organic compounds
1-Oxoisoindoline-2-carboxamide
aUniversity of the Punjab, Institute of Chemistry, Lahore 54590, Pakistan, bUniversity of Sargodha, Department of Physics, Sargodha, Pakistan, and cUniversity of Sargodha, Department of Chemistry, Sargodha, Pakistan
*Correspondence e-mail: dmntahir_uos@yahoo.com
The title molecule, C9H8N2O2, is essentially planar. The is stabilized by hydrogen bonding. An intramolecular N—H⋯O hydrogen bond results in a six-membered ring. Each molecule interacts with two others through N—H⋯O and C—H⋯O hydrogen bonding, resulting in the formation of nine-membered rings. These hydrogen bonds generate a two-dimensional polymeric network. There are also π–π interactions between the aromatic and heterocyclic rings [centroid–centroid distance 3.638 (2) Å].
Related literature
For related literature, see: Berger et al. (1999); Cignarella et al. (1981); Goddard (1977); Goddard & Levitt (1979); Maliha et al. (2007); Mancilla et al. (2007); Momose (1980); Zuman (2004).
Experimental
Crystal data
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Refinement
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Data collection: APEX2 (Bruker, 2007); cell APEX2; data reduction: SAINT (Bruker, 2007); 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) and PLATON (Spek, 2003); software used to prepare material for publication: WinGX (Farrugia, 1999) and PLATON.
Supporting information
10.1107/S1600536808004923/at2545sup1.cif
contains datablocks global, I. DOI:Structure factors: contains datablock I. DOI: 10.1107/S1600536808004923/at2545Isup2.hkl
A mixture of o-phthaldehyde (0.67 g, 200 mmol) and urea (0.30 g, 200 mmol) in 100 ml of ethanol was refluxed for 6 h. A blue color developed. The flask contents were allowed to stand for 24 h at room temperature. A white solid was separated from the solution and was washed with ethanol,ether and hexane respectively, and dried in open air. The crystals suitable for X-ray diffraction were grown in a mixture of acetone-ethanol (1:1) by slow evaporation at room temperature. The compound is soluble in DMSO, DMF, acetone, ethyl acetate, and partially soluble in ethanol and chloroform [m.p.: 493 K, yield: 55%].
H atoms were positioned geometrically, with C—H = 0.93, 0.97 Å for aromatic and methylene C-atoms and constrained to ride on their parent atoms. The H-atoms attached to N2 were taken from fourier synthesis and their coordinates were refined. The thermal parameter of all H-atoms was taken 1.2 times Ueq of the parent atom.
Data collection: APEX2 (Bruker, 2007); cell
APEX2 (Bruker, 2007); data reduction: SAINT (Bruker, 2007); 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) and PLATON (Spek, 2003); software used to prepare material for publication: WinGX (Farrugia, 1999) and PLATON (Spek, 2003).C9H8N2O2 | F(000) = 368 |
Mr = 176.17 | Dx = 1.454 Mg m−3 |
Orthorhombic, P212121 | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: P 2ac 2ab | Cell parameters from 1295 reflections |
a = 3.9839 (3) Å | θ = 1.6–28.6° |
b = 7.8732 (8) Å | µ = 0.11 mm−1 |
c = 25.651 (2) Å | T = 296 K |
V = 804.58 (13) Å3 | Needle, colourless |
Z = 4 | 0.25 × 0.12 × 0.10 mm |
Bruker KappaAPEXII CCD diffractometer | 1254 independent reflections |
Radiation source: fine-focus sealed tube | 860 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.037 |
Detector resolution: 7.40 pixels mm-1 | θmax = 28.6°, θmin = 1.6° |
ω scans | h = −3→5 |
Absorption correction: multi-scan (SADABS; Bruker, 2005) | k = −9→10 |
Tmin = 0.975, Tmax = 0.990 | l = −34→22 |
5461 measured reflections |
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)] = 0.040 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.138 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.07 | w = 1/[σ2(Fo2) + (0.0804P)2] where P = (Fo2 + 2Fc2)/3 |
1254 reflections | (Δ/σ)max < 0.001 |
124 parameters | Δρmax = 0.23 e Å−3 |
0 restraints | Δρmin = −0.22 e Å−3 |
C9H8N2O2 | V = 804.58 (13) Å3 |
Mr = 176.17 | Z = 4 |
Orthorhombic, P212121 | Mo Kα radiation |
a = 3.9839 (3) Å | µ = 0.11 mm−1 |
b = 7.8732 (8) Å | T = 296 K |
c = 25.651 (2) Å | 0.25 × 0.12 × 0.10 mm |
Bruker KappaAPEXII CCD diffractometer | 1254 independent reflections |
Absorption correction: multi-scan (SADABS; Bruker, 2005) | 860 reflections with I > 2σ(I) |
Tmin = 0.975, Tmax = 0.990 | Rint = 0.037 |
5461 measured reflections |
R[F2 > 2σ(F2)] = 0.040 | 0 restraints |
wR(F2) = 0.138 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.07 | Δρmax = 0.23 e Å−3 |
1254 reflections | Δρmin = −0.22 e Å−3 |
124 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 | ||
O1 | 0.1443 (8) | 0.5881 (3) | 0.09333 (8) | 0.0599 (8) | |
O2 | 0.3962 (6) | 0.7070 (2) | 0.24721 (7) | 0.0479 (7) | |
N1 | 0.1909 (7) | 0.7618 (2) | 0.16626 (8) | 0.0335 (6) | |
N2 | 0.3940 (9) | 0.4951 (3) | 0.18736 (10) | 0.0512 (8) | |
H2A | 0.346 (10) | 0.476 (4) | 0.1514 (13) | 0.061* | |
H2B | 0.478 (10) | 0.421 (4) | 0.2092 (14) | 0.061* | |
C1 | 0.1002 (9) | 0.7240 (3) | 0.11498 (10) | 0.0380 (7) | |
C2 | −0.0491 (8) | 0.8806 (3) | 0.09388 (10) | 0.0351 (7) | |
C3 | −0.1770 (10) | 0.9115 (4) | 0.04430 (11) | 0.0450 (8) | |
H3 | −0.1780 | 0.8269 | 0.0190 | 0.054* | |
C4 | −0.3025 (9) | 1.0715 (4) | 0.03378 (12) | 0.0491 (8) | |
H4 | −0.3903 | 1.0952 | 0.0010 | 0.059* | |
C5 | −0.2985 (9) | 1.1968 (4) | 0.07165 (12) | 0.0489 (9) | |
H5 | −0.3837 | 1.3038 | 0.0639 | 0.059* | |
C6 | −0.1693 (9) | 1.1655 (4) | 0.12114 (11) | 0.0427 (7) | |
H6 | −0.1652 | 1.2504 | 0.1463 | 0.051* | |
C7 | −0.0474 (8) | 1.0053 (3) | 0.13185 (10) | 0.0343 (7) | |
C8 | 0.1037 (9) | 0.9367 (3) | 0.18109 (9) | 0.0335 (7) | |
H8A | 0.3014 | 1.0006 | 0.1912 | 0.040* | |
H8B | −0.0569 | 0.9384 | 0.2095 | 0.040* | |
C9 | 0.3350 (8) | 0.6532 (3) | 0.20346 (10) | 0.0350 (7) |
U11 | U22 | U33 | U12 | U13 | U23 | |
O1 | 0.102 (2) | 0.0398 (11) | 0.0383 (10) | 0.0154 (14) | −0.0116 (14) | −0.0118 (9) |
O2 | 0.0734 (18) | 0.0362 (11) | 0.0340 (10) | 0.0018 (12) | −0.0113 (11) | 0.0002 (8) |
N1 | 0.0453 (16) | 0.0263 (10) | 0.0289 (10) | 0.0045 (11) | −0.0024 (10) | −0.0006 (8) |
N2 | 0.081 (2) | 0.0327 (13) | 0.0404 (13) | 0.0173 (15) | −0.0087 (15) | 0.0015 (10) |
C1 | 0.050 (2) | 0.0358 (14) | 0.0286 (12) | −0.0004 (15) | −0.0013 (13) | −0.0047 (11) |
C2 | 0.0382 (18) | 0.0348 (14) | 0.0323 (12) | 0.0001 (13) | 0.0018 (13) | 0.0021 (11) |
C3 | 0.050 (2) | 0.0502 (17) | 0.0345 (13) | 0.0036 (18) | −0.0019 (14) | 0.0011 (13) |
C4 | 0.047 (2) | 0.064 (2) | 0.0366 (13) | 0.0042 (19) | −0.0034 (14) | 0.0140 (14) |
C5 | 0.047 (2) | 0.0477 (18) | 0.0518 (17) | 0.0100 (17) | 0.0017 (16) | 0.0159 (15) |
C6 | 0.0473 (19) | 0.0352 (14) | 0.0455 (15) | 0.0051 (16) | 0.0040 (15) | 0.0022 (12) |
C7 | 0.0365 (18) | 0.0344 (14) | 0.0321 (12) | 0.0019 (13) | 0.0018 (12) | 0.0016 (11) |
C8 | 0.0437 (19) | 0.0274 (12) | 0.0293 (11) | 0.0002 (14) | 0.0001 (12) | −0.0027 (10) |
C9 | 0.0408 (18) | 0.0314 (13) | 0.0326 (12) | −0.0014 (15) | 0.0028 (13) | 0.0020 (11) |
O1—C1 | 1.218 (3) | C3—C4 | 1.382 (4) |
O2—C9 | 1.224 (3) | C3—H3 | 0.9300 |
N1—C1 | 1.396 (3) | C4—C5 | 1.385 (5) |
N1—C9 | 1.404 (3) | C4—H4 | 0.9300 |
N1—C8 | 1.470 (3) | C5—C6 | 1.392 (4) |
N2—C9 | 1.332 (3) | C5—H5 | 0.9300 |
N2—H2A | 0.95 (3) | C6—C7 | 1.379 (4) |
N2—H2B | 0.87 (3) | C6—H6 | 0.9300 |
C1—C2 | 1.472 (4) | C7—C8 | 1.500 (4) |
C2—C7 | 1.383 (4) | C8—H8A | 0.9700 |
C2—C3 | 1.392 (4) | C8—H8B | 0.9700 |
C1—N1—C9 | 128.0 (2) | C4—C5—C6 | 121.2 (3) |
C1—N1—C8 | 112.5 (2) | C4—C5—H5 | 119.4 |
C9—N1—C8 | 119.4 (2) | C6—C5—H5 | 119.4 |
C9—N2—H2A | 114 (2) | C7—C6—C5 | 118.3 (3) |
C9—N2—H2B | 120 (2) | C7—C6—H6 | 120.8 |
H2A—N2—H2B | 126 (3) | C5—C6—H6 | 120.8 |
O1—C1—N1 | 125.4 (3) | C6—C7—C2 | 120.5 (2) |
O1—C1—C2 | 128.8 (2) | C6—C7—C8 | 129.7 (2) |
N1—C1—C2 | 105.8 (2) | C2—C7—C8 | 109.8 (2) |
C7—C2—C3 | 121.4 (3) | N1—C8—C7 | 102.36 (19) |
C7—C2—C1 | 109.5 (2) | N1—C8—H8A | 111.3 |
C3—C2—C1 | 129.1 (2) | C7—C8—H8A | 111.3 |
C4—C3—C2 | 118.1 (3) | N1—C8—H8B | 111.3 |
C4—C3—H3 | 121.0 | C7—C8—H8B | 111.3 |
C2—C3—H3 | 121.0 | H8A—C8—H8B | 109.2 |
C3—C4—C5 | 120.6 (3) | O2—C9—N2 | 124.9 (3) |
C3—C4—H4 | 119.7 | O2—C9—N1 | 119.6 (2) |
C5—C4—H4 | 119.7 | N2—C9—N1 | 115.5 (2) |
C9—N1—C1—O1 | −2.8 (5) | C5—C6—C7—C8 | −179.9 (3) |
C8—N1—C1—O1 | −179.9 (3) | C3—C2—C7—C6 | −0.9 (5) |
C9—N1—C1—C2 | 178.1 (3) | C1—C2—C7—C6 | 178.8 (3) |
C8—N1—C1—C2 | 1.0 (3) | C3—C2—C7—C8 | 179.9 (3) |
O1—C1—C2—C7 | −179.5 (3) | C1—C2—C7—C8 | −0.4 (4) |
N1—C1—C2—C7 | −0.4 (4) | C1—N1—C8—C7 | −1.2 (3) |
O1—C1—C2—C3 | 0.2 (6) | C9—N1—C8—C7 | −178.5 (2) |
N1—C1—C2—C3 | 179.3 (3) | C6—C7—C8—N1 | −178.1 (3) |
C7—C2—C3—C4 | 0.2 (5) | C2—C7—C8—N1 | 0.9 (3) |
C1—C2—C3—C4 | −179.5 (3) | C1—N1—C9—O2 | −179.3 (3) |
C2—C3—C4—C5 | 0.3 (5) | C8—N1—C9—O2 | −2.4 (4) |
C3—C4—C5—C6 | −0.1 (5) | C1—N1—C9—N2 | 0.6 (5) |
C4—C5—C6—C7 | −0.6 (5) | C8—N1—C9—N2 | 177.5 (3) |
C5—C6—C7—C2 | 1.1 (5) |
D—H···A | D—H | H···A | D···A | D—H···A |
N2—H2A···O1 | 0.95 (3) | 1.91 (3) | 2.710 (3) | 140 (2) |
N2—H2B···O2i | 0.88 (3) | 2.08 (3) | 2.943 (3) | 167 (3) |
C8—H8A···O2ii | 0.97 | 2.57 | 3.447 (4) | 151 |
Symmetry codes: (i) −x+1, y−1/2, −z+1/2; (ii) −x+1, y+1/2, −z+1/2. |
Experimental details
Crystal data | |
Chemical formula | C9H8N2O2 |
Mr | 176.17 |
Crystal system, space group | Orthorhombic, P212121 |
Temperature (K) | 296 |
a, b, c (Å) | 3.9839 (3), 7.8732 (8), 25.651 (2) |
V (Å3) | 804.58 (13) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.11 |
Crystal size (mm) | 0.25 × 0.12 × 0.10 |
Data collection | |
Diffractometer | Bruker KappaAPEXII CCD diffractometer |
Absorption correction | Multi-scan (SADABS; Bruker, 2005) |
Tmin, Tmax | 0.975, 0.990 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 5461, 1254, 860 |
Rint | 0.037 |
(sin θ/λ)max (Å−1) | 0.674 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.040, 0.138, 1.07 |
No. of reflections | 1254 |
No. of parameters | 124 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.23, −0.22 |
Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997) and PLATON (Spek, 2003), WinGX (Farrugia, 1999) and PLATON (Spek, 2003).
D—H···A | D—H | H···A | D···A | D—H···A |
N2—H2A···O1 | 0.95 (3) | 1.91 (3) | 2.710 (3) | 140 (2) |
N2—H2B···O2i | 0.88 (3) | 2.08 (3) | 2.943 (3) | 167 (3) |
C8—H8A···O2ii | 0.97 | 2.57 | 3.447 (4) | 151 |
Symmetry codes: (i) −x+1, y−1/2, −z+1/2; (ii) −x+1, y+1/2, −z+1/2. |
Acknowledgements
The authors acknowledge the Higher Education Commision, Islamabad, Pakistan, for the purchase of the diffractometer.
References
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This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
A number of isoindole type compounds are known due to their wide importance in pharmaceutical industry (Berger et al., 1999; Cignarella et al., 1981). Several isoindoles have exhibited anti-inflammatory and analgesic activity (Mancilla et al., 2007). Certain substituted isoindoles have wide applications as herbicides (Goddard, 1977; Goddard et al., 1979). In continuation to our studies of ortho-phthaldehyde with various types of ureas (Maliha et al., 2007), the present compound is isolated when simple urea is reacted as given in preparation. The estimation of urea present in the biological fluids is determined with the help of color development (Momose, 1980; Zuman, 2004) when it is reacted with ortho-phthaldehyde. This fact was utilized for the formation of the title compond (I).
For comparison the best molecule is of 1-oxo-N-phenylisoindoline-2- carboxamide (Maliha et al., 2007). The bond distances in the aromatic ring (A) containing C3 are in the range of 1.379 (4) Å to 1.392 (4) Å. The formation of heterocyclic ring (B: C1/N1/C8/C7/C2) containing carbonyl group (C1?O1) and attached to ring (A), affects the bond angles in the aromatic ring. These bond angles vary in the range [118.1 (3)°-121.2 (3)°]. In this range there are three values which are compareable for diagonal atoms. The range of the bond angles in the heterocyclic ring is [1.396 (3) Å - 1.500 (4) Å], in comparison to [1.3865 (17) Å - 1.5016 (18) Å] as reported in 1-oxo-N-phenylisoindoline-2-carboxamide. The molecule is essentially planar with a maximum deviation of -0.028 (3) Å for N2. There exists an intramolecular H-bond [N2—H2A···O1], thus forming a six membered ring as shown in Fig 1. The O1-atom is not involved in intermolecular H-bonding. There exist intermolecular H-bond of N—H···O and C—H···O type as given in the Table 1. This kind of H-bond links each asymmetric unit at two places as shown in Fig 2. The distance between ring centroids of aromatic and heterocyclic is 3.638 (2) Å along the a axis, which is indication of π-π interaction.