DE121505C - - Google Patents
Info
- Publication number
- DE121505C DE121505C DENDAT121505D DE121505DA DE121505C DE 121505 C DE121505 C DE 121505C DE NDAT121505 D DENDAT121505 D DE NDAT121505D DE 121505D A DE121505D A DE 121505DA DE 121505 C DE121505 C DE 121505C
- Authority
- DE
- Germany
- Prior art keywords
- ether
- dry
- solution
- salt
- sodium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 150000001339 alkali metal compounds Chemical class 0.000 claims 1
- -1 cyclic amido ketones Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 26
- QQXLDOJGLXJCSE-KNVOCYPGSA-N tropinone Chemical compound C1C(=O)C[C@H]2CC[C@@H]1N2C QQXLDOJGLXJCSE-KNVOCYPGSA-N 0.000 description 18
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- QQXLDOJGLXJCSE-UHFFFAOYSA-N N-methylnortropinone Natural products C1C(=O)CC2CCC1N2C QQXLDOJGLXJCSE-UHFFFAOYSA-N 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 235000011118 potassium hydroxide Nutrition 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- AAJBAXNJSYYSFK-UHFFFAOYSA-N 6-amino-6-methylhept-1-en-4-one Chemical compound C(=C)CC(CC(C)(N)C)=O AAJBAXNJSYYSFK-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
- C07D451/06—Oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE121505C true DE121505C (enrdf_load_stackoverflow) |
Family
ID=390495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT121505D Active DE121505C (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE121505C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT121505D patent/DE121505C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE121505C (enrdf_load_stackoverflow) | ||
| DE65393C (de) | Verfahren zur Darstellung des Amids der Eugenolessigsäure | |
| DE134984C (enrdf_load_stackoverflow) | ||
| DE172932C (enrdf_load_stackoverflow) | ||
| DE124144C (enrdf_load_stackoverflow) | ||
| DE455590C (de) | Verfahren zur Herstellung von Menthol | |
| DE818800C (de) | Verfahren zur Gewinnung von Alkalihyposulfiten | |
| DE255030C (enrdf_load_stackoverflow) | ||
| DE446782C (de) | Verfahren zur Gewinnung des herzwirksamen Reinglykosids aus Bulbus Scillae | |
| DE64832C (de) | Verfahren zur Darstellung von Chinin und Homologen desselben aus Cuprein | |
| DE646706C (de) | Verfahren zur Darstellung substituierter 6, 7-Dioxy-1, 2, 3, 4-tetrahydroisochinolin-1-carbonsaeuren | |
| DE281007C (enrdf_load_stackoverflow) | ||
| DE202169C (enrdf_load_stackoverflow) | ||
| DE762123C (de) | Verfahren zur Herstellung von physiologisch wirksamen Abkoemmlingen des 2-Alkyl-1, 4-naphthochinons bzw. -hydrochinons | |
| DE105866C (enrdf_load_stackoverflow) | ||
| DE246207C (enrdf_load_stackoverflow) | ||
| DE1913449A1 (de) | Verfahren zur Stabilisierung von Ferrosalzen und Herstellung neuer Ferrosalzkomplexe | |
| DE305263C (enrdf_load_stackoverflow) | ||
| DE133146C (enrdf_load_stackoverflow) | ||
| DE558752C (de) | Verfahren zur Herstellung von neutralen komplexen Antimonsalzen | |
| DE205683C (enrdf_load_stackoverflow) | ||
| DE944953C (de) | Verfahren zur Herstellung eines aus dem Calciumsalz der Ca-AEthylen-diamintetraessigsaeure bestehenden Therapeutikums | |
| DE208961C (enrdf_load_stackoverflow) | ||
| DE139394C (enrdf_load_stackoverflow) | ||
| DE162912C (enrdf_load_stackoverflow) |