CH286745A - A process for preparing an aromatic diacylated hydroxy-amino-ketone. - Google Patents

A process for preparing an aromatic diacylated hydroxy-amino-ketone.

Info

Publication number
CH286745A
CH286745A CH286745DA CH286745A CH 286745 A CH286745 A CH 286745A CH 286745D A CH286745D A CH 286745DA CH 286745 A CH286745 A CH 286745A
Authority
CH
Switzerland
Prior art keywords
aromatic
ketone
hydroxy
diacylated
amino
Prior art date
Application number
Other languages
French (fr)
Inventor
Company Parke Davis
Original Assignee
Parke Davis & Co
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 Parke Davis & Co filed Critical Parke Davis & Co
Publication of CH286745A publication Critical patent/CH286745A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/02Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines

Landscapes

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

Description

  

  Procédé de préparation d'une     hydroxy-amino#cétone        diacylée    aromatique.    Dans le brevet principal, on a décrit un  procédé de préparation de la     p-nitro-a-acét-          amido   <I>-</I>     f3   <I>-</I>     acétoxypropiophénone.    Le présent  brevet a pour objet un procédé de prépara  tion d'une autre     hydroxy-amino-cétone        di-          aeylée    aromatique.

   Ce procédé est caractérisé  en ce que l'on soumet à une     acétylation,    au  moyen d'un dérivé de l'acide acétique et sous  des conditions pratiquement anhydres, de la       p-nitro-a-dichloroacétamido-p-hydroxy        propio-          phénone    de formule  
EMI0001.0014     
    On obtient de cette manière la     p-nitro-a-          dichloroacétamido-p-acétoxypropioph.énone,    qui  est une substance nouvelle, cristallisée, ayant  un point de fusion de     1.24     C.  



  Pour effectuer     l'acétylation    du groupe OH,  on peut employer comme dérivé de l'acide  acétique un halogénure ou l'anhydride de cet  acide sous des conditions anhydres. On peut  effectuer     l'acétylation    soit en présence, soit  en l'absence d'un catalyseur d'acylation, tel  qu'une base inorganique, un sel alcalin d'un  acide organique, une base organique tertiaire,  un acide aromatique     sulfonique    ou sulfurique,  un acide inorganique fort.  



       L'acétylation    peut se faire à une tempé  rature comprise entre     1:0    et 140  C environ.  On peut effectuer     l'acétylation    en présence    d'un solvant organique inerte tel que le ben  zène, l'éther de pétrole, le toluène, etc., bien       qu'il    soit plus indiqué de se passer de solvant  et d'utiliser un excès de l'agent     d'acétylation.          Exemple:     On ajoute deux gouttes d'acide     sulfurique     concentré à un mélange composé de 3,21 g de       p-nitro-a-dichloroacétamido-,l-hydroxypropio-          phénone    et de 9     em3    d'anhydride acétique.

   Le  mélange se chauffe spontanément et on dilue..  après trente minutes, la solution claire obte  nue avec quelques volumes d'eau. On brasse  le mélange jusqu'à ce que l'excès de l'an  hydride acétique soit hydrolysé et on recueille  la     p-nitro-a-dichloroacétamido-l-acétoxypropio-          phénone    solide, par filtration. Après     recris-          tallisation    dans du     benzène,    on obtient le pro  duit pur d'un point de fusion de 124  C. Ce  produit répond à la formule  
EMI0001.0036     
    Le produit obtenu par le procédé selon  l'invention a une valeur particulière pour la  préparation de composés organiques possédant.  une activité antibiotique.



  A process for the preparation of an aromatic diacylated hydroxyamino # ketone. In the main patent, a process for the preparation of p-nitro-α-acet-amido <I> - </I> f3 <I> - </I> acetoxypropiophenone has been described. The present patent relates to a process for the preparation of another aromatic di-aeylated hydroxy-amino-ketone.

   This process is characterized by subjecting to acetylation, by means of an acetic acid derivative and under substantially anhydrous conditions, of p-nitro-a-dichloroacetamido-p-hydroxy propiophenone. formula
EMI0001.0014
    In this way, p-nitro-a-dichloroacetamido-p-acetoxypropioph.enone is obtained, which is a new, crystalline substance with a melting point of 1.24 C.



  In order to effect the acetylation of the OH group, a halide or anhydride of this acid can be employed as the derivative of acetic acid under anhydrous conditions. The acetylation can be carried out either in the presence or in the absence of an acylation catalyst, such as an inorganic base, an alkali salt of an organic acid, a tertiary organic base, an aromatic sulfonic or sulfuric acid. , a strong inorganic acid.



       The acetylation can take place at a temperature of between 1: 0 and 140 ° C. approximately. Acetylation can be carried out in the presence of an inert organic solvent such as benzene, petroleum ether, toluene, etc., although it is more appropriate to dispense with the solvent and use an excess. acetylating agent. Example: Two drops of concentrated sulfuric acid are added to a mixture composed of 3.21 g of p-nitro-a-dichloroacetamido-, 1-hydroxypropiophenone and 9 em3 of acetic anhydride.

   The mixture heats up spontaneously and is diluted .. after thirty minutes, the clear solution obtained naked with a few volumes of water. The mixture is stirred until the excess acetic anhydride is hydrolyzed and the solid p-nitro-α-dichloroacetamido-1-acetoxypropiophenone is collected by filtration. After recrystallization from benzene, the pure product is obtained with a melting point of 124 C. This product corresponds to the formula
EMI0001.0036
    The product obtained by the process according to the invention has particular value for the preparation of organic compounds possessing. antibiotic activity.

 

Claims (1)

REVENDICATION: Procédé de préparation d'une hydroxy- amino-cétone diacylée aromatique, caractérisé en ce que l'on soumet â une acétylation, au moyen d'un dérivé de l'acide acétique et sous des conditions pratiquement anhydres, CLAIM: Process for the preparation of an aromatic diacylated hydroxy-amino-ketone, characterized in that it is subjected to acetylation, by means of an acetic acid derivative and under practically anhydrous conditions, de la p-nitro-a-dichloroacétamido - f-hydroxypropio- s phénone de formule EMI0002.0008 La p-nitro-a-dichloroacétamido-P-acétoxy- propiophénone obtenue est une substance cris tallisée ayant un point de fusion de 124 C. SOUS-REVENDICATIONS 1. Procédé selon la revendication, caracté risé en ce que le dérivé de l'acide acétique est. un halogénure de cet acide. 2. Procédé selon la revendication, caracté risé en ce que le dérivé de l'acide acétique est. l'anhydride acétique. 3. p-nitro-a-dichloroacetamido - f-hydroxypropio- s phenone of the formula EMI0002.0008 The p-nitro-a-dichloroacetamido-P-acetoxy-propiophenone obtained is a crystallized substance having a melting point of 124 C. SUB-CLAIMS 1. Process according to claim, characterized in that the acid derivative acetic is. a halide of this acid. 2. Method according to claim, character ized in that the derivative of acetic acid is. acetic anhydride. 3. Procédé selon la revendication, caracté risé en ce que l'on effectue ladite acétylation en présence d'un catalyseur d'acylation. 4. Procédé selon la revendication et les sous-revendications 2 et 3, caractérisé en ce que ledit catalyseur est l'acide sulfurique. Process according to claim, characterized in that said acetylation is carried out in the presence of an acylation catalyst. 4. Process according to claim and sub-claims 2 and 3, characterized in that said catalyst is sulfuric acid.
CH286745D 1948-08-24 1949-03-14 A process for preparing an aromatic diacylated hydroxy-amino-ketone. CH286745A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US286745XA 1948-08-24 1948-08-24
CH282087T 1949-03-14

Publications (1)

Publication Number Publication Date
CH286745A true CH286745A (en) 1952-10-31

Family

ID=25732139

Family Applications (1)

Application Number Title Priority Date Filing Date
CH286745D CH286745A (en) 1948-08-24 1949-03-14 A process for preparing an aromatic diacylated hydroxy-amino-ketone.

Country Status (1)

Country Link
CH (1) CH286745A (en)

Similar Documents

Publication Publication Date Title
EP0038480B1 (en) Process for the preparation of 1-(4-hydroxyphenyl)-3-butanone and intermediate compounds for this process
CH286745A (en) A process for preparing an aromatic diacylated hydroxy-amino-ketone.
Mosher et al. Benzene ring substituted 2-acetyl-1, 3-indandiones
CA1152103A (en) Purification process and preparation of itanoxone suitable for therapeutic use
CH402835A (en) Process for preparing hydroxybenzaldehydes
CH289888A (en) Process for preparing an aromatic acylamidodiol.
CH302796A (en) Process for preparing pseudo-1-p-nitrophenyl-2-acetamido-propanediol-1,3.
CH237879A (en) Process for the preparation of -dimethyl-ss-cyclohexylethylamine.
CH288998A (en) Process for preparing N-methyl-N&#39;-benzhydryl-piperazine.
CH222733A (en) Process for the preparation of a derivative of para-amino-benzene-sulfonamide.
CH268051A (en) Process for preparing 1-methyl-4-piperazine-N, N-diethyl-carboxamide.
CH222734A (en) Process for the preparation of a derivative of para-amino-benzene-sulfonamide.
CH323174A (en) Process for preparing a steroid carrying an aldehyde function in position 17
CH284721A (en) Process for preparing an aromatic acylamidodiol, nitrated in the nucleus.
CH222732A (en) Process for the preparation of a derivative of para-amino-benzene-sulfonamide.
CH288942A (en) Process for preparing an aromatic acylamidodiol.
CH408917A (en) Process for the preparation of sulfonic acid halides and sulfonic acid amides of indole and its derivatives
JPS6131090B2 (en)
CH288991A (en) Process for preparing an aromatic acylamidodiol, nitrated in the nucleus.
CH205678A (en) Process for the preparation of 2- (para-amino-benzenesulfamido) -pyridine.
BE615918A (en)
CH316152A (en) Process for the preparation of colchicoside acetate
CH294899A (en) Process for preparing a mixture of the cis and trans isomers of vitamin A.
BE816271A (en) Therapeutic indole alkaloids - prepd from vincadifformine
DE2063503A1 (en) 2- (1-butyn-3-yl-oxy) aniline