CH102277A - Process for the preparation of a new pyrazolone derivative. - Google Patents

Process for the preparation of a new pyrazolone derivative.

Info

Publication number
CH102277A
CH102277A CH102277DA CH102277A CH 102277 A CH102277 A CH 102277A CH 102277D A CH102277D A CH 102277DA CH 102277 A CH102277 A CH 102277A
Authority
CH
Switzerland
Prior art keywords
acetic acid
hot
new
parts
preparation
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH102277A publication Critical patent/CH102277A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole 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
    • C07D231/18One oxygen or sulfur atom
    • C07D231/20One oxygen atom attached in position 3 or 5
    • C07D231/22One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
    • C07D231/261-Phenyl-3-methyl-5- pyrazolones, unsubstituted or substituted on the phenyl ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Herstellung eines neuen     Pyrazolonderivates.       Es wurde     gefunden,    dass sich das     m-Ami-          dobenzolsulfa,mid        @duröh        Dia,zotieren    und hier  auf durch Reduzieren der     Diazaverbindung     in das     m-Sulfamidophenylhydrazin    überfüh  ren lässt,     welches    mit     Acetessigester    zum     1-          (3'-Sulfaanido)-phonyl-3-methyl-    5     -pyrazolon     kondensiert werden kann.

   Dieses ist ein wert  voller     Ausgangsstoff    zur Herstellung von  Farbstoffen und pharmazeutischen Produk  ten.  



       Beisyriel:     17,2 Gewichtsteile m -     Amidobenzolsulf-          amid,    in 25 Teilen     kochendem        Wasser    gelöst,  werden mit 28 Gewichtsteilen konzentrierter  Salzsäure versetzt und mit Eis und 7 Teilen  Nitrit bei 0       diazatiert.    Die     Diazolösung     giesst man .zu einer auf<B>10'</B> gekühlten wässe  rigen     Sulfitlösung,    enthaltend 25 Teile     Na-          triumbisulfit    und 20 Teile konzentrierte Na  tronlauge.

   Die erstgelbe, bald fast farblos  werdende Lösung wird bis zur beginnenden       Kristallisation    eingedampft und noch heiss  mit 20 Teilen konzentrierter Salzsäure ver  setzt. Nach dem Abtreiben der schwefligen  Säure     überlässt    man die Lösung der Kristalli-         sation,    wobei sich in guter Ausbeute das     m-          Sulfamidophenylhydrazin    als inneres . Salz       abscheidet.     



  Zur Kondensation mit     Acetessigester     braucht die     Hydrazinverbindung    nicht abge  schieden zu werden, sondern man verwendet  die von der schwefligen Säure befreite, abge  kühlte Lösung, neutralisiert sie mit Soda bis  zur eben noch kongosauren Reaktion, ver  dünnt sie ,auf 150-200 Teile und versetzt  sie nach und nach mit 13 Teilen     Acetessig-          ester,    wobei das     m-Sulfamidophenylhydrazon          ,des        Acetessi.gesters    anfangs etwas harzig,  bald aber kristallinisch ausfällt.

   Durch all  mählichen Zusatz von 26 Teilen konzentrier  ter Natronlauge geht dieses mit leicht gelb  lich-bräunlieher Farbe in Lösung und wird  beim Erwärmen ,auf etwa<B>60'</B> in das     1-(3'-          Sulfa-mido)-phenyl-3-methyl-5-pyrazolon    ver  wandelt, das durch Versetzen .mit 23 Teilen  konzentrierter !Salzsäure bis zur eben kongo  sauren Reaktion anfangs etwas harzig, bald  aber fest werdend, gefällt wird. Durch Um  kristallisieren ,aus viel kochendem Wasser.  oder aus verdünnter Essigsäure, aus Nitro-           Benzol        usw.,    kann es vollständig gereinigt  werden. Es bildet leicht     gelbliche    Kristalle  vom F.

   P. 199  , ist schwer löslich in kaltem       Wasser,    Alkohol, verdünnter Essigsäure, Ni  trobenzol, ziemlich schwer löslich in heissem  -Wasser oder Alkohol, leicht löslich in heisser,  verdünnter Essigsäure oder heissem     Nitroben-          zol,    und ebenfalls leicht löslich in wässerigen       Alkalien    und Mineralsäuren.



  Process for the preparation of a new pyrazolone derivative. It has been found that the m-Amidobenzolsulfa, mid @ duröh Dia, can be converted here by reducing the diaza compound into the m-Sulfamidophenylhydrazine, which with acetoacetate to 1- (3'-sulfaanido) -phonyl- 3-methyl-5-pyrazolone can be condensed.

   This is a valuable raw material for the manufacture of dyes and pharmaceutical products.



       For example: 17.2 parts by weight of m-amidobenzene sulfamide, dissolved in 25 parts of boiling water, are mixed with 28 parts by weight of concentrated hydrochloric acid and diazatized at 0 with ice and 7 parts of nitrite. The diazo solution is poured into an aqueous sulfite solution, cooled to 10%, containing 25 parts of sodium bisulfite and 20 parts of concentrated sodium hydroxide solution.

   The first yellow, soon becoming almost colorless solution is evaporated until crystallization begins and is still hot with 20 parts of concentrated hydrochloric acid. After the sulphurous acid has been driven off, the solution is left to crystallize, with the m-sulfamidophenylhydrazine being the internal one in good yield. Salt separates.



  For condensation with acetoacetic ester, the hydrazine compound does not need to be separated, but you use the freed from the sulphurous acid, cooled solution, neutralize it with soda until the Congo acid reaction is just a little bit, dilute it to 150-200 parts and add it gradually with 13 parts of acetoacetic ester, the m-sulfamidophenylhydrazone, of acetoaceti.gesters, initially somewhat resinous, but soon precipitating crystalline.

   The gradual addition of 26 parts of concentrated sodium hydroxide solution dissolves it with a slightly yellowish-brownish color and, when heated to about <B> 60 '</B>, becomes the 1- (3'-sulfa-mido) - phenyl-3-methyl-5-pyrazolone, which is initially somewhat resinous, but soon solidifies, by adding 23 parts of concentrated hydrochloric acid to the Congo-acidic reaction. By order to crystallize, from plenty of boiling water. or from dilute acetic acid, from nitro-benzene, etc., it can be completely cleaned. It forms slightly yellowish crystals of F.

   P. 199, is sparingly soluble in cold water, alcohol, dilute acetic acid, nitrobenzene, fairly sparingly soluble in hot water or alcohol, easily soluble in hot, dilute acetic acid or hot nitrobenzene, and also easily soluble in aqueous alkalis and Mineral acids.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Pyrazolonderivates, dadurch gekennzeichnet, class man .das m-Amidobenzolsulfamid durch Diazotieren und hierauf durch Reduzieren der Diazoverbindung in das m-Sulfamidophe- nylhy drazin überführt und dieses mit Aeei_:- essigester kondensiert. PATENT CLAIM: Process for the production of a new pyrazolone derivative, characterized in that the m-amidobenzene sulfamide is converted into the m-sulfamidophenylhydrazine by diazotization and then by reducing the diazo compound and this is condensed with acetic acid ester. Das neue Pyra.zolon- derivat: 1-(3'-Sulfa.mido)-phenyl-3-methyl-ä- pyrazolon bildet leicht gelbliche Kristalle vom F. P. 199 , ist schwer löslich in kaltem Wasser, Alkohol, verdünnter Essigsäure, Ni trobenzol, ziemlich schwer löslich in heissem Wasser oder Alkohol, leicht löslich in heisser, verdünnter Essigsäure oder heissem Nitroben- zol und ebenfalls leicht löslich in wässerigen Alkalien und Mineralsäuren. The new pyra.zolone derivative: 1- (3'-sulfa.mido) -phenyl-3-methyl-a-pyrazolone forms slightly yellowish crystals of FP 199, is sparingly soluble in cold water, alcohol, dilute acetic acid, and nitrobenzene , rather sparingly soluble in hot water or alcohol, easily soluble in hot, dilute acetic acid or hot nitrobenzene and also easily soluble in aqueous alkalis and mineral acids.
CH102277D 1922-11-11 1922-11-11 Process for the preparation of a new pyrazolone derivative. CH102277A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH102277T 1922-11-11

Publications (1)

Publication Number Publication Date
CH102277A true CH102277A (en) 1924-01-02

Family

ID=4360827

Family Applications (1)

Application Number Title Priority Date Filing Date
CH102277D CH102277A (en) 1922-11-11 1922-11-11 Process for the preparation of a new pyrazolone derivative.

Country Status (1)

Country Link
CH (1) CH102277A (en)

Similar Documents

Publication Publication Date Title
CH102277A (en) Process for the preparation of a new pyrazolone derivative.
CH104472A (en) Process for the preparation of a new pyrazolone derivative.
CH104469A (en) Process for the preparation of a new pyrazolone derivative.
CH104467A (en) Process for the preparation of a new pyrazolone derivative.
CH104471A (en) Process for the preparation of a new pyrazolone derivative.
CH104468A (en) Process for the preparation of a new pyrazolone derivative.
CH104470A (en) Process for the preparation of a new pyrazolone derivative.
CH104473A (en) Process for the preparation of a new pyrazolone derivative.
AT152837B (en) Process for the preparation of 2.4-dioxo-3.3-dialkyl-1.2.3.4-tatrahydropyridines.
DE539806C (en) Process for the preparation of isopropylallylbarbituric acid
CH204708A (en) Process for the preparation of an amino alcohol.
AT129783B (en) Process for the preparation of 2-oxymethylbenzimidazolaric acids.
DE740249C (en) Process for the preparation of aryl-methyl-pyrazolones
DE484763C (en) Process for the preparation of mercury compounds of the pyrazolone series
AT69290B (en) Process for the preparation of yellow azo dyes.
AT52937B (en) Process for the preparation of 3-nitro-4-oxyarylarsinic acids.
CH237779A (en) Process for the preparation of 1- (2&#39;-sulfo-phenyl) -5-methyl-pyrazolone- (3).
CH143889A (en) Process for the preparation of an o-cyanarylrhodane compound.
CH171984A (en) Process for the preparation of an azo compound.
CH107521A (en) Process for the production of a new azo dye.
CH122759A (en) Process for the production of a new indigoid dye.
CH107520A (en) Process for the production of a new azo dye.
CH168010A (en) Process for the preparation of 1-phenyl-3-methyl-4-sec-butylpyrazolone.
CH143891A (en) Process for the preparation of an o-cyanarylrhodane compound.
CH181160A (en) Process for the preparation of a new heterocyclic sulfonic acid.