GB807875A - New indole derivatives - Google Patents
New indole derivativesInfo
- Publication number
- GB807875A GB807875A GB440556A GB440556A GB807875A GB 807875 A GB807875 A GB 807875A GB 440556 A GB440556 A GB 440556A GB 440556 A GB440556 A GB 440556A GB 807875 A GB807875 A GB 807875A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aldehyde
- indole
- nitrovinyl
- nitrovinylindole
- benzyloxy
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
The invention comprises indole derivatives of the formula <FORM:0807875/IV (b)/1> wherein the ring A may optionally be substituted by halogen, alkyl, alkoxy or aralkoxy radicals and wherein R represents hydrogen or an alkyl radical. The compounds are prepared by heating indole-3-aldehydes of the formula <FORM:0807875/IV (b)/2> with a nitroparaffin, preferably in the presence of a basic substance as catalyst. The nitroparaffin reactant is preferably nitromethane, nitroethane, nitropropane or nitro-octane. Suitable catalysts are ammonium acetate, methylamine, n-butylamine and benzylamine. (The Provisional Specification additionally specifies piperidine as a catalyst.) Specified indole-3-aldehyde reactants are indole-3-aldehyde, 5-methoxyindole-3-aldehyde, 6-methoxyindole-3-aldehyde, 5 - benzyloxyindole - 3 - aldehyde, 6 - benzyloxyindole - 3 - aldehyde, 5 - methylindole-3-aldehyde and 5-chloroindole-3-aldehyde. The reaction may be conducted in the presence of a solvent or diluent, such as acetic acid, b -ethoxyethanol or dimethylformamide, or in the presence of an excess of nitroparaffin reactant. The examples describe the preparation of 6-benzyloxy-3-b -nitrovinylindole, 5-benzyloxy - 3 - b - nitrovinylindole, 5 - benzyloxy - 3 - (b - methyl - b - nitrovinyl) - indole, 5 - benzyloxy - 3 - (b - ethyl - b - nitrovinyl) - indole, 5 - benzyloxy - 3 - (b - n - heptyl - b - nitrovinyl)-indole, 5 - methoxy - 3 - (b - methyl - b - nitrovinyl) - indole, 5 - methyl - 3 - b - nitrovinylindole, 5-chloro-3-b -nitrovinylindole, 3-b -nitrovinylindole, 3 - (b - methyl - b - nitrovinyl)-indole and 3-(b -ethyl-b -nitrovinyl)-indole. 5 - Methylindole-3-aldehyde and 5-chloroindole-3-aldehyde are prepared by reacting dimethylformamide with 5-methylindole or 5-chloroindole respectively in presence of phosphorus oxychloride. Specification 807,620 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB440556A GB807875A (en) | 1956-02-13 | 1956-02-13 | New indole derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB440556A GB807875A (en) | 1956-02-13 | 1956-02-13 | New indole derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB807875A true GB807875A (en) | 1959-01-21 |
Family
ID=9776578
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB440556A Expired GB807875A (en) | 1956-02-13 | 1956-02-13 | New indole derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB807875A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3050530A (en) * | 1962-08-21 | Improved process for the preparation of | ||
CN110746340A (en) * | 2019-11-07 | 2020-02-04 | 上海易恩化学技术有限公司 | Synthetic method of 5-methoxy-2-methyltryptamine |
-
1956
- 1956-02-13 GB GB440556A patent/GB807875A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3050530A (en) * | 1962-08-21 | Improved process for the preparation of | ||
CN110746340A (en) * | 2019-11-07 | 2020-02-04 | 上海易恩化学技术有限公司 | Synthetic method of 5-methoxy-2-methyltryptamine |
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