GB950528A - Improvements in or relating to lysergic acid derivatives - Google Patents
Improvements in or relating to lysergic acid derivativesInfo
- Publication number
- GB950528A GB950528A GB35478/61A GB3547861A GB950528A GB 950528 A GB950528 A GB 950528A GB 35478/61 A GB35478/61 A GB 35478/61A GB 3547861 A GB3547861 A GB 3547861A GB 950528 A GB950528 A GB 950528A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- radical
- lysergic
- derivatives
- compounds
- 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
- C07D457/00—Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid
- C07D457/04—Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 8
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises lysergic acid derivatives of general formula: <FORM:0950528/C2/1> in which R1 is a C1-4 alkyl radical, each of R2 and R3 is a hydrogen atom, a C1-4 alkyl or hydroxyalkyl radical or a monocyclic aryl radical, and \sG signifies the radical -CH=C< or <FORM:0950528/C2/2> ; and their acid addition salts; and a process for preparing these compounds in which the corresponding lysergic acid azide is heated to form the isocyanate, which is reacted with an amino compound <FORM:0950528/C2/3> , and, if desired, salification is effected with an organic or inorganic acid. The azides are prepared from the corresponding lysergic and dihydrolysergic acid hydrazides using hydrochloric acid and sodium nitrite solution, and the hydrazides in turn are prepared by heating 1-substituted derivatives of natural ergot alkaloids, or their dihydro derivatives, with anhydrous hydrazine. In the examples the amines used in the preparation of the carbamides are anilene, diethylamine and (+)-butaolamine -(21). Pharmaceutical compositions, having sedative, serotonin inhibiting and/or blood pressure lowering action, comprise the compounds of the invention together with inert carriers. Specification 948,203 is referred to.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1142660A CH392533A (en) | 1960-10-12 | 1960-10-12 | Process for the production of new urea derivatives |
CH263561 | 1961-03-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB950528A true GB950528A (en) | 1964-02-26 |
Family
ID=25690994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35478/61A Expired GB950528A (en) | 1960-10-12 | 1961-10-02 | Improvements in or relating to lysergic acid derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB950528A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4692452A (en) * | 1985-06-12 | 1987-09-08 | Spofa, Spojene Podniky Pro Zdravotnickou Vyrobu | Method for treatment of endometritis in mammalian females |
-
1961
- 1961-10-02 GB GB35478/61A patent/GB950528A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4692452A (en) * | 1985-06-12 | 1987-09-08 | Spofa, Spojene Podniky Pro Zdravotnickou Vyrobu | Method for treatment of endometritis in mammalian females |
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