CH625242A5 - - Google Patents
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- Publication number
- CH625242A5 CH625242A5 CH982477A CH982477A CH625242A5 CH 625242 A5 CH625242 A5 CH 625242A5 CH 982477 A CH982477 A CH 982477A CH 982477 A CH982477 A CH 982477A CH 625242 A5 CH625242 A5 CH 625242A5
- Authority
- CH
- Switzerland
- Prior art keywords
- vincamine
- apovincamine
- epivincamine
- process according
- starting
- Prior art date
Links
- 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 claims description 45
- 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 claims description 22
- 229960002726 vincamine Drugs 0.000 claims description 22
- 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 claims description 20
- 229950006936 apovincamine Drugs 0.000 claims description 20
- OZDNDGXASTWERN-UHFFFAOYSA-N apovincamine Natural products C1=CC=C2C(CCN3CCC4)=C5C3C4(CC)C=C(C(=O)OC)N5C2=C1 OZDNDGXASTWERN-UHFFFAOYSA-N 0.000 claims description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- RXPRRQLKFXBCSJ-HLAWJBBLSA-N 16-epivincamine Chemical class C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@@](O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-HLAWJBBLSA-N 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000002841 Lewis acid Substances 0.000 claims description 5
- 150000007517 lewis acids Chemical class 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 2
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 claims 2
- 229930013930 alkaloid Natural products 0.000 claims 2
- 150000003797 alkaloid derivatives Chemical class 0.000 claims 2
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 claims 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 claims 1
- -1 benzene anhydrides Chemical class 0.000 claims 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 claims 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910020667 PBr3 Inorganic materials 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- IPNPIHIZVLFAFP-UHFFFAOYSA-N phosphorus tribromide Chemical compound BrP(Br)Br IPNPIHIZVLFAFP-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- JSLDLCGKZDUQSH-RTBUJCADSA-N 19-epivindolinine Natural products O=C(OC)[C@H]1[C@@]23[C@H](C)[C@]4([C@@H]5N(CC=C4)CC[C@]25c2c(N3)cccc2)C1 JSLDLCGKZDUQSH-RTBUJCADSA-N 0.000 description 1
- WSGYTJNNHPZFKR-UHFFFAOYSA-N 3-hydroxypropanenitrile Chemical compound OCCC#N WSGYTJNNHPZFKR-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 241000511964 Tabernaemontana Species 0.000 description 1
- KILNDJCLJBOWAN-UHFFFAOYSA-N Tabersonine Natural products CCC12CC(=C3N(C)c4cc(OC)ccc4C35CCN(CC=C1)C25)C(=O)OC KILNDJCLJBOWAN-UHFFFAOYSA-N 0.000 description 1
- 241000863480 Vinca Species 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Chemical compound C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930005303 indole alkaloid Natural products 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- FNGGIPWAZSFKCN-ACRUOGEOSA-N tabersonine Chemical compound N1C2=CC=CC=C2[C@]2([C@H]34)C1=C(C(=O)OC)C[C@]3(CC)C=CCN4CC2 FNGGIPWAZSFKCN-ACRUOGEOSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000006257 total synthesis reaction Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- FNGGIPWAZSFKCN-UHFFFAOYSA-N xi-tabersonine Natural products N1C2=CC=CC=C2C2(C34)C1=C(C(=O)OC)CC3(CC)C=CCN4CC2 FNGGIPWAZSFKCN-UHFFFAOYSA-N 0.000 description 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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Saccharide Compounds (AREA)
Priority Applications (19)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH982477A CH625242A5 (enrdf_load_stackoverflow) | 1977-08-10 | 1977-08-10 | |
| IT26420/78A IT1200363B (it) | 1977-08-10 | 1978-08-02 | Procedimento di preparazione della apovincamina a partire da vincamina e da epivincamina |
| DE19782833967 DE2833967A1 (de) | 1977-08-10 | 1978-08-03 | Verfahren zur herstellung von apovincamin |
| BE189715A BE869537A (fr) | 1977-08-10 | 1978-08-04 | Procede de preparation de l'apovincamine a partir de la vincamine et de l'epivincamine |
| AT0571278A AT365590B (de) | 1977-08-10 | 1978-08-07 | Verfahren zur herstellung von apovincamin |
| NL787808302A NL7808302A (nl) | 1977-08-10 | 1978-08-08 | Werkwijze voor het bereiden van apovincamine uit vinca- mine en epivincamine. |
| AU38743/78A AU3874378A (en) | 1977-08-10 | 1978-08-08 | Preparation of apovincamine from vincamine and epivincamine |
| CA308,873A CA1100135A (en) | 1977-08-10 | 1978-08-08 | Method for the preparation of apovincamine from vincamine and epivincamine |
| HU78CO355A HU176218B (en) | 1977-08-10 | 1978-08-09 | Process for preparing apovincamine from vincamine or epivincamine |
| DK351478A DK351478A (da) | 1977-08-10 | 1978-08-09 | Fremgangsmaade til fremstilling af apovincamin |
| FR7823463A FR2400023A1 (fr) | 1977-08-10 | 1978-08-09 | Procede de preparation de l'apovincamine a partir de la vincamine et de l'epivincamine |
| SE7808521A SE7808521L (sv) | 1977-08-10 | 1978-08-09 | Apovinkamin |
| GB7832887A GB2003860B (en) | 1977-08-10 | 1978-08-09 | Method for the preparation of apovincamine from vincamine and epivincamine |
| ES472469A ES472469A1 (es) | 1977-08-10 | 1978-08-10 | Procedimiento para la preparacion de apovincamina |
| JP9676978A JPS5452100A (en) | 1977-08-10 | 1978-08-10 | Method of producing apovincamine from vincamine and epivincamine |
| FI782447A FI782447A7 (fi) | 1977-08-10 | 1978-08-10 | Foerfarande foer framstaellning av apovinkamin ur vinkamin och epivinkamin |
| AR273263A AR216684A1 (es) | 1977-08-10 | 1978-08-10 | Procedimiento para la preparacion de apovincamina |
| ZA00784536A ZA784536B (en) | 1977-08-10 | 1978-08-10 | A method for the preparation of apovincamine from vincamine and epivincamine |
| OA56577A OA06023A (fr) | 1977-08-10 | 1978-08-10 | Procédé de préparation de l'apovincamine à partir de la vincamine et de l'épivincamine. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH982477A CH625242A5 (enrdf_load_stackoverflow) | 1977-08-10 | 1977-08-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH625242A5 true CH625242A5 (enrdf_load_stackoverflow) | 1981-09-15 |
Family
ID=4356032
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH982477A CH625242A5 (enrdf_load_stackoverflow) | 1977-08-10 | 1977-08-10 |
Country Status (19)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU532001B2 (en) * | 1978-11-20 | 1983-09-15 | Sumitomo Chemical Company, Limited | Polycyclic indole derivatives |
| FR2468605A1 (fr) * | 1979-10-30 | 1981-05-08 | Richter Gedeon Vegyeszet | Procede de preparation d'ester de l'acide apovincaminique |
| DE2944036C2 (de) * | 1979-10-31 | 1986-11-06 | Richter Gedeon Vegyészeti Gyár R.T., Budapest | Verfahren zur Herstellung von Apovincaminsäureestern |
-
1977
- 1977-08-10 CH CH982477A patent/CH625242A5/it not_active IP Right Cessation
-
1978
- 1978-08-02 IT IT26420/78A patent/IT1200363B/it active
- 1978-08-03 DE DE19782833967 patent/DE2833967A1/de not_active Withdrawn
- 1978-08-04 BE BE189715A patent/BE869537A/xx unknown
- 1978-08-07 AT AT0571278A patent/AT365590B/de not_active IP Right Cessation
- 1978-08-08 NL NL787808302A patent/NL7808302A/xx not_active Application Discontinuation
- 1978-08-08 AU AU38743/78A patent/AU3874378A/en active Pending
- 1978-08-08 CA CA308,873A patent/CA1100135A/en not_active Expired
- 1978-08-09 FR FR7823463A patent/FR2400023A1/fr active Granted
- 1978-08-09 GB GB7832887A patent/GB2003860B/en not_active Expired
- 1978-08-09 DK DK351478A patent/DK351478A/da not_active Application Discontinuation
- 1978-08-09 SE SE7808521A patent/SE7808521L/xx unknown
- 1978-08-09 HU HU78CO355A patent/HU176218B/hu unknown
- 1978-08-10 AR AR273263A patent/AR216684A1/es active
- 1978-08-10 FI FI782447A patent/FI782447A7/fi not_active Application Discontinuation
- 1978-08-10 ES ES472469A patent/ES472469A1/es not_active Expired
- 1978-08-10 JP JP9676978A patent/JPS5452100A/ja active Pending
- 1978-08-10 ZA ZA00784536A patent/ZA784536B/xx unknown
- 1978-08-10 OA OA56577A patent/OA06023A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SE7808521L (sv) | 1979-02-11 |
| FR2400023A1 (fr) | 1979-03-09 |
| DE2833967A1 (de) | 1979-03-01 |
| BE869537A (fr) | 1978-12-01 |
| GB2003860B (en) | 1982-03-03 |
| AR216684A1 (es) | 1980-01-15 |
| ATA571278A (de) | 1981-06-15 |
| IT7826420A0 (it) | 1978-08-02 |
| JPS5452100A (en) | 1979-04-24 |
| CA1100135A (en) | 1981-04-28 |
| HU176218B (en) | 1981-01-28 |
| OA06023A (fr) | 1981-06-30 |
| NL7808302A (nl) | 1979-02-13 |
| ES472469A1 (es) | 1979-03-16 |
| FI782447A7 (fi) | 1979-02-11 |
| ZA784536B (en) | 1979-08-29 |
| IT1200363B (it) | 1989-01-18 |
| GB2003860A (en) | 1979-03-21 |
| DK351478A (da) | 1979-02-11 |
| FR2400023B1 (enrdf_load_stackoverflow) | 1982-07-30 |
| AU3874378A (en) | 1980-02-14 |
| AT365590B (de) | 1982-01-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |