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ES429319A1 - Pyridine derivatives - Google Patents

Pyridine derivatives

Info

Publication number
ES429319A1
ES429319A1 ES429319A ES429319A ES429319A1 ES 429319 A1 ES429319 A1 ES 429319A1 ES 429319 A ES429319 A ES 429319A ES 429319 A ES429319 A ES 429319A ES 429319 A1 ES429319 A1 ES 429319A1
Authority
ES
Spain
Prior art keywords
formula
see formula
see
pyridine derivatives
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
ES429319A
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.)
A Christiaens SA
Original Assignee
A Christiaens 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
Application filed by A Christiaens SA filed Critical A Christiaens SA
Publication of ES429319A1 publication Critical patent/ES429319A1/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/70—Sulfur atoms
    • C07D213/71—Sulfur atoms to which a second hetero atom is attached

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A procedure for preparing 2-phenylaminopyridine derivatives of the formula: **(See formula)** wherein R1 represents an amino radical or an acylamino radical, R2, R3, R4, R5 and R6 each represent hydrogen or a chlorine, nitro, alcohol or trifluoromethyl group, which comprises reacting a 2-chloro-pyridin-3- sulfonamide or a 2-chloropyridin-3-N-acylsulfonamide of the formula: **(See formula)** wherein R1 has the meanings indicated above with a substituted aromatic amine of the formula: **(See formula)** where R2, R3, R4, and R5 have the meanings given above, in the presence of copper powder, by heating to temperatures of 150-200ºC, and as long as it is possible and desirable to form a salt by reaction with an inorganic or organic base. (Machine-translation by Google Translate, not legally binding)
ES429319A 1973-08-17 1974-08-16 Pyridine derivatives Expired ES429319A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3901873A GB1470780A (en) 1973-08-17 1973-08-17 Pyridine derivatives

Publications (1)

Publication Number Publication Date
ES429319A1 true ES429319A1 (en) 1976-08-16

Family

ID=10407102

Family Applications (1)

Application Number Title Priority Date Filing Date
ES429319A Expired ES429319A1 (en) 1973-08-17 1974-08-16 Pyridine derivatives

Country Status (10)

Country Link
JP (1) JPS5070371A (en)
AT (1) AT336016B (en)
BE (1) BE818618A (en)
DE (1) DE2438967A1 (en)
ES (1) ES429319A1 (en)
FR (1) FR2240733B1 (en)
GB (1) GB1470780A (en)
LU (1) LU70744A1 (en)
NL (1) NL7411012A (en)
SE (1) SE7410422L (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19824232A1 (en) * 1998-05-29 1999-12-02 Bayer Ag Pyridodithiazine dioxides

Also Published As

Publication number Publication date
FR2240733A1 (en) 1975-03-14
DE2438967A1 (en) 1975-02-20
BE818618A (en) 1975-02-10
NL7411012A (en) 1975-02-19
FR2240733B1 (en) 1978-07-28
LU70744A1 (en) 1974-12-10
SE7410422L (en) 1975-02-18
JPS5070371A (en) 1975-06-11
ATA664474A (en) 1976-08-15
GB1470780A (en) 1977-04-21
AT336016B (en) 1977-04-12

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