Dimerisation, rhodium complex formation and rearrangements of N-heterocyclic carbenes of indazoles

  1. Zong Guan1,
  2. Jan C. Namyslo1,
  3. Martin H. H. Drafz1,
  4. Martin Nieger2 and
  5. Andreas Schmidt1

1Clausthal University of Technology, Institute of Organic Chemistry, Leibnizstrasse 6, D-38678 Clausthal-Zellerfeld, Germany
2University of Helsinki, Laboratory of Inorganic Chemistry, Department of Chemistry, P.O. Box 55 (A.I. Virtasen aukio 1), FIN-00014 University of Helsinki, Finland

  1. Corresponding author email

Associate Editor: C. Stephenson
Beilstein J. Org. Chem. 2014, 10, 832–840. https://doi.org/10.3762/bjoc.10.79
Received 25 Jan 2014, Accepted 21 Mar 2014, Published 10 Apr 2014


Deprotonation of indazolium salts at low temperatures gives N-heterocyclic carbenes of indazoles (indazol-3-ylidenes) which can be trapped as rhodium complexes (X-ray analysis). In the absence of Rh, the indazol-3-ylidenes spontaneously dimerize under ring cleavage of one of the N,N-bonds and ring closure to an indazole–indole spiro compound which possesses an exocyclic imine group. The E/Z isomers of the imines can be separated by column chromatography when methanol is used as eluent. We present results of a single crystal X-ray analysis of one of the E-isomers, which equilibrate in solution as well as in the solid state. Heating of the indazole–indole spiro compounds results in the formation of quinazolines by a ring-cleavage/ring-closure sequence (X-ray analysis). Results of DFT calculations are presented.

Keywords: E/Z isomerism; indazol-3-ylidene; mesomeric betaine; pyrazole; quinazoline; Rh complex


As a result of their biochemical and pharmacological significance, there has been a considerably growing interest in indazoles in recent years, which is reflected in several book chapters and review articles dealing with syntheses [1-4], synthetic potentials [4], and biological activities [4,5] of this ring system. In view of the rapid development of the class of N-heterocyclic carbenes (NHC) [6-12] it is not unexpected, that attention was also directed towards the NHCs of indazole which have been generated and applied in heterocyclic synthesis (vide infra) as well as in complex chemistry [13]. Undoubtedly the N-heterocyclic carbenes of imidazole, imidazoline and the triazoles play the most important roles as ligands in metal-organic chemistry [14] or as organocatalysts [15,16]. The N-heterocyclic carbenes of indazole (and pyrazole [17,18]), however, have a chemistry of their own which set them apart from the NHCs of the aforementioned ring systems. Portions of that field have been covered in recent review articles [18,19]. The N-heterocyclic carbene of indazole 3 has been generated by thermal decarboxylation of indazolium-3-carboxylates 1 [20] which belong to the class of pseudo-cross-conjugated heterocyclic mesomeric betaines (Scheme 1). Its properties have been calculated [20,21] and examined by means of vibrational spectroscopy [21]. It was shown that pseudo-cross-conjugated mesomeric betaines decarboxylate readily in the absence of stabilizing effects such as hydrogen bonds to protic solvents or water of crystallization [18,19]. Thus, the Gibbs free energy difference for the decarboxylation of 1,2-dimethylindazolium-3-carboxylate under standard conditions (25 °C, 1 atm) was found to be 3.4 kcal/mol [20]. Alternatively, indazolium salts 2 can be deprotonated by various bases to give indazol-3-ylidenes 3 [22].


Scheme 1: Generation of indazol-3-ylidenes.

The chemistry of indazol-3-ylidene, which is a singlet carbene, is due to the considerable donor strength of the carbene atom which has a calculated Mulliken charge of 0.009 [20]. Moreover, the ability to cleave the N–N single bond, which was calculated to have a bond length of 144.6 pm in 1,2-dimethylindazol-3-ylidene [20] (N–N1H-indazole = 138.4 pm [3]) and a stretching force constant of 4.23 mdyn Å−1 [21], opens the access to several heterocyclic transformation products (vide infra). Finally, the synthetic potential is governed by the electrophilic properties of the iminium group of indazolium salts which result from protonation of the carbene. As a consequence, the synthetic potential of indazol-3-ylidene not only strongly depends on the choice of potential reaction partners, but also on its substitution pattern and the reaction conditions. As examples, when N1 is substituted with a methyl group, the carbene can be trapped by elemental sulfur, isocyanates, and isothiocyanates which form indazolethione 4, indazolium-3-amidate 5, and indazolium-3-thioamidate 6, respectively [23] (Scheme 2). Aliphatic ketones surprisingly give stable 1:1 adducts 7 [20,24]. α-Bromo acetophenones induce an unexpected ring enlargement to cinnolines 8 [25]. New ring systems such as 9 [25] and 10 [26] were prepared on treatment of indazol-3-ylidene with acetylenes.


Scheme 2: Reaction products of indazol-3-ylidenes in heterocycle synthesis.

Indazol-3-ylidenes which possess an aryl ring at N1 rearrange to give substituted acridines by a ring-cleavage/pericyclic ring-closure reaction sequence (2AB11) (Scheme 3). It proved to be advantageous to start these rearrangements from indazolium salts which are readily available by copper-catalyzed aryl couplings or Buchwald–Hartwig reactions [22]. Pyrazol-3-ylidenes rearrange similarly to quinolines [17].


Scheme 3: Syntheses of acridines from indazol-3-ylidenes.

We report here on two unexpected rearrangements of indazol-3-ylidene, and trapping reactions of the N-heterocyclic carbene with rhodium.

Results and Discussion

On trying to deprotonate the indazolium salts 12a–e with potassium 2-methylbutan-2-olate in anhydrous dichloromethane at −80 °C to the N-heterocyclic carbene I in the absence of trapping reagents we unexpectedly obtained a mixture of two compounds which are in equilibrium, when the reaction was allowed to warm to room temperature (Scheme 4). From the NMR spectra of the mixture it was apparent that neither the 3,3'-biindazolylidene II nor its trans isomer had formed, as signals between δ = 91.7 ppm and 94.0 ppm were detected by 13C NMR spectroscopy which are neither in agreement with structure II nor with its trans isomer. Mass spectrometric examinations, however, clearly showed the peaks of dimerized species of the carbene I, because the molecular peaks correspond to twice the mass of the salts 12ae minus two hydrogen atoms, respectively. We were able to separate the mixtures of the reactions of 12a,c,d by column chromatography employing methanol as eluent, and to characterize the separated species. The species in equilibrium proved to be spiro[indazole-3,2'-indolines], the exocyclic imine groups of which form Z- and E-isomers 13ae and 14ae, respectively. The equilibration of 14b is too fast so that a separation of a pure sample failed. The iodo derivative 13e gave low yields and despite of intense efforts we were not able to obtain the compounds in pure form. Solutions of pure samples of the E/Z-isomers 13a–d and 14a,c,d, respectively, equilibrated slowly in chloroform solutions to give stable ratios after several days at rt. These results are summarized in Table 1.


Scheme 4: Dimerisation of indazol-3-ylidenes to spiro compounds.

Table 1: Equilibrium between 13a–d and 14a–d in chloroform.

Compounds Ratioa Time (d)
13a/14a 10 : 7 12
13b/14b 5 : 1 2
13c/14c 1 : 1 18
13d/14d 10 : 9 9

aRatios determined by 1H NMR spectroscopy in CDCl3 at rt.

The isomers 13a–e and 14a–e gave identical IR spectra, but the NMR spectra differ considerably (Figure 1). In the NMR spectra the Z-isomers 13a–e show two distinct methyl groups at δ = 3.27 ppm and δ = 2.60 ppm in CDCl3, respectively, as well as two different phenyl rings. The methyl groups of the isomeric spiro compounds 14a,c,d appear at δ = 3.74 ppm and – as overlapped signal – at δ = 2.60 ppm in the 1H NMR spectra measured in CDCl3. On conversion of the exocyclic imine groups from the Z- into the E-configuration (1314), the methyl groups move from a position above the plane of the indazole ring into a position in the plane of the indole ring. This change from vertical to horizontal interactions of aromatics on the methyl groups explains the considerable downfield shift of their 1H NMR resonance frequencies on ZE isomerisation. The following scheme presents diagnostic peak assignments of the 1H and 13C NMR spectra, taken at 400 and 100 MHz in CDCl3, respectively.


Figure 1: Diagnostic 1H and 13C NMR chemical shifts of the Z and E configuration isomer in CDCl3.

According to DFT calculations the conversion of 13a to 14a requires an activation energy of ΔG# = +79 kJ/mol (ΔE = +89 kJ/mol) while the two species do not differ in energy (ΔE < 1 kJ/mol). In comparison the inversions of the two nitrogen atoms within the indazole ring (vide infra) require less than 50 kJ/mol. Transition with such low activation energies are not inhibited at room temperature, so the last mentioned inversions are not observable in NMR spectra at standard temperature conditions.

The spiro compound 14c crystallized from a saturated solution in n-hexane so that we were able to perform a single crystal X-ray analysis. The compound crystallized monoclinic. As expected, neither the pyrrole ring nor the pyrazole ring is planar as evidenced by the dihedral angles C9–N10–C11–C16 = −159.47(12)° and C9–N1–N2–C3 = 15.22(13)° (crystallographic numbering; Figure 2). The pyramidalization of the nitrogen atoms N1 and N10 cause an anti conformation of the methyl group attached to N1 and the 3-chlorophenyl ring attached to N10. The latter is twisted with respect to the indole moiety [C11–N10–C27–C28 = 41.85(18)°]. As N2 is also pyramidalized, the methyl group at N1 and the 3-chlorophenyl ring at N2 adopt an anti conformation as well. The exocyclic imine has a bond length of 127.13(17) pm and this value corresponds to a typical Csp2=N imine bond. Correspondingly, the dihedral angle C16–C17–N18–C19 is only −1.3(2)°. The dihedral angle C15–C16–C17–N18, however, is 6.3(3)° so that the imine group is slightly twisted out of the plane of the indole´s phenyl ring. In the single crystal of 14c, the imine adopts an E configuration as already predicted by the NMR investigations.


Figure 2: Molecular structure of 14c, displacement parameters are drawn at 50% probability level.

The mechanism of this new rearrangement can be either postulated by dimerization of the N-heterocyclic carbene I to give II followed by ring-cleavage of one of the indazole rings to III (pathways A and C, Scheme 4), or as nucleophilic attack of the carbene I to the iminium group of the salts 12a–e followed by ring-cleavage and deprotonation to give betaine III (pathway B). As a matter of fact, cross-experiments between 13a and the chlorophenyl derivative 13b failed in refluxing THF for 4 h as well as in refluxing chloroform under irradiation for 8 h, as no monochloro compound was detectable. Obviously, once the dimerized species is formed under these conditions, there is no equilibrium between the free N-heterocyclic carbene I and its dimers II or III. A closer inspection of the structures reveals that the intermediary betaines III are representatives of the aforementioned class of pseudo-cross-conjugated heterocyclic mesomeric betaines. Thus the intermediates III are related to indazolium-3-carboxylates, -amidates, and -thioamidates shown in Scheme 1 and Scheme 2. The neutralization of the charges in cross-conjugated as well as in pseudo-cross-conjugated mesomeric betaines by inter- or intramolecular cycloadditions are typical reactions [18,19].

To prove the initial formation of an N-heterocyclic carbene in this reaction we tried trapping reactions starting from 12a and 12e with carbonylbis(triphenylphosphine)rhodium(I) chloride under otherwise unchanged reaction conditions. Indeed, stable complexes were formed as yellow crystals in either case which were fully characterized (Scheme 5). The carbene atom of 15e was detected at 191.4 ppm by 13C NMR spectroscopy. A comparison of the stretching frequencies of the CO ligands (15a: 2009 cm−1, 15e: 1994 cm−1) indicated very strong donor strengths of these indazol-3-ylidenes as already postulated earlier on comparing different stretching frequencies of selected 5-membered NHCs [27] or 13C NMR resonance frequencies of several palladium carbene complexes [28].


Scheme 5: Rhodium complex formation.

We were able to obtain single crystals of 15e to perform an X-ray analysis (Figure 3). Suitable single crystals were obtained by slow evaporation of a concentrated solution in dichloromethane/iPrOH. The complex crystallized monoclinic. The Rh–Ccarbene and Rh–CCO bond lengths [Rh1–C1 and Rh1–C10; crystallographic numbering] were determined to be 206.0(2) pm and 186.3(3) pm, respectively. The p-iodophenyl substituent is twisted by −50.7(4)° from the plane of the indazole ring [C4–N2–C1–C53].


Figure 3: Structure of the cation of 15e, displacement parameters are drawn at 50% probability level.

Another type of rearrangement occurred on heating the dimerized carbenes 13a–d/14a–d in xylene, as the substituted quinazolines 16a–d were isolated in reasonable yields (Scheme 6). The mechanism can be rationalized by formation of an ylide by 1,7-H-shift from the mesomeric betaine III, followed by ring cleavage of the indazole ring and subsequent ring-closure of the resulting 1,6-dipole to give the quinazolines 16a–d.


Scheme 6: Rearrangement of the spiro compounds on heating.

Single crystals of 16b suitable for an X-ray analysis were obtained by slow evaporation of a saturated solution in methanol. This compound crystallized monoclinic. A molecular structure is shown in Figure 4. In the single crystal the NH group of the aniline (N18–H) forms a hydrogen bond to the imine group (N25) so that an almost planar six-membered ring is formed. The dihedral angle C11–C12–C17–N18 (crystallographic numbering) was determined to be 0.5(2)°. This six-membered ring is almost perpendicularly twisted in relation to the quinazoline ring [N1–C10–C11–C12 = −92.65(17)°].


Figure 4: Molecular structure of 16b, displacement parameters are drawn at 50% probability level.


The N-heterocyclic carbene of indazole, indazol-3-ylidene, displays a chemistry of its own which differs from the chemistry of N-heterocyclic carbenes of other ring systems. At low temperatures it can be trapped as a rhodium complex. Without trapping reagents it dimerizes under ring-cleavage to form two isomeric spiro compounds possessing E- and Z-configurated methylimine groups. Heating of the carbene dimer results in the formation of novel quinazolines.


General considerations: All reactions for the dimerisation and the rearrangement were carried out under an atmosphere of nitrogen in oven-dried glassware. Flash-chromatography was performed with silica gel 60 (0.040–0.063 mm). Nuclear magnetic resonance (NMR) spectra were obtained with a Bruker Avance 400 and Bruker Avance III 600 MHz. 1H NMR spectra were recorded at 400 MHz or 600 MHz. 13C NMR spectra were recorded at 100 MHz or 150 MHz, with the solvent peak or tetramethylsilane used as the internal reference. Multiplicities are described by using the following abbreviations: s = singlet, d = doublet, t = triplet, q = quartet, and m = multiplet. FTIR spectra were obtained on a Bruker Vector 22 in the range of 400 to 4000 cm−1. The mass spectra were measured with a Varian 320 MS Triple Quad GC–MS/MS with a Varian 450-GC. The electrospray ionization mass spectra (ESIMS) were measured with an Agilent LCMSD series HP 1100 with APIES. Melting points are uncorrected and were determined in an apparatus according to Dr. Tottoli (Büchi). The HRMS spectra were measured on a Bruker Daltonik Tesla-Fourier transform-ion cyclotron resonance mass spectrometer with electrospray ionisation. Yields are not optimized. Compounds 12a, 12b, 12c and 12e were described in an earlier publication [22]. 1-(4-Bromophenyl)-1H-indazole was prepared by the method B which we described earlier [22] and was isolated in better yield (85%) than in the literature (40%) [29]. All density-functional theory (DFT)-calculations were carried out by using the Jaguar 7.7.107 software running on Linux 2.6.18-238.el5 SMP (x86_64) on two AMD Phenom II X6 1090T processor workstations (Beowulf-cluster) parallelized with OpenMPI 1.3.4. MM2 optimized structures were used as starting geometries. Complete geometry optimizations were carried out on the implemented LACVP* (Hay–Wadt effective core potential (ECP) basis on heavy atoms, N31G6* for all other atoms) basis set and with the B3LYP density functional. All calculated structures were proven to be true minima by the absence of imaginary frequencies or transition states by the occurrence of one negative frequency. Plots were obtained using Maestro 9.1.207, the graphical interface of Jaguar. Inversion barriers have been calculated fully relaxed, fixating one torsion angle around the inverted center, and optimizing all remaining degrees of freedom. Torsion angles were modified in steps of 10°.

Thermodynamic corrections were estimated from unscaled frequencies, using standard formulae in the ideal gas harmonic oscillator approximation as implemented in Jaguar, and refer to a standard state of 298.15 K and 1 mol/dm3 concentration.

Crystal structure determinations of 14c, 15e, 16b

The single-crystal X-ray diffraction study was carried out on a Bruker-Nonius Kappa-CCD at 123(2) K using MoKα radiation (λ = 0.71073 Å). Direct Methods (SHELXS-97) [30] were used for structure solution and refinement was carried out using SHELXL-2013 [30] (full-matrix least-squares on F2). Hydrogen atoms were localized by difference electron density determination and refined using a riding model (H(N) free). Semi-empirical absorption corrections were applied. In 15e one of the 3 solvent molecules CH2Cl2 is disordered. For more information see the Supporting Information File 1.

14c: yellow, C25H22Cl2N4, M = 485.39, crystal size 0.45 × 0.25 × 0.15 mm, monoclinic, space group P21/c (no. 14): a = 13.522(1) Å, b = 14.131(1) Å, c = 12.306(1) Å, β = 94.16(1)°, V = 2345.2(3) Å3, Z = 4, ρ(calc) = 1.375 Mg m−3, F(000) = 1008, µ = 0.302 mm−1, 38867 reflections (2θmax = 55°), 5367 unique [Rint = 0.028], 309 parameters, R1 (for 4546 I > 2σ(I)) = 0.032, wR2 (all data) = 0.086, GOOF = 1.05, largest diff. peak and hole 0.339 / −0.294 e Å−3.

15e: yellow, C51H41IN2OP2Rh+ –PF6 · 3CH2Cl2, M = 1389.36, crystal size 0.35 × 0.25 × 0.15 mm, monoclinic, space group P21/n (no. 14): a = 14.314(1) Å, b = 26.691(2) Å, c = 15.045(1) Å, β = 99.43(1)°, V = 5670.3(7) Å3, Z = 4, ρ(calc) = 1.627 Mg m−3, F(000) = 2768, µ = 1.273 mm−1, 91339 reflections (2θmax = 55°), 12976 unique [Rint = 0.021], 685 parameters, 70 restraints, R1 (for 11838 I > 2σ(I)) = 0.032, wR2 (all data) = 0.086, GOOF = 1.09, largest diff. peak and hole 1.473/−1.377 e Å−3.

16b: colourless, C28H22Cl2N4, M = 485.39, crystal size 0.30 × 0.24 × 0.06 mm, monoclinic, space group P21/n (no. 14): a = 14.690(1) Å, b = 7.488(1) Å, c = 21.484(2) Å, β = 90.75(1)°, V = 2363.0(4) Å3, Z = 4, ρ(calc) = 1.364 Mg m−3, F(000) = 1008, µ = 0.300 mm−1, 36379 reflections (2θmax = 55°), 5408 unique [Rint = 0.034], 311 parameters, 1 restraints, R1 (for 4414 I > 2σ(I)) = 0.040, wR2 (all data) = 0.093, GOOF = 1.05, largest diff. peak and hole 0.325/−0.278 e Å−3.

Crystallographic data (excluding structure factors) for the structures reported in this work have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-972482 (14c), CCDC-972481 (15e), and CCDC-972483 (16b). Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge DB2 1EZ, UK (Fax: int.code+(1223)336-033; e-mail: deposit@ccdc.cam.ac.uk).

General procedure for the preparation of the indazole carbene dimers 13/14

A solution of 2.0 mmol of the indazolium salts 12a–e in 20 mL of dichloromethane was cooled to −80 °C. Then 1.2 mL of a 2 M solution of potassium 2-methylbutan-2-olate in THF was added dropwise within 30 minutes. The reaction mixture was then evaporated to dryness and extracted twice with 20 mL of petroleum ether, respectively. After evaporation of the solvent in vacuo the crude reaction product was purified by flash column chromatography (silica gel; methanol) and dried in vacuo. The isomers 13 and 14 have Rf values of approximately 0.4 and 0.2 on silica gel in MeOH, respectively.

(Z)-N-(2-Methyl-1,1'-diphenyl-1,2-dihydrospiro[indazole-3,2'-indolin]-3'-ylidene)methanamine (13a)

Yield: 152 mg (37%) of a yellow solid; mp 74–75 °C; 1H NMR (400 MHz, CDCl3) δ 7.68 (dd, J = 7.5, 0.6 Hz, Ar-H, 1H), 7.29–7.25 (m, 2H, Ar-H), 7.23–7.06 (m, 9H, Ar-H), 6.96 (dd, J = 8.6, 1.2 Hz, 2H, Ar-H), 6.89–6.83 (m, 2H, Ar-H), 6.71 (d, J = 8.1 Hz, 1H, Ar-H), 6.58 (d, J = 8.1 Hz, 1H, Ar-H), 3.27 (s, 3H, CH3), 2.60 (s, 3H, CH3) ppm; 13C NMR (100 MHz, CDCl3) δ 166.5, 153.5, 149.0, 145.8, 140.7, 133.0, 129.4, 129.1, 129.0, 127.6, 125.8, 125.7, 124.9, 124.5, 123.7, 123.5, 122.5, 121.9, 119.2, 110.1, 109.5, 91.8, 39.8, 35.1 ppm; IR (ATR): 3051, 2952, 2891, 2855, 1655, 1605, 1590, 1450, 1354, 1312, 1271, 1191, 1151, 1000, 922, 856, 697, 681, 480 cm−1; ESIMS: m/z (%) = 417 [M + H+]; HRESIMS: C28H25N4 calcd for 417.2079; found: 417.2075.

(E)-N-(2-Methyl-1,1'-diphenyl-1,2-dihydrospiro[indazole-3,2'-indolin]-3'-ylidene)methanamine 14a

Yield: 106 mg (25%) of a yellow solid; mp 79–80 °C; 1H NMR (400 MHz, CDCl3) δ 7.81 (d, J = 7.5 Hz, 1H, Ar-H), 7.30–7.27 (m, 1H, Ar-H), 7.25–7.21 (m, 2H, Ar-H), 7.19–7.13 (m, 6H, Ar-H), 7.10–7.06 (m, 2H, Ar-H), 6.97–6.95 (m, 2H, Ar-H), 6.91 (ddd, J = 7.4, 7.4, 0.8 Hz, 1H, Ar-H), 6.83–6.77 (m, 2H, Ar-H), 6.62 (d, J = 8.0 Hz, 1H, Ar-H), 3.75 (s, 3H, CH3), 2.59 (s, 3H, CH3) ppm; 13C NMR (100 MHz, CDCl3) δ 168.1, 155.3, 149.1, 147.0, 140.2, 133.2, 129.4, 129.0, 128.9, 128.8, 128.1, 127.7, 126.1, 125.3, 124.3, 123.8, 121.8, 118.3, 118.1, 111.1, 109.6, 93.8, 40.7, 35.8 ppm; IR (ATR): 3034, 2950, 2888, 2858, 1655, 1605, 1590, 1450, 1355, 1312, 1272, 1192, 1152, 999, 921, 857, 697, 681, 480 cm−1; ESIMS: m/z (%) = 417 [M + H+]; HRESIMS: C28H25N4 calcd for 417.2079; found: 417.2075.

General procedure for the preparation of the rhodium complexes 15

A solution of 0.2 mmol of the indazolium salts 12a and 12e, respectively, and 0.2 mmol of carbonylbis(triphenylphosphine)rhodium(I) chloride in 20 mL of THF was cooled to −80 °C. Then, 0.1 mL of a 2 M solution of potassium 2-methylbutan-2-olate in THF was added dropwise. The reaction mixture was then stirred overnight at room temperature. Yellow solids formed which were filtered off, washed with 2 mL of ethylacetate, and dried in vacuo.

Carbonyl-bis(triphenylphosphine)(2-methyl-1-phenyl-1H-indazole-3-ylidene)rhodium(I) hexafluorophosphate (15a)

Yield: 73 mg (36%) of yellow crystals; dec. 240 °C; 1H NMR (400 MHz, DMSO-d6) δ 7.67 (d, J = 8.3 Hz, 1H), 7.62–7.60 (m, 3H), 7.56–7.39 (m, 31H), 7.04–6.97 (m, 3H), 6.77 (d, J = 8.3 Hz, 1H), 3.23 (s, 3H) ppm; 13C NMR (150 MHz, DMSO-d6) δ 139.2, 133.5 (t, J = 6.0 Hz), 132.4 (t, J = 23.0 Hz), 132.3, 132.1, 131.0, 130.9, 130.3, 128.9 (t, J = 4.3 Hz), 128.7, 127.7, 126.2, 122.2, 109.6, 40.2 ppm; IR (ATR): 2009, 1498, 1479, 1436, 1308, 1095, 861, 833, 741, 641, 557, 498 cm−1; ESIMS: m/z (%) = 863 [M +]; HRESIMS: C51H42N2OP2Rh calcd for 863.1827; found: 863.1827.

General procedure for the rearrangements of the indazole carbene dimers to 16

A solution of 1.0 mmol of the dimers of the indazole carbenes 13a/13b/13d in 20 mL of xylene was stirred at reflux temperature for 3 hours. After the solvent was distilled off in vacuo, the crude product was purified by flash column chromatography (petroleum ether: ethyl acetate = 3:1) and dried in vacuo.

2-((Methylimino)(1-phenyl-1,2-dihydroquinazolin-4-yl)methyl)-N-phenylaniline 16a

Yield 233 mg (56%) of yellow crystals; mp 146–147 °C. 1H NMR (400 MHz, CDCl3) δ 11.74 (bs, 1H, NH), 7.46–7.42 (m, 2H, Ar-H), 7.38–7.28 (m, 8H, Ar-H), 7.24–7.16 (m, 3H, Ar-H), 7.11–7.05 (m, 2H, Ar-H), 6.97 (d, J = 8.3 Hz, 1H, Ar-H), 6.77 (t, J = 7.6 Hz, 1H, Ar-H), 6.65 (t, J = 7.6 Hz, 1H, Ar-H), 5.51 (s, 2H, CH2), 3.41 (s, 3H, CH3) ppm; 13C NMR (100 MHz, CDCl3) δ 169.4, 164.6, 146.7, 145.1, 144.1, 141.8, 133.3, 132.1, 129.7, 129.4, 127.3, 124.9, 123.5, 122.8, 122.2, 120.1, 119.2, 118.6, 116.9, 116.0, 114.0, 66.6, 40.1 ppm; IR (ATR): 3025, 2968, 2856, 1714, 1589, 1524, 1482, 1448, 1319, 1174, 740, 693, 638, 518 cm−1. ESIMS: m/z (%) = 417 [M + H+]. HRESIMS: C28H25N4 calcd for 417.2079; found: 417.2080.

Supporting Information

Supporting Information File 1: Synthetic procedures, characterization data, X-ray data and NMR spectra.
Format: PDF Size: 1.6 MB Download


Dr. Gerald Dräger, University of Hannover, Germany, is thankfully acknowledged for measuring the HRESIMS spectra.


  1. Stadlbauer, W. In Science of Synthesis; Neier, R., Ed.; Thieme Verlag: Stuttgart, Germany, 2002; Vol. 12, pp 227–324.
    Return to citation in text: [1]
  2. Elguero, J. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford, U.K., 1996; Vol. 3, pp 1–75.
    Return to citation in text: [1]
  3. Stadlbauer, W. In Houben-Weyl, Methoden der Organischen Chemie; Schaumann, E., Ed.; Thieme Verlag: Stuttgart, Germany, 1994; Vol. E8b, pp 764–864.
    Return to citation in text: [1] [2]
  4. Schmidt, A.; Beutler, A.; Snovydovych, B. Eur. J. Org. Chem. 2008, 4073–4095. doi:10.1002/ejoc.200800227
    Return to citation in text: [1] [2] [3]
  5. Cerecetto, H.; Gerpe, A.; González, M.; Arán, V. J.; Ochoa de Ocáriz, C. Mini-Rev. Med. Chem. 2005, 5, 869–878. doi:10.2174/138955705774329564
    Return to citation in text: [1]
  6. Arduengo, A. J., III; Harlow, R. L.; Kline, M. J. Am. Chem. Soc. 1991, 113, 361–363. doi:10.1021/ja00001a054
    Return to citation in text: [1]
  7. Breslow, R. J. Am. Chem. Soc. 1958, 80, 3719–3726. doi:10.1021/ja01547a064
    Return to citation in text: [1]
  8. Wanzlick, H.-W. Angew. Chem. 1962, 74, 129–134. doi:10.1002/ange.19620740402
    Return to citation in text: [1]
  9. Öfele, K. J. Organomet. Chem. 1968, 12, P42. doi:10.1016/S0022-328X(00)88691-X
    Return to citation in text: [1]
  10. Kühl, O. Functionalised N-Heterocyclic Carbene Complexes; John Wiley & Sons: Chichester, U.K., 2010. doi:10.1002/9780470685839
    Return to citation in text: [1]
  11. Diez-Gonzalez, S. N-Heterocyclic Carbenes: From Laboratory Curiosities to Efficient Synthetic Tools; Royal Society of Chemistry: Cambridge, U.K., 2011.
    Return to citation in text: [1]
  12. Nolan, S. P. N-Heterocyclic Carbenes in Synthesis; Wiley-VCH: Weinheim, Germany, 2002.
    Return to citation in text: [1]
  13. Yuan, D.; Huynh, H. V. Organometallics 2011, 31, 405–412. doi:10.1021/om2010029
    Return to citation in text: [1]
  14. Mata, J. A.; Poyatos, M. Curr. Org. Chem. 2011, 15, 3309–3324. doi:10.2174/138527211797247969
    Return to citation in text: [1]
  15. Grossmann, A.; Enders, D. Angew. Chem., Int. Ed. 2012, 124, 320–332. doi:10.1002/anie.201105415
    Return to citation in text: [1]
  16. Zhao, Q. W.; Curran, D. P.; Malacria, M.; Fensterbank, L.; Goddard, J. P.; Lacôte, E. Chem.–Eur. J. 2011, 17, 9911–9914. doi:10.1002/chem.201101822
    Return to citation in text: [1]
  17. Schmidt, A.; Münster, N.; Dreger, A. Angew. Chem., Int. Ed. 2010, 122, 2851–2854. doi:10.1002/anie.200905436
    Return to citation in text: [1] [2]
  18. Schmidt, A.; Guan, Z. Synthesis 2012, 3251–3268. doi:10.1055/s-0032-1316787
    Return to citation in text: [1] [2] [3] [4]
  19. Schmidt, A.; Wiechmann, S.; Freese, T. ARKIVOC 2013, No. i, 424–469. doi:10.3998/ark.5550190.p008.251
    Return to citation in text: [1] [2] [3]
  20. Schmidt, A.; Merkel, L.; Eisfeld, W. Eur. J. Org. Chem. 2005, 2124–2130. doi:10.1002/ejoc.200500032
    Return to citation in text: [1] [2] [3] [4] [5] [6]
  21. Schmidt, A.; Snovydovych, B.; Casado, J.; Quirante, J. J.; López Navarrete, J. T.; Ramírez, F. J. Phys. Chem. Chem. Phys. 2009, 11, 341–348. doi:10.1039/b812597j
    Return to citation in text: [1] [2] [3]
  22. Guan, Z.; Wiechmann, S.; Drafz, M.; Hübner, E.; Schmidt, A. Org. Biomol. Chem. 2013, 11, 3558–3567. doi:10.1039/c3ob40379c
    Return to citation in text: [1] [2] [3] [4]
  23. Schmidt, A.; Beutler, A.; Habeck, T.; Mordhorst, T.; Snovydovych, B. Synthesis 2006, 1882–1894. doi:10.1055/s-2006-942367
    Return to citation in text: [1]
  24. Schmidt, A.; Habeck, T.; Snovydovych, B.; Eisfeld, W. Org. Lett. 2007, 9, 3515–3518. doi:10.1021/ol0713739
    Return to citation in text: [1]
  25. Schmidt, A.; Snovydovych, B.; Gjikaj, M. Synthesis 2008, 2798–2804. doi:10.1055/s-2008-1067215
    Return to citation in text: [1] [2]
  26. Schmidt, A.; Snovydovych, B.; Hemmen, S. Eur. J. Org. Chem. 2008, 4313–4320. doi:10.1002/ejoc.200800456
    Return to citation in text: [1]
  27. Jothibasu, R.; Huynh, H. V. Chem. Commun. 2010, 46, 2986–2988. doi:10.1039/b925977e
    Return to citation in text: [1]
  28. Huynh, H. V.; Han, Y.; Jothibasu, R.; Yang, J. A. Organometallics 2009, 28, 5395–5404. doi:10.1021/om900667d
    Return to citation in text: [1]
  29. Lebedev, A. Y.; Khartulyari, A. S.; Voskoboynikov, A. Z. J. Org. Chem. 2005, 70, 596–602. doi:10.1021/jo048671t
    Return to citation in text: [1]
  30. Sheldrick, G. M. Acta Crystallogr., Sect. A 2008, A64, 112–122. doi:10.1107/S0108767307043930
    Return to citation in text: [1] [2]

© 2014 Guan et al; licensee Beilstein-Institut.
This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)

Back to Article List

Other Beilstein-Institut Open Science Activities

Keep Informed

RSS Feed

Subscribe to our Latest Articles RSS Feed.


Follow the Beilstein-Institut


Twitter: @BeilsteinInst