CH279838A - Process for the preparation of a new aldehyde derivative. - Google Patents
Process for the preparation of a new aldehyde derivative.Info
- Publication number
- CH279838A CH279838A CH279838DA CH279838A CH 279838 A CH279838 A CH 279838A CH 279838D A CH279838D A CH 279838DA CH 279838 A CH279838 A CH 279838A
- Authority
- CH
- Switzerland
- Prior art keywords
- works
- aldehyde derivative
- preparation
- new
- nicotinic acid
- Prior art date
Links
Landscapes
- Pyridine Compounds (AREA)
Description
Verfahren zur Herstellung eines neuen Aldehydderivates. Gegenstand des Patentes ist ein Verfahren zur Herstellung eines neuen Aldehydderivates, welches dadurch gekennzeichnet ist, dass man auf Nicotinsäure-oxymethylamid Methylchlorid einwirken lässt. Die Umsetzung wird vorzugs weise bei erhöhter Temperatur und in einem geschlossenen Gefäss, in An- oder Abwesen heit von Lösungsmitteln, durchgeführt. Das so erhaltene Nl-Chlor-N1-methyl-nicotinsäure- oxymethylamid bildet farblose Kristalle, die bei 160 bis 161 schmelzen und in Wasser und Alkohol gut, in Äther und Aceton wenig löslich sind.
Die neue Verbindung soll als Chemotherapeuticum und als Zwischenpro dukt Verwendung finden. Beispiel: 43,7 g Nicotinsäure-oxymethylamid wer den in 500 cm.3 Dioxan aufgeschlämmt und im Autoklaven mit 60 g Methylehlorid bei 100 bis 120 25 Stunden geschüttelt.
Nach dem Abkühlen wird die aus der Lö sung auskristallisierte Masse abgesogen und mit Dioxan und Äther gewaschen. Nach dem Umfällen aus Alkohol-Aceton erhält man 45,1 g des bei 160 bis 161 schmelzenden Nl- Chlor-N1-methyl-nieotinsäure-oxymethylamids, was einer Ausbeute von 78 1/a der Theorie ent spricht. Die neue Verbindung bildet farblose Kristalle, die in Wasser und Alkohol gut, in Äther, Aceton und Dioxan wenig löslich sind.
Process for the preparation of a new aldehyde derivative. The subject of the patent is a process for the production of a new aldehyde derivative, which is characterized in that the nicotinic acid oxymethylamide methyl chloride is allowed to act. The reaction is preferably carried out at elevated temperature and in a closed vessel, in the presence or absence of solvents. The Nl-chloro-N1-methyl-nicotinic acid-oxymethylamide thus obtained forms colorless crystals which melt at 160 to 161 and are readily soluble in water and alcohol, but not very soluble in ether and acetone.
The new compound is said to be used as a chemotherapeutic agent and as an intermediate product. Example: 43.7 g of nicotinic acid oxymethylamide who slurried in 500 cm.3 of dioxane and shaken in the autoclave with 60 g of methyl chloride for 100 to 120 hours.
After cooling, the mass which has crystallized out of the solution is suctioned off and washed with dioxane and ether. After reprecipitation from alcohol-acetone, 45.1 g of Nl-chloro-N1-methyl-nieotinic acid-oxymethylamide, melting at 160 to 161, are obtained, which corresponds to a yield of 78 1 / a of theory. The new compound forms colorless crystals which are readily soluble in water and alcohol, but not very soluble in ether, acetone and dioxane.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH276857T | 1949-07-12 | ||
CH279838T | 1949-07-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH279838A true CH279838A (en) | 1951-12-15 |
Family
ID=25731730
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH279838D CH279838A (en) | 1949-07-12 | 1949-07-12 | Process for the preparation of a new aldehyde derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH279838A (en) |
-
1949
- 1949-07-12 CH CH279838D patent/CH279838A/en unknown
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