CH281037A - Process for the preparation of p-isopropylureido-benzalthiosemicarbazone. - Google Patents
Process for the preparation of p-isopropylureido-benzalthiosemicarbazone.Info
- Publication number
- CH281037A CH281037A CH281037DA CH281037A CH 281037 A CH281037 A CH 281037A CH 281037D A CH281037D A CH 281037DA CH 281037 A CH281037 A CH 281037A
- Authority
- CH
- Switzerland
- Prior art keywords
- benzalthiosemicarbazone
- isopropylureido
- preparation
- weight
- parts
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung von p-Isopropylureido-benzalthiosemicarbazon. Clegenstand der vorliegenden Erfindung ist ein Verfahren zur Herstellung von p-Iso- propylureido-benzalthiosemicarbazon der For mel
EMI0001.0004
welches dadurch gekennzeichnet ist, dass man (Ion 1sopropylester der Isoeyansäure auf p Ainino-berizalt.hiosenricarbazon einwirken lässt. Die Umsetzung wird vorzugsweise in einem Lösungsmittel, wie z. B. Pyridin, Aceton, Di- oxan, vorgenommen.
<I>.</I> Beispiel: 9 Gewichtsteile p-Anrino-benzalthiosemi- earbazon werden in 40 Gewichtsteilen Pvridin rrelöst und finit 6 Gewichtsteilen Isopropyliso- cyanat vermischt. Das Cxemisch wird nun über Nacht stehen gelassen und darauf in ver dünnte Salzsäure gerührt, wobei sich das Kondensationsprodukt. als dickes Öl abschei det.
Dieses wird abgetrennt, in verdünnter Natronlauge aufgenommen, die Lösung nach Zusatz von Tierkohle filtriert und das Filtrat mit Essigsäure angesäuert, wobei sich das Kondensationsprodukt als langsam erstarren des Öl ausscheidet. Nach einigem Stehen wird das feste Produkt abgesaugt, getrocknet und aus einem Gemisch von Essigester und Benzol umkristallisiert. Man erhält das p-Isopropyl- ureido-benzalthiosemicarbazon als gelbliches Pulver vom Zersetzungspunkt 198 .
Es soll als Heilmittel verwendet werden.
Process for the preparation of p-isopropylureido-benzalthiosemicarbazone. The present invention is a process for the preparation of p-isopropylureido-benzalthiosemicarbazone of the formula
EMI0001.0004
which is characterized in that (ion isopropyl ester of isoeyanoic acid is allowed to act on p amino-berizalt.hiosenricarbazone. The reaction is preferably carried out in a solvent such as pyridine, acetone, dioxane.
<I>. </I> Example: 9 parts by weight of p-anrino-benzalthiosemi-earbazon are dissolved in 40 parts by weight of pvridine and finely 6 parts by weight of isopropyl isocyanate are mixed. The mixture is then left to stand overnight and then stirred in dilute hydrochloric acid, the condensation product being formed. separates out as thick oil.
This is separated off, taken up in dilute sodium hydroxide solution, the solution is filtered after adding animal charcoal and the filtrate is acidified with acetic acid, the condensation product separating out as the oil slowly solidify. After standing for a while, the solid product is filtered off with suction, dried and recrystallized from a mixture of ethyl acetate and benzene. The p-isopropylureido-benzalthiosemicarbazone is obtained as a yellowish powder with a decomposition point of 198.
It is said to be used as a remedy.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH281037T | 1949-12-21 | ||
CH278134T | 1949-12-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH281037A true CH281037A (en) | 1952-02-15 |
Family
ID=25731807
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH281037D CH281037A (en) | 1949-12-21 | 1949-12-21 | Process for the preparation of p-isopropylureido-benzalthiosemicarbazone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH281037A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8765802B2 (en) | 2007-06-12 | 2014-07-01 | Provid Pharmaceuticals, Inc. | Kinase inhibitors, compositions thereof, and methods of use therewith |
-
1949
- 1949-12-21 CH CH281037D patent/CH281037A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8765802B2 (en) | 2007-06-12 | 2014-07-01 | Provid Pharmaceuticals, Inc. | Kinase inhibitors, compositions thereof, and methods of use therewith |
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