CH159585A - Process for preparing an asymmetric arsenobenzene compound. - Google Patents
Process for preparing an asymmetric arsenobenzene compound.Info
- Publication number
- CH159585A CH159585A CH159585DA CH159585A CH 159585 A CH159585 A CH 159585A CH 159585D A CH159585D A CH 159585DA CH 159585 A CH159585 A CH 159585A
- Authority
- CH
- Switzerland
- Prior art keywords
- compound
- arsenobenzene
- asymmetric
- acid
- preparing
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung einer asymmetrischen Arsenobenzolverbindung. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung einer asym metrischen Arsenobenzolverbindung, welches dadurch gekennzeichnet ist, dass man 3-Acetyl- amino-4-oxybenzolarsinsäure zusammen mit. 3 - Aoetylami no - 4 -phenoxyessigsäure-1-arsin- säure reduziert.
Das neue Verfahrensprodukt ist ein in Wasser klar und mit neutraler Reaktion lös liches Pulver. Die Lösung hat den Vorzug, haltbar und sowohl bei intravenöser, als auch bei subkutaner bezw. intramuskulärer Injek tion gut wirksam und sehr gut verträglich zu sein.
<I>Beispiel:</I> 13,7 gr- 3-Acetylamino-4-oxybenzolarsin- säure, gelöst in 31 ein' 2 n.Natronlauge und 31 cm' Wasser, werden mit einer Lösung von 16,6 gr 3-Acetylamino-4-phenoxyessig- säure-1-arsinsäure in 56 em3 2 n.Natronlauge und 56 ems Wasser gemischt und die Mi- schung nach Zugabe von 500 cm' Wasser bei 65 mit 195 gr Hydrosulfit reduziert.
Die abgeschiedene Arsenoverbindung wird mit 150 cm' Methylalkohol angeteigt und dazu 75 cm' Wasser von 50 gegeben. Durch Einrühren der filtrierten Lösung in 5 Vo lumenteile Aceton scheidet man das Präparat in fester Form ab. Es löst sich klar und neutral in Wasser.
Process for preparing an asymmetric arsenobenzene compound. The present invention relates to a method for preparing an asymmetrical arsenobenzene compound, which is characterized in that 3-acetylamino-4-oxybenzolaric acid is used together with. 3 - Aoetylami no - 4 -phenoxyacetic acid-1-arsic acid reduced.
The new process product is a powder that is clear in water and has a neutral reaction. The solution has the advantage of being durable and with both intravenous and subcutaneous bezw. intramuscular injection to be effective and very well tolerated.
<I> Example: </I> 13.7 gr- 3-acetylamino-4-oxybenzolar acid, dissolved in 31 a '2N sodium hydroxide solution and 31 cm' water, are mixed with a solution of 16.6 gr 3- Acetylamino-4-phenoxyacetic acid-1-arsic acid was mixed in 56 cubic meters of 2N sodium hydroxide solution and 56 cubic meters of water and the mixture was reduced after adding 500 cm of water at 65 with 195 g of hydrosulfite.
The separated arsenic compound is made into a paste with 150 cm 'of methyl alcohol and 75 cm' of water of 50% is added. The preparation is deposited in solid form by stirring the filtered solution into 5 parts by volume of acetone. It dissolves clearly and neutrally in water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE159585X | 1930-07-22 | ||
CH156268T | 1932-12-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH159585A true CH159585A (en) | 1933-01-15 |
Family
ID=25716735
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH159585D CH159585A (en) | 1930-07-22 | 1931-07-15 | Process for preparing an asymmetric arsenobenzene compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH159585A (en) |
-
1931
- 1931-07-15 CH CH159585D patent/CH159585A/en unknown
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