ES408180A1 - Un procedimiento para la preparacion de esteres de alcaloi-des del tipo de la eburnamina. - Google Patents
Un procedimiento para la preparacion de esteres de alcaloi-des del tipo de la eburnamina.Info
- Publication number
- ES408180A1 ES408180A1 ES408180A ES408180A ES408180A1 ES 408180 A1 ES408180 A1 ES 408180A1 ES 408180 A ES408180 A ES 408180A ES 408180 A ES408180 A ES 408180A ES 408180 A1 ES408180 A1 ES 408180A1
- Authority
- ES
- Spain
- Prior art keywords
- acid
- halide
- converted
- group
- salts
- 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
Links
- VLFDXKBCNKXRBE-YTQUADARSA-N (+)-Isoeburnamine Natural products O[C@@H]1n2c3c(c4c2[C@H]2[C@@](CC)(C1)CCC[N+]2CC4)cccc3 VLFDXKBCNKXRBE-YTQUADARSA-N 0.000 title abstract 2
- HONLKDDLTAZVQV-NZSAHSFTSA-N Eburnamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@H]3[C@@]4(CC)C[C@@H](O)N5C2=C1 HONLKDDLTAZVQV-NZSAHSFTSA-N 0.000 title abstract 2
- HONLKDDLTAZVQV-UHFFFAOYSA-N eburnamine Natural products C1=CC=C2C(CCN3CCC4)=C5C3C4(CC)CC(O)N5C2=C1 HONLKDDLTAZVQV-UHFFFAOYSA-N 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 150000003839 salts Chemical group 0.000 abstract 6
- RXPRRQLKFXBCSJ-GIVPXCGWSA-N vincamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@](O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-GIVPXCGWSA-N 0.000 abstract 6
- -1 alkaloid esters Chemical class 0.000 abstract 4
- OZDNDGXASTWERN-CTNGQTDRSA-N Apovincamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C=C(C(=O)OC)N5C2=C1 OZDNDGXASTWERN-CTNGQTDRSA-N 0.000 abstract 3
- UXMCFEBDJVHVNH-HOJAQTOUSA-N ac1l52id Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@](O)(C(O)=O)N5C2=C1 UXMCFEBDJVHVNH-HOJAQTOUSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 229950006936 apovincamine Drugs 0.000 abstract 3
- OZDNDGXASTWERN-UHFFFAOYSA-N apovincamine Natural products C1=CC=C2C(CCN3CCC4)=C5C3C4(CC)C=C(C(=O)OC)N5C2=C1 OZDNDGXASTWERN-UHFFFAOYSA-N 0.000 abstract 3
- ZFCQLDAGNBFMJQ-QUCCMNQESA-N apovincaminic acid Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C=C(C(O)=O)N5C2=C1 ZFCQLDAGNBFMJQ-QUCCMNQESA-N 0.000 abstract 3
- RXPRRQLKFXBCSJ-UHFFFAOYSA-N dl-Vincamin Natural products C1=CC=C2C(CCN3CCC4)=C5C3C4(CC)CC(O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-UHFFFAOYSA-N 0.000 abstract 3
- 150000004820 halides Chemical class 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 229960002726 vincamine Drugs 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- 239000002585 base Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 2
- 239000011707 mineral Substances 0.000 abstract 2
- 150000007522 mineralic acids Chemical class 0.000 abstract 2
- 150000007524 organic acids Chemical class 0.000 abstract 2
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 229910000102 alkali metal hydride Inorganic materials 0.000 abstract 1
- 150000008046 alkali metal hydrides Chemical class 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229930013930 alkaloid Natural products 0.000 abstract 1
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 150000001502 aryl halides Chemical class 0.000 abstract 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 125000000075 primary alcohol group Chemical group 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D461/00—Heterocyclic compounds containing indolo [3,2,1-d,e] pyrido [3,2,1,j] [1,5]-naphthyridine ring systems, e.g. vincamine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HURI454A HU163434B (enrdf_load_stackoverflow) | 1971-11-03 | 1971-11-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES408180A1 true ES408180A1 (es) | 1976-02-16 |
Family
ID=11000880
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES408180A Expired ES408180A1 (es) | 1971-11-03 | 1972-11-02 | Un procedimiento para la preparacion de esteres de alcaloi-des del tipo de la eburnamina. |
Country Status (28)
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2259612B1 (enrdf_load_stackoverflow) * | 1974-01-31 | 1977-09-09 | Synthelabo | |
| HU171662B (hu) * | 1975-07-18 | 1978-02-28 | Richter Gedeon Vegyeszet | Sposob poluchenija novykh, opticheski aktivnykh proizvodnykh apovinkaminola i ikh kislotnykh adduktov |
| US4122179A (en) * | 1976-06-03 | 1978-10-24 | Enrico Corvi Mora | Acid addition salts of vincamine and apovincamine |
| HU177370B (en) * | 1977-07-27 | 1981-09-28 | Richter Gedeon Vegyeszet | Process for producing new bracket-cross-bracket-vincaminol-esters |
| JPS55100383A (en) * | 1979-01-25 | 1980-07-31 | Sumitomo Chem Co Ltd | Preparation of novel nitrogen-containing polycyclic compound |
| AU532001B2 (en) * | 1978-11-20 | 1983-09-15 | Sumitomo Chemical Company, Limited | Polycyclic indole derivatives |
| CH645269A5 (en) * | 1979-08-16 | 1984-09-28 | Richter Gedeon Vegyeszet | Medicine for the skin, and process for its production |
| JPS56161388A (en) | 1980-05-16 | 1981-12-11 | Nippon Zoki Pharmaceut Co Ltd | Novel vincamine derivative |
| IT1148733B (it) * | 1980-11-14 | 1986-12-03 | Medea Res Srl | Derivati della vincamina,metodo per la sua preparazione e composizione farmaceutiche che lo contengono |
| HU192013B (en) * | 1984-04-25 | 1987-04-28 | Richter Gedeon Vegyeszet | Process for production of new aporincavinol esther derivatives |
| HU191938B (en) * | 1984-07-11 | 1987-04-28 | Andras Vedres | Process for production of new derivatives of 9 and 11 nitro-apovincamin acid |
| ES8604956A1 (es) * | 1985-11-20 | 1986-03-16 | Covex Sa | Procedimiento de obtencion del ester etilico del acido apo- vincaminico |
-
0
- BE BE790837D patent/BE790837A/xx not_active IP Right Cessation
-
1971
- 1971-11-03 HU HURI454A patent/HU163434B/hu unknown
-
1972
- 1972-09-25 AT AT821872A patent/AT322118B/de not_active IP Right Cessation
- 1972-09-27 ZA ZA726619A patent/ZA726619B/xx unknown
- 1972-09-28 AU AU47179/72A patent/AU469544B2/en not_active Expired
- 1972-09-28 IL IL40457A patent/IL40457A/en unknown
- 1972-09-28 GB GB4489272A patent/GB1405127A/en not_active Expired
- 1972-09-28 NO NO3470/72A patent/NO136714C/no unknown
- 1972-10-02 DD DD165983A patent/DD101895A5/xx unknown
- 1972-10-17 FR FR7236735A patent/FR2158229B1/fr not_active Expired
- 1972-10-18 PL PL1972173980A patent/PL84613B1/pl unknown
- 1972-10-18 PL PL1972158330A patent/PL83604B1/pl unknown
- 1972-10-20 RO RO7272589A patent/RO62453A/ro unknown
- 1972-10-20 RO RO7200080703A patent/RO63055A/ro unknown
- 1972-10-20 CH CH1537172A patent/CH580628A5/xx not_active IP Right Cessation
- 1972-10-21 EG EG439/72A patent/EG10707A/xx active
- 1972-10-23 FI FI2929/72A patent/FI56687C/fi active
- 1972-10-27 IN IN1758/72A patent/IN138719B/en unknown
- 1972-10-27 SE SE7213934A patent/SE402460B/xx unknown
- 1972-10-30 JP JP47108028A patent/JPS5132640B2/ja not_active Expired
- 1972-10-30 NL NLAANVRAGE7214672,A patent/NL171584C/xx not_active IP Right Cessation
- 1972-11-01 BG BG021764A patent/BG20602A3/xx unknown
- 1972-11-01 BG BG023710A patent/BG22830A3/xx unknown
- 1972-11-01 DK DK540472AA patent/DK140552B/da not_active IP Right Cessation
- 1972-11-01 BG BG023711A patent/BG25515A3/xx unknown
- 1972-11-02 DE DE2265138A patent/DE2265138C3/de not_active Expired
- 1972-11-02 DE DE2253750A patent/DE2253750C3/de not_active Expired
- 1972-11-02 SU SU7201845297A patent/SU578005A3/ru active
- 1972-11-02 ES ES408180A patent/ES408180A1/es not_active Expired
- 1972-11-02 DE DE2265169A patent/DE2265169C3/de not_active Expired
- 1972-11-02 CA CA155,420A patent/CA991187A/en not_active Expired
- 1972-11-03 YU YU2735/72A patent/YU36738B/xx unknown
- 1972-11-03 CS CS727419A patent/CS191208B2/cs unknown
-
1979
- 1979-01-04 KE KE2912A patent/KE2912A/xx unknown
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