CH151182A - Process for the preparation of a crystallized, readily soluble and stable benzylmorphine salt. - Google Patents
Process for the preparation of a crystallized, readily soluble and stable benzylmorphine salt.Info
- Publication number
- CH151182A CH151182A CH151182DA CH151182A CH 151182 A CH151182 A CH 151182A CH 151182D A CH151182D A CH 151182DA CH 151182 A CH151182 A CH 151182A
- Authority
- CH
- Switzerland
- Prior art keywords
- benzylmorphine
- crystallized
- preparation
- salt
- stable
- Prior art date
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Darstellung eines kristallisierten, leichtlöslichen und beständigen Benzylmorphinsalzes. Die vorliegende Erfindung betrifft ein Ver fahren zur Darstellung eines kristallisierten, leichtlöslichen, beständigen Benzylinorphin- salzes, welches dadurch gekennzeichnet ist, dass man Benzylmorphinbase und Äthansulfon- säure aufeinander einwirken lässt.
<I>Beispiel:</I> 100 gr Benzylmorphin werden in 300 cm-' absolutem Alkohol gelöst und mit 10(f cms einer 30 %igen alkoholischen Ätharisulfon- säure versetzt. Beim Verdünnen mit trockenem Äther kristallisiert der grösste Teil des äthan- sulfonsauren Benzylmorphins in Drusen aus; durch Einengen der Mutterlauge wird der liest des Salzes gewonnen.
Ein Teil desselben löst sich in 0,7 Teilen Wasser von 200 zu einer neutral reagieren den Flüssigkeit. Das ätbansulfonsaure Benzyl- morphin verfärbt sich bei langsamem Erhitzen gegen 190 0 und schmilzt unter Braunfärbung bei 201-202 0.
Die Analyse ergab <B>0,2192</B> gr Substanz: 4,39 cm3 n/10 H2S04 nach Kjeldahl 7,110 mgr ,i 3,352 mgr BaS04 mikroanalytisch C19H18NOS. ((:H2. CrH6). C2116S03H Ber. N 2,88%; S 6,61%;
Gef. N 2,81%; S 6,48 0%. Das Produkt ergibt Reaktionen des Benzyl- morphins.
Process for the preparation of a crystallized, readily soluble and stable benzylmorphine salt. The present invention relates to a method for preparing a crystallized, easily soluble, stable benzylinorphine salt, which is characterized in that benzylmorphine base and ethanesulfonic acid are allowed to act on one another.
<I> Example: </I> 100 g of benzylmorphine are dissolved in 300 cm- 'absolute alcohol and mixed with 10 (f cms of a 30% alcoholic etharisulphonic acid. When diluted with dry ether, most of the ethane sulphonic acid crystallizes Benzylmorphine in drusen; the extract of the salt is obtained by concentrating the mother liquor.
A part of it dissolves in 0.7 parts of water from 200 to a neutral reacting liquid. The benzylmorphine ätbansulfonsaure discolored when slowly heated to 190 0 and melts with a brown color at 201-202 0.
The analysis resulted in <B> 0.2192 </B> gr substance: 4.39 cm3 n / 10 H2S04 according to Kjeldahl 7.110 mgr, i 3.352 mgr BaS04 microanalytically C19H18NOS. ((: H2. CrH6). C2116S03H calc. N 2.88%; S 6.61%;
Found N 2.81%; S 6.48 0%. The product results in reactions of benzylmorphine.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE151182X | 1929-05-24 | ||
CH148913T | 1930-05-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151182A true CH151182A (en) | 1931-11-30 |
Family
ID=25715289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151182D CH151182A (en) | 1929-05-24 | 1930-05-23 | Process for the preparation of a crystallized, readily soluble and stable benzylmorphine salt. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151182A (en) |
-
1930
- 1930-05-23 CH CH151182D patent/CH151182A/en unknown
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