CH202661A - Process for the preparation of an azo compound of acidic character. - Google Patents

Process for the preparation of an azo compound of acidic character.

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Publication number
CH202661A
CH202661A CH202661DA CH202661A CH 202661 A CH202661 A CH 202661A CH 202661D A CH202661D A CH 202661DA CH 202661 A CH202661 A CH 202661A
Authority
CH
Switzerland
Prior art keywords
sep
azo compound
preparation
acidic character
acid
Prior art date
Application number
Other languages
German (de)
Inventor
Schering A G
Original Assignee
Schering 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 Schering Ag filed Critical Schering Ag
Publication of CH202661A publication Critical patent/CH202661A/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Darstellung einer     Azoverbindung        sauren-Charakters.            Durch    die     DRP    Nr. 607587, Nr. 610320  und Nr. 638701 sind bereits     Verbindungen    be  kannt geworden,     in    denen des     eine    an die       Azobrüeke        gebundene        Keims.    eine in     p-Stel-          lung    oder zwei in beliebiger Stellung     befind-          liche        Sulfonsäureamidgruppen    besitzt,

       wäh-          rend        der        andere    an die     Azobrücke        gebundene          Rest        ausser        andern    Gruppen ein     kerngebun-          denes        Stickstoffatom,    das     ringförmig    gebun  den sein     kann,    besitzen     mmss.     



       Es    wurde     nun        gefunden,        .dass        im        ldtzt-          genannten    Kern     die        Anwesenheit    ödes gefor  derten kerngebundenen oder auch     ringförmig     gebundenen     ,Stiekstoffatomes    nicht erforder  lich ist,     um    zu     hochbaiktericiden    Verbindun  gen zu gelangen.

   Im Gegenteil     zeichnen        sieb     die nach vorliegenden Verfahren     erhaltenen          Verbindungen    durch ihre     besonderen        bakte-          riziden    Eigenschaften aus.

   Als     Kupplungs-          komponente        werden        kupplungsfähige        stiek-          stoiefreie        Verbindungen    der     Naphthalinreihe,          insbesondere        Naphtholsulfonsäuren        benutzt.     



  Als     diazotierte        Komponenten    mit einer  
EMI0001.0064     
  
    Sulfons@äureamidgruppe <SEP> eignen <SEP> sich <SEP> die <SEP> in
<tb>  den <SEP> obergenannten <SEP> Patentschriften <SEP> bereits
<tb>  beschriebenen <SEP> Verbindungen, <SEP> wie <SEP> p-Amino  benzolsulfonamid, <SEP> p-Aminabenzohsulfo#nalkyl  amde <SEP> und <SEP> andere.
<tb>  



  Die <SEP> neuen <SEP> Verbindungen, <SEP> .zeichnen <SEP> sich
<tb>  ausserdem <SEP> durch <SEP> die <SEP> hohe <SEP> Wasserlöslichkeit
<tb>  iluer <SEP> Salze <SEP> und <SEP> Neutralität <SEP> voji <SEP> deren <SEP> Lösun  gen: <SEP> aus, <SEP> die <SEP> sie <SEP> besonders <SEP> geeignet <SEP> zur <SEP> in  travenösen, <SEP> Anwendung <SEP> erscheinen <SEP> lassen.
<tb>  



  Gegenstand <SEP> des <SEP> vorliegenden <SEP> Patentes <SEP> ist
<tb>  nun <SEP> ein <SEP> Verfahren <SEP> zur <SEP> Herstellung <SEP> einer
<tb>  Azoverbindung <SEP> sauren <SEP> Charakters., <SEP> dadurch
<tb>  gekennzeichnet, <SEP> dass <SEP> . <SEP> man <SEP> diazotiertes <SEP> 4  Amino#benzolsulfonamid <SEP> mit <SEP> 2-Naphthol-6. <SEP> 8  disulfons@ärure <SEP> kuppelt. <SEP> Die <SEP> neue <SEP> Verbindung
<tb>  ist <SEP> die <SEP> 4-Sulfamido-phenylazo-1'-(2'-ogynaph  thalin-6',8'adisulfons;äure). <SEP> Sie <SEP> soll <SEP> als. <SEP> Arz  neimittel <SEP> Verwendung <SEP> finden. <SEP>   <I>Beispiel:

  </I>
<tb>  Durch <SEP> Kupplung <SEP> einer <SEP> Lösung <SEP> von <SEP> 17,2 <SEP> g
<tb>  diazotiertem <SEP> 4-Aminobenzolsulfonamid <SEP> und       
EMI0002.0001     
  
    einer <SEP> Lösung <SEP> von <SEP> 34,$ <SEP> g <SEP> 2-naphthol-6 <SEP> . <SEP> $  disu-Ifonoaurem <SEP> Natrium <SEP> wird <SEP> nach <SEP> üblicher
<tb>  Aufarbeitung,das <SEP> Dinatriumsalz <SEP> der <SEP> 4-,Sulf  amidophenylazo-1'-(2'-oxynaphthalin-6',8'-di  sulfonsäure) <SEP> in <SEP> orange <SEP> roten, <SEP> wasserlöslichen,
<tb>  in <SEP> organisohen <SEP> Lösungsmitteln <SEP> unlöslichen
<tb>  Nadeln <SEP> erhalten. <SEP> Die <SEP> Ausbeute <SEP> beträgt <SEP> 38 <SEP> g.



  Process for the preparation of an azo compound of acidic character. Through the DRP No. 607587, No. 610320 and No. 638701, compounds have already become known in which the one germ bound to the azo bridge. has one in the p-position or two sulfonic acid amide groups in any position,

       while the other radical bonded to the azo bridge, apart from other groups, have a nucleus-bonded nitrogen atom which can be bonded in a ring shape.



       It has now been found that in the ldtzt-mentioned core the presence of desolate, required core-bound or ring-shaped bound nitrogen atoms is not necessary in order to achieve highly alkaline compounds.

   On the contrary, the compounds obtained by the present process are distinguished by their particular bactericidal properties.

   Coupling components that are capable of coupling, stalk-free compounds of the naphthalene series, in particular naphtholsulfonic acids, are used.



  As diazotized components with a
EMI0001.0064
  
    Sulfonic @ acid amide group <SEP> are suitable <SEP> are <SEP> the <SEP> in
<tb> the <SEP> above <SEP> patent specifications <SEP> already
<tb> described <SEP> compounds, <SEP> such as <SEP> p-Amino benzenesulfonamide, <SEP> p-Aminabenzohsulfo # nalkyl amde <SEP> and <SEP> others.
<tb>



  The <SEP> new <SEP> connections, <SEP> .mark <SEP> themselves
<tb> also <SEP> through <SEP> the <SEP> high <SEP> water solubility
<tb> iluer <SEP> salts <SEP> and <SEP> neutrality <SEP> voji <SEP> their <SEP> solutions: <SEP> off, <SEP> the <SEP> they <SEP> especially <SEP> suitable <SEP> for <SEP> in intravenous, <SEP> application <SEP> make <SEP> appear.
<tb>



  The subject of <SEP> of the <SEP> present <SEP> patent <SEP> is
<tb> now <SEP> a <SEP> process <SEP> for <SEP> production <SEP> a
<tb> Azo compound <SEP> acidic <SEP> character., <SEP> thereby
<tb> marked, <SEP> that <SEP>. <SEP> man <SEP> diazotized <SEP> 4 amino # benzenesulfonamide <SEP> with <SEP> 2-naphthol-6. <SEP> 8 disulfons @ ärure <SEP> couples. <SEP> The <SEP> new <SEP> connection
<tb> <SEP> is the <SEP> 4-sulfamido-phenylazo-1 '- (2'-ogynaph thalin-6', 8'adisulfonic acid). <SEP> you <SEP> should <SEP> as. <SEP> Medicines <SEP> Find use <SEP>. <SEP> <I> Example:

  </I>
<tb> Through <SEP> coupling <SEP> of a <SEP> solution <SEP> of <SEP> 17.2 <SEP> g
<tb> diazotized <SEP> 4-aminobenzenesulfonamide <SEP> and
EMI0002.0001
  
    a <SEP> solution <SEP> of <SEP> 34, $ <SEP> g <SEP> 2-naphthol-6 <SEP>. <SEP> $ disu-Ifonoaurem <SEP> Sodium <SEP> becomes more common <SEP> after <SEP>
<tb> Work-up, the <SEP> disodium salt <SEP> the <SEP> 4-, sulfamidophenylazo-1 '- (2'-oxynaphthalene-6', 8'-disulfonic acid) <SEP> in <SEP> orange < SEP> red, <SEP> water-soluble,
<tb> Insoluble in <SEP> organic <SEP> solvents <SEP>
<tb> needles <SEP> received. <SEP> The <SEP> yield <SEP> is <SEP> 38 <SEP> g.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung einer Azo- verbindung sauren Charakters, dadurch ge- EMI0002.0006 kennzeichnet, <SEP> daU <SEP> mau <SEP> cliazotiertes <SEP> 4-Amino ben:zolsulfonamid <SEP> mit <SEP> 2.-Naphthol-6.8-di sulfonsäure <SEP> kuppelt. <tb> Die <SEP> neue <SEP> Verbindung, <SEP> die <SEP> 4-Sulfa.mido phenylazo-1'-(2'-oxynaphthaJin-6',8'-.di6ulfo#n säure) <SEP> stellt <SEP> in <SEP> Form <SEP> ihres <SEP> Dinatriumsalzes <tb> orangerote, <SEP> wasserlösliche, <SEP> in <SEP> organischen <SEP> Lö sungsmitteln <tb> Nadeln <SEP> dar. PATENT CLAIM: Process for the production of an azo compound of acidic character, thereby EMI0002.0006 indicates, <SEP> daU <SEP> mau <SEP> cliazotized <SEP> 4-amino ben: zolsulfonamide <SEP> couples with <SEP> 2.-naphthol-6.8-disulfonic acid <SEP>. <tb> The <SEP> new <SEP> compound, <SEP> the <SEP> 4-sulfa.mido phenylazo-1 '- (2'-oxynaphthaJin-6', 8 '-. di6ulfo # n acid) <SEP > represents <SEP> in <SEP> form <SEP> of your <SEP> disodium salt <tb> orange-red, <SEP> water-soluble, <SEP> in <SEP> organic <SEP> solvents <tb> needles <SEP>.
CH202661D 1936-12-30 1937-12-08 Process for the preparation of an azo compound of acidic character. CH202661A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE202661X 1936-12-30

Publications (1)

Publication Number Publication Date
CH202661A true CH202661A (en) 1939-01-31

Family

ID=5772598

Family Applications (1)

Application Number Title Priority Date Filing Date
CH202661D CH202661A (en) 1936-12-30 1937-12-08 Process for the preparation of an azo compound of acidic character.

Country Status (1)

Country Link
CH (1) CH202661A (en)

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