GB1505427A - Quinoline derivatives - Google Patents

Quinoline derivatives

Info

Publication number
GB1505427A
GB1505427A GB2328676A GB2328676A GB1505427A GB 1505427 A GB1505427 A GB 1505427A GB 2328676 A GB2328676 A GB 2328676A GB 2328676 A GB2328676 A GB 2328676A GB 1505427 A GB1505427 A GB 1505427A
Authority
GB
United Kingdom
Prior art keywords
optionally substituted
hydrogen
aralkyl
halogen
nitrogen
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
GB2328676A
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.)
Chinoin Private Co Ltd
Original Assignee
Chinoin Gyogyszer es Vegyeszeti Termekek Gyara Zrt
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 Chinoin Gyogyszer es Vegyeszeti Termekek Gyara Zrt filed Critical Chinoin Gyogyszer es Vegyeszeti Termekek Gyara Zrt
Publication of GB1505427A publication Critical patent/GB1505427A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • C07D215/233Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Quinoline Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

1505427 Quinoline derivatives CHINOIN GYOGYSZER ES VEGYASZETI TERMEKEK GYARA RT 4 June 1976 [6 June 1975] 23286/76 Heading C2C Novel quinoline derivatives having the general formula wherein n is 0 or 1; R is hydrogen, optionally substituted alkyl, optionally substituted alkenyl or optionally substituted aralkyl; R<SP>1</SP> is hydrogen, halogen, optionally substituted alkyl optionally substituted aryl, optionally substituted aralkyl, optionally substituted cycloalkyl of cycloalkylalkyl, optionally substituted amino, hydroxy, optionally substituted alkoxy, optionally substituted aralkoxy, optionally substituted acyl, nitro, carboxylic acid, carboxylic acid derivative, or an optionally substituted five-, six- or seven-membered heterocyclic ring containing one, two or three nitrogen heteroatoms and being attached to the quinoline ring through one of the nitrogen atoms; R<SP>2</SP> is hydrogen, halogen, optionally substituted alkyl, optionally substituted aralkyl, optionally substituted aryl, optionally substituted amino, nitro, hydroxy, optionally substituted alkoxy, optionally substituted aralkoxy or optionally substituted aryloxy; R<SP>3</SP> is hydrogen, halogen, optionally substituted alkyl, optionally substituted aralkyl, optionally substituted aryl, optionally substituted amino, hydroxyl, optionally substituted alkoxy, or optionally substituted aryloxy; or R<SP>2</SP> and R<SP>3</SP> may form together with the 5,6-, 6,7- or 7,8-side of the quinoline ring an optionally substituted five-, six- or seven-membered ring optionally containing one or two heteroatoms selected from oxygen, sulphur and nitrogen; and when n = 0, and R<SP>3</SP> is attached to 3-position of the quinoline ring, R<SP>3</SP> and R may form together an optionally substituted -(CH 2 ) m -chain, wherein: m is 2, 3 or 4; R<SP>4</SP> is hydrogen, optionally substituted alkyl, optionally substituted aryl, optionally substituted aralkyl or optionally substituted cycloalkyl or cycloalkylalkyl; R<SP>5</SP> is hydrogen, optionaly substituted alkyl, optionally substituted aryl or optionally substituted aralkyl; Y is an aromatic heterocyclic ring, containing a tertiary nitrogen atom, and being attached through the nitrogen, or Y is a trialkylamino group; Z is an anion; X is oxygen or sulphur, and salts thereof where such can exist, are prepared by either (a) reacting a compound of the formula with an aromatic tertiary base or trialkylamine YH in the presence of a halogen, or (b) reacting a compound of the formula with an aromatic tertiary base or trialkylamine YH, and optionally replacing the halide ion Z- with another anion. The above processes are preferably carried out at a temperature of from 50‹ to 150‹ C. The novel compounds possess fungicidal, insecticidal and herbicidal properties.
GB2328676A 1975-06-06 1976-06-04 Quinoline derivatives Expired GB1505427A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU75CI00001584A HU172342B (en) 1975-06-06 1975-06-06 Process for preparing pyridinium-alkanoyl-quinoline derivatives

Publications (1)

Publication Number Publication Date
GB1505427A true GB1505427A (en) 1978-03-30

Family

ID=10994569

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2328676A Expired GB1505427A (en) 1975-06-06 1976-06-04 Quinoline derivatives

Country Status (5)

Country Link
JP (1) JPS51146475A (en)
DK (1) DK247876A (en)
FI (1) FI761584A (en)
GB (1) GB1505427A (en)
HU (1) HU172342B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU1783492A (en) * 1991-05-30 1993-01-08 Tokyo Tanabe Company Limited Quinoline derivative and production thereof

Also Published As

Publication number Publication date
DK247876A (en) 1976-12-07
JPS51146475A (en) 1976-12-16
HU172342B (en) 1978-08-28
FI761584A (en) 1976-12-07

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Legal Events

Date Code Title Description
PS Patent sealed
746 Register noted 'licences of right' (sect. 46/1977)
PCNP Patent ceased through non-payment of renewal fee