DE134308C - - Google Patents
Info
- Publication number
- DE134308C DE134308C DENDAT134308D DE134308DA DE134308C DE 134308 C DE134308 C DE 134308C DE NDAT134308 D DENDAT134308 D DE NDAT134308D DE 134308D A DE134308D A DE 134308DA DE 134308 C DE134308 C DE 134308C
- Authority
- DE
- Germany
- Prior art keywords
- carbonate
- phenol
- parts
- quinine
- solution
- 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
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound 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 claims description 14
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 12
- 229930013930 alkaloid Natural products 0.000 claims description 10
- 235000001258 Cinchona calisaya Nutrition 0.000 claims description 7
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 claims description 7
- 229960000948 quinine Drugs 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- -1 alkaloid carbonic acid esters Chemical class 0.000 claims description 3
- 150000003797 alkaloid derivatives Chemical class 0.000 claims description 3
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- ORUJFMPWKPVXLZ-UHFFFAOYSA-N guaiacol carbonate Chemical compound COC1=CC=CC=C1OC(=O)OC1=CC=CC=C1OC ORUJFMPWKPVXLZ-UHFFFAOYSA-N 0.000 claims description 2
- 229950010370 guaiacol carbonate Drugs 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 239000003929 acidic solution Substances 0.000 claims 2
- 238000002844 melting Methods 0.000 claims 2
- 230000008018 melting Effects 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 239000002585 base Substances 0.000 claims 1
- BZNOBTGZGLOUCO-UHFFFAOYSA-N bis(5-methyl-2-propan-2-ylphenyl) carbonate Chemical compound CC(C)C1=CC=C(C)C=C1OC(=O)OC1=CC(C)=CC=C1C(C)C BZNOBTGZGLOUCO-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 1
- KMPWYEUPVWOPIM-KODHJQJWSA-N cinchonidine Chemical compound C1=CC=C2C([C@H]([C@H]3[N@]4CC[C@H]([C@H](C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-KODHJQJWSA-N 0.000 claims 1
- KMPWYEUPVWOPIM-UHFFFAOYSA-N cinchonidine Natural products C1=CC=C2C(C(C3N4CCC(C(C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-UHFFFAOYSA-N 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 235000015250 liver sausages Nutrition 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000001953 recrystallisation Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000004651 carbonic acid esters Chemical class 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- QIIPQYDSKRYMFG-UHFFFAOYSA-N phenyl hydrogen carbonate Chemical class OC(=O)OC1=CC=CC=C1 QIIPQYDSKRYMFG-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 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)
Publications (1)
Publication Number | Publication Date |
---|---|
DE134308C true DE134308C (enrdf_load_stackoverflow) |
Family
ID=402445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT134308D Active DE134308C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE134308C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT134308D patent/DE134308C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE134308C (enrdf_load_stackoverflow) | ||
DE2019865A1 (de) | Stoff zur Stabilisierung von Fluessig-Kristall-Stoffen gegen die Bildung von echten Feststoffen sowie Verfahren zur Herstellung eines solchen Stoffes | |
DE2019864A1 (de) | Stoff zur Stabilisierung von Fluessig-Kristall-Stoffen gegen die Bildung von echte Feststoffen sowie Verfahren zur Herstellung und Verwendung eines solchen Stoffes | |
DE489117C (de) | Verfahren zur Darstellung von C-Alkylresorcinen | |
DE568675C (de) | Verfahren zur Herstellung von O-Alkyl-, Oxyalkyl- oder Alkylaminoalkylaethern des Harmols oder Harmalols | |
DE1282430C2 (de) | Verfahren zur herstellung eines kakaobutter enthaltenden fettgemisches mit niederem schmelztemperaturbereich | |
DE118352C (enrdf_load_stackoverflow) | ||
DE1961861B2 (de) | Verfahren zur gewinnung von hellen, farbstabilen fettsaeuren | |
DE289454C (enrdf_load_stackoverflow) | ||
DE654458C (de) | Verfahren zur Herstellung von Indigweiss bzw. dessen Alkalisalzen | |
DE1039063B (de) | Verfahren zur Herstellung eines antipyretisch wirksamen, substituierten 1, 2-Diphenyl-3, 5-dioxo-pyrazolidins und dessen Salzen | |
DE80501C (enrdf_load_stackoverflow) | ||
DE2533898C3 (de) | glukosidpalmitaten | |
DE443245C (de) | Verfahren zur Herstellung von Benzoylekgoninallylesterhydrohalogeniden | |
DE138845C (enrdf_load_stackoverflow) | ||
DE2403664C3 (de) | Verfahren zur Reindarstellung von Naphthalin | |
AT285602B (de) | Verfahren zur Herstellung von neuen Thiazolderivaten | |
DE720160C (de) | Verfahren zur Darstellung von 6-Aminodihydrocinchonin und -dihydrocinchonidin | |
DE1468175C (de) | Verfahren zur Herstellung von zucker freien Reaktionsprodukten aus Rohrzucker und langkettigen Fettsaureestern | |
DE204922C (enrdf_load_stackoverflow) | ||
DE629298C (de) | UEberfuehrung von Ferrophosphor in Trialkaliorthophosphate | |
DE245142C (enrdf_load_stackoverflow) | ||
DE575470C (de) | Verfahren zur Darstellung von C, C-disubstituierten Derivaten der Barbitursaeure | |
DE633981C (de) | Verfahren zur Herstellung wohldefinierter kristalliner Nitrate des Phenylquecksilberhydroxyds | |
DE752752C (de) | Verfahren zur Herstellung von im Ring A aromatisierten Steroidverbindungen |