GB888535A - Indole compounds - Google Patents
Indole compoundsInfo
- Publication number
- GB888535A GB888535A GB38759A GB38759A GB888535A GB 888535 A GB888535 A GB 888535A GB 38759 A GB38759 A GB 38759A GB 38759 A GB38759 A GB 38759A GB 888535 A GB888535 A GB 888535A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- methyl
- alkyl
- acetic acid
- ethyl
- 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
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an alkyl or cycloalkyl radical attached to the ring nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
The invention comprises compounds of the formula <FORM:0888535/IV (b)/1> (wherein R is an alkyl radical of at most 8 carbon atoms and R1 is a dialkylaminoalkoxycarbonyl group) and acid-addition salts and quaternary ammonium compounds thereof; and their preparation by reacting a 1-alkyl-3-phenyl-2-indole acetic acid chloride or alkyl ester with a dialkylaminoalkanol. Examples are given. Ethyl 1-methyl-3-phenyl-2-indoleacetate is prepared from ethyl phenylacetoacetate and 1-phenyl-1-methyl-hydrazin sulphate in presence of sodium acetate and acetic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB38759A GB888535A (en) | 1959-01-05 | 1959-01-05 | Indole compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB38759A GB888535A (en) | 1959-01-05 | 1959-01-05 | Indole compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB888535A true GB888535A (en) | 1962-01-31 |
Family
ID=9703515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB38759A Expired GB888535A (en) | 1959-01-05 | 1959-01-05 | Indole compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB888535A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4105777A (en) * | 1976-01-21 | 1978-08-08 | Roussel Uclaf | Indoles |
-
1959
- 1959-01-05 GB GB38759A patent/GB888535A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4105777A (en) * | 1976-01-21 | 1978-08-08 | Roussel Uclaf | Indoles |
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