GB2010833A - Homoeburnamine preparation - Google Patents
Homoeburnamine preparationInfo
- Publication number
- GB2010833A GB2010833A GB7845967A GB7845967A GB2010833A GB 2010833 A GB2010833 A GB 2010833A GB 7845967 A GB7845967 A GB 7845967A GB 7845967 A GB7845967 A GB 7845967A GB 2010833 A GB2010833 A GB 2010833A
- Authority
- GB
- United Kingdom
- Prior art keywords
- homoeburnamine
- preparation
- isomers
- salt
- reducing
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
(+) or (-) isomers of homoeburnamine are prepared by reacting a 1-ethyl- 2,3,4,6,7-hexahydro-indolo-(2,3-a)- quinolizinium salt with acrolein to provide an intermediate 3,4-dehydro- homoeburnamine salt, and reducing the intermediate to the appropriate homoeburnamine. The resulting isomer is dependent on the reducing agent used. The products are useful as intermediates in the synthesis of (+/-) vincamine and of its isomers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7845967A GB2010833B (en) | 1977-11-25 | 1978-11-24 | Homoerburnamine preparation |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4920077 | 1977-11-25 | ||
GB7845967A GB2010833B (en) | 1977-11-25 | 1978-11-24 | Homoerburnamine preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2010833A true GB2010833A (en) | 1979-07-04 |
GB2010833B GB2010833B (en) | 1982-04-15 |
Family
ID=26266425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7845967A Expired GB2010833B (en) | 1977-11-25 | 1978-11-24 | Homoerburnamine preparation |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2010833B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4285865A (en) * | 1979-08-06 | 1981-08-25 | Richter Gedeon Vegyeszeti Gyar Rt | Process for the preparation of halogenated 15-hydroxy-E-homoeburnane compounds |
US4285950A (en) * | 1979-08-13 | 1981-08-25 | Richter Gedeon Vegyeszeti Gyar Rt | 10-halo-E-homoeburnane derivatives, a process for the preparation thereof, a process for the use thereof as vasodilators, and vasodilating compositions thereof |
FR2492380A1 (en) * | 1980-10-17 | 1982-04-23 | Richter Gedeon Vegyeszet | Optical antipodes of 14-oxo-E-homo-eburnane derivs. - useful as intermediates for cerebral vasodilators and their multistage prepn. from n-halo-pentanoyl-tryptophan derivs. |
EP0050492A1 (en) * | 1980-10-17 | 1982-04-28 | Richter Gedeon Vegyeszeti Gyar R.T. | 1,1-Disubstituted-hexahydro-indolo(2,3-a)quinolizine derivatives and their use in the enantioselective synthesis of optically active 14-oxo-E-homo-eburnane derivatives |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3507328B1 (en) * | 2016-08-30 | 2022-07-20 | Dow Global Technologies LLC | Method of attenuating concentration of acrolein |
-
1978
- 1978-11-24 GB GB7845967A patent/GB2010833B/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4285865A (en) * | 1979-08-06 | 1981-08-25 | Richter Gedeon Vegyeszeti Gyar Rt | Process for the preparation of halogenated 15-hydroxy-E-homoeburnane compounds |
US4285950A (en) * | 1979-08-13 | 1981-08-25 | Richter Gedeon Vegyeszeti Gyar Rt | 10-halo-E-homoeburnane derivatives, a process for the preparation thereof, a process for the use thereof as vasodilators, and vasodilating compositions thereof |
US4399069A (en) * | 1980-10-12 | 1983-08-16 | Richter Gedeon Vegyeszeti Gyar Rt. | Process for an enantioselective synthesis of optically active 14-oxo-E-homo-eburnane derivatives |
FR2492380A1 (en) * | 1980-10-17 | 1982-04-23 | Richter Gedeon Vegyeszet | Optical antipodes of 14-oxo-E-homo-eburnane derivs. - useful as intermediates for cerebral vasodilators and their multistage prepn. from n-halo-pentanoyl-tryptophan derivs. |
EP0050492A1 (en) * | 1980-10-17 | 1982-04-28 | Richter Gedeon Vegyeszeti Gyar R.T. | 1,1-Disubstituted-hexahydro-indolo(2,3-a)quinolizine derivatives and their use in the enantioselective synthesis of optically active 14-oxo-E-homo-eburnane derivatives |
Also Published As
Publication number | Publication date |
---|---|
GB2010833B (en) | 1982-04-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |