CH90807A - Process for the preparation of a derivative of nicotinic acid. - Google Patents
Process for the preparation of a derivative of nicotinic acid.Info
- Publication number
- CH90807A CH90807A CH90807DA CH90807A CH 90807 A CH90807 A CH 90807A CH 90807D A CH90807D A CH 90807DA CH 90807 A CH90807 A CH 90807A
- Authority
- CH
- Switzerland
- Prior art keywords
- nicotinic acid
- derivative
- preparation
- diethylamine
- water
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Description
Verfahren zur Herstellung eines Derivates der Nikotinsäure. Es wurde gefunden, dass- man zu einem Derivat der Nikotinsäure gelangen kann, wenn man Verbindungen" welche den Ni- kotinsä.Lirerest enthalten, z. B. Nikotinsäure halogenide, mit Diäthylamin behandelt.
Das so entstehende Nikotinsäurediäthyl- a,mid stellt ein gelbliches 01 vom Siedepunkt <B>280' (175'</B> bei 25 mm Druck) dar, welches in Wasser und organischen Lösungsmitteln leicht löslich ist und aits' der wässerigen Lö sung durch konzentrierte Alkalilauge ausge schieden wird.
Die neue Verbindung besitzt wertvolle therapeutische Eigenschaften.
Beispiel: Nikotinsäurechlorid wird mit der äqui- v aleiiten Menge Diätliylaminchlorhydrat zwei Stunden im O1bad auf<B>160'</B> erhitzt. Es er folgt lebhafte Entwicklung von Salzsäure dämpfen. Die Schmelze wird in Wasser ge löst, mit Kaliumhydroxydlösung 1; 1 ver setzt und mit Äther ausgeschüttelt.
Die Ätherlösung wird über Atzkali. getrocknet und der Äther - abdestilliert. Das zurück bleibende rohe Nikotiusäurediäthylamid wird dilrch Destillation im Vakuum gereinigt.
Process for the preparation of a derivative of nicotinic acid. It has been found that a derivative of nicotinic acid can be obtained if compounds which contain the nicotinic acid residue, for example nicotinic acid halides, are treated with diethylamine.
The resulting nicotinic acid diethyl amide is a yellowish oil with a boiling point of <B> 280 '(175' </B> at 25 mm pressure), which is easily soluble in water and organic solvents and passes through the aqueous solution concentrated alkali lye is excreted.
The new compound has valuable therapeutic properties.
Example: Nicotinic acid chloride is heated to <B> 160 '</B> in an O1 bath for two hours with the equivalent amount of diethylamine chlorohydrate. It follows lively development of hydrochloric acid steam. The melt is dissolved in water, with potassium hydroxide solution 1; 1 relocated and shaken out with ether.
The ethereal solution is via Atzkali. dried and the ether - distilled off. The remaining crude Nicotius acid diethylamide is purified by distillation in vacuo.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH90807T | 1920-07-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH90807A true CH90807A (en) | 1921-09-16 |
Family
ID=4348128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH90807D CH90807A (en) | 1920-07-21 | 1920-07-21 | Process for the preparation of a derivative of nicotinic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH90807A (en) |
-
1920
- 1920-07-21 CH CH90807D patent/CH90807A/en unknown
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