Facile synthesis of 2-phenylquinoline-4-carboxamide derivatives with variant structural features

Article abstract of DOI:10.3987/COM-14-12939

The quinoline scaffold is an important class of heterocyclic compounds that possesses diverse chemotherapeutic activities. Thus, the 2-phenylquinoline-4- carboxamide derivatives containing a variety of moieties, such as 2-(2-furanyl)-1,3,4-oxadiazole, N-(2-methylphenyl)-4-(3-pyridinyl)-2- pyrimidinamine, 4,4′-bithiazole, purine, adamantine and resorcinol, have been designed and synthesized via Suzuki coupling, acid-base coupling and other typical reactions.

Full text of DOI:10.3987/COM-14-12939

HETEROCYCLES, Vol. 89, No. 3, 2014
693
HETEROCYCLES, Vol. 89, No. 3, 2014, pp. 693 - 708. © 2014 The Japan Institute of Heterocyclic Chemistry
Received, 11th January, 2014, Accepted, 29th January, 2014, Published online, 6th February, 2014
DOI: 10.3987/COM-14-12939
FACILE SYNTHESIS OF 2-PHENYLQUINOLINE-4-CARBOXAMIDE
DERIVATIVES WITH VARIANT STRUCTURAL FEATURES
Rafiqul Islam,a Md. Imran Hossain,a Yoshinari Okamoto,b Tomohisa
Nagamatsu,a Kensaku Anraku,a and Tadashi Okawaraa,*
a Department of Medical Technology, Kumamoto Health Science University, 325
Izumi-machi, Kumamoto 861-5598, Japan; b Department of Bioorganic Medicinal
Chemistry, Faculty of Life Sciences, Kumamoto University, Kumamoto 862-0973,
Japan; E-mail: okawara@kumamoto-hsu.ac.jp
Abstract – The quinoline scaffold is an important class of heterocyclic
compounds that possesses diverse chemotherapeutic activities. Thus, the
2-phenylquinoline-4-carboxamide derivatives containing a variety of moieties,
such as 2-(2-furanyl)-1,3,4-oxadiazole, N-(2-methylphenyl)-4-(3-pyridinyl)-2-
pyrimidinamine, 4,4'-bithiazole, purine, adamantine and resorcinol, have been
designed and synthesized via Suzuki coupling, acid-base coupling and other
typical reactions.
INTRODUCTION
Signal transducer and activator of transcription 3 (STAT3), a member of the STAT protein family, is a
latent cytosolic transcription factor, that is widely recognized as a master regulator of crucial steps in
cellular proliferation and survival, metastasis and angiogenesis, and immune evasion.1-7 STAT3 is
frequently over activated in various human cancers including prostate, breast, head and neck cancers, but
not in normal epithelial cells.1-7 Thus, STAT3 signaling pathway has been validated as a promising target
for development of anticancer therapeutics.1-8 Since most of the currently available chemotherapy options
aim to initiate apoptosis, cancer cells have an intrinsic resistance to current treatment strategies. Therefore,
the design and synthesis of organic compounds with the ability to disrupt STAT3-mediated anti-apoptotic
gene expression is an important approach to search potential and selective anticancer drugs.
In the field of medicinal chemistry, synthesis of biologically active heterocyclic scaffolds is one of the
continuing interests, since most of the therapeutic drugs are derived from heterocyclic structures. The
quinoline nucleus is a significant class of heterocyclic compounds found in many synthetic and natural
products with promising biological activities.9-16 Development of new synthetic drugs based on quinoline

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HETEROCYCLES, Vol. 89, No. 3, 2014
scaffold remains as an active research area, since the structural modification of a privileged moiety with
therapeutic ability greatly alters its potency. Recently in a communication, we have reported the
identification of N-[2-(1,3,4-oxadiazolyl)]quinoline-4-carboxamide (STX-0119)17 as STAT3 inhibitor by
virtual screening strategy combining molecular docking studies and cell-line assays.
Our ongoing interest in the synthesis of heterocyclic compounds with therapeutic ability has prompted us
to further investigate the more functionalized quinoline derivatives. Hence in this paper, we report the
synthesis of a range of novel 2-phenylquinoline-4-carboxamide derivatives (I–V) containing few other
biologically important scaffolds (Figure 1).
3
H
N
R
H
N
O
O
O
O
2
1
O
O
O
R
O
(CH )n
2
N
H
N
H
N
N
N
N
N
N
R
N
N
II
I
STX-0119
R
N
H
N
N
R
N
H
N
N
N
H
N
O
Me
O
S
N
S
R
O
NH
N
O
N
H
R
N
N
V
III
IV
Figure 1
RESULTS AND DISCUSSION
Synthesis of requisite intermediates 3a-d was accomplished as illustrated in Scheme 1. The Pfitzinger
condensation18,19 of an appropriate isatin (1a-d) and acetophenone (2) in the presence of potassium
hydroxide in aqueous ethanol under reflux followed by neutralization afforded the corresponding
2-phenylquinoline-4-carboxylic acids (3a-d). Conversion of carboxylic acids (3a-c) to the corresponding
acid chlorides (4a-c) was carried out by treating with excess oxalyl chloride in the presence of a catalytic
amount of N,N-dimethylformamide (DMF) in dichloromethane at room temperature.
The acid chloride 4a was treated with various commercially available amines (5a-f), such as the 3-, 6- and
7-aminoquinoline, 1-aminoadamantane, 6-aminopurine (adenine), and 4-aminoresorcinol, in the presence
of triethylamine (Et3N) in dehydrated THF/DMF at elevated temperature to produce the corresponding
target compounds 6a-f in good yields as outlined in Scheme 2. Preparation of 6a-f took place smoothly in

HETEROCYCLES, Vol. 89, No. 3, 2014
695
O
O
O
OH
R
i
Me
R
O
+
N
H
N
1a-d
2
3a-d
a: R = H; b: R = Cl; c: R = I; d: R = OCF3
O
Cl
O
OH
ii
R
R
N
N
4a-c
3a-c
Scheme 1. Reagents and conditions: i, KOH, EtOH, water, 80-90 oC 18-36 h; ii, oxalyl
chloride, DMF, CH2Cl2, rt, overnight.
COCl
N
H
N
H
N
NH
H N
2
2
N
O
(CH )n
2
(CH )n
2
O
7a-c
ii
N
4a
8a-c
a: n = 3; b: n = 4; c: n = 7
R NH2
i
H
N
5a-f
O
NH
2
O
9
iii
H
N
O
O
H
N
R
O
N
H
O
N
N
6a-f
10
iv
d: R=
a: R=
N
N
N
H
N
O
NH
b: R=
c: R=
NH
e: R=
f: R=
2
N
N
N
N
HO
OH
11
Scheme 2. Reagents and conditions: i, Et3N, THF/DMF, reflux/(80-90 oC), 1.5-16 h; ii, Et3N, THF,
reflux, 1.5 h; iii, Et3N, THF, 40-50 oC, 2 h; iv, F3CCO2H, CH2Cl2, rt, 8 h.

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HETEROCYCLES, Vol. 89, No. 3, 2014
THF except 6e due to its less reactivity and solubility in the reaction condition. Thus, preparation of 6e
was carried out at higher temperature (80-90 °C) in DMF. In order to increase the
quinoline-4-carboxamide functionality in a single molecule, bis quinoline-4-carboxamides (8a-c) were
prepared in excellent yields by treating 4a with an appropriate diamine (7a-c) in the presence of Et3N in
THF under reflux. Under similar reaction condition, intermediate 4a was also reacted with
N-(4-aminobutyl)carbamic acid tert-butyl ester (9) to give compound 10 in 66% yield. Removal of
tert-butyl carbamate (Boc) group from compound 10 was accomplished with trifluoroacetic acid in
CH2Cl2 at room temperature to give compound 11 in 73% yield.
H
N
O
OH
O
O
O
H N
2
I
O
N
O
i
I
N
N
+
N
N
B
N
12
3c
13
H
N
OH
OH
O
O
O
Ar
Ar
N
N
14a-c
a: R = C6H5
b: R = 4-Me-C6H4
c: R = 3,5-(MeO)2-C6H3
N
ii
15a-c
Scheme 3. Reagents and conditions: i, DIPEA, HBTU, HOBt, DMF, rt, 3 d; ii, Pd(OAc)2, Xphos, K3PO4,
BuOH, 100 oC, 2 d.
A lot of efforts have been directed toward the modification of quinoline scaffold to improve biological
activities, though most of them have been accomplished either at the 2- or 4-position. Only a very little
structural modification especially aryl group alteration at the 6-position along with the 4-position has
been attained. Besides, hydrophobicity of drug is highly crucial for cell permeability. To raise the
hydrophobic character in few of our target compounds, we incorporated aryl functionality at the
6-position of N-[5-(2-furanyl)-1,3,4-oxadiazol-2-yl]-2-phenylquinoline-4-carboxamide (STX-0119) by
Suzuki-coupling reaction as delineated in Scheme 3. The acid-base coupling reaction of
6-iodoquinoline-4-carboxylic acid (3c) with 2-amino-5-(2-furyl)-1,3,4-oxadiazole (12) using coupling
reagents O-(benzotriazolyl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU) and
1-hydroxybenzotriazole (HOBt), and base N,N-diisopropylethylamine (DIPEA) in DMF at room
temperature furnished 6-iodo derivative 13 of STX-0119 in 62% yield. Subsequent Suzuki-coupling
reaction of 13 with appropriate arylboronic acid 14a-c using K3PO4, Pd(OAc)2 and
2-(dicyclohexylphosphino)-2',4',6'-triisopropyl-1,1'-biphenyl (Xphos) in butanol at 100 °C gave the
corresponding 6-aryl derivatives 15a-c in 41-57% yields.

HETEROCYCLES, Vol. 89, No. 3, 2014
697
O
O
i
Me
N
Me
Me
N
N
N
17
16
iii
N
N
NH
Me
Me
NH
ii
Me
O N
2
NH
NH
O N
2
2
NO
2
H N
2
18
20
19
N
H
N
N
N
N
Me
N
N
iv
O
NH
3a-d
NH
a: R = H
b: R = Cl
c: R = I
R
v
Me
N
NH
2
d: R = OCF3
22a-d
21
Scheme 4. Reagents and conditions: i, N,N-dimethylformamide dimethyl acetal, reflux, overnight;
ii, cyanamide, HNO3, EtOH, water, reflux, 2 d; iii, BuOH, reflux, 18 h, aq. NaOH; iv, H2, Pd-C,
THF-MeOH, rt, overnight; v, DIPEA, HBTU, HOBt, DMF, rt, 2 d.
The N-(2-methylphenyl)-4-(3-pyridinyl)-2-pyrimidinamine is an important fragment of recognized cell
specific anticancer drugs such as Imatinib20 and Nilotinib.21 Hence, we have tried to prepare few
compounds consisting of 2-phenylquinolines and above mentioned moiety as outlined in Scheme 4. The
necessary amine 21 was prepared starting from 3-acetylpyridine (16) and 6-methyl-3-nitroaniline (18)
according the reported method22 with modification. 16 was converted to 17 by treating with excess
N,N-dimethylformamide dimethyl acetal under reflux. On the other hand, aniline (18) was reacted with
cyanamide and nitric acid in aqueous ethanol to produce the corresponding guanidinium nitrate salt,
which on neutralization gave the free guanidine, 19. The majority of literature procedures use
guanidinium nitrate salt directly in next step followed in situ neutralization with alkali solution. The
condensation of 17 and free guanidine 19 in butanol under reflux afforded N-(2-methyl-5-nitrophenyl)-4-
(3-pyridinyl)-2-pyrimidinamine (20) in 87% yield, which on reduction with hydrogen using Pd-C as
catalyst in a mixture of methanol and THF at room temperature gave the desired amine 21 (88%). Finally,
the target compounds 22a-d were synthesized in 64-72% yields by coupling 21 with an appropriate acid
3a-d using HBTU, HOBt in the presence of DIPEA in DMF at room temperature.

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HETEROCYCLES, Vol. 89, No. 3, 2014
H N
NH
2
2
O
O
S
N
S
NH
Br
2
H N
2
N
Br
S
i
O
N
23
24
Cl
N
R
R
H
N
O
S
N
24
ii
N
S
O
N
H
4a-c
a: R = H; b: R = Cl; c: R = I
N
25a-c
R
Scheme 5. Reagents and conditions: i, MeOH, reflux, overnight, DMF-NH4OH; ii, Et3N, THF-DMF,
reflux, overnight.
Synthesis of the N,N'-[4,4'-bithiazole]-2,2'-diylbis-2-phenylquinoline-4-carboxamides (25a-c) was carried
out as outlined in Scheme 5. Treatment of the 1,4-dibromo-2,3-butanedione (23) with thiourea in
methanol followed by neutralization with ammonia solution afforded the 4,4'-bithiazole]-2,2'-diamine
(24) intermediate. Subsequent reaction of 24 with an appropriate quinoline-4-carbonyl chloride (4a-c) in
the presence of Et3N in a mixture of dehydrated THF and DMF under reflux produced the target
compounds 25a-c in 61-68% yields.
1
All new compounds have been characterized by elemental combustion analyses, and H-NMR and mass
1
spectral data. In the case of compounds 6e, peak for one NH proton was not visible in the H-NMR
spectrum due to high acidity.
In conclusion, we have synthesized series of novel 2-phenylquinoline-4-carboxamides containing other
significant moieties in the hope of searching STAT3 inhibitor. For this purpose, typical reactions
including Suzuki coupling and acid-base coupling have been employed, and efficient procedures have
been developed. Further synthesis of more derivatives and biological evaluation are currently ongoing,
and will be reported in due course.
EXPERIMENTAL
Melting points were obtained on a digital melting point apparatus (Round Science, RFS-10, Japan) and
1
were uncorrected. H-NMR spectra were recorded on a 300 MHz spectrometer (JNM-AL 300, JEOL).
The chemical shifts were reported in ppm (δ) relative to TMS. Coupling constants (J) were given in hertz
(Hz), and multiplicities were expressed as follows: s (singlet), br s (broad singlet), d (doublet), t (triplet),
q (quartet), quin (quintet), dd (doublet of doublet) and m (multiplet). Mass spectra were recorded on a
Microflex Maldi-TOF mass spectrometer (Bruker Daltonics). Elemental analyses were performed on a
J-Science LAB JM10 apparatus. Column chromatography was performed on Silica Gel G60 F254

HETEROCYCLES, Vol. 89, No. 3, 2014
699
(Merck).
General procedure for the preparation of 2-phenylquinoline-4-carboxylic acids (3a-d)
An appropriate isatin (1a-d) (14 mmol) and acetophenone (2) (16.5 mmol) were added to a solution of
KOH (35 mmol) in 20% aqueous EtOH (50 mL). The reaction mixture was stirred at 80-90 °C for 18-36
h. Evaporation of solvent afforded a residue, which was dissolved in minimum water. The resulting
solution was washed with Et2O (2 × 20 mL). The ice-cold aqueous layer was acidified with HCl/AcOH.
The resulting precipitate was collected by filtration followed by washing with water to give 3a-d in
49-84% yields.
2-Phenylquinoline-4-carboxylic acid (3a)
1
Yield: 74%; off-white solid; mp 212–213 ºC (DMF-H2O) (Lit.,23 209–210 ºC); H-NMR (DMSO-d6): δ
7.55 (br s, 3H), 7.69 (t, J = 8.4 Hz, 1H), 7.84 (t, J = 8.4 Hz, 1H), 8.16 (d, J = 8.6 Hz, 1H), 8.28 (d, J = 8.8
Hz, 2H), 8.46 (s, 1H), 8.65 (d, J = 8.6 Hz, 1H), 14.03 (br s, 1H); TOF mass (M+H)+ (m/z): 250.18.
6-Chloro-2-phenylquinoline-4-carboxylic acid (3b)
1
Yield: 54%; off-white solid; mp 244–245 ºC (EtOAc) (Lit.,24 241–243 ºC); H-NMR (DMSO-d6): δ
7.51-7.59 (m, 3H), 7.82 (dd, J = 8.8, 2.2 Hz, 1H), 8.15 (d, J = 8.8 Hz, 1H), 8.27 (d, J = 8.2 Hz, 2H), 8.52
(s, 1H), 8.76 (d, J = 2.2 Hz, 1H), 14.13 (br s, 1H); TOF mass (M+H)+ (m/z): 284.12.
6-Iodo-2-phenylquinoline-4-carboxylic acid (3c)
1
Yield: 49%; pale yellow solid; mp 249-250 ºC (EtOAc) (Lit.,25 249–250 ºC); H-NMR (DMSO-d6): δ
7.54 (br s, 3H), 7.89 (d, J = 8.6 Hz, 1H), 8.07 (d, J = 8.6 Hz, 1H), 8.25 (br s, 2H), 8.48 (s, 1H), 9.11 (s,
1H), 14.08 (br s, 1H); TOF mass (M+H)+ (m/z): 376.04.
2-Phenyl-6-trifluoromethoxyquinoline-4-carboxylic acid (3d)
1
Yield: 84%; pale yellow solid; mp 197–198 ºC (n-hexane-EtOAc); H-NMR (DMSO-d6): δ 7.56 (br s,
3H), 7.82 (d, J = 9.1 Hz, 1H), 8.27 (br s, 3H), 8.57 (s, 1H), 8.71 (s, 1H), 14.18 (br s, 1H); TOF mass
(M+H)+ (m/z): 334.14.
General procedure for the preparation of 2-phenyl-4-quinolinecarbonyl chlorides (4a-c)
An appropriate 2-phenylquinoline-4-carboxylic acid (3a-c) (5 mmol) was suspended in dehydrated
CH2Cl2 (50 mL), and the mixture was cooled to -5 to 0 °C. Oxalyl chloride (1 mL) was added dropwise
with stirring over 15 min to the cold reaction mixture. To it was added DMF (2 drops), and stirring was

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HETEROCYCLES, Vol. 89, No. 3, 2014
continued at -5 to 0 °C for 1 h. Ice-bath was removed, and the mixture was stirred at rt for overnight.
Evaporation of solvent under reduced pressure afforded the crude acid chlorides (4a-c), which were used
directly in the next step.
General procedure for the preparation of 2-phenylquinoline-4-carboxamides (6a-d)
To an ice-cold solution of an appropriate amine (5a-d) (1.05 mmol) and Et3N (0.3 mL) in dehydrated
THF (30 mL) was added the acid chloride (4a) (1 mmol). The reaction mixture was then heated under
reflux for 2 h. Solvent was removed under reduced pressure. Water (20 mL) was added to the residue
followed by addition of 10% aqueous Na2CO3 (2 mL). The mixture was stirred for 30 min. The resulting
precipitate was filtered, washed with water, dried and recrystallized from an appropriate solvent to afford
6a-d (81-89%).
N-(6-Quinolinyl)-2-phenylquinoline-4-carboxamide (6a)
1
Yield: 85%; off-white solid; mp 241–242 ºC (EtOH-H2O); H-NMR (DMSO-d6): δ 7.51-7.62 (m, 4H),
7.68 (t, J = 7.6 Hz, 1H), 7.87 (t, J = 7.4 Hz, 1H), 7.99 (d, J = 8.1 Hz, 1H), 8.06 (d, J = 8.4 Hz, 1H), 8.21 (t,
J = 8.8 Hz, 2H), 8.37-8.4 (m, 4H), 8.67 (s, 1H), 8.85 (s, 1H), 11.16 (s, 1H); TOF mass (M+H)+ (m/z):
376.26; Anal. Calcd for C25H17N3O: C, 79.98; H, 4.56; N, 11.19. Found: C, 80.17; H, 4.56; N, 11.05.
N-(7-Quinolinyl)-2-phenylquinoline-4-carboxamide (6b)
1
Yield: 81%; off-white solid; mp 246–247 ºC (EtOH-H2O); H-NMR (DMSO-d6): δ 7.55-7.64 (m, 4H),
7.70 (t, J = 7.6 Hz, 1H), 7.84-7.89 (m, 2H), 7.99 (d, J = 8.4 Hz, 2H), 8.19 (d, J = 8.2 Hz, 1H), 8.27 (d, J =
8.2 Hz, 1H), 8.42 (d, J = 6.9 Hz, 2H), 8.56 (s, 1H), 8.62 (d, J = 8.6 Hz, 1H), 8.95 (s, 1H), 11.01 (s, 1H);
TOF mass (M+H)+ (m/z): 376.24; Anal. Calcd for C25H17N3O·1/8H2O: C, 79.50; H, 4.60; N, 11.13.
Found: C, 79.45; H, 4.79; N, 11.02.
N-(3-Quinolinyl)-2-phenylquinoline-4-carboxamide (6c)
1
Yield: 88%; off-white solid; mp 210–211 ºC (EtOH-H2O); H-NMR (DMSO-d6): δ 7.54-7.73 (m, 6H),
7.87 (t, J = 7.7 Hz, 1H), 8.03 (t, J = 7.3 Hz, 2H), 8.19 (d, J = 8.4 Hz, 1H), 8.26 (d, J = 8.4 Hz, 1H), 8.39
(d, J = 7.7 Hz, 2H), 8.48 (s, 1H), 8.98 (s, 1H), 9.11 (s, 1H), 11.30 (s, 1H); TOF mass (M+H)+ (m/z):
376.16; Anal. Calcd for C25H17N3O: C, 79.98; H, 4.56; N, 11.19. Found: C, 80.15; H, 4.67; N, 11.21.
N-(1-Adamantanyl)-2-phenylquinoline-4-carboxamide (6d)
1
Yield: 89%; white solid; mp 257–258 ºC (n-hexane-EtOAc); H-NMR (DMSO-d6): δ 1.69 (br s, 6H),
2.09 (br s, 3H), 2.16 (br s, 6H), 7.47-7.53 (m, 3H), 7.63 (t, J = 8.2 Hz, 1H), 7.78 (t, J = 8.2 Hz, 1H), 7.99

HETEROCYCLES, Vol. 89, No. 3, 2014
701
(s, 1H), 8.05-8.12 (m, 2H), 8.27-8.31 (m, 3H); TOF mass (M+H)+ (m/z): 383.28; Anal. Calcd for
C26H26N2O: C, 81.64; H, 6.85; N, 7.32. Found: C, 81.78; H, 6.89; N, 7.21.
N-(9H-Purin-6-yl)-2-phenylquinoline-4-carboxamide (6e)
To a suspension of adenine (5e) (149 mg, 1.1 mmol) and Et3N (0.3 mL) in a dehydrated DMF (10 mL)
was added the acid chloride (4a) (268 mg, 1 mmol) at room temperature. The reaction mixture was then
heated at 80-90 °C for 16 h. Acetic acid (1 mL) was added to the cooled reaction mixture, and it was
poured into water (80 mL). The resulting precipitate was filtered, washed with water and dried. The crude
solid mass was purified by flash column chromatography on silica gel using EtOAc as eluent to give 6e
(231 mg, 63%) as pale yellow solid; mp 164–165 ºC (DMF-H2O); 1H-NMR (DMSO-d6): δ 7.52-7.57 (m,
3H), 7.69 (t, J = 8.1 Hz, 1H), 7.87 (t, J = 7.3 Hz, 1H), 8.19 (d, J = 8.4 Hz, 1H), 8.34-8.37 (m, 3H), 8.49 (s,
1H), 8.58 (s, 1H), 8.75 (s, 1H), 12.22 (br s, 1H); TOF mass (M+H)+ (m/z): 367.17; Anal. Calcd for
C21H14N6O·4/3H2O: C, 64.61; H, 4.30; N, 21.53. Found: C, 64.43; H, 4.29; N, 21.18.
N-(2,4-Dihydroxyphenyl)-2-phenylquinoline-4-carboxamide (6f)
To an ice-cold solution of 2,4-dihydroxyanilinium chloride (5f) (170 mg, 1.05 mmol) and Et3N (0.4 mL)
in dehydrated THF (30 mL) was added the acid chloride (4a) (268 mg, 1 mmol). The mixture was heated
under reflux for 1.5 h. Solvent was removed under reduced pressure, and water (20 mL) was added to the
residue. The precipitated solid was filtered, washed with water and dried. The crude solid mass was
purified by flash column chromatography on silica gel using EtOAc:CH2Cl2 (1:6) as eluent to give 6f
(175 mg, 49%) as tan solid; mp 264–265 ºC; 1H-NMR (DMSO-d6): δ 6.28 (dd, J = 8.4, 2.6 Hz, 1H), 6.40
(d, J = 2.6 Hz, 1H), 7.39 (d, J = 8.4 Hz, 1H), 7.51-7.67 (m, 4H), 7.83 (t, J = 8.4 Hz, 1H), 8.13 (d, J = 8.4
Hz, 1H), 8.24-8.38 (m, 4H), 9.28 (s, 1H), 9.55 (s, 1H), 9.86 (s, 1H); TOF mass (M+H)+ (m/z): 357.13;
Anal. Calcd for C22H16N2O3·5/6H2O: C, 71.15; H, 4.79; N, 7.54. Found: C, 71.17; H, 4.95; N, 7.46.
General procedure for the preparation of bis(2-phenylquinoline-4-carboxamides) (8a-c)
Compounds 8a-c were prepared in 79-86% yields by reacting the acid chloride 4a (1 mmol) with the
appropriate diamine (7a-c) (0.5 mmol) in the presence of Et3N (0.3 mL) following the general procedure
described for the preparation of 6a-d.
1,3-Bis(2-phenylquinoline-4-carbonylamino)propane (8a)
Yield: 81%; off-white solid; mp 244–245 ºC (DMF-H2O); 1H-NMR (DMSO-d6): δ 1.8 (quin, J = 5.9 Hz,
2H), 3.54 (br s, 4H), 7.51-7.56 (m, 6H), 7.63 (t, J = 8.0 Hz, 2H), 7.82 (t, J = 8.0 Hz, 2H), 8.13 (d, J = 8.4
Hz, 2H), 8.19 (s, 2H), 8.24 (d, J = 8.4 Hz, 2H), 8.31 (d, J = 8.1 Hz, 4H), 8.94 (br s, 2H); TOF mass

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(M+H)+ (m/z): 537.32; Anal. Calcd for C35H28N4O2: C, 78.34; H, 5.26; N, 10.44. Found: C, 78.50; H,
5.22; N, 10.29.
1,4-Bis(2-phenylquinoline-4-carbonylamino)butane (8b)
Yield: 79%; white solid; mp 285–286 ºC (DMF-H2O); 1H-NMR (DMSO-d6): δ 1.76 (br s, 4H), 3.46 (br s,
4H), 7.50-7.54 (m, 6H), 7.60 (t, J = 8.1 Hz, 2H), 7.80 (t, J = 8.1 Hz, 2H), 8.09-8.13 (m, 4H), 8.19 (t, J =
8.6 Hz, 2H), 8.27-8.3 (m, 4H), 8.92 (br s, 2H); TOF mass (M+H)+ (m/z): 551.29; Anal. Calcd for
C36H30N4O2: C, 78.52; H, 5.49; N, 10.17. Found: C, 78.44; H, 5.53; N, 10.01.
1,7-Bis(2-phenylquinoline-4-carbonylamino)heptane (8c)
1
Yield: 86%; white solid; mp 183–184 ºC (n-hexane-EtOAc); H-NMR (DMSO-d6): δ 1.43 (br s, 6H),
1.63 (br s, 4H), 3.38 (br s, 4H), 7.50-7.64 (m, 8H), 7.79 (t, J = 8.0 Hz, 2H), 8.09-8.17 (m, 6H), 8.29 (d, J
= 8.6 Hz, 4H), 8.83 (br s, 2H); TOF mass (M+H)+ (m/z): 593.40; Anal. Calcd for C39H36N4O2: C, 79.03;
H, 6.12; N, 9.45. Found: C, 79.13; H, 6.10; N, 9.32.
{4-[(2-Phenylquinoline-4-carbonyl)amino]butyl}carbamic acid tert-butyl ester (10)
To an ice-cold suspension of the acid chloride 4a (535 mg, 2 mmol) in dehydrated THF (40 mL) were
added Et3N (0.6 mL) and a solution of N-(4-aminobutyl)carbamic acid tert-butyl ester (9) (377 mg, 2
mmol) in THF (10 mL) dropwise, successively. The reaction mixture was heated at 40-50 °C for 2 h.
Solvent was evaporated under reduced pressure. The residue was taken up in water (30 mL), and
extracted with EtOAc (3 × 50 mL). The combined organic layer was washed with 5% aqueous NaHCO3,
water and brine, dried over MgSO4 and evaporated to dryness under reduced pressure. The crude amide
was recrystallized from a mixture of EtOAc and n-heptane to give 10 (554 mg, 66%) as pale yellow solid;
mp 108–109 ºC; 1H-NMR (DMSO-d6): δ 1.36 (s, 9H), 1.47-1.56 (m, 4H), 2.78 (br s, 2H), 3.37 (br s, 2H),
6.84 (br s, 1H), 7.51-7.55 (m, 4H), 7.81 (t, J = 7.4 Hz, 1H), 8.09 (s, 1H), 8.15 (d, J = 9.1 Hz, 2H), 8.31 (d,
J = 9.1 Hz, 2H), 8.84 (br s, 1H); TOF mass (M+H)+ (m/z): 420.37; Anal. Calcd for C25H29N3O3·5/16H2O:
C, 70.63; H, 7.02; N, 9.88. Found: C, 70.87; H, 7.05; N, 9.49.
N-(4-Aminobutyl)-2-phenylquinoline-4-carboxamide (11)
To a solution of 10 (420 mg, 1 mmol) in dry CH2Cl2 (20 mL) was added 30% TFA in CH2Cl2 (10 mL).
The reaction mixture was then stirred at rt for 8 h, and the volatiles were removed under reduced pressure.
To the residue were added dehydrated THF (30 mL) and anhydrous K2CO3 (1 g). The mixture was stirred
for 1 h at rt and filtered. Solvent was removed under reduced pressure, and the residue was recrystallized
from a mixture of n-heptane and THF to give 11 (233 mg, 73 %) as white solid; mp 178–179 ºC

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1
(n-hexane-THF); H-NMR (DMSO-d6): δ 1.64 (br s, 4H), 2.86 (br s, 2H), 3.50 (br s, 4H), 7.52-7.65 (m,
4H), 7.83 (t, J = 8.1 Hz, 1H), 8.09-8.18 (m, 3H), 8.28 (d, J = 7.9 Hz, 2H), 8.93 (s, 1H); TOF mass
(M+H)+ (m/z): 320.26; Anal. Calcd for C20H21N3O·(CF3COOH + 3H2O)/4: C, 68.13; H, 6.34; N, 11.63.
Found: C, 68.28; H, 6.54; N, 11.63.
N-[5-(2-Furanyl)-1,3,4-oxadiazol-2-yl]-6-iodo-2-phenylquinoline-4-carboxamide (13)
To a solution of 6-iodo-2-phenylquinoline-4-carboxylic acid (3c) (375 mg, 1 mmol) in dehydrated DMF
(15 ml) were added HBTU (759 mg, 2 mmol) and anhydrous HOBt (270 mg, 2 mmol) at rt under
nitrogen. The resulting solution was stirred at rt for 30 min. DIPEA (258 mg, 2 mmol) was added, and the
solution was stirred for another 30 min. Finally, 2-amino-5-(2-furyl)-1,3,4-oxadiazole (12) (265 mg, 1.75
mmol) was added, and the solution was stirred at rt for 3 d. The solution was poured into cold water (100
mL), and the resulting precipitate was filtered, washed well with water and dried. Recrystallization of
crude mass from a mixture of DMF-water gave 13 (315 mg, 62%) as pale yellow solid; mp 241–242 ºC;
1H-NMR (DMSO-d6): δ 6.81 (dd, J = 3.4, 1.8 Hz, 1H), 7.31 (d, J = 3.4 Hz, 1H), 7.54-7.63 (m, 3H), 7.94
(d, J = 7.8 Hz, 1H), 8.05 (s, 1H), 8.13 (d, J = 7.8 Hz, 1H), 8.34 (d, J = 7.2 Hz, 2H), 8.52 (s, 1H), 8.69 (s,
1H), 12.88 (br s, 1H); TOF mass (M+H)+ (m/z): 509.06; Anal. Calcd for C22H13IN4O3: C, 51.99; H, 2.58;
N, 11.02. Found: C, 52.00; H, 2.78; N, 10.83.
General procedure for the Suzuki coupling reactions to prepare N-[5-(2-furanyl)-
1,3,4-oxadiazol-2-yl]-6-aryl-2-phenylquinoline-4-carboxamides (15a-c)
A mixture of the 6-iodo compound 13 (203 mg, 0.4 mmol), an appropriate phenylboronic acid (14a-c)
(0.8 mmol), anhydrous K3PO4 (212 mg, 1 mmol), Xphos (4.8 mg, 10 mol) and BuOH (20 mL) was
degassed. To the mixture was added Pd(OAc)2 (1.1 mg, 5 mol), and it was heated at 100 °C under
nitrogen for 2 d. The mixture was filtered and washed with EtOAc (15 mL× 2). The combined filtrate was
concentrated to dryness under reduced pressure. Then the crude material was dissolved in EtOAc (75 mL),
and the solution was washed with 5% aqueous NaHCO3, water, and brine. The organic layer was dried
with MgSO4, filtered, and concentrated to give crude solid mass, which was purified by column
chromatography on silica gel using a mixture of CH2Cl2 and methanol (35:1) as eluent to give 15a-c in
41-57% yield.
N-[5-(2-Furanyl)-1,3,4-oxadiazol-2-yl]-2,6-diphenylquinoline-4-carboxamide (15a)
Yield: 49%; yellow solid; mp 226–227 ºC (n-hexane-EtOAc); 1H-NMR (DMSO-d6): δ 6.77 (s, 1H), 7.23
(br s, 2H), 7.51-7.58 (m, 6H), 7.76-7.82 (m, 2H), 8.01 (s, 1H), 8.14-8.22 (m, 2H), 8.35 (d, J = 7.8 Hz, 2H),
8.49 (s, 1H), 12.77 (br s, 1H); TOF mass (M+H)+ (m/z): 459.24; Anal. Calcd for C28H18N4O3·H2O: C,

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HETEROCYCLES, Vol. 89, No. 3, 2014
70.58; H, 4.23; N, 11.76. Found: C, 70.62; H, 4.27; N, 11.51.
N-[5-(2-Furanyl)-1,3,4-oxadiazol-2-yl]-2-phenyl-6-(p-tolyl)-quinoline-4-carboxamide (15b)
Yield: 41%; pale yellow solid; mp 154–155 ºC (n-hexane-EtOAc); 1H-NMR (DMSO-d6): δ 2.36 (s, 3H),
6.80 (dd, J = 3.4, 1.8 Hz, 1H), 7.28-7.33 (m, 3H), 7.57-7.71 (m, 5H), 8.05 (s, 1H), 8.22-8.27 (m, 2H),
8.35 (d, J = 7.4 Hz, 2H), 8.51 (s, 2H), 12.83 (br s, 1H); TOF mass (M+H)+ (m/z): 473.28; Anal. Calcd for
C29H20N4O3·H2O: C, 71.01; H, 4.52; N, 11.42. Found: C, 70.87; H, 4.38; N, 11.49.
N-[5-(2-Furanyl)-1,3,4-oxadiazol-2-yl]-6-(3,5-dimethoxyphenyl)-2-phenylquinoline-4-carboxamide
(15c)
Yield: 57%; yellow solid; mp 213–214 ºC (n-hexane-EtOAc); 1H-NMR (DMSO-d6): 3.75 (s, 6H), 6.51 (s,
1H), 6.71-6.83 (m, 3H), 7.21 (s, 1H), 7.52 (br s, 3H), 8.04 (s, 1H), 8.13 (br s, 2H), 8.29 (d, J = 7.6 Hz,
2H), 8.45 (s, 2H), 12.78 (br s, 1H); TOF mass (M+H)+ (m/z): 519.28; Anal. Calcd for
C30H22N4O5·6/7H2O: C, 67.48; H, 4.48; N, 10.49. Found: C, 67.83; H, 4.39; N, 10.10.
N-(2-Methyl-5-nitrophenyl)-4-(3-pyridinyl)-2-pyrimidinamine (20)
Firstly, 17 was prepared in 82% yield by refluxing 16 (3.63 g, 30 mmol) in N,N-dimethylformamide
dimethyl acetal (10 mL) for overnight followed by evaporation of volatiles and recrystallization from
n-hexane-EtOAc. Secondly, nitrate salt of 19 was prepared by treating a mixture of 18 (10 g, 65.7 mmol),
68% nitric acid (4.8 mL) and EtOH (30 mL) with a solution of cyanamide (4.3 g, 102 mmol) in water (4.3
mL) under reflux for 2 d followed by filtering and washing with EtOAc. The crude salt was suspended
portion-wise into 2% aqueous NaOH solution (300 mL) and stirred at rt for overnight. The resulting
precipitate was filtered and washed with water to afford free guanidine 19 (9.7 g, 76%). Finally a mixture
of 17 (2.5 g, 14.2 mmol) and crude 19 (2.5 g, 12.9 mmol) in BuOH (20 mL) was heated under reflux for
18 h and cooled to rt. Separated precipitate was filtered, washed with water and dried to give 20, which
was used directly in the next step without further purification. Yield: 3.44 g (87%); yellow solid; mp
1
196–197 ºC (DMF-H2O) (Lit.,26 196–197 ºC); H-NMR (DMSO-d6): δ 2.42 (s, 3H), 7.48-7.58 (m, 3H),
7.88 (d, J = 8.4 Hz, 1H), 8.47 (d, J = 8.1 Hz, 1H), 8.61 (d, J = 5.1 Hz, 1H), 8.70 (d, J = 5.1 Hz, 1H), 8.80
(s, 1H), 9.22 (s, 1H), 9.31 (s, 1H); TOF mass (M+H)+ (m/z): 308.14.
N-(5-Amino-2-methylphenyl)-4-(3-pyridinyl)-2-pyrimidinamine (21)
To a suspension of 20 (2.0 g, 6.5 mmol) in a mixture of MeOH (30 mL) and THF (70 mL) was added
10% Pd/C (600 mg) under nitrogen. After two vacuum/H2 cycles to replace nitrogen inside the reaction
flask with hydrogen, the reaction mixture was stirred at rt under hydrogen atmosphere for overnight. The

HETEROCYCLES, Vol. 89, No. 3, 2014
705
mixture was filtered through a pad of celite, and the filtrate was concentrated under reduced pressure. The
residue was recrystallized from a mixture of n-hexane and EtOAc to give 21 (1.59 g, 88% yield) as bright
yellow solid; mp 140–141 ºC (Lit.,26 142–144 ºC); 1H-NMR (DMSO-d6): δ 2.04 (s, 3H), 4.86 (br s, 2H),
6.33 (d, J = 7.7 Hz, 1H), 6.77 (s, 1H), 6.85 (d, J = 7.8 Hz, 1H), 7.35 (d, J = 5.1 Hz, 1H), 7.48-7.54 (m,
1H), 8.39 (d, J = 7.8 Hz, 1H), 8.45 (d, J = 5.1 Hz, 1H), 8.69 (br s, 2H), 9.23 (s, 1H); TOF mass (M+H)+
(m/z): 278.18.
General procedure for the preparation of N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-
phenyl]-2-phenylquinoline-4-carboxamides (22a-d)
To a solution of an appropriate quinoline-4-carboxylic acid (3a-d) (0.6 mmol) in dehydrated DMF (10
mL) were added HBTU (455 mg, 1.2 mmol) and anhydrous HOBt (162 mg, 1.2 mmol) at rt, and the
resulting solution was stirred for 30 min. To the solution was added DIPEA (194 mg, 1.5 mmol), and it
was stirred for another 30 min. Finally, 21 (250 mg, 0.9 mmol) was added and stirring at rt was continued
for 2 d. Reaction mixture was poured into cold water (100 mL), and resulting precipitate was filtered,
washed well with water and dried. Recrystallization of crude solid mass from a mixture of DMF and
water afforded 22a-d in 64-72% yields.
N
-[4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-2-phenylquinoline-4-carboxamide (22a)
Yield: 72%; yellow solid; mp 241–242 ºC; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H), 7.25 (d, J = 8.4 Hz, 1H),
7.43 (d, J = 5.1 Hz, 1H), 7.49-7.59 (m, 5H), 7.67 (t, J = 8.1 Hz, 1H), 7.85 (t, J = 8.1 Hz, 1H), 8.15 (d, J =
8.4 Hz, 2H), 8.22 (s, 1H), 8.34-8.38 (m, 3H), 8.47-8.53 (m, 2H), 8.68 (d, J = 8.1 Hz, 1H), 9.03 (s, 1H),
9.31 (s, 1H), 10.79 (s, 1H); TOF mass (M+H)+ (m/z): 509.25; Anal. Calcd for C32H24N6O: C, 75.57; H,
4.76; N, 16.52. Found: C, 75.52; H, 4.81; N, 16.30.
N
-[4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-6-chloro-2-phenylquinoline-4-carboxamide
(22b)
Yield: 69%; pale yellow solid; mp 259–260 ºC; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H), 7.26 (d, J = 8.4 Hz,
1H), 7.43 (d, J = 5.1 Hz, 1H), 7.50-7.59 (m, 5H), 7.86 (d, J = 9.1 Hz, 1H), 8.16-8.25 (m, 3H), 8.36 (d, J =
7.7 Hz, 2H), 8.43 (s, 1H), 8.48-8.53 (m, 2H), 8.68 (s, 1H), 9.03 (s, 1H), 9.31 (s, 1H), 10.83 (s, 1H); TOF
mass (M+H)+ (m/z): 543.31; Anal. Calcd for C32H23ClN6O·1/2H2O: C, 69.62; H, 4.38; N, 15.22. Found:
C, 69.59; H, 4.62; N, 15.04.
N
-[4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-6-iodo-2-phenylquinoline-4-carboxamide
(22c)

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HETEROCYCLES, Vol. 89, No. 3, 2014
Yield: 64%; yellow solid; mp 299–300 ºC; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H), 7.26 (d, J = 8.2 Hz, 1H),
7.43-7.56 (m, 6H), 7.93 (d, J = 8.6 Hz, 1H), 8.09 (d, J = 8.6 Hz, 1H), 8.18 (s, 1H), 8.33-8.39 (m, 3H),
8.51 (br s, 2H), 8.59 (s, 1H), 8.68 (s, 1H), 9.04 (s, 1H), 9.301 (s, 1H), 10.82 (s, 1H); TOF mass (M+H)+
(m/z): 635.12; Anal. Calcd for C32H23IN6O: C, 60.58; H, 3.65; N, 13.25. Found: C, 60.69; H, 3.74; N,
13.02.
N
-[4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-6-trifluoromethoxy-2-phenylquinoline-
4-carboxamide (22d)
Yield: 66%; pale yellow solid; mp 249–250 ºC; 1H-NMR (DMSO-d6): δ 2.26 (s, 3H), 7.27 (d, J = 8.4 Hz,
1H), 7.45-7.59 (m, 6H), 7.86 (d, J = 8.7 Hz, 1H), 8.19 (br s, 2H), 8.32 (d, J = 8.1 Hz, 1H), 8.39 (d, J = 7.8
Hz, 2H), 8.49 (br s, 3H), 8.67 (s, 1H), 9.03 (s, 1H), 9.30 (s, 1H), 10.84 (s, 1H); TOF mass (M+H)+ (m/z):
593.28; Anal. Calcd for C33H23F3N6O2: C, 66.89; H, 3.91; N, 14.18. Found: C, 66.91; H, 4.13; N, 14.07.
4,4'-Bithiazole]-2,2'-diamine (24)
A mixture of 1,4-dibromo-2,3-butanedione (23) (4.51 g, 18.5 mmol) and thiourea (2.82 g, 37 mmol) in
dehydrated MeOH (80 mL) was heated under reflux for overnight. The reaction mixture was cooled,
filtered and washed with EtOH to give hydrobromide salt of 24. The salt was dissolved in DMF by
heating and the hot solution was made basic with aqueous NH3. Water was added to the hot mixture and
cooled. The precipitated solid mass was collected by filtration followed by washing with water to give 24
(2.82 g, 77%) as off-white solid; mp 264–266 ºC (DMF-H2O) (Lit.,27 263–265ºC); 1H-NMR (DMSO-d6):
δ 6.59 (s, 2H), 6.98 (br s, 4H); TOF mass (M+H)+ (m/z): 199.07.
General procedure for the preparation of N,N'-[4,4'-bithiazole]-2,2'-diylbis-2-phenylquinoline-
4-carboxamide (25a-c)
To a solution of 24 (99 mg, 0.5 mmol) and Et3N (0.4 mL) in a mixture of dehydrated THF (30 mL) and
DMF (7 mL) was added an appropriate acid chloride 4a-c (1.2 mmol). The reaction mixture was then
heated under reflux for overnight. The reaction mixture was concentrated to about 6/7 mL under reduced
pressure, and was poured into water (30 mL). The resulting precipitate was filtered, washed with water
and dried. The crude solid mass was purified by column chromatography on silica gel using a mixture of
CH2Cl2 and MeOH (40:1) as eluent to give 25a-c in 61-68% yield.
N,N'-[4,4'-Bithiazole]-2,2'-diylbis-2-phenylquinoline-4-carboxamide (25a)
Yield: 66%; pale yellow solid; mp >300 ºC (DMF-H2O); 1H-NMR (DMSO-d6): δ 7.51-7.56 (m, 8H), 7.61
(t, J = 8.1 Hz, 2H), 7.87 (t, J = 7.8 Hz, 2H), 8.18 (d, J = 8.4 Hz, 2H), 8.29 (d, J = 8.1 Hz, 2H), 8.39 (d, J =

HETEROCYCLES, Vol. 89, No. 3, 2014
707
7.3 Hz, 4H), 8.52 (s, 2H), 13.33 (br s, 2H); TOF mass (M+H)+ (m/z): 661.23; Anal. Calcd for
C38H24N6O2S2·1/3H2O: C, 68.45; H, 3.73; N, 12.60. Found: C, 68.77; H, 3.93; N, 12.26.
N,N'-[4,4'-Bithiazole]-2,2'-diylbis-6-chloro-2-phenylquinoline-4-carboxamide (25b)
Yield: 68%; pale yellow solid; mp >300 ºC (DMF-H2O); 1H-NMR (DMSO-d6): δ 7.52-7.58 (m, 8H), 7.86
(d, J = 8.6 Hz, 2H), 8.13 (d, J = 8.6 Hz, 2H), 8.37 (br s, 6H), 8.57 (s, 2H), 13.38 (br s, 2H); TOF mass
(M+H)+ (m/z): 729.05; Anal. Calcd for C38H22Cl2N6O2S2·1/3H2O: C, 62.04; H, 3.11; N, 11.42. Found: C,
61.86; H, 3.09; N, 11.24.
N,N'-[4,4'-Bithiazole]-2,2'-diylbis-6-iodo-2-phenylquinoline-4-carboxamide (25c)
Yield: 61%; yellow solid; mp >300 ºC (DMF-H2O); 1H-NMR (DMSO-d6): δ 7.53-7.58 (m, 8H), 7.93 (d, J
= 8.8 Hz, 2H), 8.11 (d, J = 8.8 Hz, 2H), 8.37 (d, J = 7.1 Hz, 4H), 8.55 (s, 2H), 8.71 (s, 2H), 13.38 (br s,
2H); TOF mass (M+H)+ (m/z): 912.94; Anal. Calcd for C38H22I2N6O2S2·1/4H2O: C, 49.77; H, 2.47; N,
9.16. Found: C, 49.89; H, 2.59; N, 9.11.
ACKNOWLEDGEMENTS
The authors wish to thank Professor Masami Otsuka, Department of Bioorganic Medicinal Chemistry,
Faculty of Life Sciences, Kumamoto University, Japan for arranging facilities to measure NMR spectrum
and elemental analyses.
REFERENCES
1. J. E. Darnell, Jr., Nat. Rev. Cancer, 2002, 2, 740.
2. J. Bromberg and J. E. Darnell, Jr., Oncogene, 2000, 19, 2468.
3. H. Yu and R. Jove, Nat. Rev. Cancer, 2004, 4, 97.
4. J. Turkson and R. Jove, Oncogene, 2000, 19, 6613.
5. R. Buettner, L. B. Mora, and R. Jove, Clin. Cancer Res., 2002, 8, 945.
6. J. E. Darnell, Jr., I. M. Kerr, and G. R. Stark, Science, 1994, 264, 1415.
7. T. Bowman, R. Garcia, J. Turkson, and R. Jove, Oncogene, 2000, 19, 2474.
8. S. Becker, B. Groner, and C. W. Muller, Nature, 1998, 394, 145.
9. D. Paris, M. Cottin, P. Demonchaux, G. Augert, P. Dupassieux, P. Lenoir, M. J. Peck, and D.
Jasserand, J. Med. Chem., 1995, 38, 669.
10. A. A. Alhaider, M. A. Abdelkader, and E. J. Lien, J. Med. Chem., 1985, 28, 1394.
11. R. Musiol, J. Jampilek, K. Kralova, D. S. Richardson, D. Kalinowski, B. Podeszwa, J. Finster, H.
Niedbala, A. Palka, and J. Polanski, Bioorg. Med. Chem., 2007, 15, 1280.

708
HETEROCYCLES, Vol. 89, No. 3, 2014
12. M. Robert, J. Josef, B. Vladimir, S. Luis, N. Halina, P. Barbara, P. Anna, M.-M. Katarzyna, O.
Barbara, and P. Jaroslaw, Bioorg. Med. Chem., 2006, 14, 3592.
13. C. R. Gardner, R. Deacon, V. James, F. Parker, and P. Budhram, Eur. J. Pharm., 1987, 142, 285.
14. S. Juan, Z. Hui, Y. Zhong-Ming, and Z. Hai-Liang, Eur. J. Med. Chem., 2013, 60, 23.
15. S. K. Srivastava, A. Jha, S. K. Agarwal, R. Mukherjee, and A. C. Burman, Anti-Cancer Agents Med.
Chem., 2007, 7, 685.
16. C. M. Hall, H. G. Johnson, and J. B. Wright, J. Med. Chem., 1974, 17, 685.
17. K. Matsuno, Y. Masuda, Y. Uehara, H. Sato, A. Muroya, O. Takahashi, T. Yokotagawa, T. Furuya,
T. Okawara, M. Otsuka, N. Ogo, T. Ashizawa, C. Oshita, S. Tai, H. Ishii, Y. Akiyama, and A. Asai,
ACS Med. Chem. Lett., 2010, 1, 371.
18. J. Li, J. Chen, C. Gui, L. Zhang, Y. Qin, Q. Xu, J. Zhang, H. Liu, X. Shen, and H. Jiang, Bioorg.
Med. Chem., 2006, 14, 2209.
19. C.-C. Peng, J. L. Cape, T. Rushmore, G. J. Crouch, and J. P. Jones, J. Med. Chem., 2008, 51, 8000.
20. R. Roskoski, Jr., Biochem. Biophys. Res. Commun., 2003, 309, 709.
21. U. Rix, O. Hantschel, G. Dürnberger, L. L. R. Rix, M. Planyavsky, N. V. Fernbach, I. Kaupe, K. L.
Bennett, P. Valent, J. Colinge, T. Köcher, and G. Superti-Furgal, Blood, 2007, 110, 4055.
22. Z. Szakacs, S. Beni, Z. Varga, L. Orfi, G. Keri, and B. Noszal, J. Med. Chem., 2005, 48, 249.
23. A. E. M. Saeed and S. A. Elhadi, Synth. Commun., 2011, 41, 1435.
24. L.-M. Wang, L. Hu, H.-J. Chen, Y.-Y. Sui, and W. Shen, J. Fluorine Chem., 2009, 130, 406.
25. W. Borsche, H. Weussmann, and A. Fritzsche, Ber. Dtsch. Chem. Ges., 1924, 57B, 1770.
26. S. Chang, S.-L. Yin, J. Wang, Y.-K. Jing, and J.-H. Dong, Molecules, 2009, 14, 4166.
27. B. W. Lee and S. D. Lee, Tetrahedron Lett., 2000, 41, 3883.