CH158122A - Process for the preparation of 1-methyl-2-oxyacetic acid benzimidazole-5-arsic acid. - Google Patents
Process for the preparation of 1-methyl-2-oxyacetic acid benzimidazole-5-arsic acid.Info
- Publication number
- CH158122A CH158122A CH158122DA CH158122A CH 158122 A CH158122 A CH 158122A CH 158122D A CH158122D A CH 158122DA CH 158122 A CH158122 A CH 158122A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- methyl
- arsic
- preparation
- benzimidazole
- Prior art date
Links
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
Verfahren zur Darstellung von 1-Methyl-2-ogyessigsäurebenzimidazol-66-arsinsäure. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung von 1- Methyl-2-oxyessigsäurebenzimidazol- 5 - arsin- säure, welches dadurch gekennzeichnet ist, dass man 1-Methylbenzimidazolon-5-arsin- säure mit Halogenessigsäure umsetzt.
Das neue Verfahrensprodukt ist aus Was ser umkristallisierbar und hat den Schmelz punkt<B>308'</B> unter Zersetzung. Es findet als Heilmittel oder als Zwischenprodukt für die Herstellung von Heilmitteln Verwendung.
<I>Beispiel:</I> 90 gr 1-Methyl-benzimidazolon-5-arsin- säure werden in 200 cm' Wasser und 83 cm3 Natronlauge (40 B6) gelöst und zur Lösung 32 gr Chloressigsäure gegeben.
Nach andert halbstündigem Kochen am Rüekflusskühler setzt man nochmals 32 gr Chloressigsäure und 58 cm3 Natronlauge (40 B6) zu und kocht eine weitere Stunde. Dann wird ab- gekühlt, mit konzentrierter Salzsäure auf schwach eureuma-alkalisch abgestumpft und filtriert. Aus dem Filtrat wird mit konzen trierter Salzsäure die 1-Methyl-2-oxyessig- säurebenzimidazol-5-arsinsäure abgeschieden. Die Säure wird aus Wasser (1 :6) um kristallisiert.
Ausbeute an umkristallisierter Säure: 80 gr Fp. 308 C unter Zersetzung.
Process for the preparation of 1-methyl-2-ogyacetic acid benzimidazole-66-arsic acid. The present invention relates to a process for the preparation of 1-methyl-2-oxyacetic acid benzimidazole-5-arsic acid, which is characterized in that 1-methylbenzimidazolone-5-arsic acid is reacted with haloacetic acid.
The new process product can be recrystallized from water and has a melting point <B> 308 '</B> with decomposition. It is used as a remedy or as an intermediate in the manufacture of medicines.
<I> Example: </I> 90 g of 1-methylbenzimidazolone-5-arsic acid are dissolved in 200 cm 'of water and 83 cm3 of sodium hydroxide solution (40 B6) and 32 g of chloroacetic acid are added to the solution.
After boiling for one and half hours on the reflux condenser, another 32 grams of chloroacetic acid and 58 cm3 of sodium hydroxide solution (40 B6) are added and the mixture is boiled for another hour. Then it is cooled, blunted with concentrated hydrochloric acid to weakly eureuma-alkaline and filtered. 1-methyl-2-oxyacetic acid benzimidazole-5-arsic acid is separated off from the filtrate with concentrated hydrochloric acid. The acid is crystallized from water (1: 6).
Yield of recrystallized acid: 80 g. Mp. 308 C with decomposition.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE158122X | 1930-07-22 | ||
CH155449T | 1931-07-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH158122A true CH158122A (en) | 1932-10-31 |
Family
ID=25716577
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH158122D CH158122A (en) | 1930-07-22 | 1931-07-14 | Process for the preparation of 1-methyl-2-oxyacetic acid benzimidazole-5-arsic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH158122A (en) |
-
1931
- 1931-07-14 CH CH158122D patent/CH158122A/en unknown
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