Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536801004548/bt6025sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536801004548/bt6025Isup2.hkl |
CCDC reference: 162823
Key indicators
- Single-crystal X-ray study
- T = 293 K
- Mean (C-C) = 0.003 Å
- R factor = 0.043
- wR factor = 0.120
- Data-to-parameter ratio = 17.5
checkCIF results
No syntax errors found ADDSYM reports no extra symmetry
Alert Level C:
REFLT_03 From the CIF: _diffrn_reflns_theta_max 27.55 From the CIF: _reflns_number_total 3858 TEST2: Reflns within _diffrn_reflns_theta_max Count of symmetry unique reflns 4086 Completeness (_total/calc) 94.42% Alert C: < 95% complete
0 Alert Level A = Potentially serious problem
0 Alert Level B = Potential problem
1 Alert Level C = Please check
The title compound was prepared according to the method of Chilmonczyk et al. (1997).
Data collection: KM-4 Software (Kuma, 1993); cell refinement: KM-4 Software; data reduction: DATAPROC (Kuma, 1998); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: XP in SHELXTL/PC (Sheldrick, 1990) and ORTEP-3 (Farrugia, 1997); software used to prepare material for publication: SHELXL97.
C15H19ClN3O3+·Cl−·H2O | Z = 2 |
Mr = 378.25 | F(000) = 396 |
Triclinic, P1 | Dx = 1.420 Mg m−3 |
a = 7.122 (2) Å | Mo Kα radiation, λ = 0.71073 Å |
b = 8.809 (2) Å | Cell parameters from 99 reflections |
c = 15.178 (3) Å | θ = 5–60° |
α = 95.98 (2)° | µ = 0.39 mm−1 |
β = 99.34 (2)° | T = 293 K |
γ = 107.43 (2)° | Plate, colourless |
V = 884.6 (4) Å3 | 0.49 × 0.42 × 0.04 mm |
Kuma KM-4 diffractometer | 3418 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.014 |
Graphite monochromator | θmax = 27.6°, θmin = 2.5° |
ω–2θ scans | h = −1→9 |
Absorption correction: ψ scan (North et al., 1968) | k = −11→11 |
Tmin = 0.831, Tmax = 0.985 | l = −19→19 |
4747 measured reflections | 3 standard reflections every 100 reflections |
3858 independent reflections | intensity decay: 1.1% |
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)] = 0.043 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.120 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.04 | w = 1/[σ2(Fo2) + (0.0656P)2 + 0.312P] where P = (Fo2 + 2Fc2)/3 |
3858 reflections | (Δ/σ)max = 0.001 |
221 parameters | Δρmax = 0.35 e Å−3 |
0 restraints | Δρmin = −0.38 e Å−3 |
C15H19ClN3O3+·Cl−·H2O | γ = 107.43 (2)° |
Mr = 378.25 | V = 884.6 (4) Å3 |
Triclinic, P1 | Z = 2 |
a = 7.122 (2) Å | Mo Kα radiation |
b = 8.809 (2) Å | µ = 0.39 mm−1 |
c = 15.178 (3) Å | T = 293 K |
α = 95.98 (2)° | 0.49 × 0.42 × 0.04 mm |
β = 99.34 (2)° |
Kuma KM-4 diffractometer | 3418 reflections with I > 2σ(I) |
Absorption correction: ψ scan (North et al., 1968) | Rint = 0.014 |
Tmin = 0.831, Tmax = 0.985 | 3 standard reflections every 100 reflections |
4747 measured reflections | intensity decay: 1.1% |
3858 independent reflections |
R[F2 > 2σ(F2)] = 0.043 | 0 restraints |
wR(F2) = 0.120 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.04 | Δρmax = 0.35 e Å−3 |
3858 reflections | Δρmin = −0.38 e Å−3 |
221 parameters |
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. |
x | y | z | Uiso*/Ueq | ||
N1 | 0.1505 (2) | −0.54719 (17) | −0.23337 (10) | 0.0340 (3) | |
C1 | 0.1150 (3) | −0.4469 (2) | −0.30356 (13) | 0.0451 (4) | |
H1A | −0.0193 | −0.4422 | −0.3098 | 0.068* | |
H1B | 0.2078 | −0.3392 | −0.2862 | 0.068* | |
C2 | 0.1388 (4) | −0.5231 (3) | −0.39256 (14) | 0.0559 (5) | |
H2A | 0.1230 | −0.4586 | −0.4387 | 0.084* | |
H2B | 0.2725 | −0.5296 | −0.3848 | 0.084* | |
O1 | 0.0002 (3) | −0.6810 (2) | −0.42041 (11) | 0.0657 (5) | |
C3 | 0.0337 (4) | −0.7799 (3) | −0.35624 (17) | 0.0588 (6) | |
H3A | −0.0603 | −0.8866 | −0.3764 | 0.088* | |
H3B | 0.1665 | −0.7873 | −0.3526 | 0.088* | |
C4 | 0.0116 (3) | −0.7161 (2) | −0.26318 (15) | 0.0486 (5) | |
H4A | 0.0474 | −0.7818 | −0.2210 | 0.073* | |
H4B | −0.1250 | −0.7208 | −0.2638 | 0.073* | |
C5 | 0.1299 (3) | −0.4825 (2) | −0.14208 (12) | 0.0379 (4) | |
H5A | −0.0050 | −0.4802 | −0.1458 | 0.057* | |
H5B | 0.1520 | −0.5536 | −0.1006 | 0.057* | |
C6 | 0.2702 (3) | −0.3143 (2) | −0.10655 (12) | 0.0363 (4) | |
H6 | 0.3970 | −0.2956 | −0.1267 | 0.044* | |
O2 | 0.1872 (2) | −0.19594 (15) | −0.14219 (8) | 0.0406 (3) | |
C7 | 0.2094 (3) | −0.0743 (2) | −0.07528 (12) | 0.0369 (4) | |
O3 | 0.1696 (2) | 0.04529 (17) | −0.08899 (10) | 0.0508 (4) | |
N2 | 0.2859 (2) | −0.11091 (17) | 0.00459 (10) | 0.0370 (3) | |
C8 | 0.3015 (3) | −0.2717 (2) | −0.00396 (12) | 0.0396 (4) | |
H8A | 0.1984 | −0.3454 | 0.0186 | 0.059* | |
H8B | 0.4308 | −0.2710 | 0.0267 | 0.059* | |
N3 | 0.3085 (2) | −0.01072 (18) | 0.08314 (10) | 0.0362 (3) | |
C9 | 0.3730 (3) | −0.0571 (2) | 0.15540 (12) | 0.0375 (4) | |
H9 | 0.4039 | −0.1575 | 0.1514 | 0.056* | |
C10 | 0.4031 (3) | 0.0378 (2) | 0.24492 (12) | 0.0358 (4) | |
C11 | 0.3085 (3) | 0.1509 (2) | 0.26179 (14) | 0.0462 (4) | |
H11A | 0.2220 | 0.1740 | 0.2133 | 0.055* | |
C12 | 0.3394 (3) | 0.2327 (3) | 0.34890 (14) | 0.0499 (5) | |
H12A | 0.2692 | 0.3074 | 0.3616 | 0.060* | |
Cl1 | 0.49991 (10) | 0.29961 (7) | 0.52778 (3) | 0.05808 (17) | |
C13 | 0.4646 (3) | 0.2012 (2) | 0.41802 (12) | 0.0410 (4) | |
C14 | 0.5620 (3) | 0.0909 (3) | 0.40260 (13) | 0.0480 (5) | |
H14A | 0.6514 | 0.0723 | 0.4517 | 0.058* | |
C15 | 0.5287 (3) | 0.0087 (2) | 0.31643 (13) | 0.0464 (4) | |
H15A | 0.5925 | −0.0713 | 0.3056 | 0.056* | |
Cl2 | 0.57484 (7) | 0.43716 (6) | 0.78472 (4) | 0.04856 (15) | |
O4 | 0.8155 (3) | 0.6712 (2) | 0.97204 (12) | 0.0684 (5) | |
H41 | 0.8130 | 0.7755 | 0.9863 | 0.082* | |
H42 | 0.7142 | 0.6181 | 0.9226 | 0.082* | |
H1 | 0.279 (4) | −0.545 (3) | −0.2297 (15) | 0.045 (6)* |
U11 | U22 | U33 | U12 | U13 | U23 | |
N1 | 0.0278 (7) | 0.0367 (7) | 0.0391 (7) | 0.0137 (6) | 0.0066 (6) | 0.0045 (6) |
C1 | 0.0471 (11) | 0.0479 (10) | 0.0433 (10) | 0.0218 (9) | 0.0042 (8) | 0.0096 (8) |
C2 | 0.0632 (14) | 0.0600 (13) | 0.0395 (10) | 0.0186 (11) | 0.0017 (9) | 0.0041 (9) |
O1 | 0.0585 (10) | 0.0719 (11) | 0.0519 (9) | 0.0141 (8) | −0.0069 (7) | −0.0065 (8) |
C3 | 0.0539 (13) | 0.0471 (11) | 0.0651 (14) | 0.0086 (10) | 0.0096 (11) | −0.0099 (10) |
C4 | 0.0410 (10) | 0.0392 (10) | 0.0600 (12) | 0.0057 (8) | 0.0128 (9) | 0.0008 (8) |
C5 | 0.0356 (9) | 0.0389 (9) | 0.0411 (9) | 0.0124 (7) | 0.0126 (7) | 0.0061 (7) |
C6 | 0.0316 (8) | 0.0385 (9) | 0.0411 (9) | 0.0143 (7) | 0.0085 (7) | 0.0063 (7) |
O2 | 0.0453 (7) | 0.0401 (7) | 0.0383 (6) | 0.0189 (6) | 0.0044 (5) | 0.0062 (5) |
C7 | 0.0328 (8) | 0.0367 (9) | 0.0411 (9) | 0.0109 (7) | 0.0076 (7) | 0.0063 (7) |
O3 | 0.0648 (9) | 0.0439 (7) | 0.0496 (8) | 0.0282 (7) | 0.0061 (7) | 0.0104 (6) |
N2 | 0.0379 (8) | 0.0338 (7) | 0.0396 (7) | 0.0136 (6) | 0.0054 (6) | 0.0046 (6) |
C8 | 0.0428 (10) | 0.0370 (9) | 0.0407 (9) | 0.0176 (7) | 0.0050 (7) | 0.0054 (7) |
N3 | 0.0334 (7) | 0.0336 (7) | 0.0397 (7) | 0.0091 (6) | 0.0069 (6) | 0.0036 (6) |
C9 | 0.0380 (9) | 0.0326 (8) | 0.0419 (9) | 0.0111 (7) | 0.0091 (7) | 0.0055 (7) |
C10 | 0.0379 (9) | 0.0312 (8) | 0.0385 (9) | 0.0099 (7) | 0.0100 (7) | 0.0077 (7) |
C11 | 0.0514 (11) | 0.0473 (10) | 0.0460 (10) | 0.0259 (9) | 0.0058 (8) | 0.0105 (8) |
C12 | 0.0600 (13) | 0.0481 (11) | 0.0527 (11) | 0.0333 (10) | 0.0128 (9) | 0.0069 (9) |
Cl1 | 0.0827 (4) | 0.0555 (3) | 0.0443 (3) | 0.0324 (3) | 0.0202 (3) | 0.0025 (2) |
C13 | 0.0505 (11) | 0.0358 (9) | 0.0403 (9) | 0.0163 (8) | 0.0153 (8) | 0.0062 (7) |
C14 | 0.0598 (12) | 0.0530 (11) | 0.0400 (9) | 0.0322 (10) | 0.0070 (9) | 0.0093 (8) |
C15 | 0.0579 (12) | 0.0476 (10) | 0.0436 (10) | 0.0322 (9) | 0.0094 (9) | 0.0070 (8) |
Cl2 | 0.0353 (2) | 0.0457 (3) | 0.0667 (3) | 0.02008 (19) | 0.0035 (2) | 0.0074 (2) |
O4 | 0.0858 (13) | 0.0567 (10) | 0.0671 (10) | 0.0391 (9) | 0.0027 (9) | 0.0014 (8) |
N1—C5 | 1.489 (2) | C7—O3 | 1.199 (2) |
N1—C1 | 1.490 (2) | C7—N2 | 1.358 (2) |
N1—C4 | 1.493 (2) | N2—N3 | 1.364 (2) |
N1—H1 | 0.91 (2) | N2—C8 | 1.448 (2) |
C1—C2 | 1.502 (3) | C8—H8A | 0.9600 |
C1—H1A | 0.9600 | C8—H8B | 0.9600 |
C1—H1B | 0.9600 | N3—C9 | 1.274 (2) |
C2—O1 | 1.417 (3) | C9—C10 | 1.467 (2) |
C2—H2A | 0.9600 | C9—H9 | 0.9721 |
C2—H2B | 0.9600 | C10—C11 | 1.384 (3) |
O1—C3 | 1.411 (3) | C10—C15 | 1.387 (3) |
C3—C4 | 1.515 (3) | C11—C12 | 1.389 (3) |
C3—H3A | 0.9600 | C11—H11A | 0.9601 |
C3—H3B | 0.9600 | C12—C13 | 1.370 (3) |
C4—H4A | 0.9600 | C12—H12A | 0.9600 |
C4—H4B | 0.9600 | Cl1—C13 | 1.7385 (19) |
C5—C6 | 1.502 (2) | C13—C14 | 1.375 (3) |
C5—H5A | 0.9600 | C14—C15 | 1.375 (3) |
C5—H5B | 0.9600 | C14—H14A | 0.9599 |
C6—O2 | 1.453 (2) | C15—H15A | 0.9600 |
C6—C8 | 1.527 (2) | O4—H41 | 0.9276 |
C6—H6 | 0.9738 | O4—H42 | 0.9227 |
O2—C7 | 1.351 (2) | ||
C5—N1—C1 | 113.56 (14) | O2—C6—H6 | 104.6 |
C5—N1—C4 | 110.35 (14) | C5—C6—H6 | 111.7 |
C1—N1—C4 | 109.60 (15) | C8—C6—H6 | 112.0 |
C5—N1—H1 | 107.9 (14) | C7—O2—C6 | 110.16 (13) |
C1—N1—H1 | 105.4 (14) | O3—C7—O2 | 122.80 (17) |
C4—N1—H1 | 109.9 (14) | O3—C7—N2 | 128.42 (17) |
N1—C1—C2 | 109.08 (16) | O2—C7—N2 | 108.76 (15) |
N1—C1—H1A | 109.6 | C7—N2—N3 | 119.48 (14) |
C2—C1—H1A | 108.8 | C7—N2—C8 | 112.95 (15) |
N1—C1—H1B | 110.2 | N3—N2—C8 | 126.64 (14) |
C2—C1—H1B | 110.5 | N2—C8—C6 | 100.83 (14) |
H1A—C1—H1B | 108.7 | N2—C8—H8A | 112.1 |
O1—C2—C1 | 111.5 (2) | C6—C8—H8A | 110.7 |
O1—C2—H2A | 109.7 | N2—C8—H8B | 111.2 |
C1—C2—H2A | 111.2 | C6—C8—H8B | 112.5 |
O1—C2—H2B | 108.5 | H8A—C8—H8B | 109.3 |
C1—C2—H2B | 107.8 | C9—N3—N2 | 115.62 (15) |
H2A—C2—H2B | 108.1 | N3—C9—C10 | 121.65 (16) |
C3—O1—C2 | 109.93 (17) | N3—C9—H9 | 119.4 |
O1—C3—C4 | 112.23 (19) | C10—C9—H9 | 118.9 |
O1—C3—H3A | 108.9 | C11—C10—C15 | 118.73 (17) |
C4—C3—H3A | 109.5 | C11—C10—C9 | 123.38 (17) |
O1—C3—H3B | 109.3 | C15—C10—C9 | 117.87 (16) |
C4—C3—H3B | 109.2 | C10—C11—C12 | 120.21 (18) |
H3A—C3—H3B | 107.6 | C10—C11—H11A | 120.3 |
N1—C4—C3 | 109.69 (17) | C12—C11—H11A | 119.5 |
N1—C4—H4A | 108.5 | C13—C12—C11 | 119.58 (17) |
C3—C4—H4A | 109.0 | C13—C12—H12A | 119.8 |
N1—C4—H4B | 110.7 | C11—C12—H12A | 120.6 |
C3—C4—H4B | 110.5 | C12—C13—C14 | 121.18 (17) |
H4A—C4—H4B | 108.5 | C12—C13—Cl1 | 119.97 (15) |
N1—C5—C6 | 113.23 (14) | C14—C13—Cl1 | 118.84 (15) |
N1—C5—H5A | 108.6 | C15—C14—C13 | 118.93 (18) |
C6—C5—H5A | 107.7 | C15—C14—H14A | 121.2 |
N1—C5—H5B | 109.2 | C13—C14—H14A | 119.9 |
C6—C5—H5B | 109.9 | C14—C15—C10 | 121.35 (17) |
H5A—C5—H5B | 108.0 | C14—C15—H15A | 119.4 |
O2—C6—C5 | 110.87 (14) | C10—C15—H15A | 119.3 |
O2—C6—C8 | 104.76 (13) | H41—O4—H42 | 109.0 |
C5—C6—C8 | 112.42 (15) | ||
C1—N1—C5—C6 | −58.3 (2) | C6—C8—N2—N3 | −177.81 (15) |
N1—C5—C6—O2 | 83.06 (17) | C8—N2—N3—C9 | 8.9 (2) |
C5—C6—O2—C7 | 134.99 (15) | C5—N1—C1—C2 | −179.81 (16) |
C6—O2—C7—N2 | −5.40 (19) | N1—C1—C2—O1 | 60.0 (2) |
O2—C7—N2—N3 | −175.44 (14) | C1—C2—O1—C3 | −61.2 (2) |
C7—N2—N3—C9 | 177.06 (16) | C2—O1—C3—C4 | 59.3 (2) |
N2—N3—C9—C10 | −179.53 (15) | O1—C3—C4—N1 | −56.3 (2) |
N3—C9—C10—C11 | 21.5 (3) | C3—C4—N1—C5 | 179.78 (17) |
N3—C9—C10—C15 | −160.41 (18) | O2—C7—N2—C8 | −5.7 (2) |
C4—N1—C5—C6 | 178.24 (15) | C7—N2—C8—C6 | 13.38 (19) |
N1—C5—C6—C8 | −160.06 (14) | N2—C8—C6—O2 | −15.35 (17) |
C5—C6—C8—N2 | −135.83 (15) | C8—C6—O2—C7 | 13.49 (18) |
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1···Cl2i | 0.91 (2) | 2.13 (2) | 3.0359 (17) | 174 (2) |
O4—H42···Cl2 | 0.92 | 2.36 | 3.217 (2) | 154 |
O4—H41···O3ii | 0.93 | 2.06 | 2.873 (2) | 146 |
O4—H41···N3ii | 0.93 | 2.72 | 3.506 (2) | 143 |
O4—H41···O3iii | 0.93 | 3.36 | 3.807 (3) | 112 |
C1—H1B···O2 | 0.96 | 2.46 | 2.989 (3) | 115 |
C5—H5B···O4iv | 0.96 | 2.31 | 3.245 (3) | 163 |
C9—H9···Cl2iv | 0.97 | 2.78 | 3.666 (2) | 153 |
Symmetry codes: (i) x, y−1, z−1; (ii) −x+1, −y+1, −z+1; (iii) x+1, y+1, z+1; (iv) −x+1, −y, −z+1. |
Experimental details
Crystal data | |
Chemical formula | C15H19ClN3O3+·Cl−·H2O |
Mr | 378.25 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 293 |
a, b, c (Å) | 7.122 (2), 8.809 (2), 15.178 (3) |
α, β, γ (°) | 95.98 (2), 99.34 (2), 107.43 (2) |
V (Å3) | 884.6 (4) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.39 |
Crystal size (mm) | 0.49 × 0.42 × 0.04 |
Data collection | |
Diffractometer | Kuma KM-4 diffractometer |
Absorption correction | ψ scan (North et al., 1968) |
Tmin, Tmax | 0.831, 0.985 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 4747, 3858, 3418 |
Rint | 0.014 |
(sin θ/λ)max (Å−1) | 0.651 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.043, 0.120, 1.04 |
No. of reflections | 3858 |
No. of parameters | 221 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.35, −0.38 |
Computer programs: KM-4 Software (Kuma, 1993), KM-4 Software, DATAPROC (Kuma, 1998), SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), XP in SHELXTL/PC (Sheldrick, 1990) and ORTEP-3 (Farrugia, 1997), SHELXL97.
C6—O2—C7—N2 | −5.40 (19) | N2—C8—C6—O2 | −15.35 (17) |
O2—C7—N2—C8 | −5.7 (2) | C8—C6—O2—C7 | 13.49 (18) |
C7—N2—C8—C6 | 13.38 (19) |
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1···Cl2i | 0.91 (2) | 2.13 (2) | 3.0359 (17) | 174 (2) |
O4—H42···Cl2 | 0.92 | 2.36 | 3.217 (2) | 153.7 |
O4—H41···O3ii | 0.93 | 2.06 | 2.873 (2) | 145.5 |
O4—H41···N3ii | 0.93 | 2.72 | 3.506 (2) | 143.3 |
O4—H41···O3iii | 0.93 | 3.36 | 3.807 (3) | 112.0 |
C1—H1B···O2 | 0.96 | 2.46 | 2.989 (3) | 114.8 |
C5—H5B···O4iv | 0.96 | 2.31 | 3.245 (3) | 163.2 |
C9—H9···Cl2iv | 0.97 | 2.78 | 3.666 (2) | 152.7 |
Symmetry codes: (i) x, y−1, z−1; (ii) −x+1, −y+1, −z+1; (iii) x+1, y+1, z+1; (iv) −x+1, −y, −z+1. |
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In the Pharmaceutical Research Institute in Warsaw, a series of deriatives of 3-amino-2-oxazolidinone have been prepared (Chilmonczyk et al., 1997). It has recently been found that the oxazolidinone derivative 5-morpholinmethyl-3-(4-chloridebenzylidenamino)-2-oxazolidinone is a potential psychotropic drug (Chilmonczyk, 1995). Preliminary clinical data show that the compound exhibits antidepressive activity in humans (Rybakowski & Araszkiewicz, 1999). It is generally accepted that a specific energetically preferred conformation of a compound (so-called bioactive conformation) decides about the nature of interactions with its molecular target – pharmacological receptor. Therefore, it is of basic importance to get an insight into molecular parameters such as charge distribution, most preferred conformation or distances between specified points within a molecule (Krzywda et al., 2000).
A perspective view of the title structure, (I), together with the atom-numbering scheme are shown in Fig. 1. A l l interatomic distances are normal. The oxazolidinone ring exist in a conformation of an almost ideal half-chair, which can be deduced from the asymmetry parameters (Duax & Norton, 1975). Values and placement of asymmetry parameters are showed in Fig. 2.
The primary place of molecular interaction with an acid residue within a putative receptor site can be detected by hydrogen bonds. The structure of the title compound is assembled by strong and weak hydrogen bonds, to a three-dimensional infinite framework (Fig. 3). The water O4 atom acts as a donor for one strong and three weak intermolecular hydrogen bonds. All these weak hydrogen bonds are created via the same H atom (H41), however, in the difference Fourier map there is no orientational disorder resulting from these. In addition, O4 acts as an acceptor for two intermolecular weak hydrogen bonds with C5 and Cl2. Also noteworthy is the fact that there is a proton transfer from hydrochloric acid to N1 which is stabilized by a weak N1—H1···Cl1 hydrogen bond. In addition, in the structure, intramolecular hydrogen bonds exist linking C1 and O2 which provide additional stabilization of the molecule, creating a fused three-membered ring system.