Synthesis and herbicidal activity of 5-(4-hydroxybenzyl)-2- thioxoimidazolidin-4-one esters

Article abstract of DOI:10.3390/molecules16042833

A series of novel 5-(4-hydroxybenzyl)-2-thioxoimidazolidin-4-one esters were synthesized under mild conditions by the reaction of 5-(4-hydroxybenzyl)-2- thioxoimidazolidin-4-one and carboxylic acids with DCC and DMAP as the promoters. Their structures wer

Full text of DOI:10.3390/molecules16042833

Molecules 2011, 16, 2833-2845; doi:10.3390/molecules16042833
OPEN ACCESS
molecules
ISSN 1420-3049
www.mdpi.com/journal/molecules
Article
Synthesis and Herbicidal Activity of 5-(4-Hydroxybenzyl)-2-
Thioxoimidazolidin-4-one Esters
Jintao Han 1, Jinmin Wang 1, Hongbo Dong 1, Jianping Lei 1, Mingan Wang 1,2,* and
Jianxin Fang 2
1
Department of Applied Chemistry, China Agricultural University, Beijing 100193, China
2
State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
* Author to whom correspondence should be addressed; E-Mail: wangma@cau.edu.cn;
Tel.: +86-10-62734093.
Received: 28 February 2011; in revised form: 16 March 2011/ Accepted: 25 March 2011 /
Published: 30 March 2011
Abstract: A series of novel 5-(4-hydroxybenzyl)-2-thioxoimidazolidin-4-one esters were
synthesized under mild conditions by the reaction of 5-(4-hydroxybenzyl)-2-
thioxoimidazolidin-4-one and carboxylic acids with DCC and DMAP as the promoters.
1
Their structures were confirmed by H-NMR, IR, ESI-MS and elemental analysis. The
preliminary bioassy results indicated that some of compounds exhibit good herbicidal
activity against Zea mays, Triticum aestivum and Arabidopsis thaliana. The further
greenhouse test showed that compounds 6-16 and 6-28 have 60%, 50% and 50% efficacy
against Stellaria media, Echinochloa crus-galli and Setaria viridis at 1,000 g/ha,
respectively.
Keywords: 5-(4-hydroxybenzyl)-2-thioxoimidazolidin-4-one esters; synthesis; herbicidal
activity
1. Introduction
Hydantoins and 2-thiohydantoin derivatives are an important class of biologically active molecules.
They have not only been used in medicinal chemistry as anti-HSV [1], antidiabetic [2,3], or
HDL-cholesterol modulators [4], but also used as fungicides [5] and herbicides [6,7] in agrochemical
research. Among these hydantoin derivatives, hydantocidin (1) has generated great interest of chemists

Molecules 2011, 16
2834
because of its excellent herbicide activity and low toxicity [8]. It is a non selective phytotoxin with an
efficacy similar to that of glyphosate in contolling many common annual weeds [8].
2-Thiohydantocidin (2) was also synthesized and found to have similar herbicidal activity [9]. Cseke
and Waters [10,11] found that hydantocidin acts as a proherbicide, which is phosphorylated at the 5’
position in vivo. In the phosphorylated form 3, it strongly binds to its target enzyme, adenylosuccinate
synthetase (AdSS, EC 6.3.3.4) [12-14], a new herbicidal target. This finding led to a great of attention
being paid toward this compound or its analogues as potential lead compounds in the discovery of new
commercial herbicides [15-18]. In the investigation of 5’-phosphohydantocidin analogues as AdSS
inhibitors, Crouse found that 4 had significant inhibition against Arabidopsis, with an I50 value of
0.005 mg/L, and inhibition against eight grass and broadleaf weed species with post GR50 values of
16.6 mg/L, which are much higher than those of 0.5 mg/L and 29 mg/L obtained for hydantocidin [19].
In our laboratory, a virtual screen model was set up based on the docking method of inhibitors with
AdSS, and compared with the crystal structure of the AdSS-hydantocidin complex [14,20]. As a
continuation of our ongoing project aimed at looking for novel biologically imidazolinedione
heterocyclic compounds [21-23], a series of novel 5-(4-hydroxybenzyl)-2-thioxoimidazolidin-4-one
esters were synthesized, and their activities were evaluated. Herein, we would like to report the
synthesis and biological activity of the title compounds.
Scheme 1. The synthetic route to compounds 6.
O
O
X
O
O
HO
HO
P
O
HN
HN
Cl
O
HN
O
O
O
OH
NH
NH
NH
O
O
O
OHOH
OH OH
OHOH
1 X = O; 2 X = S
4
3
O
S
O
O
H2N C NH2
RCOOH
NH2
NH
NH
R
O
CH2
HO
CH2
HO
CH2
oil bath
COOH
N
N
DCC, DMAP
S
S
H
H
6
5
2. Results and Discussion
5-(4-Hydroxybenzyl)-2-thioxoimidazolidin-4-one (5) was prepared by heating L-tyrosine and
thiourea in an oil bath under reflux according to the reported method [24]. Compound 5 reacted at
room temperature with various substituted benzoic acids with DCC and DMAP as catalysts to give the
1
target compounds 6 in yields of 27-74%. Their structures were confirmed by IR, H-NMR, ESI-MS
and elemental analysis. As reported before [21], when acetic anhydride or benzoyl chloride were used,
compounds 7 and 8 (Figure 1) were produced as byproducts.
Figure 1. Reaction byproducts 7 and 8.
O
O
NH
NH
CH2
CH2
Ac
Bz
O
O
N
N
S
S
Ac
7
8
Bz

Molecules 2011, 16
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The herbicidal values of the title compounds against Zea mays, Triticum aestivum and Arabidopsis
thaliana at the dosages of 200 μg/mL were assayed, and compared with the commercially available
herbicide metazachlor as positive control according to the method described in the Experimental
section. The activity data are listed in Table 1.
Table 1. The inhibition ratios (%) of 6 against Z. mays, T. aestivum and A. thaliana at 200 g/mL.
Z. mays
Height
T. aestivum
A. thaliana
Compd.
R
Root
-
Height
Root
-
Germination
CK
-
-
0
metazachlor
6-1
79.0
-14.5
32.8
26.6
3.9
83.0
-6.7
66.3
44.5
-16.3
-30.2
-11.6
11.2
5.9
78.6
-3.6
-22.9
-11.1
20.6
48.4
-2.9
-10.9
24.7
3.7
77.7
20.9
-8.5
16.2
16.3
57.9
10.7
20.9
53.4
10.6
47.5
-48
70
10
20
10
20
30
20
20
30
40
70
60
40
40
50
50
40
30
60
60
50
20
50
50
40
10
5
CH3-
4-FC6H4-
6-2
6-3
C6H5-
6-4
3-NO2C6H4-
2-FC6H4-
6-5
-19.4
19.6
6.7
6-6
2,4-(OCH3)2C6H3-
2,3-(OCH3)2C6H3-
2-ClC6H4-
6-7
6-8
53.4
63.6
41.7
14.7
23.5
36.7
54.4
62.8
100
6-9
2-NO2C6H4-
3-ClC6H4-
7.6
6-10
6-11
6-12
6-13
6-14
6-15
6-16
6-17
6-18
6-19
6-20
6-21
6-22
6-23
6-24
6-25
6-26
6-27
6-28
6-29
6-30
6-31
6-32
6-33
6-34
22.1
22.0
8.6
8.8
4-BrC6H4-
5.2
4-ClC6H4-
-12.9
-15. 8
-3.7
-14.8
-24.6
25.1
1.27
5.8
-13.6
7.0
3,4-Cl2C6H3-
4-Cl-3-NO2C6H3-
3-CH3C6H4-
4-NO2C6H4-
4-OCH3C6H4-
4-CH3C6H4-
2-CH3C6H4-
3,4-(OCH3)2C6H3-
C6H5CH2-
24.1
44.2
61.3
100
2.6
12.7
-25.8
32.2
16.8
20.7
43.1
42.1
99.6
79.1
99.6
59.7
3.2
33.5
27.9
53.2
57.9
53.9
65.5
-26.2
16.4
22.1
42.4
30.9
77.4
27.8
11.6
52.7
45.5
70.1
72.8
17.8
38.7
33.5
64.2
58.1
74.9
-29.0
59.4
19.9
48.7
22.5
88.0
71.0
-24.7
77.9
71.5
77.3
60.7
26.1
34.9
97.8
81.3
95.2
42.3
20.9
55.5
100
2,4-Cl2C6H3OCH2-
2-OCH3C6H4-
4-ClC6H4OCH2-
3,4,5-(OCH3)3C6H2-
4-C6H5C6H4-
4-t-C4H9C6H4-
1-C10H7CH2-
3,5-(NO2)2C6H3-
2-C4H3S-
25.9
56.7
18.8
15.5
2.5
10
10
5
86.2
-1.2
33.8
65.5
50.2
27.5
20
10
5
C6H5CH=CH-
3,5-(CF3)2C6H3CH2-
4-FC6H4CH2-
2-C4H3O-
32.7
86.6
30.3
20
40

Molecules 2011, 16
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The preliminary bioassay results showed that some of the compounds 6 possess good herbicidal
activity. For example, compounds 6-16, 6-28, 6-33 and 6-34 exhibited more than 70% inhibitory
activity against the height growth of Z. mays, and compounds 6-16, 6-22, 6-28, 6-29, 6-31, 6-32 and 6-
33 exhibited more than 70% inhibitory activity against the root growth of Z. mays, while compounds
6-22, 6-23, 6-24, 6-28 and 6-29 showed more than 75% inhibitory activity against the height growth of
T. aestivum, and compounds 6-22, 6-23, 6-24 and 6-33 showed more than 75% inhibitory activity
against the root growth of T. aestivum. These values are almost equal to or better than those of
metazachlor, the commercially available herbicide. Also the inhibitory ratios of 6-10, 6-11, 6-18 and
6-19 are equal or close to those of metazachlor against the germination of A. thaliana, the A. thaliana
leaves exhibited yellowing and withering symptoms after germination. These results indicated that
these compounds have selectivity as potential herbicide. Compared with the results in the previous
paper [21,22], the inhibitory activities of 6 against Z. mays, T. aestivum and A. thaliana were
increased, the growth promotion activities were inhibited, which showed the thiohydantoin ring is
more helpful to increase the herbicidal activity than hydantoin ring. Comparison the activities of 7 and
8 with those of 6-1 and 6-3, they are greatly decreased due to the loss one of the N-H groups in the
thiohydantoin ring, which is consistent with the results in the previous paper [21,22] and the X-ray
structure of the AdSS-hydantocidin complex [14]. Further greenhouse tests showed that 6-16 and 6-28
have 60%, 50% and 50% efficacy against Stellaria media, Echinochloa crus-galli and Setaria viridis
at the dosage of 1,000 g/ha when used as a pre-emergence treatment, but no significant efficacy was
observed with 0%, 0% and 0% efficacy against S. media, E. crus-galli and S. viridis when used as a post-
emergence treatment. Further structure modifications are under investigation.
3. Experimental
3.1. General
Meting points were measured on a Yanagimoto apparatus (Yanagimoto MFG CO., Japan) and are
uncorrected. Elemental analysis was performed on a Vario EL instrument (Elementar Vario Micro
1
Cube, Germany). The H NMR spectra were recorded at room temperature on a Bruker DPX 300
spectrometer with DMSO-d6 as a solvent and TMS as an internal standard. IR spectra were obtained on
a Shimadzu IR-435 instrument with KBr plates. ESI-MS were analyzed on an Agilent 1100 LC-MSD-Trap
instrument. Herbicidal activity tests were carried out in a RXZ-380B illumination incubator (Jiangnan
Equipment Factory, Ningbo, Zhejiang, China).
3.2. Synthesis
3.2.1. Synthesis of 5-[(4-hydroxyphenyl)methyl]-2-thioxoimidazolidin-4-one (5)
A mixture of L-tyrosine (5.4 g, 30 mmol) and thiourea (6.9 g, 90 mmol) was placed in a flask and
heated under stirring with the oil bath. The oil bath temperature was controlled at 180-190 °C, and
about 5 min later the homogenous liquid started to fume. After 15 minutes, the reaction was complete
as monitored by TLC. The flask was allowed to cool down and water (20 mL) was added when the
flask was still warm. The solution was reheated to dissolve all the solids and allowed to cool to room

Molecules 2011, 16
2837
temperature, then placed in a refrigerator for 4 h. The crystals of compound 5 were removed by vacuum
filtration, and the mother liquid was extracted with ethyl acetate and further purified by flash column
chromatography. Finally, 5.3 g product was obtained (80% yield), m.p.208-210 °C (211 °C, lit [24]).
1H-NMR (DMSO-d6, 300 MHz ) : 11.39 (s, 1H, NH), 10.01 (s, 1H, NH), 9.25 (s, 1H, OH), 6.94 (d, J = 8.7
Hz, 2H, Ar-H), 6.63 (d, J = 8.7 Hz, 2H, Ar-H), 4.45 (dd, J = 3.9, 4.8 Hz, 1H, CH), 2.85-2.87 (m, 2H,
CH2). IR: 3440, 3289, 1752, 1744, 1615, 1595, 1441, 1260, 1061 cm-1.
3.2.2. General Procedure for the Synthesis of Compounds 6
To a stirred solution of 5-[(4-hydroxy phenyl)methyl]-2-thioxoimidazolidin-4-one (5, 2 mmol) and
a substituted benzoic acid (2.4 mmol) in dry actone (25 mL), DCC (0.49 g, 2.4 mmol) and DMAP
(0.02 g, 0.2 mmol) were added at room temperature. After about 8 h, the reaction is almost complete
as monitored by TLC. After filtration and concentration under vacuum, the crude product was purified
by column chromatography on silica gel (petroleum ether-EtOAc 5:1-2:1) or recrystallized from
ethanol to give yellow solid compounds 6.
1
5-[[4-(Acetyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-1). Yield 65%, mp: 209-211 °C. H-
NMR (DMSO-d6) δ: 2.24 (s, 3H, CH3), 2.97 (m, 2H, CH2), 4.55 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.04 (d,
J = 8.7 Hz, 2H, Ar-H), 7.19 (d, J = 8.7 Hz, 2H, Ar-H), 10.09 (s, 1H, NH), 11.50 (s, 1H, NH); IR: 3450,
3172, 1745, 1732, 1608, 1555, 1363, 1289, 1008 cm-1. Anal calcd. for C12H12N2O3S: C, 54.53, H, 4.58,
N, 10.60; found: C, 54.65, H, 4.54, N, 10.57.
5-[[4-(4-Fluorobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-2). Yield 59%, mp: 197-198 °C. 1H-
NMR (DMSO-d6): δ 3.02 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.0 Hz, 1H, CH), 7.27-7.19 (m, 4H, Ar-H),
7.41-8.22 (m, 4H, Ar-H), 10.12 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3448, 3163, 1752, 1739, 1605,
1550, 1386, 1265, 1070 cm-1. Anal calcd. for C17H13FN2O3S: C, 59.29, H,3.81, N, 8.13; found: C,
59.23, H, 3. 88, N, 8.18.
1
5-[4-(Benzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-3). Yield 60%, mp: 198-199 °C. H-
NMR (DMSO-d6): δ 3.02 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.27-7.19 (m, 4H, Ar-H),
7.60-8.14 (m, 5H, Ar-H), 10.12 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3467, 3255, 1763, 1739,
1606,1588, 1446, 1260, 1015 cm-1. Anal calcd. for C17H14N2O3S: C, 62.56, H, 4.32, N, 8.58; found: C,
62.33, H, 4.38, N, 8.39.
5-[[4-(3-Nitrobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-4). Yield 59%, mp: 210-211 °C.
1H- NMR (DMSO-d6): δ3.01-3.03 (m, 2H, CH2), 4.60 (dd, J = 4.2, 5.0 Hz, 1H, CH), 7.25-7.31 (m, 4H,
Ar-H), 7.89-7.94 (m, 3H, Ar-H), 8.52-8.60 (m, 2H, Ar-H), 8.77-8.79 (m, 1H, Ar-H), 10.13 (s, 1H,
NH), 11.53 (s, 1H, NH); IR: 3446, 3154, 1702, 1729, 1614, 1541, 1350, 1250, 1005 cm-1. Anal calcd.
for C17H13FN3O5S: C, 54.98, H, 3.53, N, 11.31; found: C, 55.02, H, 3. 73, N, 11.08.
5-[[4-(2-Fluorobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-5). Yield 30%, mp: 199-200 °C. 1H-
NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.20-7.28 (m, 4H,

Molecules 2011, 16
2838
Ar-H), 7.38-7.47 (m, 2H, Ar-H), 7.74-7.81 (m, 1H, Ar-H), 8.06-8.12 (m, 1H, Ar-H), 10.12 (s, 1H,
NH), 11.52 (s, 1H, NH); IR: 3447, 3162, 1737, 1728, 1613, 1547, 1454, 1298, 1065 cm-1. Anal calcd.
for C17H13FN2O3S: C, 59.29, H, 3.81, N, 8.13; found: C, 59.23, H, 3. 88, N, 8.18.
5-[[4-(2,4-Dimethoxybenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-6). Yield 27%, mp:
169-171 °C. 1H-NMR (DMSO-d6): δ 3.00-3.03 (m, 2H, CH2), 3.85 (s, 3H, OCH3), 3.86 (s, 3H, OCH3),
4.58 (dd, J = 5.1, 4.2 Hz, 1H, CH), 6.64-6.70 (m, 2H, Ar-H), 7.11 (d, J = 8.4 Hz, 2H, Ar-H), 7.23 (d, J
= 8.4 Hz, 2H, Ar-H), 7.93 (d, J = 8.7 Hz, 1H, Ar-H), 10.11 (s, 1H, NH), 11.50 (s, 1H, NH); IR: 3459,
3138, 1739, 1732, 1605, 1555, 1405, 1246, 1010 cm-1. Anal calcd. for C19H18N2O5S: C, 59.06, H,
4.70, N, 7.25; found: C, 59.07, H, 4.75, N, 7.15.
5-[[4-(2,3-Dimethoxybenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-7). Yield 34%, mp:
191-193 °C. 1H-NMR (DMSO-d6): δ 3.01-3.03(m, 2H, CH2), 3.82 (s, 3H, OCH3), 3.87 (s, 3H, OCH3 ),
4.58-4.60 (m, 1H, CH), 7.17-7.27 (m, 5H, Ar-H), 7.33-7.42 (m, 2H, Ar-H), 10.12 (s, 1H, NH), 11.52
(s, 1H, NH); IR: 3450, 3173, 1737, 1728, 1586, 1525, 1384, 1274, 1043 cm-1. Anal calcd. for
C19H18N2O5S: C, 59.06, H, 4.70, N, 7.25; found: C, 58.82, H, 4.77, N, 7.32.
5-[[4-(2-Chlorobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-8). Yield 47%, mp: 196-198 °C. 1H-
NMR (DMSO-d6): δ 3.01-3.04 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.21-7.29 (m, 4H, Ar-
H), 7.52-7.57 (m , 1H, Ar-H), 7.65-7.68 (m, 2H, Ar-H), 8.05-8.09 (m, 1H, Ar-H), 10.12 (s, 1H, NH),
11.50 (s, 1H, NH); IR: 3447, 3178, 1741, 1730, 1590, 1439, 1398, 1293, 1038 cm-1. Anal calcd. for
C17H13ClN2O3S: C, 56.59, H, 3.63, N, 7.76; found: C, 56.68, H, 3.73, N, 7.68.
1
5-[[4-(2-Nitrobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-9). Yield 51%, mp: 213-214 °C. H-
NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 4.58 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.19 (d, J = 8.4 Hz,
2H, Ar-H), 7.30 (d, J = 8.4 Hz, 2H, Ar-H), 7.88-7.98 (m, 2H, Ar-H), 8.07-8.11 (m, 1H, Ar-H), 8.17-
8.20 (m, 1H, Ar-H), 10.12 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3345, 3169, 1741, 1728, 1610, 1537,
1398, 1294, 1060 cm-1. Anal calcd. for C17H13N3O5S: C, 54.98, H, 3.53, N, 11.31; found: C, 54.22, H,
3.57, N, 12.31.
5-[[4-(3-Chlorobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-10). Yield 42%, mp: 192-
193 °C. 1H-NMR (DMSO-d6): δ 3.02-3.04 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.21-7.28 (m,
4H, Ar-H), 7.62-7.67 (m , 1H, Ar-H), 7.81-7.85 (m, 1H, Ar-H), 8.06-8.11 (m, 2H, Ar-H), 10.12 (s, 1H,
NH), 11.51 (s, 1H, NH); IR: 3343, 3155, 1741, 1735, 1625, 1546, 1408, 1289, 1017 cm-1. Anal calcd.
for C17H13ClN2O3S: C, 56.59, H, 3.63, N, 7.76; found: C, 56.62, H, 3.72, N, 7.70.
5-[[4-(4-Bromobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-11). Yield 47%, mp: 242-
244 °C. 1H-NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.20-7.28 (m,
4H, Ar-H), 7.82 (m, 2H, Ar-H), 8.03-8.06 (m, 2H, Ar-H), 10.13 (s, 1H, NH), 11.52 (s, 1H, NH); IR:
3288, 3142, 1770, 1741, 1604, 1515, 1382, 1266, 1066 cm-1. Anal calcd. for C17H13BrN2O3S: C,
50.38, H, 3.23, N, 6.91; found: C, 50.31, H, 3.55, N, 6.99. ESI-MS m/z: 405, 407 [M+H]+.

Molecules 2011, 16
2839
5-[[4-(4-Chlorobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-12). Yield 42%, mp: 226-
228 °C. 1H-NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.20-7.28 (m,
4H, Ar-H), 7.67-7.71 (m, 2H, Ar-H), 8.11-8.15 (m, 2H, Ar-H), 10.14 (s, 1H, NH), 11.53 (s, 1H, NH);
IR: 3152, 3167, 1738, 1729, 1600, 1592, 1400, 1263, 1077 cm-1. Anal calcd. for C17H13ClN2O3S: C,
56.59, H, 3.63, N, 7.76; found: C, 56.86, H, 3.86, N, 7.73.
5-[[4-(3,4-Dicholorobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-13). Yield 53%, mp:
200-202 °C. 1H-NMR (DMSO-d6): δ 3.02-3.04 (m, 2H, CH2), 4.58 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.22-
7.29 (m, 4H, Ar-H), 7.64-7.68 (dd, J = 2.1, 8.6 Hz, 1H, Ar-H), 7.88 (d, J = 2.1 Hz, 1H, Ar-H), 8.12 (d,
J = 8.6 Hz, 2H, Ar-H), 10.13 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3348, 3150, 1752, 1741, 1584, 1546,
1400, 1240, 1096 cm-1. Anal calcd. for C17H12Cl2N2O3S: C, 51.66, H, 3.06, N, 7.09; found: C, 52.25,
H, 3.42, N, 7.26.
5-[[4-(4-Chloro-3-nitro-benzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-14). Yield 41%, mp:
230-232 °C. 1H-NMR (DMSO-d6): δ 2.98-3.04 (m, 2H, CH2), 4.58 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.18-
7.30 (m, 4H, Ar-H), 8.02 (d, J = 8.5 Hz, 1H, Ar-H), 8.36 (dd, J = 2.0, 8.5 Hz, 1H, Ar-H), 8.72 (d, J =
2.0 Hz, 1H, Ar-H), 10.13 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3443, 3154, 1762, 1735, 1602, 1541,
1402, 1240, 1093 cm-1. Anal calcd. for C17H12ClN3O5S: C, 50.31, H, 2.98, N, 10.35; found: C, 50.62,
H, 3.20, N, 10.34.
5-[[4-(3-Methylbenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-15). Yield 51%, mp: 163-
165 °C. 1H-NMR (DMSO-d6): δ 2.42 (s, 1H, CH3), 3.02-3.04 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.0 Hz,
1H, CH), 7.27-7.17 (m, 4H, Ar-H), 7.46-7.58 (m, 2H, Ar-H), 7.91-7.95 (m, 2H, Ar-H), 10.13 (s, 1H,
NH), 11.53 (s, 1H, NH); IR: 3459, 3188, 1754, 1743, 1604, 1545, 1382, 1266, 1026 cm-1. Anal calcd.
for C18H16N2O3S: C, 63.51, H, 4.74, N, 8.23; found: C, 63.24, H, 4. 92, N, 8.32.
5-[[4-(4-Nitrobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-16). Yield 42%, mp: 246-248 °C. 1H-
NMR (DMSO-d6): δ 3.02-3.04 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.25-7.28 (m, 4H,
Ar-H), 8.35-8.44 (m, 4H, Ar-H), 10.13 (s, 1H, NH), 11.53 (s, 1H, NH); IR: 3281, 3158, 1759, 1732,
1603, 1523, 1395, 1269, 1082 cm-1. Anal calcd. for C17H13N3O5S: C, 54.98, H, 3.53, N, 11.31; found:
C, 55.13, H, 3.82, N, 11.03.
5-[[4-(4-Methoxybenzoyloxy)pheny]methyl]-2-thioxo-4-imidazolidinone (6-17). Yield 61%, mp: 226-
228 °C. 1H NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 3.87 (s, 3H, OCH3), 4.58 (dd, J = 4.2, 5.1 Hz,
1H, CH), 7.10-7.19 (m, 4H, Ar-H), 7.23-7.26 (m, 2H, Ar-H), 8.05-8.10 (m, 2H, Ar-H), 10.12 (s, 1H,
NH), 11.51 (s, 1H, NH); IR: 3281, 3158, 1759, 1732, 1603, 1523, 1395, 1269, 1070 cm-1. Anal calcd.
for C17H13N3O5S: C, 54.98, H, 3.53, N, 11.31; found: C, 55.13, H, 3.82, N, 11.03. ESI-MS m/z: 357
[M+H]+, 379 [M+Na]+.
5-[[4-(4-Methylbenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-18). Yield 52%, mp: 234-
236 °C. 1H-NMR (DMSO-d6): δ 2.43 (s, 3H, CH3), 3.02-3.04 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz,
1H, CH), 7.17-7.27 (m, 4H, Ar-H), 7.40 (d, J = 8.5 Hz, 2H, Ar-H), 8.01 (d, J = 8.5 Hz, 2H, Ar-H),

Molecules 2011, 16
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10.12 (s, 1H, NH), 11.51 (s, 1H, NH); IR: 3350, 3188, 1762, 1740, 1604, 1515, 1382, 1266, 1066 cm-1.
Anal calcd. for C18H16N2O3S: C, 63.51, H, 4.74, N, 8.23; found: C, 63.63, H, 4.84, N, 8.17. ESI-MS m/z:
341 [M+H]+, 363 [M+Na]+.
5-[[4-(2-Methylbenzoyloxy)phenylmethyl]-2-thioxo-4-imidazolidinone (6-19). Yield 35%, mp: 190-192 °C.
1H-NMR (DMSO-d6): δ 2.59 (s, 1H, CH3), 3.01-3.03 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH),
7.17-7.28 (m, 4H, Ar-H), 7.37-7.42 (m, 2H, Ar-H), 7.55-7.60 (m, 1H, Ar-H), 8.04-8.08 (m, 1H, Ar-H),
10.12 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3348, 3162, 1760, 1737, 1601, 1545, 1398, 1266, 1046 cm-1.
Anal calcd. for C18H16N2O3S: C, 63.51, H, 4.74, N, 8.23; found: C, 63.53, H, 4.79, N, 8.21.
5-[[4-(3,4-Dimethoxybenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-20). Yield 44%, mp:
228-230 °C. 1H-NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 3.84 (s, 3H, OCH3), 3.87 (s, 3H, OCH3),
4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.14-7.26 (m, 5H, Ar-H), 7.58 (d, J = 2.0 Hz, 1H, Ar-H), 7.76-7.79
(m, 1H, Ar-H), 10.12 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3498, 3186, 1758, 1749, 1596, 1520, 1409,
1279, 1017 cm-1. Anal calcd. for C19H18N2O5S: C, 59.06, H, 4.70, N, 7.25; found: C, 58.94, H, 4.62,
N, 7.21. ESI-MS m/z: 385 [M-H]-.
5-[[4-(Phenylacetyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-21). Yield 39%, mp: 160-162 °C. 1H-
NMR (DMSO-d6): δ 2.97-2.99 (m, 2H, CH2), 3.94 (s, 2H, CH2Ar), 4.58 (dd, J = 4.2, 5.1 Hz, 1H, CH),
7.03-7.19 (m, 4H, Ar-H), 7.28-7.37 (m, 5H, Ar-H), 10.12 (s, 1H, NH), 11.52 (s, 1H, NH); IR: 3378,
3159, 1756, 1748, 1548, 1507, 1320, 1199, 1010 cm-1. Anal calcd. for C18H16N2O3S: C, 63.51, H,
4.74, N, 8.23; found: C, 63.45, H, 4.77, N, 8.19. ESI-MS m/z: 339 [M-H]-.
5-[[4-(2,4-Dichlorophenoxyacetyl)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-22). Yield 60%, mp:
150-152 °C. 1H-NMR (DMSO-d6): δ 2.98-3.01 (m, 2H, CH2), 4.58 (dd, J = 4.2, 5.1 Hz, 1H, CH), 5.23
(s, 2H, OCH2), 7.10-7.29 (m, 5H, Ar-H), 7.38-7.63 (m, 2H, Ar-H), 10.11 (s, 1H, NH), 11.51 (s, 1H,
NH); IR: 3450, 3150, 1752, 1743, 1552, 1489, 1308, 1201, 1089 cm-1. Anal calcd. for
C18H14Cl2N2O4S: C, 50. 83, H, 3.32, N, 6.59; found: C, 50.86, H, 3.51, N, 6.75. ESI-MS m/z: 425, 423
[M-H]-.
5-[[4-(2-Methoxybenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-23). Yield 58%, mp: 158-160 °C.
1H-NMR (DMSO-d6): δ 2.86-2.88 (m, 2H, CH2), 3.87 (s, 3H, OCH3), 4.57 (dd, J = 4.2, 5.0 Hz, 1H,
CH), 6.96-7.17 (m, 3H, Ar-H), 7.21-7.26 (m, 3H, Ar-H), 7.60-7.66 (m, 1H, Ar-H), 7.87-7.90 (m, 1H,
Ar-H), 10.10 (s, 1H, NH), 11.51 (s, 1H, NH); IR: 3470, 3173, 1842, 1760, 1593, 1487, 1348, 1253,
1047 cm-1. Anal calcd. for C18H16N2O4S: C, 60. 66, H, 4.53, N, 7.86; found: C, 60.39, H, 4.57, N,
7.95.
5-[[4-(4-Chlorophenoxyacetyl)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-24). Yield 53%, mp:
184-186 °C. 1H-NMR (DMSO-d6): δ 2.99-3.01 (m, 2H, CH2), 4.57 (dd, J = 4.2, 5.1 Hz, 1H, CH), 5.08
(s, 2H, OCH2), 7.04-7.11 (m, 4H, Ar-H), 7.23 (d, J = 8.6 Hz, 2H, Ar-H), 7.34-7.38 (d, J = 8.6 Hz, 2H,
Ar-H), 10.11 (s, 1H, NH), 11.51 (s, 1H, NH); IR: 3435, 3149, 1850, 1737, 1547, 1495, 1320, 1170,

Molecules 2011, 16
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1072 cm-1. Anal calcd. for C18H15ClN2O4S: C, 55. 31, H, 3.87, N, 7.17; found: C, 55.48, H, 4.16, N,
7.29.
5-[[4-(3,4,5-Trimethoxybenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-25). Yield 56%,
1
mp: 194-196 °C. H-NMR (DMSO-d6): δ 3.01-3.04 (m, 2H, CH2), 3.77 (s, 3H, OCH3), 3.88 (s, 6H,
OCH3), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.17-7.27 (m, 4H, Ar-H), 7.41 (s, 2H, Ar-H), 10.12 (s, 1H,
NH), 11.51 (s, 1H, NH); IR: 3432, 3275, 1845, 1747, 1592, 1519, 1335, 1204, 1092 cm-1. Anal calcd.
for C20H20N2O6S: C, 57. 68, H, 4.84, N, 6.73; found: C, 57.36, H, 4.93, N, 6.67.
5-[[4-(4-Phenylbenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-26). Yield 58%, mp: 226-228 °C.
1H-NMR (DMSO-d6): δ 3.02-3.04 (m, 2H, CH2), 4.59 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.21-7.29 (m, 4H,
Ar-H), 7.43-7.57 (m, 3H, Ar-H), 7.78-7.93 (m, 4H, Ar-H), 8.19-8.22 (m, 2H, Ar-H), 10.13 (s, 1H,
NH), 11.53 (s, 1H, NH); IR: 3440, 3149, 1854, 1735, 1604, 1544, 1401, 1196, 1072 cm-1. Anal calcd.
for C23H18N2O3S: C, 68. 64, H, 4.51, N, 6.96; found: C, 68.63, H, 4.44, N, 6.95.
5-[[4-(4-tert-Butylbenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-27). Yield 48%, mp: 237-
239 °C. 1H-NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 4.57 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.19-7.27 (m,
4H, Ar-H), 7.61-7.64 (m, 2H, Ar-H), 8.04-8.07 (m, 2H, Ar-H), 10.12 (s, 1H, NH), 11.52 (s, 1H, NH);
IR: 3440, 3159, 1852, 1741, 1607, 1547, 1402, 1197, 1073 cm-1. Anal calcd. for C21H22N2O3S: C, 65.
95, H, 5.80, N, 7.32; found: C, 65.81, H, 5.76, N, 7.29. ESI-MS m/z: 381 [M-H]-.
5-[[4-(1-Naphthylacetoxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-28). Yield 51%, mp: 179-181 °C. 1H-
NMR (DMSO-d6): δ 3.03-3.05 (m, 2H, CH2), 4.43 (s, 2H, CH2), 4.55 (dd, J = 4.2, 5.0 Hz, 1H, CH),
7.01-7.20 (m, 4H, Ar-H), 7.50-7.65 (m, 4H, Ar-H), 7.89-8.09 (m, 3H, Ar-H), 10.11 (s, 1H, NH), 11.51
(s, 1H, NH); IR: 3446, 3150, 1853, 1739, 1601, 1548, 1403, 1199, 1150, 1090 cm-1. Anal calcd. for
C22H18N2O3S: C, 67. 67, H, 4.65, N, 7.17; found: C, 67.30, H, 4.73, N, 7.29. ESI-MS m/z: 389 [M-H]-.
5-[[4-(3,5-Dinitrobenzoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-29). Yield 41%, mp: 236-238 °C.
1H-NMR (DMSO-d6): δ 3.03-3.05 (m, 2H, CH2), 4.61 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.28-7.35 (m, 4H,
Ar-H), 9.07-9.12 (m, 3H, Ar-H), 10.15 (s, 1H, NH), 11.55 (s, 1H, NH); IR: 3448, 3209, 1860, 1751,
1629, 1540, 1352, 1157, 1087 cm-1. Anal calcd. for C17H12N4O7S: C, 49. 04, H, 2.90, N, 13.46; found:
C, 49.26, H, 3.21, N, 13.35.
5-[[4-(2-Thenoyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-30). Yield 46%, mp: 208-210 °C.
1H-NMR (DMSO-d6): δ 3.02-3.05 (m, 2H, CH2), 4.60 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.18-7.24 (m, 4H,
Ar-H), 7.26-7.33 (m, 1H, Thienyl-H), 8.01-8.11 (m, 2H, Thienyl-H), 10.11 (s, 1H, NH), 11.51 (s, 1H,
NH); IR: 3445, 3209, 1781, 1733, 1612, 1546, 1408, 1211, 1056 cm-1. Anal calcd. for C15H12N2O3S2:
C, 54. 20, H, 3.64, N, 8.43; found: C, 53.74, H, 3.45, N, 8.33.
1
5-[[4-(Phenylacryloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-31). Yield 40%, mp: 204-206 °C. H-
NMR (DMSO-d6): δ 3.00-3.02 (m, 2H, CH2), 4.58 (dd, J = 4.2, 5.1 Hz, 1H, CH), 6.86 (d, J = 15.9 Hz,
1H, H-C=), 7.13 (d, J = 8.5 Hz, Ar-H), 7.24 (d, J = 8.5 Hz, Ar-H), 7.46-7.48 (m, 3H, Ar-H), 7.79-7.89

Molecules 2011, 16
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(m, 3H, Ar-H+H-C=), 10.17 (s, 1H, NH), 11.48 (s, 1H, NH); IR: 3440, 3150, 1780, 1739, 1630, 1548,
1502, 1185, 1156 cm-1. Anal calcd. for C19H16N2O3S: C, 64. 76, H, 4.58, N, 7.95; found: C, 64.64, H,
4.63, N, 8.03. ESI-MS m/z: 351 [M-H]-.
5-[[4-(3,5-bis(Trifluoromethyl)phenylacetoxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-32). Yield
62%, mp: 161-163 °C. 1H-NMR (DMSO-d6): δ 2.49-2.52 (m, 2H, CH2), 4.27 (s, 2H, CH2), 4.56 (dd, J
= 4.2, 5.1 Hz, 1H, CH), 7.09 (d, J = 8.6 Hz, 2H, Ar-H), 7.22 (d, J = 8.6 Hz, 2H, Ar-H), 8.04 (s, 1H, Ar-
H), 8.16 (s, 2H, Ar-H), 10.08 (s, 1H, NH), 11.49 (s, 1H, NH); IR: 3442, 3168, 1782, 1747, 1546, 1502,
1391, 1290, 1086 cm-1. Anal calcd. for C20H14F6N2O4S: C, 50. 42, H, 2.96, N, 5.88; found: C, 50.80,
H, 3.26, N, 6.01.
5-[[4-(4-Fluorophenylacetoxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-33). Yield 52%, mp:
175-177 °C. 1H-NMR (DMSO-d6): δ 2.97-2.99 (m, 2H, CH2), 3.95 (s, 2H, CH2), 4.55 (dd, J = 4.2, 5.0
Hz,, 1H, CH), 7.03 (d, J = 8.5 Hz, 2H, Ar-H), 7.15-7.22 (m, 4H, Ar-H), 7.39-7.44 (m, 2H, Ar-H),
10.07 (s, 1H, NH), 11.48 (s, 1H, NH); IR: 3446, 3171, 1779, 1748, 1602, 1548, 1491, 1286, 1090 cm-1.
Anal calcd. for C18H15FN2O3S: C, 60. 32, H, 4.22, N, 7.82; found: C, 60.46, H, 4.46, N, 8.08. ESI-MS
m/z: 357 [M-H]-.
5-[[4-(2-Furylformyloxy)phenyl]methyl]-2-thioxo-4-imidazolidinone (6-34). Yield 74%, mp: 173-175 °C.
1H- NMR (DMSO-d6): δ 3.01-3.03 (m, 2H, CH2), 4.61 (dd, J = 4.2, 5.1 Hz, 1H, CH), 7.21-7.28 (m,
4H, Ar-H), 7.62-7.67 (m, 1H, Fu-H), 7.81-7.84 (m, 1H, Fu-H), 8.06-8.11 (m, 1H, Fu-H), 10.12 (s, 1H,
NH), 11.51 (s, 1H, NH); IR: 3485, 3151, 1784, 1738, 1545, 1468, 1399, 1204, 1012 cm-1. Anal calcd.
for C15H12N2O4S: C, 56. 96, H, 3.82, N, 8.86; found: C, 56.94, H, 4.07, N, 9.09.
3.2.3. Synthesis of Compound 7
To a stirred solution of 5-[(4-hydroxy phenyl)methyl]-2-thioxoimidazolidin-4-one (5, 2 mmol) and
acetic anhydride (4 mmol) in dry actone (25 mL) and DMAP (0.02 g, 0.2 mmol) were added at room
temperature. After about 10 h, the reaction is almost complete as monitored by TLC. After
concentration under vacuum, the crude product was purified by column chromatography on silica gel
(petroleum ether-EtOAc 3:1-2:1) to afford pale yellow solid compound 7, yield 51%. Compound 7,
mp: 138-139 °C. IR: 3492, 3217, 3016, 2932, 1774, 1724, 1510, 1498, 1353, 1287, 1202, 1215, 1073,
1
1030 cm-1. H NMR (DMSO-d6): δ 12.45 (s, 1H), 7.056.98 (m, 4H), 4.93 (dd, J = 5.7, 2.7 Hz, 1H),
3.35 (dd, J = 14.1, 5.7 Hz, 1H), 3.11 (dd, J = 14.1, 2.7 Hz, 1H), 2.70 (s, 3H), 2.23 (s, 3H). Anal calcd
for C14H14N2O4S: C, 54.95, H, 4.66, N, 9.03; found: C, 54.89, H, 4.61, N, 9.14.
3.2.4. Synthesis of Compound 8
To a stirred solution of 5-[(4-hydroxyphenyl)methyl]-2-thioxoimidazolidin-4-one (5, 2 mmol) in
dry acetone (25 mL), benzoyl chloride (4 mmol) in 5 mL acetone and DMAP (0.02 g, 0.2 mmol) were
added at 0 °C. Heated to reflux for 9 h after addition, the reaction is almost complete as monitored by
TLC. After filtration and concentration under vacuum, the crude product was purified by column

Molecules 2011, 16
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chromatography on silica gel (petroleum ether-EtOAc 4:1-2:1) to produce pale yellow solid compound
8, yield 64%. Compound 8, mp: 173-174. IR: 3458, 3067, 2893, 2773, 1764, 1651, 1595, 1499, 1349,
1214, 1067, 1012 cm-1. 1H NMR (DMSO-d6): δ 12.64 (s, 1H), 8.168.13 (m, 2H), 7.787.73 (m, 1H),
7.647.51 (m, 3H), 7.41~7.29 (m, 4H), 7.24~7.13 (m, 4H), 5.34 (dd, J = 5.7, 3.0 Hz, 1H), 3.41~3.34
(m, 2H). Anal calcd for C24H18N2O4S: C, 66.99, H, 4.28, N, 6.53; found: C, 66.96, H, 4.21, N, 6.51.
3.3. Bioassay of Herbicidal Activities
Herbicidal activity tests of compounds 6 were carried out in an illumination incubator. Ten seeds of
Zea mays and five seeds of Triticum aestivum were chosen for the tests. Seedlings were grown in a
plate containing a piece of filter paper and 2 mL solution of the tested compound (200 mg/L).
Arabidopsis thaliana seeding were grown in 24-well sterile microliter plates, each well contained five
sterilized Arabidopsis thaliana seedings and 100 μL solution of the tested compound (200 mg/L).
Distilled water and metazachlor were used as the blank and positive control. The herbicidal activity
was assessed as the inhibitory ratio in comparison with distilled water in the range from 0 to 100%.
The tests were run triplicate for each compounds, the results were averaged and given in Table 1. The
greenhouse test were performed according to pre-emergence and post-emergence treatment,
Echinochloa crus-galli, Lolium multiflorum, Poa annua, Setaria viridis, Abutilon theophrasti,
Amaranthus retoflexus, Matricaria chamomilla, Stellaria media were used as the target weeds.
Acknowledgements
These projects were financed by the Natural Science Foundation of China (No. 20772150) and
State Key Laboratory of Elemento-organic Chemistry, Nankai University (Nos. 200902 and 201003).
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Sample Availability: Samples of the compounds 6-1-6-34 are available from the authors.
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