Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S0108270111031155/em3042sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S0108270111031155/em3042Isup2.hkl |
CCDC reference: 846646
For related literature, see: Bernstein et al. (1995); Chen et al. (2011); Kastelic et al. (2010); Munshi & Guru Row (2006); Schultheiss & Newman (2009); Sweetman et al. (2007).
Equimolar amounts of fluconazole (100 mg, 0.33 mmol) and salicylic acid (45.1 mg, 0.33 mmol) were dissolved in acetonitrile (3.0 ml) by mixing at 323 K. After cooling to ambient temperature, the solvent was allowed to evaporate slowly. Colourless crystals of (I) appeared after 72 h.
All H atoms were initially found in a difference Fourier map, but they were repositioned in their calculated positions and refined using a riding model. Aromatic H atoms were permitted to ride with C—H = 0.93 Å and Uiso(H) = 1.2Ueq(C), H atoms bonded to O with O—H = 0.82 Å and Uiso(H) = 1.5Ueq(O), and H atoms of the CH2 group with C—H = 0.97 Å and Uiso(H) = 1.2Ueq(C).
Data collection: COLLECT (Nonius, 1998); cell refinement: DENZO and SCALEPACK (Otwinowski & Minor, 1997); data reduction: DENZO and SCALEPACK (Otwinowski & Minor, 1997); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008) and PLATON (Spek, 2009).
C13H12F2N6O·C7H6O3 | Z = 2 |
Mr = 444.40 | F(000) = 460 |
Triclinic, P1 | Dx = 1.446 Mg m−3 |
Hall symbol: -P 1 | Mo Kα radiation, λ = 0.71073 Å |
a = 6.8522 (2) Å | Cell parameters from 4060 reflections |
b = 10.5580 (4) Å | θ = 1–27.5° |
c = 14.3009 (6) Å | µ = 0.12 mm−1 |
α = 82.862 (3)° | T = 150 K |
β = 84.892 (2)° | Prismatic, colourless |
γ = 86.091 (3)° | 0.18 × 0.16 × 0.15 mm |
V = 1020.80 (6) Å3 |
Nonius KappaCCD area-detector diffractometer | 3385 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.028 |
Graphite monochromator | θmax = 27.4°, θmin = 3.4° |
ω scans at κ = 55° | h = −8→8 |
8238 measured reflections | k = −13→13 |
4579 independent reflections | l = −18→18 |
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) = 0.114 | H-atom parameters constrained |
S = 1.03 | w = 1/[σ2(Fo2) + (0.0516P)2 + 0.286P] where P = (Fo2 + 2Fc2)/3 |
4579 reflections | (Δ/σ)max < 0.001 |
292 parameters | Δρmax = 0.23 e Å−3 |
0 restraints | Δρmin = −0.23 e Å−3 |
C13H12F2N6O·C7H6O3 | γ = 86.091 (3)° |
Mr = 444.40 | V = 1020.80 (6) Å3 |
Triclinic, P1 | Z = 2 |
a = 6.8522 (2) Å | Mo Kα radiation |
b = 10.5580 (4) Å | µ = 0.12 mm−1 |
c = 14.3009 (6) Å | T = 150 K |
α = 82.862 (3)° | 0.18 × 0.16 × 0.15 mm |
β = 84.892 (2)° |
Nonius KappaCCD area-detector diffractometer | 3385 reflections with I > 2σ(I) |
8238 measured reflections | Rint = 0.028 |
4579 independent reflections |
R[F2 > 2σ(F2)] = 0.044 | 0 restraints |
wR(F2) = 0.114 | H-atom parameters constrained |
S = 1.03 | Δρmax = 0.23 e Å−3 |
4579 reflections | Δρmin = −0.23 e Å−3 |
292 parameters |
Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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 > 2σ(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. |
x | y | z | Uiso*/Ueq | ||
C10 | 0.2580 (2) | 0.34959 (15) | 0.29105 (11) | 0.0214 (3) | |
O1 | 0.07917 (16) | 0.42443 (11) | 0.28560 (8) | 0.0255 (3) | |
H1 | 0.0209 | 0.4221 | 0.3384 | 0.038* | |
F2 | 0.56548 (14) | 0.15618 (10) | 0.33173 (9) | 0.0436 (3) | |
F4 | 0.13257 (18) | −0.16925 (10) | 0.41991 (9) | 0.0508 (3) | |
C1 | 0.2242 (2) | 0.21160 (14) | 0.33335 (11) | 0.0209 (3) | |
C2 | 0.3774 (2) | 0.12039 (16) | 0.34912 (12) | 0.0283 (4) | |
C3 | 0.3528 (3) | −0.00678 (17) | 0.37904 (13) | 0.0344 (4) | |
H3 | 0.4591 | −0.0648 | 0.3897 | 0.041* | |
C4 | 0.1629 (3) | −0.04356 (16) | 0.39231 (13) | 0.0330 (4) | |
C5 | 0.0038 (3) | 0.03938 (16) | 0.37807 (13) | 0.0313 (4) | |
H5 | −0.1229 | 0.0112 | 0.3876 | 0.038* | |
C6 | 0.0366 (2) | 0.16730 (16) | 0.34885 (11) | 0.0254 (3) | |
H6 | −0.0706 | 0.2250 | 0.3394 | 0.030* | |
O1S | −0.41051 (17) | 0.37408 (11) | −0.02620 (9) | 0.0302 (3) | |
O2S | −0.29626 (16) | 0.17181 (11) | −0.03183 (9) | 0.0310 (3) | |
H2S | −0.2115 | 0.1947 | −0.0016 | 0.047* | |
C11S | −0.4229 (2) | 0.26734 (15) | −0.05132 (11) | 0.0233 (3) | |
O21S | −0.73928 (17) | 0.45112 (11) | −0.09975 (9) | 0.0325 (3) | |
H21S | −0.6434 | 0.4572 | −0.0705 | 0.049* | |
C1S | −0.5854 (2) | 0.23845 (15) | −0.10572 (11) | 0.0224 (3) | |
C2S | −0.7373 (2) | 0.33159 (15) | −0.12520 (11) | 0.0234 (3) | |
C3S | −0.8966 (2) | 0.30116 (16) | −0.17059 (12) | 0.0276 (4) | |
H3S | −0.9978 | 0.3624 | −0.1832 | 0.033* | |
C4S | −0.9044 (2) | 0.18029 (17) | −0.19687 (12) | 0.0291 (4) | |
H4S | −1.0118 | 0.1606 | −0.2267 | 0.035* | |
C5S | −0.7540 (3) | 0.08771 (16) | −0.17939 (12) | 0.0302 (4) | |
H5S | −0.7592 | 0.0069 | −0.1983 | 0.036* | |
C6S | −0.5964 (2) | 0.11684 (16) | −0.13363 (12) | 0.0285 (4) | |
H6S | −0.4962 | 0.0547 | −0.1212 | 0.034* | |
C21 | 0.4020 (2) | 0.41730 (16) | 0.34217 (11) | 0.0260 (4) | |
H21A | 0.5270 | 0.3683 | 0.3421 | 0.031* | |
H21B | 0.4238 | 0.5010 | 0.3078 | 0.031* | |
N21 | 0.32956 (19) | 0.43207 (13) | 0.43930 (9) | 0.0239 (3) | |
N22 | 0.3401 (2) | 0.33195 (14) | 0.50916 (10) | 0.0311 (3) | |
C23 | 0.2546 (3) | 0.38283 (17) | 0.58286 (13) | 0.0316 (4) | |
H23 | 0.2385 | 0.3364 | 0.6424 | 0.038* | |
N24 | 0.1915 (2) | 0.50788 (14) | 0.56605 (10) | 0.0306 (3) | |
C25 | 0.2419 (2) | 0.53436 (16) | 0.47433 (12) | 0.0266 (4) | |
H25 | 0.2191 | 0.6135 | 0.4393 | 0.032* | |
C11 | 0.3419 (2) | 0.35202 (15) | 0.18702 (11) | 0.0241 (3) | |
H11A | 0.3416 | 0.4397 | 0.1572 | 0.029* | |
H11B | 0.4766 | 0.3170 | 0.1848 | 0.029* | |
N11 | 0.22649 (18) | 0.27812 (12) | 0.13536 (9) | 0.0219 (3) | |
N12 | 0.28188 (19) | 0.15352 (13) | 0.12599 (10) | 0.0255 (3) | |
C13 | 0.1353 (2) | 0.11649 (16) | 0.08485 (12) | 0.0264 (4) | |
H13 | 0.1314 | 0.0341 | 0.0687 | 0.032* | |
N14 | −0.01002 (19) | 0.20836 (13) | 0.06786 (10) | 0.0258 (3) | |
C15 | 0.0523 (2) | 0.30860 (15) | 0.10112 (11) | 0.0244 (3) | |
H15 | −0.0150 | 0.3882 | 0.1007 | 0.029* |
U11 | U22 | U33 | U12 | U13 | U23 | |
C10 | 0.0181 (7) | 0.0233 (8) | 0.0232 (8) | −0.0005 (6) | −0.0011 (6) | −0.0054 (6) |
O1 | 0.0252 (6) | 0.0263 (6) | 0.0243 (6) | 0.0052 (5) | −0.0021 (5) | −0.0037 (5) |
F2 | 0.0182 (5) | 0.0378 (6) | 0.0738 (8) | 0.0020 (4) | −0.0038 (5) | −0.0050 (5) |
F4 | 0.0628 (8) | 0.0223 (6) | 0.0662 (8) | −0.0076 (5) | −0.0067 (6) | 0.0031 (5) |
C1 | 0.0211 (7) | 0.0225 (8) | 0.0200 (8) | 0.0006 (6) | −0.0019 (6) | −0.0062 (6) |
C2 | 0.0187 (8) | 0.0310 (9) | 0.0359 (10) | −0.0007 (6) | −0.0030 (7) | −0.0072 (7) |
C3 | 0.0333 (9) | 0.0266 (9) | 0.0430 (11) | 0.0063 (7) | −0.0077 (8) | −0.0048 (8) |
C4 | 0.0434 (10) | 0.0195 (8) | 0.0361 (10) | −0.0041 (7) | −0.0048 (8) | −0.0015 (7) |
C5 | 0.0278 (9) | 0.0301 (9) | 0.0365 (10) | −0.0073 (7) | −0.0023 (7) | −0.0031 (7) |
C6 | 0.0222 (8) | 0.0278 (9) | 0.0263 (8) | −0.0006 (6) | −0.0016 (6) | −0.0046 (7) |
O1S | 0.0289 (6) | 0.0236 (6) | 0.0406 (7) | −0.0012 (5) | −0.0070 (5) | −0.0104 (5) |
O2S | 0.0248 (6) | 0.0260 (6) | 0.0454 (8) | 0.0032 (5) | −0.0123 (5) | −0.0123 (5) |
C11S | 0.0207 (8) | 0.0227 (8) | 0.0260 (8) | −0.0004 (6) | 0.0018 (6) | −0.0044 (6) |
O21S | 0.0328 (7) | 0.0215 (6) | 0.0452 (8) | 0.0038 (5) | −0.0129 (6) | −0.0080 (5) |
C1S | 0.0215 (8) | 0.0223 (8) | 0.0233 (8) | −0.0016 (6) | 0.0001 (6) | −0.0034 (6) |
C2S | 0.0271 (8) | 0.0194 (8) | 0.0232 (8) | −0.0015 (6) | 0.0005 (6) | −0.0024 (6) |
C3S | 0.0259 (8) | 0.0281 (9) | 0.0284 (9) | 0.0012 (6) | −0.0053 (7) | −0.0011 (7) |
C4S | 0.0283 (9) | 0.0340 (9) | 0.0261 (9) | −0.0057 (7) | −0.0057 (7) | −0.0038 (7) |
C5S | 0.0325 (9) | 0.0269 (9) | 0.0333 (9) | −0.0041 (7) | −0.0040 (7) | −0.0097 (7) |
C6S | 0.0256 (8) | 0.0257 (9) | 0.0345 (9) | 0.0030 (6) | −0.0039 (7) | −0.0068 (7) |
C21 | 0.0251 (8) | 0.0272 (9) | 0.0266 (9) | −0.0057 (6) | 0.0009 (7) | −0.0071 (7) |
N21 | 0.0240 (7) | 0.0244 (7) | 0.0242 (7) | −0.0032 (5) | −0.0019 (5) | −0.0056 (5) |
N22 | 0.0364 (8) | 0.0280 (8) | 0.0285 (8) | −0.0047 (6) | −0.0015 (6) | −0.0013 (6) |
C23 | 0.0311 (9) | 0.0362 (10) | 0.0282 (9) | −0.0076 (7) | −0.0005 (7) | −0.0053 (7) |
N24 | 0.0234 (7) | 0.0388 (9) | 0.0319 (8) | −0.0029 (6) | −0.0029 (6) | −0.0126 (6) |
C25 | 0.0238 (8) | 0.0277 (9) | 0.0303 (9) | −0.0016 (6) | −0.0041 (7) | −0.0095 (7) |
C11 | 0.0215 (8) | 0.0256 (8) | 0.0261 (8) | −0.0047 (6) | −0.0002 (6) | −0.0063 (7) |
N11 | 0.0217 (6) | 0.0211 (7) | 0.0229 (7) | 0.0003 (5) | −0.0005 (5) | −0.0043 (5) |
N12 | 0.0266 (7) | 0.0233 (7) | 0.0268 (7) | 0.0042 (5) | −0.0008 (6) | −0.0077 (6) |
C13 | 0.0266 (8) | 0.0248 (8) | 0.0288 (9) | −0.0004 (6) | −0.0022 (7) | −0.0072 (7) |
N14 | 0.0238 (7) | 0.0248 (7) | 0.0296 (8) | −0.0001 (5) | −0.0033 (6) | −0.0066 (6) |
C15 | 0.0250 (8) | 0.0234 (8) | 0.0244 (8) | 0.0035 (6) | −0.0024 (6) | −0.0035 (6) |
C10—O1 | 1.4149 (18) | C3S—H3S | 0.9300 |
C10—C1 | 1.531 (2) | C4S—C5S | 1.389 (2) |
C10—C21 | 1.541 (2) | C4S—H4S | 0.9300 |
C10—C11 | 1.544 (2) | C5S—C6S | 1.382 (2) |
O1—H1 | 0.8200 | C5S—H5S | 0.9300 |
F2—C2 | 1.3610 (18) | C6S—H6S | 0.9300 |
F4—C4 | 1.3611 (19) | C21—N21 | 1.456 (2) |
C1—C6 | 1.388 (2) | C21—H21A | 0.9700 |
C1—C2 | 1.389 (2) | C21—H21B | 0.9700 |
C2—C3 | 1.374 (2) | N21—C25 | 1.331 (2) |
C3—C4 | 1.374 (3) | N21—N22 | 1.3641 (19) |
C3—H3 | 0.9300 | N22—C23 | 1.315 (2) |
C4—C5 | 1.364 (2) | C23—N24 | 1.360 (2) |
C5—C6 | 1.390 (2) | C23—H23 | 0.9300 |
C5—H5 | 0.9300 | N24—C25 | 1.326 (2) |
C6—H6 | 0.9300 | C25—H25 | 0.9300 |
O1S—C11S | 1.2351 (19) | C11—N11 | 1.4531 (19) |
O2S—C11S | 1.3043 (18) | C11—H11A | 0.9700 |
O2S—H2S | 0.8200 | C11—H11B | 0.9700 |
C11S—C1S | 1.483 (2) | N11—C15 | 1.334 (2) |
O21S—C2S | 1.3551 (19) | N11—N12 | 1.3635 (18) |
O21S—H21S | 0.8200 | N12—C13 | 1.313 (2) |
C1S—C6S | 1.400 (2) | C13—N14 | 1.358 (2) |
C1S—C2S | 1.404 (2) | C13—H13 | 0.9300 |
C2S—C3S | 1.393 (2) | N14—C15 | 1.324 (2) |
C3S—C4S | 1.380 (2) | C15—H15 | 0.9300 |
O1—C10—C1 | 111.57 (12) | C5S—C4S—H4S | 119.6 |
O1—C10—C21 | 109.56 (12) | C6S—C5S—C4S | 119.32 (15) |
C1—C10—C21 | 114.49 (13) | C6S—C5S—H5S | 120.3 |
O1—C10—C11 | 103.97 (12) | C4S—C5S—H5S | 120.3 |
C1—C10—C11 | 109.65 (12) | C5S—C6S—C1S | 120.98 (15) |
C21—C10—C11 | 106.99 (12) | C5S—C6S—H6S | 119.5 |
C10—O1—H1 | 109.5 | C1S—C6S—H6S | 119.5 |
C6—C1—C2 | 115.91 (14) | N21—C21—C10 | 112.27 (13) |
C6—C1—C10 | 121.15 (13) | N21—C21—H21A | 109.1 |
C2—C1—C10 | 122.61 (14) | C10—C21—H21A | 109.1 |
F2—C2—C3 | 116.63 (14) | N21—C21—H21B | 109.1 |
F2—C2—C1 | 119.05 (15) | C10—C21—H21B | 109.1 |
C3—C2—C1 | 124.30 (15) | H21A—C21—H21B | 107.9 |
C4—C3—C2 | 116.42 (15) | C25—N21—N22 | 109.90 (14) |
C4—C3—H3 | 121.8 | C25—N21—C21 | 128.99 (15) |
C2—C3—H3 | 121.8 | N22—N21—C21 | 121.07 (13) |
F4—C4—C5 | 118.57 (16) | C23—N22—N21 | 101.93 (14) |
F4—C4—C3 | 118.22 (16) | N22—C23—N24 | 115.47 (16) |
C5—C4—C3 | 123.21 (16) | N22—C23—H23 | 122.3 |
C4—C5—C6 | 118.08 (16) | N24—C23—H23 | 122.3 |
C4—C5—H5 | 121.0 | C25—N24—C23 | 102.08 (14) |
C6—C5—H5 | 121.0 | N24—C25—N21 | 110.62 (15) |
C1—C6—C5 | 122.08 (15) | N24—C25—H25 | 124.7 |
C1—C6—H6 | 119.0 | N21—C25—H25 | 124.7 |
C5—C6—H6 | 119.0 | N11—C11—C10 | 110.92 (12) |
C11S—O2S—H2S | 109.5 | N11—C11—H11A | 109.5 |
O1S—C11S—O2S | 123.05 (14) | C10—C11—H11A | 109.5 |
O1S—C11S—C1S | 121.94 (14) | N11—C11—H11B | 109.5 |
O2S—C11S—C1S | 115.01 (13) | C10—C11—H11B | 109.5 |
C2S—O21S—H21S | 109.5 | H11A—C11—H11B | 108.0 |
C6S—C1S—C2S | 118.98 (14) | C15—N11—N12 | 110.02 (13) |
C6S—C1S—C11S | 121.00 (14) | C15—N11—C11 | 129.44 (13) |
C2S—C1S—C11S | 119.92 (14) | N12—N11—C11 | 120.12 (13) |
O21S—C2S—C3S | 117.50 (14) | C13—N12—N11 | 102.48 (12) |
O21S—C2S—C1S | 122.78 (14) | N12—C13—N14 | 114.48 (14) |
C3S—C2S—C1S | 119.70 (14) | N12—C13—H13 | 122.8 |
C4S—C3S—C2S | 120.16 (15) | N14—C13—H13 | 122.8 |
C4S—C3S—H3S | 119.9 | C15—N14—C13 | 103.38 (13) |
C2S—C3S—H3S | 119.9 | N14—C15—N11 | 109.63 (14) |
C3S—C4S—C5S | 120.84 (15) | N14—C15—H15 | 125.2 |
C3S—C4S—H4S | 119.6 | N11—C15—H15 | 125.2 |
D—H···A | D—H | H···A | D···A | D—H···A |
O2S—H2S···N14 | 0.82 | 1.79 | 2.6012 (17) | 168 |
O21S—H21S···O1S | 0.82 | 1.89 | 2.6082 (16) | 146 |
O1—H1···N24i | 0.82 | 2.07 | 2.8190 (18) | 152 |
C15—H15···O21Sii | 0.93 | 2.31 | 3.2077 (19) | 163 |
C25—H25···F4iii | 0.93 | 2.32 | 3.184 (2) | 155 |
Symmetry codes: (i) −x, −y+1, −z+1; (ii) −x−1, −y+1, −z; (iii) x, y+1, z. |
Experimental details
Crystal data | |
Chemical formula | C13H12F2N6O·C7H6O3 |
Mr | 444.40 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 150 |
a, b, c (Å) | 6.8522 (2), 10.5580 (4), 14.3009 (6) |
α, β, γ (°) | 82.862 (3), 84.892 (2), 86.091 (3) |
V (Å3) | 1020.80 (6) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.12 |
Crystal size (mm) | 0.18 × 0.16 × 0.15 |
Data collection | |
Diffractometer | Nonius KappaCCD area-detector diffractometer |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 8238, 4579, 3385 |
Rint | 0.028 |
(sin θ/λ)max (Å−1) | 0.647 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.044, 0.114, 1.03 |
No. of reflections | 4579 |
No. of parameters | 292 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.23, −0.23 |
Computer programs: COLLECT (Nonius, 1998), DENZO and SCALEPACK (Otwinowski & Minor, 1997), SHELXS97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997), SHELXL97 (Sheldrick, 2008) and PLATON (Spek, 2009).
D—H···A | D—H | H···A | D···A | D—H···A |
O2S—H2S···N14 | 0.82 | 1.79 | 2.6012 (17) | 167.5 |
O21S—H21S···O1S | 0.82 | 1.89 | 2.6082 (16) | 145.8 |
O1—H1···N24i | 0.82 | 2.07 | 2.8190 (18) | 151.8 |
C15—H15···O21Sii | 0.93 | 2.31 | 3.2077 (19) | 162.9 |
C25—H25···F4iii | 0.93 | 2.32 | 3.184 (2) | 154.6 |
Symmetry codes: (i) −x, −y+1, −z+1; (ii) −x−1, −y+1, −z; (iii) x, y+1, z. |
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An important goal of the solid-state formulation development of drugs with multicomponent crystalline phases is a search for new pharmaceutical cocrystal forms. A pharmaceutical cocrystal can be defined as a multicomponent crystal system of the active pharmaceutical ingredient (API) with another pharmaceutically acceptable molecule, both existing as solids under ambient conditions. The presence of a cocrystal former in a solid form can have an impact on the chemical and physical properties of APIs, which can lead to improved and optimized drug formulations. Thus, cocrystals have become a complementary tool in addition to polymorphs, pseudopolymorphs (solvates) and salts in the development of pharmaceuticals in solid form (Schultheiss & Newman, 2009; Chen et al., 2011, and references therein).
Fluconazole is a wide-spectrum triazole antifungal agent used in the treatment of localized candidiasis and systematic therapy of candidial infections, dermatophytic fungal infections and cryptococcal meningitis. It is commonly used as an accompanying therapy for immunodeficient patients with AIDS or cancer and patients taking immunodepresive agents (Sweetman et al., 2007). It is only slightly soluble in water. Thus, its cocrystallization with pharmaceutically acceptable cocrystal formers presents an attractive option to increase its solubility. Along these lines, we have focused our research on the preparation of new fluconazole cocrystals and have recently reported the crystal structures of three fluconazole cocrystals with three dicarboxylic acids, namely maleic, glutaric and fumaric acids (Kastelic et al., 2010). We have extended our research to the preparation and investigation of further fluconazole cocrystals, not only with aliphatic dicarboxylic acids which proved to be appropriate cocrystal formers, but also with aromatic and/or monocarboxylic acids. We present here the crystal structure of a 1:1 cocrystal of fluconazole and salicylic acid, (I).
The asymmetric unit of (I) consists of one fluconazole and one salicylic acid molecule (Fig. 1), both in their neutral forms. An intramolecular hydrogen bond of type S(6) (Bernstein et al., 1995) is observed in the salicylic acid group, with the OH group at the ortho position as donor and the carbonyl O atom of the carboxylic acid group as the acceptor. The hydrogen-bonding details are given in Table 1. The fluconazole and salicylic acid molecules each form homomeric centrosymmetric dimers via hydrogen bonds. The two fluconazole molecules, related by an inversion centre, are linked through an O—H···N hydrogen bond, forming an R22(14) motif. The fluconazole OH group serves as the hydrogen-bond donor to triazole atom N24 at position 4 of an adjacent fluconazole molecule. The salicylic acid molecules form centrosymmetric head-to-tail dimers through O—H···O interactions between neighbouring molecules, involving the ortho-OH group as the hydrogen-bond donor to the carbonyl O atom of an adjacent salicylic acid molecule, forming an R22(4) motif. Such a pattern differs from the hydrogen-bonding motif observed in the crystal structure of pure salicylic acid, where the typical head-to-tail interaction through the carboxylic acid groups is observed (Munshi et al., 2006). Thus, the carboxylic acid OH group remains available for further hydrogen-bond formation in (I). Indeed, the fluconazole and salicylic acid dimers in (I) are linked through an intermolecular O—H···N hydrogen bond, involving the carboxylic acid OH group and triazole atom N14 of an adjacent fluconazole moiety (Fig. 2). In this way, an infinite zig-zag tape of alternating fluconazole and salicylic acid dimers is formed, which runs along the ac diagonal. Additionally, two short C—H···X intermolecular contacts were observed (Table 1). The C15—H15···O21S(-x-1, -y+1, -z) contact connects the fluconazole and salicylic acid moieties within the tape and thus stabilizes its formation. F atoms (F4) protrude from the tape on both sides. The C25—H25···F4(x, y+1, z) interaction brings the adjacent parallel tapes closer and increases the dimensionality to a three-dimensional supramolecular structure.