ES397215A1 - Biocidal pyridine derivatives - Google Patents

Biocidal pyridine derivatives

Info

Publication number
ES397215A1
ES397215A1 ES397215A ES397215A ES397215A1 ES 397215 A1 ES397215 A1 ES 397215A1 ES 397215 A ES397215 A ES 397215A ES 397215 A ES397215 A ES 397215A ES 397215 A1 ES397215 A1 ES 397215A1
Authority
ES
Spain
Prior art keywords
general formula
biocidal
pyridine derivatives
equal
radical
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
ES397215A
Other languages
Spanish (es)
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.)
Evonik Operations GmbH
Original Assignee
TH Goldschmidt AG
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 TH Goldschmidt AG filed Critical TH Goldschmidt AG
Publication of ES397215A1 publication Critical patent/ES397215A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Cosmetics (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Procedure for obtaining pyridine-derived biocidal compounds of the general formula **(See formula)** where X represents a hydrogen radical or a bromine radical in the 5th or 6th position of the pyridine ring, n is equal to 2 or 3 and 1 is equal to 0, 1 or 2, characterized in that the reaction is caused chemistry of 1 mole of the compound of the general formula, **(See formula)** wherein Y represents a chlorine or bromine radical, with 1 to 4 moles of an amine of the general formula C8H17 [NH- (CH2) n] m -NH2 wherein n and m have the indicated significance at a temperature between 100 and 180ºC, in the presence of an acid acceptor. (Machine-translation by Google Translate, not legally binding)
ES397215A 1970-11-10 1971-11-09 Biocidal pyridine derivatives Expired ES397215A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19702055209 DE2055209C3 (en) 1970-11-10 1970-11-10 Microbicidal pyridine derivatives

Publications (1)

Publication Number Publication Date
ES397215A1 true ES397215A1 (en) 1974-05-01

Family

ID=5787665

Family Applications (1)

Application Number Title Priority Date Filing Date
ES397215A Expired ES397215A1 (en) 1970-11-10 1971-11-09 Biocidal pyridine derivatives

Country Status (9)

Country Link
AT (1) AT310168B (en)
BE (1) BE775057A (en)
CH (1) CH560685A5 (en)
DE (1) DE2055209C3 (en)
ES (1) ES397215A1 (en)
FR (1) FR2113695A5 (en)
GB (1) GB1317353A (en)
IT (1) IT1050194B (en)
NL (1) NL7115467A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004077954A1 (en) 2003-03-05 2004-09-16 Byocoat Enterprises, Inc., Antimicrobial solution and process

Also Published As

Publication number Publication date
DE2055209C3 (en) 1974-11-21
GB1317353A (en) 1973-05-16
NL7115467A (en) 1972-05-15
DE2055209A1 (en) 1972-05-25
FR2113695A5 (en) 1972-06-23
AT310168B (en) 1973-09-25
CH560685A5 (en) 1975-04-15
BE775057A (en) 1972-03-01
DE2055209B2 (en) 1974-04-18
IT1050194B (en) 1981-03-10

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