ES430059A1 - Process for preparing vincamine nicotinate salt - Google Patents

Process for preparing vincamine nicotinate salt

Info

Publication number
ES430059A1
ES430059A1 ES430059A ES430059A ES430059A1 ES 430059 A1 ES430059 A1 ES 430059A1 ES 430059 A ES430059 A ES 430059A ES 430059 A ES430059 A ES 430059A ES 430059 A1 ES430059 A1 ES 430059A1
Authority
ES
Spain
Prior art keywords
vincamine
nicotinate salt
nicotinic acid
preparing
preparing vincamine
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
Application number
ES430059A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Laboratorios Roger SA
Original Assignee
Laboratorios Roger SA
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 Laboratorios Roger SA filed Critical Laboratorios Roger SA
Priority to ES430059A priority Critical patent/ES430059A1/en
Priority to BE2054552A priority patent/BE833147A/en
Priority to GB37110/75A priority patent/GB1481386A/en
Priority to FR7528890A priority patent/FR2284609A1/en
Publication of ES430059A1 publication Critical patent/ES430059A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or 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 to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • C07D213/80Acids; Esters in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D461/00Heterocyclic compounds containing indolo [3,2,1-d,e] pyrido [3,2,1,j] [1,5]-naphthyridine ring systems, e.g. vincamine

Abstract

Procedure for obtaining a new nicotinic acid derivative of formula: **(See formula)** characterized by consisting of the direct reaction of nicotinic acid with vincamine in a common polar solvent, such as methanol, leaving it to stand, and subsequent evaporation of it in vacuo. (Machine-translation by Google Translate, not legally binding)
ES430059A 1974-09-14 1974-09-14 Process for preparing vincamine nicotinate salt Expired ES430059A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
ES430059A ES430059A1 (en) 1974-09-14 1974-09-14 Process for preparing vincamine nicotinate salt
BE2054552A BE833147A (en) 1974-09-14 1975-09-08 PROCESS FOR OBTAINING A NEW NICOTINIC ACID DERIVATIVE
GB37110/75A GB1481386A (en) 1974-09-14 1975-09-09 Process for preparing vincamine nicotinate salt
FR7528890A FR2284609A1 (en) 1974-09-14 1975-09-12 PROCESS FOR OBTAINING A NICOTINE COMPOUND OF VINCAMINE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES430059A ES430059A1 (en) 1974-09-14 1974-09-14 Process for preparing vincamine nicotinate salt

Publications (1)

Publication Number Publication Date
ES430059A1 true ES430059A1 (en) 1976-10-16

Family

ID=8467549

Family Applications (1)

Application Number Title Priority Date Filing Date
ES430059A Expired ES430059A1 (en) 1974-09-14 1974-09-14 Process for preparing vincamine nicotinate salt

Country Status (4)

Country Link
BE (1) BE833147A (en)
ES (1) ES430059A1 (en)
FR (1) FR2284609A1 (en)
GB (1) GB1481386A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES446755A1 (en) * 1976-03-31 1977-06-01 Ferrer Int Vincamine salt and a process for its production
US4122179A (en) * 1976-06-03 1978-10-24 Enrico Corvi Mora Acid addition salts of vincamine and apovincamine
US20040067986A1 (en) * 2002-10-04 2004-04-08 Nathan Sassover Neuro-degenerative inhibitor, neuro-endocrine modulator, and neuro-cerebral metabolism enhancer

Also Published As

Publication number Publication date
GB1481386A (en) 1977-07-27
FR2284609A1 (en) 1976-04-09
BE833147A (en) 1975-12-31
FR2284609B3 (en) 1978-05-05

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