DE129452C - - Google Patents
Info
- Publication number
- DE129452C DE129452C DE1900129452D DE129452DA DE129452C DE 129452 C DE129452 C DE 129452C DE 1900129452 D DE1900129452 D DE 1900129452D DE 129452D A DE129452D A DE 129452DA DE 129452 C DE129452 C DE 129452C
- Authority
- DE
- Germany
- Prior art keywords
- alkaloids
- china
- salol
- alkali
- dilute
- 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.)
- Expired - Lifetime
Links
- 229930013930 alkaloids Natural products 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims 1
- 238000006011 modification reaction Methods 0.000 claims 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N Phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 229960000969 phenyl salicylate Drugs 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- 239000001576 FEMA 2977 Substances 0.000 description 1
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical class C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 1
- 229960003110 Quinine Sulfate Drugs 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- QIIPQYDSKRYMFG-UHFFFAOYSA-N phenyl hydrogen carbonate Chemical class OC(=O)OC1=CC=CC=C1 QIIPQYDSKRYMFG-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- RONWGALEIBILOG-VMJVVOMYSA-N quinine sulfate Chemical compound [H+].[H+].[O-]S([O-])(=O)=O.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 RONWGALEIBILOG-VMJVVOMYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
- C07D453/04—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT12014D AT12014B (e) | 1900-12-04 | 1902-04-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE129452C true DE129452C (e) |
Family
ID=397915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1900129452D Expired - Lifetime DE129452C (e) | 1900-12-04 | 1900-12-04 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE129452C (e) |
-
1900
- 1900-12-04 DE DE1900129452D patent/DE129452C/de not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE129452C (e) | ||
| DE615638C (de) | Verfahren zur Darstellung von organischen Wismutverbindungen | |
| DE686243C (de) | Verfahren zur Herstellung von Abkoemmlingen der Pyridin-2, 3-dicarbonsaeure | |
| DE95622C (e) | ||
| DE704297C (de) | Verfahren zur Darstellung von neutralen, oelloeslichen und sterilisierbaren organischen Wismutsalzen | |
| DE531518C (de) | Verfahren zur Darstellung aliphatisch-aromatischer Oxyketone | |
| DE716579C (de) | Verfahren zur Herstellung von Esteramiden der Mandelsaeure | |
| DE855248C (de) | Verfahren zur Herstellung von aliphatischen Phosphorsaeureesteramiden | |
| DE719535C (de) | Verfahren zur Herstellung von neutralen N-suebstituierten Abkoemmlingen des Tropasaeureamids | |
| DE683061C (de) | Herstellung photographischer Schichttraeger aus Cellulosederivaten | |
| DE725537C (de) | Verfahren zur Herstellung von p-Acylaminobenzolsulfonsaeureamidverbindungen | |
| DE555410C (de) | Verfahren zur Darstellung von 4-Oxy-5-nitroisophthalsaeure | |
| DE810028C (de) | Verfahren zur Herstellung von Phenyl-1-aethanolamin-2 | |
| AT277247B (de) | Verfahren zur herstellung der dischwefelsaeureestersalze des 4,4'-dihydroxy-diphenyl-(2"-pyridyl)-methans | |
| AT160304B (de) | Verfahren zur Darstellung öllöslicher Wismutsalze. | |
| DE1138765B (de) | Verfahren zur Herstellung der Kaffeesaeureester der Chinasaeure | |
| DE223796C (e) | ||
| DE213459C (e) | ||
| DE571591C (de) | Verfahren zur Herstellung therapeutisch wirksamer Camphersaeurepraeparate | |
| AT33110B (de) | Verfahren zur Darstellung von Alkyloxyazetylverbindungen von Alkoholen der hydroaromatischen Reihe. | |
| DE268982C (e) | ||
| DE548813C (de) | Verfahren zur Herstellung von Diacetonalkohol | |
| DE492509C (de) | Verfahren zur Herstellung von Borneol aus Nopinen | |
| DE764747C (de) | Verfahren zur Herstellung von Derivaten des Androstandiols-3, 17 und des Androstendiols-3, 17 | |
| AT160725B (de) | Verfahren zur Herstellung von Säureamiden bzw. -ureiden. |