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

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 66| Part 5| May 2010| Pages o1125-o1126
https://doi.org/10.1107/S1600536810014017

(2S*)-2-Ammonio-3-(1H-indol-3-yl)propionate pyridine-2,4-di­carboxylic acid ethanol solvate

Kai Dia*

aCollege of Chemistry and Chemical Engineering, Qiqihar University, Qiqihar 161006, People's Republic of China
*Correspondence e-mail: dikai09@sohu.com

(Received 18 March 2010; accepted 15 April 2010; online 21 April 2010)

In the title compound, C11H12N2O2·C7H5NO4·C2H6O, the (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid is present in the zwitterionic form. In the crystal structure, 2-amino-3-(1H-indol-3-yl)propionic acid mol­ecules and pyridine-2,4-dicarb­oxylic acid mol­ecules are linked through strong inter­molecular O—H⋯O and N—H⋯O hydrogen bonds, forming layers parallel to (100). The layers are linked through the ethanol mol­ecules via somewhat weaker inter­molecular O—H⋯O and N—H⋯O hydrogen bonds, forming thus a three-dimensional network. Weak C—H⋯O and N—H⋯N hydrogen bonding and π–π inter­actions between the aromatic rings are also present.

Related literature

For supra­molecular structures with imino, carboxyl­ate and pyridine groups inter­connected via inter­molecular hydrogen bonds, see: Broker & Tiekink (2010[Broker, G. A. & Tiekink, E. R. T. (2010). Acta Cryst. E66, o705.]); Hemamalini & Fun (2010[Hemamalini, M. & Fun, H.-K. (2010). Acta Cryst. E66, o689-o690.]); Narimani & Yamin (2010[Narimani, L. & Yamin, B. M. (2010). Acta Cryst. E66, o669.]); Pourayoubi et al. (2010[Pourayoubi, M., Toghraee, M., Rheingold, A. L. & Golen, J. A. (2010). Acta Cryst. E66, o844.]). For a description of the Cambridge Structural Database, see: Allen (2002[Allen, F. H. (2002). Acta Cryst. B58, 380-388.]). For hydrogen bonding, see: Desiraju & Steiner (1999[Desiraju, G. R. & Steiner, T. (1999). The Weak Hydrogen Bond in Structural Chemistry and Biology, IUCr Monographs on Crystallography, Vol. 9, p. 13. Oxford University Press.]).

[Scheme 1]

Experimental

Crystal data

  • C11H12N2O2·C7H5NO4·C2H6O

  • Mr = 417.41

  • Triclinic, P 1

  • a = 7.0320 (14) Å

  • b = 7.7590 (16) Å

  • c = 9.5800 (19) Å

  • α = 85.44 (3)°

  • β = 81.89 (3)°

  • γ = 71.84 (3)°

  • V = 491.34 (19) Å3

  • Z = 1

  • Mo Kα radiation

  • μ = 0.11 mm−1

  • T = 298 K

  • 0.27 × 0.23 × 0.22 mm
Data collection

  • Bruker SMART 1000 CCD diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996[Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.]) Tmin = 0.971, Tmax = 0.977

  • 4115 measured reflections

  • 2092 independent reflections

  • 1815 reflections with I > 2σ(I)

  • Rint = 0.024
Refinement

  • R[F2 > 2σ(F2)] = 0.045

  • wR(F2) = 0.109

  • S = 1.02

  • 2092 reflections

  • 285 parameters

  • 6 restraints

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.18 e Å−3

  • Δρmin = −0.22 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
N3—H3C⋯N1i 0.89 2.15 3.032 (4) 170
N3—H3B⋯O7ii 0.89 1.90 2.787 (4) 171
N3—H3A⋯O3 0.89 2.01 2.894 (4) 170
N2—H2A⋯O5iii 0.90 (1) 2.06 (2) 2.922 (4) 161 (4)
O7—H7⋯O5iii 0.86 (1) 1.96 (3) 2.762 (4) 155 (5)
O1—H1⋯O6iii 0.90 (5) 1.58 (6) 2.479 (3) 177 (5)
O4—H4⋯O2iv 0.88 (1) 1.79 (2) 2.611 (3) 155 (5)
C20—H20A⋯O6v 0.97 2.59 3.200 (6) 122
Symmetry codes: (i) x, y-1, z; (ii) x-1, y, z+1; (iii) x, y, z-1; (iv) x, y, z+1; (v) x+1, y, z-1.

Table 2
π–π inter­actions (Å)

Cg1, Cg2 and Cg3 are the centroids of the N2,C9,C8,C14,C15 (pyrrole), C8–C13 (benzene) and N1,C1–C5 (pyridine) rings, respectively.
Cg1⋯Cg3i 3.665 (2) Cg2⋯Cg3i 3.722 (2)
Cg1⋯Cg3ii 3.683 (2) Cg2⋯Cg3ii 3.701 (2)
Symmetry codes: (i) 1 + x, −1 + y, z; (ii) x, −1 + y, z.

Data collection: SMART (Bruker, 1998[Bruker (1998). SAINT and SMART. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Bruker, 1998[Bruker (1998). SAINT and SMART. Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.]).

Supporting information

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S1600536810014017/fb2190sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810014017/fb2190Isup2.hkl

checkCIF report


Comment top

Supramolecular assemblies are interesting field in the design of new and complicated materials. The compounds bearing imino, carboxylate and pyridine groups readily form supramolecular structures via intermolecular hydrogen bonds (Pourayoubi et al., 2010; Broker & Tiekink, 2010; Hemamalini & Fun, 2010; Narimani & Yamin, 2010). The present paper reports a new supramolecular structure of the title compound.

The title compound consists of (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid molecule in the zwitterionic form, pyridine-2,4-dicarboxylic acid molecule and ethanol molecule (Fig. 1). In the crystal structure, (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid molecules and pyridine-2,4-dicarboxylic acid molecules are linked via the strong intermolecular O—H···O and intermolecular N—H···O hydrogen bonds (Desiraju & Steiner, 1999), see Tab. 1. These molecules form layers parallel to the plane (1 0 0). The layers are further linked with ethanol molecules via weaker intermolecular O–H···O hydrogen bonds (Tab. 1) forming the three-dimensional network (Fig. 2). There is also a C–H···O weak hydrogen bond (Tab. 1). Moreover, there are also π-electron ring—π-electron ring interactions in the structure that are specified in Tab. 2 (Spek, 2009).

The difference electron density map contained some peaks in the vicinity of O5 and O6 along the direction O1-H1 and O7-H7. However, the C18-O5 (1.235 (4) Å) and C18-O6 (1.242 (4) Å) distances corresponded well to the unprotonated C-O distances in the carboxyl group. The search in the Cambridge Crystallographic Database (version 5.31 with addenda up to February 26, 2010; Allen, 2002) has revealed that the average C-O distance in the carboxyl is 1.251 (1) Å from 1269 observations, <i. e.> close to the distances C18-O5 and C18-O6.

Related literature top

For supramolecular structures with imino, carboxylate and pyridine groups interconnected via intermolecular hydrogen bonds, see: Broker & Tiekink (2010); Hemamalini & Fun (2010); Narimani & Yamin (2010); Pourayoubi et al. (2010). For a description of the Cambridge Structural Database, see: Allen (2002). For hydrogen bonding, see: Desiraju & Steiner (1999).

Experimental top

Equimolar quantities (1.0 mmol each) of (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid (L-tryptophan) (204 mg) and pyridine-2,4-dicarboxylic acid (167 mg) were mixed in solution (50 ml) of ethanol and water (v:v = 1:1). The mixture was stirred at room temperature for 3 h to give a colourless solution. After keeping the solution in air for 15 d, colourless block-shaped crystals with average size of 0.3 mm × 0.2 mm × 0.2 mm developed.

Refinement top

All the H atoms have been observed in the difference electron density maps. The atoms attached to C atoms were have been constrained: Caryl-H, Cmethylene-H, Cmethyl-H = 0.93, 0.97, 0.96 Å, respectively. Uiso(Haryl)=1.2Ueq(Caryl), Uiso(Hmethylene)=1.2Ueq(Cmethylene), Uiso(Hmethyl)=1.5Ueq(Cmethyl). The hydrogens from N3 have also been constrained: Nammonium-H = 0.89 Å; Uiso(H)=1.5Ueq(N3). The hydrogens involved in the strongest hydrogen bonds (Tab. 1) have been treated differently: The positional parameters of H1 have been refined freely; those of H4 and H7 with the distance restraints 0.88 (1) and 0.85 (1) Å, respectively, H2A with the distance restraint 0.90 (1) Å. The values for these distance restraints have been retrieved from the Cambridge Crystallographic Database (version 5.31 with addenda up to February 26, 2010; Allen, 2002) on the reliably determined structures. The displacement parameters Uiso of H1, H4, H7 and H2A equaled 1.5×Ueq of the respective carrier atoms. In the absence of significant anomalous scattering effects 1628 Friedel pairs have been merged. The absolute structure has been determined from known configuration of (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid (L-tryptophan) used in the preparation.

Structure description top

Supramolecular assemblies are interesting field in the design of new and complicated materials. The compounds bearing imino, carboxylate and pyridine groups readily form supramolecular structures via intermolecular hydrogen bonds (Pourayoubi et al., 2010; Broker & Tiekink, 2010; Hemamalini & Fun, 2010; Narimani & Yamin, 2010). The present paper reports a new supramolecular structure of the title compound.

The title compound consists of (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid molecule in the zwitterionic form, pyridine-2,4-dicarboxylic acid molecule and ethanol molecule (Fig. 1). In the crystal structure, (2S*)-2-amino-3-(1H-indol-3-yl)propionic acid molecules and pyridine-2,4-dicarboxylic acid molecules are linked via the strong intermolecular O—H···O and intermolecular N—H···O hydrogen bonds (Desiraju & Steiner, 1999), see Tab. 1. These molecules form layers parallel to the plane (1 0 0). The layers are further linked with ethanol molecules via weaker intermolecular O–H···O hydrogen bonds (Tab. 1) forming the three-dimensional network (Fig. 2). There is also a C–H···O weak hydrogen bond (Tab. 1). Moreover, there are also π-electron ring—π-electron ring interactions in the structure that are specified in Tab. 2 (Spek, 2009).

The difference electron density map contained some peaks in the vicinity of O5 and O6 along the direction O1-H1 and O7-H7. However, the C18-O5 (1.235 (4) Å) and C18-O6 (1.242 (4) Å) distances corresponded well to the unprotonated C-O distances in the carboxyl group. The search in the Cambridge Crystallographic Database (version 5.31 with addenda up to February 26, 2010; Allen, 2002) has revealed that the average C-O distance in the carboxyl is 1.251 (1) Å from 1269 observations, <i. e.> close to the distances C18-O5 and C18-O6.

For supramolecular structures with imino, carboxylate and pyridine groups interconnected via intermolecular hydrogen bonds, see: Broker & Tiekink (2010); Hemamalini & Fun (2010); Narimani & Yamin (2010); Pourayoubi et al. (2010). For a description of the Cambridge Structural Database, see: Allen (2002). For hydrogen bonding, see: Desiraju & Steiner (1999).

Computing details top

Data collection: SMART (Bruker, 1998); cell refinement: SAINT (Bruker, 1998); data reduction: SAINT (Bruker, 1998); 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
[Figure 1] Fig. 1. The constituing molecules of the title structure, showing 30% probability displacement ellipsoids and the atom-numbering scheme.
[Figure 2] Fig. 2. Molecular packing of the compound, viewed along the b axis. The hydrogen bonds are shown as dashed lines.
(2S*)-2-Ammonio-3-(1H-indol-3-yl)propionate pyridine-2,4-dicarboxylic acid ethanol solvate top
Crystal data top
C11H12N2O2·C7H5NO4·C2H6OZ = 1
Mr = 417.41F(000) = 220
Triclinic, P1Dx = 1.411 Mg m−3
Hall symbol: P 1Mo Kα radiation, λ = 0.71073 Å
a = 7.0320 (14) ÅCell parameters from 1200 reflections
b = 7.7590 (16) Åθ = 2.7–24.0°
c = 9.5800 (19) ŵ = 0.11 mm−1
α = 85.44 (3)°T = 298 K
β = 81.89 (3)°Block, colourless
γ = 71.84 (3)°0.27 × 0.23 × 0.22 mm
V = 491.34 (19) Å3
Data collection top
Bruker SMART 1000 CCD
diffractometer		2092 independent reflections
Radiation source: fine-focus sealed tube1815 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.024
ω scansθmax = 27.0°, θmin = 2.2°
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)		h = −8→8
Tmin = 0.971, Tmax = 0.977k = −9→9
4115 measured reflectionsl = −12→12
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.045Hydrogen site location: difference Fourier map
wR(F2) = 0.109H atoms treated by a mixture of independent and constrained refinement
S = 1.02 w = 1/[σ2(Fo2) + (0.0628P)2]
where P = (Fo2 + 2Fc2)/3
2092 reflections(Δ/σ)max < 0.001
285 parametersΔρmax = 0.18 e Å−3
6 restraintsΔρmin = −0.22 e Å−3
78 constraints
Crystal data top
C11H12N2O2·C7H5NO4·C2H6Oγ = 71.84 (3)°
Mr = 417.41V = 491.34 (19) Å3
Triclinic, P1Z = 1
a = 7.0320 (14) ÅMo Kα radiation
b = 7.7590 (16) ŵ = 0.11 mm−1
c = 9.5800 (19) ÅT = 298 K
α = 85.44 (3)°0.27 × 0.23 × 0.22 mm
β = 81.89 (3)°
Data collection top
Bruker SMART 1000 CCD
diffractometer		2092 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)		1815 reflections with I > 2σ(I)
Tmin = 0.971, Tmax = 0.977Rint = 0.024
4115 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0456 restraints
wR(F2) = 0.109H atoms treated by a mixture of independent and constrained refinement
S = 1.02Δρmax = 0.18 e Å−3
2092 reflectionsΔρmin = −0.22 e Å−3
285 parameters
Special details top

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
xyzUiso*/Ueq
O10.2726 (4)0.7005 (3)0.5137 (3)0.0503 (7)
H10.276 (7)0.635 (7)0.439 (6)0.075*
O20.1776 (6)0.9447 (4)0.3743 (3)0.0725 (10)
O30.2236 (5)0.7586 (4)1.0219 (3)0.0560 (8)
O40.1597 (5)1.0309 (3)1.1063 (2)0.0509 (7)
H40.175 (7)0.970 (6)1.187 (3)0.076*
O50.5693 (4)0.2870 (4)1.3453 (3)0.0522 (7)
O60.2941 (4)0.5149 (4)1.3097 (3)0.0554 (8)
O70.9134 (4)0.3938 (4)0.3005 (3)0.0601 (8)
H70.831 (6)0.332 (6)0.301 (6)0.090*
N10.1492 (4)1.1892 (3)0.8482 (3)0.0316 (6)
N20.5947 (4)0.2711 (4)0.6481 (3)0.0396 (7)
H2A0.582 (7)0.304 (6)0.5569 (17)0.059*
N30.2260 (4)0.3869 (3)1.0847 (3)0.0304 (6)
H3A0.20960.50391.06290.046*
H3B0.13050.37631.15340.046*
H3C0.21740.33161.00900.046*
C10.1801 (5)1.0105 (4)0.8599 (3)0.0274 (6)
C20.2031 (5)0.9032 (4)0.7466 (3)0.0288 (7)
H20.22920.77830.75970.035*
C30.1866 (5)0.9845 (4)0.6140 (3)0.0302 (7)
C40.1478 (5)1.1699 (5)0.6004 (3)0.0362 (8)
H4A0.13291.22990.51280.043*
C50.1316 (5)1.2645 (4)0.7195 (3)0.0346 (7)
H50.10681.38950.70900.042*
C60.2122 (5)0.8722 (5)0.4871 (3)0.0400 (8)
C70.1919 (5)0.9201 (4)1.0033 (3)0.0329 (7)
C80.6594 (5)0.0930 (5)0.8419 (3)0.0311 (7)
C90.6549 (5)0.0934 (5)0.6954 (3)0.0341 (7)
C100.7065 (6)−0.0663 (5)0.6231 (4)0.0451 (9)
H100.7036−0.06420.52630.054*
C110.7617 (6)−0.2262 (5)0.6995 (5)0.0502 (10)
H110.7968−0.33490.65350.060*
C120.7666 (6)−0.2308 (6)0.8447 (5)0.0510 (10)
H120.8051−0.34200.89380.061*
C130.7152 (5)−0.0727 (5)0.9160 (4)0.0402 (8)
H130.7178−0.07671.01300.048*
C140.6009 (5)0.2784 (4)0.8802 (3)0.0314 (7)
C150.5622 (5)0.3797 (5)0.7600 (4)0.0354 (7)
H150.51940.50590.75440.043*
C160.5926 (5)0.3425 (5)1.0252 (3)0.0368 (8)
H16A0.57050.47261.01910.044*
H16B0.72230.28561.05900.044*
C170.4276 (5)0.3016 (4)1.1330 (3)0.0303 (7)
H170.45310.16991.14230.036*
C180.4303 (5)0.3726 (5)1.2774 (3)0.0349 (7)
C190.7449 (10)0.7082 (7)0.2595 (6)0.0880 (18)
H19A0.66500.66990.20220.132*
H19B0.85660.73290.20080.132*
H19C0.66350.81620.30660.132*
C200.8210 (7)0.5635 (6)0.3650 (5)0.0608 (11)
H20A0.91830.59390.41290.073*
H20B0.71010.55430.43500.073*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
O10.0771 (19)0.0433 (16)0.0285 (13)−0.0102 (14)−0.0109 (12)−0.0145 (11)
O20.128 (3)0.066 (2)0.0212 (13)−0.0198 (19)−0.0207 (15)−0.0064 (13)
O30.105 (2)0.0348 (14)0.0324 (14)−0.0252 (15)−0.0166 (14)0.0061 (11)
O40.100 (2)0.0418 (15)0.0188 (11)−0.0313 (15)−0.0099 (13)0.0001 (10)
O50.0589 (17)0.0725 (19)0.0293 (13)−0.0211 (14)−0.0158 (12)−0.0036 (13)
O60.0627 (18)0.0611 (18)0.0423 (16)−0.0106 (14)−0.0094 (13)−0.0298 (13)
O70.0569 (18)0.0624 (19)0.0623 (19)−0.0243 (14)0.0092 (15)−0.0139 (15)
N10.0417 (15)0.0273 (14)0.0255 (13)−0.0086 (11)−0.0053 (11)−0.0044 (11)
N20.0477 (17)0.0486 (18)0.0227 (14)−0.0155 (14)−0.0048 (12)0.0021 (13)
N30.0396 (15)0.0306 (14)0.0244 (13)−0.0147 (12)−0.0020 (10)−0.0080 (10)
C10.0315 (15)0.0293 (15)0.0226 (14)−0.0100 (12)−0.0040 (11)−0.0028 (12)
C20.0369 (16)0.0255 (15)0.0235 (15)−0.0069 (13)−0.0046 (12)−0.0063 (12)
C30.0294 (16)0.0399 (18)0.0219 (14)−0.0090 (14)−0.0053 (12)−0.0062 (13)
C40.047 (2)0.0393 (19)0.0226 (16)−0.0142 (16)−0.0075 (14)0.0034 (14)
C50.0436 (18)0.0273 (16)0.0329 (17)−0.0100 (14)−0.0083 (14)0.0030 (13)
C60.050 (2)0.046 (2)0.0230 (18)−0.0117 (17)−0.0045 (15)−0.0066 (15)
C70.0490 (19)0.0331 (19)0.0219 (15)−0.0177 (15)−0.0084 (13)−0.0028 (13)
C80.0297 (16)0.0371 (17)0.0276 (15)−0.0126 (13)0.0003 (12)−0.0050 (13)
C90.0324 (17)0.0437 (19)0.0283 (16)−0.0144 (15)−0.0017 (13)−0.0053 (15)
C100.051 (2)0.056 (2)0.0306 (18)−0.0194 (18)0.0049 (15)−0.0206 (17)
C110.046 (2)0.044 (2)0.061 (3)−0.0128 (18)0.0051 (19)−0.022 (2)
C120.051 (2)0.038 (2)0.059 (3)−0.0112 (17)0.0027 (19)−0.0013 (18)
C130.043 (2)0.040 (2)0.0339 (18)−0.0092 (16)−0.0002 (14)0.0002 (16)
C140.0327 (17)0.0356 (17)0.0255 (15)−0.0096 (14)0.0001 (12)−0.0075 (13)
C150.0391 (18)0.0355 (18)0.0319 (17)−0.0134 (15)0.0004 (14)−0.0025 (14)
C160.0455 (19)0.0410 (19)0.0288 (17)−0.0209 (15)0.0004 (14)−0.0071 (14)
C170.0397 (17)0.0310 (16)0.0241 (15)−0.0147 (13)−0.0050 (12)−0.0051 (12)
C180.0426 (19)0.046 (2)0.0233 (15)−0.0229 (16)−0.0025 (13)−0.0059 (14)
C190.122 (5)0.070 (4)0.056 (3)−0.013 (3)−0.001 (3)0.002 (3)
C200.061 (3)0.074 (3)0.046 (2)−0.023 (2)0.0042 (19)−0.013 (2)
Geometric parameters (Å, º) top
O1—C61.282 (5)C5—H50.9300
O1—H10.90 (5)C8—C131.390 (5)
O2—C61.199 (4)C8—C91.408 (5)
O3—C71.205 (4)C8—C141.430 (5)
O4—C71.310 (4)C9—C101.389 (5)
O4—H40.875 (11)C10—C111.364 (6)
O5—C181.235 (4)C10—H100.9300
O6—C181.242 (4)C11—C121.393 (6)
O7—C201.422 (5)C11—H110.9300
O7—H70.855 (11)C12—C131.374 (5)
N1—C51.326 (4)C12—H120.9300
N1—C11.333 (4)C13—H130.9300
N2—C151.367 (4)C14—C151.352 (5)
N2—C91.370 (5)C14—C161.500 (4)
N2—H2A0.899 (11)C15—H150.9300
N3—C171.488 (4)C16—C171.534 (4)
N3—H3A0.8900C16—H16A0.9700
N3—H3B0.8900C16—H16B0.9700
N3—H3C0.8900C17—C181.534 (4)
C1—C21.381 (4)C17—H170.9800
C1—C71.493 (4)C19—C201.472 (7)
C2—C31.376 (4)C19—H19A0.9600
C2—H20.9300C19—H19B0.9600
C3—C41.377 (5)C19—H19C0.9600
C3—C61.509 (4)C20—H20A0.9700
C4—C51.378 (5)C20—H20B0.9700
C4—H4A0.9300
C6—O1—H1113 (3)C10—C11—C12121.7 (4)
C7—O4—H4110 (3)C10—C11—H11119.2
C20—O7—H7112 (4)C12—C11—H11119.2
C5—N1—C1116.2 (3)C13—C12—C11120.7 (4)
C15—N2—C9108.7 (3)C13—C12—H12119.6
C15—N2—H2A128 (3)C11—C12—H12119.6
C9—N2—H2A123 (3)C12—C13—C8119.4 (3)
C17—N3—H3A109.5C12—C13—H13120.3
C17—N3—H3B109.5C8—C13—H13120.3
H3A—N3—H3B109.5C15—C14—C8106.3 (3)
C17—N3—H3C109.5C15—C14—C16128.1 (3)
H3A—N3—H3C109.5C8—C14—C16125.6 (3)
H3B—N3—H3C109.5C14—C15—N2110.7 (3)
N1—C1—C2123.8 (3)C14—C15—H15124.7
N1—C1—C7118.4 (3)N2—C15—H15124.7
C2—C1—C7117.8 (3)C14—C16—C17114.1 (3)
C3—C2—C1118.8 (3)C14—C16—H16A108.7
C3—C2—H2120.6C17—C16—H16A108.7
C1—C2—H2120.6C14—C16—H16B108.7
C2—C3—C4118.3 (3)C17—C16—H16B108.7
C2—C3—C6120.5 (3)H16A—C16—H16B107.6
C4—C3—C6121.2 (3)N3—C17—C18109.6 (3)
C3—C4—C5118.5 (3)N3—C17—C16110.3 (3)
C3—C4—H4A120.7C18—C17—C16110.3 (3)
C5—C4—H4A120.7N3—C17—H17108.8
N1—C5—C4124.3 (3)C18—C17—H17108.8
N1—C5—H5117.8C16—C17—H17108.8
C4—C5—H5117.8O5—C18—O6127.7 (3)
O2—C6—O1125.9 (3)O5—C18—C17117.1 (3)
O2—C6—C3120.3 (3)O6—C18—C17115.1 (3)
O1—C6—C3113.8 (3)C20—C19—H19A109.5
O3—C7—O4123.2 (3)C20—C19—H19B109.5
O3—C7—C1122.3 (3)H19A—C19—H19B109.5
O4—C7—C1114.5 (3)C20—C19—H19C109.5
C13—C8—C9118.6 (3)H19A—C19—H19C109.5
C13—C8—C14134.3 (3)H19B—C19—H19C109.5
C9—C8—C14107.1 (3)O7—C20—C19111.0 (4)
N2—C9—C10130.7 (3)O7—C20—H20A109.4
N2—C9—C8107.2 (3)C19—C20—H20A109.4
C10—C9—C8122.1 (3)O7—C20—H20B109.4
C11—C10—C9117.6 (3)C19—C20—H20B109.4
C11—C10—H10121.2H20A—C20—H20B108.0
C9—C10—H10121.2
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N3—H3C···N1i0.892.153.032 (4)170
N3—H3B···O7ii0.891.902.787 (4)171
N3—H3A···O30.892.012.894 (4)170
N2—H2A···O5iii0.90 (1)2.06 (2)2.922 (4)161 (4)
O7—H7···O5iii0.86 (1)1.96 (3)2.762 (4)155 (5)
O1—H1···O6iii0.90 (5)1.58 (6)2.479 (3)177 (5)
O4—H4···O2iv0.88 (1)1.79 (2)2.611 (3)155 (5)
C20—H20A···O6v0.972.593.200 (6)122
Symmetry codes: (i) x, y−1, z; (ii) x−1, y, z+1; (iii) x, y, z−1; (iv) x, y, z+1; (v) x+1, y, z−1.

Experimental details

Crystal data
Chemical formulaC11H12N2O2·C7H5NO4·C2H6O
Mr417.41
Crystal system, space groupTriclinic, P1
Temperature (K)298
a, b, c (Å)7.0320 (14), 7.7590 (16), 9.5800 (19)
α, β, γ (°)85.44 (3), 81.89 (3), 71.84 (3)
V (Å3)491.34 (19)
Z1
Radiation typeMo Kα
µ (mm−1)0.11
Crystal size (mm)0.27 × 0.23 × 0.22
Data collection
DiffractometerBruker SMART 1000 CCD
diffractometer
Absorption correctionMulti-scan
(SADABS; Sheldrick, 1996)
Tmin, Tmax0.971, 0.977
No. of measured, independent and
observed [I > 2σ(I)] reflections		4115, 2092, 1815
Rint0.024
(sin θ/λ)max (Å−1)0.639
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.045, 0.109, 1.02
No. of reflections2092
No. of parameters285
No. of restraints6
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å−3)0.18, −0.22

Computer programs: SMART (Bruker, 1998), SAINT (Bruker, 1998), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N3—H3C···N1i0.892.153.032 (4)169.6
N3—H3B···O7ii0.891.902.787 (4)171.1
N3—H3A···O30.892.012.894 (4)169.7
N2—H2A···O5iii0.899 (11)2.059 (19)2.922 (4)161 (4)
O7—H7···O5iii0.855 (11)1.96 (3)2.762 (4)155 (5)
O1—H1···O6iii0.90 (5)1.58 (6)2.479 (3)177 (5)
O4—H4···O2iv0.875 (11)1.79 (2)2.611 (3)155 (5)
C20—H20A···O6v0.972.593.200 (6)121.5
Symmetry codes: (i) x, y−1, z; (ii) x−1, y, z+1; (iii) x, y, z−1; (iv) x, y, z+1; (v) x+1, y, z−1.
Overview of π-electron—π-electron ring interactions (Å) in the structure top
Cg1, Cg2 and Cg3 are the centroids of the N2,C9,C8,C14,C15 (pyrrole), C8–C13 (benzene) and N1,C1–C5 (pyridine), respectively.
Cg···CgdistanceCg···Cgdistance
Cg1···Cg3i3.665 (2)Cg2···Cg3i3.722 (2)
Cg1···Cg3ii3.683 (2)Cg2···Cg3ii3.701 (2)
Symmetry codes: (i) 1+x, -1+y, z; (ii) x, -1+y, z.
 

References

First citationAllen, F. H. (2002). Acta Cryst. B58, 380–388.  Web of Science CSD CrossRef CAS IUCr Journals Google Scholar
 First citationBroker, G. A. & Tiekink, E. R. T. (2010). Acta Cryst. E66, o705.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationBruker (1998). SAINT and SMART. Bruker AXS Inc., Madison, Wisconsin, USA.  Google Scholar
 First citationDesiraju, G. R. & Steiner, T. (1999). The Weak Hydrogen Bond in Structural Chemistry and Biology, IUCr Monographs on Crystallography, Vol. 9, p. 13. Oxford University Press.  Google Scholar
 First citationHemamalini, M. & Fun, H.-K. (2010). Acta Cryst. E66, o689–o690.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationNarimani, L. & Yamin, B. M. (2010). Acta Cryst. E66, o669.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationPourayoubi, M., Toghraee, M., Rheingold, A. L. & Golen, J. A. (2010). Acta Cryst. E66, o844.  Web of Science CrossRef IUCr Journals Google Scholar
 First citationSheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.  Google Scholar
 First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationSpek, A. L. (2009). Acta Cryst. D65, 148–155.  Web of Science CrossRef CAS IUCr Journals Google Scholar

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ISSN: 2056-9890
Volume 66| Part 5| May 2010| Pages o1125-o1126
https://doi.org/10.1107/S1600536810014017
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