Synthesis and in vitro growth inhibition of 2-allylphenol derivatives against Phythopthora cinnamomi rands

Article abstract of DOI:10.3390/molecules24224196

Phytophthora cinnamomi is a phytopathogen that causes extensive damage in different crops, and therefore, produces important economic losses all around the world. Chemical fungicides are a key factor for the control of this disease. However, ecological an

Full text of DOI:10.3390/molecules24224196

molecules
Article
Synthesis and In Vitro Growth Inhibition of
2-Allylphenol Derivatives Against
Phythopthora cinnamomi Rands
Andrés F. Olea 1 , Luis Espinoza 2 , Claudia Sedan 3, Mario Thomas 3, Rolando Martínez 3
,
Marco Mellado 4 , Héctor Carrasco 1,
*
and Katy Díaz 2,
*
1
Instituto de Ciencias Químicas Aplicadas, Facultad de Ingeniería, Universidad Autónoma de Chile,
El Llano Subercaseaux 2801, Santiago CP 8900000, Chile; andres.olea@uautonoma.cl
Departamento de Química, Universidad Técnica Federico Santa María, Avenida España 1680,
Valparaíso CP 2340000, Chile; luis.espinozac@usm.cl
2
3
Departamento de Ciencias Químicas, Facultad de Ciencias Exactas, Universidad Andrés Bello, Quillota 910,
Viña del Mar CP 2520000, Chile; claudiasedan@hotmail.com (C.S.); m.thomaselgueda@gmail.com (M.T.);
rmartinez@unab.cl (R.M.)
Instituto de Química, Facultad de Ciencias, Pontificia Universidad Católica de Valparaíso, Avenida
Universidad 330, Curauma, Valparaíso CP 2340000, Chile; marco.mellado@pucv.cl
Correspondence: hector.carrasco@uautonoma.cl (H.C.); katy.diaz@usm.cl (K.D.)
4
*
ꢀꢁꢂꢀꢃꢄꢅꢆꢇ
ꢀꢁꢂꢃꢄꢅꢆ
Received: 3 October 2019; Accepted: 16 November 2019; Published: 19 November 2019
Abstract: Phytophthora cinnamomi is a phytopathogen that causes extensive damage in different crops,
and therefore, produces important economic losses all around the world. Chemical fungicides are
a key factor for the control of this disease. However, ecological and environmental considerations,
as well as the appearance of strains that are resistant to commercial fungicides, have prompted
the quest for new antifungal agents which are of low ecological impact. In this work, a series
of new 2-allylphenol derivatives was synthesized, and their structures were confirmed by FT-IR,
NMR, and MS. Some of the synthesized compounds, more specifically nitro derivatives, exhibit
strong growth inhibition of P. cinnamomi with EC50 as low as 10.0 µg/mL. This level of activity
is similar to that exhibited by METALAXYL MZ 58 WP, a commonly-used commercial fungicide;
therefore, these compounds might be of agricultural interest due to their potential use as fungicides
against P. cinnamomi. The results indicate that this activity depends on the chemical structures of the
2-allylphenol derivatives, and that it is strongly enhanced in molecules where nitro and hydroxyl
groups adopt a -para configuration. These effects are discussed in terms of the electronic distribution
of the aromatic ring induced by substituent groups.
Keywords: pest control; Phytophthora cinnamomi; fungicide; 2-allylphenol; structure–activity relationship
1. Introduction
Diseases of plants caused by species of the genus Phytophthora represent some of the most
devastating crop diseases worldwide. All known species of Phytophthora are plant pathogens [
It has worldwide distribution and a host range approaching 5000 species [ ]. In addition to causing
substantial economic loss in agriculture, forestry, and horticulture, the inadvertent introduction of
Phytophthora cinnamomi has had disastrous consequences for natural ecosystems and biodiversity [ ].
1].
2,3
4
The scale of P. cinnamomi distribution, its ability to survive for years in soil or symptomless plants,
and the extent of plant susceptibility make the management of P. cinnamomi diseases challenging
and difficult. Based on these facts, P. cinnamomi has been ranked in the top ten Oomycete plant
pathogens [3].
Molecules 2019, 24, 4196; doi:10.3390/molecules24224196
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In addition, Phytophthora shows important structural differences with respect to true fungi, which
induce changes in the mechanism and efficacy of fungicides to control this phytopathogen. In other
words, compounds that exhibit antifungal activity have no effect against oomycetes. The most
commonly-used chemicals to control P. cinnamomi are metalaxyl or mefenoxam (phenylamides) and
phosphite (a phosphonate and active ingredient in fosetyl-Al). However, the development of resistance
to chemical fungicides have been detected, mainly in soils that have been treated for long periods with
these antifungal compounds [5,6]. Thus, it is of great interest to find new chemical compounds that are
active against these species and, hopefully, harmless for both people and the environment. From this
point of view, the study of secondary metabolites and their hemisynthetic derivatives emerges as
an interesting alternative to be explored. In this line, we have previously studied the antifungal
activity of a series of phenols with side alkyl chains, such as geranylated phenols [7–10] and eugenol
derivatives [11]. In these studies, it has been shown that fungicide activity depends on the nature,
number, and position of substituents in the aromatic ring.
On the other hand, 2-allylphenol (2-AP) is a synthetic fungicide molecule that is structurally
related to eugenol, and mimics the compound ginkgol found in gingko fruit (Gingko biloba L.). Recently,
it has been shown that its fungicide activity against Botrytis cinerea is associated with increasing the cell
respiration, i.e., mycelial oxygen uptake increases by 19.58% and 24.56% at 2-AP concentrations of
5 and 10 ppm, respectively [12]. Additionally, at 150 ppm, the oxygen consumption rate decreases
by 77.49% in comparison with the control. These results indicated that at low concentrations, 2-AP
increases cellular metabolism, whereas at high concentrations, it induces cell death [12]. Recently,
the inhibition of mycelial growth of Ramulispora cerealis, Pythium aphanidermatum, Valsa mali, and
B. cinerea by 2-AP derivatives, 2-(2-hydroxypropyl)phenol and 2-(3-hydroxypropyl)phenol has been
assessed [13]. The results indicate that the chemical modification of the side allyl chain influences the
antifungal activity, i.e., EC50 values of 2-(2-hydroxypropyl) were lower (1.0 to 23.5 ppm) than those
measured for 2-allylphenol (8.2 to 48.8 ppm) [14].
Thus, these results suggest that 2-AP and its derivatives could be an interesting means by which
to obtain new antifungal agents. We have previously shown that the antifungal activity of eugenol
on B. cinerea is enhanced by the presence of nitro groups in the aromatic ring [15]. This effect was
attributed to the increasing reactivity of the nitro derivative and production of reactive oxygen species
(ROS) in an enzymatic-mediated process. Thus, herein we report on the synthesis of a series of 2-AP
derivatives in which nitro groups were attached to the aromatic ring. The growth inhibition effect
on P. cinnamoni was evaluated for all these compounds. The results indicate that the highest activity
corresponds to nitro derivatives adopting a –para configuration of nitro and hydroxyl groups.
2. Results and Discussion
A series of nine new derivatives of 2-AP (1), compounds 2–10 in Figure 1, have been synthesized
and characterized by spectroscopic methods.
The reactions used to synthesize these derivatives are depicted in Scheme 1. Briefly, compounds
, and were obtained from 2-AP following standard reactions. Reaction yields of 96% and 67% were
obtained for compounds and , respectively. The nitration of 2-AP leads to a mixture of compounds
and with low yields (20% and 21%). To improve the reaction yield of compound , an alternative
synthetic procedure was used to get with a 72% yield. Similarly, the nitration of generates a mixture
of and with low yields (4% and 7%). Methyl ethers and 10 are obtained by the reaction of phenols
and with dimethylsulfate with high reaction yields, i.e., 67% and 78% respectively. Compound is
obtained by the treatment of with potassium carbonate in methanol (80% yield). Finally, nitration of
2 leads to nitroacetate derivatives 5 and 7, with 4% and 7% reaction yields, respectively.
2,
4
9
2
3
4
9
4
4
2
5
7
6
4
9
8
7

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Figure 1. Chemical structures of 2-AP (1) and new synthesized derivatives (2–10).
Scheme 1. Synthesis of new 2-AP derivatives. Conditions: (a) HNO3/H2SO4, CH2Cl2, 0 ◦C. 30 min;
(b) Ac2O, DMAP, CH2Cl2, r.t 2.5 h; (c) NaNO3/KHSO4, SiO2/H2O (1:1), r.t 24 h; (d) dimethylsulfate,
(CH3)2CO, reflux overnight; (e) K2CO3, MeOH, r.t 4 h.
Growth Inhibition of 2-AP and Its Derivatives Against Phytophthora cinnamomi In Vitro
The antifungal activities of 2-AP and its derivatives against P. cinnamomi were determined by
measuring mycelial growth inhibition in the absence and presence of different concentrations of
all the assayed compounds. The results indicate that the inhibitory effect increases with increasing
concentration and depends on the chemical structure of 2-AP derivatives. A typical measurement is
shown in Figure 2 for compound 9.

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Figure 2. In vitro effect of 2-allyl-4,6-dinitrophenol (
at different concentrations: ( ) 0 g/mL (Negative control); (
(e) METALAXYL MZ 48 WP at 10 µg/mL, used as positive control.
9
) on mycelial growth of Phytophthora cinnamomi
a
µ
b
) 10 g/mL; ( ) 25 g/mL; ( ) 50 g/mL;
µ
c
µ
d
µ
The percentages of inhibition (%I) were calculated for each concentration, and EC50 values
(concentration causing 50% inhibition of mycelial growth) were obtained from fitting data to a
dose-response curve (see Experimental section). The EC50 values for all assayed compounds are given
in Table 1.
Table 1. EC50 values of 2-AP and its synthetic derivatives on the in vitro mycelial growth of P. cinnamomi.
These values were estimated by measuring the colony diameter after 144 h of incubation.
a
EC50 (µg/mL) ± SD b
Compounds
R c
1
2
3
155 ± 1.45
360 ± 1.27
I
0.9404
0.9312
i
4
5
6
180 ± 1.42
105 ± 1.70
I
0.9327
0.9878
i
7
8
9
10
10 ± 1.43
10 ± 0.15
9 ± 1.77
80 ± 2.00
7.5 ± 0.64
0.9185
0.9973
0.9805
0.9996
0.9999
Metalaxil MZ 48 WP (C+)
EC50, concentration causing 50% mycelial growth inhibition; b SD, Standard Deviation; R c Pearson’s correlation
a
coefficient; i: Inactive compound.
Interestingly, 2-AP has been assayed against various fungal plant pathogens; its EC50 values
range from 8 µg/mL (Rhizoctonia cerealis) to 49 µg/mL (B. cinerea) [14]. However, to the best of our
knowledge, this is the first report of 2-AP activity against P. cinnamomi, and the EC50 value obtained in
this work is three times higher than that measured for B. cinerea. This variability on antifungal activity
suggests that the action mechanism of 2-AP changes from one fungal species to another. In addition,
the results shown in Table 1 indicate that growth inhibition of P. cinnamomi (EC50 values) is clearly
dependent on the chemical structure of 2-AP derivatives. For example, a two-fold increase in EC50
values is observed by acetylation of hydroxyl group (compare
more important when the hydroxyl group is replaced by a methoxy group in compound
1
and
2
). This activity decrease is even
. On the
3
other hand, the introduction of nitro groups in the aromatic ring of 2-AP brings about the opposite
effect, depending on its relative position to the hydroxyl group, i.e., activity slightly decreases with
substitution in the -ortho position (compares
is attached in the -para position to the hydroxyl group (compares
is observed in nitro derivatives where the hydroxyl group has been replaced by acetyl or methoxy
groups. For example, the completely inactive methoxy derivative ( ) becomes slightly active by adding
a nitro group in the -ortho position ( ), but an even more drastic activity increase is obtained by
moving the nitro group to the -para position (10). For acetyl derivatives, the -para isomer is one
order of magnitude more active than the -ortho isomer (compares and ). Thus, it seems that this
1
and
4), whereas it increases 15 times when a nitro group
1
and ). Interestingly, a similar effect
8
3
6
5
7
structural configuration of 2-AP nitro derivatives enhances the antifungal activity, independently of the
presence of a hydroxyl group in the -para position. These results suggest that the structural features
of 2-AP derivatives determining their antifungal activity are mainly associated with the distribution

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of substituent groups in the aromatic ring, instead of the presence or absence of a particular group.
Similar results were obtained for the inhibition of P. cinnamomi by a series of geranylated phenols [ 16].
8,
Thus, it seems that the mechanism of action on this fungus involves the whole molecule and depends
on the electronic distribution existing on the aromatic ring. To confirm this hypothesis, a study of the
electronic properties of 2-AP derivatives was carried out. Maps of the molecular electronic potential
were obtained after the optimization of chemical structure by molecular mechanics methods. Figure 3
shows charge distribution maps obtained for compounds
derivatives of 2-AP, respectively).
1, 4, and 8 (2-AP, ortho- and para- nitro
Figure 3. Charge distribution map: (A) compound 1; (B) compound 4; (C) compound 8. Red
and blue represent negative and positive charges, respectively. Charge variation is represented by
intermediate colors.
The electrostatic potential map obtained for 2-AP (1) shows the existence of a positive charge area
in the vicinity of carbon atoms C1 and C6, due to the presence of the hydroxyl group. For the o-nitro
derivative (compound 4) the introduction of a nitro group in C6 decreases the positive charge in this
area (change from blue to green) due to an intra-molecular hydrogen bond and induces the appearance
of a negative charge around oxygen of the nitro group. This drastic change in charge polarity induces
a slight decrease on activity, i.e., EC50 increases from 155 to 180 µg/mL (compounds 1 and 4, Table 1).
Therefore, it seems that positively- or negatively-charged areas are required for these molecules to bind
electrostatically to P. cinnamomi. On the other hand, for the most active derivative, the map shows both
positive and negative surfaces located on opposite sides of the aromatic ring. As consequence, EC50 of
8 (p-nitro isomer) is more than one order of magnitude lower than that obtained for 4 (o-isomer). Thus,
a polar surface involving the whole molecule seems to be a main structural requirement for activity.
Metalaxyl is a systemic fungicide which is highly selective to oomycetes that has no effect on
respiration [17]. These results have been attributed to the alteration of biosynthesis or membrane
structure caused by the presence of cellulose instead of chitin in the cell membrane [17]. Similarly,
the antifungal activity of eugenol and its nitro-derivatives against B. cinerea has been explained by the
ability of these compounds to interact with the cell wall of the fungus, spreading inside the hypha
and interfering in the enzymatic activity responsible for the growth of the fungus [15,18]. This ability
has been attributed to the molecular lipophilicity, measured by ClogP (calculated logarithm of the
partition coefficient of the molecule between octanol and aqueous phase), and the chemical reactivity
of the nitro groups [19]. Thus, to determine whether the growth inhibition of P. cinnamomi by 2-AP
derivatives follows a similar mechanism, the values of ClogP were calculated for all 2-AP derivatives.
The ClogP values were in the range of 2.3 to 2.9 and were similar to those calculated for other antifungal
agents [20]; however, no correlation between activity and ClogP was found. These results suggest
that activity against P. cinnamomi is determined mainly by the reactivity of nitro derivatives, which is
closely related to the electronic distribution in the whole molecule.

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3. Experimental Section
3.1. General Information
Unless otherwise stated, all chemical reagents purchased (Merck, Darmstadt, Germany or Aldrich,
St. Louis, MO, USA) were of the highest commercially-available purity and were used without previous
purification. IR spectra were obtained in a Thermo Scientific Nicolet Impact 6700 FT-IR spectrometer
1
using KBr pellets or as thin films, frequencies are reported in cm−1. H- and 13C-NMR (DEPT 135 and
DEPT 90) were performed on a Bruker Avance 400 Digital NMR spectrometer, operating at 400.1 MHz
for 1H and 100.6 MHz for 13C. Spectra were recorded in CDCl3 solutions, and are referenced to the
residual peaks of CHCl3,
are reported in ppm and coupling constants (J) are given in Hz. Chemical shifts are reported in
(ppm downfield from the TMS resonance) and coupling constants (J) are given in Hz. GC–MS was
carried out using a SHIMADZU GCMS-QP2010 instrument (Tokyo, Japan) using a 30 m 0.25 mm id.,
0.25 m Rtx-5MS capillary column with helium as carrier gas to 1.61 mL/min. The column temperature
δ = 7.26 ppm and δ
= 77.0 ppm for 1H and 13C, respectively. Chemical shifts
δ
δ
×
µ
program was 60 ◦C for 1 min at 5 ◦C/min, then increased to 285 ◦C for 2 min at 15 ◦C/min. Silica gel
(Merck 200–300 mesh) was used for column chromatography (CC) and silica gel plates GF-254 for thin
layer chromatography (TLC). TLC spots were detected by UV light and by heating after spraying with
25% H2SO4 in H2O.
3.2. Synthesis of 2-AP Derivatives
The synthetic pathways to obtain the nine new derivatives of 2-AP are shown in Scheme 1. General
and specific information is given below. Pure compounds were obtained by CC, and new compounds
were characterized and verified by spectroscopic methods.
3.2.1. Methylation Reactions
Phenols 1, 4, and 9 were reacted with dimethyl sulfate to give methyl ethers 3, 6, and 10 by the
following synthetic procedure. To a stirred solution of phenol in dry acetone (50–100 mL) was added
potassium carbonate and dimethyl sulfate. The reaction was left to continue overnight under reflux.
After this period, the complete disappearance of the starting product was confirmed by TLC (ethyl
acetate/hexane; 1:3 by volume). The crude product of the reaction is diluted in acetone (30 mL) and
water (50 mL), and then extracted with dichloromethane (3
vacuum evaporated. The pure product was obtained by CC (ethyl acetate/hexane; 1:9 by volume).
×
50 mL), dried with anhydrous, and
3.2.2. Nitration Procedure
Nitro derivatives 4, 9, and 5, 7 were obtained from 2-AP and compound 2, respectively, by reaction
with sulfonitric mixture (2 mL of concentrated nitric acid, 6 mL of concentrated sulfuric acid and 2 mL
of water). To a stirred and cooled (2 ◦C) solution of phenol in dichloromethane (10 mL) was carefully
added the sulfonitric mixture (2 mL). The reaction was left to continue for 30 min and then interrupted
by adding water (10 mL). The complete disappearance of the starting product was confirmed by
TLC (ethyl acetate/hexane; 1:3 by volume). The organic layer was washed with water (3
eliminate the excess of acid, dried with anhydrous Na2SO4, filtered, and the solvent was evaporated at
×
10 mL) to
low pressure. Pure products were separated by CC (ethyl acetate/hexane; 1:9 by volume).
3.2.3. Preparation of 2-Allylphenyl Acetate (2)
This compound was obtained by the acetylation of 2-AP. To a stirred solution of 2-AP (5.0 g,
37 mmol) in dichloromethane (10 mL) was added 4-N,N-dimethylaminopyridine (DMAP) (0.487 g,
3.98 mmol) and acetic anhydride (15.5 mL, 0.16 mol). The reaction proceeded for 2.5 h at room
temperature. After this period, the complete disappearance of the starting product was confirmed by
means of TLC (ethyl acetate/hexane; 1:3 by volume). The reaction was stopped by adding a 10% solution

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of potassium hydrogen sulfate (50 mL). The reaction crude product was extracted with dichloromethane,
and the organic phase was washed with water (3 20 mL), dried with anhydrous Na2SO4, and vacuum
evaporated. The pure product (yellow oil) was obtained by CC (ethyl acetate/hexane; 1:9 by volume).
Compound
(6.31 g, 96% yield): IR (cm−1): 3076 (=C-H); 1756 (C=O); 1637 (C=C); 1367 (-CH2); 1197
×
2
(C-O); 1168 (C-O-C). 1H-NMR: 7.24–7.16 (2H, m, H-3 and H-5); 7.05–7.03 (2H, m, H-4 and H6); 5.95–5.65
(1H, m, H-20); 5.09–5.05 (2H, m, H-30); 3.31 (2H, d, J = 6.6 Hz, H-10); 2.28 (3H, s, OCH3). 13C-NMR:
148.9 (C-1); 135.8 (C-20); 131.8 (C-2); 130.3 (C-3); 127.3 (C-4); 126.0 (C-5); 122.3 (C-6); 116.1 (C-30); 34.6
(C-10); 20.8(CH3). EI-MS (+) m/z 176 [M+] (100%).
3.2.4. Preparation of 1-Allyl-2-Methoxybenzene (3)
This compound was obtained by the methylation of 2-AP (1.0 g, 5.71 mmol) in the presence of dry
acetone (120 mL), potassium carbonate (5.5 g, 39.8 mmol) and dimethyl sulfate (4.85 mL, 51.1 mmol).
Compound 3
(yellow oil) was obtained by CC (0.735 g, 67% yield): IR (cm−1): 3080 (=C-H); 1768 (C=O);
1522 (C=C); 1344 (CH3); 1184 (C-O); 1166 (C-O-C). 1H-NMR: 7.25 (1H, dd, J = 8.8 and 7.5 Hz, H-3); 7.18
(1H, t, J = 9.0 Hz, H-5); 6.93 (1H, t, J = 7.4 Hz, H-4); 6.88 (1H, d, J = 8.2 Hz, H-6); 6.09–5.99 (1H, m, H-20);
5.11–5.06 (2H, m, H-30); 3.85 (3H, s, CH3CO); 3.42 (2H, d, J = 6.6 Hz, H-10). 13C-NMR: 157.2 (C-1); 137.0
(C-20); 129.7 (C-5); 128.6 (C-2); 127.3 (C-3); 120.5 (C-4); 115.3 (C-30); 110.3 (C-6); 55.3 (OCH3); 34.2 (C-10).
EI-MS (+) m/z non-detected.
3.2.5. Preparation of 2-Allyl-6-Nitrophenol (4) and 2-Allyl-4,6-Dinitrophenol (9)
The nitration of 2-AP (1.0 g, 7.42 mmol) was performed in dichloromethane (5 mL) with sulfonitric
◦
mixture (2 mL) at 2 C. Two fractions were obtained by CC. Fraction I: Compound
4
; reddish oil
4
(285 mg, 21% yield); Fraction II: Compound
9; brown oil (342 mg, 20% yield). Compound
: IR (cm−1):
3201 (OH); 3085 (=C-H); 2977 (C-H); 1609 (C=C); 1539 (-NO2); 1448 (C=C); 1329 (N=O); 1249 (C-O-C).
1H-NMR: 10.90 (s, 1H, OH); 7.99 (1H, d, J = 8.6 Hz, H-5); 7.46 (1H, d, J = 7.3 Hz, H-3); 6.92 (1H, t, J = 8.0
Hz, H-4); 6.03–5.93 (1H, m, H-20); 5.13–5.09 (2H, m, H-30); 3.48 (2H, d, J = 6.5 Hz, H-10).13C-NMR: 153.3
(C-6); 137.5 (C-3); 135.1 (C-20); 131.4 (C-1); 123.1 (C-5); 119.5 (C-4); 112.5 (C-3); 116.8 (C-30); 33.6 (C-10).
EI-MS (+) m/z 179 [M +] (100%) Compound
(C=C); 1331 (CH2); 1552 (-NO2); 1432 (N=O). 1H-NMR: 11.40 (1H, s, OH); 8.95 (1H, d, J = 2.7 Hz, H-5);
9
: IR (cm−1): 3218 (OH); 3105 (=C-H); 2921 (C-H); 1610
8.34 (1H, d, J = 2.2 Hz, H-3); 6.03–5.93 (1H, m, H-20); 5.27–5.19 (2H, m, H-30); 3.57 (2H, d, J = 6.6 Hz
,
H-10). 13C-NMR: 157.3 (C-1); 139.7 (C-4); 133.8 (C-6); 133.2 (C-20); 130.9 (C-3); 119.7 (C-5); 118.7 (C-30);
33.6 (C-10). EI-MS (+) m/z 224 [M+] (100%).
Because of the low reaction yield obtained with the previous reaction, the following alternative
synthetic path was used to obtain compound 4. First, 2-AP (5.0 g, 37 mmol) was dissolved in
dichloromethane (100 mL) and added to a mixture containing potassium hydrogen sulfate (18.3 g,
0.134 mol), sodium nitrate (12.2 g, 0.144 mol), and wet silica (14.25 g, 50% w/w). The mixture was stirred
under reflux for 24 h. The complete disappearance of the starting product was confirmed by TLC
(ethyl acetate/hexane; 1:3 by volume). The solid product was filtered through silica and washed with
dichloromethane; the solvent was evaporated in a vacuum to yield a reddish oil. The pure product
(4.8 g, 72% yield) was obtained by CC (ethyl acetate/hexane; 1:9 by volume).
3.2.6. Preparation of 2-Allyl-6-Nitrophenyl Acetate (5) and 2-Allyl-4-Nitrophenyl Acetate (7)
Nitration of compound
sulfonitric mixture (2 mL) at 2 ◦C. Two fractions were obtained by CC. Fraction I: Compound
oil (47 mg, 4% yield); Fraction II: Compound ; reddish oil (87 mg, 7% yield). Compound
: IR (cm−1):
2
(1.0 g 5.71 mmol) was carried out in dichloromethane (8 mL) using
5; yellow
7
5
3080 (=C-H); 2930 (C-H); 1768 (C=O); 1522 (N-O); 1344 (N-O); 1184 (C-O); 1165 (C-O-C). 1H-NMR:
7.95 (1H, dd, J = 8.2 and 6.6 Hz, H-5); 7.54 (1H, dd, J = 7.7 and 6.4 Hz, H-3); 7.32 (1H, t, J = 15.8
Hz, H-4); 5.92–5.82 (1H, m, H-20); 5.15–5.07 (2H, m, H-30); 3.38 (2H, d, J = 6.6 Hz, H-10); 2.37 (3H, s,
CH3CO).13C-NMR: 168.3 (CO); 142.4 (C-1); 135.9 (C-6); 135.5 (C-3); 134.5 (C-20); 121.0 (C-2); 117.5 (C-30);
34.4 (C-10); 20.7 (CH3CO). EI-MS (+) m/z 43 (CH3CO); 179 (C9H8NO3); 221 [M+] Compound
7: IR

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(cm−1): 3085 (=C-H); 2915 (C-H); 1767(C=O); 1638 (C=C); 1521 (N-O); 1344 (N-O); 1183 (C-O); 1166
(C-O-C). 1H-NMR: 8.14–8.10 (2H, m, H-3 and H-5); 7.23 (1H, d, J = 8.8 Hz, H-6); 5.93–5.83 (1H, m, H-20);
5.16 (1H, dd, J = 9.9 and 0.8 Hz H-3a0); 5.12 (1H, dd, J = 15.8 and 1.3 Hz, H-30b); 3.37 (2H, d, J = 6.6 Hz,
H-10); 2.34 (3H, s, CH3CO) 13C-NMR: 168.2 (CO); 153.6 (C-4); 145.5 (C-1); 134.0 (C-20); 133.8 (C-2); 125.6
(C-3); 123.3 (C-6); 122.8 (C-5); 117.7 (C-30); 34.3(C-10); 20.8 (CH3CO). EI-MS (+) m/z equal Compound
5.
3.2.7. Preparation of 1-Allyl-2-Methoxy-3-Nitrobenzene (6)
Compound
(2.5 g, 18.1 mmol) and dimethylsulfate (2 mL, 21 mmol). Compound
CC (418 mg, 78% yield). Compound
: IR (cm−1): 3085 (=C-H); 2937 (C-H); 1602 (NO2); 1523 (C=C);
4
(0.5 g, 2.23 mmol) was methylated in dry acetone (45 mL) with potassium carbonate
6
(reddish oil) was obtained by
6
1353 (N=O). 1H-NMR: 7.63 (1H, d, J = 1.6 Hz, H-4); 7.43 (1H, m, H-5); 7.15 (1H, t, J = 7.8 Hz, H-6);
6.00–5.90 (2H, m, H-20); 5.15–5.06 (2H, m, H-30); 3.88 (3H, s, CH3CO); 3.48 (2H, d, J = 7.7 Hz, H-10).
13C-NMR: 151.4 (C-2); 144.2 (C-3); 136.4 (C-1);135.7 (C-20); 135.0 (C-6); 123.8 (C-5); 123.4 (C-4); 117.0
(C-30); 62.6 (OCH3); 33.5 (C-10). EI-MS (+) m/z 193 [M+] (100%).
3.2.8. Preparation of 2-Allyl-4-Nitrophenol (8)
A solution containing
was stirred for 4 h at room temperature; then, HCl (0.1 M) was added to achieve pH = 2. The organic
phase was extracted with CH2Cl2 (3 15 mL), washed with water, dried over Na2SO4, filtered, and
evaporated. Subsequently, the mixture was purified by CC eluting with hexane + ethyl acetate mixtures
of increasing polarity. Compound
; yellow oil (87 mg, 80% yield): IR (cm−1): 3353 (O-H); 2929 (C-H);
7 (100 mg, 0.452 mmol) in methanol (5 mL) and K2CO3 (14 mg, 0.10 mmol)
×
8
2361 (C=C); 1586 (NO2); 1493 (C=C); 1334 (N=O); 1280 (C-O). 1H-NMR: 8.06 (1H, d, J = 7.5 Hz, H-3);
8.05 (1H, dd, J = 7,5 Hz, H-5); 6.88 (1H, d, J = 9.1 Hz, H-6); 6.03–5.99 (2H, m, OH and H-20); 5.26–5.19
(2H, m, H-30); 3.46 (2H, d, J = 6.2 Hz, H-10); 13C-NMR: 159.7 (C-1); 141.6 (C-4); 134.6 (C-20); 126.4 (C-2);
126.3 (C-3); 124.3 (C-5); 118.0 (C-30); 115.8 (C-6); 34.6 (C-10). EI-MS (+) m/z 179 [M+] (100%).
3.2.9. Preparation of 1-Allyl-6-Methoxy-3,5-Dinitrobenzene (10)
Compound 10 was obtained by methylation of 9 (530 mg, 2.37 mmol) with dimethylsulfate
(1.6 mL, 16.9 mmol) in dry acetone (36 mL) and presence of potassium carbonate (1.63 g, 11.8 mmol).
Compound 10 (reddish oil) was obtained by CC (380 mg, 67% yield). Compound 10: IR (cm−1): 3094
(=C-H); 2924 (C-H); 1593 (C=C); 1530 (-NO2); 1477 (C=C); 1342 (N=O); 1264 (C-O-C). 1H-NMR: 8.57
(1H, d, J = 2.8 Hz, H-4); 8.30 (1H, d, J = 2.8 Hz, H-2); 6.00–5.90 (m, 1H, H-20); 5.26 (1H, dd, J = 10.2 and
1.2 Hz, H-3a’); 5.17 (1H, d, J = 17.0 and 1.4 Hz, H-2b0); 3.98 (3H, s, OCH3); 3.55 (2H, d, J = 6.6 Hz, H-10).
13C-NMR: 156.3 (C-6); 143.0 (C-3); 142.4 (C-1); 138.4 (C-20); 133.9 (C-5); 128.8 (C-2); 119.5 (C-4); 63.0
(OCH3); 33.8 (C-30). EI-MS (+) m/z 238 [M+] (100%).
3.3. Antifungal Activity of 2-Allylphenol and Derivatives Against Phytophthora Cinnamomi In Vitro
The antifungal activity of all studied compounds (
1–10) against P. cinnamomi were tested according
to a procedure previously reported [ ]. Briefly, each compound was dissolved in an ethanol (5% v/v)
8
solution and added to petri dishes (d = 50 mm) containing a potato dextrose agar medium (PDA,
◦
5 mL) at 50 C. The final concentrations of all the assayed compounds were: 10, 25, 50, 150, and
250
µ
g/mL. Solvent (1% ethanol) was taken as the negative control (C ), whereas METALAXIL MZ 48
−
WP (ANASAC, Santiago, Chile) commercial fungicide was used as positive control (C+) at the same
concentrations and under the same conditions as those of the tested compounds. A mycelium agar
disc (d = 4 mm) of the pathogen fungi was placed upside down in the center of PDA and incubated for
six days at 23 ◦C in the dark. Colony diameters were measured when the colonies on the C
plates
covered 100% of the agar surface. The inhibition percentages of mycelial growth for each compound
were calculated by using a previously-described method [16]. Each treatment was replicated three
times, and each assay was repeated twice. The effective concentration that inhibited mycelium growth
−

Molecules 2019, 24, 4196
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by 50% (EC50) was obtained for each compound by fitting %I and concentration to a dose-response
equation (see Figure 4). The fit analysis was performed using the Origin 8.0 software.
Figure 4. Inhibition data obtained for compound 9 fitted to a dose-response curve.
3.4. Computational Details
All 2-AP derivatives synthetized were optimized using Gaussian 09 and the DFT-B3LYP-6-31G (d,p)
basis set, and verified by frequency calculations (without imaginary frequency) in gas phase calculus.
After optimization, the electrostatic potential map of each compound was plotted. The lipophilicity
index (CLogP) were obtained after molecular mechanic (MM) optimization using ChemDraw 3D 15.0.
4. Conclusions
In this work, a series of phenylpropanoids derived from 2-AP was synthetized and evaluated
for its antifungal properties on mycelial growth of P. cinnamomi. The results show that some of these
compounds are as effective as metalaxil, a commonly-used commercial fungicide, at inhibiting the
mycelial growth of P. cinnamomi. The growth inhibition of the parent compound (2-AP) changes by
attaching electron-acceptor groups to the aromatic ring, or by chemical modification of the hydroxyl
group. In addition, this activity is strongly enhanced in those molecules where nitro and hydroxyl
groups adopt a -para configuration. These effects are mainly attributed to changes in the electronic
distribution on the aromatic ring induced by substituent groups.
It is worth mentioning that few known fungicides exhibit activity against P. cinnamomi at such
low concentrations, which convert these molecules in potential precursors of useful fungicides for
agricultural applications focused to control the infection caused for P. cinnamomi. However, further
work is needed to increase the yields of reactions, leading to the most active compounds, and to
determine the mechanism of action of these nitro derivatives.
Author Contributions: C.S., M.T., H.C. and R.M. collaborated in the synthesis and purification of 2-AP derivatives,
H.C., K.D., L.E., M.M. and A.F.O. collaborated in the discussion of structure-activity relationship, and writing of
the manuscript; K.D. supervised the biological work and wrote the biological component of this manuscript; M.M.
supervised molecular electronic studies; H.C., K.D. and A.F.O. collaborated in the discussion and interpretation of
the results, manuscript redaction, and corrections.
Funding: The authors are grateful to FONDECYT for financial support of this work under Grant 1170706.
Conflicts of Interest: The authors declare no conflict of interest.

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Sample Availability: Samples of the compounds 1–10 are available from the authors.
©
2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).