Efficient synthesis of N-Substituted 4-arylquinoline derivatives using ZnCl2 or ZrO2

Article abstract of DOI:10.3987/COM-12-12467

N-Substituted 7,8-dihydro-7,7-dimethyl-4-arylquinolin-5(1H,4H,6H)-ones 4a-l have been reported by one-pot reaction of cinnamaldehyde derivatives, dimedone and various amines in the presence of ZnCl₂ or ZrO₂ in fairly high yields.

Full text of DOI:10.3987/COM-12-12467

HETEROCYCLES, Vol. 85, No. 6, 2012, pp. -. © 2012 The Japan Institute of Heterocyclic Chemistry
Received, 18th March, 2012, Accepted, 23rd April, 2012, Published online, 2nd May, 2012
DOI: 10.3987/COM-12-12467
EFFICIENT SYNTHESIS OF N-SUBSTITUTED 4-ARYLQUINOLINE
DERIVATIVES USING ZnCl2 or ZrO2

Afsaneh Zonouzi, Roghieh Mirzazadeh, Azadeh Peivandi, and Shahrzad
Dehdari
School of Chemistry, University College of Science, University of Tehran, Tehran,
Iran, E-mail: zonouzi@khayam.ut.ac.ir
Abstract - N-Substituted 7,8-dihydro-7,7-dimethyl-4-arylquinolin-5 (1H,4H,6H)-
ones 4a-l have been reported by one-pot reaction of cinnamaldehyde derivatives,
dimedone and various amines in the presence of ZnCl2 or ZrO2 in fairly high
yields.
The preparation of 1,4-dihydropridines by classical Hantzsch synthesis, a one-pot condensation of an
aldehyde with alkyl acetoacetate and ammonia, was developed more than one hundred years ago.1 Up to
now some reports on modification of Hantzsch reaction have been published.2-10 Also it has been shown
some substituted 1,4-dihyropyridine derivatives exhibit biological activity.3-7 The classical methods for
the synthesis of 1,4-dihyropyridines almost involved long reaction time, harsh reaction conditions, and
use of a large quality of volatile organic solvents or microwave irradiation and generally achieved the
products in low to moderate yields and sometimes had been reported as by-product. In 2006 Sivamurugan
and co-workers had reported the synthesis of 1,4-dihyropyridine derivatives using aldehydes, 1,3-
diketones and ammonium acetate in the presence of Zn[L-proline]2 and microwave irradiation.8 Wu and
co-workers had reported synthesis of α-flouro substituted amidines using ZnCl2.9 They reported 1,4-
dihydropyridines as by-product. In 2007 Moreau and co-workers used p-TSA for the synthesis of N-
substituted 1,4-dihydropyridine derivatives.10
We have recently reported one-pot procedure for heterocyclic frameworks,11-14 here we wish to report
multi-component and one-pot reaction of cinnamaldehyde derivatives 1, primary amine 2 and dimedone 3
(5,5-dimethyl-1,3-cyclohexanedione) in the presence of ZnCl2, ZrO2 and p-toluenesulfonic acid (p-TSA)
as catalyst. In this reaction N-substituted-4-arylquinolin-5-ones 4 were achieved in fairly good yields 68-
88% (Scheme 1).
In previous reports enamine was produced using ammonia and aldehyde then enamine attacked to α,β-

O
O
C6H4R
O
ZnCl2 or ZrO2
EtOH, heat
H
R'NH2
+
+
O
N
R
1
2
3
R'
4
R = H, 4-NO2, 4-OMe
R' = Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, PhCH2, PhCH2CH2
Scheme 1
unsaturated carbonyl compound as a nucleophile. While in this research we used α,β-unsaturated imine
(produced by cinnamaldehyde derivatives and primary amines) as a Michael acceptor. Michael addition
of enolate ion of dimedone 3 (1,3-dicarbonyl compound) to this imine in the presence of Lewis acid
produced the N-substituted-4-arylquinolin-5-ones, which is a new modification of Hantzsch reaction.
Moreover dimedone 3 is still desired for the synthesis of fused heterocyclic compounds.15
We have found when cinnamaldehyde, dimedone and primary amine (PhCH2CH2NH2) in the presence of
ZnCl2 were used simultaneously only (E)-3-hydroxy-5,5-dimethyl-2-(3-phenylprop-2-en-1-yl)cyclohex-
2-en-1-one was produced.16 In this research, enolate ion is produced initially by using 1-2 drops of a
suitable base like triethylamine then this enolate is added to imine of cinnamaldehyde and primary amine.
Meanwhile we have used primary amines instead of ammonia or ammonium salts for synthesis of some
N-substituted-4-arylylquinoline derivatives.
On the other hand this one-pot reaction did not process without using acid as catalyst. Lewis acids (ZnCl2,
ZrO2) also p-TSA were used as catalyst in different amounts. Solvents (toluene, p-xylene, H2O and
EtOH) have been investigated in this procedure. The results for compound 4a are compared in Table 1.
Table 1. Effect of solvents on the synthesis of compound 4a using ZnCl2, ZrO2 and
P-TSA
Catalyst
(mol %)
EtOH
(Yield %)
p-Xylene
(Yield %)
Toluene
(Yield %)
H2O
(Yield %)
ZnCl2
5
68
52
48
-
10
20
88
87
70
62
62
55
10
5
ZrO2
5
58
76
78
45
65
60
40
58
54
-
10
20
5
5
p-TSA
5
35
28
22
-
10
20
42
40
30
32
25
25
-
-

As shown in table 1, for the synthesis of compound 4a, EtOH was the best solvent and p-TSA was not so
effective, therefore, ZnCl2 and ZrO2 have been chosen as the catalyst and EtOH as solvent. The different
amounts of ZnCl2 and ZrO2 on the reaction times and yields of compounds 4a-l have been examined too
(Table 2). Obviously for both catalysts 10 mol% was better than 5 mol% and 20 mol% of both catalysts
was similar to 10 mol%.
1
13
Structures 4 were assigned on the basis of their elemental analysis, IR, H NMR, C NMR and mass
spectral data. The mass spectra of these compounds 4a-l displayed molecular ion peaks at the appropriate
1
m/z values. The H NMR and 13C NMR spectra of 4a-l displayed absorption in agreement with their
structures. (Experimental Section)
The reaction described here is a new modification of Hantzsch reaction which represent an efficient entry
for the synthesis of N-substituted-7,8-dihydro-7,7-dimethyl-4-arylquinolin-5(1H,4H,6H)-ones.
Inexpensive Lewis acid (ZnCl2 and ZrO2) catalyzed this reaction. Further investigations of this method
are currently in progress to establish its scope and utility.
EXPERIMENTAL
Chemicals and solvents were obtained from Merck (Germany) and Fluka (Switzerland) and were used
without further purification. Columns chromatography were performed on silica Gel (0.015-0.04 mm,
mesh-size) and TLC on percolated plastic sheets (25 DCUV-254) respectively. Melting points were
measured on Barnstead Electrothermal melting point apparatus and are not corrected. Elemental analysis
for C, H and N were performed using a Thermo Finnigan Flash EA1112 instrument. IR spectra were
measured on a Bruker EQUINOX 55 spectrophotometer as ATR method. 1H NMR and 13C NMR spectra
were determined in CDCl3 on a Bruker 500 spectrophotometer and chemical shifts were expressed in ppm
downfield from tetramethyl silane. Mass spectra were recorded on a Finnigan-MAT 8430 spectrometer at
an ionization potential of 70 ev.
General procedure for the synthesis of compounds 4
To a magnetically stirred solution of cinnamaldehyde derivatives 1 (4 mmol) in EtOH (10 mL), amines 2
(4 mmol) was added gently and stirred for 20-30 min. Then a mixture of dimedone 3 (4 mmol) and 1-2
drops of triethylamine were added to the above reaction mixture. Catalyst was added according to Table 2
in this stage. The reaction mixture was refluxed for 12-14 h. The product was purified by column
chromatography using silica gel and EtOAc: n-hexane (1:4) as co-solvent.

7,8-Dihydro-1,7,7-trimethyl-4-phenylquinolin-5(1H,4H,6H)-one (4a): yellow liquid; νmax (KBr): 3024,
1
2958 (C-H), 1718 (C=O), 1616, 1551 (C-N) cm-1; H NMR (CDCl3, 500 MHz): δH 1.00, 1.12 (6H, 2s,
2CH3), 2.18-2.20 (2H, d, J = 7.70 Hz, 2H8), 2.40-2.42 (2H, d, J = 16.02 Hz, 2H6), 3.16 (3H, s, CH3-N),
4.69-4.70 (1H, d, J = 5.35 Hz, CH-Ph), 5.07-5.09 (1H, d of d, J = 8.12 Hz, J = 5.35 Hz, H3), 5.96-5.98
(1H, d, J = 8.12 Hz, H2), 7.13-7.16, 7.26-7.32 (5H, 2m, aromatic) ppm. 13C NMR (CDCl3, 125 MHz): δC
27.78, 30.46 (2CH3), 29.71 (CMe2), 38.46 (CH-Ph), 36.91, 40.32 (2CH2), 50.30 (CH3-N), 109.32
(olefinic carbon), 110.01 (olefinic CH), 126.32, 127.96, 128.62, 130.20 (aromatic); 148.19 (=CH-N),
152.72 (=C-N), 195.52 (C=O) ppm; MS: m/z: 267 (M+), 252 (M+-CH3), 190 (M+-Ph), 175 (M+-CH3, Ph),
77. Anal. Calcd for C18H21NO: C, 80.86; H, 7.92; N, 5.24. Found: C, 80.84; H, 7.95; N, 5.21.
1-Ethyl-7,8-dihydro-7,7-dimethyl-4-phenylquinolin-5(1H,4H,6H)-one (4b): yellow liquid; νmax (KBr):
3020, 2956 (C-H), 1711 (C=O), 1612, 1552 (C-N) cm-1; 1H NMR (CDCl3, 500 MHz): δH 1.02, 1.14 (6H,
2s, 2CH3), 1.04 (3H, t, CH3 of C2H5N), 2.17-2.199 (2H, d, J = 7.72 Hz, 2H8), 2.41-2.43 (2H, d, J = 16.04
Hz, 2H6), 3.25-3.29 (2CH2, q, J = 7.71 Hz, CH2 of C2H5N), 4.68-4.69 (1H, d, J = 5.35 Hz, CH-Ph), 5.08-
5.10 (1H, d of d, J = 8.13 Hz, J = 5.35 Hz, H3), 5.97-5.99 (1H, d, J = 8.13 Hz, H2), 7.12-7.15, 7.25-7.31
13
(5H, 2m, aromatic) ppm. C NMR (CDCl3, 125 MHz): δC 21.12, 27.73, 30.15 (3CH3), 28.97 (CMe2),
36.74, 40.12 (2CH2), 38.41 (CH-Ph), 52.32 (CH2 of C2H5N), 109.51 (olefinic carbon), 111.02 (olefinic
CH), 126.03, 127.56, 128.42, 129.85 (aromatic), 147.61 (=CH-N), 151.93 (=C-N), 195.23 (C=O) ppm;
MS: m/z: 281 (M+), 266 (M+-CH3), 204 (M+-77), 77, 43. Anal. Calcd for C19H23NO: C, 81.10; H, 8.24; N,
4.98. Found: C, 81.12; H, 8.26; N, 4.95.
7,8-Dihydro-7,7-dimethyl-4-phenyl-1-propylquinolin-5(1H,4H,6H)-one (4c): yellow liquid; νmax
1
(KBr): 3029, 2960 (C-H), 1716 (C=O), 1616, 1550 (C-N) cm-1; H NMR (CDCl3, 500 MHz): δH 0.94,
1.12 (6H, 2s, 2CH3), 1.01-1.02 (3H, t, CH3 of propyl), 1.69-1.74 (2H, m, CH2 of propyl), 2.20-2.22 (2H,
d, J = 7.75 Hz, 2H8), 2.42-2.44 (2H, d, J = 16.02 Hz, 2H6), 3.26-3.30, 3.48-3.52 (2H, 2m, CH2-N), 4.71-
4.72 (1H, d, J = 5.35 Hz, CH-Ph), 5.10-5.13 (1H, d of d, J = 8.13 Hz, J = 5.35 Hz, H3), 6.00-6.02 (1H, d,
13
J = 8.12 Hz, H2), 7.14-7.17, 7.27-7.34 (5H, 2m, aromatic) ppm. C NMR (CDCl3, 125 MHz): δC 11.49
(CH3 of propyl), 24.17 (CH2 of propyl), 27.72, 30.34 (2CH3), 30.12(CMe2), 37.05, 39.84 (2CH2), 37.69
(CH-Ph), 52.19 (CH2-N), 109.39 (olefinic carbon), 110.31 (olefinic CH), 126.29, 127.99, 128.60, 129.12
(aromatic), 147.24 (=CH-N), 151.85 (=C-N), 195.59 (C=O) ppm; MS: m/z: 295 (M+), 280 (M+-CH3), 218
(M+-Ph), 203 (M+-CH3, Ph), 77, 43. Anal. Calcd for C20H25NO: C, 81.31; H, 8.53; N, 4.74. Found: C,
81.30; H, 8.54; N, 4.77.
7,8-Dihydro-1-isopropyl-7,7-dimethyl-4-phenylquinolin-5(1H,4H,6H)-one (4d): yellow liquid; νmax
1
(KBr): 3023, 2963 (C-H), 1714 (C=O), 1616, 1556 (C-N) cm-1; H NMR (CDCl3, 500 MHz): δH 1.03,
1.14 (6H, 2s, 2CH3), 1.47-1.56 (6H, 2d, J = 6.68 Hz), 2.20-2.22 (2H, d, J = 7.75 Hz, 2H8), 2.40-2.42 (2H,
d, J = 16.03 Hz, 2H6), 3.37-3.83 (1H, m, CH-N), 4.58-4.59 (1H, d, J = 5.35 Hz, CH-Ph), 5.18-5.20 (1H, d

of d, J = 8.17 Hz, J = 5.35 Hz, H3), 5.98-6.01 (1H, d, J = 8.17 Hz, H2), 7.15-7.18, 7.28-7.35 (5H, 2m,
13
aromatic) ppm. C NMR (CDCl3, 125 MHz): δC 25.16, 25.63 (2CH3 of i-prop), 27.38, 30.16 (2CH3),
30.23 (CMe2), 37.13 (CH-Ph), 37.46, 40.05 (2CH2), 52.25 (CH-N), 110.05 (olefinic carbon), 112.11
(olefinic CH), 126.13, 127.85, 128.76, 129.99 (aromatic), 150.20 (=CH-N), 154.37 (=C-N), 196.02 (C=O)
ppm; MS: m/z: 295 (M+), 280 (M+-CH3), 218 (M+-Ph), 203 (M+-Ph, Me), 77, 57. Anal. Calcd for
C20H25NO: C, 81.31; H, 8.53; N, 4.74. Found: C, 81.32; H, 8.52; N, 4.77.
1-Butyl-7,8-dihydro-7,7-dimethyl-4-phenylquinolin-5(1H,4H,6H)-one (4e): yellow liquid; νmax (KBr):
3027, 2959 (C-H), 1717 (C=O), 1615, 1549 (C-N) cm-1; 1H NMR (CDCl3, 500 MHz): δH 1.01, 1.12 (6H,
2s, 2CH3), 1.02-1.03 (3H, t, CH3 of n-butyl), 1.41-1.44 (2H, six, CH2-Me of n-butyl), 1.62-1.67 (2H, m,
CH2-Et of n-butyl), 2.20-2.23 (2H, d, J = 7.71 Hz, 2H8), 2.41-2.44 (2H, d, J = 16.07 Hz, 2H6), 3.26-3.32,
3.48-3.54 (2H, 2m, CH2-N), 4.69-4.70 (1H, d, J = 5.37 Hz, CH-Ph), 5.09-5.11 (1H, d of d, J = 8.18 Hz, J
13
= 5.37 Hz, H3), 5.98-6.00 (1H, d, J = 8.18 Hz, H2), 7.13-7.16, 7.27-7.32 (5H, 2m, aromatic) ppm. C
NMR (CDCl3, 125 MHz): 14.26 (CH3 of n-butyl), 20.27 (CH2-Me of n-butyl), 27.75, 30.12 (2CH3), 30.32
(CMe2), 33.06 (CH2-Et of n-butyl), 32.39, 39.81 (2CH2), 37.03 (CH-Ph), 50.38 (CH2-N), 109.38 (olefinic
carbon), 110.39 (olefinic CH), 126.30, 127.98, 128.59, 129.11 (aromatic), 148.30 (=CH-N), 151.96 (=C-
N), 195.61 (C=O) ppm; MS: m/z: 309 (M+), 294 (M+-CH3), 232 (M+-Ph), 176 (M+-Ph, C4H8), 77, 57, 41.
Anal. Calcd for C21H27NO: C, 81.51; H, 8.79; N, 4.53. Found: C, 81.49; H, 8.78; N, 4.55.
7,8-Dihydro-1-isobutyl-7,7-dimethyl-4-phenylquinolin-5(1H,4H,6H)-one (4f): yellow liquid; νmax
1
(KBr): 3025, 2958 (C-H), 1711 (C=O), 1616, 1547 (C-N) cm-1; H NMR (CDCl3, 500 MHz): δH 0.99,
1.12 (6H, 2s, 2CH3 ), 1.01-1.02, 1.09-1.10 (6H, 2d, J = 3.96 Hz, 2CH3 of i-butyl), 1.94-1.99 (1H, m, CH
of i-butyl), 2.19-2.20 (2H, d, J = 7.72 Hz, 2H8), 2.26-2.28 (2H, d, J = 16.05 Hz, 2H6), 3.00-3.05, 3.38-
3.41 (2H, 2 d of d, J = 14.54 Hz, J = 7.54 Hz, CH2N), 4.71-4.72 (1H, d, J = 5.39 Hz, CH-Ph); 5.07-5.10
(1H, d of d, J = 7.70 Hz, J = 5.39 Hz, H3), 5.96-5.98 (1H, d, J = 7.70 Hz, H2); 7.13-7.16, 7.28-7.38 (5H,
2m, aromatic) ppm. 13C NMR (CDCl3, 125 MHz): δC 20.26, 20.46 (2CH3 of i-butyl) 27.56, 30.32 (2
CH3); 30.50 (CMe2), 32.40 (CH of i-butyl), 36.96 (CH-Ph), 38.14, 40.10 (2CH2), 57.88 (CH-N), 109.20
(olefinic carbon), 109.86 (olefinic CH), 126.29, 127.98, 128.61, 129.74 (aromatic), 148.25 (=CH-N),
152.27 (=C-N), 195.81 (C=O) ppm; MS: m/z: 309 (M+), 2294 (M+-CH3), 232 (M+-77), 84, 77, 43. Anal.
Calcd for C21H27NO: C, 81.51; H, 8.79; N, 4.53. Found: C, 81.50; H, 8.77; N, 4.56.
1-Benzyl-7,8-dihydro-7,7-dimethyl-4-phenylquinolin-5(1H,4H,6H) one (4g): yellow liquid; νmax
1
(KBr): 3031, 2978 (C-H), 1718 (C=O); 1621, 1563 (C-N) cm-1; H NMR (CDCl3, 500 MHz): δH 0.93,
1.03 (6H, 2s, 2CH3 ), 2.22-2.25 (2H, d, J = 7.75 Hz, 2H8), 2.40-2.43 (2H, d, J = 16.09 Hz, 2H6), 4.64 (2H,
s, CH2-Ph), 4.77-4.78 (1H, d, J = 5.34 Hz, CH-Ph), 5.14-5.16 (1H, d of d, J = 7.51 Hz, J = 5.34 Hz, H3),
6.07-6.08 (1H, d, J = 7.51 Hz, H2), 7.16-7.19, 7.27-7.31, 7.36-7.38, 7.42-7.45 (10H, 4m, aromatic) ppm.
13C NMR (CDCl3, 125 MHz): δC 27.93, 29.83 (2 CH3); 31.98 (CMe2), 32.49, 39.90 (2CH2), 37.09 (CH-

Ph), 53.91 (CH2 of benzyl), 109.33 (olefinic carbon), 110.46 (olefinic CH), 126.39, 126.44, 128.13,
128.18, 128.64, 129.45, 129.75, 137.91 (aromatic), 148.93 (=CH-N), 152.22 (=C-N), 195.88 (C=O) ppm;
+
MS: m/z: 343 (M+), 328 (M+-CH3), 252 (M+-91), 105 (Ph-CH2N+), 91 (PhCH2 ), 77. Anal. Calcd for
C24H25NO: C, 83.93; H, 7.34; N, 4.08. Found: C, 83.90; H, 7.35; N, 4.10.
7,8-Dihydro-7,7-dimethyl-1-phenethyl-4-phenylquinolin-5(1H,4H,6H) one (4h): yellow liquid; νmax
1
(KBr): 3038, 2956 (C-H), 1712 (C=O); 1610, 1564 (C-N) cm-1; H NMR (CDCl3, 500 MHz): δH 0.83,
1.02 (6H, 2s, 2CH3 ), 2.09-2.12 (2H, d, J = 7.81 Hz, 2H8), 2.16-2.18 (2H, d, J = 16.01 Hz, 2H6), 2.91-2.98
(2H, m, -CH2-Ph), 3.76-3.77, 4.70-4.71 (2H, 2m, CH2-N), 4.70-4.71 (1H, d, J = 5.30 Hz, CH-Ph), 5.12-
5.15 (1H, d of d, J = 7.25 Hz, J = 5.30 Hz, H3), 6.00-6.01 (1H, d, J = 7.25 Hz, H2), 7.15-7.18, 7.23-7.25,
13
7.27-7.32, 7.35-7.38 (10H, 4m, aromatic) ppm. C NMR (CDCl3, 125 MHz): δC 27.41, 30.49 (2 CH3),
31.95 (CMe2), 32.05, 39.87 (2CH2), 37.04 (CH2-benzyl), 37.12 (CH-Ph), 51.72 (CH2-N), 109.28 (olefinic
carbon), 110.77 (olefinic CH), 126.32, 127.42, 128.04, 128.48, 128.58, 129.24, 129.47, 138.12
(aromatic), 148.22 (=CH-N), 151.92 (=C-N), 195.72 (C=O) ppm; MS: m/z: 357 (M+), 342 (M+-CH3), 280
+
+
(M+-Ph), 105 (Ph-C2H4 ), 91 (PhCH2 ), 77. Anal. Calcd for C25H27NO: C, 83.99; H, 7.61; N, 3.92. Found:
C, 83.98; H, 7.60; N, 3.95.
1-Ethyl-7,8-dihydro-7,7-dimethyl-4-(4-nitrophenyl)quinolin-5(1H,4H,6H)-one (4i): orange liquid; νmax
1
(KBr): 3030, 2968 (C-H), 1722 (C=O), 1616, 1561 (C-N), 1525, 1340 (NO2) cm-1; H NMR (CDCl3, 500
MHz): δH 1.04, 1.16 (6H, 2s, 2CH3), 1.06 (3H, t, CH3 of C2H5N), 2.18-2.21 (2H, d, J = 7. 85 Hz, 2H8),
2.42-2.45 (2H, d, J = 15.98 Hz, 2H6), 3.27-3.31 (2CH2, q, J = 8.10 Hz, CH2 of C2H5N), 4.69-4.70 (1H, d,
J = 5.85 Hz, CH-Ph), 5.21-5.23 (1H, d of d, J = 9.01 Hz, J = 5.53Hz, H3), 6.00-6.02 (1H, d, J = 8.15 Hz,
13
H2), 7.58-7.61, 8.32-8.36 (4H, 2m, aromatic) ppm. C NMR (CDCl3, 125 MHz): δC 21.14, 27.79, 30.28
(3CH3), 29.01, 32.18 (3CH3), 31.18 (CMe2), 37.76, 40.93 (2CH2), 41.11 (CH-Ph), 52.05 (CH2 of C2H5N),
110.21 (olefinic carbon), 112.51 (olefinic CH), 124.42, 128.19, 129.56, 150.18 (aromatic), 148.63 (=CH-
N), 152.98 (=C-N), 196.59 (C=O) ppm; MS: m/z: 326 (M+), 311 (M+-CH3), 280 (M+-NO2), 265 (M+-CH3,
NO2), 107 (C6H5NO+), 43. Anal. Calcd for C19H22N2O3: C, 69.92; H, 6.7; N, 8.58. Found: C, 69.91; H,
6.78; N, 8.60.
1-Benzyl-7,8-dihydro-7,7-dimethyl-4-(4-nitrophenyl)quinolin-5(1H,4H,6H)-one (4j): orange liquid;
ν
max (KBr): 3033, 2972 (C-H), 1727 (C=O), 1617, 1563 (C-N), 1526, 1339 (NO2) cm-1; 1H NMR (CDCl3,
500 MHz): δH 1.04, 1.17 (6H, 2s, 2CH3), 4.65 (2H, s, CH2Ph), 4.91-4.92 (1H, d, J = 5.38 Hz, CH-Ar),
5.35-5.36 (1H, d of d, J = 7.60 Hz, J = 5.51 Hz, H3), 6.16-6.17 (1H, d, J = 7.50 Hz, H2), 7.17-7.19, 7.30-
7.32, 7.38-7.43, 8.32-8.36 (9H, 4m, aromatic) ppm. 13C NMR (CDCl3, 125 MHz): δC 27.15, 32.38,
(2CH3), 31.29 (CMe2), 37.91, 41.02(2CH2), 41.83 (CH-Ph), 52.19 (CH2 of benzyl), 110.31 (olefinic
carbon), 112.60 (olefinic CH), 125.00, 126.54, 128.12, 128.36, 128.50, 129.65, 150.47 (aromatic), 148.81
(=CH-N), 153.01 (=C-N), 196.59 (C=O) ppm; MS: m/z: 388 (M+), 373 (M+-CH3), 297 (M+-Ph-CH2), 91

+
(PhCH2 ), 77, 43. Anal. Calcd for C24H24N2O3: C, 74.21; H, 6.23; N, 7.21. Found: C, 74.20; H, 6.21; N,
7.23.
1-Ethyl-7,8-dihydro-4-(4-methoxyphenyl)-7,7-dimethylquinolin-5(1H,4H,6H)-one (4k): light yellow
1
liquid; νmax (KBr): 3019, 2953 (C-H), 1717 (C=O), 1611, 1550 (C-N), 1211, 1198 (C-O) cm-1; H NMR
(CDCl3, 500 MHz): δH 1.02, 1.15 (6H, 2s, 2CH3), 1.05 (3H, t, CH3 of C2H5N), 2.16-2.181 (2H, d, J = 7.75
Hz, 2H8), 2.42-2.44 (2H, d, J = 15.99 Hz, 2H6), 3.25-3.27 (2CH2, q, J = 7.65 Hz, CH2 of C2H5N), 3.79
(3H, S, OCH3) 4.68 (1H, d, J = 5.41 Hz, CH-Ph), 5.09-5.11 (1H, d of d, J = 8.11 Hz, J = 5.34Hz, H3),
5.98-6.00 (1H, d, J = 8.13 Hz, H2), 7.22-7.27, 7.76-7.98 (4H, 2m, aromatic) ppm. 13C NMR (CDCl3, 125
MHz): δC 21.13, 27.70, 30.11 (3CH3), 29.95 (CMe2), 36.75, 40.27 (2CH2), 38.43 (CH-Ph), 52.36 (CH2 of
EtN), 55.88 (OCH3),110.15 (olefinic carbon), 111.49 (olefinic CH), 126.73, 131.26, 131.48, 138.22,
148.75 (aromatic), 147.68 (=CH-N), 151.98 (=C-N), 195.38 (C=O) ppm; MS: m/z: 311 (M+), 296 (M+-
CH3), 280 (M+-OCH3), 189(M+-CH3, Ph), 107, 43. Anal. Calcd for C20H25NO2: C, 77.14; H, 8.09; N,
4.50. Found: C, 77.13; H, 8.10; N, 4.52.
1-Benzyl-7,8-dihydro-4-(4-methoxyphenyl)-7,7-dimethylquinolin-5(1H,4H,6H)-one (4l): yellow
1
liquid; νmax (KBr): 3029, 2965 (C-H), 1723 (C=O), 1613, 1556 (C-N), 1216, 1199 (C-O) cm-1; H NMR
(CDCl3, 500 MHz): δH 1.02, 1.16 (6H, 2s, 2CH3), 2.17-2.19 (2H, d, J = 7.70 Hz, 2 H8), 2.43-2.45 (2H, d,
J = 15.80 Hz, 2H6), 3.01-3.04 (2H, m, CH2Ph), 3.77-3.79, 4.71-4.72 (2H, 2m, CH2N), 3.81 (3H, S,
OCH3), 4.65 (1H, d, J = 5.62 Hz, H2, CHPh), 5.08-5.10 (1H, d of d, J = 8.13 Hz, J = 5.60 Hz, H3), 5.97-
5.99 (1H, d, J = 8.17 Hz, H2), 7.16-7.18, 7.30-7.24, 7.26-7.35, 7.40-7.67-7.99 (9H, 4m, aromatic) ppm.
13C NMR (CDCl3, 125 MHz): δC 27.93, 30.97 (2CH3), 31.05 (CMe2), 36.14, 39.81 (2CH2), 38.75 (CH-
Ph), 51.94 (CH2-N), 56.91 (OCH3), 110.26 (olefinic carbon), 112.23 (olefinic CH), 127.43, 128.06,
128.85, 129.24, 131.45, 131.63, 138.43, 149.06 (aromatic), 148.85 (=CH-N), 152.08 (=C-N), 197.01
(C=O) ppm; MS: m/z: 373 (M+), 358 (M+-CH3), 342 (M+-OCH3), 266 (M+-Ph), 107, 105, 92, 43. Anal.
Calcd for C25H27NO2: C, 80.40; H, 7.29; N, 3.75. Found: C, 80.39; H, 7.27; N, 3.78.
ACKNOWLEDGEMENTS
We wish to thank the Iran National Science Foundation (INSF) for the financial support.
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