EP0261226A1 - Use of malonic acid derivative compounds for increasing crop yield - Google Patents

Use of malonic acid derivative compounds for increasing crop yield

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Publication number
EP0261226A1
EP0261226A1 EP87902946A EP87902946A EP0261226A1 EP 0261226 A1 EP0261226 A1 EP 0261226A1 EP 87902946 A EP87902946 A EP 87902946A EP 87902946 A EP87902946 A EP 87902946A EP 0261226 A1 EP0261226 A1 EP 0261226A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
substituted
ring system
unsubstituted
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP87902946A
Other languages
German (de)
French (fr)
Inventor
Charles David Fritz
Anson Richard Cooke
David Treadway Manning
James Joseph Cappy
Thomas Neil Wheeler
Barbara Auxier Moore
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rhone Poulenc Nederland BV
Rhone Poulenc BV
Original Assignee
Rhone Poulenc Nederland BV
Rhone Poulenc BV
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Publication of EP0261226A1 publication Critical patent/EP0261226A1/en
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
    • C07C233/15—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • 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
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
    • A01N37/04—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof polybasic
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A01N37/30—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the groups —CO—N< and, both being directly attached by their carbon atoms to the same carbon skeleton, e.g. H2N—NH—CO—C6H4—COOCH3; Thio-analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
    • A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • C07C233/04—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C233/07—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members 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
    • C07D261/14—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D277/38—Nitrogen atoms
    • C07D277/44—Acylated amino or imino radicals
    • C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62—Benzothiazoles
    • C07D277/68—Benzothiazoles 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 in position 2
    • C07D277/82—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
    • C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C07D285/135—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms

Definitions

  • This invention relates to the use of malonic acid derivative compounds for increasing crop yield. This invention further relates to novel malonic acid derivative compounds and processes for the preparation thereof.
  • malonic acid derivative compounds have been known for some time in the art. See, for example, U.S. Patent 2,504,896 and U.S. Patent 3,254,108. Some malonic acid derivative compounds have been described in the art as capable of providing certain plant growth regulating responses such as prevention of fruit drop, rooting of cuttings and formation of parthenogenetic fruit.
  • U.S. Patent 3,072,473 describes N-arylmalonamic acids and their esters and salts, N, N'-diarylmalonamides, N-alkyl-N-arylmalonamic acids and their esters and salts, and N, N'-dialkyl-N, N'-diarylmalonamides which may be useful as plant growth reguiants and herbicides.
  • Japanese Patent 84 39,803 (1984) describes malonic acid anilide derivative compounds which may be useful as plant growth regulators. The plant growth regulating properties of substituted malonyl monoanilides are described by Shindo, N. and Kato, M., Meiji Daigaku Noogaku-bu Kenkyu Hokoku, Vol. 63, pp. 41-58 (1984).
  • This invention relates to a method for increasing crop yield which comprises applying to the crop an effective amount, sufficient to increase crop yield, of a compound having the formula:
  • This invention also relates to novel malonic-sacId derivative compounds and to processes for the prepartion of said compounds.
  • this invention relates to a method of increasing crop yield by use of certain malonic add derivative compounds. More particularly, this invention involves a method for increasing crop yield which comprises applying to the crop an effective amount, sufficient to increase crop yield, of a compound having the formula: wherei n :
  • R 1 and R 2 are independently a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents (Z) are the same or different and are one or more hydrogen, halogen, alkylcarbonyl, alkylcarbonylalkyl, formyl, alkoxycarbonylalkyl, alkoxycarbonylalkylthio, polyhaloalkenylthio, thiocyano, propargylthlo, hydroxyimino, alkoxyimino, trialkylsilyloxy, aryldialkylsilyloxy, triarylsilyloxy, formamidino, alkylsulfamido, dlalkylsulfamid
  • R 1 and R 2 are independently hydrogen or derivative salts, or a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z as hereinbefore defined;
  • Y 1 and Y 2 are independently a substituted or unsubstituted heteroatom in which the permissible substituents are Z as hereinbefore defined; Y 3 and Y 4 are independently hydrogen, or a substituted or unsubstituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination, or halogen, alkylcarbonyl, formyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkoxycarbonylalkyIthio, polyhaloalkenylthio, thiocyano, propargylthio, trialkylsilyloxy, aryldialkylsilyloxy, triarylsilyloxy, formamidino, alkylsulfamido, dialkylsulfamido, alkoxysulfonyl, polyhaloalkoxysulfonyl,
  • Y 5 and Y 6 are independently oxygen or sulfur;
  • X is a covalent single bond or double bond, a substituted or unsubstituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z as hereinbefore defined;
  • R 3 is a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents are Z as hereinbefore defined;
  • R 3 is a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituent
  • the alkyl-containlng moieties in formula 1 may contain from about 1 to about 100 carbon atoms or greater, preferably from about 1 to about 30 carbon atoms, and more preferably from about 1 to about 20 carbon atoms.
  • the polysaccharide moiety may contain up to about 50 carbon atoms. It is appreciated that all compounds encompassed within formula 1 are compounds having no unfilled bonding positions.
  • R 1 and R 2 are independently other than hydrtogen, alkyl or aryl when both Y 1 and Y 2 are
  • hydrogen or derivative salts refer to hydrogen or any appropriate derivative salt substituents which may be substituted therefore.
  • Illustrative derivative salt substituents include, for example, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, alkali metals, alkaline earth metals and the like including mixtures thereof.
  • Monocyclic ring systems encompassed by R 1 , R 2 and R 3 in formula 1 may be represented by generalized formula 2 as follows:
  • B 1 represents a saturated or unsaturated carbon atom and A 1 represents a ring-forming chain of atoms which together with B 1 forms a cyclic system containing from 0 to 3 double bonds or from 0 to 2 triple bonds.
  • a 1 may contain entirely from 2 to 12 carbon atoms, may contain a combination of from 1 to 11 carbon atoms and from 1 to 4 heteroatoms which may be selected independently from N, O, S, P or other heteroatoms, or may contain 4 ring-forming heteroatoms alone.
  • Monocyclic ring systems encompassed by Y 3 and Y 4 linked together in formula 1 may include any monocyclic ring system of R 1 , R 2 and R 3 appropriately positioned in formula 1.
  • Ring-forming heteroatoms may in some cases bear oxygen atoms as in aromatic N-oxides and ring systems containing the sulfinyl, sulfonyl, selenoxlde and phosphine oxide moieties.
  • Selected carbon atoms contained in cycles formed by B 1 and A 1 containing at least 3 ring-forming atoms may bear carbonyl, thlocarbonyl, substituted or unsubstituted imino groups or substituted or unsubstituted methylidene groups.
  • the group designated as Z represents one or more substituents selected independently from among the group of substituents defined for Z herein.
  • Bicycllc ring systems encompassed by R 1 , R 2 and R 3 in formula 1 may be represented by generalized formulae 3 and 4 as follows:
  • B 2 and B 3 may be independently a saturated or unsaturated carbon atom or a saturated nitrogen atom, A 2 and A 3 independently represent the ring-forming chains of atoms described below and
  • Z represents one or more substituents selected independently from among the group of substituents defined for Z herein.
  • Combinations of A 2 and A 3 may contain in combination with B 2 or B 3 from 0 to 5 double bonds.
  • a 2 and A 3 independent of B 2 and B 3 . may contain entirely from 1 to 11 carbon atoms, may contain a combination of 1 to 3 heteroatoms which may be selected independently from among N, O, S, P or other heteroatoms together with from 1 to 10 carbon atoms or may contain from 1-3 ring-forming heteroatoms alone.
  • Ring-forming heteroatoms may in some cases bear oxygen atoms, as in aromatic N-oxides and ring systems containing the sulfinyl, sulfonyl. selenoxide and phosphine oxide groups.
  • Selected carbon atoms contained in A 2 and A 3 may bear carbonyl, thiocarbonyl, substituted or unsubstituted imino groups or substituted or unsubstituted methylidene groups.
  • Bicyclic ring systems encompassed by Y 3 and Y 4 linked together in formula 1 may include any bicyclic ring system of R 1 , R 2 and R 3 appropriately positioned in formula 1.
  • bicyclic ring systems defined for R 1 , R 2 , R 3 and Y 3 and Y 4 linked together may be spirocyclic ring systems and are not limited to the fused bicyclic structures of formulae 3 and 4.
  • Spirocyclic ring systems may be saturated or unsaturated carbocyclic or heterocyclic and may be independently substituted by one or more substituents Z as defined herein.
  • Polycyclic ring systems i.e., greater than 2 rings, encompassed by R 1 , R 2 and R 3 in formula 1 may be represented by generalized formulae 5 , 6, 7 and 8 as follows:
  • B 4 , B 5 , B 6 and B 7 may be independently a saturated or unsaturated carbon atom or a saturated nitrogen atom, and A 4 , A 5 , A 6 and A 7 independently represent ring forming chains of atoms which may contain together with one or the other (but not both) of their two associated bridgehead atoms, from 0-2 double bonds.
  • Z represent one or more substituents selected independently from among the group of substituents defined for Z herein.
  • the ring-forming elements of A 4 , A 5 , A 6 and A 7 independent of B 4 , B 5 , B 6 and B 7 may contain from 1-11 carbon atoms, may contain a combination of from 1-10 carbon atoms and from 1-3 heteroatoms which may be selected independently from among N, O, S, P or other heteroatoms, or may contain from 1-3 heteroatoms alone. Ring-forming heteroatoms may in some cases bear oxygen atoms as in aromatic N-oxides and ring systems containing the sulfinyl, sulfonyl, selenoxide and phosphine oxide groups.
  • the group A 6 may at times be defined as a bond.
  • Selected carbon atoms contained in A 4 , A 5 , A 6 and A 7 may bear one or more carbonyl, thiocarbonyl or substituted or unsubstituted imino groups.
  • the groups B 10 represent independently a saturated or unsaturated carbon atom or a saturated nitrogen atom.
  • the group B 11 may represent a saturated or unsaturated carbon atom or a nitrogen or phosphorous atom.
  • the groups A 8 , A 9 and A 10 represent ring-forming chains of atoms which may contain together with 1 of the groups B 8 , B 9 , B 10 and B 11 from 0-2 double bonds.
  • the ring-forming elements of groups A 8 , A 9 and A 10 independent of groups B 8 , B 9 , B 10 and B 11 may contain from 2-10 carbon atoms, may contain from 1-10 carbon atoms in combination with 1-3 heteroatoms which may be selected independently from among N, O, S, P or other heteroatoms, or may contain from 2-3 heteroatoms alone. Ring-forming heteroatoms may in some cases bear oxygen atoms as in aromatic N-oxides and in ring systems containing the sulfinyl, sulfonyl, selenoxide and phosphine oxide groups. Selected carf'n atoms contained in groups A 8 , A 9 and A 10 may bear one or more carbonyl, thiocarbonyl or substituted or unsubstituted imino groups.
  • polycyclic ring systems defined for R 1 , R 2 , R 3 and Y 3 and Y 4 linked together may be spirocyclic ring systems and are not limited to the fused polycyclic structures of formulae 5, 6, 7 and 8.
  • Spirocyclic ring systems may be saturated or unsaturated, carbocyclic or heterocyclic and may be independently substituted by one or more substituents Z as defined herein.
  • Polycyclic ring systems encompassed by Y 3 and Y 4 linked together in formula 1 may include any polycyclic ring system of R 1 , R 2 and R 3 appropriately positioned in formula 1.
  • Bridged bicyclic structures encompassed by R 1 , R 2 and R 3 in formula 1 may be represented by generalized formulae 9, 10, and 11 as follows:
  • B 12 and B 13 may be independently a saturated carbon atom optionally substituted by Z or a nitrogen atom, and the groups A 11 , A 12 and A 13 independently represent ring-forming chains of atoms which may contain, Independently of B 12 and B 13 , from 0-2 double bonds.
  • the groups Z represent one or more substituents selected Independently from among the groups of substituents defined for Z herein.
  • the ring-forming elements of A 11 , A 12 and A 13 may contain entirely from 1-11 carbon atoms, may contain a combination of from 1-10 carbon atoms and from 1-3 heteroatoms which may be selected Independently from among N, O, S, P or other heteroatoms, or may contain from 1-3 heteroatoms alone with the proviso that when one of the groups A 11 , A 12 and A 13 is a single heteroatom, the other two groups should contain two or more ring-forming atoms.
  • a second proviso is that when one or both of the groups B 12 and B 13 is nitrogen, the groups A 11 , A 12 and A 13 should contain at least two saturated ring-forming atoms.
  • Ring-forming heteroatoms may in some cases bear oxygen atoms as in the sulfinyl, sulfonyl, selenoxide and phosphine oxide moieties.
  • Selected carbon atoms contained in A 11 , A 12 and A 13 may bear one or more carbonyl, thiocarbonyl or substituted or unsubstituted imino groups.
  • Bridged bicyclic structures encompassed by Y 3 and Y 4 linked together in formula 1 may include any bicyclic bridged system of R 1 , R 2 and R 3 appropriately positioned in formula 1.
  • formula 1 encompasses a wide variety of malonic acid derivative compounds.
  • Illustrative malonic acid derivative compounds within the scope of formula 1 which may be used for increasing crop yield are included in Tables 1 through 11 below.
  • novel malonic acid derivative compounds of this invention can be depicted by the following formulae:
  • Y 11 is O, S or NR wherein R 7 is hydrogen or alkyl
  • Y 12 is O, S, NH or N (alkyl); and R 6 is ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dlalkylaminoalkyl, aryl, mercaptoalkyl, alkylthloalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulflnylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalky
  • Z 2 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio.
  • Y 13 is O, S or NR 9 wherein R 9 is hydrogen or alkyl
  • Y 14 is O, S, NH or N (alkyl);
  • Y 15 and Y 16 are Independently hydrogen, alkyl, halogen, alkoxy, alkylthio, alkenyl, alkynyl, hydroxy, cyano, nitro, formyl, amino, alkylcarbonyl, dialkoxyalkyl, alkylcarbonylamino, formylamino, hydroxyalkyl, haloalkyl or polyhaloalkyl provided that when Y 15 is alkyl then Z 2 is not halogen or polyhaloalkyl at the para- position, and further provide that at least one of Y 15 and Y 16 is other than hydrogen;
  • Y 15 and Y 16 may be linked together to form a substituted or unsubstituted heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated; and
  • R 8 is hydrogen or R 6 ;
  • Y 17 is O, S or NR 11 wherein R 11 is hydrogen or alkyl
  • Y 18 is O or S
  • Y 19 and Y 20 are independently hydrogen, alkyl, alkoxy, alkylthio, halogen, haloalkyl or polyhaloalkyl; or
  • Y 19 and Y 20 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated; and
  • R 10 is hydrogen or R 6 ;
  • R 1 and R 2 are independently a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated; or
  • R 1 and R 2 are independently hydrogen or derivative salts, or a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination;
  • Y 1 and Y 2 are independently a substituted or unsubstituted heteroatom
  • Y 3 and Y 4 are linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated; and
  • Y 5 and Y 6 are independently oxygen or sulfur; in which the permissible substituents for formulae
  • Novel malonic acid derivative compounds within the scope of formula (iv) above can be depicted by the following formulae:
  • Y 21 is O, S or N R 13 wherein R 13 is hydrogen or alkyl
  • Y 22 is O, S, NH or N (alkyl);
  • Y 23 , Y 24 , Y 25 and Y 26 are independently hydrogen, alkyl or halogen
  • R 12 is hydrogen or R 6 ;
  • Y 27 is O, S or NR 15 wherein R 15 is hydrogen or alkyl
  • Y 28 is O S, NH or N (alkyl);
  • Y 29 , Y 30 , Y 31 , Y 32 , Y 33 and Y 34 are independently hydrogen, alkyl or halogen; and R 14 is hydrogen or R 6 ;
  • Y 35 is O, S or NR 17 wherein R 17 is hydrogen or alkyl
  • Y 36 is O or S; and R 16 is hydrogen or R 6 , in which the permissible substituents for formulae (v) through (vii) are as described for Z above for formulae (i) through (iv).
  • the malonic acid derivative compounds encompassed within formula 1 and the intermediate compounds used in the preparation thereof can be prepared by conventional methods known in the art and many may be available from various suppliers.
  • the novel malonic acid derivative compounds of formulae (i) through (vii) above which may used in the method of this invention may be prepared by reacting appropriate starting ingredients in accordance with conventional procedures described in the art as illustrated below.
  • novel malonic acid derivative compounds of formula (i) can be prepared by the following general reaction scheme:
  • novel malonic acid derivative compounds of formula (ii) can be prepared by the following general reaction scheme:
  • novel malonic add derivative compounds of formula (iii) can be prepared by the following general reaction scheme:
  • R 10 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (iii) including process conditions are described for example by Richter,
  • novel malonic acid derivative compounds of formula (iv) can be prepared by the following general reaction scheme:
  • Y 6 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (iv) including process conditions are described for example by Richter, G.H., supra, according to the known Schotten-Baumann procedure.
  • novel malonic acid derivative compounds of formula (v) can be prepared by the following general reaction scheme:
  • Y 26 and R 12 are as defined hereinabove.
  • novel malonic acid derivative compounds of formula (vi) can be prepared by the following general reaction scheme:
  • novel malonic acid derivative compounds of formula (vii) can be prepared by the following general-reaction scheme:
  • the malonic acid derivative compounds of formula 1 have been found to significantly increase crop yield in comparison with untreated crops at similar conditions.
  • the malonic acid derivative compounds used in this invention are substantially non-phytotoxic to growing plants.
  • an effective amount of a malonic acid derivative compound for increasing crop yield refers to a yield enhancing effective amount of the compound sufficient to increase crop yield.
  • the effective amount of compound can vary over a wide range depending on the particular compound employed, the particular crop to be treated, environmental and climatic conditions, and the like.
  • the amount of compound used preferably does not cause substantial phytotoxicity, e.g., foliar burn, chlorosis or necrosis, to the crop.
  • the compound can preferably be applied to plants and crops at a concentration of from about 0.01 to 15 pounds of compound per acre as more fully described below.
  • compositions containing the compounds as the active ingredient will usually comprise a carrier and/or diluent, either liquid or solid.
  • Suitable liquid diluents or carriers include water, petroleum distillates, or other liquid carriers with or without surface active agents.
  • Liquid concentrates can be prepared by dissolving one of these compounds with a nonphytotoxic solvent such as acetone, xylene, nitrobenzene, cyclohexanone or dimethyl formamide and dispersing the active ingredients in water with the aid of suitable surface active emulsifying and dispersing agents.
  • dispersing and emulsifying agents are dictated by the nature of the composition and the ability of the agent to facilitate the dispersion of the active ingredient. Generally, it is desirable to use as little of the agent as is possible, consistent with the desired dispersion of the active ingredient in the spray so that rain does not re-emulsify the active ingredient after it is applied to the plant and wash it off the plant.
  • Nonionic, anionic, or cationic dispersing and emulsifying agents may be employed, for example, the condensation products of alkylene oxides with phenol and organic acids, alkyl aryl sulfonates, complex ether alcohols, quaternary ammonium compounds, and the like.
  • the active ingredient is dispersed in and on an appropriately divided solid carrier such as clay, talc, bentonite, diatomaceous earth, fuller's earth, and the like.
  • an appropriately divided solid carrier such as clay, talc, bentonite, diatomaceous earth, fuller's earth, and the like.
  • the aforementioned dispersing agents as well as lignosulfonates can be included.
  • the required amount of the active ingredient contemplated herein can be applied per acre treated in from 1 to 200 gallons or more of liquid carrier and/or diluent or In from about 5 to 500 pounds of inert solid carrier and/or diluent.
  • concentration in the liquid concentrate will usually vary from about 5 to 95 percent by weight and in the solid formulations from about 0.5 to about 90 percent by weight.
  • Satisfactory sprays or dusts for general use contain from about 0.001 to about 100 pounds of active ingredient per acre, preferably from about 0.01 to about 15 pounds of active ingredient per acre, and more preferably from about 0.1 to about 5 pounds of active ingredient per acre.
  • Formulations useful in the conduct of this invention can also contain other optional ingredients such as stabilizers or other biologically active compounds, insofar as they do not impair or reduce the activity of the active ingredient and do not harm the plant being treated.
  • Other biologically active compounds include, for example, one or more insecticidal, herbicidal, fungicidal, nematicidal, miticidal, plant growth regulators or other known compounds. Such combinations may be used for the known or other purpose of each ingredient and may provide a synergistic effect.
  • the malonic acid derivative compounds of formula 1 are preferably applied to plants and crops under average or normal growing conditions.
  • the malonic acid derivative compounds used in this invention can be applied during the plant vegetative growth phase or the plant reproductive growth phase to obtain increased crop yield. It may be desirable for some crops to apply the malonic acid derivative compounds at the reproductive growth phase including, for example, the early flower stage, fruit set stage or full flower bloom stage. In other crops, it may be desirable to apply the malonic acid derivative compounds at the vegetative growth phase.
  • the application timing will in general depend upon the particular crop to be treated.
  • An increase in crop yield can be attributable, for example, to various plant growth effects such as increased branching (increased reproductive sites), early pod (fruit) set, increased blossom set and inhibition of blossom (flower and fruit) abscission during early stages of plant reproductive development.
  • increased crop yield refers to an increase in the raw agricultural commodity in terms of harvestable yield, e.g., bushels of seeds, bales of cotton and the like. It may be possible to have an increased harvestable yield for a treated crop in comparison with an untreated crop, yet the total crop biomass may be less for the treated crop.
  • harvestable yield as used herein may be inclusive of total crop biomass, e.g., bushels of corn per acre and the like.
  • Treatment of certain crops such as alfalfa with the malonic acid derivative compounds of formula 1 may also increase the crop nutritional value, e.g., total digestable nutrients (TDN).
  • TDN total digestable nutrients
  • plants and crops refer in general to any agronomic or horticultural crops, ornamentals and turfgrasses.
  • Illustrative of plants and crops which can be treated by the malonic acid derivative compounds of formula 1 according to the method of this invention include, for example, corn, cotton, sweet potatoes, white potatoes, alfalfa, wheat, rye, rice, barley, oats, sorghum, dry beans, soybeans, sugar beets, sunflowers, tobacco, tomatoes, canola, deciduous fruit, citrus fruit, tea, coffee, olives, pineapple, cocoa, banana, sugar cane, oil palm, herbaceous bedding plants, woody shrubs, turfgrasses, ornamental plants, evergreens, trees, flowers, and the like.
  • the malonic acid derivative compounds contemplated herein are effective for increasing crop yields. Such compounds have a high margin of safety in that when used in sufficient amount to provide a yield enhancing effect, they do not burn or injure the crop or plant, and they resist weathering which indudes wash-off caused by rain, decomposition by ultraviolet light, oxidation, or hydrolysis in the presence of moisture or, at least, such decomposition, oxidation, and hydrolysis as would materially decrease the desirable yield enhancing characteristic of the active ingredient or impart undesirable characteristics, for instance, phytotoxicity, to the active ingredients. Mixtures of the active compounds can be employed if desired as well as combinations of the active compounds with other biologically active compounds or ingredients as indicated above.
  • Example I Preparation of ethyl 3-[(4-fluorophenyl)amino]- 3-oxopropanoate Into a nitrogen-purged, air-stirred reaction flask was charged 4.44 grams (0.04 mole) of 4-fluoroaniline, 4.05 grams (0.04 mole) of triethylamine and 200 mmiliters of tetrahydrofuran solvent. A 6.02 gram (0.04 mole) portion of ethyl malonyl chloride was added rapidly with stirring at room temperature followed by a few milliliters of tetrahydrofuran. The temperature rose to 42°C and triethylamine hydrochloride separated therefrom.
  • Example II In a similar manner Compounds 2-76 were prepared and identified in Table A.
  • Example III Preparation of ethyl 1-(2-methyl-4,5-dichlorophenylaminocarbonyl)cyclopropanecarboxylate Into a nitrogen-purged round bottom flask was charged 5.53 grams (0.03 mole) of 2-methyl-4,5-dichloroaniline, 3.18 grams (0.03 mole) of triethylamine and 190 milliliters of tetrahydrofuran solvent. With vigorous stirring, a 5.55 gram (0.03 mole) portion of ethyl 1-chlorocarbonylcyclopropanecarboxylate prepared in Example XVIII was added in one portion, after which the mixture was stirred at ambient temperature for a six-hour period.
  • Example IV In a manner similar to that employed in Example III, Compounds 78-96 were prepared and identified in Table B.
  • Example V Preparation of 3-[(4-bromo-2-methylphenyl)- amino]-3-oxopropanoic acid
  • a 6.0 gram (0.02 mole) portion of ethyl 3-[(4-bromo-2-methylphenyl)amino]-3-oxopropanoate prepared in Example I (Compound No. 75) was dissolved in approximately 80 milliliters of ethanol and 1.2 grams (0.03 mole) of sodium hydroxide pellets were added to the resulting mixture. The mixture was stirred for four hours and then allowed to stand overnight. The mixture was then evaporated to drynoss and water added to give a yellow cloudy solution.
  • Example VI In a manner similar to that employed in Example V, Compounds 98-109 were prepared.
  • Example VII Preparation of 1-(2-methyl-4.5-dichlorophenylaminocarbonyl)cvclopropanecarboxylic acid
  • a solution containing 0.34 gram (0.006 mole) of potassium hydroxide and 0.109 gram (0.006 mole) of water in 80 millniters of ethanol was prepared in a 250 milliliter round bottom flask.
  • a solution of ethyl 1-(2-methyl-4,5-dichlorophenylaminocarbonyl)cyclopropanecarboxylate prepared in Example III in a small volume of ethanol was added and the mixture allowed to stir with warming to room temperature over a 72 hour period.
  • Example IX Preparation of ethyl 1-(4-bromo-2-methylphen ⁇ laminocarbonyl)cyclobutanecarboxylate Into a nitrogen-purged reaction flask was charged 2.74 grams (0.01 mole) of 4-bromo-2-methylaniline and 1.49 grams (0.01 mole) of triethylamine dissolved in 200 milliliters of tetrahydrofuran. With vigorous stirring, 2.80 grams (0.01 mole) of ethyl 1-chlorocarbonylcyclobutanecarboxylate prepared in Example XIX were added and the resulting mixture stirred at ambient temperature for 6 hours. A precipitate of triethylamine hydrochloride was removed by filtration.
  • Example XI Preparation of 1-(3,5-dichlorophenylaminocarbonyl)cyclobutanecarboxylic acid A 2.0 gram (0.006 mole) portion of ethyl 1-(3,5-dichlorophenylaminocarbonyl)cyclobutanecarboxylate prepared in Example X (Compound 130) was hydrolyzed in the presence of water (0.114 gram, 0.006 mole) and ethanolic potassium hydroxide (0.355 gram, 0.006 mole).
  • Example XII In a manner similar to that employed in Example XI, Compounds 136-139 were prepared and identified in Table F below.
  • Example XIII Preparation of ethyl 1-(4-bromo-2-methylphenylaminocarbonyl)cyclopentanecarboxylate
  • Ethyl 1-chlorocarbonylcyclopentanecarboxylate (3.10 grams, 0.02 mole) prepared in Example XX, 4-bromo-2-methylaniline (2.82 grams, 0.02 mole) and triethylamine (1.53 grams, 0.02 mole) were reacted in tetrahydrofuran (200 milliliters) under conditions similar to that described in Example I to give 2.40 grams (0.007 mole) of ethyl 1-(4-bromo-2-methylphenylaminocarbonyl)cyclopentanecarboxylate (Compound 140) which, after recrystallization from hexane, had a melting point of 64°C-67oC.
  • Example XIV Preparation of ethyl 2-(4-bromo-2- methylphenylaminocarbonyl)butanoate
  • Ethyl 2-(chlorocarbonyl)butanoate (5.8 grams, 0.03 mole), 4-bromo-2-methylaniline (5.0 grams, 0.03 mole) and triethylamine (3.27 grams, 0.03 mole) were reacted under conditions similar to that described for Example I to give 7.4 grams (0.02 mole) of ethyl 2-(4-bromo-2-methylphenylaminocarbonyl)butanoate (Compound 141) as a white solid having a melting point of 98°C-100°C.
  • Example XV In a manner similar to Example XIV, Compounds 142-152 were prepared and identified in Table G below.
  • Example XVI Preparation of 3-[(4-bromo-2-methylphenyl)- amino]-2-bromo-2-methyl-3-oxopropanoic acid
  • Example XVII Preparation of N-butyl 3-[(4-bromo-2- methylphenyl)amino]-3-oxopropanamide
  • Example XIX Preparation of ethyl 1-chlorocarbonylcyclobutanecarboxylate Diethyl 1,1-cyclobutanedicarboxylate (20.0 grams, 0.10 mole) was saponified with 6.59 grams (0.10 mole) of potassium hydroxide in a mixture of 200 milliliters of ethanol and 1.80 grams (0.10 mole) of water and worked up to give the monocarboxylic acid which was reacted with thionyl chloride (8.86 grams, 0.07 mole) in methylene chloride solution as described in Example XVIII.
  • Example XX Preparation of ethyl 1-chlorocarbonylcyclopentanecarboxylate
  • a 10 gram (0.05 mole) portion of diethyl 1,1-cyclopentanedicarboxylate was converted into 5.67 grams (0.03 mole) of ethyl 1-chlorocarbonylcydopentanecarboxylate (Compound 157).
  • NMR analysis of the product indicated the following:
  • Example XXII Preparation of ethyl 3-[(4-chlorophenyl)amino1-3- oxopropanoate 4-Chloroanlline (25.4 grams, 0.20 mole) and diethyl malonate (48 grams, 0.30 mole) were reacted in a manner similar to the procedure described by A.K. Sen and P. Sengupta, Jour. Indian Chem. Soc. 46 (9), 857-859 (1969).
  • Example XXIII Preparation of ethyl 3-[(4-methylthiazol-2-yl) aminol-3-oxopropanoate
  • 2-amino-4-methylthiazole was reacted with ethyl malonyl chloride employing triethylamine as the acid acceptor in tetrahydrofuran solution.
  • the ethyl 3-[(4-methylthiazol-2-y1)amino]-3-oxopropanoate product (Compound 160) (7.5 grams, 0.03 mole) was obtained as an off-white solid having a melting point of 138°C-141°C.
  • Example XXIV In a manner similar to Example XXIII, Compounds 161-173 were prepared and identified in Table H below.
  • Example XXV Preparation of ethyl 2-chlorocarbonyl-3- methyl-2-butenoate Diethyl isopropylidenemalonate (30 grams, 0.15 mole) was saponified with 10.0 grams (0.15 mole) of potassium hydroxide in 200 milliliters of ethanol solution and worked up to give the monocarboxylic acid which was then reacted with thionyl chloride (10 mllimters, 0.1 mole) in methylene chloride solution in a manner similar to the procedure described in Example XVIII. Removal of solvent gave 9.6 grams (0.05 mole) of ethyl 2-chlorocarbonyl-3-methyl-2-butenoate. NMR analysis of the residue product in CDCI 3 solution indicated complete conversion of the carboxylic acid to the acid chloride as evidenced by absence of a downfield carboxylic acid proton. This compound is referred to hereinafter as Compound 174.
  • Example XXVI Preparation of ethyl 2-[(4-bromo-2-methylphenyl)- aminocarbonyl]-3-methyl-2-butenoate
  • ethyl 2-chlorocarbonyl-3-methyl-2-butenoate 9.6 grams, 0.05 mole
  • 4-bromo-2-methylaniline 5.3 grams, 0.03 mole
  • triethylamine 4.0 mnimters, 0.03 mole
  • Example XXVII Preparation of 3,4-dichloro-2,5-dimethylannine A solution of 5.0 grams (0.03 mole) of 3,4-dichloro-2,5-dimethyl-1-nitrobenzene in 70 milliliters of ethanol was hydrogenated at room temperature at 50 psi in the presence of 0.25 gram of 10% palladium on activated carbon as a catalyst. Working up the reaction mixture gave 1.21 grams (0.006 mole) of 3,4-dichloro-2,5-dimethylaniline (Compound 176) as a yellow solid having a melting point of 72°C-76°C.
  • Part A Preparation of 2,2-dimethyl-N-(4-chloro- 2-metho ⁇ yphenyl)propanamide
  • the resulting mixture was stirred for two hours at room temperature.
  • Triethylamine hydrochloride precipitated and was filtered off and the filtrate vacuum stripped to give a dark liquid which was taken up in methylene chloride.
  • Part B Preparation of 2,2-dimethyl-N- (4,5-dichloro-2-methoxyphenyl)propanamide Into a stirred solution containing 6.82 grams (0.03 mole) of 2,2-dimethyl-N-(4-chloro-2-methoxyphenyl)propanamide prepared in Part A in 150 miliniters of chloroform was added 3.81 grams (0.03 mole) of sulfuryl chloride over a 40 minute period. The resulting reaction mixture was heated under reflux for a 3 day period, each day cooling the mixture and adding an additional 3.81 grams (0.03 mole) of sulfuryl chloride before continuing the reflux. At the end of 3 days, thin layer chromatographic analysis of the mixture indicated the reaction to be complete.
  • Part C Preparation of 4.5-dichloro-2- methoxyanlline
  • the 2,2-dimethyl-N-(4,5-dichloro-2-methoxyphenyl)propanamide (3.70 grams, 0.01 mole) prepared in Part B was dissolved in ethanol: 12N HCl (1:1), the mixture heated under reflux overnight and then freed of volatiles under rotary evaporation.
  • Example IX A 3.0 gram (0.009 mole) portion of ethyl l-(4-bromo-2-methylphenylaminocarbonyl)cyclobutanecarboxylate prepared in Example IX (Compound 129) was hydrolyzed in a manner similar to that described in Example XI to give 2.19 grams (0.007 mole) of 1-(4-bromo-2-methylphenylaminocarbonyl)cyclobutanecarboxylic acid, Compound 181, having a melting point of 154°C-155°C.
  • Example LIII 3,5-Dichloroaniline (2.69 grams, 0.02 mole) and ethyl (chlorocarbonyl)methoxyacetate (3.0 grams, 0.02 mole), prepared in Example LIII (Compound 211), were reacted in the presence of triethylamine (1.68 grams, 0.02 mole) in 200 milliliters of methylene chloride in a manner similar to that described in Example I to give 1.34 grams (0.004 mole) of ethyl 3-[(3,5-dichlorophenyl)amino]-2-methoxy-3-oxopropanoate, Compound 213, having a melting point of 89.5°C-92.5°C.
  • Dimethyl methoxymalonate (50.0 grams, 0.3 mole) was saponified with potassium hydroxide (17.3 grams, 0.3 mole) in a mixture of 500 milliliters of methanol and 5.55 grams (0.3 mole) of water according to the general procedure of Example VII but employing a reaction period of approximately 16 hours.
  • the reaction mixture was evaporated free of solvents and the residue dissolved in water and extracted twice with ether to remove any unreacted diester.
  • the aqueous layer was then saturated with potassium chloride, acidified with 2H HCl and extracted twice with ethyl ether.
  • t-Butyl methyl methoxymalonate (7.57 grams, 0.04 mole), prepared in Part A, was saponified with potassium hydroxide (2.45 g, 0.04 mole) in a mixture of 25 milliliters of methanol and 668 microliters (0.04 mole) of water according to the general procedure of Example VII but employing a reaction period of 20 hours. Workup according to the general method of Example VII gave 5.42 grams (0.03 mole) of mono-t-butyl methoxymalonate. NMR analysis of the product indicated the following:
  • a 50 milliliter round-bottom flask was equipped with a magnetic stirring bar and a reflux condenser with N 2 inlet.
  • the flask was charged with 183.0 grams (1.07 mole) of bis(trimethylsilyl) acetylene and 0.40 gram (0.001. mole) of cupric acetylacetonate.
  • Using an oil bath the temperature of the stirred mixture was raised to 145°C.
  • Using a syringe pump 39.3 grams (0.21 mole) of diethyl diazomalonate were added over 36 hours. Heating at 1450C was continued for an additional 12 hours after all of the diazomalonate had been added.
  • the excess bis(trimethylsilyl)acetylene was removed by vacuum distillation.
  • a 500 milliliter round-bottom flask was equipped with a magnetic stirrer and N 2 inlet.
  • the flask was charged with 21.0 grams (0.07 mole) of diethyl bis (2,3-trimethylsilyl)cyclopropene-1,1-dicarboxylate, 125 milliters of acetonitrile, 12.2 grams (0.21 mole) of anhydrous KF, and 6.50 grams (0.02 mole) of dicyclohexano-18-crown-6 ether.
  • the mixture was stirred 6 hours at room temperature.
  • the mixture was filtered and the filtrate concentrated under reduced pressure to a deep red oil. This oil was taken up in 100 milliliters of methanol and stirred 24 hours at room temperature.
  • a 250 milliliter round-bottom flask was equipped with a magnetic stirring bar and an addition funnel with N 2 inlet.
  • the flask was charged with 6.15 grams (0.03 mole) of diethylcyclopropene-1,1-dicarboxylate and 50 milliliters of ethanol.
  • the stirred mixture was cooled in an ice bath and a solution of 1.33 grams (0.03 mole) of NaOH in 5.0 milliliters of water was added dropwise.
  • the mixture was allowed to come to room temperature and stirred for 3 days.
  • the reaction mixture was concentrated to 1/4 of the original volume under reduced pressure, diluted with ice water, and extracted twice with ether.
  • the flask was charged with1.30 grams (0.008 mole) of mono-ethyl cyclopropene-1,1-dicarboxylate, 50 milliliters of dry THF, 2.3 grams (0.02 mole) of potassium carbonate (anhydrous), and 450 milligrams of dicyclohexano-18-crown-6 ether.
  • the stirred reaction mixture was cooled to 00C, and 0.90 gram (0.008 mole) of ethyl chloroformate in 10 milliliters of THF was added dropwise. The mixture was stirred for 2 1/2 hours at 00C.
  • Plant axillary stimulation may be indicative of increased plant reproductive sites resulting in increased plant biomass and/or increased crop yield. Treatment of plants with certain malonic acid derivative compounds such as those compounds identified in Table I below results in enhanced axillary stimulation.
  • Solutions of the test compounds identified in Table I were prepared by dissolving 68.8 milligrams of the particular compound in 5.5 milliliters of acetone and then adding water to a final volume of 11.0 miimiters. If clouding of the solution occurred as the water was added, the use of water was discontinued and acetone was added to a final volume of 11.0 milliliters.
  • the resulting stock solutions contained 6255 parts per million by weight of the particular compound.
  • the test concentrations in parts of the test compound per million parts by weight of final solution employed in the axillary stimulation tests in Table I were obtained by appropriate dilution of the stock suspensions with acetone and water (50/50 volume/volume).
  • a water-acetone solution containing no test compound was also sprayed on a flat.
  • all of the flats of plants were placed in a greenhouse at a temperature of 80°F ⁇ 5°F and humidity of 50 percent ⁇ 5 percent.
  • Visual Indications of axillary stimulation activity were observed and recorded 10 to 14 days after treatment.
  • Enhancement-Wheat Solutions of Compound 75 were prepared by dissolving either 0.48 grams, 0.96 grams or 1.92 grams of the compound into 800 milliliters acetone. Water plus 0.2 percent by volume of Surfelk spray adjuvant were added to each of the above solutions to a final volume of 1600 milliliters. Surfelk spray adjuvant is commercially available from Union Carbide Corporation, Danbury, Connecticut.
  • the above formulations were applied to each plot by use of a carbon dioxide backpack sprayer set at about 30 psig air pressure.
  • the planting, application and harvesting times for each crop are detailed in Table J.
  • the harvested wheat crops for yield determination included the inner 20 feet of the middle 4 rows in each plot (5 feet in from ends of the middle 4 rows). The values obtained for each plot in each repetition were averaged to obtain the results in Table J.
  • Solutions of Compound 75 were prepared by dissolving either 70 milligrams, 140 milligrams or 280 milligrams of the compound into 87 milliliters of acetone. Water plus 0.2 percent by volume of Triton X-100 surfactant were added to each of the above solutions to a final volume of 174 milliliters. Triton X-100 surfactant is commercially available from Rohm and Haas Company, Phildelphla, Pennsylvania.
  • the above formulations were applied to each plot by use of a carbon dioxide backpack sprayer set at about 30 psig air pressure.
  • the planting, applicaton and harvesting times are detailed in Table L.
  • the harvested soybean crops for yield determinaton included the inner 10 feet of the middle 2 rows in each plot (5 feet in from ends of the middle 2 rows).
  • the values obtained for each plot (kilograms of soybeans/plot) in each repetition were averaged to obtain the results in Table L.
  • Table L demonstrate that treatment of soybean plants with certain malonic acid derivative compounds at certain rates provides significantly increased yields in comparison with untreated control soybean plants. As demonstrated in Table L, in addition to an increase in actual yield (kilograms of soybeans/plot), the treated soybean plants exhibited an increased number of pods per plant in comparison with untreated control soybean plants.
  • Solutions of Compound 75 were prepared by dissolving either 0.75 grams or 1.5 grams of the compound into 125 milliliters acetone. Water was added to each of the above solutions to a final volume of 250 milliliters.
  • Table M demonstrate that treatment of soybean plants with certain malonic acid derivative compounds at certain rates provides significantly increased yields in comparison with untreated control soybean plants. As demonstrated in Table M, in addition to an increase in actual yield (kilograms of soybeans/plot), the treated soybean plants exhibited an increased number of pods per plant in comparison with untreated control soybean plants.
  • Example XLIII Effect of Representative Malonic Acid Derivative Compounds on Crop Yield Enhancement-Snapbeans Solutions of Compound 75 were prepared by dissolving either 1.56 milligrams, 3.13 milligrams or 6.25 milligrams of the compound in 5 milliliters of acetone and then adding water to a final volume of 10 milliliters.
  • Increased chlorophyll content can be an indication of increased photosynthetic activity resulting in increased biomass and/or increased crop yield.
  • Treatment of plants with certain malonic acid derivative compounds, e.g., Compound 75, as described hereinafter results in enhanced levels of chlorophyll.
  • Solutions of Compound 75 were prepared by dissolving either 1.56 milligrams, 6.25 milligrams or 25.0 milligrams of the compound in 5 milliliters of acetone and then adding water to a final volume of 10 milliliters.
  • Nitrate reductase is a substrate-lnducible enzyme which mediates the conversion of nitrate to nitrite.
  • the inducible nature of nitrate reductase and the dependence of the enzyme level on substrate level provides the plant with a mechanism for controlling growth.
  • Nitrate reductase catalyzes the rate-limiting step in the conversion of nitrate into proteins.
  • increased levels of nitrate reductase may indicate increased potential for grain and protein production. See, for example, Beevers, L. and R.H. Hageman, 1969, Nitrate Reduction in Higher Plants, Annual Review of Plant Physiology 20: 495-522.
  • Solutions of Compound 75 were prepared by dissolving either 1.56 milligrams, 6.25 milligrams or 25.0 milligrams of the compound 1n 5 milliliters of acetone and then adding water to a final volume of 10 milliliters.
  • nitrate released into the medium was determined by removing a 0.2 milliliter aliquot from each beaker and placing it in a test tube. Into the test tube was added 0.25 milliliters of 1 percent (weight/volume) sulfanilamide in 3N HCl and 0.25 milliliters of 0.02 percent (weight/volume) N-(1-naphthyl)- ethylenediamine dihydrochloride.
  • test tubes were allowed to stand for 20 minutes before mesuring the optical densities at 540 nanometers on a Beckman DB spectrophotometer.
  • Nitrate reductase activity was expressed as micromoles ( M) of nitrite formed per gram of fresh leaf weight per hour.
  • the values obtained for the control and Compound 75 were averaged to obtain the results in Table P below.
  • Test compounds identified in Table Q below were prepared by dissolving the compounds in acetone/water (50:50 volume/volume) containing 0.05 percent volume/volume of Triton X-100 surfactant commercially available from Rhom and Haas Company, Philadelphia, Pennsylvania. As detailed below, these solutions of test compounds were applied to wheat at a concentration of 0.06, 0.12, 0.25, 0.50 and 1.0 pounds of active ingredient per acre.
  • Wheat seeds (var. Olaf) were planted in a sandy loam soil in flats having the following dimensions: 5.5 inches In width x 9.0 inches in length x 3.0 inches in height. The wheat seeds were sown in 2 different arrangements as follows: 4 rows (5 inches in length) per flat, 10 seeds per row (Flat No. 1); and 2 rows (5 inches in length) per flat, 5 seeds per row (Flat No. 2). Eleven days after planting at the 2-3 leaf growth stage of wheat, each concentration of the test compounds identified in Table Q was applied to a separate flat as a foliar spray by use of an aspirated spray apparatus set at 10 psig air pressure (all flats sprayed at a concentration of 120 gallons per acre).
  • the number of vegetative shoots per seed was determined by actual count. The results reported in Table Q reflect the average of 3 repetitions. The percent increase tillering is based upon the untreated control.

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Abstract

Composés dérivés d'acide malonique, procédés pour leur préparation et leur utilisation afin d'augmenter les récoltes.Compounds derived from malonic acid, processes for their preparation and their use in order to increase harvests.

Description

Use of Malonic Acid Derivative Compounds for Increasing Crop Yield
Brief Summary of the Invention Technical Field
This invention relates to the use of malonic acid derivative compounds for increasing crop yield. This invention further relates to novel malonic acid derivative compounds and processes for the preparation thereof.
Background of the Invention
Certain malonic acid derivative compounds have been known for some time in the art. See, for example, U.S. Patent 2,504,896 and U.S. Patent 3,254,108. Some malonic acid derivative compounds have been described in the art as capable of providing certain plant growth regulating responses such as prevention of fruit drop, rooting of cuttings and formation of parthenogenetic fruit.
U.S. Patent 3,072,473 describes N-arylmalonamic acids and their esters and salts, N, N'-diarylmalonamides, N-alkyl-N-arylmalonamic acids and their esters and salts, and N, N'-dialkyl-N, N'-diarylmalonamides which may be useful as plant growth reguiants and herbicides. Japanese Patent 84 39,803 (1984) describes malonic acid anilide derivative compounds which may be useful as plant growth regulators. The plant growth regulating properties of substituted malonyl monoanilides are described by Shindo, N. and Kato, M., Meiji Daigaku Noogaku-bu Kenkyu Hokoku, Vol. 63, pp. 41-58 (1984).
However, certain malonic acid derivative compounds and the use of malonic acid derivative compounds for increasing crop yield as described herein have not been disclosed in the art.
Accordingly, it is an object of this invention to provide a method for the use of malonic acid derivative compounds to increase crop yield. It is another object of this invention to provide novel malonic acid derivative compounds and processes for the preparation thereof. These and other objects will readily become apparent to those skilled in the art in light of the teachings herein set forth.
Disclosure of the Invention
This invention relates to a method for increasing crop yield which comprises applying to the crop an effective amount, sufficient to increase crop yield, of a compound having the formula:
wherein R1, R2, Y1, Y2, Y3, Y4, Y5 and Y6 are as defined hereinafter, This invention also relates to novel malonic-sacId derivative compounds and to processes for the prepartion of said compounds.
Detailed Description As indicated above, this invention relates to a method of increasing crop yield by use of certain malonic add derivative compounds. More particularly, this invention involves a method for increasing crop yield which comprises applying to the crop an effective amount, sufficient to increase crop yield, of a compound having the formula: wherei n :
R1 and R2 are independently a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents (Z) are the same or different and are one or more hydrogen, halogen, alkylcarbonyl, alkylcarbonylalkyl, formyl, alkoxycarbonylalkyl, alkoxycarbonylalkylthio, polyhaloalkenylthio, thiocyano, propargylthlo, hydroxyimino, alkoxyimino, trialkylsilyloxy, aryldialkylsilyloxy, triarylsilyloxy, formamidino, alkylsulfamido, dlalkylsulfamido, alkoxysulfonyl, polyhaloalkoxysulfonyl, hydroxy, amino, azido, azo, aminocarbonyl, alkylaminocarbonyl, hydrazino, dialkylaminocarbonyl, amlnothiocarbonyl, alkylamlnothiocarbonyl, dialkylaminothiocarbonyl, nitro, cyano, hydroxycarbonyl and derivative salts, formamido, alkyl, alkoxy, polyhaloalkyl, polyhaloalkoxy, alkoxycarbonyl, substituted amino in which the permissible substituents are the same or different and are one or two propargyl, alkoxyalkyl, alkylthioalkyl, alkyl, alkenyl, haloalkenyl or polyhaloalkenyl; alkylthio, polyhaloalkylthio, alkylsulfinyl, polyhaloalkylsulfinyl, alkylsulfonyl, polyhaloalkylsulfonyl, alkylsulfonylamino, alkylcarbonylamino, polyhaloalkylsulfonylamino, polyhaloalkylcarbonylamino, trialkylsilyl, aryldialkylsilyl, triarylsilyl, sulfonic acid and derivative salts, phosphonic acid and derivative salts, alkoxycarbonylamino, alkylaminocarbonyloxy, didlkylaminocarbonyloxy, alkenyl, polyhaloalkenyl, alkenyloxy, alkynyl, alkynyloxy, polyhaloalkenyloxy, polyhaloalkynyl, polyhaloalkynyloxy, polyf luoroalkanol, cyanoalkylamino, semicarbazonomethyl, alkoxycarbonylhydrazonomethyl, alkoxyiminomethyl, unsubstituted or substituted aryloxyiminomethyl, hydrazonomethyl, unsubstituted or substituted arylhydrazonomethyl, a hydroxy group condensed with a mono-, di- or polysaccharide, haloalkyl, haloalkenyl, haloalkynyl, alkoxyalkyl, aryloxy, aralkoxy, arylthio, aralkylthio, alkylthioalkyl, arylthioalkyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, haloalkenyloxy, haloalkynyloxy, haloalkynylthio, haloalkenylsulfonyl, polyhaloalkenylsulfonyl, isocyano, aryloxysulfonyl, propargyloxy, aroyl, haloacyl, polyhaloacyl, aryloxycarbonyl, aminosulfonyl, alkylamlnosulfonyl, dialkylaminosulfonyl, arylamlnosulfonyl, carboxyalkoxy, carboxyalkylthio, alkoxycarbonylalkoxy, acyloxy, haloacyloxy, polyhaloacyloxy, aroyloxy, alkylsulfonyloxy, alkenylsulfonyloxy, arylsulfonyloxy, haloalkylsulfonyloxy, polyhaloalkylsulfonyloxy, aroylamino, haloacylamino, alkoxycarbonyloxy, arylsulfonylamino, aminocarbonyloxy, cyanato, isocyanato, isothiocyano, cycloalkylamino, trialkylammonium, arylamino, aryl(alkyl)amino, aralkylamino, alkoxyalkylphosphinyl, alkoxyalkylphosphinothioyl, alkylhydroxyphosphinyl, dialkoxyphosphino, hydroxyamino, alkoxyamino, aryloxyamino, aryloxyimino, oxo, thiono, diazo, alkylidene, alkylimino, hydrazono, semicarbazono, dialkylsulfoniurn, dialkylsulfuranylidene, dialkyloxosulfuranylidene, -X, = X, -X = R3, = X-R3,
R1 and R2 are independently hydrogen or derivative salts, or a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z as hereinbefore defined;
Y1 and Y2 are independently a substituted or unsubstituted heteroatom in which the permissible substituents are Z as hereinbefore defined; Y3 and Y4 are independently hydrogen, or a substituted or unsubstituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination, or halogen, alkylcarbonyl, formyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkoxycarbonylalkyIthio, polyhaloalkenylthio, thiocyano, propargylthio, trialkylsilyloxy, aryldialkylsilyloxy, triarylsilyloxy, formamidino, alkylsulfamido, dialkylsulfamido, alkoxysulfonyl, polyhaloalkoxysulfonyl, hydroxy, amino, hydrazino, azo, aminocarbonyl, alkylaminocarbonyl, azido, dialkylarninocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, nitro, cyano, hydroxycarbonyl and derivative salts, formamido, alkyl, alkoxy, polyhaloalkyl, polyhaloalkoxy, alkoxycarbonyl, substituted amino in which the permissible substituents are the same or different and are one or two propargyl, alkoxyalkyl, alkylthioalkyl, alkyl, alkenyl, haloalkenyl or polyhaloalkenyl; alkylthlo, polyhaloalkylthio, alkylsulfinyl, polyhaloalkylsulfinyl, alkylsulfonyl, polyhaloalkylsulfonyl, alkylsulfonylamino, alkylcarbonylamlno, polyhaloalkylsulfonylamino, polyhaloalkylcarbonylamino, trialkylsilyl, aryldialkylsilyl, triarylsilyl, sulfonic acid and derivative salts, phosphonic acid and derivative salts, alkoxycarbonylamino, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkenyl, polyhaloalkenyl, alkenyloxy, alkynyl, alkynyloxy, polyhaloalkenyloxy, polyhaloalkynyl, polyhaloalkynyloxy, polyfluoroalkanol, cyanoalkylamino, semicarbazonomethyl, alkoxycarbonylhydrazonomethyl, alkoxyiminomethyl, unsubstituted or substituted aryloxyiminomethyl, hydrazonomethyl, unsubstituted or substituted arylhydrazonomethyl, a hydroxy group condensed with a mono-, di- or polysaccharide, haloalkyl, haloalkenyl, haloalkynyl, alkoxyalkyl, aryloxy, aralkoxy, arylthio, aralkylthio, alkylthioalkyl, arylthioalkyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, haloalkenyloxy, haloalkynyloxy, haloalkynylthio, haloalkenylsulfonyl, polyhaloalkenylsulfonyl, isocyano, aryloxysulfonyl, propargyloxy, aroyl, haloacyl, polyhaloacyl, aryloxycarbonyl, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, arylaminosulfonyl, carboxyalkoxy, carboxyalkylthio, alkoxycarbonylalkoxy, acyloxy, haloacyloxy, polyhaloacyloxy, aroyloxy, alkylsulfonyloxy, alkenylsulfonyloxy, arylsulfonyloxy, haloalkylsulfonyloxy, polyhaloalkylsulfonyloxy, aroylamino, haloacylamino, alkoxycarbonyloxy, arylsulfonylamino, aminocarbonyloxy, cyanato, isocyanato, isothiocyano, cycloalkylamino, trialkylammonium, arylamino, aryl(alkyl)amino, aralkylamino, alkoxyalkylphosphinyl, alkoxyalkylphosphinothioyl, alkylhydroxyphosphinyl, dialkoxyphosphino, hydroxyamino, alkoxyamino, aryloxyamino, -X, -X = R3,
in which the permissible substituents are Z as hereinbefore defined; or Y3 and Y4 taken together are oxo, thiono, diazo, = X or = X - R3, or substituted or unsubstituted alkylidene, alkylimino, hydrazono, dialkylsulfonium, dialkyloxosulfuranylidene, semicarbazono, hydroxyimino, alkoxyimino or aryloxyimino in which the permissible substituents are Z as hereinbefore defined; Y3 and Y4 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a blcyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents are Z as hereinbefore defined;
- Y5 and Y6 are independently oxygen or sulfur; wherein:
X is a covalent single bond or double bond, a substituted or unsubstituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z as hereinbefore defined; R3 is a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents are Z as hereinbefore defined; R3 is a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z as hereinbefore defined; Y7 and Y10 are independently oxygen or sulfur; Y8 and Y9 are independently oxygen, sulfur, amino or a covalent single bond; and R4 and R5 are independently hydrogen or substituted or unsubstituted alkyl, alkenyl, alkynyl, polyhaloalkyl, phenyl or benzyl in which the permissible substituents are Z as hereinbefore defined.
The alkyl-containlng moieties in formula 1 may contain from about 1 to about 100 carbon atoms or greater, preferably from about 1 to about 30 carbon atoms, and more preferably from about 1 to about 20 carbon atoms. The polysaccharide moiety may contain up to about 50 carbon atoms. It is appreciated that all compounds encompassed within formula 1 are compounds having no unfilled bonding positions. In regard to the malonic acid derivative compounds used in this invention, it is preferred that R1 and R2 are independently other than hydrtogen, alkyl or aryl when both Y1 and Y2 are
-NH-.
As used herein, hydrogen or derivative salts refer to hydrogen or any appropriate derivative salt substituents which may be substituted therefore. Illustrative derivative salt substituents include, for example, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, alkali metals, alkaline earth metals and the like including mixtures thereof.
Monocyclic ring systems encompassed by R1, R2 and R3 in formula 1 may be represented by generalized formula 2 as follows:
wherein B1 represents a saturated or unsaturated carbon atom and A1 represents a ring-forming chain of atoms which together with B1 forms a cyclic system containing from 0 to 3 double bonds or from 0 to 2 triple bonds. A1 may contain entirely from 2 to 12 carbon atoms, may contain a combination of from 1 to 11 carbon atoms and from 1 to 4 heteroatoms which may be selected independently from N, O, S, P or other heteroatoms, or may contain 4 ring-forming heteroatoms alone.
Monocyclic ring systems encompassed by Y3 and Y4 linked together in formula 1 may include any monocyclic ring system of R1, R2 and R3 appropriately positioned in formula 1.
Ring-forming heteroatoms may in some cases bear oxygen atoms as in aromatic N-oxides and ring systems containing the sulfinyl, sulfonyl, selenoxlde and phosphine oxide moieties.
Selected carbon atoms contained in cycles formed by B1 and A1 containing at least 3 ring-forming atoms may bear carbonyl, thlocarbonyl, substituted or unsubstituted imino groups or substituted or unsubstituted methylidene groups.
The group designated as Z represents one or more substituents selected independently from among the group of substituents defined for Z herein.
Bicycllc ring systems encompassed by R1, R2 and R3 in formula 1 may be represented by generalized formulae 3 and 4 as follows:
wherein B2 and B3 may be independently a saturated or unsaturated carbon atom or a saturated nitrogen atom, A2 and A3 independently represent the ring-forming chains of atoms described below and
Z represents one or more substituents selected independently from among the group of substituents defined for Z herein. Combinations of A2 and A3 may contain in combination with B2 or B3 from 0 to 5 double bonds. A2 and A3, independent of B2 and B3. may contain entirely from 1 to 11 carbon atoms, may contain a combination of 1 to 3 heteroatoms which may be selected independently from among N, O, S, P or other heteroatoms together with from 1 to 10 carbon atoms or may contain from 1-3 ring-forming heteroatoms alone.
Ring-forming heteroatoms may in some cases bear oxygen atoms, as in aromatic N-oxides and ring systems containing the sulfinyl, sulfonyl. selenoxide and phosphine oxide groups. Selected carbon atoms contained in A2 and A3 may bear carbonyl, thiocarbonyl, substituted or unsubstituted imino groups or substituted or unsubstituted methylidene groups.
Bicyclic ring systems encompassed by Y3 and Y4 linked together in formula 1 may include any bicyclic ring system of R1, R2 and R3 appropriately positioned in formula 1.
In regard to structures encompassed within formulae 3 and 4, it is noted as follows:
(a) When B2 and B3 are both nitrogen, the groups A2 and A3 should each contain no fewer than three ring atoms;
(b) When B2 but not B3 is nitrogen, either of A2 or A3 should contain at least three ring atoms and the other at least two ring atoms;
(c) When either of groups A2 or A3 contains fewer than three ring atoms, the other should contain at least three ring atoms and the bridgehead atoms should be saturated;
(d) When the group A2 or A3 contains a carbon atom bearing a carbonyl, thiocarbonyl, imino or methylidene group, it should together with B2 and B3 form a cycle having at least four members; (e) When a annular double bond is exocyclic to either of the two rings represented in structures 3 and 4, it should be contained in a ring containing at least five members and be exocyclic to a ring containing at least five members; and
(f) When a group A2 or A3 is joined to the bridgehead atoms B2 and B3 by 2 double bonds, the group A2 or A3 is understood to contain one double bond and the bridgehead atoms are considered to be unsaturated.
It is recognized that bicyclic ring systems defined for R1, R2, R3 and Y3 and Y4 linked together may be spirocyclic ring systems and are not limited to the fused bicyclic structures of formulae 3 and 4. Spirocyclic ring systems may be saturated or unsaturated carbocyclic or heterocyclic and may be independently substituted by one or more substituents Z as defined herein.
Polycyclic ring systems, i.e., greater than 2 rings, encompassed by R1, R2 and R3 in formula 1 may be represented by generalized formulae 5 , 6, 7 and 8 as follows:
wherein B4, B5, B6 and B7 may be independently a saturated or unsaturated carbon atom or a saturated nitrogen atom, and A4, A5, A6 and A7 independently represent ring forming chains of atoms which may contain together with one or the other (but not both) of their two associated bridgehead atoms, from 0-2 double bonds. The groups
Z represent one or more substituents selected independently from among the group of substituents defined for Z herein.
The ring-forming elements of A4, A5, A6 and A7 independent of B4, B5, B6 and B7 may contain from 1-11 carbon atoms, may contain a combination of from 1-10 carbon atoms and from 1-3 heteroatoms which may be selected independently from among N, O, S, P or other heteroatoms, or may contain from 1-3 heteroatoms alone. Ring-forming heteroatoms may in some cases bear oxygen atoms as in aromatic N-oxides and ring systems containing the sulfinyl, sulfonyl, selenoxide and phosphine oxide groups. The group A6 may at times be defined as a bond. Selected carbon atoms contained in A4, A5, A6 and A7 may bear one or more carbonyl, thiocarbonyl or substituted or unsubstituted imino groups. On structure 8 the groups B8, B9 and
B10 represent independently a saturated or unsaturated carbon atom or a saturated nitrogen atom. The group B11 may represent a saturated or unsaturated carbon atom or a nitrogen or phosphorous atom. The groups A8, A9 and A10 represent ring-forming chains of atoms which may contain together with 1 of the groups B8, B9, B10 and B11 from 0-2 double bonds.
The ring-forming elements of groups A8, A9 and A10 independent of groups B8, B9, B10 and B11 may contain from 2-10 carbon atoms, may contain from 1-10 carbon atoms in combination with 1-3 heteroatoms which may be selected independently from among N, O, S, P or other heteroatoms, or may contain from 2-3 heteroatoms alone. Ring-forming heteroatoms may in some cases bear oxygen atoms as in aromatic N-oxides and in ring systems containing the sulfinyl, sulfonyl, selenoxide and phosphine oxide groups. Selected carf'n atoms contained in groups A8, A9 and A10 may bear one or more carbonyl, thiocarbonyl or substituted or unsubstituted imino groups.
It is recognized that polycyclic ring systems defined for R1, R2, R3 and Y3 and Y4 linked together may be spirocyclic ring systems and are not limited to the fused polycyclic structures of formulae 5, 6, 7 and 8. Spirocyclic ring systems may be saturated or unsaturated, carbocyclic or heterocyclic and may be independently substituted by one or more substituents Z as defined herein. Polycyclic ring systems encompassed by Y3 and Y4 linked together in formula 1 may include any polycyclic ring system of R1, R2 and R3 appropriately positioned in formula 1.
Bridged bicyclic structures encompassed by R1, R2 and R3 in formula 1 may be represented by generalized formulae 9, 10, and 11 as follows:
wherein B12 and B13 may be independently a saturated carbon atom optionally substituted by Z or a nitrogen atom, and the groups A11, A12 and A13 independently represent ring-forming chains of atoms which may contain, Independently of B12 and B13, from 0-2 double bonds. The groups Z represent one or more substituents selected Independently from among the groups of substituents defined for Z herein.
The ring-forming elements of A11, A12 and A13, independent of B12 and B13, may contain entirely from 1-11 carbon atoms, may contain a combination of from 1-10 carbon atoms and from 1-3 heteroatoms which may be selected Independently from among N, O, S, P or other heteroatoms, or may contain from 1-3 heteroatoms alone with the proviso that when one of the groups A11, A12 and A13 is a single heteroatom, the other two groups should contain two or more ring-forming atoms. A second proviso is that when one or both of the groups B12 and B13 is nitrogen, the groups A11, A12 and A13 should contain at least two saturated ring-forming atoms.
Ring-forming heteroatoms may in some cases bear oxygen atoms as in the sulfinyl, sulfonyl, selenoxide and phosphine oxide moieties. Selected carbon atoms contained in A11, A12 and A13 may bear one or more carbonyl, thiocarbonyl or substituted or unsubstituted imino groups.
Bridged bicyclic structures encompassed by Y3 and Y4 linked together in formula 1 may include any bicyclic bridged system of R1, R2 and R3 appropriately positioned in formula 1.
It is readily apparent that formula 1 encompasses a wide variety of malonic acid derivative compounds. Illustrative malonic acid derivative compounds within the scope of formula 1 which may be used for increasing crop yield are included in Tables 1 through 11 below.
It is appreciated that the particular compounds listed in Tables 1 through 11 hereinabove are illustrative of malonic add derivative compounds which can be used for increasing crop yield according to this invention. This invention is not to be construed as being limited only to the use of these compounds; but rather, this invention includes the use of those malonic add derivative compounds encompassed within formula 1 hereinabove.
The novel malonic acid derivative compounds of this invention can be depicted by the following formulae:
wherein:
Z1 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl,polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y11 is O, S or NR wherein R7 is hydrogen or alkyl;
Y12 is O, S, NH or N (alkyl); and R6 is ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dlalkylaminoalkyl, aryl, mercaptoalkyl, alkylthloalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulflnylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthloalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylaminoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl;
wherei n :
Z2 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio. arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y13 is O, S or NR9 wherein R9 is hydrogen or alkyl;
Y14 is O, S, NH or N (alkyl);
Y15 and Y16 are Independently hydrogen, alkyl, halogen, alkoxy, alkylthio, alkenyl, alkynyl, hydroxy, cyano, nitro, formyl, amino, alkylcarbonyl, dialkoxyalkyl, alkylcarbonylamino, formylamino, hydroxyalkyl, haloalkyl or polyhaloalkyl provided that when Y15 is alkyl then Z2 is not halogen or polyhaloalkyl at the para- position, and further provide that at least one of Y15 and Y16 is other than hydrogen;
Y15 and Y16 may be linked together to form a substituted or unsubstituted heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated; and
R8 is hydrogen or R6;
wherein:
Z3 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y17 is O, S or NR11 wherein R11 is hydrogen or alkyl;
Y18 is O or S;
Y19 and Y20 are independently hydrogen, alkyl, alkoxy, alkylthio, halogen, haloalkyl or polyhaloalkyl; or
Y19 and Y20 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated; and
R10 is hydrogen or R6; and
wherein:
R1 and R2 are independently a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated; or
R1 and R2 are independently hydrogen or derivative salts, or a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination;
- Y1 and Y2 are independently a substituted or unsubstituted heteroatom;
Y3 and Y4 are linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated; and
Y5 and Y6 are independently oxygen or sulfur; in which the permissible substituents for formulae
(i) through (iv) above are Z, as hereinbefore defined.
Novel malonic acid derivative compounds within the scope of formula (iv) above can be depicted by the following formulae:
wherein :
Z4 is Independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamlno, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n Is a value of from 0 to 5;
Y21 is O, S or N R13 wherein R13 is hydrogen or alkyl;
Y22 is O, S, NH or N (alkyl);
Y23, Y24, Y25 and Y26 are independently hydrogen, alkyl or halogen; and
R12 is hydrogen or R6; or
wherein:
Z5 is Independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y27 is O, S or NR15 wherein R15 is hydrogen or alkyl;
Y28 is O S, NH or N (alkyl);
Y29, Y30, Y31, Y32, Y33 and Y34 are independently hydrogen, alkyl or halogen; and R14 is hydrogen or R6;
wherein:
Z6 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y35 is O, S or NR17 wherein R17 is hydrogen or alkyl;
Y36 is O or S; and R16 is hydrogen or R6 , in which the permissible substituents for formulae (v) through (vii) are as described for Z above for formulae (i) through (iv).
The malonic acid derivative compounds encompassed within formula 1 and the intermediate compounds used in the preparation thereof can be prepared by conventional methods known in the art and many may be available from various suppliers. The novel malonic acid derivative compounds of formulae (i) through (vii) above which may used in the method of this invention may be prepared by reacting appropriate starting ingredients in accordance with conventional procedures described in the art as illustrated below.
The novel malonic acid derivative compounds of formula (i) can be prepared by the following general reaction scheme:
Scheme I
wherein Z1, n, Y11, Y12 and R6 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (i) including process conditions are described for example by Richter, G.H., Textbook of Organic Chemistry, Third Edition, John Wiley and Sons, New York, p. 486. In the Schotten-Baumann procedure described therein, cold aqueous sodium hydroxide is illustrated as the acid acceptor.
The novel malonic acid derivative compounds of formula (ii) can be prepared by the following general reaction scheme:
Scheme II
wherein Z2, n, Y13, Y14, Y15, Y16 and R8 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (ii) including process conditions are described for example by Richter,
G.H., supra, according to the known Schotten-Baumann procedure.
The novel malonic add derivative compounds of formula (iii) can be prepared by the following general reaction scheme:
Scheme III
wherein Z3, n, Y17 , Y18, Y19 , Y20 and
R10 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (iii) including process conditions are described for example by Richter,
G.H., supra, according to the known Schotten-Baumann procedure.
The novel malonic acid derivative compounds of formula (iv) can be prepared by the following general reaction scheme:
Scheme IV
wherein R1, R2, Y1, Y2, Y3, Y4, Y5 and
Y6 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (iv) including process conditions are described for example by Richter, G.H., supra, according to the known Schotten-Baumann procedure.
The novel malonic acid derivative compounds of formula (v) can be prepared by the following general reaction scheme:
Scheme V
wherein Z4, n, Y21, Y22, Y23, Y24, Y25,
Y26 and R12 are as defined hereinabove.
Reactions of this general type for preparing malonic acid derivative compounds of formula (v) including process conditions are described for example by
Richter, G.H., supra, according to the known
Schotten-Baumann procedure. The novel malonic acid derivative compounds of formula (vi) can be prepared by the following general reaction scheme:
Scheme VI
wherein Z5, n, Y27, Y28, Y29, Y30, Y31 , Y32, Y33, Y34 and R14 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (vi) Including process conditions are described for example by Richter, G.H., supra, according to the known Schotten-Baumann procedure.
The novel malonic acid derivative compounds of formula (vii) can be prepared by the following general-reaction scheme:
Scheme VI I
wherein Z6, n, Y35, Y36 and Y16 are as defined hereinabove. Reactions of this general type for preparing malonic acid derivative compounds of formula (vii) including process conditions are described for example by Richter, G.H., supra, according to the known Schotten-Baumann procedure.
In addition to the above, other illustrative procedures which can be employed in preparing malonic add derivative compounds encompassed within formula 1 and intermediate compounds used in the preparation thereof are described, for example, in the following: Breslow, D.S. et al., Jour. Amer. Chem. Soc. 66, 1286-1288 (1944); Svendsen, A. and Boll, P.M., Jour. Org. Chem. 40, 1927-1932 (1975); Sen, A.K. and Sengupta, P., J. Ind. Chem. Soc. 46, (9), 857-859 (1969); Thlers, R. and Van Dormael, A., Bull. Soc. Chim. Belg. 61, 245-252 (1952); Brown, R.F.C., Austral. Jour. of Chem. 8, 121-124 (1955); U.S. Patent 3,951,996; United Kingdom Patent 1,374,900; Chiriac, C.I., Revue Romaine de Chimie 25, (3), 403-405 (1980); Weiner, N., Org. Syn. Coll., Vol. II, 279-282 (1950), Sixth Printing, John Wiley & Sons, New York; Block, Jr., Paul, Org. Syn. Coll. Vol. V, 381-383 (1973), John Wiley and Sons, New York; Reliquet, F. et al., Phos. and Sulfur 24, 279-289 (1985); Palmer, C.S. and McWherter, P.W., Org. Syn. Coll. Vol. I, 245-246 (1951), Second Edition, John Wiley and Sons, New York; Staudinger, H. and Becker, H., Berichte 50, 1016-1024 (1917); Purrington, S.T. and Jones, W.A., J. Org. Chem. 48, 761-762 (1983); Kitazume, T. et al., Chem. Letters (1984) 1811-1814; Wolff, I.A. et al., Synthesis (1984), 732-734; Zamblto, A.J. and Howe, E.E.., Org. Syn. Coll. Vol. V, 373-375 (1973), John Wiley and Sons, New York; and Hartung, W.H. et al., Org. Syn. Coll. Vol. V, 376-378, John Wiley and Sons, New York.
Still other illustrative procedures which can be employed in preparing malonic acid derivative compounds encompassed within formula 1 and intermediate compounds used in the preparation thereof are described, for example, in the following: Rathke, M.W. and Cowan, P.J., J. Org. Chem. 50, 2622-2624 (1985); Fones, W.S., Org. Syn. Coll. Vol. IV, 293 (1963), John Wiley and Sons, New York; Gompper, R. and Topfl, W., Chem. Ber. 95, 2861-2870 (1962); Gompper, R. and Kunz, R., Chem. Ber. 99, 2900-2904 (1966); Ono, N. et al., J. Org. Chem. 50, 2807-2809 (1985); U.S. Patent 4,154,952; Blankenship, C. and Paquette, L.A., Synth. Comm. 14, (11), 983-987 (1984); Baldwin, J.E. et al., Tet. Lett. 26, (4), 481-484 (1985); Kawabata, N. et al., Bull. Chem. Soc. Jpn. 55, (8), 2687-2688 (1982); Bodanszky, M. and du Vignaud, V., J. Am. Chem. Soc. 81, 5688-5691 (1959); Neelakantan, S. et al., Tetrahedron 21, 3531-3536 (1965); U.S. Patent 4,020,099; Japan Patent Application 148,726 (1979); Fuson, R.C., Advanced Organic Chemistry, p. 202 (1950), John Wiley and Sons, New York; Duty, R.C., Anal. Chem. 49, (6), 743-746 (1977); Korner, G., Contradi, Atti acad. Llncei 22, I, 823-836 (CA. 8, 73 (1914)); Schimelpfenig, C.W., J. Chem. Soc. Perk. Trans. I, 1977 (10), 1129-1131; Kim, Y.S. et al., Taehan Hwahak Hoechi 18, (4), 278-288 (1974); German Patent 2,449,285; U.S. Patent 3,962,336; and U.S. Patent 3,992,189.
Copending U.S. Patent Application Serial No. (D-15328), filed on an even date herewith, describes the use of malonic acid derivative compounds of formula 1 for retarding plant growth. Copending U.S. Patent Application Serial No. (D-15298), filed on an even date herewith, describes synergistic plant growth regulator compositions containing (i) an ethylene response or an ethylene-type response Inducing agent and (ii) a malonic acid derivative compound of formula 1. Both of these applications are incorporated herein by reference.
The malonic acid derivative compounds of formula 1 have been found to significantly increase crop yield in comparison with untreated crops at similar conditions. In addition, the malonic acid derivative compounds used in this invention are substantially non-phytotoxic to growing plants.
As used herein, an effective amount of a malonic acid derivative compound for increasing crop yield refers to a yield enhancing effective amount of the compound sufficient to increase crop yield. The effective amount of compound can vary over a wide range depending on the particular compound employed, the particular crop to be treated, environmental and climatic conditions, and the like. The amount of compound used preferably does not cause substantial phytotoxicity, e.g., foliar burn, chlorosis or necrosis, to the crop. In general, the compound can preferably be applied to plants and crops at a concentration of from about 0.01 to 15 pounds of compound per acre as more fully described below.
The malonic acid derivative compounds contemplated by formula 1 can be employed according to a variety of conventional methods known to those skilled in the art. Compositions containing the compounds as the active ingredient will usually comprise a carrier and/or diluent, either liquid or solid. Suitable liquid diluents or carriers include water, petroleum distillates, or other liquid carriers with or without surface active agents. Liquid concentrates can be prepared by dissolving one of these compounds with a nonphytotoxic solvent such as acetone, xylene, nitrobenzene, cyclohexanone or dimethyl formamide and dispersing the active ingredients in water with the aid of suitable surface active emulsifying and dispersing agents.
The choice of dispersing and emulsifying agents and the amount employed are dictated by the nature of the composition and the ability of the agent to facilitate the dispersion of the active ingredient. Generally, it is desirable to use as little of the agent as is possible, consistent with the desired dispersion of the active ingredient in the spray so that rain does not re-emulsify the active ingredient after it is applied to the plant and wash it off the plant. Nonionic, anionic, or cationic dispersing and emulsifying agents may be employed, for example, the condensation products of alkylene oxides with phenol and organic acids, alkyl aryl sulfonates, complex ether alcohols, quaternary ammonium compounds, and the like.
In the preparation of wettable powder or dust compositions, the active ingredient is dispersed in and on an appropriately divided solid carrier such as clay, talc, bentonite, diatomaceous earth, fuller's earth, and the like. In the formulation of the wettable powders, the aforementioned dispersing agents as well as lignosulfonates can be included.
The required amount of the active ingredient contemplated herein can be applied per acre treated in from 1 to 200 gallons or more of liquid carrier and/or diluent or In from about 5 to 500 pounds of inert solid carrier and/or diluent. The concentration in the liquid concentrate will usually vary from about 5 to 95 percent by weight and in the solid formulations from about 0.5 to about 90 percent by weight. Satisfactory sprays or dusts for general use contain from about 0.001 to about 100 pounds of active ingredient per acre, preferably from about 0.01 to about 15 pounds of active ingredient per acre, and more preferably from about 0.1 to about 5 pounds of active ingredient per acre.
Formulations useful in the conduct of this invention can also contain other optional ingredients such as stabilizers or other biologically active compounds, insofar as they do not impair or reduce the activity of the active ingredient and do not harm the plant being treated. Other biologically active compounds include, for example, one or more insecticidal, herbicidal, fungicidal, nematicidal, miticidal, plant growth regulators or other known compounds. Such combinations may be used for the known or other purpose of each ingredient and may provide a synergistic effect.
The malonic acid derivative compounds of formula 1 are preferably applied to plants and crops under average or normal growing conditions. The malonic acid derivative compounds used in this invention can be applied during the plant vegetative growth phase or the plant reproductive growth phase to obtain increased crop yield. It may be desirable for some crops to apply the malonic acid derivative compounds at the reproductive growth phase including, for example, the early flower stage, fruit set stage or full flower bloom stage. In other crops, it may be desirable to apply the malonic acid derivative compounds at the vegetative growth phase. The application timing will in general depend upon the particular crop to be treated.
Such compounds are useful in agriculture, horticulture and related fields for increasing crop yield. An increase in crop yield can be attributable, for example, to various plant growth effects such as increased branching (increased reproductive sites), early pod (fruit) set, increased blossom set and inhibition of blossom (flower and fruit) abscission during early stages of plant reproductive development. As used herein, increased crop yield refers to an increase in the raw agricultural commodity in terms of harvestable yield, e.g., bushels of seeds, bales of cotton and the like. It may be possible to have an increased harvestable yield for a treated crop in comparison with an untreated crop, yet the total crop biomass may be less for the treated crop. However, harvestable yield as used herein may be inclusive of total crop biomass, e.g., bushels of corn per acre and the like. Treatment of certain crops such as alfalfa with the malonic acid derivative compounds of formula 1 may also increase the crop nutritional value, e.g., total digestable nutrients (TDN).
As used herein, plants and crops refer in general to any agronomic or horticultural crops, ornamentals and turfgrasses. Illustrative of plants and crops which can be treated by the malonic acid derivative compounds of formula 1 according to the method of this invention include, for example, corn, cotton, sweet potatoes, white potatoes, alfalfa, wheat, rye, rice, barley, oats, sorghum, dry beans, soybeans, sugar beets, sunflowers, tobacco, tomatoes, canola, deciduous fruit, citrus fruit, tea, coffee, olives, pineapple, cocoa, banana, sugar cane, oil palm, herbaceous bedding plants, woody shrubs, turfgrasses, ornamental plants, evergreens, trees, flowers, and the like.
The malonic acid derivative compounds contemplated herein are effective for increasing crop yields. Such compounds have a high margin of safety in that when used in sufficient amount to provide a yield enhancing effect, they do not burn or injure the crop or plant, and they resist weathering which indudes wash-off caused by rain, decomposition by ultraviolet light, oxidation, or hydrolysis in the presence of moisture or, at least, such decomposition, oxidation, and hydrolysis as would materially decrease the desirable yield enhancing characteristic of the active ingredient or impart undesirable characteristics, for instance, phytotoxicity, to the active ingredients. Mixtures of the active compounds can be employed if desired as well as combinations of the active compounds with other biologically active compounds or ingredients as indicated above.
This invention is illustrated by the following examples. Example I Preparation of ethyl 3-[(4-fluorophenyl)amino]- 3-oxopropanoate Into a nitrogen-purged, air-stirred reaction flask was charged 4.44 grams (0.04 mole) of 4-fluoroaniline, 4.05 grams (0.04 mole) of triethylamine and 200 mmiliters of tetrahydrofuran solvent. A 6.02 gram (0.04 mole) portion of ethyl malonyl chloride was added rapidly with stirring at room temperature followed by a few milliliters of tetrahydrofuran. The temperature rose to 42°C and triethylamine hydrochloride separated therefrom. The mixture was then stirred at ambient temperature and the triethylamine hydrochloride filtered off, washed with solvent and dried to give 5.2 grams (0.04 mole). The filtrate was freed of solvent and the resulting purple solid dissolved in methylene chlorlde, washed with 2N HCl (3 × 75 milliliters), and water (2 × 75 mmmters), and then dried and stripped to give a crude solid product. Recrystallization from ethyl acetate- cyclohexane followed by flash column chromatography gave 3.47 grams (0.015 mole) of ethyl 3-[(4-fluoro- phenyl)amino] -3-oxopropanoate (Compound 1) having a melting point of 68°C-71°C.
Example II In a similar manner Compounds 2-76 were prepared and identified in Table A.
Example III Preparation of ethyl 1-(2-methyl-4,5-dichlorophenylaminocarbonyl)cyclopropanecarboxylate Into a nitrogen-purged round bottom flask was charged 5.53 grams (0.03 mole) of 2-methyl-4,5-dichloroaniline, 3.18 grams (0.03 mole) of triethylamine and 190 milliliters of tetrahydrofuran solvent. With vigorous stirring, a 5.55 gram (0.03 mole) portion of ethyl 1-chlorocarbonylcyclopropanecarboxylate prepared in Example XVIII was added in one portion, after which the mixture was stirred at ambient temperature for a six-hour period. A precipitate of triethylamine hydrochloride was then filtered off and the filtrate vacuum stripped to give a light yellow solid. The solid was taken up in ether and the solution water-washed, dried over magnesium sulfate, and solvent evaporated to give a yellow powder. Recrystallization from ethyl acetate-hexane gave 4.51 grams (0.01 mole) of ethyl 1-(2-methyl-4,5-dichlorophenylaminocarbonyl)cyclopropanecarboxylate (Compound 77) having a melting point of 105°C-107°C.
Example IV In a manner similar to that employed in Example III, Compounds 78-96 were prepared and identified in Table B.
Example V Preparation of 3-[(4-bromo-2-methylphenyl)- amino]-3-oxopropanoic acid A 6.0 gram (0.02 mole) portion of ethyl 3-[(4-bromo-2-methylphenyl)amino]-3-oxopropanoate prepared in Example I (Compound No. 75) was dissolved in approximately 80 milliliters of ethanol and 1.2 grams (0.03 mole) of sodium hydroxide pellets were added to the resulting mixture. The mixture was stirred for four hours and then allowed to stand overnight. The mixture was then evaporated to drynoss and water added to give a yellow cloudy solution. This solution was extracted with methylene chloride and then acidified with 10% hydrochloric acid causing a white precipitate to form. The white precipitate was worked up to give 1.8 grams (0.01 mole) of 3-[(4-bromo-2-methylphenyl)-amino]-3-oxopropanoic acid (Compound 97) as a white solid having a melting point of 163°C-165°C.
Example VI In a manner similar to that employed in Example V, Compounds 98-109 were prepared.
Example VII Preparation of 1-(2-methyl-4.5-dichlorophenylaminocarbonyl)cvclopropanecarboxylic acid A solution containing 0.34 gram (0.006 mole) of potassium hydroxide and 0.109 gram (0.006 mole) of water in 80 millniters of ethanol was prepared in a 250 milliliter round bottom flask. With cooling to a temperature of 0°C in an ice/NaCl bath and stirring, a solution of ethyl 1-(2-methyl-4,5-dichlorophenylaminocarbonyl)cyclopropanecarboxylate prepared in Example III in a small volume of ethanol was added and the mixture allowed to stir with warming to room temperature over a 72 hour period. The mixture was vacuum evaporated to give a white solid residue which was dissolved in water and extracted twice with ether. The ether extracts were discarded. The water solution was acidified to a pH of 2 with 25% HCl solution causing separation of a solid which was taken up into ether, and the acidified aqueous phase was extracted four times. The combined ether extracts were dried over magnesium sulfate and vacuum evaporated to give a white solid. This white solid was water-washed and dried in a vacuum oven to give 1.85 grams (0.006 mole) of 1-(2-methyl-4,5-dichlorophenylaminocarbonyi)cyclopropanecarboxylic acid (Compound 110) having a melting point of 248°C-251°C. Example VIII In a manner similar to Example VII, other Compounds 111-128 were prepared and identified in Table D below.
Example IX Preparation of ethyl 1-(4-bromo-2-methylphenγlaminocarbonyl)cyclobutanecarboxylate Into a nitrogen-purged reaction flask was charged 2.74 grams (0.01 mole) of 4-bromo-2-methylaniline and 1.49 grams (0.01 mole) of triethylamine dissolved in 200 milliliters of tetrahydrofuran. With vigorous stirring, 2.80 grams (0.01 mole) of ethyl 1-chlorocarbonylcyclobutanecarboxylate prepared in Example XIX were added and the resulting mixture stirred at ambient temperature for 6 hours. A precipitate of triethylamine hydrochloride was removed by filtration. The filtrate was vacuum stripped and the residue taken up in methylene chloride. This solution was washed successively with 2N HCl (2 x 75 millinters) and water, and then dried over magnesium sulfate. Rotary evaporation gave a crude product which was flash chromatographed on silica using 7:3 hexane-ethyl acetate to give 3.68 grams (0.01 mole) of ethyl 1-(4-bromo-2-methylphenylaminocarbonyl)cyclobutanecarboxylate (Compound 129) as a white solid. A small sample which was recrystallized from hexane had a melting point of 61°C-64°C.
Example X
In a manner similar to Example IX, Compounds 130-134 were prepared and identified in Table E below.
Example XI Preparation of 1-(3,5-dichlorophenylaminocarbonyl)cyclobutanecarboxylic acid A 2.0 gram (0.006 mole) portion of ethyl 1-(3,5-dichlorophenylaminocarbonyl)cyclobutanecarboxylate prepared in Example X (Compound 130) was hydrolyzed in the presence of water (0.114 gram, 0.006 mole) and ethanolic potassium hydroxide (0.355 gram, 0.006 mole). The potassium salt of the acid was then acidified with 25% HCl solution and worked up in a manner similar to that described in Example VII to give 0.92 gram (0.003 mole) of 1-(3,5-dichlorophenylaminocarbonyl)cyclobutanecarboxylic acid (Compound 135) as a beige-colored solid having a melting point of 159°C-160°C.
Example XII In a manner similar to that employed in Example XI, Compounds 136-139 were prepared and identified in Table F below.
Example XIII Preparation of ethyl 1-(4-bromo-2-methylphenylaminocarbonyl)cyclopentanecarboxylate Ethyl 1-chlorocarbonylcyclopentanecarboxylate (3.10 grams, 0.02 mole) prepared in Example XX, 4-bromo-2-methylaniline (2.82 grams, 0.02 mole) and triethylamine (1.53 grams, 0.02 mole) were reacted in tetrahydrofuran (200 milliliters) under conditions similar to that described in Example I to give 2.40 grams (0.007 mole) of ethyl 1-(4-bromo-2-methylphenylaminocarbonyl)cyclopentanecarboxylate (Compound 140) which, after recrystallization from hexane, had a melting point of 64°C-67ºC.
Example XIV Preparation of ethyl 2-(4-bromo-2- methylphenylaminocarbonyl)butanoate Ethyl 2-(chlorocarbonyl)butanoate (5.8 grams, 0.03 mole), 4-bromo-2-methylaniline (5.0 grams, 0.03 mole) and triethylamine (3.27 grams, 0.03 mole) were reacted under conditions similar to that described for Example I to give 7.4 grams (0.02 mole) of ethyl 2-(4-bromo-2-methylphenylaminocarbonyl)butanoate (Compound 141) as a white solid having a melting point of 98°C-100°C.
Example XV In a manner similar to Example XIV, Compounds 142-152 were prepared and identified in Table G below.
Example XVI Preparation of 3-[(4-bromo-2-methylphenyl)- amino]-2-bromo-2-methyl-3-oxopropanoic acid A 1.25 gram (0.003 mole) portion of ethyl 3-[(4-bromo-2-methylphenyl)amino]-2-bromo-2-methyl-3-oxopropanoate prepared in Example XV (Compound 144) was hydrolyzed with water (0.06 gram, 0.003 mole) and ethanolic potassium hydroxide (0.21 gram, 0.003 mole). The potassium salt of the acid was then acidified with concentrated HCl and worked up in a manner similar to that described in Example VII to give 1.04 grams (0.003 mole) of 3-[(4-bromo-2-methylphenyl)amino]-2-bromo-2-methyl-3-oxopropanoic acid (Compound 153) as a white solid having a melting point of 133°C-136°C.
Example XVII Preparation of N-butyl 3-[(4-bromo-2- methylphenyl)amino]-3-oxopropanamide A mixture of 4.90 grams (0.02 mole) of ethyl 3-[(4-bromo-2-methylphenyl)amino]-3-oxopropanoate prepared in Example I (Compound No. 75), 358 grams (4.9 moles) of n-butylamine , 150 milimters of ethanol and 5 drops of water was stirred at room temperature for about 16 hours. After this period, rotary evaporation gave a crude product as a white solid. The white solid was recrystallized from ethyl acetate-hexane to give 3.08 grams (0.009 mole) of N-butyl 3-[(4-bromo-2-methylphenyl)amino]-3- oxopropanamide (Compound 154) having a melting point of 123°C-125°C. Example XVIII
Preparation of ethyl 1-chlorocarbonylcyclopropanecarboxylate
Into a stirred solution containing 15.1 grams (0.27 mole) of potassium hydroxide in 240 milliliters of ethanol and 4.83 grams (0.27 mole) of water was added dropwise, with cooling at a temperature of 0°C, 50.0 grams (0.27 mole) of dlethyl 1,1-cyclopropanedicarboxylate. The mixture was stirred for about 16 hours at room temperature. Solvent was removed under reduced pressure to give a white residue which was dissolved in water and extracted with ether. The water solution was acidified to a pH of 2 with 25% aqueous hydrochloric acid and the organic acid was extracted from the aqueous suspension with ethyl ether (4 x 400 milliliters). The ether extract was dried over magnesium sulfate and vacuum stripped to give the monocarboxylic acid as a clear liquid. The clear liquid was dissolved in 300 mmiliters of methylene chloride after which 74 grams (0.62 mole) of thionyl chloride were added, and the resulting mixture was then heated under reflux for approximately 16 hours. Volatiles were removed under reduced pressure to give 45.7 grams (0.25 mole) of ethyl 1-chlorocarbonylcyclopropanecarboxylate (Compound 155). NMR analysis of the product indicated the following:
NMR (CDCl3): 1.22-1.50 (t, 3H), 1.75
(s, 4H), 4.1-4.52 (q, 2H) ppm. Example XIX Preparation of ethyl 1-chlorocarbonylcyclobutanecarboxylate Diethyl 1,1-cyclobutanedicarboxylate (20.0 grams, 0.10 mole) was saponified with 6.59 grams (0.10 mole) of potassium hydroxide in a mixture of 200 milliliters of ethanol and 1.80 grams (0.10 mole) of water and worked up to give the monocarboxylic acid which was reacted with thionyl chloride (8.86 grams, 0.07 mole) in methylene chloride solution as described in Example XVIII. Removal of the solvent gave 7.48 grams (0.04 mole) of ethyl 1-chlorocarbonylcydobutanecarboxylate. NMR analysis of the product indicated the following: NMR (CDCl3): 1.10-1.44 (t, 3H), 1.7-2.85 (m, 6H), 4.05-4.5 (q, 2H). ppm.
Example XX Preparation of ethyl 1-chlorocarbonylcyclopentanecarboxylate In a manner similar to the procedure described in Example XVIII, with the exception that refluxing with thionyl chloride in methylene chloride was conducted for only a 2 hour period, a 10 gram (0.05 mole) portion of diethyl 1,1-cyclopentanedicarboxylate was converted into 5.67 grams (0.03 mole) of ethyl 1-chlorocarbonylcydopentanecarboxylate (Compound 157). NMR analysis of the product indicated the following:
NMR (CDCl3): 1.10-1.49 (t, 3H), 1.56-2.48 (m, 8H), 4.0-4.5 (q, 2H) ppm. Example XXI
Preparation of ethyl 2-bromo-2-chlorocarbonylpropanoate
In a manner similar to the procedure described in Example XVIII, except that refluxing with thionyl chloride in methylene chloride solution was conducted only for a 6 hour period followed by standing at room temperature for about 16 hours, a 25.0 gram (0.10 mole) portion of diethyl 2-bromo-2-methylmalonate was converted into 12.94 grams (0.05 mole) of ethyl 2-bromo-2-chlorocarbonylpropanoate (Compound 158). This compound was employed in the preparation of Compound Nos. 144-148 and 152 in Example XV. NMR analysis of the product indicated the following:
NMR (CDCl3): 1.10-1.47 (t, 3H),
2.05-2.17 (s pair, 3H), 4.05-4.55 (q pair,
2H) ppm.
Example XXII Preparation of ethyl 3-[(4-chlorophenyl)amino1-3- oxopropanoate 4-Chloroanlline (25.4 grams, 0.20 mole) and diethyl malonate (48 grams, 0.30 mole) were reacted in a manner similar to the procedure described by A.K. Sen and P. Sengupta, Jour. Indian Chem. Soc. 46 (9), 857-859 (1969). The reaction afforded a greenish colored solid which was recrystallized from toluene-hexane (1:1) and then from isopropyl ether to give 9.0 grams (0.04 mole) of ethyl 3-[(4-chlorophenyl)amino]-3-oxopropanoate (Compound 159) as white crystals having a melting point of 82°C-83°C. Example XXIII Preparation of ethyl 3-[(4-methylthiazol-2-yl) aminol-3-oxopropanoate In a manner similar to the procedure described in Example I, 2-amino-4-methylthiazole was reacted with ethyl malonyl chloride employing triethylamine as the acid acceptor in tetrahydrofuran solution. The ethyl 3-[(4-methylthiazol-2-y1)amino]-3-oxopropanoate product (Compound 160) (7.5 grams, 0.03 mole) was obtained as an off-white solid having a melting point of 138°C-141°C.
Example XXIV In a manner similar to Example XXIII, Compounds 161-173 were prepared and identified in Table H below.
Example XXV Preparation of ethyl 2-chlorocarbonyl-3- methyl-2-butenoate Diethyl isopropylidenemalonate (30 grams, 0.15 mole) was saponified with 10.0 grams (0.15 mole) of potassium hydroxide in 200 milliliters of ethanol solution and worked up to give the monocarboxylic acid which was then reacted with thionyl chloride (10 mllimters, 0.1 mole) in methylene chloride solution in a manner similar to the procedure described in Example XVIII. Removal of solvent gave 9.6 grams (0.05 mole) of ethyl 2-chlorocarbonyl-3-methyl-2-butenoate. NMR analysis of the residue product in CDCI3 solution indicated complete conversion of the carboxylic acid to the acid chloride as evidenced by absence of a downfield carboxylic acid proton. This compound is referred to hereinafter as Compound 174.
Example XXVI Preparation of ethyl 2-[(4-bromo-2-methylphenyl)- aminocarbonyl]-3-methyl-2-butenoate In a manner similar to the procedure described in Example I, ethyl 2-chlorocarbonyl-3-methyl-2-butenoate (9.6 grams, 0.05 mole) prepared in Example XXV, 4-bromo-2-methylaniline (5.3 grams, 0.03 mole) and triethylamine (4.0 mnimters, 0.03 mole) were reacted to give 2.9 grams (0.009 mole) of ethyl 2-[(4-bromo- 2-methylphenyl)aminocarbonyl]-3-methyl-2-butenoate (Compound 175) as a white solid having a melting point of 116ºC-119ºC. Example XXVII Preparation of 3,4-dichloro-2,5-dimethylannine A solution of 5.0 grams (0.03 mole) of 3,4-dichloro-2,5-dimethyl-1-nitrobenzene in 70 milliliters of ethanol was hydrogenated at room temperature at 50 psi in the presence of 0.25 gram of 10% palladium on activated carbon as a catalyst. Working up the reaction mixture gave 1.21 grams (0.006 mole) of 3,4-dichloro-2,5-dimethylaniline (Compound 176) as a yellow solid having a melting point of 72°C-76°C.
Example XXVIII Preparation of 4.5-dichloro-2-methoxyaniline
Part A: Preparation of 2,2-dimethyl-N-(4-chloro- 2-methoχyphenyl)propanamide Into a stirred solution containing 10.0 grams (0.06 mole) of 4-chloro-2-methoxyaniline and 6.42 grams (0.06 mole) of triethylamine in 200 milliliters of tetrahydrofuran was added 7.65 grams (0.06 mole) of trimethylacetyl chloride in a small amount of tetrahydrofuran solvent. The resulting mixture was stirred for two hours at room temperature. Triethylamine hydrochloride precipitated and was filtered off and the filtrate vacuum stripped to give a dark liquid which was taken up in methylene chloride. This solution was washed with 2N HCl (2 x 100 milliliters), then with water (1 x 100 miimiters), dried over magnesium sulfate and solvent evaporated to give a crude product which was crystallized from hexane to give 6.82 grams (0.03 mole) of 2,2-dimethyl-N-(4-chloro-2-methoxyphenyl)propanamide as a first and second crop. NMR analysis of the product indicated the following:
NMR (CDCI3): 1.32 (s, 9H), 3.91 (s, 3H), 6.83-7.08 (m, 2H), 8.28-8.52 (d, 2H) ppm.
Part B: Preparation of 2,2-dimethyl-N- (4,5-dichloro-2-methoxyphenyl)propanamide Into a stirred solution containing 6.82 grams (0.03 mole) of 2,2-dimethyl-N-(4-chloro-2-methoxyphenyl)propanamide prepared in Part A in 150 miliniters of chloroform was added 3.81 grams (0.03 mole) of sulfuryl chloride over a 40 minute period. The resulting reaction mixture was heated under reflux for a 3 day period, each day cooling the mixture and adding an additional 3.81 grams (0.03 mole) of sulfuryl chloride before continuing the reflux. At the end of 3 days, thin layer chromatographic analysis of the mixture indicated the reaction to be complete. Volatiles were removed from the reaction mixture and 3.70 grams (0.01 mole) of 2,2-dimethyl-N-(4,5-dichloro-2-methoxyphenyl)-propanamide (Compound 177) recovered as a light yellow-orange solid by flash column chromatography eluting with dlchloromethane. NMR analysis of this product indicate the following:
NMR (CDCI3): 1.34 (s, 9H), 3.92 (s, 3H), 6.94 (s, H), 8.08 (br s H) , 8.67 (s, H) ppm. Part C: Preparation of 4.5-dichloro-2- methoxyanlline The 2,2-dimethyl-N-(4,5-dichloro-2-methoxyphenyl)propanamide (3.70 grams, 0.01 mole) prepared in Part B was dissolved in ethanol: 12N HCl (1:1), the mixture heated under reflux overnight and then freed of volatiles under rotary evaporation. Partition between 2N HCl and dichloromethane gave an acid-soluble fraction which was worked up to give 1.1 grams (0.01 mole) of pure 4,5-dichloro-2-methoxyaniline as determined by thin layer chromatographic analysis. The dichloromethane fraction from above was freed of solvent giving starting material which was again refluxed overnight with ethanol: 12N HCl and worked up to give an additional 1.2 grams (0.01 mole) of pure 4,5-dichloro-2-methoxyaniline as determined by thin layer chromatographic analysis. NMR analysis of the product indicated the following:
NMR (COCI3):63.88 (s, 5H) , 6.73-6.90
(d, 2H) ppm.
Example XXIX
Preparation of 1-(4-bromo-2-methylphenylaminocarbonyl)cyclobutanecarboxylic acid
A 3.0 gram (0.009 mole) portion of ethyl l-(4-bromo-2-methylphenylaminocarbonyl)cyclobutanecarboxylate prepared in Example IX (Compound 129) was hydrolyzed in a manner similar to that described in Example XI to give 2.19 grams (0.007 mole) of 1-(4-bromo-2-methylphenylaminocarbonyl)cyclobutanecarboxylic acid, Compound 181, having a melting point of 154°C-155°C.
Example XXX
Preparation of ethyl (chlorocarbonyl)methoxyacetate
Part A. Preparation of diethyl methoxymalonate
A mixture of 50.4 grams (0.3 mole) of dimethyl methoxymalonate, para-toluenesulfonic acid (2.76 grams) and 300 milliliters of ethanol was heated under reflux for a period of about 24 hours. Volatile materials were then removed under reduced pressure, employing a water bath at about 25°C. A second 300 mmniter-portion of ethanol was added and the mixture then refluxed for about 5 hours after which it was stirred at room temperature for an approximate 64-hour period. Removal of ethanol from the mixture under reduced pressure gave 61.0 grams (0.3 mole) of diethyl methoxymalonate, employed in the subsequent steps without purification. Part B. Preparation of mono-ethyl methoxymalonate
A mixture of 30.0 grams (0.2 mole) of diethyl methoxymalonate (Part A, above), 8.85 grams (0.2 mole) of potassium hydroxide, 2.84 grams (0.2 mole) of water and 300 milliliters of ethanol was stirred at room temperature for about 72 hours and volatiles then removed under reduced pressure. The residue was dissolved in water and the pH of the solution adjusted to 10 by addition of potassium hydroxide. The solution was saturated with potassium chloride and extracted with methylene chloride (3x100 milliliters) to remove unsaponified diester. Acidification to pH=1 and continuous extraction with methylene chloride afforded 9.45 grams (0.06 mole) of mono-ethyl methoxymalonate as a liquid.
Part C. Preparation of ethyl (chlorocarbonyl) methoxyacetate
A mixture of 5.88 grams (0.04 mole) of mono-ethyl methoxymalonate from Part B, above, 8.63 grams (0.07 mole) of thionyl chloride and 150 millinters of methylene chloride was stirred for about 17 hours and then evaporated free of volatile materials. As NMR examination indicated the reaction to be incomplete, the above thionyl chloride treatment in methylene chloride was repeated for a period of about 65 hours. A third treatment with 8.63 grams of thionyl chloride in 150 milliliters of methylene chloride was finally given, refluxing for a period of approximately 7 hours. Removal of volatiles under reduced pressure gave 6.0 grams (0.03 mole) of ethyl (chlorocarbonyl) methoxyacetate, Compound 211. NMR analysis of the product indicated the following:
Η NMR (CDCI3 )δ 1.16-1.53(t, 3H, CH3) , 3.58(s, 3H, CH3O), 4.13-4.56 (q, 2H, CH2) 4.62 (s, H, CH) ppm.
Example XXXI
Preparation of ethyl 3-[(3,5-dichlorophenyl)aminol-2-methoxy-3-oxopropanoate
3,5-Dichloroaniline (2.69 grams, 0.02 mole) and ethyl (chlorocarbonyl)methoxyacetate (3.0 grams, 0.02 mole), prepared in Example LIII (Compound 211), were reacted in the presence of triethylamine (1.68 grams, 0.02 mole) in 200 milliliters of methylene chloride in a manner similar to that described in Example I to give 1.34 grams (0.004 mole) of ethyl 3-[(3,5-dichlorophenyl)amino]-2-methoxy-3-oxopropanoate, Compound 213, having a melting point of 89.5°C-92.5°C.
Example XXXII Preparation of mono-methyl methoxymalonate
Dimethyl methoxymalonate (50.0 grams, 0.3 mole) was saponified with potassium hydroxide (17.3 grams, 0.3 mole) in a mixture of 500 milliliters of methanol and 5.55 grams (0.3 mole) of water according to the general procedure of Example VII but employing a reaction period of approximately 16 hours. The reaction mixture was evaporated free of solvents and the residue dissolved in water and extracted twice with ether to remove any unreacted diester. The aqueous layer was then saturated with potassium chloride, acidified with 2H HCl and extracted twice with ethyl ether. As this procedure enabled recovery of only a minor amount of product the aqueous phase was then subjected to three 16-hour periods of continuous liquid-liquid extraction with methylene chloride, adjusting the pH from 4 to 1 at the beginning of the second extraction period. Workup of the combined extracts gave 29.24 grams (0.2 mole) of mono-methyl methoxymalonate, Compound 214. NMR analysis of the product indicated the following:
Η NMR (COCI3) δ 3.54(s, 3H, alpha CH3O), 3.86(s, 3H, ester CH3O) , 4.51 (s, H, CH), 9.36(s, H, CO2H) ppm.
Example XXXIII
Preparation of methyl 3-[(4-bromo-2-fluorophenyl)aminol-2-methoxy-3-oxopropanoate
To a stirred mixture of 2.78 grams (0.02 mole) of mono-methyl methoxymalonate prepared in Example LVI (Compound 214) and 3.56 grams (0.02 mole) of 4-bromo-2-fluoroaniline in approximately 100 milliliters of dry tetrahydrofuran was fed dropwise a solution of 3.87 grams (0.02 mole) of 1,3-dicyclohexylcarbodiimide in about 30 milliliters of dry tetrahydrofuran, while cooling the reaction mixture in an ice-water bath. The reaction mixture was allowed to warm slowly to room temperature and stirring continued for an approximate 65-hour period. The precipitated 1,3-dicyclohexylurea by-product (3.15 grams) was removed by filtration and the filtrate vacuum evaporated and the residue dissolved in methylene chloride. The latter solution was extracted with dilute HCl and then water, then dried (MgSO4) and solvent vacuum evaporated to give a colorless liquid. Flash column chromatography of the latter on silica, eluting with hexane-ethyl acetate (7:3) gave, after workup, a liquid which crystallized on standing. Recrystallization from hexane containing a small amount of ethyl acetate gave 2.3 grams (0.01 mole) of methyl 3-[(4-bromo-2-fluorophenyl)amino]¬-2-methoxy-3-oxopropanaote, Compound 215, having a melting point of 51°C-53°C.
Example XXXIV
In a manner similar to that employed in Example XXXIII, other compounds were prepared. The structures and andlytical data for Compounds 216 through 219 are set forth in TableHa below.
Example XXXV
Preparation of t-butyl 3-[(3,5-dichlorophenyl)amino]
-2-methoxy-3-oxopropanoate
Part A Preparation of t-butyl methyl methoxymalonate
To a stirred solution of 9.26 grams (0.06 mole) of methyl (chlorocarbonyl)methoxyacetate in 25 milliliters of carbon tetrachloride was added a mixture of 4.94 grams (0.07 mole) of anhycrous t-butyl alcohol, 4.50 milliliters (0.06 mole) of pyridine and 25 milliliters of carbon tetrachloride over an approximate 20-minute period, with cooling to 0°C-5°C by an ice bath. On completing the addition, the cooling bath was removed and the mixture allowed to stir for a 4-hour period at ambient temperature after which pyridine hydrochloride was removed from the mixture by filtration. The filtrate was diluted with 100 milliliters of methylene chloride and partitioned with 100 milliliters of saturated aqueous sodium bicarbonate following which the organic phase was extracted with cold 10% hydrochloric acid (3 x 100 milliliters), then with cold water (3 x 100 milliliters) after which it was dried (MgSO4) and solvents then flash evaporated. The residue was vacuum distilled to give 7.57 grams (0.04 mole) of t-butyl methyl methoxymalonate having a boiling point of 93.5°C-95°C at 4.0 mm Hg. Part B Preparation of mono-t-butyl methoxymalonate
t-Butyl methyl methoxymalonate (7.57 grams, 0.04 mole), prepared in Part A, was saponified with potassium hydroxide (2.45 g, 0.04 mole) in a mixture of 25 milliliters of methanol and 668 microliters (0.04 mole) of water according to the general procedure of Example VII but employing a reaction period of 20 hours. Workup according to the general method of Example VII gave 5.42 grams (0.03 mole) of mono-t-butyl methoxymalonate. NMR analysis of the product indicated the following:
'H NMR (COCI3) δ 1.45(s, 9H, t-butyl), 3.58(s, 3H, CH3O), 4.45(s, H, CH), 10.51(s, H, CO2H) ppm.
Part C Preparation of t-butyl 3-[(3,5-dichlorophenyl)aminol-2-methoxy-3-oxopropanoate
Mono-t-butyl methoxymalonate (5.42 grams, 0.03 mole), prepared in Part B, 3,5-dichloroaniline (4.62 grams, 0.03 mole) and 1,3-dicyclohexylcarbodiimide (5.88 grams, 0.03 mole) were reacted in a manner similar to. that described in Example LVII to give 2.92 grams (0.009 mole) of t-butyl 3-[(3,5-dichlorophenyl)amino]-2-methoxy-3-oxopropanoate having a melting point of 129.5°C-131.5°C.
Example XXXVI
Preparation of methyl 3-[(3,5-dichlorophenyl)amino]-2-methoxy-3-thioxopropanoate
A mixture of 3.50 grams (0.01 mole) of methyl 3-[(3,5-dichlorophenyl)amino]-2-methoxy-3-oxopropanoate (Compound 233, Example LXX), 2.42 grams (0.006 mole) of 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide and 35 milliliters of anhydrous 1,1-dimethoxyethane was stirred at room temperature for a period of about 20 hours after which stirring was continued with testing at 55°C for a 168-hour interval. Solvent was removed from the reaction mixture under reduced pressure and the residue worked up by flash column chromatography to give 2.31 grams (0.007 mole) of methyl 3-[(3,5-dichloro-phenyl)amino]-2-methoxy-3-thioxopropanoate, Compound 238, having a melting point of 144°C-147°C.
Example XXXVII Preparation of 2-cyclopropeny -1-carboethoxy-1-[N- (2-methyl-4-bromophenyl)]carboxamide
Part A. Preparation of diethyl bis(2,3-trimethylsilyl)cyclopropene-1,1-dicarboxylate
A 50 milliliter round-bottom flask was equipped with a magnetic stirring bar and a reflux condenser with N2 inlet. The flask was charged with 183.0 grams (1.07 mole) of bis(trimethylsilyl) acetylene and 0.40 gram (0.001. mole) of cupric acetylacetonate. Using an oil bath the temperature of the stirred mixture was raised to 145°C. Using a syringe pump 39.3 grams (0.21 mole) of diethyl diazomalonate were added over 36 hours. Heating at 1450C was continued for an additional 12 hours after all of the diazomalonate had been added. The excess bis(trimethylsilyl)acetylene was removed by vacuum distillation. The residue product was purified by flash chromatography eluting with 80:20 hexane-ethyl acetate to give 17.0 grams (0.05 mole) of diethyl bis(2,3-trimethylsilyl)cyclopropene-1,1-dicarboxylate as a yellow liquid. NMR analysis of the product indicated the following: 'H NMR (CDCI3): δ 0.23(s,18H), 1.20 (t, 6H),4,17(q, 4H) ppm.
Part B. Preparation of diethyl cyclopropene-1,1- dicarboxylate
A 500 milliliter round-bottom flask was equipped with a magnetic stirrer and N2 inlet. The flask was charged with 21.0 grams (0.07 mole) of diethyl bis (2,3-trimethylsilyl)cyclopropene-1,1-dicarboxylate, 125 milliters of acetonitrile, 12.2 grams (0.21 mole) of anhydrous KF, and 6.50 grams (0.02 mole) of dicyclohexano-18-crown-6 ether. The mixture was stirred 6 hours at room temperature. The mixture was filtered and the filtrate concentrated under reduced pressure to a deep red oil. This oil was taken up in 100 milliliters of methanol and stirred 24 hours at room temperature. The methanol was removed under vacuum and the residue purified by flash column chromatography to give 6.25 grams (0.02 mole) of diethyl cyclo propene-1,1-dicarboxylate as a yellow oil. NMR analysis of the product indicated the following: 'H NMR (CDCl3): δ 1.25 (t, 6H) , 4.23 (q, 4H); 7.08 (s, 2H).
Part C. Preparation of mono-ethyl cyclopropene-1,1- dicarboxylate
A 250 milliliter round-bottom flask was equipped with a magnetic stirring bar and an addition funnel with N2 inlet. The flask was charged with 6.15 grams (0.03 mole) of diethylcyclopropene-1,1-dicarboxylate and 50 milliliters of ethanol. The stirred mixture was cooled in an ice bath and a solution of 1.33 grams (0.03 mole) of NaOH in 5.0 milliliters of water was added dropwise. The mixture was allowed to come to room temperature and stirred for 3 days. The reaction mixture was concentrated to 1/4 of the original volume under reduced pressure, diluted with ice water, and extracted twice with ether. The basic aqueous phase was acidified with ice cold 10% HCl, and extracted three times with ethyl acetate. The ethyl acetate was dried (MgSO4) and the solvent removed under reduced pressure to leave an orange colored solid. This was recrystallized from hexaneethyl acetate to give 3.65 grams (0.02 mole) of monoethyl cyclopropene-1,1-dicarboxylate as a light yellow solid having a melting point of 76.00C-77.50C. NMR analysis of the product indicated the following:
'H NMR (COCl3): δ 1.20 (t, 3H), 4.25 (q, 2H), 6.80 (s, 2H), 11.5 (br s, 1H) ppm. Part D. Preparation of 1-carboethoxy-1-ethoxycarbonyloxycarbonyl-2-cyclopropene A 250 milliliter round-bottom flask was equipped with a magnetic stirrer and an addition funnel with N2 inlet. The flask was charged with1.30 grams (0.008 mole) of mono-ethyl cyclopropene-1,1-dicarboxylate, 50 milliliters of dry THF, 2.3 grams (0.02 mole) of potassium carbonate (anhydrous), and 450 milligrams of dicyclohexano-18-crown-6 ether. The stirred reaction mixture was cooled to 00C, and 0.90 gram (0.008 mole) of ethyl chloroformate in 10 milliliters of THF was added dropwise. The mixture was stirred for 2 1/2 hours at 00C. At this time an aliquot from the reaction mixture showed a very strong anhydride carbonyl stretch at 1820 cm-1 in the infrared indicating the formation of the mixed anhydride 1-carboethoxy-1-ethoxycarbonyloxycarbonyl-2-cyclopropene. The balance of the reaction mixture containing the mixed anhydride was carried on to Part E.
Part E. Preparation of 2-cyclopropenyl-1-carboethoxy-1-[N-(2-methy1-4-bromophenv1)] carboxamide
A solution of 1.40 grams (0.0075 mole) of 2-methyl-4-bromoaniline in 10 milliliters of tetrahydrofuran was added dropwise to the reaction mixture from part D at 00C. The mixture was allowed to come to room temperature and stirred for 2 hours. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to give an orange colored solid. This solid was washed with ether and recrystallized from hexane-ethyl acetate to give 1.5 grams (0.004 mole) of 2-cyclopropenyl-1-carboethoxy-1-[N-(2-methyl-4-bromophenyl)]carboxamide, Compound 256, as a white crystalline solid having a melting point of 1510C-1530C.
Example XXXVIII
Effect of Representative Malonic Acid Derivative Compounds on Crop Yield Enhancement- Plant Axillary Stimulation
Plant axillary stimulation may be indicative of increased plant reproductive sites resulting in increased plant biomass and/or increased crop yield. Treatment of plants with certain malonic acid derivative compounds such as those compounds identified in Table I below results in enhanced axillary stimulation.
Solutions of the test compounds identified in Table I were prepared by dissolving 68.8 milligrams of the particular compound in 5.5 milliliters of acetone and then adding water to a final volume of 11.0 miimiters. If clouding of the solution occurred as the water was added, the use of water was discontinued and acetone was added to a final volume of 11.0 milliliters. The resulting stock solutions contained 6255 parts per million by weight of the particular compound. The test concentrations in parts of the test compound per million parts by weight of final solution employed in the axillary stimulation tests in Table I were obtained by appropriate dilution of the stock suspensions with acetone and water (50/50 volume/volume). Seeds of snapbeans, wheat, velvetleaf, cucumber, sunflower, flax, buckwheat, tomato, perennial rye, marigold, soybean, barnyard grass, wild oats and pea were planted in a sandy loam soil in a flat having the following dimensions: 3.5 inches in width x 7.9 inches in length x 1.0 inches in height. Twelve to fourteen days after planting at the time the first trifoliolate of leaf snapbean was at least 3.0 centimeters long, each concentration of the test compounds identified in Table I was applied to one flat as a foliar spray by use of an aspirated spray apparatus set at 10 psig air pressure (all flats sprayed at a rate of 4 pounds per acre). As a control, a water-acetone solution containing no test compound was also sprayed on a flat. When dry, all of the flats of plants were placed in a greenhouse at a temperature of 80°F ± 5°F and humidity of 50 percent ± 5 percent. Visual Indications of axillary stimulation activity were observed and recorded 10 to 14 days after treatment.
Visual observations of axillary stimulation were recorded employing a system of numerical ratings. Numerical ratings from "0" to "10" were used to designate the degree of axillary stimulation activity observed in comparison with the untreated control. A "0" rating indicates no visible response, a "5" rating indicates 50 percent more axillary stimulation than the control, and a "10" rating indicates 100 percent more axillary stimulation than the control. This rating system indicates the degree of axillary bud growth on broadleaf plants and the degree of tillering on grasses in comparison with an untreated control. The results are reported in Table I.
TABLE I
Effect of Representative Malonic Acid
Derivative Compounds on Crop Yield Enhancement - Axillary Stimulation on Snapbean Plants
Compound Axillary Stimulation
No. Rating
Control 0 1 1
2 2
3 1 5 1
8 1
9 1 11 1 15 1
21 1
22 5
23 2
24 2
25 1
26 3
27 1
28 1
34 5
35 1
36 1
37 1
38 1 40 1 TABLE I (Cont.)
Effect of Representative Malonic Acid Derivative Compounds on Crop Yield Enhancement Axillary Stimulation on Snapbean Plants
Compound Axillary Stimulation No. Rating
43 1 46 3 47 1 50 1 57 1 58 1 66 1 67 2 68 2 69 2 70 2 71 1 75 6 79 1 80 1 82 1 83 1 84 1 86 1 88 1 90 1 92 1 95 1 TABLE I ( Cont . )
Effect of Representati ve Malonic Acid
Derivative Compounds on Crop Yield Enhancement - Axillary Stimulation on Snapbean Plants
Compound Axillary Stimulation
No. Rating
98 1
99 1
100 1
101 1
102 2 105 1
107 1
108 1
110 2
111 2
112 1
114 2
11 5 1
116 1
117 1
120 1
121 1
122 1
123 1
125 2
126 2 129 1 135 1 TABLE I (Cont.)
Effect of Representative Malonic Acid
Derivative Compounds on Crop Yield Enhancement -
Axillary Stimulation on Snapbean Plants
Compound Axillary Stimulation No. Rating
140 1 141 2 144 2 145 1 146 1 148 2 149 1 150 1 159 2 168 1 173 1 175 4
TABLE I
Effect of Representative Malonic Acid Derivative
Compounds on Crop Yield Enhancement - Axillary Stimulation on Wheat
Compound Axillary Stimulation No. Rating
Control 0 1 2
2 1 14 2
22 1
66 3
67 3
69 1
88 1
96 4
97 3
83 2 175 1 144 1 129 1 116 1 117 1 121 1 146 1 145 1 The results in Table I demonstrate that treatment of plants with certain malonic acid derivative compounds provides signficantly enhanced axillary stimulation which may be indicative of increased plant reproductive sites resulting in increased plant biomass and/or increased crop yield.
Example XXXIX Effect of Representative Malonic Acid Derivative Compounds on Crop Yield
Enhancement-Wheat Solutions of Compound 75 were prepared by dissolving either 0.48 grams, 0.96 grams or 1.92 grams of the compound into 800 milliliters acetone. Water plus 0.2 percent by volume of Surfelk spray adjuvant were added to each of the above solutions to a final volume of 1600 milliliters. Surfelk spray adjuvant is commercially available from Union Carbide Corporation, Danbury, Connecticut.
The above formulations were applied to wheat by utilizing a statistical treatment procedure involving 42 separate plots. Each plot consisted of 8 rows individually 30 feet in length and about 0.75 feet between rows. The entire plot was treated with the prepared solutions containing the active ingredient identified in Table J below. The experiment was designed as a randomized complete block of six different repetitions in which each repetition included the following: (1) an untreated control;
(2) treatment with 0.48 grams/plot of Compound 75 at time T1 designated in Table J;
(3) treatment with 0.96 grams/plot of Compound 75 at time T1 designated in Table J;
(4) treatment with 1.92 grams/plot of Compound 75 at time T1 designated in Table J;
(5) treatment with 0.48 grams/plot of Compound 75 at time T2 designated in Table J;
(6) treatment with 0.96 grams/plot of Compound 75 at time T2 designated in Table J; and
(7) treatment with 1.92 grams/plot of Compound 75 at time T2 designated in Table J.
The above formulations were applied to each plot by use of a carbon dioxide backpack sprayer set at about 30 psig air pressure. The planting, application and harvesting times for each crop are detailed in Table J. The harvested wheat crops for yield determination included the inner 20 feet of the middle 4 rows in each plot (5 feet in from ends of the middle 4 rows). The values obtained for each plot in each repetition were averaged to obtain the results in Table J.
Two weeks prior to harvest, the wheat plants from 2 separate 1 square foot sections of each plot were sampled (subsamples) and the number of inflorescences and seeds per inflorescence were determined. The values of the subsamples per plot together with the values obtained for each plot in each repetition were averaged to obtain the results in Table J.
The results in Table J demonstrate that treatment of wheat with certain malonic acid derivative compounds provides significantly increased yields in comparison with untreated control wheat. As demonstrated in Table J, the increased yield may be attributable to an increase in the number of inflorescences or an increase in the number of seeds per inflorescence or a combination thereof.
Example XL
Effect of Representative Malonic Acid Derivative
Compounds on Crop Yield
Enhancement-Alfalfa
Solutions of Compound 75 were prepared by dissolving either 70 milligrams, 140 milligrams or 280 milligrams of the compound into 87 milliliters of acetone. Water plus 0.2 percent by volume of Triton X-100 surfactant were added to each of the above solutions to a final volume of 174 milliliters. Triton X-100 surfactant is commercially available from Rohm and Haas Company, Phildelphla, Pennsylvania.
The above formulations were applied to alfalfa by utilizing a statistical treatment procedure involving 24 separate plots. Each plot measured 5 feet by 10 feet. The entire plot was treated with the prepared solutions containing the active Ingredient in Table K below. The experiment was designed as a randomized complete block of six different repetitions in which each repetition included the following: (1) an untreated control;
(2) treatment with 70 milligrams per plot of Compound 75 at 45 days after planting;
(3) treatment with 140 milligrams per plot of Compound 75 at 45 days after planting; and
(4) treatment with 280 milligrams per lot of Compound 75 at 45 days after planting.
The above formulations were applied by use of a carbon dioxide bicycle sprayer set at about 30 psig air pressure. Three weeks after treatment, eight plants per plot were harvested. The plants were separated into stems and leaves. placed in a drying oven and dried for a period of 48 hours at a temperature of 90°C. The leaf and stem components were weighed separately and these results are reported in Table K. Total dry weight and leaf/stem ratio were calculated from the leaf and stem dry weight data and these results are reported in Table K. The values obtained for each plot in each repetition were averaged to obtain all of the results in Table K.
The results in Table K demonstrate that treatment of alfalfa with certain malonic acid derivative compounds provides significantly increased yields in comparison with untreated control alfalfa. As demonstrated in Table K, the treated alfalfa exhibited an increase in leaf dry weight, a decrease in stem dry weight and an increase in total dry weight (leaf and stem) in comparison with untreated control alfalfa. A significant increase in leaf-stem ratio for treated alfalfa versus untreated control alfalfa is demonstrated by the results in Table K.
Example XLI
Effect of Representative Malonic Acid Derivative Compounds on Crop Yield Enhancement-Soybeans Solutions of Compound 75 were prepared by dissolving either 0.39 grams, 0.78 grams or 1.56 grams of the compound into 650 milliliters acetone. Water plus 0.2 percent by volume of Surfelk spray adjuvant were added to each of the above solutions to a final volume of 1300 millinters. Surfelk spray adjuvant is commercially available from Union Carbide Corporation, Danbury, Connecticut.
The above formulations were applied to soybean plants by utilizing a statistical treatment procedure involving 42 separate plots. Each plot consisted of 4 rows individually 20 feet in length and about 3 feet between rows. The middle two rows of each plot were treated with the prepared solutions containing the active ingredient identified in Table L below. The experiment was designated as a randomized complete block of six different repetitions in which each repetition included the following:
(1) an untreated control;
(2) treatment with 0.39 grams/plot of Compound 75 at time T1 designated in Table L;
(3) treatment with 0.78 grams/plot of Compound 75 at time T1 designated in Table L;
(4) treatment with 1.56 grams/plot of Compound 75 at time T1 designated 1n Table L;
(5) treatment with 0.39 grams/plot of Compound 75 at time T2 designated in Table L;
(6) treatment with 0.7 grams/plot of Compound 75 at time T2 designated in Table L; and
(7) treatment with 1.56 grams/plot of Compound 75 at time T2 designated in Table L.
The above formulations were applied to each plot by use of a carbon dioxide backpack sprayer set at about 30 psig air pressure. The planting, applicaton and harvesting times are detailed in Table L. The harvested soybean crops for yield determinaton included the inner 10 feet of the middle 2 rows in each plot (5 feet in from ends of the middle 2 rows). The values obtained for each plot (kilograms of soybeans/plot) in each repetition were averaged to obtain the results in Table L.
Four weeks following the applications at time T2, eight soybean plants were sampled from each plot to determine the number of fruits (pods) per plant. The values obtained for each plant were averaged to obtain the results in Table L.
The results in Table L demonstrate that treatment of soybean plants with certain malonic acid derivative compounds at certain rates provides significantly increased yields in comparison with untreated control soybean plants. As demonstrated in Table L, in addition to an increase in actual yield (kilograms of soybeans/plot), the treated soybean plants exhibited an increased number of pods per plant in comparison with untreated control soybean plants.
Example XLII Effect of Representative Malonic Acid Derivative Compounds on Crop Yield
Enhancement-Soybeans
Solutions of Compound 75 were prepared by dissolving either 0.75 grams or 1.5 grams of the compound into 125 milliliters acetone. Water was added to each of the above solutions to a final volume of 250 milliliters.
The above formulations were applied to soybean plants by utilizing a statistical procedure involving 36 separate plots. Each plot consisted of 4 rows individually 25 feet in length and 2.5 feet between rows. The middle two rows of each plot were treated with the prepared solutions containing the active ingredient identified in Table M below. The experiment was designed as a split-plot design with six different repetitions. The experiment was divided Into two blocks as follows: Block 1 consisted of those plots treated at first flower and Block 2 consisted of those plots treated at 3 weeks after first flower. Randomized within each block were:
(1) an untreated control;
(2) treatment with 0.75 grams of Compound
75; and
(3) treatment with 1.5 grams of Compound
75.
The above formulations were applied to each plot by use of a carbon dioxide backpack sprayer set at about 30 psig air pressure. The planting, application and harvesting times are detailed in Table M. The middle two rows of each plot were harvested for yield determinations. The values obtained for each plot in each repetition were averaged to obtain the results in Table M.
Four weeks prior to harvest, 5 soybean plants were sampled from each plot to determine the number of fruits (pods) per plant. The values obtained for each plant were averaged to obtain the results in Table M.
The results in Table M demonstrate that treatment of soybean plants with certain malonic acid derivative compounds at certain rates provides significantly increased yields in comparison with untreated control soybean plants. As demonstrated in Table M, in addition to an increase in actual yield (kilograms of soybeans/plot), the treated soybean plants exhibited an increased number of pods per plant in comparison with untreated control soybean plants.
Example XLIII Effect of Representative Malonic Acid Derivative Compounds on Crop Yield Enhancement-Snapbeans Solutions of Compound 75 were prepared by dissolving either 1.56 milligrams, 3.13 milligrams or 6.25 milligrams of the compound in 5 milliliters of acetone and then adding water to a final volume of 10 milliliters.
Into 10.2 centimeter diameter plastic pots containing a perlite-vermicullte potting mix (1:2 volume/volume) were sown three snapbean seeds (Phaseolus vulgaris var. Cranberry). Five to seven days after planting, the plants were thinned to one plant per pot. Ten to twelve days after planting at the time of full expansion of the primary leaves, each concentration of Compound 75 (each pot was sprayed with 1 milliliter of solution) was applied to 10 snapbean plants as a foliar spray by use of an aspirated spray apparatus set at 10 psig air pressure. Untreated plants were included as controls. When dry, all of the plants were placed in a Sherer Model FAL22R controlled environment chamber with day/night temperatures of 80°F/65°F and a daily 15 hour photoperiod. Sixty-seven days after planting, the plants were removed from the controlled environment chamber, harvested and the total number of fruits (pods) per plant was determined. The values obtained for each plant were averaged to obtain the results in Table N below.
TABLE N
Effect of Representative Malonic Acid Derivative Compounds on Crop Yield Enhancement - Snapbeans
Compound Concentration No. of Fruit (pods) No. (ppm) per Plant
Control -- 34
Compound 75 156 44
313 45
625 44
The results in Table N demonstrate that treatment of snapbean plants with certain malonic acid derivative compounds provides significantly increased yields in comparison with untreated control snapbean plants. A significant increase in the number of fruit (pods) per treated snapbean plants versus untreated control snapbean plants is demonstrated by the results in Table N.
Example XLIV
Effect of Representative Malonic Acid Derivative Compounds on Plant Chlorophyll Content
Increased chlorophyll content can be an indication of increased photosynthetic activity resulting in increased biomass and/or increased crop yield. Treatment of plants with certain malonic acid derivative compounds, e.g., Compound 75, as described hereinafter results in enhanced levels of chlorophyll.
Solutions of Compound 75 were prepared by dissolving either 1.56 milligrams, 6.25 milligrams or 25.0 milligrams of the compound in 5 milliliters of acetone and then adding water to a final volume of 10 milliliters.
Into 10.2 centimeter diameter plastic pots containing a perlite-vermiculite potting mix (1:2 volume/volume) were sown three snapbean seeds (Phaseolus vulgaris var. Cranberry). Five to seven days after planting, the plants were thinned to one plant per pot. Eleven days after planting at the time of full expansion of the primary leaves, each concentration of Compound 75 (each pot was sprayed with 1 mlinnter of solution) was applied to 10 snapbean plants as a foliar spray by use of an aspirated spray apparatus set at 10 psig air pressure. Untreated plants were included as controls. When dry, all of the plants were placed in a greenhouse at a temperature of 80°F ± 5°F and humidity of 50 percent ± 5 percent. Eleven days following treatment, 15 disks (10 millimeters diameter) were punched from the primary leaves of each plant. Each set of 15 disks were weighed, placed in a test tube and stored on ice in a dark environment. Each set of disks were then homogenized in a Waring blender with 20 milliliters of a solution containing 80 percent acetone/20 percent water (volume/volume). The resulting suspensions were centrifuged at a temperature of
0°C-2°C at 12,000 X g (g = 980 cm sec-2) for a period of 5 minutes. The supernatant containing the chlorophyll was saved and the absorbance of light of the solutions at 645 nanometers (nm) and 663 nanometers (nm) was determined by spectrophotometric analysis. Total chlorophyll (milligrams chlorophyll/grams leaf tissue) was calculated according to the following equation:
milligrams (20.2)(absorbance at 645 nm) + of chlorophyll = (8.02)(absorbance at 663 nm) grams of leaf weight of leaf disks (grams) tissue
The values obtained for the control and Compound 75 were averaged to obtain the results in Table 0 below.
The results in Table 0 demonstrate that treatment of plants with certain malonic acid derivative compounds provides significantly increased levels of plant chlorophyll in comparison with untreated control plants. This increase in plant chlorophyll content may be indicative of increased plant biomass and/or increased crop yield.
Example XLV
Effect of Representative Malonic Acid
Derivative Compounds on Plant
Nitrate Reductase Content
Nitrate reductase is a substrate-lnducible enzyme which mediates the conversion of nitrate to nitrite. The inducible nature of nitrate reductase and the dependence of the enzyme level on substrate level provides the plant with a mechanism for controlling growth. Nitrate reductase catalyzes the rate-limiting step in the conversion of nitrate into proteins. Thus, increased levels of nitrate reductase may indicate increased potential for grain and protein production. See, for example, Beevers, L. and R.H. Hageman, 1969, Nitrate Reduction in Higher Plants, Annual Review of Plant Physiology 20: 495-522.
Solutions of Compound 75 were prepared by dissolving either 1.56 milligrams, 6.25 milligrams or 25.0 milligrams of the compound 1n 5 milliliters of acetone and then adding water to a final volume of 10 milliliters.
Into 10.2 centimeter diameter plastic pots containing perlite-vermiculite potting mix (1:2 volume/volume) were sown three snapbean seeds (Phaseolus vulgaris var. Cranberry). Five to seven days after planting, the plants were thinned to one plant per pot. Eleven days after planting at the time of full expansion of the primary leaves, each concentration of Compound 75 (each pot was sprayed with 1 milliliter of solution) was applied to 10 snapbean plants as a foliar spray by use of an aspirated spray apparatus set at 10 psig air pressure. Untreated plants were included as controls. When dry, all of the plants were placed in a greenhouse at a temperature of 80°F ± 5°F and humidity of 50 percent ± 5 percent. Seven days after treatment, groups of 5 disks (diameter of 1 centimeter each) were cut at random from the primary leaves. The disks were weighed and then infiltrated under vacuum twice for about 3 minutes in 30 miimiter beakers containing 10 milliliters of a particular medium. The medium consisted of 0.1 M phosphate buffer (pH 7.5), 0.02 M postassium nitrate and 0.1 percent (volume/volume) Triton X-100. Triton X-100 surfactant is commercially available from Rohm and Haas Company, Philadelphia, Pennsylvania.
The beakers were then covered and incubated for 90 minutes at a temperature of 32°C. At the beginning of the incubation period and at 20 minutes and 80 minutes into the incubation period, nitrate released into the medium was determined by removing a 0.2 milliliter aliquot from each beaker and placing it in a test tube. Into the test tube was added 0.25 milliliters of 1 percent (weight/volume) sulfanilamide in 3N HCl and 0.25 milliliters of 0.02 percent (weight/volume) N-(1-naphthyl)- ethylenediamine dihydrochloride. The test tubes were allowed to stand for 20 minutes before mesuring the optical densities at 540 nanometers on a Beckman DB spectrophotometer. Nitrate reductase activity was expressed as micromoles ( M) of nitrite formed per gram of fresh leaf weight per hour. The values obtained for the control and Compound 75 were averaged to obtain the results in Table P below.
The results in Table P demonstrate that treatment of plants with certain malonic acid derivative compounds provides significantly increased levels of nitrate reductase in comparison with untreated control plants. This increase in plant nitrate reductase content may be indicative of increased plant protein production and/or increased crop yield.
Example XLVI
Effects of Representative Malonic Acid Derivative
Compounds on Crop Yield
Enhancement - Wheat Tillering
Solutions of the test compounds identified in Table Q below were prepared by dissolving the compounds in acetone/water (50:50 volume/volume) containing 0.05 percent volume/volume of Triton X-100 surfactant commercially available from Rhom and Haas Company, Philadelphia, Pennsylvania. As detailed below, these solutions of test compounds were applied to wheat at a concentration of 0.06, 0.12, 0.25, 0.50 and 1.0 pounds of active ingredient per acre.
Wheat seeds (var. Olaf) were planted in a sandy loam soil in flats having the following dimensions: 5.5 inches In width x 9.0 inches in length x 3.0 inches in height. The wheat seeds were sown in 2 different arrangements as follows: 4 rows (5 inches in length) per flat, 10 seeds per row (Flat No. 1); and 2 rows (5 inches in length) per flat, 5 seeds per row (Flat No. 2). Eleven days after planting at the 2-3 leaf growth stage of wheat, each concentration of the test compounds identified in Table Q was applied to a separate flat as a foliar spray by use of an aspirated spray apparatus set at 10 psig air pressure (all flats sprayed at a concentration of 120 gallons per acre). As a control, a water-acetone solution containing no test compound was also sprayed on separate flats. When dry, all of the flats were placed in a greenhouse at a temperature of 80°F ± 5°F and humidity of 50 percent ± 5 percent. Measured indications of tillering activity were observed and recorded 15 days after treatment for wheat sown in Flat No. 1 arrangements and 20 days after treatment for wheat sown in Flat No. 2 arrangements.
The number of vegetative shoots per seed was determined by actual count. The results reported in Table Q reflect the average of 3 repetitions. The percent increase tillering is based upon the untreated control.
The results in Table Q demonstrate that treatment of wheat with certain malonic acid derivative compounds provides significantly increased tillering in comparison with untreated control wheat.

Claims

Claims
1. A method of increasing crop yield which comprises applying to the crop an effective amount, sufficient to increase crop yield, of a compound having the formula:
wherein:
R1 and R2 are independently a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents (Z) are the same or different and are one or more hydrogen, halogen, alkylcarbonyl, alkylcarbonylalkyl, formyl, alkoxycarbonylalkyl, alkoxycarbonylalkylthio, polyhaloalkenylthlo, thlocyano, propargylthio, hydroxyimlno, alkoxyimlno, trialkylsilyloxy, aryldialkylsilyloxy, triarylsilyloxy, formamidino,
alkylsulfamido, dialkylsulfamido, alkoxysulfonyl, polyhaloalkoxysulfonyl, hydroxy, amino, azido, azo, aminocarbonyl, alkylaminocarbonyl, hydrazino, dialkylaminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylamlnothiocarbonyl, nitro, cyano, hydroxycarbonyl and derivative salts, formamido, alkyl, alkoxy, polyhaloalkyl, polyhaloalkoxy, alkoxycarbonyl, substituted amino in which the permissible substituents are the same or different and are one or two propargyl, alkoxyalkyl, alkylthloalkyl, alkyl, alkenyl, haloalkenyl or polyhaloalkenyl; alkylthio, polyhaloalkylthio, alkylsulfinyl, polyhaloalkylsulfinyl, alkylsulfonyl, polyhaloalkylsulfonyl, alkylsulfonylamino, dlkylcarbonylamino, polyhaloalkylsulfonylamino, polyhaloalkylcarbonylamino, trialkylsilyl, aryldialkylsilyl, triarylsilyl, sulfonic acid and derivative salts, phosphonic acid and derivative salts, alkoxycarbonylamino, alkylaminocarbonyloxy, dlalkylaminocarbonyloxy, alkenyl, polyhaloalkenyl, alkenyloxy, alkynyl, alkynyloxy, polyhaloalkenyloxy, polyhaloalkynyl, polyhaloalkynyloxy, polyfluoroalkanol, cyanoalkylamino, semicarbazonomethyl, alkoxycarbonylhydrazonomethyl, alkoxyiminomethyl, unsubstituted or substituted aryloxyiminomethyl, hydrazonomethyl, unsubstituted or substituted arylhydrazonomethyl, a hydroxy group condensed with a mono-, di- or polysaccharide, haloalkyl, haloalkenyl, haloalkynyl, alkoxyalkyl, aryloxy, aralkoxy, arylthio, aralkylthio, alkylthioalkyl, arylthioalkyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, haloalkenyloxy, haloalkynyloxy, haloalkynylthio, haloalkenylsulfonyl, polyhaloalkenylsulfonyl, isocyano, aryloxysulfonyl, propargyloxy, aroyl, haloacyl, polyhaloacyl, aryloxycarbonyl, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, arylaminosulfonyl, carboxyalkoxy, carboxyalkylthio, alkoxycarbonylalkoxy, acyloxy, haloacyloxy, polyhaloacyloxy, aroyloxy, alkylsulfonyloxy, alkenylsulfonyloxy, arylsulfonyloxy, haloalkylsulfonyloxy, polyhaloalkylsulfonyloxy, aroylamino, haloacylamino, alkoxycarbonyloxy, arylsulfonylamino, aminocarbonyloxy, cyanato, isocyanato, isothiocyano, cycloalkylamino, trialkylammonium, arylamino, aryl(alkyl)amino, aralkylamino, alkoxyalkylphosphinyl, alkoxyalkylphosphinothioyl, alkylhydroxyphosphinyl, dialkoxyphosphino, hydroxyamino, alkoxyamino, aryloxyamino, aryloxyimino, oxo, thiono, diazo, alkylidene, alkylimino, hydrazono, semicarbazono, dialkylsulfonium, dialkylsulfuranylidene, dialkyloxosulfuranylidene,
-X, = X, -X = R3, = X-R3,
or
R1 and R2 are independently hydrogen or derivative salts, or a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z;
Y1 and Y2 are independently a substituted or unsubstituted heteroatom in which the permissible substituents are;
Y3 and Y4 are independently hydrogen, or a substituted or unsubstituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination, or halogen, alkylcarbonyl, formyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkoxycarbonylalkylthio, polyhaloalkenylthio, thiocyano, propargylthio, trialkylsilyloxy, aryldialkylsilyloxy, triarylsilyloxy, formamidino, alkylsulfamido, dialkylsulfamido, alkoxysulfonyl, polyhaloalkoxysulfonyl, hydroxy, amino, hydrazino, azo, aminocarbonyl, alkylaminocarbonyl, azido, dialkylaminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, nitro, cyano, hydroxycarbonyl and derivative salts, formamido, alkyl, alkoxy, polyhaloalkyl, polyhaloalkoxy, alkoxycarbonyl, substituted amino in which the permissible substituents are the same or different and are one or two propargyl, alkoxyalkyl, alkylthioalkyl, alkyl, alkenyl, haloalkenyl or polyhaloalkenyl; alkylthio, polyhaloalkylthio, alkylsulfinyl, polyhaloalkylsulfinyl, alkylsulfonyl, polyhaloalkylsulfonyl, alkylsulfonylamino, alkylcarbonylamino, polyhaloalkylsulfonylamino, polyhaloalkylcarbonylamino, trialkylsilyl, aryldlalkylsilyl, triarylsilyl, sulfonic acid and derivative salts, phosphonic acid and derivative salts, alkoxycarbonylamino, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkenyl, polyhaloalkenyl, alkenyloxy, alkynyl, alkynyloxy, polyhaloalkenyloxy, polyhaloalkynyl, polyhaloalkynyloxy, polyfluoroalkanol, cyanoalkylamino, semicarbazonomethyl, alkoxycarbonylhydrazonomethyl, alkoxyiminomethyl, unsubstituted or substituted aryloxyiminomethyl, hydrazonomethyl, unsubstituted or substituted arylhydrazonomethyl, a hydroxy group condensed with a mono-, di- or polysacoharide, haloalkyl, haloalkenyl, haloalkynyl, alkoxyalkyl, aryloxy, aralkoxy, arylthio, aralkylthio, alkylthioalkyl, arylthioalkyl, arylsulfinyl, arylsulfonyl, haloalkylsulfinyl, haloalkylsulfonyl, haloalkenyloxy, haloalkynyloxy, haloalkynylthio, haloalkenylsulfonyl, polyhaloalkenylsulfonyl, isocyano, aryloxysulfonyl, propargyloxy, aroyl, haloacyl, polyhaloacyl, aryloxycarbonyl, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, arylaminosulfonyl, carboxyalkoxy, carboxyalkylthio, alkoxycarbonylalkoxy, acyloxy, haloacyloxy, polyhaloacyloxy, aroyloxy, alkylsulfonyloxy, alkenylsulfonyloxy, arylsulfonyloxy, haloalkylsulfonyloxy, polyhaloalkylsulfonyloxy, aroylamino, haloacylamino, alkoxycarbonyloxy, arylsulfonylamino, amlnocarbonyloxy, cyanato, isocyanato, isothiocyano, cycloalkylamino, trialkylammonium, arylamino, aryl(alkyl)amino, aralkylamino, alkoxyalkylphosphinyl, alkoxyalkylphosphinothioyl, alkylhydroxyphosphinyl, dialkoxyphosphino, hydroxyamino, alkoxyamino, aryloxyamino,
-X, -X = R3,
or
in which the permissible substituents are Z; or Y3 and Y4 taken together are oxo, thiono, diazo, = X or = X - R3, or substituted or unsubstituted alkylidene, alkylimino, hydrazono, dialkylsulfonium, dialkylsulfuranylidene, dialkyloxosulfuranylidene, semicarbazono, dialkylsulfonium, dialkylsulfuranylidene, dialkyloxosulfuranylidene, hydroxylmino, alkoxyimino or aryloxyimino in which the permissible substituents are Z; or Y3 and Y4 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents are; and Y5 and Y6 are independently oxygen or sulfur; wherein:
X is a covalent single bond or double bond, a substituted or unsubstituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z;
R3 is a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents are Z; or R3 is a substituted heteroatom or substituted carbon atom, or a substituted or unsubstituted, branched or straight chain containing two or more carbon atoms or heteroatoms in any combination in which the permissible substituents are Z;
Y7 and Y10 are independently oxygen or sulfur;
Y8 and Y9 are independently oxygen, sulfur, amino or a covalent single bond; and
R4 and R5 are independently hydrogen or substituted or unsubstituted alkyl, alkenyl, alkynyl, polyhaloalkyl, phenyl or benzyl in which the permissible substituents are Z;
2. The method of claim 1 in which the compound has the formula:
wherein: R1, R2, Y1, Y2, Y5, Y6 and are as defined in Claim 1 and Y3 and Y4 taken together are oxo, thiono, diazo, = X or = X - R3, or substituted or unsubstituted alkylidene, alkylimino, hydrazono, dialkylsulfonium, dialkyloxosulfonium, semicarbazono, dialkylsulfonium, dialkyloxosulfonium, hydroxyimino, alkoxyimino or aryloxyimino in which the permissible substituents are Z.
3. The method of claim 1 in which the compound has the formula:
whe rein:
R1, R2, Y1 , Y2 , Y5, Y6 and Z are as defined in Claim 1 and
Y3 and Y4 are linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system, and a bridged ring system which may be saturated or unsaturated in which the permissible substituents are Z.
4. The method of claim 1 in which the compound has the formula:
wherein:
Z' is the same or different and is one 8 or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'38 is O, S, NH or N (alkyl); and R' is hydrogen, ammonium, alkylammonium, 7 polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted alkyl, hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, mercaptoalkyl, alkylthloalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsuIfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylaminoalkyl, cyanoamlnoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible substituents are Z as defined in Claim 1.
5. The method of claim 1 in which the compound has the formula:
Z'9 is the same or different and is one or more hydrogen, or substituted of unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'39 is O, S, NH or N (alkyl); and
R'8 is a derivative salt, or Z as defined in Claim 1.
6. The method of claim 1 in which the compound has the formula:
wherein:
Z'10 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'40 is O, S, NH or N (alkyl);
Y'4 and Y'5 are independently hydrogen or substituted or unsubstituted halogen, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, cyano, nitro, formyl, amino, hydroxy, alkylcarbonyl, dialkoxyalkyl, alkylcarbonylamino, formylamino, hydroxyalkyl, polyhaloalkyl or haloalkyl; or Y'4 and Y'5 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated, and
R'9 is hydrogen, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly (hydroxyalkyl)ammonlum, an alkali metal or alkaline earth metal or substituted or unsubstituted alkyl, hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, mercaptoalkyl, alkylthioalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylaminoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, amlnosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible substituents are Z as defined in Claim 1.
7. The method of claim 1 in which the compound has the formula:
wherein:
Z'11 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'6 is hydrogen or alkyl;
Y'7, Y'8, Y'9 and Y'10 are independently hydrogen, halogen or alkyl;
Y'41 is O, S, NH or N (alkyl); and
R'10 is hydrogen, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted alkyl, hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, mercaptoalkyl, alkylthioalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylaminoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible subsitutents are Z as defined in Claim 1.
8. The method of claim 1 in which the compound has the formula:
wherein:
Z'12 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'11, Y'12, Y'13, Y'14, Y'15 and Y'16 are independently hydrogen,halogen or alkyl;
Y'42 is O, S, NH or N (alkyl); and R'11 is hydrogen, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl) ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted alkyl, hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, mercaptoalkyl, alkylthioalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsuIfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylaminoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible substituents are Z as defined in Claim 1.
9. The method of claim 1 in which the compound has the formula:
wherein :
Z'13 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'17 is hydrogen or alkyl;
Y'18, Y'19, Y' 20 and Y'21 are
Independently hydrogen, halogen or alkyl;
Y'43 is O, S, NH or N (alkyl); and R'12 is a derivative salt, or Z as defined in Claim 1.
10. The method of claim 1 in which the compound has the formula:
wherei n :
Z '14 i s the same or di fferent and i s one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'21, Y'22, Y'23, Y'24, Y'25 and
Y'26 are independently hydrogen, halogen or alkyl;
Y'44 is O, S, NH or N (alkyl); and
R'13 is a derivative salt, or Z as defined in Claim 1.
11. The method of claim 1 in which the compound has the formula:
wherein:
Z'15 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'27 is O, S, NH or N (alkyl);
Y'28 completes a substituted or unsubstituted, carbocylic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated;
Y'45 is O, S, NH or N (alkyl); and
R' 14 is a derivative salt, or Z as defi ned i n Claim 1 .
12. The method of claim 1 in which the compound has the formula:
wherein :
Z'16 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'29 is O, S, NH or N (alkyl);
Y'30 and Y'31 are independently hydrogen, or substituted or unsubstituted halogen, alkenyl, alkynyl, alkyl, alkoxy, alkylthio, cyano, nitro, formyl, amino, hydroxy, alkylcarbonyl, dialkoxyalkyl, alkylcarbonylamino, formylamino, hydroxyalkyl, polyhaloalkyl or haloalkyl; or Y'30 and Y'31 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated;
Y'46 is O, S, NH or N (alkyl); and R'15 is a derivative salt, or Z as defined in Claim 1.
13. The method of claim 1 in which the compound has the formula:
wherein:
Z'17 is the same or different and is one or more hydrogen, or substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-;
Y'32 is O, S, N or N (alkyl);
Y'33 and Y'34 are independently hydrogen, or substituted or unsubstituted halogen, alkyl, alkoxy, alkylthio, polyhaloalkyl or haloalkyl; or Y'33 and Y'34 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated;
Y'47 is O, S, NH or N (alkyl), and
R'16 is a derivative salt, or Z as defined in Claim 1.
14. The method of claim 1 in which the compound has the formula:
wherein:
R'17 is a substituted or unsubstituted heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, or polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated;
Y'35 is O, S, N or N (alkyl);
Y'36 and Y'37 are independently hydrogen, or substituted or unsubstituted halogen, alkenyl, alkynyl, alkyl, alkoxy, alkylthio, cyano, nitro, formyl, amino, hydroxy, alkylcarbonyl, dialkoxyalkyl, alkylcarbonylamino, formylamino, hydroxyalkyl, polyhaloalkyl or haloalkyl; or
Y'36 and Y'37 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated;
Y'48 is O, S, N or N (alkyl); and
R'18 is a derivative salt, or Z as defined in Claim 1.
15. The method of claim 1 in which the compound has the formula:
16. The method of claim 1 in which the compound has the formula:
17. The method of claim 1 in which the compound has the formula:
18. The method of claim 1 in which the compound has the formula:
19. The method of claim 1 in which the compound has the formula:
20. The method of claim 1 in which the compound has the formula:
21. The method of claim 1 in which the compound has the formula:
22. The method of claim 1 in which the compound has the formula:
23. The method of claim 1 in which the compound has the formula:
24. The method of claim 1 in which the compound has the formula:
25. A method of increasing crop yield which comprises applying to the crop an effective amount, sufficient to increase crop yield, of a compound of claim 33.
26. The method of claim 1 wherein the compound is applied to the crop in an amount sufficient to Increase crop yield without causing substantial phytotoxicity.
27. The method of claim 1 wherein the compound 1s applied to the crop at a period prior to the plant reproductive growth phase.
28. The method of claim 1 wherein the compound is applied to the crop at a period during the plant reproductive growth phase.
29. The method of claim 1 wherein the compound is applied to the crop at a concentration of from about 0.001 to about 100 pounds of compound per acre.
30. The method of claim 1 wherein the compound 1s applied to the crop at a concentration of from about 0.01 to about 15 pounds of compound per acre.
31. The method of claim 1 wherein the crop is any agronomic or horticultural crop, ornamental or turfgrass.
32. The method of claim 1 wherein the crop is selected from corn, cotton, sweet potatoes, white potatoes, alfalfa, wheat, rye, rice, barley, oats, sorghum, dry beans, soybeans, sugar beets, sunflowers, tobacco, tomatoes, canola, deciduous fruit, dtrus frut, tea, coffee, olives, pineapple, banana, sugar cane, cocoa, oil palm, herbaceous bedding plants, woody shrubs, turfgrasses, ornamental plants, evergreens, trees and flowers.
33. A compound having the formula selected from the following:
wherein:
Z1 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y11 is O, S or NR wherein R7 is hydrogen or alkyl;
Y12 is O, S, NH or N (alkyl); and
R6 is ammonium, alkylammonlum, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dlalkylaminoalkyl, aryl, mercaptoalkyl, alkylthloalkyl, arylthloalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthloalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamlno, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylamlnoalkyl, cyanoamlnoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylallyl;
wherein:
Z3 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y17 is O, S or NR11 wherein R11 is hydrogen or alkyl;
Y18 is O or S;
Y19 and Y20 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated; and
R10 is hydrogen, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted alkyl, hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, mercaptoalkyl, alkylthloalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylal , alkylsulfinylalkyl, acylalkyl, aroylalkyl, dia xyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nltroalkyl, alkylldeneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylamlnoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible substituents are Z as defined in Claim 1.
34. The compound of claim 33 having the formula:
wherein:
Z1 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl. polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from O to 5;
Y11 is O, S or NR, wherein R7 is hydrogen or alkyl;
Y12 is O, S, NH or N (alkyl); and
R6 is ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dlalkylaminoalkyl, aryl, mercaptoalkyl, alkylthloalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylideneamlno, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylamlnoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible substituents are as defined for Z in claim 33.
35. The compound of claim 33 having the formula:
wherein:
Z3 is independently substituted or unsubstituted halogen, haloalkyl, polyhaloalkyl, polyhaloalkoxy, alkyl, alkoxy, alkylthio, alkylsulfonyl, alkylsulfinyl, aryl, aryloxy, arylthio, arylsulfonyl, nitro, cyano, dialkoxyphosphinyl, acyl, aroyl, alkoxycarbonyl, alkoxycarbonylalkyl, acylamino, sulfonylamino, alkylsulfonylamino, acyloxy, alkenyl or -CH=CHCH=CH-; n is a value of from 0 to 5;
Y17 is O, S or NR wherein R11 is hydrogen or alkyl;
Y18 is O or S;
Y19 and Y20 may be linked together to form a substituted or unsubstituted, carbocyclic or heterocyclic ring system selected from a monocyclic aromatic or nonaromatic ring system, a bicyclic aromatic or nonaromatic ring system, a polycyclic aromatic or nonaromatic ring system and a bridged ring system which may be saturated or unsaturated; and R10 is hydrogen, ammonium, alkylammonium, polyalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium, an alkali metal or alkaline earth metal or substituted or unsubstituted alkyl, hydroxyalkyl, alkoxyalkyl, alkoxycarbonylalkyl, alkylaminoalkyl, dlalkylaminoalkyl, aryl, mercaptoalkyl, alkylthioalkyl, arylthioalkyl, aryloxyalkyl, alkylsulfonylalkyl, alkylsulfinylalkyl, acylalkyl, aroylalkyl, dialkoxyphosphinylalkyl, diaryloxyphosphinylalkyl, hydroxyalkylthioalkyl, hydroxyalkylsulfonylalkyl, alkoxyalkylthioalkyl, alkoxyalkylsulfonylalkyl, poly(oxyalkylene)alkyl, cyanoalkyl, nitroalkyl, alkylldeneamino, carbamoylalkyl, alkylcarbamoylalkyl, dialkylcarbamoylalkyl, aminoalkyl, acylaminoalkyl, acyloxyalkyl, alkoxycarbonylaminoalkyl, cyanoaminoalkyl, carbamoyloxyalkyl, alkylcarbamoyloxyalkyl, dialkylcarbamoyloxyalkyl, alkoxycarbonyloxyalkyl, alkoxycarbonylthioalkyl, aminosulfonylalkyl, alkylaminosulfonylalkyl or dialkylaminosulfonylalkyl; in which the permissible substituents are as defined for Z in claim 33.
36. The compound of claim 33 having the formula:
37. A composition for increasing crop yield comprising an acceptable carrier and an effective amount, sufficient to increase crop yield, of a compound of claim 33.
38. The method of claim 1 in which the compound is used in combination with one or more other biologically active compounds.
39. The method of claim 1 in which the compound is a derivative salt.
40. The method of claim 39 in which the derivative salt is selected from an alkali metal, an alkaline earth metal, ammonium, alkylammonium, polyhaloalkylammonium, hydroxyalkylammonium, poly(hydroxyalkyl)ammonium or mixtures thereof..
EP87902946A 1986-03-31 1987-03-30 Use of malonic acid derivative compounds for increasing crop yield Withdrawn EP0261226A1 (en)

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US5292937A (en) * 1986-03-31 1994-03-08 Rhone-Poulenc Inc. Use of malonic acid derivative compounds for retarding plant growth
HU201455B (en) * 1986-03-31 1990-11-28 Rhone Poulenc Bv Synergetic compositions regulating the growth of plants
WO1987005898A2 (en) * 1986-03-31 1987-10-08 Rhone-Poulenc Nederlands B.V. Use of malonic acid derivative compounds for retarding plant growth
JP2715559B2 (en) * 1989-06-26 1998-02-18 富士電機株式会社 High voltage generation circuit
EP1033365B1 (en) 1999-03-03 2002-09-25 Basf Aktiengesellschaft Diureides and their use
EP2052612A1 (en) 2007-10-24 2009-04-29 Bayer CropScience AG Herbicide combination
DE102008037629A1 (en) 2008-08-14 2010-02-18 Bayer Cropscience Ag Herbicide combination with dimethoxytriazinyl-substituted difluoromethanesulfonylanilides
CN102531787B (en) * 2012-01-17 2013-07-17 山东省农业科学院作物研究所 Preparation for improving wheat dry and hot wind resistance and application method thereof
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US3254108A (en) * 1963-02-18 1966-05-31 Eastman Kodak Co Process for preparation of arylimino propionates
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