br2ⁱⁱ	3.5758 (6)	C13···H2^vi	3.4377
O2···O2ⁱⁱⁱ	2.981 (4)	C13···H3^vi	3.2974
O2···O1	2.802 (4)	C14···H6ⁱⁱ	3.1729
O2···N2ⁱⁱⁱ	3.317 (4)	C14···H2a^iv	3.1287
O2···C9ⁱⁱ	3.513 (4)	C14···H2bⁱⁱⁱ	3.4607
O2···C14^iv	3.461 (5)	C14···H3^vi	3.4954
O2···C15ⁱⁱⁱ	3.591 (4)	C15···H5^vi	3.5171
O2···C15^iv	3.441 (4)	C15···H6ⁱⁱ	2.9843
O2···C7ⁱⁱ	3.235 (4)	C15···H2a^iv	3.2156
O1···O2	2.802 (4)	C15···H2bⁱⁱⁱ	2.6491
O1···C9^v	3.573 (4)	C15···H10^iv	2.9333
O1···C10^v	3.599 (4)	C8···H3^v	3.5002
O1···C14^iv	3.245 (4)	C7···H2bⁱ	3.5859
O1···C15^iv	3.407 (4)	C6···H7^vi	3.4036
N1···C9^vi	3.543 (4)	C5···H8^vi	3.3410
N1···C10^vi	3.579 (4)	C4···H1^vii	3.5635
N1···C11^vi	3.584 (4)	C4···H7^v	3.2202
N1···C12^vi	3.548 (4)	C3···H7^ix	3.2679
N1···C16^vi	3.501 (4)	C3···H7^v	3.1868
N1···C8^vi	3.504 (4)	C3···H8^ix	3.5317
N2···O2ⁱⁱⁱ	3.317 (4)	C2···H6^v	3.2008
N2···C9^vi	3.433 (4)	C2···H7^v	3.5484
N2···C15^iv	3.549 (4)	C2···H9^iv	3.5608
C9···O2ⁱ	3.513 (4)	C2···H2a	3.4792
C9···O1^v	3.573 (4)	C1···H6^v	3.2005
C9···N1^vi	3.543 (4)	C1···H7^vi	3.5052
C9···N2^vi	3.433 (4)	C1···H9^iv	3.2966
C9···C16^vi	3.566 (5)	C1···H2a	2.8785
C9···C7^v	3.531 (4)	H1···Br2^viii	3.3259
C9···C6^v	3.494 (5)	H1···C11^ix	3.2864
C9···C1^v	3.500 (5)	H1···C13^ix	3.4564
C10···O1^v	3.599 (4)	H1···C4^vii	3.5635
C10···N1^vi	3.579 (4)	H1···H1^viii	3.4915
C10···C6^v	3.435 (4)	H1···H7^ix	2.4008
C10···C2^v	3.417 (5)	H1···H7^v	3.4186
C10···C1^v	3.216 (4)	H1···H8^ix	2.6504
C11···N1^vi	3.584 (4)	H2···Br1ⁱ	3.0863
C11···C7^vi	3.438 (5)	H2···O2ⁱ	2.9874
C11···C6^v	3.577 (4)	H2···C12^v	3.3776
C11···C6^vi	3.455 (4)	H2···C13^vi	3.4377
C11···C5^v	3.430 (5)	H2···H8^vi	3.2389
C11···C4^v	3.386 (5)	H2···H2aⁱ	3.2590
C11···C3^v	3.503 (5)	H2···H2bⁱ	3.0600
C12···N1^vi	3.548 (4)	H4···C9^v	3.5576
C12···C7^vi	3.204 (4)	H4···C9^vi	3.4525
C12···C6^vi	3.570 (4)	H4···C10^vi	3.3478
C12···C5^v	3.395 (4)	H4···C11^vi	3.5395
C16···N1^vi	3.501 (4)	H4···H5^v	3.3911
C16···C9^vi	3.566 (5)	H4···H2a	3.1151
C16···C8^vi	3.504 (4)	H4···H2bⁱⁱⁱ	3.4361
C16···C7^vi	3.512 (4)	H4···H10^iv	3.1944
C13···C7^vi	3.545 (5)	H5···O2ⁱ	2.5933
C14···O2^iv	3.461 (5)	H5···O2^v	3.4645
C14···O1^iv	3.245 (4)	H5···O1^v	3.4254
C15···O2ⁱⁱⁱ	3.591 (4)	H5···N1^v	3.5727
C15···O2^iv	3.441 (4)	H5···N2^vi	3.1676
C15···O1^iv	3.407 (4)	H5···C16^vi	3.4957
C15···N2^iv	3.549 (4)	H5···C15^vi	3.5171
C15···C15^iv	3.553 (5)	H5···H4^v	3.3911
C8···N1^vi	3.504 (4)	H5···H2aⁱ	3.3155
C8···C16^vi	3.504 (4)	H5···H2a^v	3.1946
C8···C8^vi	3.251 (4)	H5···H2bⁱ	3.1505
C8···C7^v	3.382 (4)	H5···H2b^v	3.0498
C7···O2ⁱ	3.235 (4)	H5···H10ⁱ	2.9431
C7···C9^v	3.531 (4)	H6···Br1^v	3.5893
C7···C11^vi	3.438 (5)	H6···O1^v	3.4300
C7···C12^vi	3.204 (4)	H6···O1^vi	3.5961
C7···C16^vi	3.512 (4)	H6···C14ⁱ	3.1729
C7···C13^vi	3.545 (5)	H6···C15ⁱ	2.9843
C7···C8^v	3.382 (4)	H6···C2^v	3.2008
C6···C9^v	3.494 (5)	H6···C1^v	3.2005
C6···C10^v	3.435 (4)	H6···H9ⁱ	2.8425
C6···C11^v	3.577 (4)	H6···H2a^v	3.2544
C6···C11^vi	3.455 (4)	H6···H2b^v	3.0578
C6···C12^vi	3.570 (4)	H6···H10ⁱ	2.5189
C5···C11^v	3.430 (5)	H7···Br2^xi	3.1930
C5···C12^v	3.395 (4)	H7···C6^vi	3.4036
C4···C11^v	3.386 (5)	H7···C4^v	3.2202
C3···C11^v	3.503 (5)	H7···C3^xi	3.2679
C3···C3^vii	3.553 (5)	H7···C3^v	3.1868
C2···C10^v	3.417 (5)	H7···C2^v	3.5484
C1···C9^v	3.500 (5)	H7···C1^vi	3.5052
C1···C10^v	3.216 (4)	H7···H1^xi	2.4008
Br2···H1	2.9246	H7···H1^v	3.4186
Br2···H2	2.9386	H8···Br2^v	3.3349
Br1···H1	2.8453	H8···Br1^xi	3.3429
O1···H4	1.9019	H8···C5^vi	3.3410
N1···H5	2.6838	H8···C3^xi	3.5317
N2···H4	2.3054	H8···H1^xi	2.6504
N2···H9	3.2262	H8···H2^vi	3.2389
C9···H4	3.1744	H9···Br2^xii	3.1799
C9···H7	3.2758	H9···Br1^iv	3.1411
C9···H3	2.6758	H9···O2^iv	3.4986
C11···H5	3.2439	H9···O1^iv	2.6114
C11···H8	2.7263	H9···C10ⁱⁱ	3.5628
C12···H6	3.2712	H9···C2^iv	3.5608
C12···H9	3.2986	H9···C1^iv	3.2966
C16···H4	2.4811	H9···H6ⁱⁱ	2.8425
C16···H5	3.2915	H9···H2a^iv	2.9358
C16···H7	3.2635	H2a···Br1	3.2207
C16···H8	3.3035	H2a···O2ⁱⁱⁱ	3.2332
C16···H10	3.1514	H2a···O1	1.8607
C13···H7	2.6451	H2a···C14^iv	3.1287
C13···H10	3.2352	H2a···C15^iv	3.2156
C15···H4	3.5810	H2a···C2	3.4792
C15···H8	3.2635	H2a···C1	2.8785
C8···H6	3.2335	H2a···H2ⁱⁱ	3.2590
C8···H3	2.6218	H2a···H4	3.1151
C7···H2	2.5738	H2a···H5ⁱⁱ	3.3155
C7···H5	2.7450	H2a···H5^v	3.1946
C6···H4	2.4512	H2a···H6^v	3.2544
C5···H1	3.2960	H2a···H9^iv	2.9358
C5···H3	2.5606	H2a···H2bⁱⁱⁱ	3.0958
C3···H2	3.2649	H2a···H10^iv	3.0931
C1···H1	3.3264	H2a···H3ⁱⁱ	3.0138
C1···H2	3.3407	H2b···O2ⁱⁱⁱ	2.9125
C1···H4	2.4574	H2b···O1	3.2329
C1···H3	3.3243	H2b···N2ⁱⁱⁱ	2.4795
H2···H3	2.3548	H2b···C16ⁱⁱⁱ	3.1593
H4···H5	3.4942	H2b···C14ⁱⁱⁱ	3.4607
H4···H3	2.6355	H2b···C15ⁱⁱⁱ	2.6491
H5···H6	2.2800	H2b···C7ⁱⁱ	3.5859
H5···H3	2.1835	H2b···H2ⁱⁱ	3.0600
H6···H7	2.3672	H2b···H4ⁱⁱⁱ	3.4361
H7···H8	2.5302	H2b···H5ⁱⁱ	3.1505
H8···H9	2.3801	H2b···H5^v	3.0498
H9···H10	2.2819	H2b···H6^v	3.0578
Br2···H1^viii	3.3259	H2b···H2aⁱⁱⁱ	3.0958
Br2···H7^ix	3.1930	H2b···H2bⁱⁱⁱ	3.1439
Br2···H8^v	3.3349	H2b···H10ⁱⁱⁱ	2.7953
Br2···H9^x	3.1799	H2b···H3ⁱⁱ	2.7509
Br1···H2ⁱⁱ	3.0863	H10···O2^iv	3.4704
Br1···H6^v	3.5893	H10···O1^iv	2.9448
Br1···H8^ix	3.3429	H10···N2^iv	2.7204
Br1···H9^iv	3.1411	H10···C9ⁱⁱ	3.2816
Br1···H2a	3.2207	H10···C10ⁱⁱ	3.0491
O2···H2ⁱⁱ	2.9874	H10···C15^iv	2.9333
O2···H5ⁱⁱ	2.5933	H10···H4^iv	3.1944
O2···H5^v	3.4645	H10···H5ⁱⁱ	2.9431
O2···H9^iv	3.4986	H10···H6ⁱⁱ	2.5189
O2···H2aⁱⁱⁱ	3.2332	H10···H2a^iv	3.0931
O2···H2bⁱⁱⁱ	2.9125	H10···H2bⁱⁱⁱ	2.7953
O2···H10^iv	3.4704	H10···H10^iv	2.5278
O2···H3ⁱⁱ	2.3043	H3···O2ⁱ	2.3043
O1···H5^v	3.4254	H3···C12^vi	3.2196
O1···H6^v	3.4300	H3···C16^vi	3.3870
O1···H6^vi	3.5961	H3···C13^vi	3.2974
O1···H9^iv	2.6114	H3···C14^vi	3.4954
O1···H2a	1.8607	H3···C8^v	3.5002
O1···H2b	3.2329	H3···H2aⁱ	3.0138
O1···H10^iv	2.9448	H3···H2bⁱ	2.7509

C8—N1—C7	126.9 (3)	Br1—C2—C1	118.04 (19)
C16—N2—C15	117.5 (3)	C3—C2—C1	122.9 (3)
C10—C9—C8	119.6 (3)	O1—C1—C6	122.4 (3)
C9—C10—C11	120.9 (3)	O1—C1—C2	123.1 (3)
C10—C11—C12	120.9 (3)	C6—C1—C2	114.5 (3)
C11—C12—C16	119.0 (3)	H2a—O2—H2b	104.997
C11—C12—C13	124.0 (3)	C8—N1—H4	118.703
C16—C12—C13	117.0 (3)	C7—N1—H4	114.421
N2—C16—C12	123.1 (3)	C10—C9—H5	118.165
N2—C16—C8	117.8 (3)	C8—C9—H5	122.173
C12—C16—C8	119.1 (3)	C9—C10—H6	117.050
C12—C13—C14	119.8 (3)	C11—C10—H6	122.057
C13—C14—C15	118.6 (3)	C10—C11—H7	122.229
N2—C15—C14	123.9 (3)	C12—C11—H7	116.883
N1—C8—C9	123.8 (3)	C12—C13—H8	121.326
N1—C8—C16	115.6 (3)	C14—C13—H8	118.840
C9—C8—C16	120.5 (3)	C13—C14—H9	125.339
N1—C7—C6	122.7 (3)	C15—C14—H9	116.025
C7—C6—C5	117.7 (3)	N2—C15—H10	118.045
C7—C6—C1	120.1 (3)	C14—C15—H10	118.053
C5—C6—C1	122.0 (3)	N1—C7—H3	118.643
C6—C5—C4	119.2 (3)	C6—C7—H3	118.650
Br2—C4—C5	120.9 (2)	C6—C5—H2	119.587
Br2—C4—C3	117.73 (19)	C4—C5—H2	120.964
C5—C4—C3	121.2 (3)	C4—C3—H1	121.379
C4—C3—C2	120.2 (3)	C2—C3—H1	118.393
Br1—C2—C3	119.0 (2)

C8—N1—C7—C6	178.3 (3)	C12—C16—C8—C9	−0.6 (4)
C7—N1—C8—C9	−3.4 (5)	C12—C13—C14—C15	0.6 (5)
C7—N1—C8—C16	176.7 (3)	C13—C14—C15—N2	1.0 (5)
C16—N2—C15—C14	−1.3 (5)	N1—C7—C6—C5	−178.0 (3)
C15—N2—C16—C12	−0.1 (4)	N1—C7—C6—C1	−2.1 (5)
C15—N2—C16—C8	−178.2 (3)	C7—C6—C5—C4	176.6 (3)
C10—C9—C8—N1	−179.5 (3)	C7—C6—C1—O1	2.5 (5)
C10—C9—C8—C16	0.4 (4)	C7—C6—C1—C2	−176.5 (3)
C8—C9—C10—C11	0.0 (5)	C5—C6—C1—O1	178.2 (3)
C9—C10—C11—C12	−0.3 (5)	C5—C6—C1—C2	−0.7 (4)
C10—C11—C12—C16	0.1 (5)	C1—C6—C5—C4	0.8 (5)
C10—C11—C12—C13	−179.3 (3)	C6—C5—C4—Br2	−175.0 (3)
C11—C12—C16—N2	−177.8 (3)	C6—C5—C4—C3	0.1 (5)
C11—C12—C16—C8	0.3 (4)	Br2—C4—C3—C2	174.29 (19)
C11—C12—C13—C14	177.5 (3)	C5—C4—C3—C2	−1.0 (5)
C16—C12—C13—C14	−1.8 (4)	C4—C3—C2—Br1	−175.4 (3)
C13—C12—C16—N2	1.6 (4)	C4—C3—C2—C1	1.0 (5)
C13—C12—C16—C8	179.7 (3)	Br1—C2—C1—O1	−2.7 (4)
N2—C16—C8—N1	−2.5 (4)	Br1—C2—C1—C6	176.26 (16)
N2—C16—C8—C9	177.6 (3)	C3—C2—C1—O1	−179.2 (3)
C12—C16—C8—N1	179.3 (3)	C3—C2—C1—C6	−0.2 (4)

Symmetry codes: (i) x, y−1, z; (ii) x, y+1, z; (iii) −x, −y+1, −z+2; (iv) −x+1, −y+1, −z+2; (v) −x, −y, −z+2; (vi) −x+1, −y, −z+2; (vii) −x, −y, −z+1; (viii) −x−1, −y, −z+1; (ix) x−1, y, z−1; (x) x−1, y−1, z−1; (xi) x+1, y, z+1; (xii) x+1, y+1, z+1.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O2—H2a···O1	0.95	1.86	2.802 (4)	171
N1—H4···O1	0.83	1.90	2.592 (4)	140
N1—H4···N2	0.83	2.31	2.668 (3)	107
C7—H3···O2ⁱ	0.95	2.31	3.234 (4)	166

Symmetry code: (i) x, y−1, z.

Experimental details

Crystal data
Chemical formula	C₁₆H₁₀Br₂N₂O·H₂O
M_r	424.09
Crystal system, space group	Triclinic, P1
Temperature (K)	93
a, b, c (Å)	7.0027 (8), 8.2782 (11), 12.9164 (19)
α, β, γ (°)	94.953 (9), 102.010 (5), 94.551 (6)
V (Å³)	725.99 (17)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	5.61
Crystal size (mm)	0.64 × 0.58 × 0.18

Data collection
Diffractometer	Rigaku Mercury70
Absorption correction	Multi-scan (REQAB; Rigaku, 1998)
T_min, T_max	0.145, 0.364
No. of measured, independent and observed [F² > 2σ(F²)] reflections	6768, 3281, 3070
R_int	0.049
(sin θ/λ)_max (Å⁻¹)	0.650

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.038, 0.104, 1.00
No. of reflections	3281
No. of parameters	239
No. of restraints	3
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	1.13, −1.49

Computer programs: CrystalClear (Rigaku, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), CrystalStructure (Rigaku, 2010).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O2—H2a···O1	0.950	1.861	2.802 (4)	170.6
N1—H4···O1	0.827	1.902	2.592 (4)	140.2
N1—H4···N2	0.827	2.305	2.668 (3)	107.1
C7—H3···O2ⁱ	0.950	2.305	3.234 (4)	166.07

Symmetry code: (i) x, y−1, z.

Acknowledgements

The authors thank Mr Yuta Komine for the preparation of the title compound and the Japan Private School Promotion Foundation for financial support.

References

Rigaku (1998). REQAB. Rigaku Corporation, Tokyo, Japan. Google Scholar
Rigaku (2007). CrystalClear. Rigaku Corporation, Tokyo, Japan. Google Scholar
Rigaku (2010). CrystalStructure. Rigaku Corporation, Tokyo, Japan. Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Shibahara, T., Takahashi, M., Maekawa, A. & Takagi, H. (2010). Acta Cryst. E66, o429. Web of Science CSD CrossRef IUCr Journals Google Scholar

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Volume 67| Part 12| December 2011| Page o3380

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

2,4-Di­bromo-6-[(quinolin-8-yl­amino)­methyl­­idene]cyclo­hexa-2,4-dien-1-one monohydrate

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Experimental

Crystal data

Data collection

Refinement

Supporting information

Acknowledgements

References

organic compounds

2,4-Dibromo-6-[(quinolin-8-ylamino)methylidene]cyclohexa-2,4-dien-1-one monohydrate