GB888413A - Substituted tryptamines - Google Patents
Substituted tryptaminesInfo
- Publication number
- GB888413A GB888413A GB11641/58A GB1164158A GB888413A GB 888413 A GB888413 A GB 888413A GB 11641/58 A GB11641/58 A GB 11641/58A GB 1164158 A GB1164158 A GB 1164158A GB 888413 A GB888413 A GB 888413A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloro
- methoxy
- salt
- tryptamines
- tryptamine
- 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
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
- C07D471/02—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 system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
Abstract
The invention comprises 4,5,6-trimethoxy-, 7 - chloro-, 4 - chloro - 7 - methoxy-, 6 - methoxy-7 - chloro-, 6 - chloro - 7 - methoxy-, 4,7 - dichloro- and 6,7-dichloro-tryptamine together with a process for the preparation of tryptamines of the general formula <FORM:0888413/IV (b)/1> (in which R1-R4 represent H, Cl or OCH3 with the proviso that one to three of R1-R4 must be H) by condensing an aniline diazonium salt of the formula <FORM:0888413/IV (b)/2> with a salt of 3-carboxy-2-piperidone, cyclising the resulting phenylhydrazone of 2 : 3-dioxopiperidine to give a 1-oxo-1,2,3,4-tetrahydro-b -carboline, saponifying to give a salt of a tryptamine-2-carboxylic acid, liberating the free acid and decarboxylating. Detailed examples illustrate the invention and also the use of the novel tryptamines as antimetabolites for the microbiological conversion of tryptophane to indole. Specifications 868,475, 868,477, 888,407, 888,408, 888,409, 888,410, 888,411, 888,412, 888,414 and 888,426 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR888413X | 1957-08-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB888413A true GB888413A (en) | 1962-01-31 |
Family
ID=9376766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11641/58A Expired GB888413A (en) | 1957-08-02 | 1958-04-11 | Substituted tryptamines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB888413A (en) |
-
1958
- 1958-04-11 GB GB11641/58A patent/GB888413A/en not_active Expired
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