CS216231B2 - Method of making the esters of the n-substituted acid of the 9,10-dihydrolysergic - Google Patents

Method of making the esters of the n-substituted acid of the 9,10-dihydrolysergic Download PDF

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Publication number
CS216231B2
CS216231B2 CS784790A CS479078A CS216231B2 CS 216231 B2 CS216231 B2 CS 216231B2 CS 784790 A CS784790 A CS 784790A CS 479078 A CS479078 A CS 479078A CS 216231 B2 CS216231 B2 CS 216231B2
Authority
CS
Czechoslovakia
Prior art keywords
mmol
dihydrolysergic
formula
benzene
hydrogen
Prior art date
Application number
CS784790A
Other languages
Czech (cs)
English (en)
Inventor
Rudolf Rucman
Original Assignee
Lek Tovarna Farmacevtskih
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lek Tovarna Farmacevtskih filed Critical Lek Tovarna Farmacevtskih
Publication of CS216231B2 publication Critical patent/CS216231B2/cs

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D457/00Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula:, e.g. lysergic acid
    • C07D457/04Heterocyclic 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
CS784790A 1977-07-21 1978-07-18 Method of making the esters of the n-substituted acid of the 9,10-dihydrolysergic CS216231B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
YU1819/77A YU40004B (en) 1977-07-21 1977-07-21 Praocess for preparing n-substituted esters of 9,10-dihydrlysergic acid

Publications (1)

Publication Number Publication Date
CS216231B2 true CS216231B2 (en) 1982-10-29

Family

ID=25555705

Family Applications (1)

Application Number Title Priority Date Filing Date
CS784790A CS216231B2 (en) 1977-07-21 1978-07-18 Method of making the esters of the n-substituted acid of the 9,10-dihydrolysergic

Country Status (11)

Country Link
US (1) US4230859A (de)
EP (1) EP0000533B1 (de)
JP (1) JPS5436296A (de)
AT (1) AT363195B (de)
CS (1) CS216231B2 (de)
DE (1) DE2860896D1 (de)
ES (1) ES471716A1 (de)
FI (1) FI64369C (de)
PT (1) PT68278A (de)
SU (1) SU784775A3 (de)
YU (1) YU40004B (de)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4563461A (en) * 1983-03-10 1986-01-07 Eli Lilly And Company Selective method for blocking 5HT2 receptors
FR2584721B1 (fr) * 1985-07-11 1987-10-02 Rhone Poulenc Sante Procede de preparation des derives n-methyles du dihydrolysergate de methyle ou du methoxylumilysergate de methyle
FR2584720B1 (fr) * 1985-07-11 1987-10-02 Rhone Poulenc Sante Procede de preparation de derives n-methyles de l'ergoline
US4772709A (en) * 1985-10-01 1988-09-20 Eli Lilly And Company Process of making ketoalkanol esters of dihydrolysergic acid
US4734501A (en) * 1985-10-01 1988-03-29 Eli Lilly And Company N-alkylation of dihydrolysergic acid
US4810710A (en) * 1985-10-01 1989-03-07 Eli Lilly And Company 4-hydroxycyclohexyl 1-isopropyl-9,10-dihydro-lysergate for the treatment of migraine
US4845224A (en) * 1985-10-01 1989-07-04 Eli Lilly And Company Cycloalkanol esters of dihydrolysergic acid having peripheral serotonin antagonist properties
US4939258A (en) * 1985-10-01 1990-07-03 Eli Lilly And Company Cycloalkanol esters of dihydrolysergic acid
US4847261A (en) * 1985-10-01 1989-07-11 Eli Lilly And Company Alkoxy cycloalkanol esters of dihydrolysergic acid having peripheral serotonin antagonists properties
US4683236A (en) * 1985-10-01 1987-07-28 Eli Lilly And Company Cycloalkanol esters of dihydrolysergic acid useful as 5Ht2 receptor antagonists
US4820713A (en) * 1985-10-01 1989-04-11 Eli Lilly And Company Ketoalkanol esters of dihydrolysergic acid useful as 5HT receptor antagonists
US4713384A (en) * 1985-10-01 1987-12-15 Eli Lilly And Company Selective method for blocking 5HT2 receptors
US4968802A (en) * 1985-10-01 1990-11-06 Eli Lilly And Company Process of making alkoxy cycloalkanol esters of dihydrolysergic acid
US4762842A (en) * 1985-10-01 1988-08-09 Eli Lilly And Company Selective method for blocking 5HT2 receptors
US4713385A (en) * 1985-10-01 1987-12-15 Eli Lilly And Company Alkoxy and dialkoxyalkyl esters of dihydrolysergic acid and related compounds useful as 5HT receptor antagonists
US4906639A (en) * 1985-10-01 1990-03-06 Eli Lilly And Company Cycloalkanol esters of dihydrolysergic acid
US4714704A (en) * 1985-10-01 1987-12-22 Eli Lilly And Company Alkoxy cycloalkanol esters of dihydrolysergic acid useful as 5HT receptor antagonists
US4683237A (en) * 1985-12-20 1987-07-28 Eli Lilly And Company Fluoroalkyl esters of dihydrolysergic acid useful as 5HT2 receptor antagonists
US4704396A (en) * 1985-12-20 1987-11-03 Eli Lilly And Company Phenacyl esters of 1-substituted-6-(substituted and unsubstituted) dihydrolysergic acids useful as 5HT receptor antagonists
US4704395A (en) * 1985-12-20 1987-11-03 Eli Lilly And Company Cyclic ether esters of 2-substituted-6-(substituted and unsubstituted) dihydrolysergic acid useful as 5HT receptor antagonists
US4782063A (en) * 1987-05-11 1988-11-01 Eli Lilly And Company Ergoline esters useful as serotonin antagonists
US4835159A (en) * 1987-05-11 1989-05-30 Eli Lilly And Company Ergoline esters useful as serotonin antagonists
US4981859A (en) * 1987-06-15 1991-01-01 Cycloalkylamides of (8 beta )-1-alkyl-6-(substituted)ergolines
US4931447A (en) * 1987-06-15 1990-06-05 Eli Lilly And Company Cycloalkylamides of (8β)-1-alkyl-6-(substituted) ergolines
JPH01106511U (de) * 1988-01-02 1989-07-18
JPH02125915U (de) * 1989-03-29 1990-10-17

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA631701A (en) * 1961-11-28 Sandoz A.G. Compounds of the lysergic acid series alkylated at the indol nitrogen atom
FR1175276A (fr) * 1956-05-18 1959-03-23 Sandoz Ag Nouveaux dérivés de la série de l'acide lysergique et leur préparation
CH344731A (de) * 1956-05-18 1960-02-29 Sandoz Ag Verfahren zur Herstellung von neuen, am Indolstickstoff alkylierten Derivaten der Lysergsäure-Reihe
US3228943A (en) * 1962-06-11 1966-01-11 Lumilysergol derivatives
US3232942A (en) * 1964-06-02 1966-02-01 Sandoz Ltd 1-substituted (+)-lysergol
GB1298277A (en) * 1969-04-18 1972-11-29 Sandoz Ltd Preparation of ergot peptide alkaloids
US3879554A (en) * 1970-03-20 1975-04-22 Farmaceutici Italia Use of 1,6-dimethyl-8-{62 -(5-bromonicotinoyloxymethyl)-10 {60 -methoxyergoline in treating cerebral and peripheral metabolic vascular disorders
NL159384B (nl) * 1971-03-13 1979-02-15 Farmaceutici Italia Werkwijze voor het bereiden van een geneesmiddel met een adrenolytische activiteit, alsmede werkwijze voor het bereiden van een ester van 1-methyl-10-methoxylumilysergol.
DE2330912C3 (de) * 1972-06-22 1979-01-11 Societa Farmaceutici Italia S.P.A., Mailand (Italien) Verfahren zur Herstellung von Bromergolinverbindungen

Also Published As

Publication number Publication date
PT68278A (en) 1978-08-01
FI64369C (fi) 1983-11-10
FI782081A (fi) 1979-01-22
FI64369B (fi) 1983-07-29
EP0000533B1 (de) 1981-08-05
ATA490078A (de) 1980-12-15
AT363195B (de) 1981-07-10
YU40004B (en) 1985-06-30
US4230859A (en) 1980-10-28
DE2860896D1 (en) 1981-11-05
SU784775A3 (ru) 1980-11-30
ES471716A1 (es) 1979-10-01
JPS5648512B2 (de) 1981-11-16
YU181977A (en) 1983-01-21
EP0000533A1 (de) 1979-02-07
JPS5436296A (en) 1979-03-16

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