1Department of Organic Chemistry, Semmelweis University, Hőgyes u. 7., 1092 Budapest, Hungary, Fax: +36 1 217-0851
2Department of Organic Chemistry, University of Debrecen, Debrecen, P. O. Box 20, 4010 Debrecen, Hungary
3CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zu Chong Zhi Road, Zhang Jiang Hi-Tech Park, Shanghai 201203, PR China
4Department of Inorganic and Analytical Chemistry, University of Debrecen, H-4010 Debrecen, Hungary
5Porfirin Ltd., Mikszáth K. u. 7. III/3, 4032 Debrecen, Hungary
Associate Editor: J. Aubé
Beilstein J. Org. Chem. 2014, 10, 2594–2602. https://doi.org/10.3762/bjoc.10.272
Received 28 Apr 2014, Accepted 16 Oct 2014, Published 06 Nov 2014
Condensed O,N-heterocycles containing tetrahydro-1,4-benzoxazepine and tetrahydroquinoline moieties were prepared by a regio- and diastereoselective domino Knoevenagel–[1,5]-hydride shift cyclization reaction of a 4-aryl-2-phenyl-1,4-benzoxazepine derivative obtained from flavanone. The relative configuration of products were determined by the correlation of 3JH,H coupling data with the geometry of major conformers accessed by DFT conformational analysis. Separated enantiomers of the products were characterized by HPLC-ECD data, which allowed their configurational assignment on the basis of TDDFT-ECD calculation of the solution conformers. Two compounds showed neuroprotective activities against hydrogen peroxide (H2O2) or β-amyloid25–35 (Aβ25–35)-induced cellular injuries in human neuroblastoma SH-SY5Y cells in the range of those of positive controls.
Keywords: 1,4-benzoxazepine; diastereoselective domino Knoevenagel–[1,5]-hydride shift cyclization; neuroprotective; tert-amino effect; TDDFT-ECD calculation
The 1,4-benzoxazepine structural unit and its analogues are found in several pharmacologically active derivatives such as the selective 5-HT1A agonist SUN 8399 (1) , the neuroprotective piclozotan (2) [2,3], the antihistaminic rocastine (3) [4,5], and the antihelmintic 4  (Figure 1).
We report herein the preparation of two neuroprotective condensed 2-phenyl-1,4-benzoxazepines rac-7a,b through the diastereoselective domino Knoevenagel–1,5-hydride shift cyclization reaction rac-5→rac-7a,b from the readily available 4-aryl-2-phenyl-1,4-benzoxazepine derivative, rac-5 (Scheme 1).
Ring-closure transformations involving C(sp3)–H bond functionalization in an internal redox process, particularly involving C–H bonds in α-position to a tertiary amine nitrogen atom, has attracted considerable attention due to its synthetic potential [7-11]. The intramolecular “tert-amino effect” induced cyclization consists in (1) the cleavage of the C(sp3)–H bond α to a tertiary amine nitrogen through [1,5]-hydride shift (rac-6→A) (Scheme 1) to afford the zwitterionic intermediate A and (2) subsequent 6-endo cyclization (A→rac-7a,b).
The stereoselective version of “tert-amino effect” induced cyclization using chiral metal-catalyzed [12-15] or organocatalytic [16,17] reactions and the mechanism of the stereospecific hydride transfer have been recently studied by several research groups. The synthetic potential of the diastereoselective domino Knoevenagel–[1,5]-hydride shift cyclization reaction was exploited in our present work for the preparation of condensed O,N-heterocycles with the 1,2,8,9-tetrahydro-7bH-quinolino[1,2-d][1,4]benzoxazepine skeleton, the neuroprotective activities of which were tested against hydrogen peroxide (H2O2), Alzheimer's amyloid β-peptide fragment Aβ25–35 and oxygen–glucose deprivation (OGD)-induced neurotoxicity in human neuroblastoma SH-SY5Y cells.
The starting material 4-aryl-2-phenyl-1,4-benzoxazepine (rac-5) for the domino Knoevenagel–[1,5]-hydride shift cyclization reaction was prepared from rac-flavanone (rac-8) in four steps (Scheme 2).
The Schmidt reaction of rac-8 was carried out according to the procedure of Litkey and Patonay  affording the racemic 3,4-dihydro-2-phenyl-1,4-benzoxazepine-5-one (rac-9) with high regioselectivity, which was reduced to (rac)-10 with LAH in dry THF. In the following step, the N-arylation of rac-10 was performed through a nucleophilic aromatic substitution by using 2-fluoro-5-nitrobenzaldehyde (11b) to give rac-5 containing a tertiary arylamine nitrogen in 71% yield. With the 2-chloro-5-nitrobenzaldehyde reagent, only 3% yield for rac-5 could be achieved. Subsequently rac-5 was reacted with 1,3-dimethylbarbituric acid (12), Meldrum’s acid (13) and malononitrile (14) all containing active methylene groups, which initiated a domino reaction (Scheme 2). The Knoevenagel reaction of the formyl group in rac-5 and the active methylene groups of 12–14 afforded the intermediates rac-6a–c (Scheme 1), which underwent regioselective [1,5]-hydride shift with participation of the benzylic hydrogen to result in the zwitterionic iminium ion intermediates A. The 6-endo cyclization of this intermediate gave rac-trans-7a,b with high diastereoselectivity, which was governed by the C-2 chirality center of intermediate A. In contrast to the domino reaction with 1,3-dimethylbarbituric acid (12) and Meldrum’s acid (13), the reaction with malonitrile (14) stopped at the stage of the Knoevenagel product rac-7c with MgSO4 in CHCl3 and further cyclization did not occur when heated in DMSO at 150 °C or refluxed in n-butanol.
The NMR data of 7a,b clearly indicated that they were single diastereomers and the determination of the relative configuration was carried out by the correlation of NMR data and DFT conformational analysis of cis- and trans-7a,b (Figure 2 and Figure 3).
Although the hydrogens 2-H and 15a-H of cis-7a,b are expected to point toward the same side of the molecules, the analysis of the computed solution conformers of cis-7a,b revealed that the orientation and distance (>4.6 Å) of these methine protons (Figure 3) does not allow for the detection of their NOE contact, rendering the NOE-based assignment of the relative configuration ambiguous. Similarly, no NOE correlation is expected between 2-H and 15a-H of trans-7a,b, which was also evident from the structures of their computed lowest-energy conformers (Figure 2). Accordingly, no characteristic NOE was observed between these methine protons for 7a,b, which did not help for the assignment of the relative configuration. However, in the computed solution conformers of cis-7a,b, the oxazepine ring adopts a twist boat conformation with axial 2-H showing gauche orientation with adjacent 3-H protons (e.g., ω2-Hax,C-2,C-3,3-Hax ≈ 36.2°, ω2-Hax,C-2,C-3,3-Heq ≈ −79.2° in 7a), suggesting small 3J2-H,3-H couplings.
Whereas in the computed solution conformers of trans-7a,b (Figure 2), the oxazepine ring adopts a boat conformation showing a trans-diaxial relationship with the adjacent 3-Hax. In accordance with the calculations, the measured values of the 3J2-Hax,3-H (11.5 and 3.2 Hz) corroborate that the couplings between 2-Hax and 3-Hs derive from trans-diaxial (ω2-Hax,C-2,C-3,3-Hax ≈ 180°) and gauche (ω2-Hax,C-2,C-3,3-Heq ≈ 60°) orientations, which is only feasible with the trans relative configuration of 7a,b. Thus in the course of the cyclization, the attack of the carbanion to the iminium carbon of intermediate A occurred with trans-diastereoselectivity to the C-2 phenyl group. The formation of the diastereomeric cis-7a,b could not be detected.
The chiral HPLC analysis of the products 7a,b also confirmed that the reaction took place diastereoselectively and enantiomers of trans-7a,b were separated on a Chiralpak IA column using hexane/dichloromethane as eluent and online HPLC-ECD spectra of the separated enantiomers were recorded. Due to their similar chromophoric system, the HPLC-ECD spectra of 7a and 7b were quite similar. The first-eluting enantiomer of 7a had an intense broad positive Cotton effect (CE) at 378 nm, negative ones at 314, 305, 272 nm and positive ones at 284, 279 and 224 nm (Figure 4a).
The HPLC-ECD spectrum of the first-eluting enantiomer of 7b showed similar ECD pattern with somewhat different shape and intensities in the 290–240 nm range (Figure 4b). TDDFT-ECD calculation was proved an efficient method to determine the absolute configuration of separated stereoisomers of bioactive synthetic  and natural derivatives [20,21] on the basis of their HPLC-ECD spectra.
For the configurational assignment of the separated enantiomers, TDDFT-ECD calculations were carried out on the solution conformers of (2S,15aS)-7d (N-methyl groups were replaced by hydrogens for the calculation) and (2S,15aS)-7b and computed ECD curves were compared with the measured HPLC-ECD ones of the separated enantiomers of trans-7a,b (Figure 4a and Figure 4b). The computed TDDFT-ECD spectra of (2S,15aS)-7d and (2S,15aS)-7b gave good agreement with the experimental HPLC-ECD spectra of the second-eluting enantiomers (Figure 4a,b), which allowed determining the absolute configuration of their second-eluting enantiomers (negative CEs at 370 and 371 nm, respectively) as (2S,15aS). The good agreement between the experimental HPLC-ECD and computed ECD spectra of 7a,b not only allowed the configurational assignment of their separated enantiomers but also confirmed independently the trans-diastereoselectivity of the cyclization.
The neuroprotective activities of rac-7a,b and rac-5 were tested against hydrogen peroxide (H2O2), β-amyloid-25-35 (Aβ25–35) and oxygen–glucose deprivation (OGD)-induced neurotoxicity in human neuroblastoma SH-SY5Y cells . The preliminary screenings showed that rac-7a at 10 µM concentration displayed neuroprotective activity against H2O2-induced cellular injuries in human neuroblastoma SH-SY5Y cells with 16.4% increase in cell viability (Figure 5), while 10 µM of rac-7b increased cell viability in Aβ25–35-induced neurotoxicity by 22.8% (Figure 6).
The positive controls with N-L-acetylcysteine (NAC)  and epigallocatechin gallate (EGCG)  increased cell viability by 17.3% and 22.4% in H2O2 and Aβ25–35 model, respectively. Compounds rac-7a,b and rac-5 did not show acetylcholinesterase inhibitory effect.
Regioselective domino Knoevenagel–[1,5]-hydride shift cyclization reactions of a 4-aryl-2-phenyl-1,4-benzoxazepine derivative afforded three condensed O,N-heterocycles containing tetrahydro-1,4-benzoxazepine and tetrahydroquinoline moieties. trans-Diastereoselectivity of the cyclizations was determined by the correlation of 3JH,H coupling constants with the geometry of the computed conformers, while (2R,15aR) absolute configurations of 7a,b were assigned to the separated enantiomers showing positive CE for the lowest-energy ECD transition by the comparison of the experimental HPLC-ECD spectra with those obtained by the TDDFT-ECD calculations of the solution conformers. Compound 7a showed neuroprotective activity against hydrogen peroxide (H2O2), while 7b against β-amyloid25–35 (Aβ25–35)-induced cellular injuries in human neuroblastoma SH-SY5Y cells with 16.4% and 22.8% increase in cell viability at 10 μM concentrations, respectively.
Melting points were determined on a Kofler hot-stage apparatus and are uncorrected. The NMR spectra were recorded on Bruker-AMX 500 (1H: 500 MHz; 13C: 125 MHz) and Bruker Avance II 400 (1H: 400 MHz; 13C: 100 MHz) spectrometers using TMS as internal standard. Chemical shifts were reported as δ in ppm and 3JH,H coupling constants in Hz. Chiral HPLC separation of 7a,b were performed on a Jasco HPLC system with Chiralpak IA column (5 μm, 150 × 4.6 mm, hexane/dichloromethane 80:20 or 70:30 eluents, 1 mL min−1 flow rate) and HPLC-ECD spectra were recorded in stopped-flow mode on a JASCO J-810 electronic circular dichroism spectropolarimeter equipped with a 10 mm HPLC flow cell. ECD ellipticity (Φ) values were not corrected for concentration. For an HPLC-ECD spectrum, three consecutive scans were recorded and averaged with 2 nm bandwidth, 1 s response, and standard sensitivity. The HPLC-ECD spectrum of the eluent recorded in the same way was used as background. The concentration of the injected sample was set so that the HT value did not exceed 500 V in the HT channel down to 230 nm. IR spectra were recorded on a JASCO FTIR-4100 spectrometer and absorption bands are presented as wavenumber in cm−1. Electrospay Quadrupole Time-of-Flight HRMS measurements were performed with a MicroTOF-Q type QqTOF MS instrument equipped with an ESI source from Bruker (Bruker Daltoniks, Bremen, Germany). Elementary analysis was carried with a Vario Micro V1.9.6 instrument.
Computational section: Mixed torsional/low mode conformational searches were carried out by means of the Macromodel 9.9.223 software  using OPLS-2005 force field with implicit solvent model for chloroform applying a 42 kJ/mol energy window. Geometry reoptimizations (B3LYP/6-31G(d) level in gas phase and B3LYP/TZVP level with PCM solvent model for CHCl3) and TDDFT-ECD calculations were performed with Gaussian 09  using various functionals (B3LYP, BH&HLYP, PBE0) and TZVP basis set for ECD calculations. ECD spectra were generated as the sum of Gaussians  with 2100, 2400 and 4200 cm−1 half-height width (corresponding to ca. 19, 22 and 38 nm at 300 nm) using dipole-velocity computed rotational strengths. Boltzmann distributions were estimated from the ZPVE-corrected B3LYP/6-31G(d) energies in the gas-phase calculations and from the B3LYP/TZVP energies in the PCM ones. The MOLEKEL  software package was used for visualization of the results.
Bioassay on neuroprotective activity: SH-SY5Y cells were high passages from the American Type Culture Collection and were maintained at 37 °C in a humidified atmosphere containing 5% CO2. Cells were pretreated with compounds for 2 h and then suffered cell injury by treatment with 10 µM Aβ25–35 or 100 µM H2O2 for another 24 h; to SH-SY5Y cells, pretreated with compounds before exposed to OGD for 1 h, was added 1 mg/mL glucose and 10% serum and cultured for another 24 h under normal condition. SH-SY5Y cells cultured with glucose under normal condition served as control. Cell viability was evaluated by incubating cells with 0.5 mg/mL 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) for 3 h under 5% CO2/95% air at 37 °C. After replacement of the medium with 100 µL DMSO, absorbance was read at 490 nm. Data were analyzed by one-way analysis of variance (ANOVA) and expressed as means ± SD with P < 0.05 as significance.
2-Phenyl-3,4-dihydro-1,4-benzoxazepin-5(2H)-one (rac-9): To a stirred solution of racemic flavanone (rac-8, 10.00 g, 44.63 mmol) in TFA (55 mL), sodium azide (5.80 g, 89.22 mmol) was added in two parts and the mixture was stirred for 6 h. Cold diethyl ether (200 mL) was added to the reaction mixture and stirring was continued for 1 h. The precipitated white solid was filtered and refluxed in 180 mL water for 3 h. After cooling to room temperature, it was refrigerated for 1 h, the resultant precipitate was filtered and washed with cold water. The product rac-9 was dried and isolated as white powder (8.23 g, 77%) with mp 127–129 °C. 1H NMR (400 MHz, CDCl3) δ 3.54 (m, 3-Ha, 1H), 3.66 (m 3-Hb, 1H), 5.46 (dd, J = 9.7 and 3.6 Hz, 2-H, 1H), 7.07 (d, J = 8.4 Hz, 9-H, 1H), 7.19 (m, J = 7.6 Hz, 7-H, 1H), 7.28 (bs, NH, 1H), 7.36–7.44 (m, Ph, 5H), 7.50 (m, J = 7.6 Hz, 8-H, 1H), 7.85 (dd, J = 8.0 and 1.6 Hz, 6-H, 1H); 13C NMR (100 MHz, CDCl3) δ 46.3 (C-3), 85.8 (C-2), 122.4 (C-9), 123.7 (C-7), 125.9 (C-5a), 126.3 (C-2’, C-6’), 128.5 (C-4’), 128.7 (C-3’, C-5’), 130.9 (C-6), 133.3 (C-8), 139.0 (C-1’), 154.5 (C-9a), 170.9 (C-5); IR (KBr) ν: 1462, 1665, 2917, 3075, 3203, 3307 cm−1; HRMS–ESI (m/z): [M + Na]+ calcd for C15H13NO2Na, 262.0844; found, 262.0839; Anal. calcd for C15H13NO2 (239.09): C, 75.30; H, 5.48; N, 5.85; found: C, 75.28; H, 5.49; N, 5.85.
2-Phenyl-2,3,4,5-tetrahydro-1,4-benzoxazepine (rac-10): To a stirred solution of rac-9 (8.13 g, 33.98 mmol) in dry THF (80 mL), 2.0 M lithium aluminium hydride solution in THF was added dropwise (10 mL, 0.76 g, 20.03 mmol) and the mixture was refluxed for 1.5 h. After cooling to room temperature, ethyl acetate (5 mL), methanol (5 mL) and water (50 mL) were added and the mixture was concentrated under reduced pressure. The residue was extracted with dichloromethane (3 × 50 mL). The combined organic layers were washed with water (20 mL), dried over MgSO4, filtered and concentrated under reduced pressure. The product rac-10 was isolated as yellow solid (6.12 g, 80%) with mp 73–74 °C. 1H NMR (400 MHz, CDCl3) δ 3.20 (dd, J = 14.4 and 10.0 Hz, 3-Hax, 1H), 3.37 (d, 3-Heq, 14.4 Hz, 1H), 3.96 (d, J = 14.8 Hz, 5-Ha, 1H), 4.12 (d, J = 14.8 Hz, 5-Hb, 1H), 4.66 (d, J = 10.0 Hz, 2-H, 1H), 7.04 (m, 7-H, 8-H, 2H), 7.17 (m, 6-H, 9-H, 2H), 7.31–7.43 (m, Ph, 5H); 13C NMR (100 MHz, CDCl3) δ 52.5 (C-5), 58.9 (C-3), 86.4 (C-2), 121.6 (C-9), 123.6 (C-7), 125.8 (C-2’, C-6’), 127.7 (C-8), 128.4 (C-3’, C-5’), 129.0 (C-4’, C-6), 135.6 (C-5a), 140.5 (C-1’), 159.1 (C-9a); IR (KBr) ν: 1579, 2935, 3328 cm−1; HRMS–ESI (m/z): [M + H]+ calcd for C15H16NO, 226.1232; found, 226.1235; Anal. calcd for C15H15NO (225.11): C, 79.97; H, 6.71; N, 6.22; found: C, 80.03; H, 6.76; N, 6.18.
5-Nitro-2-(2-phenyl-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl)benzaldehyde (rac-5): To the stirred solution of rac-10 (1.50 g, 6.66 mmol) in dry toluene (25 mL), anhydrous K2CO3 (1.85 g 13.39 mmol) and 2-fluoro-5-nitrobenzaldehyde (1.35 g, 7.98 mmol) were added and the mixture was refluxed for 8 h. After cooling to room temperature, K2CO3 was filtered off and toluene was removed under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate/hexane 4:1) to give rac-5 as yellow solid (1.77 g, 71%). Mp 152–156 °C; 1H NMR (400 MHz, CDCl3) δ 3.63 (dd, J = 10.8 and 13.6 Hz, 3-Hax, 1H), 4.04 (dd, J = 13.6 and 2.4 Hz, 3-Heq, 1H), 4.71 (d, J = 16.4 Hz, 5-Ha, 1H), 4.94 (d, J = 16.4 Hz, 5-Hb, 1H), 5.29 (dd, J = 10.8 and 2.4 Hz, 2-H, 1H), 7.03 (m, J = 9.6 Hz, 6-H, 9-H, 2H), 7.13 (m, 8-H, 1H), 7.26 (m, 6”-H, 7-H, 2H), 7.36–7.42 (m, Ph, 5H), 8.17 (dd, J = 9.2 Hz and 2.8 Hz, 5”-H, 1H), 8.61 (d, J = 2.8 Hz, 3”-H, 1H), 9.97 (s, CHO, 1H); 13C NMR (100 MHz, CDCl3) δ 56.1 (C-5), 64.6 (C-3), 82.7 (C-2), 117.6 (C-6”), 121.0 (C-9), 123.8 (C-7), 124.3 (C-5a), 125.9 (C-2’, C-6’), 127.5 (C-2’’), 128.1 (C-4”), 128.7 (C-8, C-3”), 129.1 (C-3’, C-5’), 129.5 (C-5”), 129.8 (C-4’), 129.8 (C-6), 138.1 (C-1’), 156.8 (C-9a), 158.2 (C-1”), 188.3 (CHO); IR (KBr) ν: 1382, 1500, 1681, 1734, 2921 cm−1; HRMS–ESI (m/z): [M + Na]+ calcd for C22H18N2O4Na, 397.1164; found, 397.1158; Anal. calcd for C22H18N2O4 (374.12): C, 70.58; H, 4.85; N, 7.48; found: C, 70.59; H, 4.89; N, 7.45.
trans-1,3-Dimethyl-11'-nitro-2'-phenyl-1',2'-dihydro-2H,7b'H,9'H-spiro[pyrimidine-5,8'-quinolino[1,2-d][1,4]benzoxazepine]-2,4,6(1H,3H)-trione (rac-trans-7a): To a stirred solution of rac-5 (100 mg, 0.27 mmol) in chloroform (5 mL), anhydrous MgSO4 (150 mg, 1.25 mmol) and 1,3-dimethylbarbituric acid (60 mg, 0.38 mmol) were added and the mixture was refluxed for 4 h. After cooling to room temperature, MgSO4 was filtered off and chloroform was removed under reduced pressure. Water (10 mL) and dichloromethane (20 mL) were added and the layers were separated. The aqueous phase was extracted with dichloromethane (2 × 10 mL). The combined organic layers were washed with concentrated NaHCO3 solution, dried over MgSO4, filtered and concentrated under reduced pressure. The oily product was triturated with ether to afford rac-trans-7a as yellow solid (131 mg, 96%) with mp 262–264 °C. 1H NMR (400 MHz, CDCl3) δ 2.91 (s, N-Me, 3H), 3.12 (d, J = 16.8 Hz, 9-Ha, 1H), 3.13 (s, N-Me, 3H), 3.87 (dd, J = 16.4 and 12.0 Hz, 3-Hax, 1H), 4.00 (d, J = 16.8 Hz, 9-Hb, 1H), 4.16 (dd, J = 12.0 and 3.2 Hz, 3-Heq, 1H), 4.81 (s, 15a-H, 1H), 5.13 (dd, J = 12.0 and 3.2 Hz, 2-H, 1H), 6.80 (d, J = 7.6 Hz, 19-H, 1H), 6.85 (d, J = 9.2 Hz, 5-H, 1H), 7.10 (m, 16-H, Ph, 3H), 7.15 (m, 17-H, 1H), 7.30–7.38 (m, 18-H, Ph, 4H), 8.08 (dd, J = 9.2 and 2.4 Hz, 6-H, 1H), 8.13 (s, 8-H, 1H); 13C NMR (100 MHz, CDCl3) δ 28.7 (Me), 28.9 (Me), 34.7 (C-9), 47.3 (C-3) 51.9 (C-10), 71.5 (C-15a), 81.2 (C-2), 109.9 (C-19), 121.5 (C-15b), 123.8 (C-5), 124.7 (C-17), 124.8 (C-6), 125.5 (C-8a), 127.0 (C-2’ and C-6’), 128.8 (C-3’ and C-5’), 129.1 (C-8), 129.9 (C-18), 132.1 (C-16), 137.6 (C-7), 138.3 (C-1’), 147.6 (C-13), 150.1 (C-19a), 151.7 (C-4a), 167.1 (C-15), 168.9 (C-11); IR (KBr) ν: 749, 988, 1326, 1683, 2926 cm−1; HRMS–ESI (m/z): [M + Na]+ calcd for C28H24N4O6Na, 535.1594; found, 535.1588; Anal. calcd for C28H24N4O6 (512.17): C, 65.65; H, 4.72; N, 10.93; found: C, 65.64; H, 4. 70; N, 10.95. (2R,15aR)-7a: retention time (tR) 10.57 min (Chiralpak IA, hexane/dichloromethane 70:30); HPLC-ECD data in hexane/dichloromethane 70:30 as λmax (Φ): 378 (8.97), 368 sh (8.71), 314 (−12.73), 305 sh (−12.73), 284 (2.21), 272 (−1.54), 239 (16.42), 224 sh (11.27). (2S,15aS)-7a: retention time (tR) 28.73 min (Chiralpak IA, hexane/dichloromethane 70:30); HPLC-ECD in hexane/dichloromethane 70:30 as λmax (Φ): 381 sh (−4.83), 370 (−5.03), 314 (7.10), 305 sh (5.68), 286 (−1.24), 270 (0.78), 239 (−9.32), 221 (−11.60).
trans-2,2-Dimethyl-11'-nitro-2'-phenyl-1',2'-dihydro-7b'H,9'H-spiro[1,3-dioxane-5,8'-quinolino[1,2-d][1,4]benzoxazepine]-4,6-dione (rac-trans-7b): To the stirred solution of rac-5 (100 mg, 0.27 mmol) in chloroform (5 mL), anhydrous MgSO4 (150 mg, 1.25 mmol) and Meldrum’s acid (54 mg, 0.31 mmol) were added and the mixture was refluxed for 6 h. After cooling to room temperature, MgSO4 was filtered off and chloroform was removed under reduced pressure. Water (10 mL) and dichloromethane (20 mL) were added and the layers were separated. The aqueous phase was extracted with dichloromethane (2 ×10 mL). The combined organic layers were washed with concentrated NaHCO3 solution, dried over MgSO4, filtered and concentrated under reduced pressure. The oily product was triturated with ether to afford rac-trans-7b as yellow solid (30 mg, 22%) with mp 130–134 °C. 1H NMR (500 MHz, CDCl3) δ 1.06 (s, Me, 3H), 1.62 (s, Me, 3H), 3.19 (d, J = 16.5 Hz, 9-Ha, 1H), 3.90 (d, J = 16.5 Hz, 9-Hb, 1H), 3.95 (dd, J = 16.5 and 11.5 Hz, 3-Hax, 1H), 4.16 (dd J = 16.5 Hz and 3.2 Hz, 3-Heq, 1H), 5.02 (s, 15a-H, 1H), 5.22 (dd, J = 11.5 Hz and 3.2 Hz, 2-H, 1H), 6.83 (d, J = 8.0 Hz, 19-H, 1H), 6.87 (d, J = 9.0 Hz, 5-H, 1H), 7.12 (m, 16-H, 1H), 7.22 (m, 17-H, 18-H, 2H), 7.27–7.35 (m, Ph, 5H), 8.09 (m, 8-H, 6-H, 2H); 13C NMR (100 MHz, CDCl3) δ 26.9 (Me), 30.5 (Me), 35.7 (C-9), 47.2 (C-3), 50.0 (C-10), 70.7 (C-15a), 80.3 (C-2), 105.5 (C-13), 110.0 (C-19), 119.5 (C-8a), 125.1 (C-5), 125.2 (C-17), 125.6 (C-6), 126.7 (C-15b), 127.2 (C-2’, C-6’), 128.6 (C-3’, C-5’), 129.0 (C-8), 131.1 (C-4’), 131.4 (C-16), 137.3 (C-7), 138.1 (C-1’), 147.7 (C-19a), 152.2 (C-4a), 164.5 (C-15), 168.2 (C-11); IR (KBr) ν: 1197, 1322, 1507, 1737, 2925 cm−1; HRMS–ESI (m/z): [M + Na]+ calcd for C28H24N2O7Na, 523.1481; found, 523.1475; Anal. calcd for C28H24N2O7 (500.16): C, 67.19; H, 4.83; N, 5.60; found: C, 67.17; H, 4.86; N, 5.59. (2R,15aR)-7b: retention time (tR) 5.96 min (Chiralpak IA, hexane/dichloromethane 70:30); HPLC-ECD data in hexane/dichloromethane 70:30 as λmax (Φ): 379 sh (10.62), 368 (10.90), 312 (−9.79), 303 sh (−7.89), 279 (6.49), 261 sh (−3.01), 251 (−3.30), 228 (15.44). (2S,15aS)-7b: retention time (tR) 14.09 min (Chiralpak IA, hexane/dichloromethane 70:30); HPLC-ECD data in hexane/dichloromethane 70:30 as λmax (Φ): 383 sh (−3.29), 371 (−3.71), 311 (3.16), 302 sh (2.75), 278 (−2.26), 260 sh (1.04), 249 (1.10), 227 (−5.51).
[5-Nitro-2-(2-phenyl-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl)benzylidene]propanedinitrile (7c): To the stirred solution of rac-5 (100 mg, 0.27 mmol) in chloroform (5 mL), anhydrous MgSO4 (150 mg, 1.25 mmol) and malononitrile (130 mg, 1.97 mmol) were added and the mixture was refluxed for 10 h. After cooling to room temperature, MgSO4 was filtered off and chloroform was removed under reduced pressure. Water (10 mL) and dichloromethane (20 mL) were added and the layers were separated. The aqueous phase was extracted with dichloromethane (2 × 10 mL). The combined organic layers were washed with concentrated NaHCO3 solution, dried over MgSO4, filtered and concentrated under reduced pressure. The oily product was triturated with ether to afford 7c as yellow solid (91 mg, 81%) with mp 152–156 °C. 1H NMR (400 MHz, CDCl3) δ 3.78 (m, 3-H, 2H), 4.50 (d, J = 15.6 Hz, 11-Ha, 1H), 4.58 (d, J = 15.6 Hz, 11-Hb, 1H), 5.06 (dd, J = 10.0 Hz and 2.4 Hz, 3-Heq, 1H), 7.15 (d, J = 8.0 Hz, 15-H, 1H), 7.16–7.26 (m, 12-H, 13-H, 14-H, 3H), 7.32 (m, 7-H, 1H), 7.41 (m, Ph, 5H), 7.75 (s, 16-H, 1H), 8.26 (dd, J = 9.2 Hz and 2.6 Hz, 7-H, 1H), 8.85 (d, J = 2.6 Hz, 9-H, 1H); 13C NMR (100 MHz, CDCl3) δ 59.4 (C-11), 63.2 (C-3), 82.9 (C-2), 84.3 (C-17), 111.8 (CN), 112.9 (CN), 119.2 (C-15), 121.5 (C-6), 121.9 (C-10), 124.5 (C-13), 125.9 (C-2’, C-6’, C-9), 128.4 (C-11a), 128.7 (C-7) 128.9 (C-3’, C-5’, C-14), 129.2 (C-4’), 129.9 (C-12), 138.2 (C-8), 141.2 (C-1’), 156.9 (C-16), 158.2 (C-15a), 158.5 (C-5) IR (KBr) ν: 759, 1222, 1335, 1488, 2227, 2923 cm−1; HRMS–ESI (m/z): [M+Na]+ calcd for C25H18N4O3Na, 445.1277; found, 445.1271; Anal. calcd for C28H18N4O3 (422.14): C, 71.08; H, 4.29; N, 13.26; found: C, 71.05; H, 4.30; N, 13.25. First eluting enantiomer of 7c: retention time (tR) 21.41 min (Chiralpak IA, hexane/dichloromethane 80:20); HPLC-ECD data in hexane/dichloromethane 80:20 as λmax (Φ): 348 (−4.21), 279 (3.84), 252 sh (1.62), 223 (2.04). Second eluting enantiomer of 7c: retention time (tR) 21.41 min (Chiralpak IA, hexane/dichloromethane 80:20); HPLC-ECD data in hexane/dichloromethane 80:20 as λmax (Φ): 356 (3.97), 281 (−3.48), 250 sh (−1.32).
|Supporting Information File 1:
Spectroscopic data and details of calculations.
Structures and populations of the in vacuo and PCM solvent model conformers, cartesian coordinates of 7b–d, 1H, 13C NMR and IR spectra are disclosed in this file.
|Format: PDF||Size: 3.2 MB||Download|
Sándor Antus thanks the Hungarian National Research Foundation (OTKA K81701) for financial support. The financial support implemented in the frame of the ÉAOP-1.1.3-12-2012-0026 is acknowledged. This work was partially supported by the European Union and the European Social Fund through the project Supercomputer, the national virtual lab (grant no.: TAMOP-4.2.2.C-11/1/KONV-2012-0010).
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