CH205678A - Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine. - Google Patents

Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine.

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Publication number
CH205678A
CH205678A CH205678DA CH205678A CH 205678 A CH205678 A CH 205678A CH 205678D A CH205678D A CH 205678DA CH 205678 A CH205678 A CH 205678A
Authority
CH
Switzerland
Prior art keywords
amino
pyridine
para
benzene
benzenesulfamido
Prior art date
Application number
Other languages
French (fr)
Inventor
Rhone-Poulenc Societ Chimiques
Original Assignee
Rhone Poulenc Chemicals
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 Rhone Poulenc Chemicals filed Critical Rhone Poulenc Chemicals
Publication of CH205678A publication Critical patent/CH205678A/en

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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
    • C07D213/76Nitrogen atoms to which a second hetero atom is attached

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

Description

  

  Procédé de préparation de la     2-(para-amino-benzène-sulfamido)-pyridine.       La présente     invention    a pour objet un  procédé de préparation de la     2-(para-amino-          benzène-sulfamido)-pyridine,    ayant pour for  mule:  
EMI0001.0005     
    Ce composé fond à 190   C;     il    est peu so  luble à froid dans l'eau, l'acétone, l'alcool;  il présente des propriétés bactéricides mar  quantes et il est susceptible     d'applications     thérapeutiques.  



  Le procédé selon     l'invention    est carac  térisé en ce que l'on fait réagir de la     2-amino-          pyridine    avec     un        halogénure    de     para-acyle-          amino-benzène-sulfonyle,.    de manière à for  mer, en     éliminant    de l'halogénure d'hydro  gène, de la     2-i(para-acyle-amino-benzène-          sulfamido)-pyridine,    puis en ce que l'on sou  met ce dernier corps à une hydrolyse pour en  éliminer le groupe acyle et obtenir la     2-(para-          amino-benzène-sulfamido)

  -pyridine.       De préférence, on fait réagir de la     2-          amino-pyridine    avec du chlorure de para  ac6tyl-amino-benzène-sulfonyle. L'hydrolyse       dela        2-(para-acyle-amino-benzène-sulfamido)-          pyridine    peut être réalisée en milieu alcalin.  



  Voici quelques exemples d'exécution du  procédé de l'invention:    <I>Exemple 1:</I>    On dissout 9,4 g de     2-amino-pyridine    dans  20 cm' de     pyridine    sèche et on ajoute à cette       solution    23,5 g de chlorure de     p-acétyl-amino-          benzène-sulfonyle;    on chauffe le mélange  obtenu au bain de vapeur. On ajoute alors  de l'eau et le précipité de     2-(p-acétyl-amino-          benzène-sulfamido-)pyridine    - point de fu  sion     224'    C - est hydrolysé à l'ébullition  avec 175 cm' d'une solution 2N de soude  caustique.

   La solution est refroidie et rendue  juste acide au tournesol par addition d'acide  chlorhydrique 2N. Le précipité de     2-(p-amino-          benzène-sulfamido)-pyridine    est séparé et     re-          cristallisé    à l'eau.     Point    de     fusion   <B>190'</B> C.      <I>Exemple 2:</I>  4,7 g de     2-amino-pyridine    sont dissous  dans 20 cm' de benzène; on ajoute 12     g    de  chlorure de     p-acétyl-amino-benzène-sulfonyle     et on laisse reposer le mélange. Le solide qui  se sépare est filtré et bouilli pendant une  heure avec 90 cm' d'une solution de soude  caustique 2N.

   Par acidification avec l'acide  acétique dilué, on précipite la     2-(p-amino-          benzène-sulfamido)-pyridine,    que l'on     recris-          tallise    dans l'acétone. Point de fusion 190   C.  <I>Exemple 3:</I>  3 g de chlorure de     p-acétyl-amino-benzène-          sulfonyle    sont mis en suspension dans 5 cm'  de chloroforme et on ajoute 1 g de     2-amino-          pyridine    dissoute dans 5 cm' d'eau. On  ajoute au mélange 2 g de carbonate de soude  anhydre et l'ensemble est agité vigoureuse  ment à. la température ordinaire pendant une  heure.

   Le mélange est dilué avec 20     cm3    d'eau,  la couche de chloroforme en même temps que  tout le solide non dissous sont séparés et le  chloroforme éliminé par distillation. Le ré  sidu est traité à l'ébullition avec 25     cm3     d'une solution de soude 2N pendant 30 mi  nutes et la solution, précipitée par addition  d'acide acétique glacial chaud jusqu'à ce  qu'elle soit acide au tournesol. Le     précipiiué     cristallin de     2-(p-amino-benzène-sulfamido)-          pyridine    est filtré et recristallisé à l'acétone.  Point de fusion: 189-190   C.

      <I>Exemple</I>  A 9,4 g de     2-amino-pyridine    :à<B>55'</B> C on  ajoute 11,6 g de chlorure de     p-acétylamino-          benzène-sulfonyle.    Quand la réaction est ter  <U>min</U>ée, le produit fondu est dissous dans  150 cm' d'une solution de soude 2N et le  mélange est bouilli à reflux pendant une  heure. Par acidification à l'acide acétique,  on précipite la 2-(p-amino-benzène-sulfamido)-         pyridine    qui fond à<B>190'</B> C, après cristalli  sation à l'alcool aqueux.



  Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine. The present invention relates to a process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine, having the following formula:
EMI0001.0005
    This compound melts at 190 C; it is not very soluble when cold in water, acetone or alcohol; it has remarkable bactericidal properties and is capable of therapeutic applications.



  The process according to the invention is characterized in that 2-amino-pyridine is reacted with a para-acyl-amino-benzene-sulfonyl halide. so as to form, by eliminating hydrogen halide, 2-i (para-acyl-amino-benzenesulfamido) -pyridine, then in that the latter body is subjected to a hydrolysis to remove the acyl group and obtain 2- (para-amino-benzene-sulfamido)

  -pyridine. Preferably, 2-amino-pyridine is reacted with para-acetyl-amino-benzenesulfonyl chloride. The hydrolysis of 2- (para-acyl-amino-benzenesulfamido) - pyridine can be carried out in an alkaline medium.



  Here are some examples of execution of the process of the invention: <I> Example 1: </I> 9.4 g of 2-amino-pyridine are dissolved in 20 cm 3 of dry pyridine and 23, 5 g of p-acetyl-amino-benzenesulfonyl chloride; the mixture obtained is heated in a steam bath. Water is then added and the precipitate of 2- (p-acetyl-amino-benzene-sulfamido-) pyridine - melting point 224 ° C - is hydrolyzed at the boiling point with 175 cm 3 of a 2N solution. of caustic soda.

   The solution is cooled and made just acidic with sunflower by adding 2N hydrochloric acid. The 2- (p-amino-benzene-sulfamido) -pyridine precipitate is separated and recrystallized from water. Melting point <B> 190 '</B> C. <I> Example 2: </I> 4.7 g of 2-amino-pyridine are dissolved in 20 cm' of benzene; 12 g of p-acetyl-amino-benzenesulfonyl chloride are added and the mixture is allowed to stand. The solid which separates is filtered off and boiled for one hour with 90 cm 3 of a 2N sodium hydroxide solution.

   By acidification with dilute acetic acid, 2- (p-amino-benzenesulfamido) -pyridine is precipitated, which is recrystallized from acetone. Melting point 190 C. <I> Example 3: </I> 3 g of p-acetyl-amino-benzenesulfonyl chloride are suspended in 5 cm 'of chloroform and 1 g of 2-amino- pyridine dissolved in 5 cm 3 of water. 2 g of anhydrous sodium carbonate are added to the mixture and the whole is stirred vigorously at. room temperature for an hour.

   The mixture is diluted with 20 cm3 of water, the chloroform layer together with all the undissolved solid are separated and the chloroform removed by distillation. The residue is boiled with 25 cm3 of a 2N sodium hydroxide solution for 30 minutes and the solution precipitated by adding hot glacial acetic acid until it is acidic to the sunflower. The crystalline precipitate of 2- (p-amino-benzene-sulfamido) - pyridine is filtered off and recrystallized with acetone. Melting point: 189-190 C.

      <I> Example </I> To 9.4 g of 2-amino-pyridine: at <B> 55 '</B> 11.6 g of p-acetylamino-benzene-sulfonyl chloride are added. When the reaction is complete, the molten product is dissolved in 150 cm 3 of a 2N sodium hydroxide solution and the mixture is boiled under reflux for one hour. By acidification with acetic acid, the 2- (p-amino-benzenesulfamido) - pyridine is precipitated, which melts at <B> 190 ° </B> C, after crystallization with aqueous alcohol.

 

Claims (1)

REVENDICATION Procédé de préparation de la 2-(para- amino-benzène-sulfamido)-pyridine, caracté risé en ce que l'on fait réagir de la. 2-amino- pyridine avec un halogénure de para-acyle- î amino -benzène-s-tilfonyle, de manière à for- mer, en éliminant de l'halogénure d'hydro gène, de la 2-(para-acyle-amino-benzène- sulfamido)-pyridine, CLAIM Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine, characterized in that the. 2-Amino-pyridine with a para-acyl-amino-benzene-s-tilfonyl halide, so as to form, removing hydrogen halide, 2- (para-acyl-amino -benzene- sulfamido) -pyridine, puis en ce que l'on sou met ce dernier corps à une hydrolyse pour en éliminer le groupe acyle et obtenir la 2-(para- amino-benzène-sulfamido) -pyridine. Cette dernière fond à 190 C; elle est peu soluble à froid dans l'eau, l'acétone, l'alcool; elle pré sente des propriétés bactéricides marquantes et elle est susceptible d'applications théra peutiques. then in that the latter body is subjected to hydrolysis in order to remove the acyl group therefrom and obtain 2- (para-amino-benzenesulfamido) -pyridine. The latter melts at 190 C; it is poorly soluble when cold in water, acetone and alcohol; it exhibits remarkable bactericidal properties and it is capable of therapeutic applications. SOUS-REVENDICATIONS: 1 Procédé selon la revendication, caractérisé en ce que l'on fait réagir de la 2-amino- pyridine avec du chlorure de para-ac6tyl- amino-benzène-sulfonyle, puis en ce que l'on soumet le corps obtenu à une hydro lyse. 2 Procédé selon la revendication, caractérisé en ce que l'on effectue l'hydrolyse en milieu alcalin. SUB-CLAIMS: 1 A method according to claim, characterized in that one reacts 2-amino-pyridine with para-acetyl-amino-benzene-sulfonyl chloride, then in that the body is subjected obtained by hydrolysis. 2 A method according to claim, characterized in that the hydrolysis is carried out in an alkaline medium. 3 Procédé selon la revendication, caractérisé en ce que l'on chauffe une solution sèche de 2-amino-pyridine dans un solvant orga nique, avec du chlorure de para-acétyl- amino-benzène-sulfonyle, puis en ce que l'on soumet le corps obtenu à une hydro lyse. 3 Process according to claim, characterized in that a dry solution of 2-amino-pyridine is heated in an organic solvent, with para-acetyl-amino-benzene-sulfonyl chloride, then in that one subjects the resulting body to hydrolysis.
CH205678D 1937-11-29 1938-11-15 Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine. CH205678A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB205678X 1937-11-29

Publications (1)

Publication Number Publication Date
CH205678A true CH205678A (en) 1939-06-30

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Application Number Title Priority Date Filing Date
CH205678D CH205678A (en) 1937-11-29 1938-11-15 Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine.

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CH (1) CH205678A (en)

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