GB1364137A - 1,3,4-oxadiazolone derivatives - Google Patents

1,3,4-oxadiazolone derivatives

Info

Publication number
GB1364137A
GB1364137A GB4133072A GB4133072A GB1364137A GB 1364137 A GB1364137 A GB 1364137A GB 4133072 A GB4133072 A GB 4133072A GB 4133072 A GB4133072 A GB 4133072A GB 1364137 A GB1364137 A GB 1364137A
Authority
GB
United Kingdom
Prior art keywords
formula
carbon atoms
compound
prepared
alkyl
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
GB4133072A
Inventor
R Boesch
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 SA
Original Assignee
Rhone Poulenc SA
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
Priority claimed from FR7132587A external-priority patent/FR2162692A5/fr
Priority claimed from FR7224327A external-priority patent/FR2205068A6/en
Application filed by Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB1364137A publication Critical patent/GB1364137A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/101,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C07D271/1131,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C243/00Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C243/00Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
    • C07C243/24Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
    • C07C243/26Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C243/28Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Paints Or Removers (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1364137 1,3,4-oxadiazolone derivatives RHONE-POULENC SA 6 Sept 1972 [9 Sept 1971 5 July 1972] 41330/72 Heading C2C The invention comprises oxadiazolone derivatives of general formula wherein R represents an alkyl radical containing 1 to 4 carbon atoms or a cycloalkyl radical containing 3 to 6 carbon atoms, R 1 and R 2 are the same or different and each represents a hydrogen or halogen atom or an alkyl radical containing 1 to 4 carbon atoms, R 3 represents a hydrogen atom, or an alkyl or alkoxy radical each containing 1 to 4 carbon atoms, and R 4 represents a carboxy radical, an alkoxycarbonyl radical in which alkyl moiety contains 1 to 4 carbon atoms, a hydromethyl radical, an alkoxymethyl radical in which the alkyl moiety contains 1 to 4 carbon atoms, or a carbamoyl group -CONR 5 R 6 , in which R 5 represents a hydrogen atom or an alkyl radical containing 1 to 4 carbon atoms, an alkenyl radical containing 2 to 4 carbon atoms or an alkoxy radical containing 1 to 4 carbon atoms, and R 6 represents a hydrogen atom or an alkyl radical containing 1 to 4 carbon atoms or an alkenyl radical containing 2 to 4 carbon atoms. Compounds of Formula I where R 4 represents carboxy, alkoxycarbonyl or alkoxymethyl may be prepared by reacting a compound of Formula II where X is a halogen atom, and R 7 is carboxy optionally salified by an alkali metal atom, or alkoxycarbonyl or alkoxymethyl in which the alkyl moiety contains 1 to 4 carbon atoms, with an oxadiazolone derivative of Formula III Compounds of Formula I where R 4 is carboxy may also be prepared by acid or alkaline hydrolysis of a compound of Formula I where R 4 is alkoxycarbonyl in which the alkyl moiety contains 1 to 4 carbon atoms. Compounds of Formula I where R 4 is -CONR 5 R 6 may be prepared by reacting a compound of Formula IV with an acid halide of Formula V where X 1 is a halogen atom. The acid halides of Formula V may be obtained by reacting thionyl chloride with a compound of Formula I where R 4 is carboxy. Compounds of Formula I where R 4 is hydroxymethyl may be prepared by reduction of a compound of Formula I where R 4 is alkoxycarbonyl in which the alkyl moiety contains 1 to 4 carbon atoms. The oxadiazolone derivatives of Formula III may be prepared by reacting phosgene with a hydrazide of Formula VI or by hydrolysis in an acid medium of a compound of Formula VII where R 8 is a C 1 to C 4 alkyl radical. The hydrazide of Formula VII may be prepared by diazotization of the corresponding amino compound followed by reduction of the diazonium salt with stannous chloride, the amino compound having first been prepared by reduction of the nitro compound. The compounds of Formula I are used in herbicidal compositions.
GB4133072A 1971-09-09 1972-09-06 1,3,4-oxadiazolone derivatives Expired GB1364137A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR7132587A FR2162692A5 (en) 1971-09-09 1971-09-09
FR7224327A FR2205068A6 (en) 1972-07-05 1972-07-05 3-(substd phenyl)-oxadiazol-2-ones - with herbicidal activity

Publications (1)

Publication Number Publication Date
GB1364137A true GB1364137A (en) 1974-08-21

Family

ID=26216605

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4133072A Expired GB1364137A (en) 1971-09-09 1972-09-06 1,3,4-oxadiazolone derivatives

Country Status (20)

Country Link
JP (2) JPS5248987B2 (en)
AR (1) AR194500A1 (en)
AT (3) AT317888B (en)
AU (1) AU463690B2 (en)
BE (1) BE788612A (en)
CA (1) CA986122A (en)
CH (3) CH561014A5 (en)
DE (1) DE2244237A1 (en)
DK (1) DK131676C (en)
EG (1) EG10717A (en)
ES (4) ES406548A1 (en)
GB (1) GB1364137A (en)
HU (1) HU165428B (en)
IL (1) IL40321A (en)
IT (1) IT967312B (en)
NL (1) NL7211949A (en)
OA (1) OA04166A (en)
RO (1) RO62265A (en)
SE (1) SE376234B (en)
SU (1) SU496735A3 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0354622A1 (en) * 1988-08-11 1990-02-14 Shell Internationale Researchmaatschappij B.V. Oxadiazolone herbicides

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2222378B1 (en) * 1973-03-22 1976-11-05 Rhone Poulenc Ind
JPS5218302A (en) * 1975-08-01 1977-02-10 Fuji Photo Film Co Ltd Magnetic sheet recording/playing method
JPS5228697A (en) * 1975-08-29 1977-03-03 Hitachi Maxell Ltd Production method of magnetic powder
JPS60171887A (en) * 1984-02-15 1985-09-05 Matsushita Electric Ind Co Ltd Solid-state color image pickup device
JPS6224896U (en) * 1985-07-30 1987-02-16
JPS6356078U (en) * 1986-09-30 1988-04-14
JP3135741B2 (en) * 1993-05-07 2001-02-19 富士写真フイルム株式会社 Abrasive body
DE19822316A1 (en) * 1998-05-19 1999-11-25 Clariant Gmbh Process for the preparation of arylhydrazines
EA039048B1 (en) 2016-03-15 2021-11-26 Сионоги Энд Ко., Лтд. Method for producing phenoxyethanol derivatives

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0354622A1 (en) * 1988-08-11 1990-02-14 Shell Internationale Researchmaatschappij B.V. Oxadiazolone herbicides

Also Published As

Publication number Publication date
DK131676B (en) 1975-08-18
IL40321A0 (en) 1972-11-28
AR194500A1 (en) 1973-07-23
CH555355A (en) 1974-10-31
JPS5248987B2 (en) 1977-12-14
JPS50140447A (en) 1975-11-11
ES406550A1 (en) 1975-09-01
ES406549A1 (en) 1976-01-16
RO62265A (en) 1977-09-15
AT317888B (en) 1974-09-25
DE2244237A1 (en) 1973-03-15
ES406551A1 (en) 1976-01-16
IL40321A (en) 1975-03-13
AT317887B (en) 1974-09-25
IT967312B (en) 1974-02-28
AT329917B (en) 1976-06-10
BE788612A (en) 1973-03-08
SE376234B (en) 1975-05-12
AU4637272A (en) 1974-03-14
JPS538699B2 (en) 1978-03-31
CA986122A (en) 1976-03-23
CH561014A5 (en) 1975-04-30
DK131676C (en) 1976-01-19
NL7211949A (en) 1973-03-13
ES406548A1 (en) 1976-01-16
ATA930373A (en) 1975-08-15
OA04166A (en) 1979-12-15
CH555849A (en) 1974-11-15
AU463690B2 (en) 1975-07-31
HU165428B (en) 1974-08-28
SU496735A3 (en) 1975-12-25
JPS4839639A (en) 1973-06-11
EG10717A (en) 1976-05-31

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee