Phenyl isothiocyanate derivatives and their production

Abstract

A compound of the formula: ##STR1## wherein X is oxygen or sulfur;R.sup.1 is hydroxy, C.sub.1 -C.sub.4 alkoxy, phenoxy, amino, C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.8 dialkylamino, C.sub.6 -C.sub.10 arylamino, tetrahydrofurfurylamino, morpholino or methylpiperazino, but when X is sulfur R.sup.1 must be amino, C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.8 dialkylamino or morpholino;R.sup.2 is C.sub.1 -C.sub.4 alkoxy or C.sub.2 -C.sub.5 alkoxycarbonyl;R.sup.3 is hydrogen C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.2 -C.sub.8 dialkylamino or halogenand its salts being useful as agricultural fungicides are provided.

Description

The present invention relates to phenyl isothiocyanate derivatives. Some phenyl isothiocyanates have heretofore been known in Belgian Pat. No. 741,448; Canadian Pat. No. 807,601; French Pat. No. 1,545,679; German Pat. No. 2,013,788; British Pat. No. 1,183,113; Japanese Patent Publication No. 4,523/1973; Japanese Patent Unexamined Publications Nos. 18,626/1975; 1,023/1977; Dutch Pat. No. 67.12996; U.S. Pat. Nos. 3,530,161; 3,887,358, etc.

More particularly, this invention is directed to a compound of the formula: ##STR2## wherein X is oxygen or sulfur;

R.sup.1 is hydroxy C.sub.1 -C.sub.4 alkoxy, phenoxy, amino, C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.8 dialkylamino, C.sub.6 -C.sub.10 arylamino, tetrahydrofurylamino, morpholino or methylpiperazino, but when X is sulfur R.sup.1 must be amino, C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.8 dialkylamino or morpholino; R.sup.2 is C.sub.1 -C.sub.4 alkoxy or C.sub.2 -C.sub.5 alkoxycarbonyl; R.sup.3 is hydrogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.2 -C.sub.8 dialkylamino or halogen; and their salts being useful as agricultural fungicides.

Giving some additional explanations to the terms in the foregoing definition, "alkyl" refers to methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl and the like; "alkoxy" refers to methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, t-butoxy and the like; "alkylamino" refers to methylamino, ethylamino, propylamino, isopropylamino, butylamino and the like; "dialkylamino" refers to dimethylamino, methylethylamino, diethylamino, ethyl-butylamino, dibutylamino and the like; "arylamino" refers to phenylamino, tolylamino, xylylamino, mesitylamino, cumenylamino and the like; "alkoxycarbonyl" refers to methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl and the like; "halogen" refers to fluoro, chloro, bromo, iodo and the like.

Up to this time, it has been known that such phenyl isothiocyanates are useful as germination regulators (Japanese Patent Unexamined Publication 1023/1977), and that p-ethoxycarbonylphenyl isothiocyanates are useful as agricultural fungicides (Canadian Pat. No. 807,601). However, the fungicidal activity of these compounds is insufficient for agricultural use.

The phenyl isothiocyanate derivatives (1) of the present invention are synthesized as shown in the following reaction scheme: ##STR3## wherein R.sup.1, R.sup.2 and R.sup.3 are each as defined above.

Route I

The isothiocyanate formation may be carried out in a conventional manner. The starting material (II) is reacted with carbon disulfide and a base (e.g. triethylamine, pyridine, dimethylamine) in an organic solvent, and the resulting intermediate is reacted with an alkyl halogenocarbonate (e.g. ethyl chlorocarbonate, methyl chlorocarbonate) with or without organic solvent. Thus phenyl isothiocyanates (Ia) are obtained.

Alternatively the phenyl isothiocyanates (Ia) are prepared by reacting the starting material (II) with a dialkylthiocarbamoyl halogenide (e.g. diethylthiocarbamoyl chloride) in an organic solvent.

The starting material (II) can be prepared by known methods. For example, 3-diethylcarbamoyl-4-methoxy-5-methylaniline is prepared from 2-methoxy-3-methyl-5-nitrobenzoyl chloride by two steps as follows: ##STR4##

Route II

The convertion of carbamoyl group into thiocarbamoyl group is carried out by treating the starting material (II) with phosphorus pentasulfide in an organic solvent. Thus, thiocarbamoyl compound (III) is obtained.

Route III

The above obtained thiocarbamoyl compound (III) is subjected to the isothiocyanate formation. This route may be carried out in accordance with the procedure given in Route I. The thiocarbamoylaniline (III) can be obtained by reducing the corresponding nitrobenzene derivative: ##STR5## wherein R.sup.1, R.sup.2 and R.sup.3 are each as defined above. Thus, another product (Ib) is obtained.

Route IV

The first product (Ia) is subjected to the thiocarbamoyl group formation. This route may be carried out by treating with phosphorus pentasulfide or with a dialkylthiocarbamoyl halogenide/aluminum chloride each in an organic solvent. Thus, the second product (Ib) is obtained, too.

Route V

The second product (Ib) is directly prepared by treating the starting material (II) with a dialkylthiocarbamoyl halogenide/aluminum chloride in an organic solvent.

Any of these reactions are carried out at a temperature of about 0.degree.-150.degree. C., preferably 45.degree.-100.degree. C. Representatives of the organic solvent include tetrahydrofuran, benzene, toluene, ethylene dichloride, methylene chloride, chlorobenzene and the like.

Presently preferred and practical embodiments of the present invention are illustratively shown in the following examples.

EXAMPLE 1

To a solution of methyl 2-methoxy-4-methyl-5-aminobenzoate (975 mg) in tetrahydrofuran (5 ml) are added triethylamine (1.52 g) and carbon disulfide (1.14 g), and the resultant mixture is stirred at room temperature for 2.5 hours. Ethyl chlorocarbonate (1.63 g) is added to the mixture, which is stirred for additional 20 minutes at room temperature. A solution of sodium hydroxide (1.2 g) in water (32 ml) is added to the mixture, which is stirred for 15 minutes. The reaction mixture is mixed with an excess amount of water and shaken with methylene chloride. The organic layer is dried over Glauber's salt and the solvent is evaporated. The residue is dissolved in methylene chloride and chromatographed on a column of silica gel. Evaporating the solvent from the elution, the residue is dissolved in isopropyl ether and n-hexane is added thereto. The precipitated crystals are filtered to give 3-methoxy-carbonyl-4-methoxy-6-methylphenyl isothiocyanate (952 mg) as crystals melting at 86.degree.-87.5.degree. C.

EXAMPLES 2-27

Using the following starting material (II), the reaction is carried out as in Example 1, whereby the corresponding product (Ia) is obtained:

______________________________________ ##STR6## IaEx. II mp(.degree.C.) orNo. R.sup.1 R.sup.2 R.sup.3a R.sup.3b IR(cm.sup.-1)______________________________________2 OMe OMe H H 78.5-79.53 OMe OMe H OMe 92-934 OMe OMe Me H 2100, 1728 (CHCl.sub.3)5 OMe OMe OMe H 64-656 OEt OMe H Me 60.5-61.57 OMe OEt H Me 91-928 O-i-Pr OMe H Me 2080, 1722 (film)9 DMA OMe H H 2100, 1630 (CHCl.sub.3)10 DMA OMe H Me 161-16211 DMA OMe H OMe 184-185.512 DMA OMe Me H 74.0-75.013 DMA OMe OMe H 2100, 1629 (CHCl.sub.3)14 OPh OMe H Me 174.5-175.515 ##STR7## OMe H Me 162.5-163.516 ##STR8## OMe H Me 155.5-156.517 NHMe OMe H Me 191.5-192.518 NHMe OMe H OMe 187-18819 NHMe OMe Me H 128-12920 NHMe OMe OMe H 129-13021 NH.sub.2 OMe H Me 206-20722 NH.sub.2 OMe H OMe 224-22623 NH.sub.2 OMe OMe H 161-16224 OMe COOEt H H 1728, 1760, 2090 (film)25 DEA OMe H H 90-9126 DEAEA OMe H Me 93-9427 OMe OMe H DMA 103-103.5______________________________________ Note: The abbreviations in the Table have the following meanings: H (hydrogen), Me (methyl group), Et (ethyl group), Pr (propyl group), Ph (phenyl group) DMA (dimethylamino group), DEA (diethylamino group), DEAEA (diethylaminoethylamino group), i (iso), mp (melting point), IR (infrared spectrum).

EXAMPLE 28

A mixture of 3-[N-(2,6-dimethylphenyl)carbamoyl]-4-methoxy-5-chloroaniline (650 mg), diethylthiocarbamoyl chloride (360 mg) and chlorobenzene (6 ml) is refluxed for 30 minutes. The reaction mixture is mixed with water and shaken with methylene chloride. The organic layer is washed with water, dried over Glauber's salt and concentrated to remove the solvent. The residue is chromatographed on a column of silica gel, which is eluted with methylene chloride. The eluted fractions are collected and the solvent is evaporated. The residue is recrystallized from ethyl acetate to give 3-[N-(2,6-dimethylphenyl)carbamoyl]-4-methoxy-5-chlorophenyl isothiocyanate (340 mg) as crystals melting at 191.degree.-192.5.degree. C.

EXAMPLE 29-33

Using the following starting material (II), the reaction is carried out as in Example 28, whereby the following product (Ia) is obtained:

______________________________________ ##STR9##Ex. II IaNo. R.sup.1 R.sup.2 R.sup.3b mp(.degree. C.)______________________________________29 OMe OMe Cl 98-9930 DMA OMe Cl 195-196.531 NHMe OMe Cl 192-19532 ##STR10## OMe Cl 167-16833 OH OMe Me 181-183______________________________________ Note: The abbreviations in the Table have the same meanings as defined above.

EXAMPLE 34

(a) To a solution of 3-dimethylcarbamoyl-4-methoxy-5-methylnitrobenzene (1.10 g) in benzene (11 ml) is added phosphorus pentasulfide (3.08 g), and the resultant mixture is refluxed for 1 hour. After sooling, the reaction mixture is mixed with icy water and shaken with ether. The organic layer is washed with water, dried over Glauber's salt and concentrated under reduced pressure to remove the solvent. The residue is chromatographed on a column of silica gel, which is eluted with benzene, methylene chloride and then methylene chloride/2% methanol in order. The eluted fractions are concentrated under reduced pressure and the residue is washed with isopropyl ether to give 3-dimethylthiocarbamoyl-4-methoxy-5-methyl-nitrobenzene (1.0 g) as crystals melting at 138.degree.-139.degree. C.

(b) To a solution of above product (0.95 g) in methanol (30 ml) is added platinum dioxide hydrate (0.20 g), and the resultant mixture is shaken in hydrogen stream, until the absorption of hydrogen stops. The reaction mixture is filtered to remove the catalyst and the filtrate is concentrated under reduced pressure. The residue is dissolved in methylene chloride, dried over Glauber's salt and the solvent is evaporated. The residue is dissolved in dry tetrahydrofuran (5 ml) to give a solution, which is mixed with triethylamine (1.13 g) and carbon disulfide (0.85 g). The resultant mixture is stirred at ordinary temperature overnight. Ethyl chlorocarbonate (1.22 g) is added to the mixture under cooling, which is stirred for 45 minutes under cooling. The mixture is treated with 10% aqueous sodium hydroxide (9 ml) and shaken with methylene chloride. The organic layer is washed with water, dried over Glauber's salt and the solvent is evaporated. The residue is chromatographed on a column of silica gel, which is eluted with methylene chloride. After evaporating the solvent, the fraction affords a brown oil (0.87 g), which is recrystallized from isopropyl ether-petroleum ether to give 3-dimethylthiocarbamoyl-4-methoxy-5-methylphenyl isothiocyanate (312 mg) as crystals melting at 74.degree.-75.degree. C.

EXAMPLE 35

To a solution of 3-dimethylcarbamoyl-4-methoxy-5-methylaniline (600 mg) in dry ethylene dichloride (12 ml) is added diethylthiocarbamoyl chloride (850 mg), and the resultant mixture is refluxed for 25 minutes. Aluminum chloride (360 mg) is added to the mixture, which is refluxed for 2 hours. After cooling, the mixture is mixed with aqueous sodium bicarbonate, stirred at room temperature for 15 minutes and shaken with methylene chloride. The organic layer is washed with water, dried over Glauber's salt and the solvent is evaporated under reduced pressure. The residue is chromatographed on a column of silica gel, which is eluted with methylene chloride. The eluted fraction is evaporated, and the residue is washed with isopropyl ether-petroleum ether to give 3-dimethylthiocarbamoyl-4-methoxy-5-methylphenyl isothiocyanate (214 mg) as crystals melting at 74.degree.-75.degree. C.

EXAMPLE 36

Using 3-diethylcarbamoyl-4-methoxyphenyl isothiocyanate (700 mg), the reaction is carried out as in Example 35, whereby 3-diethylthiocarbamoyl-4-methoxyphenyl isothiocyanate (437 mg) is obtained as colorless needles melting at 121.degree.-122.degree. C.

EXAMPLES 37-39

The following compounds are obtained by carrying out the reaction as in Example 34 (a).

______________________________________Ex.No.______________________________________37 ##STR11## m.p. 202.5-204.degree. C.38 ##STR12## m.p. 165-165.degree. C.39 ##STR13## m.p. >250.degree. C.______________________________________

The phenyl isothiocyanates (I) are useful as agricultural fungicides against various phytopathogenic fungi such as cucurbitaceae powdery mildew, cucurbitaceae downy mildew, cucurbitaceae anthracnose, rice plant blast and drooping diseases of various crops. Excellent control effect of the product (I) is illustratively shown by the following experiments. The list indicates test compounds used in the experiments.

__________________________________________________________________________Compd.No. Structural Formula Chemical Name Note__________________________________________________________________________ ##STR14## 3-Methoxycarbonyl- 4-methoxyphenyl isothiocyanat e ##STR15## 3-Methoxycarbonyl- 4-methoxy-6-methyl- phenyl isothiocyanate ##STR16## 3-Methoxycarbonyl- 4,6-dimethoxyphenyl isothiocy anate ##STR17## 3-Methoxycarbonyl- 4,5-dimethoxyphenyl isothiocy anate ##STR18## 3-Dimethylcarbamoyl- 4-methoxyphenyl isothiocyan ate ##STR19## 3-Isopropoxycarbonyl- 4-methoxy-6-methyl- phenyl isothiocyanate ##STR20## 3-Methoxycarbonyl- 4-methoxy-5-methyl- phenyl isothiocyanate ##STR21## 3-Methoxycarbonyl- 4-ethoxy-6-methyl- phenyl isothiocyanate ##STR22## 3-Ethoxycarbonyl- 4-methoxy-6-methyl- phenyl isothiocyanate10. ##STR23## Manganese ethylene bisdithiocarbamic acid (mannev) control ##STR24## N'-Dichlorofluoro- methylthio-N,N-di- methyl-N'- phenyl- sulfamide (dichlo- fluanide) control ##STR25## 6-Methyl-1,3-dithiolo- [4,5-b]-quinoxalin-2- on (quinomethionate) control ##STR26## O-Ethyl-S,S-diphenyl- phosphorodithiolate (EDDP) control ##STR27## 3-Hydroxy-5-methyl- isoxazole (hydroxyisoxazole) control__________________________________________________________________________

EXPERIMENT 1

Test for control effect against cucumber anthracnose

Seeds of cucumber (cultivar: Matsukaze) were sown in a vinyl chloride-cup of 9 cm in diameter containing soil, one seed per cup, in a greenhouse. When the primary leaf was developed, 5 ml of a solution of the test compound at a prescribed concentration was applied per cup. After application, the cups were kept at a temperature of 25.degree.-26.degree. C. and humidity of 80% for 1 day. A spore suspension of cucumber anthracnose (Colletotrichum lagenarium) was inoculated onto the aforementioned primary leaves of cucumber, five spots per leaf. The cups were kept at a temperature of 25.degree. C. and humidity of 95% for 1 day. After allowing to stand at a temperature of 25.degree. C. and humidity of 75-80% for 6 days, diseased degree in the inoculated portions was observed. Percent disease control was calculated using the following formula: ##EQU1##

Results are indicated in Table 1.

TABLE 1______________________________________ Percent DiseaseTest Compound Concentration ControlNo. (ppm) Diseased Degree (%)______________________________________1 500 0 100.02 500 0 100.03 500 0 100.04 500 0 100.08 500 0 100.09 500 0 100.010 1440 0 100.0Untreated Plot -- 25 0.0______________________________________

EXPERIMENT 2

Test for control effect against cucumber downy mildew

Seeds of cucumber (cultivar: Matsukaze) were sown in a vinyl chloride-cup of 9 cm in diameter containing soil, one seed per cup, in a greenhouse. When the primary leaf was developed, 5 ml of the solution of the test compounds at a prescribed concentration was applied per cup. After application, the cups were kept at a temperature of 20.degree.-22.degree. C. for 1 day. A spore suspension of cucumber downy mildew (Pseudoperonospora cubensis) was inoculated onto the aforementioned primary leaves of cucumber, five spots per leaf. The cups were kept at a temperature of 20.degree. C. and humidity of 95% for 10 days. Diseased degree in the inoculated portions was observed. Percent disease control was calculated using the following formula: ##EQU2##

Results are indicated in Table 2.

TABLE 2______________________________________ Percent DiseaseTest Compound Concentration ControlNo. (ppm) Diseased Degree (%)______________________________________1 500 0 1002 500 0 1003 500 0 1004 500 0 1006 500 0 1008 500 0 10011 500 0 100Untreated Plot -- 100 0______________________________________

EXPERIMENT 3

Test for control effect against cucumber powdery mildew

Seeds of cucumber (cultivar: Matsukaze) were sown in a vinyl chloride-cup of 9 cm in diameter containing soil, one seed per cup, in a greenhouse. When the primary leaf was developed, 5 ml of the solution of the test compounds at a prescribed concentration was applied per cup. After application, the cups were kept at a temperature of 25.degree.-26.degree. C. for 1 day. Leaves of cucumber infected by pathogenic fungi of the powdery mildew (Sphaerotheca fuliginea) were taken, and lesions covered with oidia were cut out in 1 square centimeter pieces. The fungi were inoculated to the primary leaves in the cups by sticking the oidia covered pieces onto them, four plots per leaf. The cups were then kept at a temperature of 25.degree.-26.degree. C. for 10 days. The oidium formation on the inoculated leaves was observed by microscope.

+: Infected spots and formation of numbers of oidia observed on the inoculated portions. -: Neither infected spot nor oidium formation observed

Results are indicated in Table 3.

TABLE 3______________________________________Test Compound ConcentrationNo. (ppm) Diseased Degree______________________________________1 500 --2 500 --3 500 --4 500 --7 500 --8 500 --12 125 --Untreated Plot -- +______________________________________

EXPERIMENT 4

Test for control effect against rice plant blast

Seedlings of rice plant (cultivar: Aichi-asahi), reared for 10 days in the greenhouse, were transplanted in a vinyl chloride-cup of 12 cm in diameter containing soil. A solution of the test compound at a prescribed concentration was applied 14 days after the transplantation. One day after the application, a spore suspension of pathogenic fungi of rice plant blast (Pyricularia oryzae) was sprayed on the leaf blade of the seedilings. The cups were kept in an infection room at a temperature of 28.degree. C. and humidity of 98% for 24 hours. Then, they were kept at a temperature of 28.degree. C. and humidity of 90% for 7 days in a greenhouse. Number of spots on the inoculated leaves was observed, and percent disease control was calculated using the following formula: ##EQU3##

Results are indicated in Table 4.

TABLE 4______________________________________ Percent DiseaseTest Compound Concentration Number of ControlNo. (ppm) Spots (%)______________________________________1 500 4 99.82 500 92 96.33 500 11 99.64 500 4 99.85 500 23 99.16 500 143 94.38 500 331 86.89 500 567 77.413 300 17 99.3Untreated Plot -- 2515 0______________________________________

EXPERIMENT 5

Test for control effect against damping-off of cucumber seedlings

One hundred and fifty ml of sterile soil was placed into a pot of 9 cm in diameter, and 20 cucumber seeds were sowed per pot. After cultivating fungi of the cucumber damping-off (Pythium aphanidermatum, Fusarium oxysoirum, Rhizoctonia solani) in a wheat bran medium for 5 days, it was mixed with sterile soil and cultured again for 2 days at a temperature of 25.degree. C. Thirty ml of the solution of the test compounds at a prescribed concentration was drenched to each pot. The pots were kept at a temperature of 28.degree. C. for 11 days in a greenhouse. Diseased degree in the treated pots was observed. Diseased degree and percent disease control were calculated using the following formulae:

Index of damping-off

1. Not germinated 2. Wilt and rot 3. Invasion more than 1/3 seedlings 4. Invasion not more than 1/3 seedlings 5. Seedlings sound ##STR28##

Results are indicated in Table 5.

TABLE 5__________________________________________________________________________ Pythium Rhizoctonia solani aphanidermatum Fusarium oxysporumTest Percent Percent PercentCom- Concen- Disease Disease Diseasepound traction Diseased Control Diseased Control Diseased ControlNo. (ppm) Degree (%) Degree (%) Degree (%)__________________________________________________________________________1 500 28.8 71.2 36.3 63.7 65.0 7.94 500 0 100 76.3 23.7 10.0 85.85 500 36.3 63.7 0 100 22.5 68.16 500 28.8 71.2 85.0 15.0 10.0 85.87 500 56.3 43.7 100 0 27.5 61.08 500 66.0 34.0 100 0 18.8 73.414 500 62.5 37.5 21.3 78.7 25.0 64.6Un-treated -- 100 0 100 0 100 0edPlot__________________________________________________________________________ Accordingly, the phenyl isothiocyanates (I) showed potent fungicidal activity against cucumber anthracnose, cucumber downy mildew, cucumber powdery mildew, rice plant blast, and damping-off of cucumber seedlings. The other compounds (I) also showed similar fungicidal activity.

The product (I) of this invention may be applied in a form suitable for agricultural fungicides, such as emulsions, solutions, wettable powders, dusts, suspensions, granules, aerosols, oils, smokes, pastes and the like. The compound (I) may be applied singly or in combination with solid or liquid carriers. Representatives of the solid carriers include clay, talc, diatomaceous earth, silica, kaolin, bentonite, pumice and the like. Examples of the liquid carriers are water, methanol, ethanol, ethylene glycol, dimethylformamide, dimethylsulfoxide, acetone, methyl ethyl ketone, cellosolve, dioxane, diglyme, and the like. If necessary, there may be added appropriate adjuvants such as emulsifiers, dispersants, spreaders, surfactants, wetting agents, stabilizers, synergists and the like. Moreover, the compound (I) may be used in combination with other agricultural chemicals such as other fungicides, germicides, insecticides, herbicides, repellents, miticides, nematocides, plant growth regulators and the like. Application rate of the compound (I) for liquid formulations is in the range of about 50-2,000 ppm, preferably 100-1,000 ppm and about 100-200 L per 10 are; and application rate for solid formulations is about 3-4 kg per 10 are.

Fungicidal compositions containing the compound (I) are illustratively shown in the following Formulations.

FORMULATION 1

Fifty parts by weight of 3-methoxycarbonyl-4-methoxyphenyl isothiocyanate, 35 parts by weight of diatomaceous earth, 10 parts by weight of white carbon, 2 parts by weight of sodium alkylbenzenesulfonate and 3 parts by weight of calcium lignin sulfonate are triturated and mixed to provide wettable powder.

FORMULATION 2

Thirty parts by weight of 3-methoxycarbonyl-4,6-dimethoxyphenyl isothiocyanate, 40 parts by weight of xylene, 20 parts by weight of cyclohexanone, and 10 parts by weight of polyoxyethylene alkyl aryl ether are mixed and stirred to provide an emulsion.

FORMULATION 3

Three parts by weight of 3-methoxycarbonyl-4,5-dimethoxyphenyl isothiocyanate, 7 parts by weight of talc and 90 parts by weight of clay are mixed and triturated to provide a dust formulation.

FORMULATION 4

Three parts by weight of 3-methoxycarbonyl-4,6-dimethoxyphenyl iosthiocyanate, 2 parts by weight of sodium alkylbenzenesulfonate, 45 parts by weight of clay and 50 parts by weight of bentonite are mixed, kneaded with a suitable amount of water and granulated by an extrusive granulator. Air-drying at 50.degree. C. and sieving through a 20-40 mesh screen provides the desired granules. Such granules are directly applied.

Further, the phenyl isothiocyanates (I) are also hopeful as antifungal agents in humans and animals. For example, 3-methoxycarbonyl-4,5-dimethoxyphenyl isothiocyanate showed a minimum inhibitory concentration of 6.2 .gamma./ml against Candida albicans M-9 in in vitro test.

Claims

1. An agricultural fungicidal composition comprising a fungicidally effective amount of a compound of the formula: ##STR29## wherein X is oxygen or sulfur;

R.sup.1 is hydroxy, phenoxy, amino, methylamino, ethylamino, propylamino, isopropylamino, butylamino, dimethylamino, methylethylamino, diethylamino, ethylbutylamino, dibutylamino, phenylamino, tolylamino, xylylamino, mesitylamino, cumenylamino, tetrahydrofurfurylamino, morpholino or methylpiperazino; but when X is sulfur R.sup.1 must be amino, methylamino, ethylamino, propylamino, isopropylamino, butylamino, dimethylamino, methylethylamino, diethylamino, ethylbutylamino, dibutylamino, or morpholino;

R.sup.2 is methoxy, ethoxy, propoxy, isopropoxy, butyoxy, isobutoxy, or t-butoxy; and

R.sup.3 is hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butuyl, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, t-butoxy, dimethylamino, methylethylamino, diethylamino, ethylbutylamino, dibutylamino, ffluorine chlorine, bromine or iodine,

or its salts and one or more agriculturally suitable carriers and/or adjuvants.

2. An agricultural fungicidal composition comprising a fungicidally effective amount of a compound of the formula: ##STR30## wherein X is oxygen or sulfur;

R.sup.1 is hydroxy, C.sub.1 -C.sub.4 alkoxy, phenoxy, amino, C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.8 dialkylamino, C.sub.6 -C.sub.10 arylamino, tetrahydrofurfurylamino, morpholino or methylpiperazino; but when X is further R.sup.1 must be amino, C.sub.1 -C.sub.4 alkylamino, C.sub.2 -C.sub.8 dialkylamino or morpholino;

R.sup.2 is C.sub.1 -C.sub.4 alkoxy or C.sub.2 -C.sub.5 alkoxycarbonyl; and

R.sup.3 is hydrogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.2 -C.sub.8 dialkylamino or halogen

or its salts and one or more agriculturally suitable carriers and/or adjuvants.

3. A composition according to claim 2 in which X is oxygen; R.sup.1 is methoxy, methylamino or dimethylamino; R.sup.2 is methoxy; and R.sup.3 is hydrogen, chlorine, methyl or methoxy.

4. A composition according to claim 2, in which the effective compound is 3-methoxycarbonyl-4-methoxyphenyl isothiocyanate.

5. A composition according to claim 2, in which the effective compound is 3-methoxycarbonyl-4,5-dimethoxyphenyl isothiocyanate.

6. A composition according to claim 2, in which the effective compound is 3-methoxycarbonyl-4-methoxy-6-chlorophenyl isothiocyanate.

7. A composition according to claim 2, in which the effective compound is 3-methoxycarbonyl-4-methoxy-5-methylphenyl isothiocyanate.

8. A composition according to claim 2, in which the effective compound is 3-dimethylcarbamoyl-4-methoxy-5-methylphenyl isothiocyanate.

9. A composition according to claim 2, wherein X is sulfur; R.sup.1 is amino, methylamino, dimethylamino or morpholino; R.sup.2 is methoxy; and R.sup.3 is hydrogen, chlorine, methyl or methoxy.

10. A composition acording to claim 8, in which the effective compound is 3-thiocarbamoyl-4,6-dimethoxyphenyl isothiocyanate.

11. A composition according to claim 8, in which the effective compound is 3-methylthiocarbamoyl-4,6-dimethoxyphenyl isothiocyanate.

12. A composition according to claim 8, in which the effective compound is 3-morpholino-thiocarbamoyl-4-methoxy-5-methylphenyl isothiocyanate.