[go: up one dir, main page]

DE881652C - Process for the preparation of p- (AEthylureido) -benzalthiosemicarbazone - Google Patents

Process for the preparation of p- (AEthylureido) -benzalthiosemicarbazone

Info

Publication number
DE881652C
DE881652C DEW1298A DEW0001298A DE881652C DE 881652 C DE881652 C DE 881652C DE W1298 A DEW1298 A DE W1298A DE W0001298 A DEW0001298 A DE W0001298A DE 881652 C DE881652 C DE 881652C
Authority
DE
Germany
Prior art keywords
benzalthiosemicarbazone
preparation
aethylureido
ethylureido
mixed
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
DEW1298A
Other languages
German (de)
Inventor
Rudolf Dr Hirt
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.)
Wander AG
Original Assignee
Wander 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 Wander AG filed Critical Wander AG
Application granted granted Critical
Publication of DE881652C publication Critical patent/DE881652C/en
Expired legal-status Critical Current

Links

Landscapes

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

Description

Verfahren zur Herstellung von p-(Äthylureido)-benzalthiosemicarbazon Es wurde gefunden, .daß p-(Äthylureido)-benzalthiosemicarbazon der Formel eine das Wachstum von Tuberkelbazillen hemmend Wirkung .entfaltet.Process for the preparation of p- (Ethylureido) -benzalthiosemicarbazone It was found that p- (Ethylureido) -benzalthiosemicarbazone of the formula has an inhibiting effect on the growth of tubercle bacilli.

Gegenstand der Erfindung ist ein Verfahren zur Herstellung dieser Verbindung, welches dadurch gekennzeichnet ist, daß man p-Aminobenzalthiotemicarbazon mit Äthylisocyanat behandelt.The invention relates to a method for producing these Compound which is characterized in that p-aminobenzalthiotemicarbazone treated with ethyl isocyanate.

Vorzugsweise wird das Verfahren in einem geeigneten Lösungsmittel, wie Pyridin. Aceton, Dioxan, durchgeführt.The process is preferably carried out in a suitable solvent, like pyridine. Acetone, dioxane.

Beispiel 32 Gewichtsteile p-Aminob-enzalthiosemicarbazon @v@erden in i 5o Gewichtsteilen Pyridin gelöst und mit i9 Gewichtsteilen Athylisocyanat versetzt. Die Lösung erwärmt sich langsam bis auf etwa 35°. Sie wird nach einstündigem Stehen noch i Stunde lang auf dem Dampfbad erwärmt und sodann in. verdünnte Salzsäure gerührt. Dabei scheidet sich ein gelbliches, bald erstarrendes Harz ab. Dieses wird abgesaugt und mit Wasser nachgewaschen. Zur Reinigung wird es nun in. etwa i 1 5°/oiger Natronlauge bei 3o bis 4o,°' aufgenomm-en. Die trübe Lösung wird mit Tierkohle versetzt und, abgesaugt. Aus -dem Filtrat wird das Produkt durch Ansäuern als gelbliches Pulver ausgefällt und nun, in der gerade nötigen -Menge kochenden Alkohols gelöst und heiß mit dem doppelten Volumen heißen Wassers vermischt und erkalten gelassen. in feinen gelblichen Kristallen aus. F.: 22o°' (Zers).Example 32 parts by weight of p-aminobenzalthiosemicarbazon @ v @ earth dissolved in 15 parts by weight of pyridine and mixed with 19 parts by weight of ethyl isocyanate. The solution slowly warms up to about 35 °. After standing for one hour, it is warmed for another hour on the steam bath and then stirred in dilute hydrochloric acid. A yellowish, soon solidifying resin separates out. This is suctioned off and washed with water. To clean it, it is then taken up in about 15% sodium hydroxide solution at 3o to 4o ° '. The cloudy solution is mixed with animal charcoal and sucked off. The product is precipitated from the filtrate as a yellowish powder by acidification and then dissolved in the just necessary amount of boiling alcohol and mixed with twice the volume of hot water and allowed to cool. in fine yellowish crystals. F .: 22o ° '(dec).

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung von p-(Äthylureido)-benzalthiosemicarbazon, dadurch gekennzeichnet, daß man p-Aminobenzalthiosemicarbazon mit Äthylisocyanat behandelt. Dabei scheidet sich das gebildete p-(Äthylureido)-bernzalthiosemicarbazon der Formel PATENT CLAIM: Process for the preparation of p- (ethylureido) -benzalthiosemicarbazone, characterized in that p-aminobenzalthiosemicarbazone is treated with ethyl isocyanate. The formed p- (ethylureido) -bernzalthiosemicarbazone of the formula is separated
DEW1298A 1949-05-24 1950-03-02 Process for the preparation of p- (AEthylureido) -benzalthiosemicarbazone Expired DE881652C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH881652X 1949-05-24

Publications (1)

Publication Number Publication Date
DE881652C true DE881652C (en) 1953-07-02

Family

ID=4544891

Family Applications (1)

Application Number Title Priority Date Filing Date
DEW1298A Expired DE881652C (en) 1949-05-24 1950-03-02 Process for the preparation of p- (AEthylureido) -benzalthiosemicarbazone

Country Status (1)

Country Link
DE (1) DE881652C (en)

Similar Documents

Publication Publication Date Title
DE1267678B (en) Process for the saponification of polyalkylene terephthalates
DE1493854B1 (en) Benzanilides and process for their preparation
DE881652C (en) Process for the preparation of p- (AEthylureido) -benzalthiosemicarbazone
DE1009623B (en) Process for the preparation of ª ‡ -oxy-1,2,5,6-tetrahydrobenzylphosphinous acid or its alkali metal salts
DE863496C (en) Process for the preparation of diesters of glycols with methane or ethanesulphonic acid
DE1143802B (en) Process for the preparation of 2-chloro-6-nitro-benzonitrile
DE904534C (en) Process for the preparation of nicotinic acid ester nitrates
CH281035A (en) Process for the preparation of p-methylureido-benzalthiosemicarbazone.
DE956047C (en) Process for the production of furano (4 ', 5': 6, 7) chromones
DE806438C (en) Process for the production of novel pentaerythritol clusters
DE828105C (en) Process for the production of bactericidal oil-soluble substances
DE962608C (en) Process for the production of phosphoric or thiophosphoric acid esters
DE907293C (en) Process for the preparation of polysulfuric acid esters and salts thereof
DE968752C (en) Process for the production of chondroitin polysulfuric acid esters
CH278134A (en) Process for the preparation of p-ethyl-ureido-benzalthiosemicarbazone.
AT163822B (en) Process for the preparation of new condensation products of sulfanilamidopyrimidines
DE941372C (en) Process for the preparation of nuclear mono-acylated phloroglucins
DE1237560B (en) Process for the preparation of cyanoformic acid ethiol esters
DE890647C (en) Process for the production of Ni-acyherren Aminoarylsulfonamiden
DE912209C (en) Process for the preparation of 1, 3, 5-triacetylbenzene
DE893949C (en) Process for the production of aliphatic urea derivatives
DE906334C (en) Process for the preparation of quinolinium compounds
DE1543687A1 (en) Process for the purification of a 6- and 7-carboxy-2-methylol-1,4-benzodioxane mixture
AT202712B (en) Process for the extraction of alkaloids
DE913895C (en) Process for the preparation of bisquaterner salts of pyridine monocarboxylic acid esters with alkylene dihalides