CH242526A - Process for the preparation of an acylated sulfonamide. - Google Patents
Process for the preparation of an acylated sulfonamide.Info
- Publication number
- CH242526A CH242526A CH242526DA CH242526A CH 242526 A CH242526 A CH 242526A CH 242526D A CH242526D A CH 242526DA CH 242526 A CH242526 A CH 242526A
- Authority
- CH
- Switzerland
- Prior art keywords
- naphthalene
- sulfonamide
- preparation
- naphthoyl
- converted
- Prior art date
Links
- 229940124530 sulfonamide Drugs 0.000 title claims description 7
- 238000000034 method Methods 0.000 title claims description 6
- 150000003456 sulfonamides Chemical class 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 4
- 230000003301 hydrolyzing effect Effects 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- SWBLLSQMOMPTMC-UHFFFAOYSA-N naphthalene-2-sulfonamide Chemical class C1=CC=CC2=CC(S(=O)(=O)N)=CC=C21 SWBLLSQMOMPTMC-UHFFFAOYSA-N 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 238000007127 saponification reaction Methods 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- -1 2-naphthalenesulfonyl Chemical group 0.000 claims 1
- 238000003776 cleavage reaction Methods 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 230000007017 scission Effects 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 1
- 229940126601 medicinal product Drugs 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines aeylierten Sulfonamides. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines- acylierten Sulfonamides. Das Verfahren ist dadurch gekennzeichnet, dass man ein substituiertes 2-Naphthalin-sulfonamid der Formel
EMI0001.0007
in der R einen durch hydrolysierende Mittel abspaltbaren Rest bedeutet, durch Verseifung in 2-N aphthalin-N-(a-naphthoyl)-sulfonamid überführt.
' Das Natriumsalz der neuen Verbindung stellt ein weisses, in Wasser mässig lösliches Pulver dar. Die Verbindung soll als Arznei mittel Verwendung finden.
<I>Beispiel:</I> 10 Teile -N-(2-Naphthalin-sulfonyl)-.a- naphthoesäureamidin. vom Schmelzpunkt und der Formel
EMI0001.0021
werden mit 100 Teilen 15 % iger Salzsäure 4 Stunden auf<I>90-100 </I> erhitzt. Nach dem Erkalten wird s.odaalkalisch gestellt, filtriert und mit Essigsäure angesäuert. Man erhält das. 2 -Naphthalin - N - (u - naphthoyl)-sulfon- amid.
Process for the preparation of an alkylated sulfonamide. The subject of the present patent is a process for the preparation of an acylated sulfonamide. The process is characterized in that a substituted 2-naphthalene sulfonamide of the formula
EMI0001.0007
in which R denotes a radical which can be split off by hydrolyzing agents, converted by saponification into 2-naphthalene-N- (a-naphthoyl) sulfonamide.
The sodium salt of the new compound is a white powder that is moderately soluble in water. The compound is said to be used as a medicinal product.
<I> Example: </I> 10 parts -N- (2-naphthalene-sulfonyl) -. A-naphthoic acid amidine. on the melting point and the formula
EMI0001.0021
are heated to <I> 90-100 </I> for 4 hours with 100 parts of 15% hydrochloric acid. After cooling, it is made soda-alkaline, filtered and acidified with acetic acid. The 2-naphthalene-N- (u-naphthoyl) -sulphonamide is obtained.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH242526T | 1943-05-21 | ||
| CH239850T | 1944-03-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH242526A true CH242526A (en) | 1946-05-15 |
Family
ID=25728455
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH242526D CH242526A (en) | 1943-05-21 | 1943-05-21 | Process for the preparation of an acylated sulfonamide. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH242526A (en) |
-
1943
- 1943-05-21 CH CH242526D patent/CH242526A/en unknown
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