US3055801A - 1-substituted pyrenes as fungicides - Google Patents

1-substituted pyrenes as fungicides Download PDF

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US3055801A
US3055801A US73997A US7399760A US3055801A US 3055801 A US3055801 A US 3055801A US 73997 A US73997 A US 73997A US 7399760 A US7399760 A US 7399760A US 3055801 A US3055801 A US 3055801A
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compound
pyrene
substituted
hydrochloride
fungi
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Dewayne C Torgeson
Marcus Erich
Joseph A Lambrech
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Union Carbide Corp
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Unin Carbide Corp
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
    • C07D295/03—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79—Acids; Esters
    • C07D213/80—Acids; Esters in position 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
    • C07C2603/42—Ortho- or ortho- and peri-condensed systems containing four condensed rings containing only six-membered rings
    • C07C2603/50—Pyrenes; Hydrogenated pyrenes

Definitions

  • This invention relates to methods and compositions for the control of fungi. More particularly, the present invention relates to methods and compositions employing l-substituted pyrenes for the control of fungi, particularly the powdery mildews that attack vegetable, fruit, and ornamental plants.
  • the l-suostituted pyrenes to which the present invention relates are substituted in the one position by an organic radical.
  • organic radicalj as used throughout this specification, includes any group of atoms, either organic or inorganic, that normally passes unchanged trom one molecule of a carbon compound to another (seehackhs Chemical Dictionary, Third Edition, McGraw-Hill Co., New York, page 714 (1944)).
  • the l-substituted pyrenes of the present invention may also be substituted in the six or eight position by an organic radical of the same or of a different kind than the orangic radical at the one position.
  • Such pyrenes may be illustrated by the structural formula:
  • R is an organic radical and R is either hydrogen or an organic radical attached at either the six or eight position.
  • fungicides are the compounds having the formula:
  • R" is an organic radical
  • R' and R"" are selected from the group consisting of hydrogen and organic radicals, at least one of said R" and R"" being hydrogen.
  • Particularly preferred are such compounds having a molecular weight of up to about 700.
  • Illustrative of such l-substituted pyrenes are:
  • the first visible sign of a powdery mildew infection is a gray to white felt-like growth on the leaves. As the disease progresses, the leaves curl and fold, and may die and drop off prematurely. The infection may spread to any succulent plant part such as the stems, fruits, and the like.
  • the powdery mildews are found in most of the Worlds agricultural areas. They attack and damage a wide range of plants. Among those attacked are cereal grains, forage, and fruit crops such as clover, apples, cherries, peaches, grapes, cantaloupes, beans, and ornamentals such as roses, lilacs, and the like.
  • the fungicides in common use today are not generally effective against the powdery mildews.
  • the l-substituted pyrenes of the present invention can be prepared by a number of methods.
  • nitropyrene can be prepared by the mild nitration of pyrene with nitric acid.
  • the acetyl and benzoylpyrcnes can be prepared by the reaction of the corresponding acid chloride with pyrene in the presence of aluminum chloride as a catalyst.
  • the novel l-aminoalkyl pyrenes may be prepared or described in copending application, Serial No.
  • the carbonyl compound and the amide may generally be present in widely varying proportions, but are preferably present in a molar ratio of from about 1:1 to about 1:10, respectively.
  • Formic acid in an amount corresponding to 0.01 to 5 mols of formic acid per mol of carbonyl compound, is preferably present during the reaction.
  • the reaction may be conducted by heating a solution of the carbonyl compound in the amide at a temperature of from about to about 250 C. for a period of from about 1 to about 100 hours, preferably at a temperature of from about to about 200 C. for a period of about 2 to 10 hours.
  • the product When neither R nor R is hydrogen, the product may be recovered as a residue by distillation of any unreacted amide and formic acid, if present.
  • the distillation is preferably conducted under vacuum.
  • the residue product is, in many cases, pure enough for use without further treatment.
  • the products may conveniently be isolated in the pure state, as the hydrochloride salts, by dissolving the crude product in a solvent such as ethyl ether, dioxane, or benzene and introducing dry hydrogen chloride gas into the solution (in an amount corresponding to at least one mole equivalent) to precipitate the l- (aminoalkyl) pyrene hydrochloride.
  • Similar salts of other anhydrous acids may also be prepared in a similar fashion.
  • the free amine can be obtained from the hydrochloride by treating it with an aqueous base, such as ammonia, and a water-immiscible solvent, such as ether or benzene. Separation of the organic layer, followed by removal of the solvent leaves the free amine as residue.
  • an aqueous base such as ammonia
  • a water-immiscible solvent such as ether or benzene
  • the crude reaction mixture when R or R or both are hydrogen, the crude reaction mixture, after removal of excess amide and formic acid, if present, contains a mixture of the desired amine and its corresponding N-forrnyl derivative.
  • the formyl derivative can be hydrolyzed by heating the crude reaction mixture with aqueous or alcoholic acid or base.
  • a convenient method comprises refluxing the crude mixture with an excess of concentrated hydrochloric acid and butanol for 2 to 100 hours, preferably from 4 to 24 hours.
  • the crude amine hydrochloride is obtained by distilling ofif hydrochloric acid, butanol, and formic acid.
  • the crude amine hydrochloride can then be treated with an aqueous base, such as ammonia, and a water-immiscible solvent, such as benzene, to give a solution of the free amino in the nonaqueous layer.
  • an aqueous base such as ammonia
  • a water-immiscible solvent such as benzene
  • the free amine can then be recovered by distilling oil the solvent, or the amine hydrochloride can be obtained by treating the solution with gaseous hydrogen chloride.
  • the monoalkylaminomethylpyrenes and monoarylaminomethylpyrenes are also prepared in two steps by catalytic reduction of the imines derived from l-pyrenecarboxaldehyde and the corresponding amine.
  • imines derived from l-pyrenecarboxaldehyde and the corresponding amine are prepared most readily by hydrogenation of the oximes of the corresponding carbonyl compounds.
  • l-thiopyrenol has been prepared by reduction of l-thiocyanopyrene with zinc and acetic acid. Oxidation of thiopyrenol with iodine gave the disulfide. Reaction of spanner 'ril g,
  • N-(l-pyrenyDmalearnic acid was obtained by reaction of the amine with maleic anhydride. Cyclization of the maleamic acid with acetic anhydride afforded the maleimide. N,N'-diacetoacetyl-1,6(or8)-diaminopyrene was synthesized by the reaction of diketene with l-aminopyrene.
  • 'lhe l-substituted pyrenes of the present invention may be applied at the rate of 0.2 to 25 pounds per acre. We have found, however, that good control of fungi is obtained when the l-substituted pyrenes are applied at the rate of 0.5 to 6 pounds per acre. They may be used alone, but are preferably employed with a carrier or diluent in the form of a solution or dispersion which can be sprayed on the plants or as a wettable powder which can be dusted on the plants.
  • Suitable solutions or dispersions for use in accordance with the present invention comprise from 1 to 95 parts by weight of a l-substituted pyrene or mixture of l-substituted pyrenes, as the active fungicidal ingredient, and from to 99 parts by weight of a liquid carrier, such as water, alcohols, ether alcohols, ketones, petroleum distillates, vegetable oils, and the like and mixtures thereof.
  • a liquid carrier such as water, alcohols, ether alcohols, ketones, petroleum distillates, vegetable oils, and the like and mixtures thereof.
  • Suitable wettable powders or dusts for use in accordance with the present invention comprise from 1 to 90 parts by weight of a l-substituted pyrene or mixture of 1-substituted pyrene, as the active fungicidal ingredient, and from to 99 parts by weight or" a solid carrier, such as clay, talc, chalk, magnesium carbonate, diatomaceous earth, pyrophyllite, and mixtures of such materials.
  • compositions may also contain dispersing or emulsifying agents, such as the condensation products of alkylene oxides with phenols and organic acids, aryl alkyl sulfonates, complex ether alcohols, mahogany soaps, and quaternary ammonium compounds.
  • dispersing or emulsifying agents such as the condensation products of alkylene oxides with phenols and organic acids, aryl alkyl sulfonates, complex ether alcohols, mahogany soaps, and quaternary ammonium compounds.
  • compositions may also contain other toxicants, such as arsenates, rotenone, pyrethrum, irnidazolines, dithiocarbamates, and mixtures of such materials.
  • toxicants such as arsenates, rotenone, pyrethrum, irnidazolines, dithiocarbamates, and mixtures of such materials.
  • aqueous suspensions were prepared containing 0.04 part (all parts by weight), 0.008 part, and 0.0016 part of the chemicals to be tested.
  • the suspensions also contained .05 part of dispersing agent, an alkyl phenyl polyethylene glycol ether, marketed under the proprietary mark Tergitol. dispersant NPX, per 100 parts of water.
  • dispersing agent an alkyl phenyl polyethylene glycol ether, marketed under the proprietary mark Tergitol. dispersant NPX, per 100 parts of water.
  • Individual bean plants of about 10 days of age that had been inoculated two to four days previously by dusting with spores of the test organism were sprayed for 30 seconds with one or another of the suspensions.
  • Check or control plants received no fungicidal spray. The plants were then placed in the greenhouse and after 10 days to two weeks the primary leaves were examined for mildew and scored as follows:
  • Concentration of t0xicant.'lhe test compounds are formulated by a standard procedure of solution in acetone, addition of an emulsifier and dilution with water. The compounds are evaluated at concentrations of 2000 and ppm.
  • ppm. means parts per million.
  • R" is an organic radical
  • R' and R"" are selectcd from the group consisting of hydrogen and organic radicals, at least one of said R and R"" being hydrogen, said compound having a molecular weight of up to about 700.
  • a method which comprises applying to fungi a fungicidal amount of pyrene substituted in the l-position by an organic radical, said substituted pyrene having a molecular weight of up to about 700.
  • a method which comprises applying to fungi a fungicidal amount of pyrene substituted in the 1- and 6- positions by an organic radical, said substituted pyrene having a molecular weight of up to about 700.
  • a method which comprises applying to fungi a fungicidal amount of pyrene substituted in the 1- and 8- positions by an organic radical, said substituted pyrene having a molecular weight of up to about 700.
  • a method which comprises applying to fungi a fungicidal amount of 1,6-dinitropyrene.
  • a method which comprises applying to fungi a fungicidal amount of 1,8-dinitropyrene.
  • a method which comprises applying to fungi a fungicidal amount of l-acetylpyrene.
  • a method which comprises applying to fungi a fungicidal amount of 1,6-dibenzoylpyrene.
  • a method which comprises applying to fungi a fungicidal amount of 1,8-dibenzoylpyrene.
  • a method which comprises applying to fungi a fungicidal amount of 1-(hydroxymethyl)pyrene.

Description

This invention relates to methods and compositions for the control of fungi. More particularly, the present invention relates to methods and compositions employing l-substituted pyrenes for the control of fungi, particularly the powdery mildews that attack vegetable, fruit, and ornamental plants.
The l-suostituted pyrenes to which the present invention relates are substituted in the one position by an organic radical. The term organic radicalj as used throughout this specification, includes any group of atoms, either organic or inorganic, that normally passes unchanged trom one molecule of a carbon compound to another (see Hackhs Chemical Dictionary, Third Edition, McGraw-Hill Co., New York, page 714 (1944)). The l-substituted pyrenes of the present invention may also be substituted in the six or eight position by an organic radical of the same or of a different kind than the orangic radical at the one position. Such pyrenes may be illustrated by the structural formula:
wherein R is an organic radical and R is either hydrogen or an organic radical attached at either the six or eight position.
Preferred for use as fungicides are the compounds having the formula:
RI!!! RI! III wherein R" is an organic radical, and R' and R"" are selected from the group consisting of hydrogen and organic radicals, at least one of said R" and R"" being hydrogen. Particularly preferred are such compounds having a molecular weight of up to about 700. Illustrative of such l-substituted pyrenes are:
Compound No. l-1,6-dinitropyrene I Compound No. 2-l,8-dinitropyrene I Compound No. 3Ethyle l pyrenalmalonate Compound No. 4-1-nitropyrene Compound No. 51-benzoylpyrene Compound No. 6--1-aminopyrene Compound No. 7-1-acetylpyrene Compound No. 8--l-phthalimidopyrene Compound No. 9N-acetylaminopyrene Compound No. 10-1,6-dibenzoylpyrene Compound No. 1l-l,8-dibenzoylpyrene Compound No. 12X-nitro-l-acetylpyrene Compound No. 133-(1-pyrenyl)acrylic acid Compound No. 14--1-thiocyanopyrene Compound No. 15-1-pyrenecarboxa.ldehyde Compound No. 16-1-acetylpyrene oxime Compound No. 17--l-(omega-nitrovinyl)pyrene 3,055,801 Patented Sept. 25, 1962 Compound No. 39--1-(N,N-diethylaminornethyl)pyrene hydrochloride Compound No. 40-l,1'-dipyreny1 disulfide Compound No. 41-1-(N-piperidinomethyl)pyrene hydrochloride Compound No. 42-1-(N-pyrrolidinomethyDpyrene hydrochloride Compound No. 431-(N,N-dimethylaminomethyl) pyrene hydrochloride Compound No. 44-1-(N,N-dibutylaminomethyl)pyrene hydrochloride Compound No. 45-1-(para-nitrobenzalamino)pyrene Compound No. 46--1-pyrenalaniline Compound No. 47-1-(N,N-dihexylaminomethyl)pyrene hydrochloride Compound No. 48-1-[N-(NmethyDpiperazinomethyll pyrene dihydrochloride Compound No. 49-1-cinnamalaminopyrene Compound No. 5 0--1-(N-an.ilinomethyl)pyrene Compound No. 5l1-(alpha-N-methy1aminoethyl) pyrene hydrochloride Compound No. 52-nButyl-l-pyrenecarboxylate Compound No. 53-l-thiopyrenol Compound No. 54-X-nitro-1-ethylpyrene Compound No. 55-1-pyrenylmercaptoacetic acid Compound No. 56N-(1-pyrenyl)maleimide Compound No. 57-N-(1-pyrenyl)maleamic acid Compound No. 58--1-m'cotinylpyrene Compound No. 591-(N,N-di-(2-ethylhexyl)aminomethyDpyrene hydrochloride Compound No. 601-(anthralamino)pyrene I Compound No. 61--1-(1-pyrenalamino) pyridine Compound No. 62-1-(hydroxymethyl)pyrene Compound No. 63--l-(N,N-diallylaminomethyl)pytene hydrochloride Compound No. 64--l-(l-naphthalamino)pyrene Compound No. 6S-1-(N-(2-pyridyl) aminomethyl) pyrene Compound No. 66-N-methyl-N,N-bis(l-pyrenylmethyl) amine hydrochloride Compound No. 67-1-pyrenalbutylamine Compound No. 68-l-(N-butylaminomethyl)pyrene Compound No. 69-1-(alpha-N-hexylaminoethyDpyrene hydrochloride Compound No. 70-1-(N-butylaminomethyDpyrene hydrochloride Compound No. 7l1-(alpha-aminoethyl)pyrene hydrochloride Compound No. 72-l-(a.lpha-aminobenzyl)pyrene hydrochloride Compound No. 73l-(aminomethyl)pyrene hydrochloride Compound No. 74-Tris(l-pyrenylmethyl)amine hydrochloride Compound No. 75-1-pyrenylidenebismorpholine Compound No. 76-l-aminopyrene hydrochloride Compound No. 77--1-(N-methylaminomethyl)pyrene Compound No. 78--l-pyrenaimethylamine Compound No. 792-( l-( l-pyrenyl) ethylmercapto) -2- imidazoline hydrochloride Compound No. 80-l-(chloromethyl)pyrene Compound No. 812-(1-pyrenylmethylmercapto)-2- imidazoline hydrochloride Compound No. 821-pyrenol Growers of fruits, vegetables, grain, and forage crops are faced with many plant disease problems. One group of diseases, caused by the powdery mildews, are particularly troublesome. The powdery mildews are obligate parasites; that is, they can grow and multiply only on a living host plant. Any plant which is forced to feed the fungus suffers a reduction in actively functioning leaf area and partial or complete destruction of leaves, stems, fruits, and other plant parts. The affected plant parts may be disfigured, stunted, or killed.
The first visible sign of a powdery mildew infection is a gray to white felt-like growth on the leaves. As the disease progresses, the leaves curl and fold, and may die and drop off prematurely. The infection may spread to any succulent plant part such as the stems, fruits, and the like.
The powdery mildews are found in most of the Worlds agricultural areas. They attack and damage a wide range of plants. Among those attacked are cereal grains, forage, and fruit crops such as clover, apples, cherries, peaches, grapes, cantaloupes, beans, and ornamentals such as roses, lilacs, and the like.
The fungicides in common use today are not generally effective against the powdery mildews.
Sulfur has been used to control powdery mildew on some crops. However, control with sulfur has never been too satisfactory because it frequently injures the fruit, buds, blossoms, or foliage of treated plants. This is particularly true in hot weather. On some crops such as grapes which are particularly sensitive to sulfur, it cannot be safely used.
We have discovered that the l-substituted pyrenes give excellent control of the powdery mildews. These materials, when properly used, are safe to both the plant and the operator applying them.
The l-substituted pyrenes of the present invention can be prepared by a number of methods. For example, nitropyrene can be prepared by the mild nitration of pyrene with nitric acid. The acetyl and benzoylpyrcnes can be prepared by the reaction of the corresponding acid chloride with pyrene in the presence of aluminum chloride as a catalyst. The novel l-aminoalkyl pyrenes may be prepared or described in copending application, Serial No. 782,624, filed December 24, 1958, to Marcus et al., by the reaction of a carbonyl compound selected from the group consisting of l-pyrenecarboxaldehyde and a l-acylpyrene, such as l-acetylpyrene and l-benzoylpyrene, with an amide having the formula HCONR R wherein NR R is selected from the group consisting of heterocyclic radicals containing from to 6 atoms in the ring and radicals of the formula wherein R and R are selected from the group consisting of hydrogen, alkyl, aryl, and pyridyl.
4 The reaction is illustrated by the following equation:
0 R1 ii-R1 OHNRaBI HCONRsR: 00:
The carbonyl compound and the amide may generally be present in widely varying proportions, but are preferably present in a molar ratio of from about 1:1 to about 1:10, respectively. Formic acid, in an amount corresponding to 0.01 to 5 mols of formic acid per mol of carbonyl compound, is preferably present during the reaction.
The reaction may be conducted by heating a solution of the carbonyl compound in the amide at a temperature of from about to about 250 C. for a period of from about 1 to about 100 hours, preferably at a temperature of from about to about 200 C. for a period of about 2 to 10 hours.
When neither R nor R is hydrogen, the product may be recovered as a residue by distillation of any unreacted amide and formic acid, if present. The distillation is preferably conducted under vacuum. The residue product is, in many cases, pure enough for use without further treatment. However, the products may conveniently be isolated in the pure state, as the hydrochloride salts, by dissolving the crude product in a solvent such as ethyl ether, dioxane, or benzene and introducing dry hydrogen chloride gas into the solution (in an amount corresponding to at least one mole equivalent) to precipitate the l- (aminoalkyl) pyrene hydrochloride. Similar salts of other anhydrous acids may also be prepared in a similar fashion.
The free amine can be obtained from the hydrochloride by treating it with an aqueous base, such as ammonia, and a water-immiscible solvent, such as ether or benzene. Separation of the organic layer, followed by removal of the solvent leaves the free amine as residue.
When R or R or both are hydrogen, the crude reaction mixture, after removal of excess amide and formic acid, if present, contains a mixture of the desired amine and its corresponding N-forrnyl derivative. The formyl derivative can be hydrolyzed by heating the crude reaction mixture with aqueous or alcoholic acid or base. A convenient method comprises refluxing the crude mixture with an excess of concentrated hydrochloric acid and butanol for 2 to 100 hours, preferably from 4 to 24 hours. The crude amine hydrochloride is obtained by distilling ofif hydrochloric acid, butanol, and formic acid. The crude amine hydrochloride can then be treated with an aqueous base, such as ammonia, and a water-immiscible solvent, such as benzene, to give a solution of the free amino in the nonaqueous layer. The free amine can then be recovered by distilling oil the solvent, or the amine hydrochloride can be obtained by treating the solution with gaseous hydrogen chloride.
The monoalkylaminomethylpyrenes and monoarylaminomethylpyrenes are also prepared in two steps by catalytic reduction of the imines derived from l-pyrenecarboxaldehyde and the corresponding amine. On the other hand (aminoalkyl), pyrenes in which R and R are both hydrogen are prepared most readily by hydrogenation of the oximes of the corresponding carbonyl compounds.
The following examples are illustrative of the preparation of the l-substituted pyrenes of the present invention.
l-thiopyrenol has been prepared by reduction of l-thiocyanopyrene with zinc and acetic acid. Oxidation of thiopyrenol with iodine gave the disulfide. Reaction of spanner 'ril g,
thiopyrenol with chloroacetic acid gave the mercaptoacetic acid derivative.
N-(l-pyrenyDmalearnic acid was obtained by reaction of the amine with maleic anhydride. Cyclization of the maleamic acid with acetic anhydride afforded the maleimide. N,N'-diacetoacetyl-1,6(or8)-diaminopyrene was synthesized by the reaction of diketene with l-aminopyrene.
'lhe l-substituted pyrenes of the present invention may be applied at the rate of 0.2 to 25 pounds per acre. We have found, however, that good control of fungi is obtained when the l-substituted pyrenes are applied at the rate of 0.5 to 6 pounds per acre. They may be used alone, but are preferably employed with a carrier or diluent in the form of a solution or dispersion which can be sprayed on the plants or as a wettable powder which can be dusted on the plants.
Suitable solutions or dispersions for use in accordance with the present invention comprise from 1 to 95 parts by weight of a l-substituted pyrene or mixture of l-substituted pyrenes, as the active fungicidal ingredient, and from to 99 parts by weight of a liquid carrier, such as water, alcohols, ether alcohols, ketones, petroleum distillates, vegetable oils, and the like and mixtures thereof.
Suitable wettable powders or dusts for use in accordance with the present invention comprise from 1 to 90 parts by weight of a l-substituted pyrene or mixture of 1-substituted pyrene, as the active fungicidal ingredient, and from to 99 parts by weight or" a solid carrier, such as clay, talc, chalk, magnesium carbonate, diatomaceous earth, pyrophyllite, and mixtures of such materials.
The above compositions may also contain dispersing or emulsifying agents, such as the condensation products of alkylene oxides with phenols and organic acids, aryl alkyl sulfonates, complex ether alcohols, mahogany soaps, and quaternary ammonium compounds.
The compositions may also contain other toxicants, such as arsenates, rotenone, pyrethrum, irnidazolines, dithiocarbamates, and mixtures of such materials.
The efiectiveness of the l-substituted pyrenes of the present invention as fungicides is demonstrated by the following experiments. The methods by which the experiments were carried out are described below and the results of the experiments are given in Table I below.
BEAN MILDEW TEST Greenhouse tests were conducted with these materials for the control of powdery mildew of beans caused by the fungus Erysiphe polygoni.
For the tests against bean mildew, aqueous suspensions were prepared containing 0.04 part (all parts by weight), 0.008 part, and 0.0016 part of the chemicals to be tested. The suspensions also contained .05 part of dispersing agent, an alkyl phenyl polyethylene glycol ether, marketed under the proprietary mark Tergitol. dispersant NPX, per 100 parts of water. Individual bean plants of about 10 days of age that had been inoculated two to four days previously by dusting with spores of the test organism were sprayed for 30 seconds with one or another of the suspensions. Check or control plants received no fungicidal spray. The plants were then placed in the greenhouse and after 10 days to two weeks the primary leaves were examined for mildew and scored as follows:
1=leaf over-run with mildew, equal to check plants. 2=many but distinctly separate spots on each leaf. 3=410 spots per leaf.
4=13 mildew spots per leaf.
5=no mildew infection.
EARLY BLIGHT TOMATO FOLIAGE DISEASE TEST Test organism-Early blight fungus Alternarin solani is the organism used in this test procedure. The organism is reared on potato dextrose agar in Petri dishes at a temperature of 20 C. Organisms used are transferred 10 days prior to testing; scraped and irradiated with ultra- 2: 25-49% control 1=0-24% control Table I Early Blight Benn Mildew (p.p.m.)
(p.p.m.) Compound Number Mtsture of 1 and 2 4 5 3 3 4 3 5 5 4 5 3 5 5 4 4 2 3 2 3 5 5 4 2 4 2 r. 10 4 t t i a s 4 5 4 3 4 4 5 4 3 4 5 4 3 3 5 3 2 4 5 3 2 l 4 5 5 2 1 3 3 2 2 5 5 5 5 2 2 5 5 4 2 2 i 4 a a 5 4 2 5 4 3 4 4 2 3 2 4 4 4 8 3 g 2 2 4 3 2 5 4 3 1 5 3 2 1 5 4 4 5 5 5 4 s i i i 4.2 4 5 5 4 violet light for 2 minutes on the seventh day following transfer.
Application of toxicant.--One tomato plant variety, Bonny Best, of a standard age and height per concentration is sprayed on a revolving turntable. One hundred to one hundred and ten ml. of the formulated water mixture of the chemical is applied to each plant by use of a Devilbis spray gun with air pressure set at 40 pounds. Application of this volume of spray takes 30 seconds. An equal volume of a water solution containing acetone and emulsifier in the same concentrations as in the fungicidal mixture but without the candidate fungicide, is also sprayed on six tomato plants and held as check or control plants. As soon as the spray has dried the plants are inoculated by again placing them on the turntable and spraying with a spore suspension of early blight, containing 25,000 to 30,000 per mll of water, for 30 seconds at 20 pounds pressure.
Concentration of t0xicant.'lhe test compounds are formulated by a standard procedure of solution in acetone, addition of an emulsifier and dilution with water. The compounds are evaluated at concentrations of 2000 and ppm.
Holding conditions.-Following inoculation :the plants are incubated for 24 hours at 72 F. and percent relative humidity. The plants are then removed from the incubation chamber and held for an additional 24 hours at room temperature.
Record of results-The total number of lesions per 11 15 magnification fields on 11 leaflets on the three top leaves of each plant are counted. A similar count is made on the control plants and the average number of lesions per plant is calculated. Control is based on a comparison of the number of lesions on the treated versus the untreated plants. Compounds are rated according to the following designations.
5=90100% control 4=70-89% control 3=50-69% control Table I-Continued Early Blight Bean Mildew (p.p.m.)
(P-P-IIL) Compound Number As used herein, unless otherwise indicated, all parts and percentages are by weight.
The term ppm. means parts per million.
Similar tests were made against early blight employing turd-cant concentrations of 1000 and 100 parts per million and against bean mildew employing toxicant concentrations of 500, 100 and 20 parts per million.
Table II Early Blight Bean Mildew (ow -l (up- Compound Numbor This application is a continuation-in-part of oo-pcnding 8 application, Serial No. 782,638, filed December 24, 1958, now abandoned.
We claim:
1. A method which comprises applying to fungi a fungicidal amount of a compound having the structurfl formula:
RI!!! RI! III wherein R" is an organic radical, R' and R"" are selectcd from the group consisting of hydrogen and organic radicals, at least one of said R and R"" being hydrogen, said compound having a molecular weight of up to about 700.
2. A method which comprises applying to fungi a fungicidal amount of pyrene substituted in the l-position by an organic radical, said substituted pyrene having a molecular weight of up to about 700.
3. A method which comprises applying to fungi a fungicidal amount of pyrene substituted in the 1- and 6- positions by an organic radical, said substituted pyrene having a molecular weight of up to about 700.
4. A method which comprises applying to fungi a fungicidal amount of pyrene substituted in the 1- and 8- positions by an organic radical, said substituted pyrene having a molecular weight of up to about 700.
5. A method which comprises applying to fungi a. fungicidal amount of l-nitropyrene.
6. A method which comprises applying to fungi a fungicidal amount of 1,6-dinitropyrene.
7. A method which comprises applying to fungi a fungicidal amount of 1,8-dinitropyrene.
8. A method which comprises applying to fungi a fungicidal amount of l-acetylpyrene.
9. A method which comprises applying to fungi a. fungicidal amount of l-benzoylpyrene.
10. A method which comprises applying to fungi a fungicidal amount of 1,6-dibenzoylpyrene.
11. A method which comprises applying to fungi a fungicidal amount of 1,8-dibenzoylpyrene.
12. A method which comprises applying to fungi a fungicidal amount of 1-(hydroxymethyl)pyrene.
13, A method which comprises applying to fungi a fungicidal amount of l-(N,N-dimethylaminomethyl)pyrene hydrochloride.
References Cited in the file of this patent UNITED STATES PATENTS 2,777,794 Kenaga Jan. 15, 1957

Claims (1)

1. A METHOD WHICH COMPRISES APPLYING TO FUNGI A FUNGICIDAL AMOUNT OF A COMPOUND HAVING THE STRUCTURAL FORMULA:
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3486900A (en) * 1965-06-02 1969-12-30 Keuffel & Esser Co Diazotype material
US3723547A (en) * 1965-10-20 1973-03-27 Ciba Geigy Corp Polysubstituted dihydropyrenes
US10975014B2 (en) * 2016-07-01 2021-04-13 Boe Technology Group Co., Ltd. Organic ligand and preparation method thereof, quantum dot structure material, quantum-dot-containing layer, and light emitting diode

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2777794A (en) * 1954-01-13 1957-01-15 Dow Chemical Co Polychlorinated pyrene as a parasiticide

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2777794A (en) * 1954-01-13 1957-01-15 Dow Chemical Co Polychlorinated pyrene as a parasiticide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3486900A (en) * 1965-06-02 1969-12-30 Keuffel & Esser Co Diazotype material
US3723547A (en) * 1965-10-20 1973-03-27 Ciba Geigy Corp Polysubstituted dihydropyrenes
US10975014B2 (en) * 2016-07-01 2021-04-13 Boe Technology Group Co., Ltd. Organic ligand and preparation method thereof, quantum dot structure material, quantum-dot-containing layer, and light emitting diode

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