FR2408601A1 - Procede d'acylation d'une aniline substituee par une lactone en l'absence d'accepteur d'acide - Google Patents

Procede d'acylation d'une aniline substituee par une lactone en l'absence d'accepteur d'acide

Info

Publication number
FR2408601A1
FR2408601A1 FR7830402A FR7830402A FR2408601A1 FR 2408601 A1 FR2408601 A1 FR 2408601A1 FR 7830402 A FR7830402 A FR 7830402A FR 7830402 A FR7830402 A FR 7830402A FR 2408601 A1 FR2408601 A1 FR 2408601A1
Authority
FR
France
Prior art keywords
absence
acid acceptor
gammabutyrolactone
dimethylphenylamino
lactone
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.)
Granted
Application number
FR7830402A
Other languages
English (en)
Other versions
FR2408601B1 (fr
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.)
Chevron USA Inc
Original Assignee
Chevron Research and Technology Co
Chevron Research 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 Chevron Research and Technology Co, Chevron Research Co filed Critical Chevron Research and Technology Co
Publication of FR2408601A1 publication Critical patent/FR2408601A1/fr
Application granted granted Critical
Publication of FR2408601B1 publication Critical patent/FR2408601B1/fr
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D307/32—Oxygen atoms
    • C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • 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
    • C07D333/26—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 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
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/36—Nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

L'INVENTION CONCERNE UN PROCEDE D'ACYLATION D'UNE ANILINE SUBSTITUEE PAR UNE LACTONE EN L'ABSENCE D'ACCEPTEUR D'ACIDE. LE PROCEDE CONSISTE A FAIRE REAGIR, EN L'ABSENCE D'UN ACCEPTEUR D'ACIDE, UN HALOGENURE D'ACYLE AVEC UNE GAMMA-BUTYROLACTONE SUBSTITUEE PAR DE L'ANILINE EN PRESENCE D'UN SOLVANT NON BASIQUE, A UNE TEMPERATURE DE 65 A 150C. AINSI, ON PREPARE LA 3-(N-CHLORACETYL-N-2,6-DIMETHYLPHENYLAMINO)- GAMMABUTYROLACTONE PAR UN PROCEDE QUI CONSISTE A FAIRE ENTRER, EN L'ABSENCE D'UNE ADDITION D'ACCEPTEUR D'ACIDE, DU CHLORURE DE CHLORACETYLE EN CONTACT AVEC LA 3-(N-2,6-DIMETHYLPHENYLAMINO) GAMMABUTYROLACTONE EN PRESENCE D'UN SOLVANT ORGANIQUE NON BASIQUE, A UNE TEMPERATURE DE 65 A 150C. LA 3-(N-2,6-DIMETHYLPHENYLAMINO)- GAMMABUTYROLACTONE EST FORMEE DE PREFERENCE PAR REACTION D'A-BROMOGAMMABUTYROLACTONE AVEC LA DIMETHYLANILINE EN PRESENCE D'EAU DANS UN SOLVANT ORGANIQUE NON BASIQUE ET LA PHASE ORGANIQUE CONTENANT LA 3-(N-2,6-DIMETHYLPHENYLAMINO)- GAMMABUTYROLACTONE EST SOUMISE DIRECTEMENT, APRES SEPARATION, A L'OPERATION D'ACETYLATION. LES COMPOSES PREPARES PAR LE COMPOSE DE L'INVENTION SONT DOUES NOTAMMENT DE PROPRIETES FONGICIDES.
FR7830402A 1977-11-01 1978-10-25 Procede d'acylation d'une aniline substituee par une lactone en l'absence d'accepteur d'acide Granted FR2408601A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US84750477A 1977-11-01 1977-11-01

Publications (2)

Publication Number Publication Date
FR2408601A1 true FR2408601A1 (fr) 1979-06-08
FR2408601B1 FR2408601B1 (fr) 1983-08-12

Family

ID=25300794

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7830402A Granted FR2408601A1 (fr) 1977-11-01 1978-10-25 Procede d'acylation d'une aniline substituee par une lactone en l'absence d'accepteur d'acide

Country Status (7)

Country Link
JP (1) JPS5470260A (fr)
BR (1) BR7807190A (fr)
CH (1) CH639966A5 (fr)
DE (1) DE2847075A1 (fr)
FR (1) FR2408601A1 (fr)
GB (1) GB2006783B (fr)
IT (1) IT1100884B (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2407210A1 (fr) * 1977-11-01 1979-05-25 Chevron Res Nouvelles 3-(n-acyl-n-arylamino)-gamma-butyro (thio)-lactones et leurs applications a la lutte fongicide
FR2415634A1 (fr) * 1978-01-28 1979-08-24 Ciba Geigy Ag Nouvelles 3-(n-hydroxyacetyl-n-phenyl)-amino-tetrahydro-2-furanones utiles comme agents microbicides
FR2485013A1 (fr) * 1980-06-23 1981-12-24 Chevron Res Procede de production de 3-(n-aryl-n-acylamino)-gamma-butyrothiolates et produits obtenus

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0016985A1 (fr) * 1979-03-16 1980-10-15 F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft Anilides substitués, procédés pour leur préparation, fongicides contenant de tels composés et utilisation de tels composés ou fongicides dans la lutte contre les champignons des plantes
US4289701A (en) * 1979-11-13 1981-09-15 Chevron Research Lactone substituted aniline preparation
DK13681A (da) * 1980-01-31 1981-08-01 Hoffmann La Roche Substituerede anilider
US4721797A (en) * 1986-09-02 1988-01-26 Ciba-Geigy Corporation Process for the preparation of N-acyl-N-alkyl-2,6-dialkyl-3-chloroanilines

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3933860A (en) * 1975-02-10 1976-01-20 Chevron Research Company 3-(N-acyl-N-arylamino) lactones

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH587605A5 (fr) * 1974-04-01 1977-05-13 Ciba Geigy Ag
US4147792A (en) * 1977-02-04 1979-04-03 Ciba-Geigy Corporation Fungicidal compositions

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3933860A (en) * 1975-02-10 1976-01-20 Chevron Research Company 3-(N-acyl-N-arylamino) lactones

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
HW1958 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2407210A1 (fr) * 1977-11-01 1979-05-25 Chevron Res Nouvelles 3-(n-acyl-n-arylamino)-gamma-butyro (thio)-lactones et leurs applications a la lutte fongicide
FR2433524A1 (fr) * 1977-11-01 1980-03-14 Chevron Res Nouvelles 3-(n-acyl-n-arylamino-gamma-butyrothiolactones et leurs applications a la lutte fongicide
FR2415634A1 (fr) * 1978-01-28 1979-08-24 Ciba Geigy Ag Nouvelles 3-(n-hydroxyacetyl-n-phenyl)-amino-tetrahydro-2-furanones utiles comme agents microbicides
FR2485013A1 (fr) * 1980-06-23 1981-12-24 Chevron Res Procede de production de 3-(n-aryl-n-acylamino)-gamma-butyrothiolates et produits obtenus

Also Published As

Publication number Publication date
FR2408601B1 (fr) 1983-08-12
JPS5470260A (en) 1979-06-05
CH639966A5 (de) 1983-12-15
DE2847075A1 (de) 1979-05-10
IT7829299A0 (it) 1978-10-31
GB2006783A (en) 1979-05-10
GB2006783B (en) 1982-02-03
IT1100884B (it) 1985-09-28
BR7807190A (pt) 1979-06-12

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