CH297272A - Process for the preparation of a diammonium compound. - Google Patents
Process for the preparation of a diammonium compound.Info
- Publication number
- CH297272A CH297272A CH297272DA CH297272A CH 297272 A CH297272 A CH 297272A CH 297272D A CH297272D A CH 297272DA CH 297272 A CH297272 A CH 297272A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- diammonium compound
- bis
- diammonium
- compound
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung einer Diammoniumverbindung. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung einer Diammonium- verbindung. Das Verfahren ist dadurch ge kennzeichnet, dass man auf 1. Mol 1,10-Bis- (ss-diä.t.liylamino-äthylmereapto)-delzan 2 Mol :ltliyljodid einwirken lässt.
Die erhaltene neue Verbindung, das 1,10- Bis -[ss -(triäthylammonium) - äthylmercapt.o]- dekan-dijodid, schmilzt bei 130-132 . Sie soll therapeutische Verwendung finden.
Beispiel: 8,09 Teile 1,10-Bis-(ss-diäthylamino-ätliyi- inercapto)-dekan in 70 Volumteilen trockenem Aeeton werden mit 3,4 Volumteilen Äthyl- jodid 14 Stunden auf 50-60 erwärmt. Nach Erkalten wird das Produkt abgesaugt und gewünschtenfalls aus Aeeton unter Zusatz von wenig abs. Methanol umkristallisiert. Es zeigt. einen Schmelzpunkt von 130-132 .
Process for the preparation of a diammonium compound. The present patent relates to a process for the production of a diammonium compound. The process is characterized in that 1,10-bis- (ss-diä.t.liylamino-äthylmereapto) -delzan is allowed to act on 1 mole: ethyl iodide.
The new compound obtained, the 1,10-bis - [ss - (triäthylammonium) - äthylmercapt.o] - decane diiodide, melts at 130-132. It should find therapeutic use.
Example: 8.09 parts of 1,10-bis- (ss-diethylamino-ätliyi- inercapto) -dekan in 70 parts by volume of dry acetone are heated with 3.4 parts by volume of ethyl iodide to 50-60 hours for 14 hours. After cooling, the product is filtered off with suction and, if desired, from acetone with the addition of a little abs. Recrystallized methanol. It shows. a melting point of 130-132.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH297272T | 1950-12-12 | ||
| CH293565T | 1950-12-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH297272A true CH297272A (en) | 1954-03-15 |
Family
ID=25733370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH297272D CH297272A (en) | 1950-12-12 | 1950-12-12 | Process for the preparation of a diammonium compound. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH297272A (en) |
-
1950
- 1950-12-12 CH CH297272D patent/CH297272A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH297272A (en) | Process for the preparation of a diammonium compound. | |
| CH297274A (en) | Process for the preparation of a diammonium compound. | |
| CH297269A (en) | Process for the preparation of a diammonium compound. | |
| CH297268A (en) | Process for the preparation of a diammonium compound. | |
| CH297279A (en) | Process for the preparation of a diammonium compound. | |
| CH297271A (en) | Process for the preparation of a diammonium compound. | |
| CH297278A (en) | Process for the preparation of a diammonium compound. | |
| CH297273A (en) | Process for the preparation of a diammonium compound. | |
| CH297270A (en) | Process for the preparation of a diammonium compound. | |
| CH297275A (en) | Process for the preparation of a diammonium compound. | |
| CH297282A (en) | Process for the preparation of a diammonium compound. | |
| CH297277A (en) | Process for the preparation of a diammonium compound. | |
| CH209554A (en) | Process for the preparation of a new derivative of an azo dye. | |
| CH297280A (en) | Process for the preparation of a diammonium compound. | |
| CH293930A (en) | Process for the preparation of a quaternary ammonium compound of a bis-aminoalkoxy-alkane. | |
| CH312054A (en) | Process for the preparation of a diammonium compound. | |
| CH312049A (en) | Process for the preparation of a diammonium compound. | |
| CH297281A (en) | Process for the preparation of a diammonium compound. | |
| CH307557A (en) | Process for the preparation of a diammonium compound. | |
| CH307564A (en) | Process for the preparation of a diammonium compound. | |
| CH293931A (en) | Process for the preparation of a quaternary ammonium compound of a bis-aminoalkoxy-alkane. | |
| CH209552A (en) | Process for the preparation of a new derivative of an azo dye. | |
| CH306906A (en) | Process for the preparation of a diammonium compound. | |
| CH310719A (en) | Process for the preparation of a quaternary ammonium compound of a bis-aminoalkoxy-alkane. | |
| CH306912A (en) | Process for the preparation of a diammonium compound. |