CH312529A - Process for the preparation of a new pyridine derivative. - Google Patents
Process for the preparation of a new pyridine derivative.Info
- Publication number
- CH312529A CH312529A CH312529DA CH312529A CH 312529 A CH312529 A CH 312529A CH 312529D A CH312529D A CH 312529DA CH 312529 A CH312529 A CH 312529A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- pyridine derivative
- new pyridine
- new
- isonicotinyl
- 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
- C07D213/86—Hydrazides; Thio or imino analogues thereof
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Description
Verfahren zur Herstellung eines neuen Pyridinderivates. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung von 1-Isonico- tinyl-2-dw -undecenoyl-hydrazin, das dadurch gekennzeichnet ist, dass Isonicotinylhydrazin mit df-Undecenoylchlorid umgesetzt wird.
Die neue Verbindung soll als Therapeuti- cum, besonders zur Bekämpfung der Tuberku lose, Verwendung finden. <I>Beispiel:</I> Man setzt tropfenweise 20,2 g dw-Undece- noylchlorid einer Lösung von 13,7 g Isonico- tinylhydrazin in 100 cm3 Siedenein Pyridin in einer solchen Geschwindigkeit zu,
dass die 1VIi- sehung trotz Entfernung der äussern Wärme- quelle unter Rückfluss weitersiedet. Nach be endetem Zusatz wird die Mischung während weiteren 10 Minuten im Sieden gehalten. Man setzt nun 100 em3 Wasser zu, worauf sich beim Abkühlen 1-Isonicotinoyl-2-undecenoyl.- hydrazin abscheidet. Die aus einem Wasser- Propanol=Gemisch umkristallisierten weissen Flocken schmelzen bei 111,5 C.
Process for the preparation of a new pyridine derivative. The present patent relates to a process for the preparation of 1-isonicotinyl-2-dw -undecenoylhydrazine, which is characterized in that isonicotinylhydrazine is reacted with df-undecenoyl chloride.
The new compound is intended to be used as a therapeutic agent, particularly to combat tuberculosis. <I> Example: </I> 20.2 g of dw-undecanoyl chloride are added dropwise to a solution of 13.7 g of isonicotinyl hydrazine in 100 cm3 of boiling point in pyridine at a rate such that
that the vision continues to boil under reflux despite the removal of the external heat source. After the addition has ended, the mixture is kept boiling for a further 10 minutes. 100 cubic meters of water are then added, whereupon 1-isonicotinoyl-2-undecenoyl.hydrazine separates out on cooling. The white flakes recrystallized from a water-propanol mixture melt at 111.5 ° C.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US312529XA | 1951-11-03 | 1951-11-03 | |
CH309035T | 1952-10-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH312529A true CH312529A (en) | 1955-12-31 |
Family
ID=25735568
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH312529D CH312529A (en) | 1951-11-03 | 1952-10-16 | Process for the preparation of a new pyridine derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH312529A (en) |
-
1952
- 1952-10-16 CH CH312529D patent/CH312529A/en unknown
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