Synthesis and substitution reactions of 4(6)-chlorodihydropyrimidines

Article abstract of DOI:10.3987/COM-11-12244

Chlorination of the corresponding ketones with phenylphosphonic dichloride (PhPOCl₂) provided ethyl 6(4)-chloro-2-methyl-4(6)-phenyl-1,4(6)- dihydropyrimidine-5-carboxylate in good yield. The cross-coupling reactions of organoboronic acids or t

Full text of DOI:10.3987/COM-11-12244

HETEROCYCLES, Vol. 83, No. 8, 2011
1807
HETEROCYCLES, Vol. 83, No. 8, 2011, pp. 1807 - 1818. © The Japan Institute of Heterocyclic Chemistry
Received, 27th April, 2011, Accepted, 31st May, 2011, Published online, 6th June, 2011
DOI: 10.3987/COM-11-12244
SYNTHESIS AND SUBSTITUTION REACTIONS OF 4(6)-CHLORO-
DIHYDROPYRIMIDINES
Hidetsura Cho,a,b Yoshizumi Yasui,c Satoshi Kobayashi,b Eunsang Kwon,a,d
Mieko Arisawa, b and Masahiko Yamaguchi b,c
aGraduate School of Science, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku,
Sendai, 980-8578, Japan. bGraduate School of Pharmaceutical Sciences, Tohoku
c
University. WPI Advanced Institute for Materials Research, Tohoku University.
dResearch and Analytical Center for Giant Molecules, Tohoku University, 6-3
Aoba, Aramaki, Aoba-ku, Sendai, 980-8578, Japan
E-mail: hcho@mail.pharm.tohoku.ac.jp
Abstract – Chlorination of the corresponding ketones with phenylphosphonic
dichloride (PhPOCl2) provided ethyl 6(4)-chloro-2-methyl-4(6)-phenyl-1,4(6)-
dihydropyrimidine-5-carboxylate in good yield. The cross-coupling reactions of
organoboronic acids or triethylborane with 1-tert-butyl 5-ethyl 4-chloro-2-
methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate
synthesized
by
regiospecific alkoxycarbonylation of the chlorinated dihydropyrimidine afforded
1,4(3,4)-dihydropyrimidines having a variety of functional groups at position-6(4)
in good to excellent yields.
INTRODUCTION
Dihydropyrimidine (DP) could theoretically be represented as nine isomers including tautomers when it
bears different substituted groups.1 Moreover, DPs in some cases are spontaneously oxidized during
isolation or storage. Therefore, they are unstable and sometimes difficult to handle. We reported
nucleophilic substitution at position-2 of 4-unsubstituted dihydropyrimidines A and B.2 Survey of the
literature reveals no report on synthesis of C having phenyl, alkyl, and aralkyl groups by substitution of a
chloro atom at position-4(6) of D. Recently, Zych has reported the synthesis of E by the Suzuki-Miyaura
cross-coupling reaction3 of 5-halo-3,4-dihydropyrimidin-2(1H)-ones F, which were given by reaction at

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HETEROCYCLES, Vol. 83, No. 8, 2011
position-5 of carboxylic acid G with oxone and sodium halide in basic aqueous methanol.4 The report
prompted us to disclose the first synthesis of various dihydropyrimidines H (and C) by the cross-coupling
reaction at position-4(6) of dihydropyrimidine D with organoboronic acids or organoborane. It was
expected that the skeleton I could be constructed by chlorination5 of J6 and that successive regiospecific
alkoxycarbonylation developed by Cho1c,1d could provide compound D. Alternatively, cyclization of
CO2R4
Me
6
1
N
R2O2C
R"R'N
CO2R4
Me
1
HN
2
4
CO2R4
5
3
CO2R4
R5
N
N
5
5
2
2
R1
N
R5
N
4
6
N
Me
Me
N
4
3
H
1
3
H
5
C
: R = Ph, Bzl, Et,
1
A:
R = NR'R", SMe
R4 = Et
B
CH=CHPh, thienyl
6
R2O2C
Me
CO2R4
Cl
1
N
X
R
CO2H
Me
HN
HN
N
5
2
O
N
Me
F:
X = Br, I
O
N
H
Me
Me
N
H
N
4
t
3
H
2
D
: R = Bu
R4 = Et
E: R = Ph etc.
G
NH2
NH
R6
a
6
CO2R4
O
CO2R4
Cl
CO2Et
R2O2C
Me
CO2R4
5
Me
1
N
CO2Et
N
N
b
2
N
R5
R5
O
Me
N
H
Me
N
H
O
4
3
H: R5 = Ph, Bzl, Et,
CH=CHPh, thienyl
R2 = tBu
K
L
I
J
Figure 1. A variety of dihydropyrimidines
amidines with compounds K having an alkyl or a phenyl group at R5should afford cyclized compounds,
while cyclization of amidines with unknown compounds L having a trans-2-phenylvinyl or a vinyl group
might give complicated compounds because of two reaction positions a and b of L. Therefore,
development of a new procedure for modification at postion-4(6) of dihydropyrimidines D or I would be
useful and convenient to obtain various new DPs C and H.

HETEROCYCLES, Vol. 83, No. 8, 2011
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Herein, we wish to disclose results of transformations using phenylphosphonic dichloride (PhPOCl2) or
POCl3 from J to I and successive substitutions at position-4(6) of D or I with organoboronic acids or
triethylborane.
RESULTS AND DISCUSSION
Treatment of benzaldehyde with 1.2 equivalents of diethyl malonate in the presence of 0.05 equivalents of
piperidine and 0.025 equivalents of benzoic acid afforded the , -unsaturated carbonyl compound in
85% yield, which was heated at reflux with 1.2 equivalents of acetamidine hydrochloride in 2 equivalents
of NaOEt in EtOH for 2 h to yield a single compound (trans: J=11.2 Hz), 5-ethyl
2-methyl-6-phenyl-1,4,5,6- tetrahydropyrimidin-4-one-5-carboxylate 1 in 67% yield.6 Generally, it is
difficult to maintain chlorinated dihydroheterocycles even under argon atmosphere. According to the
literature,5a,5b chlorination of dihydropyrazinones M, dihydropyridazinones N, dihydropyrimidin-2-ones
O, or dihydropyridines P with POCl3 did not give dihydroheterocycles because of over-chlorination and
dehydrochlorination, but yielded aromatized heterocycles m, n-1, n-2, or p, respectively (Figure 2).
However, we obtained 4(6)-chloro-1,4(6)-dihydropyrimidine 2 using excess phenylphosphonic dichloride
(PhPOCl2) (110 oC, for 5 h) as well as 5 equivalents of POCl3 (110 oC, for 4 h) in 60% yield.
Figure 2. Unsuccessful chlorination of various dihydroheterocycles
Alkoxycarbonylation of the sodium salt of 2 (prepared with 60% NaH) with 2 equivalents of di-tert-butyl
dicarbonate (Boc2O) regiospecifically furnished the sole compound 3 in 86% yield.1c,1d The chemical
structure of 3 was determined by NMR analysis (HMBC and NOE). Thus, the regiospecificity of Boc
protection was confirmed by three-bond long-range coupling (hetero-nuclear multiple bond connectivity:
HMBC) between methine protons at position-6 and the carbonyl carbon of the Boc group. Also, when the
protons of the t-Bu group (= 1.55) of 3 were irradiated, a positive NOE (0.6%) was observed at H-4 (=

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HETEROCYCLES, Vol. 83, No. 8, 2011
6.26). Suzuki-Miyaura cross-coupling reaction at position-4 of 3 with organoboronic acids or
triethylborane was carried out. Thus, the reaction of dihydropyrimidine 3 and 1.5 equivalents of
Figure 3. Dihydropyrimidines 1-5
Table 1. Optimization of the Cross Coupling Reaction at Position-4 of Dihydropyrimidine 3
5 mol% catalyst
tBuO2C
Me
CO2Et
tBuO2C
Me
CO2Et
Cl
1.5 eq. phenylboronic acid
N
N
N
N
2.0 eq. Cs2CO3 or K2CO3
THF reflux, or DMA, 60 oC
3
4a
Entry
Catalyst
5 mol% NiCl2(PPh3)2
5 mol% Pd(PPh3)4
5 mol% PdCl2(PPh3)2
5 mol% PdCl2(PPh3)2
5 mol% PdCl2(PPh3)2
Base
Solvent
THF
THF
THF
DMA
DMA
Temp (oC) Time (h) Yielda (%)
1
2
3
4
5
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
K2CO3
reflux
reflux
reflux
60
5
3
3
4
4
0 (82)a
4 (63)
34 (58)
85 (0)
60
62 (25)
a The values in parentheses show the recovered yield of compound 3.
phenylboronic acid with either bis(triphenylphosphine)nickel (II) dichloride; NiCl2(PPh3)2,
tetrakis(triphenylphosphine)palladium(0); Pd (PPh3)4, or bis(triphenylphosphine)palladium (II)
dichloride; PdCl2(PPh3)2 was examined in the presence of 2 equivalents of Cs2CO3 or K2CO3 in THF or N,
N-dimethylacetamide (DMA), respectively (Table 1).

HETEROCYCLES, Vol. 83, No. 8, 2011
1811
Initially, the reaction of 3 with phenylboronic acid did not occur under conditions of 5 mol%
NiCl2(PPh3)2 and 2 equivalents of Cs2CO3 in THF at reflux for 5 h, but resulted in recovery of the starting
material (Table 1, Entry 1). Changing the catalyst to Pd (PPh3)4, 4a was obtained in a poor yield (Entry 2).
Using 5 mol% PdCl2(PPh3)2, the cross-coupling reaction of 3 with 1.5 equivalents of phenylboronic acid
was carried out to afford compound 4a in a modest yield (Entry 3). Subsequently, the solvent was
replaced with DMA. Thus, treatment of 3 with 1.5 equivalents of phenylboronic acid in the presence of 5
o
mol% PdCl2(PPh3)2 and 2 equivalents of Cs2CO3 in DMA at 60 C provided dihydropyrimidine 4a in
85% yield (Entry 4). As the base, K2CO3 was employed instead of Cs2CO3 under the same reaction
conditions as entry 4. The yield, however, was lower than that of the reaction using Cs2CO3 (Entry 5).
Therefore, PdCl2(PPh3)2 was selected as the catalyst for the other substrates. Thus, the reactions using the
organoboronic acids with electron-donating or electron-withdrawing groups on a phenyl ring were studied.
The reaction of 3 with o-tolylboronic acid in the presence of 5 mol% PdCl2(PPh3)2 unsatisfactorily
proceeded to give 4b contaminated with a small amount of the starting material recovered, because it is
not easy to separate both starting material 3 and compound 4b by silica gel column chromatography. This
may be due to lower reactivity because of steric hindrance of the methyl group of o-tolylboronic acid.
Table 2. Cross Coupling Reaction of Dihydropyrimidines at Position-4
Entry
R
Reagent
Time (h)
Compound 4
Yield (%)
1
2
3
4
C6H5
C6H5B(OH)2
4
6
3
6
4a
4b
4c
4d
85
99a
92
69
C6H4Me-2
C6H4OMe-4
C6H4NO2-4
2-MeC6H4B(OH)2
4-MeOC6H4B(OH)2
4-NO2C6H4B(OH)2
5
4
4e
90
6
7
Et
Et3B
4
4
4f
83
91
4g
a 10 mol% of PdCl2(PPh3)2, 3 eq. of organoboronic acid, 4 eq. of Cs2CO3.
Therefore, we employed 10 mol% catalyst to consume the starting material and to complete the reaction.
Thus, compound 4b was obtained quantitatively using 10 mol% PdCl2(PPh3)2 (Table 2, Entry 2). The
reaction of 3 with 4-methoxyphenylboronic acid having an electron-donating group (OMe) furnished

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HETEROCYCLES, Vol. 83, No. 8, 2011
product 4c in excellent yield (Table 2, Entry 3), but the yield of 4d was 69% in the case of an
electron-withdrawing group (NO2) (Entry 4). The remarkable result was found that dihydropyrimidine 4e
having a trans-2-phenylvinyl group at postion-4 was provided in 90% yield, which might not be given by
the alternative cyclization reaction (Entry 5). Introduction of an ethyl group was carried out using
ethylboronic acid, but 4f was not obtained. Therefore, other reaction conditions were examined using
triethylborane, and 4f was provided in 83% yield (Entry 6). Regarding introduction of a heterocyclic
moiety, for instance, a thienyl group, the cross-coupling reaction of 3 with 3-thienylboronic acid was
performed to furnish 4g in 91% yield (Entry 7).
Table 3. Deprotection of dihydropyrimidine 4
Entry
R
Compound 5
Yield (%)
1
2
3
4
5
6
C6H5
5a
5b
5c
5d
5e
5f
96
90
86
89
78
98
C6H4Me-2
C6H4OMe-4
C6H4NO2-4
Et
7
5g
93
Subsequently, deprotection of a Boc group was performed under the reaction conditions of CF3COOH
(TFA)-CH2Cl2 at rt for 1 h. Dihydropyrimidines 5a-5g were obtained in good yields.
On the other hand, to obtain compound 5 directly, the cross-coupling reaction of 2 with phenylboronic
acid in the presence of 5 mol% PdCl2(PPh3)2 was carried out, but product 5 was not obtained and the
starting material was recovered, although the reason is unclear.
In summary, substitution of 1-tert-butyl 5-ethyl 4-chloro-2-methyl-6-phenyl-1,6-dihydropyrimidine-
1,5-dicarboxylate 3 synthesized from the corresponding ketone and phenylphosphonic dichloride
(PhPOCl2) was performed with organoboronic acids or organoborane to afford dihydropyrimidines 4
having a variety of moieties at position-4 in good yields. Deprotection of 4 with TFA provided various
5-ethyl 6(4)-substituted-2-methyl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylates 5, which may be
useful for biological applications. In addition, the cross-coupling reaction at position-4 should be useful

HETEROCYCLES, Vol. 83, No. 8, 2011
1813
because it can be applied to synthesize other dihydropyrimidines having various functional groups at
position-2, 4(6), or -5.
EXPERIMENTAL
General: Unless otherwise noted, reactions were performed under argon. Melting points were determined
on a Yanaco micro melting point apparatus and uncorrected. IR spectra were measured on a SHIMADZU
1
FTIR-8300 spectrometer. H-NMR spectra were recorded on a Varian Mercury (400 MHz) or a Bruker
AVANCE III 600 (600 MHz) with tetramethylsilane (0 ppm), CD3OD (3.30 ppm), CD3CN (1.93 ppm), or
DMSO-d6 (2.49 ppm) as an internal standard. The abbreviations of signal patterns are follows: s, singlet;
d, doublet; t, triplet; q, quartet; m, multiplet; br, broad. 13C-NMR spectra were recorded on a Varian
Mercury (400 MHz) or a Bruker AVANCE III 600 (600 MHz) with CDCl3 (77.0 ppm), CD3OD (49.0
ppm), CD3CN (1.30 ppm), or DMSO-d6 (39.7 ppm) as an internal standard. Mass spectra were recorded
on a JMS-DX303, JMS-700, or JMS-T100GC spectrometer. Flash column chromatography was
performed on silica gel 60N (Kanto, 40-60 mm) using the indicated solvent. Reactions and
chromatography fractions were monitored with pre-coated silica gel 60 F254 plates (Merck).
Ethyl 6(4)-chloro-2-methyl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylate (2): A mixture of
ethyl 2-methyl-4-phenyl-1,4,5,6-tetrahydropyrimidin-6-one-5-carboxylate 1 (633 mg, 2.43 mmol) and
phenylphosphonic dichloride (5 mL, 35.26 mmol) was heated at 110 oC for 5 h. The reaction mixture was
poured into ice-cooled saturated aqueous NaHCO3. After adding aqueous 2M NaOH, the organic
materials were extracted with EtOAc. The combined organic extracts were washed with saturated
aqueous NaHCO3 and brine, dried over Na2SO4, and concentrated under reduced pressure. The residue
was purified by silica gel column chromatography (EtOAc) to give chloride 2 (406 mg, 60%) as yellow
crystals; mp 155-156 °C (Et2O); IR (KBr) 2979, 2846, 1682, 1604, 1514, 1323, 1250, 1117 cm1;
1H-NMR (400 MHz, CD3OD)  1.11 (3H, t, J = 7.2 Hz), 1.98 (3H, s), 3.974.09 (2H, m), 5.55 (1H, s),
7.27-7.37 (5H, m); 13C-NMR (100 MHz, CD3OD)  14.4, 20.9, 57.1, 61.4, 102.8, 127.9, 129.5, 129.9,
145.4, 148.7, 161.9, 166.1; LRMS (EI) m/z 278 (M+); HRMS (EI) m/z Calcd for C14H15ClN2O2 (M+)
278.0822, Found: 278.0820.
1-tert-Butyl 5-ethyl 4-chloro-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate (3): To
sodium hydride (60% dispersion in mineral oil, 89.4 mg, 2.24 mmol) was added a solution of 2 (406 mg,
1.46 mmol) in DMF (5 mL) and a solution of di-tert-butyl dicarbonate (645 mg, 2.96 mmol) in DMF (3
mL) at 0 oC. After stirring for 30 min at rt, water was added and the organic materials were extracted with
toluene. The combined organic extracts were washed with water and brine, dried over Na2SO4, and

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HETEROCYCLES, Vol. 83, No. 8, 2011
concentrated under reduced pressure. The residue was purified by silica gel column chromatography
(n-hexane:toluene:EtOAc = 50:50:0 → 50:48:2) to give the carbamate 3 (474 mg, 86%) as pale yellow
crystals; mp 106-107 °C (n-hexane-Et2O); IR (KBr) 2981, 1724, 1693, 1558, 1369, 1230, 1151, 1091
1
cm1; H-NMR (400 MHz, CDCl3)  1.25 (3H, t, J = 7.2 Hz), 1.55 (9H, s), 2.42 (3H, s), 4.134.26 (2H,
m), 6.26 (1H, s), 7.31 (5H, brs); 13C-NMR (100 MHz, CDCl3)  14.0, 25.7, 28.0, 55.7, 61.1, 84.8, 111.5,
126.9, 128.6, 128.7, 139.2, 143.5, 151.3, 158.4, 163.7; LRMS (EI) m/z 378 (M+); HRMS (EI) m/z Calcd
for C19H23ClN2O4 (M+) 378.1346, Found: 378.1339.
1-tert-Butyl 5-ethyl 2-methyl-4,6-diphenyl-1,6-dihydropyrimidine-1,5-dicarboxylate (4a): A solution
of 3 (46.2 mg, 0.122 mmol), phenylboronic acid (22.1 mg, 0.181 mmol), bis(triphenylphosphine)-
palladium(II) dichloride PdCl2(PPh3)2 (4.5 mg, 0.0064 mmol), and Cs2CO3 (81.3 mg, 0.249 mmol) in
DMA (2 mL) was carefully degassed three times with freeze-pump-thaw cycles under argon atmosphere
o
and heated for 4 h at 60 C. The reaction mixture was diluted with water and the organic materials were
extracted with toluene. The combined organic extracts were washed with brine, dried over Na2SO4 and
concentrated under reduced pressure to give the residue, which was purified by silica gel column
chromatography (toluene:EtOAc = 10:0 → 97:3) to afford compound 4a (43.5 mg, 85%); pale yellow
crystals (needles); mp 96-97 °C (CHCl3); IR (KBr) 2979, 2933, 1707, 1572, 1371, 1230, 1138, 1032
cm1; 1H-NMR (400 MHz, CDCl3) 0.894 (3H, t, J = 7.2 Hz), 1.57 (9H, s), 2.41 (3H, s), 3.874.02 (2H,
m), 6.30 (1H, s), 7.28-7.39 (8H, m), 7.49-7.51 (2H, m); 13C-NMR (100 MHz, CDCl3)  13.5, 25.6, 28.1,
54.3, 60.5, 83.8, 114.3, 127.1, 127.8, 128.2, 128.53, 128.58, 128.64. 137.9, 139.6, 151.0, 151.9, 154.9,
166.3. LRMS (EI) m/z 420 (M+); HRMS (EI) m/z Calcd for C25H28N2O4 (M+) 420.2049, Found:
420.2053.
1-tert-Butyl 5-ethyl 2-methyl-6-phenyl-4-o-tolyl-1,6-dihydropyrimidine-1,5-dicarboxylate (4b): A
solution of 3 (45.0 mg, 0.119 mmol), o-tolylboronic acid (48.5 mg, 0.357 mmol), PdCl2(PPh3)2 (8.39 mg,
0.0120 mmol) and Cs2CO3 (156 mg, 0.479 mmol) in DMA (2.5 mL) was degassed three times with
freeze-pump-thaw cycles under argon atmosphere and heated for 6 h at 60 °C. Water was added to the
reaction mixture and the organic materials were extracted with EtOAc. The combined organic extracts
were washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure. The
residue was purified by silica gel column chromatography (n-hexane:EtOAc = 10:0 → 9:1) to give
compound 4b (51.1 mg, 99%) as a colorless oil. IR (neat) 2979, 1720, 1566, 1493, 1369, 1230, 1153,
1
1095 cm-1; H-NMR (400 MHz, CD3CN)  0.790 (3H, t, J = 7.2 Hz), 1.56 (9H, s), 2.24 (3H, brs), 2.34
(3H, s), 3.77-3.91 (2H, m), 6.26 (1H, s), 7.07-7.41 (9H, m); 13C-NMR (100 MHz, CD3CN)  13.8, 19.6,
25.8, 28.2, 54.5, 61.2, 84.9, 116.0, 126.2, 127.7, 128.7, 128.7, 129.3, 129.7, 130.5, 136.5, 139.7, 141.1,

HETEROCYCLES, Vol. 83, No. 8, 2011
1815
152.8, 153.0, 156.2, 166.3; LRMS (EI) m/z 434 (M+); HRMS (EI) m/z Calcd for C26H30N2O4 (M+)
434.2206, Found: 434.2197.
1-tert-Butyl 5-ethyl 4-p-methoxyphenyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate
(4c): pale yellow crystals; mp 57-58 °C (CHCl3); IR (KBr) 2979, 2833, 1707, 1574, 1371, 1248, 1034
1
cm1; H-NMR (400 MHz, CDCl3)  0.97 (3H, t, J = 7.2 Hz), 1.56 (9H, s), 2.39 (3H, s), 3.83 (3H, s),
3.91-4.06 (2H, m), 6.28 (1H, s), 6.89-6.92 (2H, m), 7.25-7.38 (5H, m), 7.48-7.51 (2H, m); 13C-NMR (100
MHz, CDCl3)  13.7, 25.5, 28.1, 54.4, 55.3, 60.5, 83.6, 113.2, 113.2, 127.1, 128.2, 128.6, 129.8, 130.3,
139.8, 150.6, 151.9, 154.5, 160.2, 166.5; LRMS (EI) m/z 450 (M+); HRMS (EI) m/z Calcd for
C26H30N2O5 (M+) 450.2155, Found: 450.2162.
1-tert-Butyl 5-ethyl 2-methyl-4-p-nitrophenyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate
(4d): yellow crystals; mp 97-98 °C (CHCl3); IR (KBr) 3068, 2974, 2939, 1714, 1525, 1348, 1232 cm1;
1H-NMR (400 MHz, CDCl3)  0.94 (3H, t, J = 7.2 Hz), 1.58 (9H, s), 2.43 (3H, s), 3.93-4.02 (2H, m), 6.31
(1H, s), 7.29-7.38 (5H, m), 7.65-7.67 (2H, m), 8.23-8.26 (2H, m); 13C-NMR (100 MHz, CDCl3)  13.6,
25.7, 28.1, 54.3, 60.9, 84.3, 115.7, 123.0, 127.0, 128.5, 128.8, 129.7, 139.2, 144.7, 147.7, 149.2, 151.7,
156.2, 165.3; LRMS (EI) m/z 465 (M+); HRMS (EI) m/z Calcd for C25H27N3O6 (M+) 465.1900, Found:
465.1931.
1-tert-Butyl 5-ethyl 2-methyl-6-phenyl-4-trans-styryl-1,6-dihydropyrimidine-1,5-dicarboxylate (4e):
1
a yellow oil; IR (neat) 2979, 2933, 1720, 1620, 1369, 1238, 1153 cm1; H-NMR (400 MHz, CDCl3) 
1.26 (3H, t, J = 7.2 Hz), 1.56 (9H, s), 2.44 (3H, s), 4.15-4.27 (2H, m), 6.27 (1H, s), 7.25-7.37 (8H, m),
7.59-7.61 (2H, m), 7.76 (1H, d, J = 15.6 Hz), 8.22 (1H, d, J = 15.6 Hz); 13C-NMR (100 MHz, CDCl3) 
14.2, 25.7, 28.2, 53.8, 60.6, 83.6, 111.7, 123.3, 127.2, 127.6, 128.1, 128.5, 128.57, 128.62, 137.0, 137.3,
140.0, 148.1, 151.9, 155.5, 165.6; LRMS (EI) m/z 446 (M+); HRMS (EI) m/z Calcd for C27H30N2O4 (M+)
446.2206, Found: 446.2207.
1-tert-Butyl 5-ethyl 4-ethyl-2-methyl-6-phenyl-1,6-dihydropyrimidine-1,5-dicarboxylate (4f): A
solution of 3 (53.5 mg, 0.141 mmol), triethylborane (1 M in hexane, 0.200 mL, 0.200 mmol),
PdCl2(PPh3)2 (4.5 mg, 0.00642 mmol) and Cs2CO3 (95.2 mg, 0.292 mmol) in N, N-dimethylacetamide (2
mL) was degassed twice with freeze-pump-thaw cycles under argon atmosphere and heated for 4 h at 60
oC. The reaction mixture was diluted with water and the organic materials were extracted with toluene.
The combined organic extracts were washed with water and brine, dried over Na2SO4, and concentrated
under reduced pressure. The residue was purified by silica gel column chromatography (toluene:EtOAc =

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HETEROCYCLES, Vol. 83, No. 8, 2011
10:0 → 97:3) to give compound 4f (43.7 mg, 83%); yellow crystals; mp 70-71 °C (CHCl3); IR (KBr)
2979, 2935, 1730, 1631, 1577, 1225, 1099 cm1; 1H-NMR (400 MHz, CDCl3)  1.22 (3H, t, J = 7.2 Hz),
1.23 (3H, t, J = 7.2 Hz), 1.56 (9H, s), 2.35 (3H, s), 2.71 (1H, dq, J = 7.2, 12.4 Hz), 2.88 (1H, dq, J = 7.2,
12.4 Hz), 4.09-4.21 (2H, m), 6.14 (1H, s), 7.23-7.30 (5H, m); 13C-NMR (100 MHz, CDCl3) 12.6, 14.1,
25.4, 27.1, 28.1, 53.3, 60.4, 83.6, 111.5, 127.0, 128.0, 128.4, 140.0, 151.9, 155.6, 157.1, 165.7; LRMS
(EI) m/z 372 (M+); HRMS (EI) m/z Calcd for C21H28N2O4 (M+) 372.2049, Found: 372.2045.
1-tert-Butyl 5-ethyl 2-methyl-6-phenyl-4-(thiophen-3-yl)-1,6-dihydropyrimidine-1,5-dicarboxylate
1
(4g): yellow crystals; 77-79 °C (CHCl3); IR (KBr) 3093, 2979, 2933, 1702, 1574, 1230 cm1; H-NMR
(400 MHz, CDCl3)  1.05 (3H, t, J = 7.2 Hz), 1.56 (9H, s), 2.38 (3H, s), 3.99-4.12 (2H, m), 6.28 (1H, s),
7.25-7.38 (7H, m), 7.72 (1H, dd, J1 = J2 = 2.0 Hz); 13C-NMR (100 MHz, CDCl3)  13.8, 25.5, 28.1, 54.4,
60.7, 83.7, 113.2, 124.3, 127.0, 127.1, 128.2, 128.5, 128.6, 138.0, 140.0, 145.4, 151.9, 154.8, 166.3;
LRMS (EI) m/z 426 (M+); HRMS (EI) m/z Calcd for C23H26N2O4S (M+) 426.1613, Found: 426.1606.
Deprotection of
4
with trifluoroacetic acid: 5-Ethyl 2-methyl-4,6-diphenyl-1,4(6)-
dihydropyrimidine-5-carboxylate (5a): To a stirred solution of 4a (40.1 mg, 0.0955 mmol) in CH2Cl2
o
(1 mL) was added trifluroacetic acid (0.75 mL, 10.1 mmol,) at 0 C. Stirring was continued at room
temperature for 1 h. The reaction mixture was basified with saturated aqueous NaHCO3 and extracted
with EtOAc. The combined organic layer was washed with saturated aqueous NaHCO3 and brine, dried
over Na2SO4, and concentrated under reduced pressure to leave the residue. Purification by silica gel
column chromatography (n-hexane:EtOAc:MeOH = 8:2:0 → 0:95:5) provided compound 5a (29.4 mg,
96%); colorless crystals; mp 212-213 °C (n-hexane-Et2O); IR (KBr) 3030, 2981, 2868, 2731, 1674, 1504,
1234, 1084, 966 cm-1; 1H-NMR (400 MHz, CD3CN)  0.79 (3H, t, J = 7.2 Hz), 1.93 (3H, s), 3.76 (2H, q,
J = 7.2 Hz), 5.50 (1H, s), 7.24-7.42(10H, m); 13C-NMR (100 MHz, CD3CN) 14.0, 21.4, 58.3, 60.2,
101.6, 128.0, 128.2, 128.7, 129.3, 129.4, 129.6, 138.4, 146.7, 150.1, 153.3, 167.5; LRMS (EI) m/z 320
(M+); HRMS (EI) m/z Calcd for C20H20N2O2 (M+) 320.1525, Found: 320.1526.
5-Ethyl 2-methyl-6(4)-(2-methyl)phenyl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylate (5b):
colorless crystals; mp 200-201 °C (n-hexane-Et2O); IR (KBr) 3163, 3033, 2898, 1678, 1496, 1371, 1338,
1082 cm-1; 1H-NMR (400 MHz, CD3CN)  0.74 (3H, t, J = 7.2Hz), 0.74* (t, J = 7.2Hz), 1.89* (s), 1.91
(3H, s), 2.23 (3H, s), 2.23* (s), 3.643.72 (2H, m), 3.643.72* (m), 5.51* (s), 5.54 (1H, s), 7.09-7.45 (9H,
13
m), 7.09-7.45* (m); C-NMR (100 MHz, CD3CN) 13.9, 13.9*, 19.2*, 19.5, 21.2*, 21.4, 58.5*, 59.1,
60.0, 60.0*, 101.8, 102.5*, 126.29*, 126.35, 128.0, 128.1*, 128.1, 128.1*, 128.6, 128.6*, 129.1, 129.1*,
129.3, 129.4*, 130.4, 130.5*, 136.1, 137.2*, 138.0, 138.0*, 146.9*, 147.2, 148.5, 149.2*, 152.3, 152.3*,

HETEROCYCLES, Vol. 83, No. 8, 2011
1817
166.9*, 167.0; LRMS (EI) m/z 334 (M+); HRMS (EI) m/z Calcd for C21H22N2O2 (M+) 334.1681, Found:
1
13
334.1675. (Two isomers were observed in both H-NMR and C-NMR spectra, and the signals with a
mark <*> indicate a minor isomer.2) 
5-Ethyl 2-methyl-6(4)-(4-methoxy)phenyl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylate (5c):
pale yellow crystals; mp 159-160 °C (n-hexane-Et2O); IR (KBr) 3296, 3120, 3028, 2906, 2835, 1701,
1649, 1510, 1242, 1032cm-1; 1H-NMR (400 MHz, CD3CN)  0.85 (3H, t, J = 7.2 Hz), 1.92 (3H, s),
3.73-3.85 (2H, m), 3.80 (3H, s), 5.47 (1H, s), 6.90-6.92 (2H, m), 7.24-7.41 (7H, m); 13C-NMR (100 MHz,
CD3CN) 14.1, 21.4, 56.0, 58.6, 60.2, 100.6, 114.0, 128.0, 128.1, 129.4, 130.1, 131.0, 146.8, 149.6,
152.9, 161.2, 167.7; LRMS (EI) m/z 350 (M+); HRMS (EI) m/z Calcd for C21H22N2O3 (M+) 350.1630,
Found: 350.1615.
5-Ethyl 2-methyl-6(4)-(4-nitro)phenyl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylate (5d):
yellow crystals; 83-84 °C (n-hexane-Et2O); IR (KBr) 3309, 2979, 1685, 1591, 1518, 1348, 1236, 1099
cm-1; 1H-NMR (400 MHz, CD3CN)  0.79 (3H, t, J = 7.2 Hz), 1.94 (3H, s), 3.76 (2H, q, J = 7.2 Hz), 5.51
(1H, s), 7.27-7.43(5H, m), 7.53 (2H, d, J = 8.8 Hz), 8.18 (2H, d, J = 8.8 Hz); 13C-NMR (100 MHz,
CD3CN) 13.9, 21.8, 56.3, 60.6, 104.4, 123.8, 127.9, 128.8, 129.6, 130.4, 146.2, 147.5, 148.5, 151.9,
157.0, 166.9; LRMS (EI) m/z 365 (M+); HRMS (EI) m/z Calcd for C20H19N3O4 (M+) 365.1376, Found:
365.1363.
5-Ethyl 2-methyl-6(4)-trans-styryl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylate (5e): yellow
crystals; mp 155-157 °C (n-hexane-Et2O); IR (KBr) 3386, 2979, 1691, 1618, 1589, 1552, 1493, 1219,
1049 cm-1; 1H-NMR (400 MHz, CD3CN)  1.17 (3H, t, J = 7.2 Hz), 2.01 (3H, s), 4.06 (2H, q, J = 7.2 Hz),
13
5.47 (1H, s), 7.22-7.56 (11H, m), 8.11 (1H, d, J = 15.6 Hz); C-NMR (100 MHz, CD3CN) 14.5, 22.2,
56.2, 60.8, 104.6, 124.8, 127.8, 128.2, 128.5, 129.50, 129.54, 129.9, 135.3, 137.9, 146.7, 148.9, 156.6,
167.5; LRMS (EI) m/z 346 (M+); HRMS (EI) m/z Calcd for C22H12N2O2 (M+) 346.1681, Found:
346.1669.
5-Ethyl 6(4)-ethyl-2-methyl-4(6)-phenyl-1,4(6)-dihydropyrimidine-5-carboxylate (5f): colorless
crystals (needles); mp 135-136 °C (n-hexane-AcOEt); IR (KBr) 3180, 3062, 3027, 2978, 2924, 2800,
1685, 1510, 1456, 1248, 1109 cm-1; 1H-NMR (400 MHz, CDCl3)  1.15 (3H, t, J = 7.2Hz), 1.22 (3H, t, J
= 7.6 Hz), 1.97 (3H, s), 2.65-2.82 (2H, m), 4.02-4.08 (2H, m), 5.51 (1H, s), 7.20-7.33 (5H, m); 13C-NMR
(100 MHz, CDCl3) 12.6, 14.1, 21.3, 26.0, 57.6, 59.6, 99.9, 127.1, 127.2, 128.4, 145.3, 151.4, 152.2,
166.4; LRMS (EI) m/z 272 (M+); HRMS (EI) m/z Calcd for C16H20N2O2 (M+) 272.1525, Found:

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HETEROCYCLES, Vol. 83, No. 8, 2011
272.1514.
5-Ethyl 2-methyl-4(6)-phenyl-6(4)-(thiophen-3-yl)-1,4(6)-dihydropyrimidine-5-carboxylate (5g):
pale yellow crystals; mp 167-168 °C (n-hexane-Et2O); IR (KBr) 3107, 3030, 2981, 2850, 2723, 1672,
1495, 1236, 1086 cm-1; 1H-NMR (400 MHz, CD3CN)  0.92 (3H, t, J = 7.2 Hz), 1.93 (3H, s), 3.79-3.90
(2H, m), 5.47 (1H, s), 7.12 (1H, dd, J = 1.6 , 5.2 Hz), 7.23-7.40 (6H, m), 7.50 (1H, dd, J = 1.6, 3.2Hz);
13C-NMR (100 MHz, CD3CN)  14.1, 21.5, 58.3, 60.4, 101.8, 125.4, 126.5, 128.0, 128.2, 129.4, 129.7,
138.5, 144.8, 146.6, 153.6, 167.6; LRMS (EI) m/z 326 (M+). HRMS (EI) m/z Calcd for C18H18N2O2S
(M+) 326.1089, Found: 326.1074.
ACKNOWLEDGEMENTS
The authors appreciate Mr. Takaaki Suzuki for taking the HMBC and the NOE spectra of compound 3
and thank Mr. Shin-ichiro Yoshida for his useful experiments and suggestions. This work was carried out
with the financial support of Japan Tobacco INC. to H.C. and of the Tohoku University G-COE program
‘IREMC’.
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