Preparation of azulene substituted pyrazine and quinoxaline derivatives

Article abstract of DOI:10.3987/COM-08-S(F)87

2,3-Di(2-azulenyl)pyrazines and -quinoxalines were obtained by the reaction of di(2-azulenyl)ethanedione with diamines. Cyclodehydrogenation reaction of the pyrazine and quinoxaline derivatives with manganese dioxide afforded the corresponding azulene-fus

Full text of DOI:10.3987/COM-08-S(F)87

HETEROCYCLES, Vol. 77, No. 2, 2009
1079
HETEROCYCLES, Vol. 77, No. 2, 2009, pp. 1079 - 1088. © The Japan Institute of Heterocyclic Chemistry
Received, 31st July, 2008, Accepted, 30th September, 2008, Published online, 2nd October, 2008
DOI: 10.3987/COM-08-S(F)87
PREPARATION OF AZULENE SUBSTITUTED PYRAZINE AND
QUINOXALINE DERIVATIVES
Nozomi Furuta, Takuo Mizutani, Akira Ohta, and Kunihide Fujimori*
Department of Chemistry, Faculty of Science, Shinshu University, Asahi
Matsumoto 390-8621, Japan. E-mail: kfujimo@shinshu-u.ac.jp
Abstract – 2,3-Di(2-azulenyl)pyrazines and -quinoxalines were obtained by the
reaction of di(2-azulenyl)ethanedione with diamines. Cyclodehydrogenation
reaction of the pyrazine and quinoxaline derivatives with manganese dioxide
afforded the corresponding azulene-fused quinoxaline and phenazine derivatives,
respectively.
Azulene has attracted the interest of many research groups from the standpoint of synthetic and
theoretical studies, due to its unusual properties.1 On the other hand, heterocyclic compounds, pyrazines
and quinoxalines, are of interest not only in their physical properties and chemical behavior, but also in
their physiological activities and molecular electronics.2 This paper describes the synthesis of azulene
substituted pyrazine and quinoxaline derivatives.
One of the authors (K. Fujimori) has reported the facile synthetic method and reactivities of
di(2-azulenyl)ethanedione (1).3 Compound 1 afforded 2,3-di(2-azulenyl)-5,6-dihydropyrazine (2) by the
reaction with ethylenediamine in good yield (Scheme 1). Oxidation of 2 with chloranil gave
2,3-di(2-azulenyl)pyrazine (3) in almost quantitative yield. Furthermore, compound 2 was readily
converted into 3 on a column of basic alumina with toluene.
1
2
Scheme 1
This paper is dedicated to Professor Emeritus Keiichiro Fukumoto on the occasion of his 75th birthday.

1080
HETEROCYCLES, Vol. 77, No. 2, 2009
On the other hand, the treatment of 2 with activated manganese dioxide afforded 3 and 4 in 41% and 20%
yields, respectively (Scheme 2). Formation of 4 is ascribed to the oxidative cyclodehydrogenation
reaction of 3. Actually, the treatment of 3 with activated manganese dioxide gave 4 in 36% yield.
3
4
Scheme 2
Table 1. Oxidation of compound 2
A reaction that characterizes compound 1 as an -diketone is condensation reaction with
o-phenylenediamines (5a - g) to give the corresponding quinoxaline derivatives (6a - g) (Scheme 3, Table
2). 2,3,7,8-Tetra(2-azulenyl)pyradino[2,3-g]quinoxaline (7) could not be obtained by the reaction of
6,7-diamino-2,3-di(2-azulenyl)quinoxaline (6d) with dione 1. Cyclodehydrogenation reaction of 6a with
activated manganese dioxide afforded 8 in 20% yield (Scheme 4). These novel azulene fused quinoxaline
derivatives (4, 8) are stable, showing no decomposition even after several weeks at room temperature.
5
6
Scheme 3

HETEROCYCLES, Vol. 77, No. 2, 2009
1081
Scheme 4
Table 2. Reaction of di(2-azulenyl)ethanedione (1) with o-phenylenediamines (5)

1082
HETEROCYCLES, Vol. 77, No. 2, 2009
All the spectral data and elemental analyses supported the structure of the new compounds. The structure
of 6a was also confirmed by X-ray analysis (Figure 1). Single crystals of 4 or 8 suitable for X-ray
analysis were not obtained. But the vicinal coupling constants on 1H NMR allow us to estimate the degree
of bond alternation in the seven-membered ring.4 The coupling constants (3JHH) of 4, 8 vary between
9.0-9.2 Hz across the formal C-C bonds and 10.0-10.1 Hz across the formal C=C bonds in the
seven-membered ring. These values indicate the existence of some bond alternation in the
seven-membered ring of 4, 8, although the degree is considerably smaller than that in benz[a]azulene.4
The chemical shifts of 10-H, 11-H protons in compound 4 and those of 5-H, 6-H protons in compound 8
were observed at lower field than the corresponding protons of 3 or 6a owing to anisotropic effect of
neighboring azulene ring. UV-VIS spectra of 3, 4, 6a, and 8 in dichloromethane show that the
abosorption maxima in the visible region were significantly influenced by the ring closure at the
1,1'-positions of the two azulene rings.3 The azulene-fused quinoxaline and phenazine derivatives 4, 8
exhibited the longest wavelength absorption up to 815 nm and 777 nm, respectively.
Figure 1. X-Ray molecular structure of 6a.
EXPERIMENTAL
Melting points were determined on a Yanagimoto micro-melting point apparatus and are uncorrected.
1
Spectral data were obtained on the following instruments: H-NMR: JEOL-JNM-LA300 (300 MHz), and
-LA400 (400 MHz); 13C-NMR; JEOL-JNM-LA300 (75.5 MHz), and –LA400 (100 MHz); IR: JEOL
JIR-Diamond20; MS spectroscopy: Shimadzu GCMS-QP1000EX; UV-VIS: Shimadzu UV-260.
Elemental analyses were performed on a Perkin-Elmer model 240.

HETEROCYCLES, Vol. 77, No. 2, 2009
1083
2,3-Di(2-azulenyl)-5,6-dihydropyrazine (2). A mixture of di(2-azulenyl)ethanedione (1) (307 mg,
0.99 mmol) and ethylenediamine (0.1 mL) in EtOH (120 mL) was refluxed for 30 min. Reaction mixture
was poured in water and extracted with CHCl3. The dried organic layer was concentrated and the residue
was purified by column chromatography on silica gel to afford 2 (263 mg, 79%) as dark blue needles, mp
176-178 °C and 2,3-di(2-azulenyl)pyradine (3) (51 mg, 16%) as dark bluish green plates, mp 189-190 °C.
2: 1H-NMR (300 MHz, CDCl3)  : 3.18 (4H, s, H-5, 6), 7.08 (4H, t, J = 9.7 Hz, Az -5', 7', 5'', 7''), 7.39 (4H,
s, Az -1', 3', 1'', 3''), 7.53 (2H, t, J = 9.7 Hz, Az - 6', 6'), 8.18 (4H, d, J = 9.7 Hz, Az -4', 8', 4", 8").
13C-NMR (75.5 MHz, CDCl3) : 46.1, 118.1, 123.8, 138.6, 138.7, 140.0, 145.8, 158.6. IR (KBr): 3079,
2937, 1552, 1191, 826 cm-1. MS: m/z (rel. int. %) 334 (M+, 100), 306 (18), 252 (7), 127 (Az+, 19).
UV-VIS (CH2Cl2) max (log ): 221 (4.46), 242 (4.56), 283 (4.92), 300sh (4.81), 340sh (4.08), 365 (4.03),
603 (2.96), 635 (2.95), 698sh (2.64). Anal. Calcd for C24H18N2: C, 86.20; H, 5.43; N, 8.38. Found: C,
85.99; H, 5.45; N, 8.31.
2,3-Di(2-azulenyl)pyrazine (3).
a) Oxidation using activated manganese dioxide, Method 1. A mixture of 2 (29 mg, 0.09 mmol) and
activated manganese dioxide (155 mg, 1.79 mmol) in benzene (10 mL) was stirred at rt for 41 h. To a
reaction mixture was added fresh activated manganese dioxide (160 mg, 1.85 mmol) and then the mixture
was stirred for 26 h. From the reaction mixture, excess manganese dioxide was removed by filtration. The
organic layer was concentrated and the residue was purified by column chromatography on silica gel with
CHCl3 to give 3 (8 mg, 28%) as dark bluish green plates, mp 189-190 °C. Method 2. A mixture of 2 (51
mg, 0.15 mmol) and activated manganese dioxide (260 mg, 2.99 mmol) in benzene (17 mL) was refluxed
for 20 h. After workup, the residue was purified by column chromatography on silica gel with chloroform
1
to give 3 (21 mg, 41%) and diazuleno[2,1-f:1,2-h]quinoxaline (4) (10 mg, 20%). 3: H-NMR (400 MHz,
CDCl3) : 7.10 (4H, t, J = 9.8 Hz, Az -5', 7', 5", 7"), 7.53 (2H, t, J = 9.8 Hz, Az -6', 6"), 7.53 (4H, s, Az -1',
3', 1", 3"), 8.20 (4H, d, J = 9.8 Hz, Az -4', 8', 4", 8"), 8.62 (2H, s, H-5,6). 13C-NMR (75.5 MHz, CDCl3) :
118.4, 123.5, 137.8, 137.9, 140.2, 142.0, 147.5, 150.1. IR (KBr): 3052, 1573, 1142, 818 cm-1. MS: m/z
(rel. int. %) 332 (M+, 79), 331 (100), 254 (10), 127 (Az+, 6). UV-VIS (CH2Cl2) max (log ): 278 (4.88),
320 (4.70), 391 (4.21), 595 (2.86), 635 (2.85), 698sh (2.53). Anal. Calcd for C24H16N2: C, 86.72; H, 4.85; N,
1
8.43. Found: C, 86.55; H, 4.93; N, 8.37. 4: Dark green needles; mp 198-199 °C; H-NMR (400 MHz,
CDCl3) : 7.2-7.3 (4H, m, H-7, 9, 12, 14), 7.11 (2H, t, J =9.6 Hz, H-8, 13), 8.56 (2H, s, H-5, 16), 8.58
13
(2H, d, J =10.0 Hz, H-6, 15), 9.03 (2H, s, H-2, 3), 9.53 (2H, d, J =9.0 Hz, H-10, 11). C-NMR (75.5
MHz, CDCl3) : 115.1, 123.1, 123.2, 124.0, 135.6, 136.1, 138.9, 139.0, 139.1, 139.5, 141.4, 143.5. IR
(KBr): 3054, 1571, 1213, 808 cm-1. MS: m/z (rel. int. %) 330 (M+, 100), 304 (7), 276 (5). UV-VIS
(CH2Cl2) max (log ): 237 (4.46), 275 (4.73), 321 (4.60), 358sh (4.41), 374 (4.45), 396sh (4.41), 413 (4.49),

1084
HETEROCYCLES, Vol. 77, No. 2, 2009
455 (4.06), 653 (3.05), 700sh (2.98), 815sh (2.61). Anal. Calcd for C24H14N2: C, 87.25; H, 4.27; N, 8.48.
Found: C, 87.25; H, 4.22; N, 8.59.
b) Oxidation using chloranil. A solution of 2 (51 mg, 0.15 mmol) and chloranil (37 mg, 0.15 mmol) in
xylene (15 mL) was refluxed for 2 h. To the reaction mixture was added Et2O (30 mL) and the organic
layer was washed with 1% NaOH aqueous solution for three times, dried over anhydrous MgSO4, and
concentrated under reduced pressure. The residue was purified by column chromatography on silica gel
with CHCl3 to afford 3 (50 mg, 99%) as dark green plates (mp 189-190 °C). The IR spectrum was
identical with that of the sample prepared by means of Method 1, 2 and the mixed melting point with the
sample was not depressed.
Diazuleno[2,1-f:1,2-h]quinoxaline (4). A mixture of 3 (54 mg, 0.16 mmol) and activated manganese
dioxide (267 mg, 3.07 mmol) in toluene (17 mL) was refluxed for 22 h. To a reaction mixture was added
fresh activated manganese dioxide (270 mg, 3.11 mmol) and then the mixture was stirred for 19 h. From
the reaction mixture, excess manganese dioxide was removed by filtration. The organic layer was
concentrated and the residue was purified by column chromatography on silica gel with CHCl3 to give 4
(18 mg, 36%) as dark green needles, mp 198-199 °C. The IR spectrum was identical with that of the
sample prepared by the reaction of 2 with activated manganese dioxide and the mixed melting point with
the sample was not depressed.
2,3-Di(2-azulenyl)quinoxaline (6a). A mixture of 1,2-di(2-azulenyl)ethanedione (1) (100 mg, 0.33
mmol), o-phenylenediamine (5a) (44 mg, 0.05 mmol), and molecular sieve 3Å in dry EtOH (40 mL) was
refluxed for 40 min. After work up, the residue was purified by column chromatography on silica gel with
1
benzene to afford 6a as dark blue needles (mp 213-214 °C, from EtOH) in 78% yield. H-NMR (300
MHz, CDCl3) : 7.11 (4H, t, J = 9.9 Hz, Az -5', 7', 5", 7"), 7.54 (2H, dd, J = 9.9 Hz, Az -6', 6"), 7.57 (4H,
s, Az -1', 3', 1", 3"), 7.7-7.8 (2H, m, H - 6, 7), 8.1-8.2 (2H, m, H - 5, 8), 8.23 (4H, d, J = 9.9 Hz, Az -4', 8',
4", 8"). IR (KBr): 3047, 3018, 1568, 823 cm-1. UV-VIS (CH2Cl2)max (logε): 245 (4.53), 292 (4.92),
316sh (4.73), 384 (4.38), 600 (2.90), 637 (2.89), 700 (2.56). Anal. Calcd for C28H18N2: C, 87.93; H, 4.74;
N, 7.32. Found: C, 87.86; H, 4.91; N, 7.21.
2,3-Di(2-azulenyl)-5-azaquinoxaline (6b). A mixture of 1 (50 mg, 0.16 mmol) and 2,3-diaminopyridine
(5b) (27 mg, 0.25 mmol) in dry EtOH was refluxed for 20 h. The reaction mixture was concentrated to
leave a residue. The residue was purified by column chromatography on silica gel with AcOEt-hexane
1
(1:1) to give 6b (60 mg, 97%) as dark blue needles (mp 243-245 °C). H-NMR (300 MHz, CDCl3) :
7.08 (2H, t, J = 9.9 Hz, Az -5', 7'), 7.15 (2H, t, J = 9.9 Hz, Az-5", 7"), 7.53 (1H, t, J = 9.9 Hz, Az -6'), 7.59

HETEROCYCLES, Vol. 77, No. 2, 2009
1085
(1H, t, J = 9.9 Hz, Az -6"), 7.63 (2H, s, Az -1', 3'), 7.6-7.7 (1H, m, H-7), 7.67 (2H, s, Az -1", 3"), 8.20 (2H,
d, J = 9.9 Hz, Az -4', 8'), 8.27 (2H, d, J = 9.9 Hz, Az -4", 8"), 8.52 (1H, d, J = 7.5, 1.8 Hz, H-8), 9.1-9.2
(1H, m, H-6). 13C-NMR (100 MHz, CDCl3) :118.7, 119.2, 119.4, 119.9, 123.4, 123.6, 123.7, 123.9,
124.8, 125.3, 136.3, 137.7, 138.1, 138.3, 138.4, 138.6, 138.7, 138.9, 140.1, 140.2, 146.6, 147.2, 150.0,
152.4, 153.6, 153.7, 154.4. MS: m/z (rel. int. %) 383 (M+, 79), 382 (100), 153 (16), 127 (8). IR (KBr):
3052, 3012, 1571, 822 cm-1. UV-VIS (CH2Cl2) max (logε): 248 (4.58), 283 (4.91), 313 (4.71), 388 (4.47),
604 (2.94), 641 (2.93), 699 (2.60). Anal. Calcd for C27H17N3: C, 84.57; H, 4,47; N, 10.9. Found: C, 84.31;
H, 4.74; N. 10.64.
2,3-Di(2-azulenyl)-6-azaquinoxaline (6c).
A solution of 1 (50 mg, 0.16 mmol) and
3,4-diaminopyridine (5c) (22 mg, 0.20 mmol) in dry EtOH (20 mL) was refluxed for 26 h. The reaction
mixture was treated by a method similar to that used for 6b described above to give 6c (54 mg, 87%) as
dark blue needles (mp 204-205 °C, from EtOH). 1H-NMR (400 MHz, CDCl3) : 7.14 (4H, t, J = 9.8 Hz,
Az -5', 7', 5", 7"), 7.5-7.6 (6H, m, Az -1', 3', 6', 1", 3", 6"), 8.01 (1H, d, J = 5.8 Hz, H-8), 8.25 (4H, d, J =
9.8 Hz, Az -4', 8', 4", 8"), 8.80 (1H, d, J = 5.8 Hz, H-7), 9.62 (1H, s, H-5). 13C-NMR (100 MHz, CDCl3)
: 119.0, 119.2, 121.4, 123.8, 123.9, 136.4, 138.5, 138.6, 138.9, 139.0, 140.2, 143.7, 146.7, 146.8, 147.1,
153.0, 154.5, 155.5. MS: m/z (rel. int. %) 383 (M+, 77), 382 (100), 153 (14), 127 (9). IR (KBr): 3052,
3012, 1574, 822 cm-1. UV-VIS (CH2Cl2) max (logε): 223 (4.51), 249 (4.57), 291 (4.91), 386 (4.41), 606
(2.94), 640 (2.93), 702sh (2.60). Anal. Calcd for C27H17N3: C, 84.57; H, 4.47; N, 10.96. Found: C, 84.98; H,
4.60; N, 10.82.
6,7-Diamino-2,3-(2-azulenyl)quinoxaline (6d).
A solution of 1 (100 mg, 1.74 mmol),
1,2,4,5-benzenetetramine tetrahydrochloride (5d) (83 mg, 0.29 mmol) and pyridine (0.14 mL, 1.74 mmol)
in dry EtOH (40 mL) was refluxed for 1 h. The reaction mixture was diluted with water and extracted
with CHCl3. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced
pressure to leave a residue. The residue was chromatographied on silica gel with AcOEt to give 6d (125
mg, 94%) as brown crystals (mp 190-193 °C, from EtOH). 1H-NMR (400 MHz, CDCl3) : 3.99 (4H, brs,
-NH2), 7.08 (4H, t, J = 9.8 Hz, Az - 5', 7', 5", 7"), 7.35 (2H, s, H-5, 8), 7.50 (2H, t, J = 9.8 Hz, Az -6', 6"),
7.52 (4H, s, Az -1', 3', 1", 3"), 8.18 (4H, d, J = 9.8 Hz, Az -4', 8', 4", 8"). 13C-NMR (100 MHz, CDCl3) :
110.5, 110.8, 118.7, 119.1, 123.1, 123.4, 137.1, 137.5, 138.8, 140.2, 147.6, 149.1. MS: m/z (rel. int. %)
412 (M+, 72), 411 (100), 334 (12), 205 (12). IR (KBr): 3345, 3045, 3004, 1571, 1500, 1230, 825 cm-1.
UV-VIS (CH2Cl2) max (logε): 233 (4.56), 273 (4.70), 295 (4.77), 312sh (4.71), 430 (4.55), 580 (3.06),
625 (2.97), 692 (2.68). Anal. Calcd for C28H20N4: C, 81.53; H, 4.89; N, 12.58. Found: C, 81.09; H, 4.77;
N, 12.38.

1086
HETEROCYCLES, Vol. 77, No. 2, 2009
2,3-Di(2-azulenyl)dibenzo[f,h]quinoxaline (6e). A solution of 1 (30 mg, 0.10 mmol) and
9,10-diaminophenanthlene (5e) (22.0 mg, 0.11 mmol) in dry EtOH (15 mL) was refluxed for 21 h. The
reaction mixture was diluted with water and extracted with CHCl3. The organic layer was dried over
anhydrous sodium sulfate, and concentrated under reduced pressure to leave a residue. The residue was
chromatographied on silica gel with AcOEt-hexane (1:1) to give 6e (25 mg, 75%) as yellowish green
plates (mp 275-277 °C). 1H-NMR (400 MHz, CDCl3) : 7.13 (4H, t, J = 9.8 Hz, Az -5', 7', 5", 7"), 7.55
(2H, t, J = 9.8 Hz, Az -6', 6"), 7.79 (4H, s, Az -1', 3', 1", 3"), 7.7-7.8 (4H, m, H-6, 7, 10, 11), 8.27 (4H, d, J
= 9.8 Hz, Az -4', 8', 4", 8"), 8.65 (2H, d, J = 7.8 Hz, H-8, 9), 9.41 (2H, d, J = 8.3 Hz, H-5, 12). 13C-NMR
(100 MHz, CDCl3) : 119.1, 122.8, 123.5, 125.8, 127.6, 129.3, 130.1, 131.7, 137.7, 137.8, 138.9, 140.4,
148.4, 148.9. MS: m/z (rel. int. %) 482 (M+, 87), 481 (100), 240 (21), 177 (3), 127 (2). IR (KBr): 3131,
3095, 3045, 3012, 1571, 825 cm-1. UV-VIS (CH2Cl2) max (logε): 238 (4.69), 259 (4.71), 282 (4.90), 329
(4.71), 409 (4.57), 597 (2.90), 638 (2.87), 702 (2.53), Anal. Calcd for C36H22N2: C, 89.60; H, 4.60; N,
5.81. Found: C, 89.41; H, 4.60; N, 5.79.
2,2’,3,3’-Tetra(2-azulenyl)-6,6’-biquinoxaline (6f). A solution of 1 (80 mg, 0.26 mmol) and
3,3’-diaminobenzidine (5f) (30 mg, 0.14 mmol) in dry EtOH (30 mL) was refluxed for 45 h. The reaction
mixture was treated by a method similar to that used for 6e described above to give 6f (52 mg, 54%) as
yellowish green powder (mp > 300 °C). 1H-NMR (400 MHz, CDCl3) : 7.13 (8H, t, J = 9.8 Hz, Az-5", 7",
5''', 7''', 5'''', 7'''', 5''''', 7'''''), 7.56 (4H, t, J = 9.8 Hz, Az - 6", 6''', 6'''', 6'''''), 7.62 (8H, s, Az -1", 3", 1''', 3''',
1'''', 3'''', 1''''', 3'''''), 8.26 (8H, d, J = 9.8 Hz, Az -4", 8", 4''', 8''', 4'''', 8'''', 4''''', 8'''''), 8.35 (4H d, J = 8.5 Hz,
H-7, 8, 7', 8'), 8.65 (2H, s, H-5, 5'). IR (KBr): 3091, 3012, 2991, 2970, 2924, 2850, 1571, 839 cm-1.
UV-VIS (CH2Cl2) max (logε): 250 (4.80), 298 (5.11), 418 (4.85), 599 (3.24), 638 (3.21), 708 (2.85).
Anal. Calcd for C56H34N4: C, 88.16; H, 4.49; N, 7.34. Found: C, 88.42; H, 4.68; N, 7.06.
2,3-Di(2-azulenyl)-6-benzoylquinoxaline (6g).
A solution of 1 (50 mg, 0.16 mmol) and
3,4-diaminobenzophenone (5g) (39 mg, 0.18 mmol) in dry EtOH (20 mL) was refluxed for 51 h. The
reaction mixture was treated by a method similar to that used for 6e described above to give 6g (73 mg,
1
93%) as yellowish green crystals (mp 221-222 °C). H-NMR (400 MHz, CDCl3) : 7.11 (4H, t, J = 9.8
Hz, Az -5', 7', 5'', 7"), 7.5-7.7 (5H, m, Az - 6', 6", Ph -3, 4, 5), 7.56 (2H, s, Az - 1', 3'), 7.59 (2H, s, Az -1",
3"), 7.92 (2H, d, J = 7.8 Hz, Ph -2, 6), 8.22 (2H, d, J = 9.8 Hz, Az -4', 8'), 8.23 (2H, d, J = 9.8 Hz, Az -4",
8"), 8.2-8.3 (2H, m, H-7, 8), 8.55 (2H, d, J =1.5 Hz, H-5). 13C-NMR (100 MHz, CDCl3) : 118.7, 118.9,
119.1, 119.3, 123.6, 123.9, 128.3, 128.7, 129.5, 129.9, 130.0, 130.3, 132.4, 132.9, 139.3, 138.2, 138.5,
138.7, 140.2, 143.1, 147.2, 147.3, 152.2, 152.7, 195.9. MS: m/z (rel. int. %) 486 (M+, 94), 485 (100), 381
(12), 127 (5), 108 (28), 77 (40). IR (KBr): 3055, 1654, 1572, 1167, 829 cm-1. UV-VIS (CH2Cl2) max (log

HETEROCYCLES, Vol. 77, No. 2, 2009
1087
): 249 (4.62), 296 (4.96), 298sh (4.95), 602 (2.93), 638 (2.91), 705sh (2.57). Anal. Calcd for C35H22N2O: C,
86.40; H, 4.56; N, 5.76. Found: C, 86.64; H, 4.78; N, 5.83.
Diazuleno[2,1-a:1,2-c]phenazine (8) A solution of 6a (50 mg, 0.13 mmol) and activated manganese
dioxide (230 mg, 2.65 mmol) in benzene (15 mL) was refluxed for 27 h. The reaction mixture was
purified by column chromatography on silica gel with CH2Cl2 to afford the recovered 6a (27 mg, 54%)
1
and 8 (10 mg, 20%) as yellowish brown crystals (mp 270-271 °C). H-NMR (400 MHz, CDCl3) :
7.2-7.3 (4H, m, H-2, 4, 7, 9), 7.69 (2H, t, J =9.9 Hz, H-3, 8), 7.88 (2H, m, H-14, 15), 8.40 (2H, m, H-13,
16), 8.54 (2H, d, J =10.1 Hz, H-1, 10), 8.64 (2H, s, H-11, 18), 9.35 (2H, d, J =9.2 Hz, H-5, 6). 13C-NMR
(100 MHz, CDCl3) : 116.2, 123.0, 123.7, 124.1, 129.5, 129.9, 135.5, 136.7, 139.5, 139.6, 140.0, 142.3,
143.3. MS: m/z (rel. int. %) 380 (M+, 100), 328 (1), 276 (1), 190 (13), 126 (1). IR (KBr): 3047, 1568,
1136, 760 cm-1. UV-VIS (CH2Cl2) max (logε): 265 (4.59), 312 (4.79), 330sh (4.72), 368sh (4.56), 407
(4.49), 435sh (4.33), 462 (4.24), 636sh (2.79), 719 (3.03), 777 (3.03). Anal. Calcd for C28H16N2: C, 88.14; H,
4.24; N, 7.36. Found: C, 88.14, H, 4.11, N, 7.06.
X-ray structural analysis of 6a. Reflection data were collected on a Rigaku Mercury CCD
diffractometer with Mo-K radiation ( = 0.71070 Å) at 295 K. All the structures were solved by the
direct method and refined by full-matrix least-squares method on F2 with SHELX-97.5 All non-hydrogen
atoms were refined anisotropically, and all hydrogen atoms were placed in geometrically calculated
positions and refined by using a riding model. Crystal data are as follows: C28H18N2, M = 382.44,
monoclinic, space group P21/c, a = 6.1404(18), b = 24.158(7), c = 13.302(4) Å,  = 91.849(1)°, V =
1972.2(10) Å3, Z = 4, Dc = 1.288 g cm–1, F(000) = 800, (Mo-K) = 0.76 cm–1, crystal dimensions = 0.40
 0.075 0.05 mm, 15659 reflections collected, 4501 independent (Rint = 0.0492), R1 = 0.0748 and wR2 =
0.2504 for 3200 data with I > 2(I). CCDC 695852 contains the supplementary crystallographic data for
this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre
via www.ccdc.cam.ac.uk/data_request/cif.
ACKNOWLEDGEMENT
The authors thank the Institute for Molecular Science for the carrying out the X-ray analysis of 6a.
REFERENCES AND NOTES
1. K. -P. Zeller, Azulene. In Houben-Weyl: Method der Organischen Chemie, 4th ed.; Georg Thieme:
Stuttgart, Germany, 1985; Vol.Ⅴ, Part 2C, pp. 127-418.
2. M. Tisler and B. Stanovnik, Adv. Heterocycl. Chem., 1968, 9, 211; A. E. A. Porter, Comprehensive

1088
HETEROCYCLES, Vol. 77, No. 2, 2009
Heterocyclic Chemistry, 1984,Vol. 3, Pergamon, p. 157.
3. S. Ito, A. Nomura, N. Morita, C. Kabuto, H. Kobayashi, S. Maejima, K. Fujimori, and M. Yasunami,
J. Org. Chem., 2002, 67, 7295; S. Ito, H. Hamazaki, Y. Hirasawa, A. Ohta, K. Fujimori, N. Tanaka,
and M. Shiro, Heterocycles, 2004, 62, 463.
4. D. J. Bertelli and P. Crews, Tetrahedron, 1970, 26, 4717; Y. Lu, D. M. Lemal, and J. P. Jasinski,
J. Am. Chem. Soc., 2000, 122, 2440.
5. G. M. Sheldrick, SHELX-97. Program for the Structure Solution and Refinement of Crystal
Structures, University of Göttingen, Germany, 1997.