GB954213A - New therapeutically active sulphonamides and process for their preparation - Google Patents

New therapeutically active sulphonamides and process for their preparation

Info

Publication number
GB954213A
GB954213A GB2785760A GB2785760A GB954213A GB 954213 A GB954213 A GB 954213A GB 2785760 A GB2785760 A GB 2785760A GB 2785760 A GB2785760 A GB 2785760A GB 954213 A GB954213 A GB 954213A
Authority
GB
United Kingdom
Prior art keywords
aminobenzenesulphonamido
thiazole
methyl
compounds
therapeutically active
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
GB2785760A
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 GB954213A publication Critical patent/GB954213A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D277/38Nitrogen atoms
    • C07D277/50Nitrogen atoms bound to hetero atoms
    • C07D277/52Nitrogen atoms bound to hetero atoms to sulfur atoms, e.g. sulfonamides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention comprises monoazo compounds of formula <FORM:0954213/C3/1> wherein R1 is a hydrogen atom or an acetyl group, R is a heterocyclic residue containing either a nitrogen atom and a sulphur atom or two nitrogen atoms and A is an aromatic residue which may be substituted. The compounds are therapeutically active. They are prepared by coupling a diazotised aromatic amine with a compound of formula <FORM:0954213/C3/2> The compounds are light yellow in colour. In examples the preparation of the following compounds is described: 2-(p-aminobenzenesulphonamido) - 4 - methyl - 5 - (p - chlorophenylazo) - thiazole; 2 - (p - aminobenzenesulphonamido) - 4 - methyl - 5 - (phenylazo)-thiazole; 2 - (p - aminobenzenesulphonamido)- 4 - methyl - 5 - (p - tolylazo) - thiazole; 2 - (p-acetylaminobenzenesulphonamido) - 4 - methyl- 5 - (p - chlorophenylazo) - thiazole; 2 - (p - aminobenzenesulphonamido) - 4,6 - dimethyl- 5 - (phenylazo) - pyrimidine; 2 - (p - aminobenzenesulphonamido) - 4 - methyl - 5 - (p-ethoxyphenylazo) - thiazole; 2 - (p - aminobenzenesulphonamido) - 4 - methyl - 5 - (l-naphthylazo) - thiazole; 2 - (p - aminobenzenesulphonamido) - 5 - (p - chlorophenylazo) - thiazole and 2 - (p - aminobenzenesulphonamido)-4-phenyl-5-(p-tolylazo)-thiazole. Compounds of the above formula are therapeutically active and may be used in pharmaceutical compositions. Specified compositions are wound sprayings, ointments for eyes or wounds, aqueous suspensions, aerosols and enterosolvent dragees. The compounds are effective against strepto-, staphylo- and pneumo-cocci and have some action on strains of Staphylococcus aureus haemolyticus.
GB2785760A 1959-08-17 1960-08-11 New therapeutically active sulphonamides and process for their preparation Expired GB954213A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU30659 1959-08-17

Publications (1)

Publication Number Publication Date
GB954213A true GB954213A (en) 1964-04-02

Family

ID=10949015

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2785760A Expired GB954213A (en) 1959-08-17 1960-08-11 New therapeutically active sulphonamides and process for their preparation

Country Status (1)

Country Link
GB (1) GB954213A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4406661A (en) 1980-06-06 1983-09-27 Cassella Aktiengesellschaft Process for dyeing and printing synthetic, hydrophobic fibre material with dischargeable azo disperse dye

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4406661A (en) 1980-06-06 1983-09-27 Cassella Aktiengesellschaft Process for dyeing and printing synthetic, hydrophobic fibre material with dischargeable azo disperse dye

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