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GB1337269A - Phosphorus and thiophosphorus acid ester derivatives of substituted hydantoins - Google Patents

Phosphorus and thiophosphorus acid ester derivatives of substituted hydantoins

Info

Publication number
GB1337269A
GB1337269A GB5534270A GB5534270A GB1337269A GB 1337269 A GB1337269 A GB 1337269A GB 5534270 A GB5534270 A GB 5534270A GB 5534270 A GB5534270 A GB 5534270A GB 1337269 A GB1337269 A GB 1337269A
Authority
GB
United Kingdom
Prior art keywords
formula
reacting
compound
halogen
hydantoin
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.)
Expired
Application number
GB5534270A
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB1337269A publication Critical patent/GB1337269A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
    • A01N57/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34 containing heterocyclic radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
    • C07D233/72—Two oxygen atoms, e.g. hydantoin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503—Five-membered rings
    • C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Environmental Sciences (AREA)
  • Dentistry (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

1337269 Hydantoin derivatives ESSO RESEARCH & ENG CO 20 Nov 1970 [5 Jan 1970] 55342/70 Headings C2P and C2C Novel compounds of Formula I where R 1 is C 1-4 alkyl optionally substituted by halogen or alkoxy, C 2-4 alkenyl, C 3-6 cycloalkyl, phenyl or benzyl optionally substituted by one or more halogen atoms, C 2-5 alkylcarbonyl or C 3-6 alkoxycarbonylalkyl, R 2 and R 3 are hydrogen, C 1-4 alkyl or phenyl, or R 2 and R 1 together form a tri- or tetra-methylene bridge, R 4 and R 5 are C 1-4 alkoxy or alkylthio and X is oxygen or sulphur, with the proviso that when R 1 is methyl or alkylcarbonyl, R 4 and R 5 may not both represent simultaneously methoxy or ethoxy, may be prepared by reacting a compound of Formula II with a compound of Formula III where Hal is halogen and M<SP>+n</SP> is an n-valent cation. The starting materials of Formula II may be prepared by reacting a corresponding 1- substituted or 1,5-disubstituted hydantoin with formaldehyde to form a 3-hydroxymethyl hydantoin derivative and reacting this compound with a halogenating agent. The compounds of Formula I have insecticidal and acaricidal properties and may be used as the active ingredients in conventional pesticidal compositions.
GB5534270A 1970-01-05 1970-11-20 Phosphorus and thiophosphorus acid ester derivatives of substituted hydantoins Expired GB1337269A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US80270A 1970-01-05 1970-01-05

Publications (1)

Publication Number Publication Date
GB1337269A true GB1337269A (en) 1973-11-14

Family

ID=21693087

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5534270A Expired GB1337269A (en) 1970-01-05 1970-11-20 Phosphorus and thiophosphorus acid ester derivatives of substituted hydantoins

Country Status (8)

Country Link
BE (1) BE761209A (en)
CA (1) CA930366A (en)
DE (1) DE2064474A1 (en)
FR (1) FR2090470A5 (en)
GB (1) GB1337269A (en)
IL (1) IL35731A (en)
NL (1) NL7018205A (en)
ZA (1) ZA708041B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001025216A1 (en) * 1999-10-01 2001-04-12 Basf Aktiengesellschaft 1-aryl-1,3-dihydro-imidazol-2-(thi)one derivatives, production of said compound and use as a dessicating/defoliating agent for plants

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH573920A5 (en) * 1972-12-12 1976-03-31 Ciba Geigy Ag
US4260769A (en) * 1977-04-22 1981-04-07 Interx Research Corporation 5,5-Diphenylhydantoins

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001025216A1 (en) * 1999-10-01 2001-04-12 Basf Aktiengesellschaft 1-aryl-1,3-dihydro-imidazol-2-(thi)one derivatives, production of said compound and use as a dessicating/defoliating agent for plants

Also Published As

Publication number Publication date
FR2090470A5 (en) 1972-01-14
BE761209A (en) 1971-07-05
CA930366A (en) 1973-07-17
ZA708041B (en) 1971-09-29
IL35731A0 (en) 1971-01-28
DE2064474A1 (en) 1971-07-15
IL35731A (en) 1974-05-16
NL7018205A (en) 1971-07-07

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PLNP Patent lapsed through nonpayment of renewal fees