Current Chemistry Letters 1 (2012) 59–68

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Current Chemistry Letters

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Synthesis of novel dihydropyrimidin-2(1H)-ones derivatives using lipase and their

antimicrobial activity

Bhushan N. Borse, Vasant S. Borude, and Sanjeev R. Shukla*

Department of Fibres and Textile Processing Technology, Institute of Chemical Technology (University under Section-3 of UGC Act 1956), Matunga,
Mumbai 400019, India
ARTICLE INFO ABSTRACT
Article history: A series of novel dihydropyrimidin-2(1H)-ones derivatives was synthesized by using Rhizopus
Received January 11, 2012 Oryzae lipase biocatalyst in deep eutectic solvent. The reaction is characterized by high
Received in Revised form efficiency and selectivity, short reaction time, mild and environmentally friendly reaction
Feb 19, 2011 conditions. The yields were found to be significantly higher and reuse of both the lipase and
Accepted 2 March 2011 deep eutectic solvent was possible up to four consecutive cycles. The products are found to
Available online
exhibit appreciable in vitro antibacterial activity against Echerichia coli, Pseudomonas
2 March 2012
neumoniae and in vitro antifungal activity against Aspergillus niger and Candida albicans.
Keywords:
Biological activity
Rhizopus Oryzae
Biocatalyst
Deep Eutectic Solvent
Ionic Liquids © 2012 Growing Science Ltd. All rights reserved.

1. Introduction

Dihydropyrimidin-2(1H)-ones (DHPMs) moieties are common in a variety of biologically

important natural products and potent drugs including anti-hypertensive agents, anti-carcinogenic
agents, anti-inflammatory, analgesic agents and calcium channel blockers1-3. DHPMs are also
screened as neuropeptide antagonists agents in treating anxiety and recently, as anti-oxidants4.
Barrow et al5. reported that the biologically active DHPMs derivatives exhibited α1a-adrenoceptor
antagonist properties and some of them such as monastrol showed anticancer activity against mitotic
kinesin6. Tamaddon et al.7 recently reported the synthesis of DHPMs using ammonium carbonate as
base. However, in this method both Hantzsch and Biginelli products are formed.

* Corresponding author. Tel.: +91 22-2414 5614

E-mail addresses: [email protected] (S. R. Shukla)

© 2011 Growing Science Ltd. All rights reserved.

doi: 10.5267/j.ccl.2012.3.001
60

Debache et al.8 investigated the use of triphenylphosphine as a Lewis base catalyst for the
synthesis of DHPMs derivatives. It has been also reported by using imidazole based ionic liquids
(ILs) such as water tolerant Lewis acid [bmim][FeCl4]9, [bmim]BF4 and [bmim]PF610.

Use of the ILs as a reaction medium for biocatalysis has attracted great attention in recent years,
as the processes are green and the ILs have several advantages compared to conventional reaction
media11-14. However, imidazole base ILs containing anions BF4- and PF6- are not environmentally
safe as they liberate hazardous HF gas and also their high costs and disposability problems make their
use limited15.

As an alternative approach to overcome these drawbacks, we used deep eutectic solvent (DES)
which is nontoxic, cheap, easily available and also possesses biodegradability. The used DES was a
mixture of choline chloride and urea, resulting in a very large depression of freezing point. The
solvent and physical properties of DES are similar to ILs16. Both choline chloride and urea are
naturally occurring biocompatible compounds that are environmentally safe if released back into
nature as a choline or its DES17.

Biocatalysis is an efficient and green tool for modern organic synthesis due to its high selectivity
and mild conditions18-19. Biocatalytic promiscuities provide new tool for organic synthesis and thus
expand largely the applications of enzymes. The lipase from Rhizopus Oryzae as a biocatalyst is well
known in organic synthesis due to its easy availability, selectivity and stability20. Although it has
found applications in ester hydrolysis21, knoevenagel condensation22 and mannich reaction23, the
application in synthesis of DHPMs derivatives has not been well explored.

In the last two decades, chemists have paid much attention to the clean synthesis leading to
introduction of efficient and green methodology24. Earlier we have reported the synthesis of novel
styryl colorants22 and synthesis of trisubstituted alkenes25 by using lipase as a biocatalyst. In
continuation, we report herein for the first time environmentally-benign base catalyzed synthesis of
novel DHPMs using lipase biocatalyst in DES and their antimicrobial activity.

2. Results and Discussion

X HN NH
O O Lipase, DES
Ar-CHO + + Ar Me
R Me H2N NH2 55 °C
COR

1a-g 2a-b 3a-b 4a-g

Where R= OEt, Me, X= O, S

Scheme 1: General Reaction Scheme for synthesis of DHPMs 4a-g

The reaction of aromatic aldehydes 1a, ethyl acetoacetate 2a and urea 3a was selected as a model
reaction for optimizing the reaction parameters (Scheme 1) such as molar ratio, effects of solvents,
catalysts study, catalysts amount, and reusability. Base catalyzed Biginelli reaction has been shown to
be more effective in terms of reaction time, conversion and isolated yield compared to the acid
catalyzed reaction26-30. Synthesis of DHPMs derivatives by using base catalyst has not been well
explored. Therefore, we have employed base catalyzed synthesis of DHPMs derivatives.
 B. N. Borse et al. / Current Chemistry Letters 1 (2012) 61

As shown in Table 1 (entries 1, 2) our attempt to perform the model reaction using conventional
catalyst such as K2CO3 and t-BuOK, yielded the product 4a in 65-79 % after reacting at 55 0C for 6-7
h. The model reaction using biocatalyst such as proline, L-histidine and lipase afforded the product 4a
in 80-95% yields after reacting at 55 0C for 4-5 h. The catalytic activity of the lipase biocatalyst was
found to be more than that of the corresponding biocatalyst (Table 1, entries 3, 4, 5). Lipase
biocatalysts were used in different organic transformation without need of additional coenzyme
because of their high efficiency and selectivity20, 22. Different organic solvents were also screened to
see their efficiency in the reaction. As shown in Table 1 (entries 5-9) it seems that the reaction
proceeds better in DES solvents than water, methanol, dioxane, and DMF. In the absence of the
catalyst, it affords the desired product 4a in 20 % yield after reacting at 55 0C for 7.5 h (Table 1,
entry 10).
Table 1. Effect of catalysts and solvents on product yield 4a
Entrya Catalyst (5% w/w) Solvent Time(h) Yield (%)b
1 K 2CO3 DES 7 65
2 t-BuOK DES 6 79
3 Proline DES 5 80
4 L-Histidine DES 5 88
5 Lipase DES 4 95
6 Lipase Water 8 50
7 Lipase Methanol 5 80
8 Lipase Dioxane 6 72
9 Lipase DMF 5.5 78
10 No Catalyst DES 7.5 20
Reaction Condition: aAll reactions were carried out with aldehyde 1a (2 mmol), ethyl acetoacetate (2.1
mmol), urea (2.2 mmol), catalyst (0.019g), solvent (3 ml), Temperature = 55 0C, bIsolated yields.

Use of Rhizopus oryzae lipase in DES reduced the reaction time to more than half coupled with
the yield of the product as high as 95 % (Table 1, entry 5). For further reaction optimization, the
lipase biocatalyst was used. To optimize the amount of the catalyst, the reaction was performed with
different quantity of the lipase, and we observed that 5% w/w of lipase with respect to the aldehyde
was found to be optimal (Table 2). Under the optimized conditions, various substituted aromatic
aldehydes 1a-g were reacted to obtain the corresponding products 4a-g (Table 3).

Table 2.Optimization of amount of lipase

Entrya Catalyst (% w/w) Time(h) Yield (%)b
A 3 6 80
B 5 4 95
C 7 4 95
Reaction Condition: aAll reactions were carried out with aldehyde 1a (2 mmol), ethyl acetoacetate (2.1
mmol), urea (2.2 mmol), DES (3 ml), Temperature = 55 0C, bIsolated yields.

In all the synthesized compounds disappearance of aldehydic proton at around 9.8 δ in 1H-NMR and
C-H stretching frequency at around 2750 cm-1 in IR spectra gives the evidence of product formation.
Thiourea has shown excellent reactivity to synthesis of 3,4-dihydropyrimidin-2-(1H)thione, which is
also of much interest with respect to its biological activity6. In order to make the biocatalytic
processes economical at large scale, the recyclability of both lipase and DES has to be taken into
consideration.

Recycling experiments were conducted to find out the change in activity of the catalyst after the
reaction. During this study, lipase and DES were recycled up to four times. No significant decrease in
62

the yield of the product was observed during the first recycle, whereas it continuously declined up to
75 % at the end of fourth cycle as shown in Table 4.
Table 3. Synthesis of dihydropyrimidin-2(1H)-ones (DHPMs) derivatives
Urea/
Entrya Aldehyde AMG Product Time(h) Yield,%b
Thiourea
O
O O O O HN NH
a H H 3C O H2N NH2 4 95
H3CO H3CO O O
O S
H O O S HN NH
b H 3C O H2 N NH2 4 92
H3CO
H3CO O O
O O
H O O O HN NH
c H 3C H2N NH2 4 90
H3CO
H3CO O
O O
H O O O NH
HN
H 3C O H2N NH2
d N
6 82
O
O
N

O S
H O O S NH
HN
H 3C O H2 N NH2
e 6 81
N O
O
N

O O

H O O O HN NH

N H3 C O H2 N NH2
N O O
f 6 73
O
O H HN O
O N
H
O O
O O O O O HN NH HN NH
H H H3 C O
g H2 N NH2 6 78
N
(CH2) 6 O O N O O
(CH2)5CH3
Reaction Conditions: aAll reactions were carried out with aldehyde 1a-g (2 mmol), AMG 2a-b (2.1 mmol), urea/ thiourea
(2.2 mmol), Lipase (5% w/w with respect to aldehyde), DES (3 ml), Temperature (55 0C). bIsolated yields.

Table 4. Recyclability of Lipase and DES

Entrya Recycle Yield (%)b
1 Fresh 95
2 First 93
3 Second 87
4 Third 81
5 Fourth 75
Reaction Condition: aAll reactions were carried out with aldehyde 1a (2 mmol), ethyl acetoacetate (2.1 mmol), urea (2.2
mmol), Lipase, DES, Time = 4h, Temperature = 55 0C, bIsolated yields.
 B. N. Borse et al. / Current Chemistry Letters 1 (2012) 63

All these novel DHPMs derivatives were evaluated for in vitro antibacterial activity against
Echerichia coli, Pseudomonas neumoniae, Micrococcus and in vitro antifungal activity against
Aspergillus niger and Candida albicans. Appreciable in vitro activity against the tested strains was
exhibited by all the compounds. Minimal Inhibitory Concentrations (MIC) were determined by
means of standard serial dilution method and summarized in Table 5. In all the cases, purity of the
product was confirmed by elemental analysis. The structures of the pure products were confirmed by
FT-IR, 1H-NMR, 13C-NMR, elemental analysis and Mass spectral data.

Table 5. MIC (µg/mL) determination using the modified resazurin assay

Bacterial Strains Fungal Strains
Entry Compound
E. coli P. neumoniae C. albicans A. niger
2 2 2
1 4a 2.5 × 10 2.5 × 10 2.5 × 10 2.5 × 102
2 4b 2.5 × 102 5.0 × 102 2.5 × 102 2.5 × 102
3 4c 5.0 × 102 5.0 × 102 5.0 × 102 5.0 × 102
4 4d 5.0 × 102 5.0 × 102 2.5 × 102 2.5 × 102
5 4e 2.5 × 102 5.0 × 102 2.5 × 102 2.5 × 102
6 4f 5.0 × 102 5.0 × 102 2.5 × 102 5.0 × 102
7 4g 2.5 × 102 2.5 × 102 2.5 × 102 2.5 × 102

1. Antimicrobial activities were expressed in MIC (Minimal inhibitory concentration) values.

2. (-): Inactive.
3. Bacterial strain: E. coli NCIMB 8110, Pseudomonas neumoniae
4. Fungal Strain: Candida albicans; Aspergillus niger.
5. Solvent used: DMSO (Dimethylsulphoxide).
6. Standard: Bacterial strain: Streptomycin 125µg/mL, Fungal strains: Fluconazole 125µg/ mL

A O A O O
Me + Me Me
N: H NH O
O N N + - -
B H H R1 B O
H R1 Ar R1
H
O O O O
O
1 2

A A
+
X N: NH
B O HN B O HN
X H2N NH2
NH2 OH O
O O H O O- O
HN OH
Ar Me Ar Me
Ar Me Ar Me
COR1 R1 O R1
O O R1
6 5 4
3

X
HN NH
X OH X
NH2 Ar H Me A
HN O COR1 HN NH N:
B O N
+ H
Ar Me A Ar Me
COR1 COR1 O
N:
B O N
H
7 8 9
O

O
O H2N
OH
N
Where, OH B= O R 1 = -CH 3, -OCH 2CH3
A= HN NH2
O- X= O,S

Scheme 2: Plausible Reaction Mechanism for synthesis of DHPMs 4a-g

As shown in Scheme 2 plausible reaction mechanisms were proposed for lipase catalyzed reaction,
the condensation of the active methylene group and aromatic aldehyde gives intermediates (5) which
further reacts with urea or thiourea to give DHPMs (9).
64

3. Conclusions

Environmentally benign synthesis of novel DHPMs in DES with lipase as a biocatalyst has been
reported for the first time. It is a simple, convenient and effective method for the one pot synthesis of
DHPMs. The lipase in DES gave high isolated yield of the DHPMs in a shorter reaction time and
minimizes the use of harmful organic solvents and catalysts, which are the major environmental
issues in the pharmaceutical research. Lipase is a heterogeneous catalyst, easily recoverable by simple
filtration and reused in same reaction up to four cycles without major loss in its catalytic activity. All
the synthesized compounds showed antibacterial and antifungal activity.

Acknowledgements
The Authors B. N. Borse and V. S. Borude are thankful to University Grant Commission (UGC-
SAP programme) INDIA for financial assistance.

4. Experimental

Materials and Methods

Lipase from Rhizopus oryzae having activity 41.6 U/ mg was procured from Zytex India Pvt. Ltd.
All the solvents and chemicals were procured from S. D. Fine Chemicals (India) and were used
without further purification. The reactions were monitored by TLC using 0.25 mm E- Merck silica
gel 60 F254 precoated plates, which were visualized with UV light. FT-IR spectra were recorded on
8400S Fourier Transform Infrared Spectrophotometer Shimadzu. The 1H-NMR and 13C-NMR spectra
were recorded on 300 MHz and 100 MHz on Varian Mercury Plus Spectrometer, respectively.
Chemical shifts are expressed in δ ppm using TMS as an internal standard. Coupling constants are
given in Hz. The following abbreviations are used to indicate the multiplicity: s, singlet; d, doublet; t,
triplet; q, quartet; m, multiplet; bs, broad signal. Elemental analysis was done on Harieus Rapid
Analyzer. Mass spectral data were obtained with Micromass – Q– Tof (YA105) Spectrometer.

General Procedures for the synthesis of DHPMs derivatives 4(a-g).

A mixture of 1a-g (2 mmol), active methylene group (AMG) 2a-b (2.1 mmol), urea/ thiourea 3a-
b (2.2 mmol) and lipase (5% w/w with respect to aldehydes) was stirred in DES (3 ml) at 55 0C in 25
ml round bottom flask. The progress of a reaction was monitored by TLC. After completion of the
reaction, ethyl acetate was added in reaction mass and Lipase was then filtered. The ethyl acetate and
DES layers were separated, ethyl acetate layer dried by using sodium sulphate and then distilled out
in high vacuum to afford final products which were recrystallized from methanol.

General Procedures for the synthesis of DES.

A DES solvent was prepared by previously reported simple method17 with 100% atom economy.
For DES preparation choline chloride (1 equiv.) was reacted with urea (2 equiv.) at 80 0C for 12h.
The resulting molten salt was used directly in reactions without purification.

Recyclability study of Rhizopus Oryzae Lipase and DES

Once the reaction is over, since reaction mass is diluted with ethyl acetate, lipase was recovered
by filtration and DES was immiscible with ethyl acetate, it was easily separated. Lipase and DES was
dried under vacuum. The recovered lipase and DES was loaded in the same reactor, and the fresh
reactant aldehyde 1a (2 mmol), ethyl acetoacetate (2.1 mmol), and urea (2.2 mmol) were stirred at
550C for 4h to get final product (4a), the same procedure was repeated for consecutive recycling of
the catalyst.
 B. N. Borse et al. / Current Chemistry Letters 1 (2012) 65

Determination of Antimicrobial Activity 4a-g

Incubator at 35 °C and 37 °C; pipettes of various sizes (Gilson); sterile tips, 100, 200, 500 and
1000 μL; sterile normal saline; sterile isosensitest agar (Southern Group Laboratory, SGL); antibiotic
solutions (Sigma–Aldrich); sterile solution of 10 % (v/ v) DMSO in water (Sigma– Aldrich).

Medium
Isosensitest broth was used for this antimicrobial activity study. As recommended by NCCLS31,
Mueller Hinton medium was used for antimicrobial susceptibility testing, the most of the bacterial
strains show comparable results in isosensitest medium32, 33.

Preparation of the Plates

Plates were prepared under aseptic conditions. A sterile 96 well plate was labeled. A volume of
100 μL of test material in 10 % (v/ v) DMSO (usually a stock concentration of 4 mg/ ml) was
pipetted into the first row of the plate. To all other wells, 50 μL of nutrient broth was added. Serial
dilutions were performed using a multichannel pipette. Tips were discarded after use such that each
well had 50 μL of the test material in serially descending concentrations. To each well, 10 μL of
resazurin indicator solution was added. Using a pipette 30 μL of 3.3 × strength isosensitised broth
was added to each well to ensure that the final volume was single strength of the nutrient broth.
Finally, 10 μL of bacterial suspension (5 × 106 cfu/ mL) was added to each well to achieve a
concentration of 5 × 105 cfu/ mL. Each plate was wrapped loosely with cling film to ensure that
bacteria did not become dehydrated. Each plate had a set of controls: a column with a broad-spectrum
antibiotic as positive control, a column with all solutions with the exception of the test compound,
and a column with all solutions with the exception of the bacterial solution adding 10 μL of nutrient
broth instead. The plates were prepared in triplicate and placed in an incubator set at 37 °C for 18– 24
h. The colour change was then assessed visually. Any colour changes from purple to pink or
colourless were recorded as positive. The lowest concentration at which colour change occurred was
taken as the Minimum inhibitory concentration (MIC) value. The average of three values was
calculated and that was the MIC for the test material and bacterial or fungal strain.33
Antimicrobial Activity
As shown in Table 5 all the compounds were evaluated for their antifungal as well as
antibacterial activity against the tested strains. The antibacterial activity of compounds 4a, 4b, 4e and
4g was found against E. coli and that of the compounds 4a and 4g against pseudomonas neumoniae.
Further, the antifungal activity of the compounds 4a, 4b, 4d-4g was found to be significant against
Candida albicans and that of the compounds 4a, 4b, 4d, 4e and 4g against Aspergillus niger. All the
novel compounds have good antimicrobial activity against both bacteria and fungi.

Spectral Data 4(a-g)

Ethyl-4-(6-methoxynaphthalen-2-yl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-
carboxylate Table 3, entry 4a:
FT-IR (neat, cm–1): 3358 (N-H), 1696 (C=O), 1093 (C-O).
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 1.10 (t, 3H), 2.31 (s, 3H), 2.50 (q, 2H), 3.85 (s, 3H), 5.25 (d,
J = 2.7 Hz, 1H), 7.12 (d, 1H), 7.19 (d, J = 6.5 Hz, 1H), 7.28 (d, J = 2.2 Hz, 1H), 7.35 (d, J = 6.5 Hz,
1H), 7.40 (d, J = 1.8 Hz, 1H), 7.79 (dd, J = 8.4 Hz, 1H), 7.58 (s, 1H, -NHgr), 9.20 (s, 1H, -NH gr).
13
C-NMR (100 MHz, DMSO-d6, δ ppm): 14.12, 17.88, 54.18, 55.18, 59.20, 99.22, 105.77, 118.80,
124.53, 125.38, 127.22, 128.05, 129.38, 133.64, 139.91, 148.40, 152.12, 157.26, 165.42.
Anal. Calcd. for C19H20N2O4: C, 67.05; H, 5.92; N, 8.23. Found: C, 67.12; H, 5.98; N, 8.32.
MS (EI) (m/z): 338.07 (M-).
66

Ethyl-4-(6-methoxynaphthalen-2-yl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-
carboxylate Table 3, entry 4b:
FT-IR (neat, cm–1): 3298 (N-H), 2985 (C-H), 1736 (C=O), 1663 (C=C ), 1550(C=S), 1018(C-O ).
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 1.10 (t, 3H), 1.21 (q, 2H), 2.32 (s, 3H), 3.85 (s, 3H), 5.28 (s, J
= 3.6 Hz, 1H), 7.12 (d, J = 2.5 Hz, 1H), 7.19 (d, J = 2.5 Hz, 1H), 7.28 (d, J = 2.5 Hz, 1H), 7.32 (d, J = 1.8
Hz, 1H), 7.36 (d, J = 6.9 Hz, 1H), 7.8 (d, J = 8.7 Hz, 1H), 9.85 ( s, 1H, -NH gr), 10.20 (s, 1H, -NHgr).
13
C-NMR (100 MHz, DMSO-d6, δ ppm): 14.05, 17.25, 54.33, 55.21, 59.59, 100.62, 105.79, 118.97,
124.90, 125.31, 127.39, 128.01, 129.47, 133.81, 138.54, 145.11, 157.44, 165.20, 174.10.
Anal. Calcd. for C19H20N2O3S: C, 64.02; H, 5.66; N, 7.86; S, 9.00. Found: C, 64.12; H, 5.68; N,
7.96; S, 9.18.
MS (EI) (m/z): 357.2 (M+).

5-acetyl-4-(6-methoxynaphthalen-2-yl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one Table 3,
entry 4c:
FT-IR (neat, cm–1): 3290 (N-H), 1670 (C=O), 1610 (C=C), 1083 (C-O), 1031(C-O).
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 2.10 (s, 3H), 2.36 (s, 3H), 3.83 (s, 3H), 5.45 (d, J = 3 Hz,
1H), 7.15 (d, J = 2.1 Hz, 1H), 7.28 (d, J = 1.8 Hz, 1H), 7.40 (d, J = 8.7 Hz, 1H), 7. 60 (s, 1H), 7.80
(d, J = 8.7 Hz, 2H), 7.90 (s, 1H), 9.25 (s, 1H);
13
C-NMR (100 MHz, DMSO-d6, δ ppm): 19.02, 30.35, 54.04, 55.18, 105.74, 109.41, 118.81, 124.55,
125.60, 127.39, 128.10, 129.46, 133.68, 139.28, 148.26, 152.14, 157.29, 194.48;
Anal. Calcd. for C18H18N2O3: C, 69.66; H, 5.85; N, 9.03. Found: C, 69.71; H, 5. 92; N, 9.27.
MS (EI) (m/z): 310.93 (M+).

Ethyl-4-(9-ethyl-9H-carbazol-3-yl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
Table 3, entry 4d:
FT-IR (neat, cm–1): 3340 (NH), 2817 (C-H), 1651 (C=O), 1227, 1088 (C-O);
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 1.10 (t, 3H), 1.30 (t, 3H), 2.42 (s, 3 H), 3.95 (q, 2H), 4.45
(q, 2H), 5.35 (d, J = 2.4 Hz, 1H), 7.20 (t, J = 7.6 Hz, 1H), 7.35-7.40 (dd, J = 8.4 Hz, 1.4 Hz, 2H),
7.54 (t, J = 6.9 Hz, 1 H), 7.58 (dd, J = 8.4 Hz, 1H), 8.02 (d, J = 8.7 Hz, 1H), 8.15 (d, J = 7.6 Hz, 1H),
9.20 ( S, 1H, -NH gr), 10.24 (S, 1H, -NHgr);
13
C-NMR (100 MHz, DMSO-d6, δ ppm): 13.70, 14.13, 17.86, 36.99, 54.51, 59.15, 99.93, 109.19, 109.21,
118.04, 118.74, 120.11, 121.65, 122.05, 124.36, 125.73, 135.73, 138.86, 139.84, 147.86, 152.11, 165.52;
Anal. Calcd. for C22H23N3O3: C, 70.01; H, 6.14; N, 11.13. Found: C, 70.12; H, 6.20; N, 11.33.
MS (EI) (m/z): 376.07 (M-).

Ethyl-4-(9-ethyl-9H-carbazol-3-yl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-
carboxylate Table 3, entry 4e:
FT-IR (neat, cm–1): 3180 (N-H), 2998 (C-H), 1705 (C=O), 1590 (C=S), 1100 (C-O);
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 1.10 (t, 3H), 1.30 (t, 3H), 2.40 (s, 3 H), 4.00 (q, 2H), 4.45
(q, 2H), 5.38 (d, J = 3.3 Hz, 1H), 7.20 (t, J = 7.6 Hz, 1H), 7.33 (dd, J = 7.9 Hz, 2H), 7.45 (t, J = 7.6
Hz, 1H), 7.60 (dd, J = 8.4 Hz, 1.4 Hz, 1 H), 7.92 (d, J = 1.4 Hz 1H), 8.13 (d, J = 7.6 Hz, 1H), 9.70( S,
1H, -NH gr), 10.24 (S, 1H, -NHgr);
13
C-NMR (100 MHz, DMSO-d6, δ ppm): 13.71, 14.05, 17.25, 37.01, 54.62, 59.54, 101.304, 109.236,
109.385, 118.29, 118.85, 120.16, 121.73, 121.99, 124.46, 125.87, 134.38, 139.03, 139.88, 144.63,
165.32, 173.81;
Anal. Calcd. for C22H23N3O2S: C, 67.15; H, 5.89; N, 10.68; S, 8.15; Found: C, 67.12; H, 5. 97; N,
10.92; S, 8.39.
MS (EI) (m/z): 393.07 (M+).

Diethyl-4,4'-(4,4'-(phenylazanediyl)bis(4,1-phenylene))bis(6-methyl-2-oxo-1,2,3,4-
tetrahydropyrimidine-5-carboxylate) Table 3, entry 4f:
 B. N. Borse et al. / Current Chemistry Letters 1 (2012) 67

FT-IR (neat, cm–1): 3466 (N-H), 2983 (C-H), 1738 (C=O), 1153 (C-O), 1042 (C-O);
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 1.15-1.20 ( t, 6H), 2.25 (s, 6 H), 3.95-4.05 (q, 4H), 4.75 (s,
1H), 4.85 (s, 1H), 6.75 (d, J = 8.7 Hz, 4H), 7.05 (d, J = 8.4 Hz, 4H), 7.15 (dd, J = 7.3 Hz, 2H), 7.38
(t, J = 7.6 Hz, 1H), 7.65 (d, J = 8.7 Hz, 2H), 8.80 (s, 2H), 9.70 (s, 2H);
13
C-NMR (100 MHz, DMSO-d6, δ ppm): 14.18, 14.29, 18.30, 21.67, 58.81, 59.04, 59.04, 91.78,
101.62, 101.62, 117.51, 125.51, 125.51, 126.06, 126.06, 126.52, 126.52, 128.20, 128.20, 129.01,
129.01, 129.01, 130.02, 130.02, 131.28, 131.28, 143.12, 145.51, 145.60, 152.92, 154.23, 156.83,
166.93, 168.31;
Anal. Calcd. for C34H35N5O6 : C, 66.98; H, 5.79; N, 11.49; Found C, 66.57; H, 5.82; N, 11.82.
MS (EI) (m/z): 607.16 (M-).
Diethyl-4,4'-(4,4'-(hexylazanediyl)bis(4,1-phenylene))bis(6-methyl-2-oxo-1,2,3,4-
tetrahydropyrimidine-5-carboxylate) Table 3, entry 4g:
FT-IR (neat, cm–1): 2982 (C-H), 1738 (C=O), 1666 (C=C), 1042 (C-O);
1
H-NMR (300 MHz, DMSO-d6, δ ppm): 0.88 (t, 3H), 1.15 (t, 6H), 1.10-1.35 (m, 8H), 2.25 (s, 6H),
2.50 (t ,2H), 4.15 (q, 4 H), 4.75 (s, 2H), 6.65 (d, J = 8.4, 2H), 7.12 (d, J = 8.0 Hz, 2H), 7.26 (d, J =
8.4 Hz, 2H), 7.60 (d, 2H), 8.85 (s, 2H), 9.60 (s, 2 H);
13
C NMR (100 MHz, DMSO-d6, δ ppm): 13.83, 14.16, 14.27, 18.28, 21.67, 22.07, 25.84, 26.70,
29.08, 31.01, 51.79, 51.79, 58.80, 59.01, 91.70, 101.68, 112.77, 112.77, 125.67, 125.67, 126.69,
126.69, 129.23, 131.50, 142.88, 145.60, 146.36, 152.93, 154.23, 156.83, 166.92, 168.31, 189.82,
189.82;
Anal. Calcd. for C34H43N5O6: C, 66.1; H, 7.02; N, 11.34; Found C, 65.91; H, 6.97; N, 11.68.
MS (EI) (m/z): 617.19 (M+).

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