Preparation of 4-cyano-3-methyl-1-penyl-1H-pyrazole-5-(4-bromophenyl)-nitrile imine: Regio- and stereoselective synthesis of a new class of substituted 3-pyrazolyl-2-pyrazolines and pyrazoles

Article abstract of DOI:10.3987/COM-08-11531

A regio and stereoselective preparation of a new class of substituted 3-pyrazolyl-2-pyrazolines and pyrazoles in good to excellent yields has been developed by reacting 4-cyanopyrazole-5-nitrile imine with dipolarophiles.

Full text of DOI:10.3987/COM-08-11531

HETEROCYCLES, Vol. 78, No. 4, 2009
911
HETEROCYCLES, Vol. 78, No. 4, 2009, pp. 911 - 922. © The Japan Institute of Heterocyclic Chemistry
Received, 20th August, 2008, Accepted, 28th November, 2008, Published online, 4th December, 2008
DOI: 10.3987/COM-08-11531
PREPARATION OF 4-CYANO-3-METHYL-1-PHENYL-1H-PYRAZOLE-
5-(4-BROMOPHENYL)-NITRILE IMINE: REGIO- AND
STEREOSELECTIVE SYNTHESIS OF A NEW CLASS OF
SUBSTITUTED 3-PYRAZOLYL-2-PYRAZOLINES AND PYRAZOLES
Attreyee Mukherjee and Kumar K. Mahalanabis*
Department of Chemistry, Jadavpur University, Kolkata-700032, India
kumarmahalanabis@yahoo.in; kkmahalanabis@gmail.com
Abstract - A regio and stereoselective preparation of a new class of substituted 3-
pyrazolyl-2-pyrazolines and pyrazoles in good to excellent yields has been
developed by reacting 4-cyanopyrazole-5-nitrile imine with dipolarophiles.
INTRODUCTION
The present communication reports, for the first time, a regio and stereoselective synthesis of a new class
of substituted 3-pyrazolyl-2-pyrazolines and pyrazoles required for our contemplated biological and
photophysical study. Nitrile ylides have received extensive attention and synthetic use as reactive
intermediate for the construction of heterocyclic systems.1 Hydrazonoyl halides are stable precursor of
nitrile imines which undergo facile 1,3-dipolar cycloaddition with a variety of alkenes and alkynes to
produce pyrazolines and pyrazoles respecively2 often accompanied by regio and stereoisomers. In our
case, the major constraint for successful application of this widely used protocol is the lack of a straight-
forward and efficient method to obtain 5-formyl pyrazole particularly in the presence of electron-
withdrawing substitutents. This aldehyde is the key intermediate for the generation of the desired nitrile
imine to undergo planned 1,3-dipolar cycloaddition with alkenes leading to formation of the 2-pyrazoline
ring. Reported preparation of 3-carboethoxy-5-formyl pyrazole mixed with undesirable side products
involves either hydrogenolysis of pyrazole-5-acid chloride or ozonolysis of the 5-olefinic side chain.3
While seeking new methodologies for regiospecific synthesis of trisubstituted 1,2-azoles,4-6 we have
developed a high yielding synthesis of 5-dichloromethyl-3-methyl-1-phenyl-1H-pyrazole-4-carbonitrile 1.
5-Dichloromethyl substituent present in 1 as masked formyl group, on mild acid hydrolysis, neatly
afforded the desired 5-formyl pyrazole 2 in excellent yield. Easy availability of 2, thus, allowed us a
facile entry into in situ preparation of the key intermediate, 4-cyano-3-methyl-1-phenyl-1H-pyrazole-5-

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HETEROCYCLES, Vol. 78, No. 4, 2009
(4-bromophenyl) nitrile imine 5 from 4 in the presence of triethylamine. Nitrile imine 5 was then treated
with a series of dipolarophiles to give a new class of regio and stereocontrolled substituted 3-pyrazolyl-2-
pyrazolines 6a-h and 3-pyrazolylpyrazole 7 in good to excellent yields (Scheme 1, Table1).
Nitrogen containing heterocycles in general and pyrazole and pyrazolylpyrazoline derivatives specially
possess important biological and pharmaceutical activities7 and are also useful synthetic building blocks
in organic chemistry including pyrazole-based bioactive materials.8 2-Pyrazoline derivatives, in particular,
have been effectively utilized as antibacterial, antiviral, antiparasitic, antitubercular and insectidal
agents.9-12 Some of these compounds have also anti-inflammatory, anesthetic and analgesic properties,13
and are also known to exhibit pronounced fluorescence.14 In addition, the other most interesting property
of 2-pyrazoline moiety is its use as nanoparticles.15 Bipyrazoles are useful compounds and are used as
cytotoxic, insecticide, herbicide and fungicide agents along with applications in the photographic and
paint industry.16
Aryl/heteryl pyrazolines are mostly derived from condensation of substituted chalcones with
hydrazines.17 Heteryl pyrazolines and pyrazoles have also been synthesized by the reaction of thienyl and
pyridyl hydrazonoyl halides with alkenes and alkynes respectively.18,19 A multi-step synthesis of 5-
pyrazolyl-2-pyrazoline is reported.20 Preparation of 3-pyrazolylpyrazoles by microwave assisted 1,3-
dipolar cycloaddition has been described.21 However, preparation of 3-pyrazolyl-2-pyrazolines are yet to
be reported.
RESULTS AND DISCUSSION
Highly successful introduction of an aldehyde function in excellent yield and free from undesirable side
products at C-5 of pyrazole ring in the presence of an electron-withdrawing group (-CN) allowed us to
overcome the earlier difficulties encountered in formylation in good yield at C-5 of pyrazole particularly
with electron withdrawing substituent. Pyrazole-5-aldehyde 2 thus obtained was then smoothly converted
into hydrazone 3 by treatment with phenylhydrazine reagent.22 Hydrazonoyl halides are generally
26
prepared by direct halogenation23-25 of hydrazone or treating the hydrazone with NBS/CCl4 or
Ph3P/CX427 (X = Cl, Br) respectively. In the present case, the best result was obtained when hydrazone 3
was treated with NBS in refluxing CCl4 to afford 4. The absence of -CH=N- proton signal in the 1H-NMR
spectrum of 4 is indicative of desired C-halogenation (-CBr=N-). Appearance of double doublets at δ 6.46
(J = 8.3 Hz) and δ 6.68 ppm (J = 8.8 Hz) respectively clearly demonstrates that spontaneous bromination
also occurred in the para position of the N-phenyl ring during NBS treatment of 3.
Terminal alkenes i.e. acrylonitrile, ethyl acrylate and styrene when reacted with nitrile imine 5, in
refluxing chloroform afforded 3-substituted-2-pyrazolines 6a-c with complete control of regioselectivity
in each case (Table 1). Selective incorporation of substituent at C-5 of pyrazoline ring is found to be in

HETEROCYCLES, Vol. 78, No. 4, 2009
913
compliance with the known observation that 1,3-cycloaddition of nitrile imines with terminal olefins
generally produce 5-isomer regioselectively.
CN
CHCl2
Me
Me
Me
CN
CHO
CN
20% H2SO4
reflux, 16 h
PhNHNH2
Ph
N
N
N
N
N
N
N
N
Ph
H
Ph
Ph
1
3
2
CN
Me
CN
Me
C6H4Br (p)
C6H4Br (p)
NBS/CCl4
N
Et3N
N
N
H
3
N
N
reflux, 1.5 h
N
N
Br
N
Ph
4
Ph
5
Me
CN
3
R1
4
Me
CN
3
R1
4
dipolarophile
Et3N
5
N
5
5
N
R2
R2
N
Ph
N
Ph
N
2
1
N
N
1
N
2
C6H4Br (p)
C6H4Br (p)
6a-h
7
Scheme 1
The effects of substituents on the shapes of the FOs have been elegantly derived28 and union of the
unsubstituted end of the dipolarophile with the carbon end of the dipole where larger HOMO and LUMO
coefficients respectively are located, always favours the formation of 5-substituted heterocycles.
1
The chemical shift values of methine and methylene protons of 6a-c in H-NMR are well supported by
the literature analogy.29 For structural analyses of all new compounds please see Experimental section.
Huisgen30 has demonstrated the reactivity of cyclic dipolarophiles with accurate comparisons of kinetic
and thermodynamic data. The olefinic C-H bonds of norbornene are bent in the endo direction by 3.4°,
and only a small expenditure of energy is necessary to effect the 10° cis bending to react in cycloaddition
TS geometry. Similar deformations are also found in cyclopentene. On the other hand, the C=C bond of
cyclohexene is bent in a trans fashion and considerable energy and even conformational changes are
required to cause a cis bending - a fact borne out by the lower yield of the adduct 6e.
The reaction of pyrazole-5-nitrile imine 5 with cyclic alkenes, namely norbornene, cyclopentene,
cyclohexene and N-phenylmaleimide were found to be totally stereoselective and gave exclusive cis-

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HETEROCYCLES, Vol. 78, No. 4, 2009
Table 1. Reaction of 5 with dipolarophiles
Entry no. Dipolarophile Structure
Yield (%)
70
Me
CN
1
CH2=CH-CN
6a
6b
H
H
CN
N
N
H
N
N
Ph
C6H4Br ( p)
Me
CN
H
H
N
2
CH2=CH-CO2Et
75
CO2Et
H
N
N
N
Ph
C6H4Br ( p)
Me
CN
H
H
3
4
5
CH2=CH-Ph
cyclopentene
cyclohexene
6c
6d
6e
72
75
54
Ph
H
N
N
N
N
Ph
C6H4Br ( p)
CN
Me
H
N
N
H
N
N
Ph
C6H4Br ( p)
CN
Me
H
N
N
N
H
N
Ph
C6H4Br ( p)
6
norbornene
6f
73
H
H
CN
Me
H
N
N
H
N
N
Ph
C6H4Br ( p)
O
7
8
N-phenylmaleimide
6g
6h
61
70
Ph
N
Me
CN
H
N
N
O
H
N
N
Ph
C6H4Br ( p)
Me
CN
Ph
PhCH=CHPh (trans)
H
H
N
N
Ph
N
N
Ph
C6H4Br ( p)
CN
Me
CO2Me
CO2Me
9
DMAD
7
55
N
N
N
N
Ph
C6H4Br ( p)

HETEROCYCLES, Vol. 78, No. 4, 2009
915
fused 2-pyrazoline products. Thus, in the 1H-NMR spectrum of 6f, protons (3a, 7a) appeared as doublet at
δ 3.57 (J = 9.7 Hz) and δ 4.10 ppm (J = 9.7 Hz) respectively, and no splitting was observed between 3a
and 4 and 7a and 7 protons indicating that the adduct is being produced by the attack of the dipolarophile
from the exo side.28 Similarly, cis fused adducts were also obtained with cyclopentene, cyclohexene and
N-phenylmaleimide.
Reaction of pyrazole-5-nitrile imine 5 with trans-stilbene is expected to give the cycloadduct 6h with
retention of configuration. This was indeed the case31 as evidenced from the coupling constant (J = 4.6
Hz) between C-4 and C-5 protons of 6h.
Pyrazole-5-nitrile imine 5 when reacted with dimethyl acetylenedicarboxylate neatly produced 3-
pyrazolyl pyrazole 7 in high yield.
Our interest on the photophysical study of these newly synthesized 2-pyrazoline derivatives in
homogeneous solvents with Bhattacharya et al.32 stems mainly for two reasons : to explore (i) potential
biological applications of this class of compounds in pharmaceuticals, and (ii) their use as optical
brightening agents for textile fibres, plastics and papers.33 2-Pyrazoline based nanoparticles have found
applications in optical field.34 Results of preliminary photophysical study with 6b and 6f have already
been communicated.32,35 These compounds show a strong tendency towards a hydrogen bonding
interaction with protic solvents, are highly fluorescent with high fluorescence quantum yield and exhibit
considerable solvatochromism. Presently we are exploring the photophysical behavior of these
compounds in microheterogeneous medium.
In conclusion, we have developed an efficient new route for the synthesis of a new class of
polysubstituted 3-pyrazolyl-2-pyrazolines with excellent control of regio and stereochemistry by
employing, for the first time, cyanopyrazole-5-nitrile imine in 1,3-dipolar cycloaddition with different
dipolarophiles. These compounds, in turn, on oxidative aromatization, could be easily converted to the
corresponding pyrazoles which are known to exhibit a wide range of biological activities.36, 37 Synthesis
of this new class of pyrazole-substituted-2-pyrazolines with inbuilt bromo substituent allow them to be
used as potential bromo organics in pharmaceuticals, intermediate for agrochemicals and industrially
valuable new materials38 and provides scope for elaboration to other functionality.39-42 Further, 2-
Pyrazoline derivatives are also considered to be important organic heterocyclic ‘transition’ materials
and find use in organic molecular crystals.43 Preliminary photophysical study32,35 with some of these
newly synthesized 2-pyrazoline derivatives clearly demonstrates their potential application as fluorescent
probes in some chemosensors44 and as nanoparticles in optoelectronic device.45-48

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HETEROCYCLES, Vol. 78, No. 4, 2009
EXPERIMENTAL
Melting points (°C) were determined in open capillaries and are uncorrected . All compounds were
°
crystallised from ethyl acetate- pet ether(60-80 C). IR spectra (KBr, υmax; cm-1) were taken on Hitachi
270-30 spectrometer; UV spectra (EtOH ; λmax (ε), nm) were taken on a Hitachi U-2000 spectrometer.
IH NMR and 13C NMR spectra (δ ppm ; J in Hz) in CDCl3 (otherwise stated) were recorded on Bruker
AV-300 and Spect-400 spectrometers with TMS as internal standard. Mass spectra [m/z(%)] were
recorded by a Thermo Finnigan LCQ DUO . Elemental analyses were performed on a Perkin-Elmer
240C elemental analyser. All yields (%) refer to isolated , spectroscopically pure material.
5-Formyl-3-methyl-1-phenyl-1H-pyrazole-4-carbonitrile (2)
5-(Dichloromethyl)-3-methyl-1-phenyl-1H-pyrazole-4-carbonitrile4 (1) (2.65 g, 10 mmol) in H2SO4 (20%,
30 mL) was taken in a round-bottomed flask (250 mL) and the mixture was refluxed for 16 h (monitored
by TLC, EtOAc-pet. ether(1:3). Usual work up afforded white needle-shaped crystalline material.
°
Mp 134 – 135 C. Yield (%): 75. IR (KBr): 2230, 1690, 1592, 1535 cm-1. UV (EtOH): λmax (ε) = 254
(9,769). 1H NMR (400 MHz, CDCl3): δ = 2.48 (s, 3H, Me), 7.53 (m, 5H, Ar-H), 9.90 (s, 1H, CHO). 13C
NMR (100 MHz, CDCl3): δ = 12.60, 96.79, 111.78, 125.35, 129.50, 129.99, 137.09, 141.44, 153.53,
177.29. MS m/z (%): 211 (100) [M+]. Anal. Calcd for C12H9N3O (%): C, 68.24; H, 4.29; N, 19.89. Found
(%): C, 68.46; H, 4.32; N, 19.92.
(E)-1-((4-Cyano-3-methyl-1-phenyl-1H-pyrazol-5-yl)methylene)-2-phenylhydrazine (3)
A mixture of 2 (0.633 g, 3 mmol) and phenylhydrazine reagent22 (13 mL, 9 mmol) was heated on a steam
bath for a period of 30 min. The reaction mixture was cooled and extracted with EtOAC (3x20 mL).
Usual work up afforded a yellow solid which was purified by column filtration (silica gel 60-120 mesh;
EtOAc-pet.ether (1:1) when yellow shiny crystals were isolated.
Mp 148 – 149 °C. Yield (%): 75. IR (KBr): 3264, 2212, 1571, 1551, 1526, 1388, 1338 cm-1. UV (EtOH):
1
λmax (ε) = 372 (14,639), 242 (15,843). H NMR (300 MHz, DMSO-d6): δ = 2.37 (s, 3H, Me), 6.85-7.58
(m, 10H, Ar-H), 7.72 (s, 1H, =CH) 11.02 (br, 1H, NH). 13C NMR (75 MHz, DMSO-d6): δ = 12.18, 87.89,
112.55, 114.90, 120.42, 122.27, 125.75, 129.15, 129.27, 129.59, 137.87, 144.01, 144.34, 152.30. MS m/z
(%): 300 (100) [M+]. Anal. Calcd for C18H15N5 (%): C, 71.74; H, 5.02; N, 23.24. Found (%): C, 71.46; H,
4.99; N, 23.28.
(Z)-1-(Bromo(4-cyano-3-methyl-1-phenyl-1H-pyrazol-5-yl)methylene)-2-(4-bromophenyl)hydrazine
(4)
A mixture of 3 (0.3 g, 1 mmol) and NBS (0.352 g, 2 mmol) was taken in dry carbon tetrachloride (30 mL)
and refluxed for 1.5 h. The reaction mixture was filtered hot and the organic layer was washed with water,
dried over anhydrous Na2SO4, and concentrated. The crude solid on recrystallization from a mixture (1:1)

HETEROCYCLES, Vol. 78, No. 4, 2009
917
of EtOAc and pet. ether afforded a grey solid.
Mp 160 -161 °C. Yield (%): 75. IR (KBr): 3072, 2212, 1568, 1533, 1475 cm-1. UV (EtOH): λmax (ε) = 341
(9,450), 245 (13,760). 1H NMR (300 MHz, CDCl3): δ = 2.48 (s, 3H, Me), 6.46 (d, J = 8.3, 2H), 6.68 (d, J
= 8.8, 2H), 7.13-7.47 (m, 5H, Ar-H), 8.15 (s, 1H, NH). MS m/z (%): 459 (94) [M+], 461 (60) [MH+ +1],
462 (50) [MH+ + 2]. Anal. Calcd for C18H13N5Br2 (%): C, 47.09; H, 2.85; N, 15.25. Found (%): C, 47.37;
H, 2.89; N, 15.28.
GENERAL PREPARATIVE METHOD OF 2-PYRAZOLINES 6a-h AND PYRAZOLE 7.
A mixture of 4 (0.459 g, 1 mmol), dipolarophile (1 mmol) and triethylamine (1 mmol) in dry CHCl3 (10
mL) was refluxed for 12-16 h (monitored by TLC). The reaction mixture was then washed with water
and the organic layer was dried over anhydrous Na2SO4. The crude solid, obtained on concentration of the
organic layer, was purified by column filtration (silica gel 60-120 mesh ; EtOAc-pet.ether(1:3).
5-(1-(4-Bromophenyl)-5-cyano-4,5-dihydro-1H-pyrazol-3-yl)-3-methyl-1-phenyl-1H-pyrazole-4-
carbonitrile (6a)
Yellowish-green sugar-cube crystals. Mp 199-200 °C. IR (KBr): 2224, 1575, 1355, 1124, 766, 692 cm-1.
UV (EtOH): λmax (ε) = 389 (35902), 360 (21119), 248 (24437). 1H NMR (400 MHz, CDCl3): δ = 2.50 (s,
3H, Me), 3.49-3.62 (m, 2H, H4), 4.95 (dd, J = 5.8 & 11.3, 1H, H5), 6.76 (d, J = 8.7, 2H, Ar-H), 7.39 (d, J
= 8.6, 2H, Ar-H), 7.42-7.56 (m, 5H, Ar-H). 13C NMR (100 MHz, CDCl3): δ = 12.50, 39.28, 49.73, 93.59,
113.69, 115.33, 115.59, 116.07, 126.58, 129.49, 129.90, 132.38, 136.16, 138.98, 139.34, 140.99, 153.13.
MS m/z (%): 431 (30) [MH+], 432 (26) [MH++1], 433 (30) [MH++2], 406 (100) [MH++2-HCN], 404 (92)
(MH+-HCN). Anal. Calcd for C21H15N6Br (%): C, 58.48; H, 3.51; N, 19.49. Found (%): C, 58.22; H, 3.53;
N, 19.52;
Ethyl 1-(4-bromophenyl)-3-(4-cyano-3-methyl-1-phenyl-1H-pyrazol-5-yl)-4,5-dihydro-1H-pyrazole-
5-carboxylate (6b)
Yellow needles. Mp 137-138 °C. IR (KBr) : 2220, 1740, 1590, 1479, 1366, 1199 cm-1. UV (EtOH): λmax
1
(ε) = 377 (17903), 250 (19467). H NMR (400 MHz, CDCl3): δ = 1.22 (t, J = 7.0, 3H, CH2Me), 2.47 (s,
3H, Me), 3.35 (dd, J = 6.2 & 17.6, 1H, H4), 3.56 (dd, J = 12.9 & 17.6, 1H, H4), 4.21 (q, J = 7.0, 2H,
CH2Me), 4.77 (dd, J = 5.8 & 12.9, 1H, H5), 6.62 (d, J = 9.3, 2H, Ar-H), 7.30(d, J = 9.0, 2H, Ar-H), 7.45-
7.46 (m, 2H, Ar-H), 7.53-7.54 (m, 3H, Ar-H). 13C NMR (100 MHz, CDCl3): δ = 12.49, 14.03, 38.67,
61.38, 62.20, 92.84, 113.39, 114.12, 114.95, 126.64, 129.14, 129.47, 131.96, 134.64, 139.73, 140.00,
141.98, 152.88, 169.72. MS m/z (%): 477 (30) [M+], 478 (100) [MH+], 480 (96) [M++3]. Anal. Calcd for
C23H20N5O2Br (%): C, 57.75; H, 4.21; N, 14.64. Found (%): C, 57.52; H, 4.19; N, 14.85.
5-(1-(4-Bromophenyl)-4,5-dihydro-5-phenyl-1H-pyrazol-3-yl)-3-methyl-1-phenyl-1H-pyrazole-4-

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HETEROCYCLES, Vol. 78, No. 4, 2009
carbonitrile (6c)
°
Yellowish green crystals. Mp 148-149 C. IR (KBr) : 2214, 1589, 1483, 1347, 1130 cm-1. UV (EtOH):
λ
max (ε) = 373 (5752), 245 (5315). 1H NMR (400 MHz, CDCl3): δ = 2.46 (s, 3H, Me), 3.00 (dd, J = 6.8 &
17.4, 1H, H4), 3.70 (dd, J = 12.5 & 17.5, 1H, H4), 5.23 (dd, J = 6.7 & 12.4, 1H, H5), 6.51-7.49 (m, 14H,
Ar-H). 13C NMR (100 MHz, CDCl3): δ = 12.04, 43.25, 62.98, 91.34, 111.36, 113.34, 114.19, 115.22,
125.75, 126.71, 127.81, 128.85, 129.05, 129.60, 131.55, 135.55, 138.96, 140.69, 141.05, 141.91, 151.95.
MS m/z (%): 481.9 (100) [M+], 483.9 (88) [MH+], 484.9 (25) [MH++1], 505.9 (20) [MH++Na+]. Anal.
Calcd for C26H20N5Br (%): C, 64.74; H, 4.18; N, 14.52. Found (%): C, 65.01; H, 4.20; N, 14.48.
5-((3aS,6aR)-1-(4-Bromophenyl)-1,3a,4,5,6,6a-hexahydrocyclopenta[c]pyrazol-3-yl)-3-methyl-1-
phenyl-1H-pyrazole-4-carbonitrile (6d)
°
Yellowish brown shiny crystals. Mp 197-198 C. IR (KBr): 2224, 1579, 1481, 1361, 1194, 1134, 914
1
cm-1. UV (EtOH): λmax (ε) = 253 (15833). H NMR (400 MHz, CDCl3): δ = 1.37-2.08 (m, 6H, H-4,5,6),
2.50 (s, 3H, Me), 4.1 (m, 1H, H3a), 4.66 (m, 1H, H6a), 6.62 (d, J = 8.0, 2H, Ar-H), 7.29 (d, J = 8.0, 2H,
13
Ar-H), 7.40-7.53 (m, 5H, Ar-H). C NMR (100 MHz, CDCl3): δ = 12.53, 24.44, 33.01, 33.61, 50.91,
65.68, 92.13, 112.30, 114.38, 114.79, 126.57, 129.08, 129.16, 131.83, 138.50, 140.21, 140.64, 141.42,
152.83. MS m/z (%): 445 (30) [M+], 446 (100) [MH+], 448 (98) [MH++2], 449 (26) [MH++3]. Anal.
Calcd for C23H20N5Br (%): C, 61.89; H, 4.52; N, 15.69. Found (%): C, 62.07; H, 4.54; N, 15.78.
5-((3aS,7aR)-1-(4-Bromophenyl)-3a,4,5,6,7,7a-hexahydro-1H-indazol-3-yl)-3-methyl-1-phenyl-1H-
pyrazole-4-carbonitrile (6e)
°
Light green crystals. Mp 200-201 C. IR (KBr): 2222, 1602, 1471, 1445, 1316, 1102 cm-1. UV (EtOH):
λ
max (ε) = 385 (30973), 340 (10081). 1H NMR (400 MHz, CDCl3): δ =1.18-2.04 (m, 8H, H-4,5,6,7), 2.55
(s, 3H, Me), 3.47 (m, 1H, H3a), 4.27 (m, 1H, H7a), 6.79-7.58 (m, 9H, Ar-H). MS m/z (%): 459.9 (92)
[MH+], 461.9 (100) [MH++1], 462.9 (24) [MH++2], 483.9 (17) [M+Na].+ Anal. Calcd for C24H22N5Br
(%): C, 62.61; H, 4.82; N, 15.21. Found (%): C, 62.38; H, 4.79; N, 15.19.
5-((3aS,7aR)-1-(4-Bromophenyl)-3a,4,5,6,7,7a-hexahydro-1H-4,7-methano-indazol-3-yl)-3-methyl-
1-phenyl-1H-pyrazole-4-carbonitrile (6f)
°
Yellowish brown shiny crystals. Mp 202-203 C. IR (KBr): 2224, 1575, 1484, 1367, 1295, 1152 cm-1.
UV (EtOH): λmax (ε) = 341 (12272), 255 (17888). 1H NMR (400 MHz, CDCl3): δ = 1.22-1.62 (m, 6H, H-
5,6,8), 2.49 (s, 3H, Me), 2.50 & 2.72 (each s, 2H, H4,7), 3.57 (d, J = 9.7, 1H, H3a), 4.09 (d, J = 9.7, 1H,
H7a), 6.59 (d, J = 9.0, 2H, Ar-H), 7.28 (d, J = 9.0, 2H, Ar-H), 7.42-7.53 (m, 5H, Ar-H). 13C NMR (100
MHz, CDCl3): δ = 12.52, 24.18, 27.09, 32.92, 40.71, 40.97, 55.11, 67.76, 112.18, 114.44, 114.51, 126.70,
129.07, 129.20, 131.84, 137.57, 140.28, 141.54, 152.81. MS m/z (%): 471 (38) [M+], 472 (100) [MH+],
474 (92) [MH++3]. Anal. Calcd for C25H22N5Br (%): C, 63.56; H, 4.69; N, 14.83. Found (%): C, 63.29; H,

HETEROCYCLES, Vol. 78, No. 4, 2009
919
4.72; N, 14.78.
5-((3aS,6aS)-1-(4-Bromophenyl)-1,3a,4,5,6,6a-hexahydro-4,6-dioxo-5-phenylpyrrolo[3,4-c]pyrazol-
3-yl)- 3-methyl-1-phenyl-1H-pyrazole-4-carbonitrile (6g)
°
Yellowish green crystals. Mp 152-153 C. IR (KBr) : 2224, 1721, 1586, 1487, 1368, 1187 cm-1. UV
(EtOH): λmax (ε) = 373 (398441), 286 (29547). 1H NMR (300 MHz, CDCl3): δ = 2.50 (s, 3H, Me), 4.81
(d, J = 11.2, 1H, H3a), 5.23 (d, J = 11.2, 1H, H6a), 7.21-7.51 (m, 14H, Ar-H). 13C NMR (75 MHz,
CDCl3): δ = 12.54, 29.67, 52.93, 64.20, 115.23, 116.26, 126.09, 126.60, 129.26, 129.32, 129.75, 130.69,
131.07, 132.10, 138.28, 139.28, 141.51, 153.14, 169.46, 170.21. MS m/z (%): 551 (40) [M+], 552 (60)
[MH+], 553 (40) [MH++1]. Anal.Calcd for C28H19N6O2Br (%): C, 60.99; H, 3.47; N, 15.24.. Found (%): C,
60.74; H, 3.51; N, 15.32.
5-((4S,5R)-1-(4-Bromophenyl)-4,5-dihydro-4,5-diphenyl-1H-pyrazol-3-yl)-3-methyl-1-phenyl-1H-
pyrazole-4-carbonitrile (6h)
°
Yellowish green crystals. Mp 170-171 C. IR (KBr): 2208, 1589, 1548, 1485, 1360, 1303, 1199, 1135
1
cm-1. UV (EtOH): λmax (ε) = 370 (26832), 253 (31639). H NMR (300 MHz, CDCl3): δ = 2.37 (s, 3H,
Me), 4.18 (d, J = 4.6, 1H, H4), 5.03 (d, J = 4.6, 1H, H5), 6.66-7.42 (m, 19H, Ar-H). 13C NMR (75 MHz,
CDCl3): δ = 12.46, 62.32, 73.97, 113.09, 114.07, 115.38, 125.19, 126.10, 127.18, 128.19, 128.35, 129.08,
129.20, 129.38, 129.49, 131.62, 131.87, 137.27, 138.46, 139.37, 139.72, 140.43, 141.76, 152.90. MS m/z
(%) : 557 (94) [M-H]-, 559 (100) [M+], 560 (22) [MH+]. Anal. Calcd for C32H24N5Br (%): C, 68.82; H,
4.33; N, 12.54. Found (%): C, 68.67; H, 4.23; N, 12.32.
Dimethyl 1-(4-b
dicarboxylate (7)
romophenyl)-3-(4-cyano-3-methyl-1-phenyl-1H-pyrazol-5-yl)-1H-pyrazole-4,5-
°
White amorphous solid. Mp 106-107 C. IR (KBr): 2224, 1727, 1445, 1380, 1234, 1149 cm-1. UV
1
(EtOH): λmax (ε) = 340 (9568), 256 (33384). H NMR (400 MHz, CDCl3): δ = 2.53 (s, 3H, Me), 3.63 (s,
13
3H, CO2Me), 3.80 (s, 3H, CO2Me), 7.30-7.62 (m, 9H, Ar-H). C NMR (100 MHz, CDCl3): δ = 12.64,
52.22, 53.70, 96.53, 113.36, 115.40, 123.70, 124.30, 125.49, 128.53, 129.09, 132.64, 137.29, 138.00,
138.35, 138.87, 140.30, 152.65, 160.06, 160.56. MS m/z (%): 519 (18) [M+], 520 (100) [MH+], 522 (92)
[MH++1], 523 (26) [MH++2]. Anal. Calcd for C24H18N5O4Br (%): C, 55.40; H, 3.48; N, 13.46. Found
(%): C, 55.24; H, 3.41; N, 13.35.
ACKNOWLEDGEMENTS
Partial financial assistance from Jadavpur University is gratefully acknowledged. Professor R.G.
Bhattacharyya, Jadavpur University is thanked for generous gift of some of the alkenes used in this study.
Authors are extremely grateful to Dr. W. Frostl, Novartis Pharma, Basel, Switzerland for helping us with

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HETEROCYCLES, Vol. 78, No. 4, 2009
high resolution NMR spectra and MS analysis of some of these compounds.
REFERENCES
1. J. T. Sharp, The Chemistry of Heterocyclic Compounds; vol 59, ed. by A. Padwa and W. H Pearson,
John Wiley & Sons, 2002, p. 473.
2. H. M. Hassaneen, H. A. H. Mousa, S. T. Ezmirly, and A. S. Shawali, Can. J. Chem., 1988, 66, 1386.
3. R. H. Wiley, L. C. Beur, R. Fusco, and C. H. Jaboe, Heterocyclic Compounds, 1967, p. 122.
4. S. K. Dutta Chowdhury, M. Sarkar, and K. K. Mahalanabis, J. Chem. Res., 2003, 746.
5. M. Mishra, S. K. Dutta Chowdhury, and K. K. Mahalanabis, Synth. Commum., 2004, 36, 2681.
6. K. K. Mahalanabis, S. K. Dutta Chowdhury, M. Sarkar, and M. Mishra, J. Chem. Res., 2006, 78.
7. J. Elguero, Comprehensive Heterocyclic Chemistry II: Vol 3, ed. by A. R. Katritzky and C W. Rees, E.
F. V. Scriven, Pergamon Press, Oxford, 1996, p. 1; P. Singh, K. Paul, and W. Holzer, Bioorg. Med.
Chem., 2006, 14, 5061.
8. D. Azarifar and H. Ghasemnejad, Molecules, 2003, 8, 642; C. Lamberth, Heterocycles, 2007, 21,
1467.
9. A. Singh, S. Rathod, B. N. Berad, S. D. Patil, and A. G. Dosh, Orient. J. Chem., 2000, 16, 315.
10. B. S. Holla, P. M. Akberali, and M. K. Shivananda, Farmaco, 2000, 55, 256.
11. E. Palaska, M. Aytemir, I. Tayfun, K. Erol, and E. Dilek, Eur. J. Med. Chem. Chim. Ther., 2001, 36,
539.
12. J. R. Goodell, F. Puig-Basagoiti, B. M. Forshey, P. –Y. Shi, and D. M. Ferguson, J. Med. Chem., 2006,
49, 2127; R. M. Kedar, N. N. Vidhale, and M. M. Chincholkar, Orient. J. Chem., 1997, 13, 143.
13. S. G. Kucukguzel and S. Rollas, Farmaco, 2002, 57, 583; T.-S. Jeong, K. S. Kim, S.-J. An, K.-H.
Cho, S. Lee, and W. S. Lee, Bioorg. Med. Chem. Lett., 2004, 14, 2715.
14. M. Wang, J. Zhang, J. Liu, C. Xu, and H. Ju, J. Luminescence, 2002, 99, 79; M. Jin, R. Lu, C. Y. Bao,
T. H. Xu, and Y. Y. Zhao, Optical Materials, 2004, 26, 85.
15. S. W. Oh, D. R. Zhang, and Y. S. Kang, Material Science Engineering: C, 2004, 24, 131.
16. A. Arrieta, J. R. Carrillo, F. P. Cossio, A. Diaz-Ortiz, M. J. Gomez-Escalonilla, A. de la Hoz, F.
Langa, and A. Moreno, Tetrahedron, 1998, 54, 13167.
17. D. Azarifar and M. Shaebanzadeh, Molecules, 2002, 7, 885; M. K. Bratenko, V. A Chornous, and M.
V. Vovk, Russ. J. Org. Chem., 2001, 37, 556.
18. H. M. Hassaneen, H. A. H. Mousa, N. M. Abed, and A. S. Shawali, Heterocycles, 1988, 27, 695.
19. S. Tanaka and A. Tarada, Heterocycles, 1981, 16, 717.
20. H. M. Hassaneen, A. S. Shawali, and N. M. Elwan, Heterocycles, 1990, 31, 1041.
21. A. Diaz-Ortiz, A. de la Hoz, and F. Langa, Green Chem., 2000, 2, 165.

HETEROCYCLES, Vol. 78, No. 4, 2009
921
22. A. I. Vogel, A Text Book of Practical Organic Chemistry, 3rd Edn, ELBS and Longmann, 1973, p. 121.
23. F. L. Scott, D. A. Cronin, and J. K. O’Halloran, J. Chem. Soc. (C), 1971, 2769.
24. J. C. Tobin, A. F. Hegarty, and F. L. Scott, J. Chem. Soc (B), 1971, 2198.
25. R. N. Butler and F. L. Scott, J. Chem. Soc. (C), 1968, 1711.
26. K. C. Joshi, R. Jain, and K. Sharma, Ind. J. Chem. Sec. B, 1990, 29, 895.
27. P. Wolkoff, Can. J. Chem., 1975, 53, 1333.
28. K. N. Houk and K. Yamaguchi, 1,3-Dipolar Cycladdition Chemistry, vol 2, ed. by A. Padwa, Wiley,
New York, 1984, p. 407.
29. W. Fliege, R. Huisgen, J. S. Clovis, and H. Knupfer, Chem. Ber., 1983, 116, 3039.
30. R. Huisgen, M. Seidel, G. Wallbillich, and H. Knupfer, Tetrahedron, 1962, 17, 36; R. Huisgen, P. H.
J. Ooms, M. Mingin, and N. L. Allinger, J. Am. Chem. Soc., 1980, 102, 3951.
31. R. Huisgen, H. Knupfer, R. Sustmann, G. Wallbillich, and V. Weberndörfer, Chem. Ber., 1967, 100,
1580.
32. S. Chatterjee, P. Banerjee, S. Pramanik, A. Mukhrjee, K. K. Mahalanabis, and S. C. Bhattacharyya,
Chem. Phys. Lett., 2007, 440, 313.
33. D. Xiao, L. Xi, W. Yang, H. Fu, Z. Shuai, Y. Fang, and J. Yao, J. Am. Chem. Soc., 2003, 125, 6740; J.
Barbera, K. K. Clays, R. Gimenez, S. Houbrechts, A. Persoons, and J. L. Serrano, J. Mater. Chem.,
1998, 8, 1725.
34. J. S. Yin, and Z. L. Wang, Phys. Rev. Lett., 1997, 79, 2570; H.-B. Fu, R.-M. Xie, Y.-Q. Wang, J.-N.
Yao, and Col. A. Surf, Phys. Eng. Asp., 2000, 174, 367.
35. S. Pramanik, P. Banerjee, A. Sarkar, A. Mukherjee, K. K. Mahalanabis, and S. C. Bhattacharyya,
Spectrochimica Acta
Part A: Molecular and Biomolecular Spectroscopy, 2008, doi:
10.1016/j.saa.2008.04.01.
36. M. J. Alberti, E. P. Auten, K. E. Lackey, O. B. McDonald, E. R. Wood, F. Preugschat, G. J. Cutler,
L. Kane-Carson, W. Liu, and D. K. Jung, Bioorg. Med. Chem. Lett., 2005, 15, 3778.
37. F. Shirai, H. Azami, N. Kayakiri, K.Okumura, and K. Nakamura, PCT Int. Appl. 2004, p. 436 WO
2004050632 (Chem. Abstr., 2004, 141, 54327).
38. A. Butler and J. V. Walker, Chem. Rev., 1993, 93, 1937.
39. D. Zhao, Z. Fei, T. J. Geldbach, R. Scopelliti, and P. J. Dyson, J. Am. Chem. Soc., 2004, 126, 15876.
40. Q. Yao, E. P. Kinney, and C. Zheng, Org. Lett., 2004, 6, 2997.
41. R. B. DeVashre, L. R. Moore, and K. H. J. Shaughnessy, J. Org. Chem., 2004, 69, 7919.
42. J. F. Hartwig, Angew. Chem. Int. Ed., 1998, 37, 2046.
43. E.A. Silinsh, Organic Molecular Crystals: Their Electronic States, Springer-Verlag, Berlin, 1980.
44. A. P. De Silva, H. Q. N. Gunaratne, T. Gunnlaugsson, A. J. M. Huxley, J. T. Rademacher, and T. E.

922
HETEROCYCLES, Vol. 78, No. 4, 2009
Rice, Chem. Rev., 1997, 97, 1515.
45. D. Xiao, L. Xi, W. Yang, H. Fu, Z. Shuai, Y. Fang, and J. Yao, J. Am. Chem. Soc., 2003, 125, 6740.
46. H. B. Fu and J. N. Yao, J. Am. Chem. Soc., 2001, 123, 1434.
47. S. W. Oh and Y. S. Kang, Colloids and Surfaces A: Physicochem. Eng. Aspects, 2005, 415, 257.
48. H. B. Fu, B. H. Loo, D. B. Xiao, R. M. Xie, X. H. Ji, J. N. Yao, B. W. Zhag, and L. Q. Zhang, Angew.
Chem. Int. Ed., 2002, 41, 962.