CH168032A - Process for the preparation of a therapeutically valuable derivative of veratrum acid. - Google Patents
Process for the preparation of a therapeutically valuable derivative of veratrum acid.Info
- Publication number
- CH168032A CH168032A CH168032DA CH168032A CH 168032 A CH168032 A CH 168032A CH 168032D A CH168032D A CH 168032DA CH 168032 A CH168032 A CH 168032A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- therapeutically valuable
- veratrumsäuredimethylamid
- derivative
- acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
Verfahren zur Darstellung eines therapeutisch wertvollen Derivates der Veratrumsäure. Es wurde gefunden, dass auch dem bis her nicht bekannten Veratrumsäuredimethyl- amid wertvolle therapeutische Eigenschaften zukommen. Gegenstand der vorliegenden Er findung ist ein Verfahren zur Darstellung von Veratrumsäuredimethylamid, welches da durch gekennzeichnet ist, dass man auf die Halogenide der Veratrumsäure, Dimethylamin einwirken lässt.
Das Veratrumsäuredimethylamid kristalli siert in farblosen, glänzenden Nadeln, die bei 102-1030 schmelzen. Es siedet unter einem Druck von 12 mm unzersetzt bei 203 . Es ist in kaltem Wasser leicht löslich, ebenso in Äther, Alkohol und Benzol. In Petroläther ist es schwerer löslich.
Das Veratrumsäuredimethylamid soll als Arzneimittel verwendet werden.
<I>Beispiel:</I> 20 Teile Veratroylchlorid werden in 300 Volumteilen Toluol gelöst und zu einer Lö sung von 9 Teilen Dimethylamin in 150 Volumteilen Toluol gegossen. Es fällt Di- methylaminohlorhydrat aus, das nach einigen Stunden abgetrennt wird. Nach dem Ab- destillieren des Toluols wird der Rückstand im Vakuum destilliert. Das Veratrumsäure- dimethylamid destilliert bei einem Druck von 12 mm bei 203 als farbloses 01 über, das alsbald erstarrt.
Nach dem Umkristalli- sieren aus Petroläther erhält man es in Form farbloser, glänzender Kristallnadeln, die bei 102-103 schmelzen.
Process for the preparation of a therapeutically valuable derivative of veratrum acid. It has been found that veratrumsäuredimethyl amide, which was not previously known, also has valuable therapeutic properties. The subject matter of the present invention is a process for the preparation of veratrumsäuredimethylamid, which is characterized in that dimethylamine is allowed to act on the halides of veratrumsäure.
The Veratrumsäuredimethylamid crystallized in colorless, shiny needles that melt at 102-1030. It boils undecomposed at 203 under a pressure of 12 mm. It is easily soluble in cold water, as well as in ether, alcohol and benzene. It is more difficult to dissolve in petroleum ether.
Veratrumsäuredimethylamid should be used as a drug.
<I> Example: </I> 20 parts of veratroyl chloride are dissolved in 300 parts by volume of toluene and poured into a solution of 9 parts of dimethylamine in 150 parts by volume of toluene. Dimethylamine carbohydrate precipitates and is separated off after a few hours. After the toluene has been distilled off, the residue is distilled in vacuo. The veratrum acid dimethylamide distilled over at a pressure of 12 mm at 203 as a colorless oil, which soon solidified.
After recrystallization from petroleum ether, it is obtained in the form of colorless, shiny crystal needles which melt at 102-103.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH168032T | 1932-07-20 | ||
CH163700T | 1932-07-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH168032A true CH168032A (en) | 1934-03-15 |
Family
ID=25717858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH168032D CH168032A (en) | 1932-07-20 | 1932-07-20 | Process for the preparation of a therapeutically valuable derivative of veratrum acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH168032A (en) |
-
1932
- 1932-07-20 CH CH168032D patent/CH168032A/en unknown
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