IE811832L - Indoles. - Google Patents
Indoles.Info
- Publication number
- IE811832L IE811832L IE811832A IE183281A IE811832L IE 811832 L IE811832 L IE 811832L IE 811832 A IE811832 A IE 811832A IE 183281 A IE183281 A IE 183281A IE 811832 L IE811832 L IE 811832L
- Authority
- IE
- Ireland
- Prior art keywords
- group
- alkyl
- hydrogen atom
- cycloalkyl
- represent
- Prior art date
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
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- 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
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- 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
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
- C07D209/16—Tryptamines
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
Compounds are disclosed of general formula (I> <IMAGE> wherein R1 represents a group CHO, COR8, CO2R8, CONR9R10, CSNR9R10 or SO2NR9R10, where R8 represents an alkyl, cycloalkyl, aryl or aralkyl group, R9 represents a hydrogen atom or an alkyl group, and R10 represents a hydrogen atom or an alkyl, cycloalkyl, aryl or aralkyl group; R2, R3, R4, R6 and R7, which may be the same or different, each represents a hydrogen atom or a C1-3 alkyl group; R5 represents a hydrogen atom or an alkyl, cycloalkyl, alkenyl or an aralkyl group or R4 and R5 together form an aralkylidene group or R4 and R5 together with the nitrogen atom to which they are attached form a saturated monocyclic 5- to 7-membered ring; n is zero or 1; and Alk represents an alkylene chain containing two or three carbon atoms which may be unsubstituted or substituted by not more than two C1-3 alkyl groups; with the provisos that, when n is zero and (i) R4 and R5, both represent alkyl groups, R1 does not represent the group CHO or COR8; and (ii) R1 does not represent the group SO2NH2; and physiologically acceptable salts, solvates and bioprecursors thereof. The compounds are described as potentially useful for the treatment of migraine.
[GB2083463A]
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8026288 | 1980-08-12 | ||
| GB8026287 | 1980-08-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE811832L true IE811832L (en) | 1982-02-12 |
| IE51493B1 IE51493B1 (en) | 1987-01-07 |
Family
ID=26276534
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1832/81A IE51493B1 (en) | 1980-08-12 | 1981-08-11 | Heterocyclic compounds |
Country Status (12)
| Country | Link |
|---|---|
| AU (1) | AU550010B2 (en) |
| CH (1) | CH652394A5 (en) |
| DE (1) | DE3131752A1 (en) |
| DK (1) | DK157995C (en) |
| ES (2) | ES504694A0 (en) |
| FR (1) | FR2488606A1 (en) |
| GB (1) | GB2083463B (en) |
| IE (1) | IE51493B1 (en) |
| IT (1) | IT1171450B (en) |
| NL (1) | NL8103764A (en) |
| NZ (1) | NZ197998A (en) |
| SE (1) | SE454777B (en) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1170387B (en) * | 1982-06-07 | 1987-06-03 | Glaxo Group Ltd | HETEROCYCLIC COMPOUNDS, PROCEDURE TO PREPARE THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| PT78358B (en) * | 1983-04-07 | 1986-05-30 | Smith Kline French Lab | Chemical process |
| HU196752B (en) * | 1983-12-06 | 1989-01-30 | Glaxo Group Ltd | Process for production of medical compositions containing indole-derivatives and these compounds |
| GB8332437D0 (en) * | 1983-12-06 | 1984-01-11 | Glaxo Group Ltd | Chemical compounds |
| GB8419575D0 (en) * | 1984-08-01 | 1984-09-05 | Glaxo Group Ltd | Chemical compounds |
| GB8600398D0 (en) * | 1986-01-08 | 1986-02-12 | Glaxo Group Ltd | Chemical compounds |
| GB8600397D0 (en) * | 1986-01-08 | 1986-02-12 | Glaxo Group Ltd | Chemical compounds |
| GB8607824D0 (en) * | 1986-03-27 | 1986-04-30 | Glaxo Group Ltd | Chemical compounds |
| US5225431A (en) * | 1987-10-23 | 1993-07-06 | Burroughs Wellcome Co. | Therapeutic substituted indole compounds and compositions thereof |
| SK278998B6 (en) * | 1991-02-01 | 1998-05-06 | Merck Sharp & Dohme Limited | Imidazole, triazole and tetrazole derivatives, method of producing same, their use and pharmaceutical compositons on their base |
| GB9104136D0 (en) * | 1991-02-27 | 1991-04-17 | Merck Sharp & Dohme | Therapeutic agents |
| DK0635015T3 (en) * | 1992-04-10 | 1997-03-17 | Pfizer | Acylaminoindole derivatives as 5-Htl agonists |
| GB9207930D0 (en) * | 1992-04-10 | 1992-05-27 | Pfizer Ltd | Indoles |
| GB9209882D0 (en) * | 1992-05-07 | 1992-06-24 | Glaxo Lab Sa | Compositions |
| GB9211277D0 (en) | 1992-05-28 | 1992-07-15 | Glaxo Group Inc | Pharmaceutical compositions |
| IL106445A (en) * | 1992-07-30 | 1998-01-04 | Merck Sharp & Dohme | 4-substituted 1, 2, 4-triazole derivatives, their preparation and pharmaceutical compositions containing them |
| ES2070772B1 (en) * | 1993-08-09 | 1996-02-16 | Pfizer | DERIVATIVES OF ACILAMINOINDOL |
| EP0796258A1 (en) * | 1994-12-06 | 1997-09-24 | MERCK SHARP & DOHME LTD. | Azetidine, pyrrolidine and piperidine derivatives as 5ht1 receptor agonists |
| FR2731224B1 (en) * | 1995-03-02 | 1997-05-30 | Pf Medicament | NOVEL BI-TRYPTAMINIC SULFONAMIDE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS |
| US7189753B1 (en) | 1997-11-06 | 2007-03-13 | Cady Roger K | Preemptive prophylaxis of migraine |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2870162A (en) * | 1954-04-28 | 1959-01-20 | Upjohn Co | Production of certain tryptamines and compounds produced in the process |
| FR1203195A (en) * | 1958-07-25 | 1960-01-15 | Chimiotherapie Lab Franc | Process for the preparation of a new derivative of tryptamine |
| NL7316677A (en) * | 1972-12-21 | 1974-06-25 | ||
| ZA795239B (en) * | 1978-10-12 | 1980-11-26 | Glaxo Group Ltd | Heterocyclic compounds |
-
1981
- 1981-08-11 CH CH5161/81A patent/CH652394A5/en not_active IP Right Cessation
- 1981-08-11 DK DK357281A patent/DK157995C/en not_active IP Right Cessation
- 1981-08-11 FR FR8115515A patent/FR2488606A1/en active Granted
- 1981-08-11 NL NL8103764A patent/NL8103764A/en not_active Application Discontinuation
- 1981-08-11 IE IE1832/81A patent/IE51493B1/en unknown
- 1981-08-11 DE DE19813131752 patent/DE3131752A1/en active Granted
- 1981-08-11 IT IT49085/81A patent/IT1171450B/en active
- 1981-08-11 AU AU73995/81A patent/AU550010B2/en not_active Ceased
- 1981-08-11 NZ NZ197998A patent/NZ197998A/en unknown
- 1981-08-11 ES ES504694A patent/ES504694A0/en active Granted
- 1981-08-11 SE SE8104783A patent/SE454777B/en not_active IP Right Cessation
- 1981-08-11 GB GB8124478A patent/GB2083463B/en not_active Expired
-
1982
- 1982-07-13 ES ES513934A patent/ES513934A0/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| AU550010B2 (en) | 1986-02-27 |
| AU7399581A (en) | 1982-02-18 |
| DK357281A (en) | 1982-02-13 |
| ES8405371A1 (en) | 1984-06-01 |
| ES513934A0 (en) | 1984-06-01 |
| CH652394A5 (en) | 1985-11-15 |
| DE3131752A1 (en) | 1982-06-16 |
| SE454777B (en) | 1988-05-30 |
| FR2488606A1 (en) | 1982-02-19 |
| DK157995B (en) | 1990-03-12 |
| GB2083463A (en) | 1982-03-24 |
| IT8149085A0 (en) | 1981-08-11 |
| IT1171450B (en) | 1987-06-10 |
| FR2488606B1 (en) | 1984-10-26 |
| GB2083463B (en) | 1984-05-10 |
| DK157995C (en) | 1990-08-06 |
| IE51493B1 (en) | 1987-01-07 |
| NL8103764A (en) | 1982-03-01 |
| DE3131752C2 (en) | 1992-04-23 |
| NZ197998A (en) | 1985-08-16 |
| ES8300699A1 (en) | 1982-11-01 |
| IT8149085A1 (en) | 1983-02-11 |
| ES504694A0 (en) | 1982-11-01 |
| SE8104783L (en) | 1982-02-13 |
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