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ES8603880A1 - Eburnane carboxylic acid derivative, manufacture and medicinal composition - Google Patents

Eburnane carboxylic acid derivative, manufacture and medicinal composition

Info

Publication number
ES8603880A1
ES8603880A1 ES545116A ES545116A ES8603880A1 ES 8603880 A1 ES8603880 A1 ES 8603880A1 ES 545116 A ES545116 A ES 545116A ES 545116 A ES545116 A ES 545116A ES 8603880 A1 ES8603880 A1 ES 8603880A1
Authority
ES
Spain
Prior art keywords
opt
prods
eburnane
carboxylic acid
iii
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
ES545116A
Other languages
Spanish (es)
Other versions
ES545116A0 (en
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.)
Richter Gedeon Vegyeszeti Gyar Nyrt
Original Assignee
Richter Gedeon Vegyeszeti Gyar RT
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 Richter Gedeon Vegyeszeti Gyar RT filed Critical Richter Gedeon Vegyeszeti Gyar RT
Publication of ES8603880A1 publication Critical patent/ES8603880A1/en
Publication of ES545116A0 publication Critical patent/ES545116A0/en
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/06Peri-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cephalosporin Compounds (AREA)
  • Fats And Perfumes (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

(A) 9- or 11-Amino-eburnane-carboxylic acid derivs. of formula (I) and their optical isomers and salts are new. R = NH2, NHCOR1 or NHSO2R2 in the 9 or 11 posn. R1 = H or opt. substd. 1-10C aliphatic hydrocarbyl, 3-8C cycloaliphatic hydrocarbyl, 6-14C aryl or heteroaryl R2 = opt. substd. 1-10C aliphatic hydrocarbyl or 6-14C aryl R3 = H or opt. substd. 1-10C aliphatic hydrocarbyl, 3-8C cycloaliphatic hydrocarbyl or 6-14C aryl A = OH B = H or A+B = direct bond provided that R3 is not Me when (a) R = NH2 or (b) R = 11-acetamido, A = OH and B = H. (B) Prodn. of eburnane-carboxylic acid derivs., 11-acetamido-vincamine or 9- or 11-amino-apovincamine is effected by: (a) acylating a cpd. (I) where R3 = Me or where R3 = H and A+B = bond, opt. after hydrolysis, excluding acetylation when R4 = Me, A = OH and B = H, opt. followed by (i) esterificn. or transesterificn. of prods. where R = NHCOR1 or NHSO2R2, (ii) hydrolysis of prods. where R = NHCOR1 or NHSO2R2, A = OH, B = H and R3 is other than H, and/or (iii) dehydration of prods. where A = OH and B = H (b) esterifying or transesterifying a cpd. (I) where R3 = Me or R3 = H and A+B bond, opt. followed by (i) hydrolysis of prods. where R = NH2, A = OH, B = H and R3 is other than H, (ii) dehydration of prods. where A = OH and B = H, and/or (iii) acylation of prods. where R = NH2 and R3 is as defined in (A) or is Me or (c) reducing cpds. of formula (I) where R = NO2, opt. followed by reactions as defined in (a)(i) and/or (a)(ii) or in (b)(i) and/or (a)(iii) or in (b)(ii) and/or (b)(iii). (C) Medicaments contg. cpds. (I) as defined in (A) and/or 11-acetamido-vincamine are new.
ES545116A 1984-07-11 1985-07-11 PROCEDURE FOR THE PREPARATION OF NEW RACEOMIC AND OPTICALLY ACTIVE DERIVATIVES OF ACID 9- AND 11-AMINOEBURNANO-CARBOXYLIC Granted ES545116A0 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU842703A HU191694B (en) 1984-07-11 1984-07-11 Process for production of new derivatives of amineburnan carbonic acid

Publications (2)

Publication Number Publication Date
ES8603880A1 true ES8603880A1 (en) 1986-01-01
ES545116A0 ES545116A0 (en) 1986-01-01

Family

ID=10960716

Family Applications (1)

Application Number Title Priority Date Filing Date
ES545116A Granted ES545116A0 (en) 1984-07-11 1985-07-11 PROCEDURE FOR THE PREPARATION OF NEW RACEOMIC AND OPTICALLY ACTIVE DERIVATIVES OF ACID 9- AND 11-AMINOEBURNANO-CARBOXYLIC

Country Status (18)

Country Link
JP (1) JPS6150981A (en)
KR (1) KR860001111A (en)
AU (1) AU577393B2 (en)
CS (1) CS255889B2 (en)
DD (1) DD235646A5 (en)
DK (1) DK317985A (en)
ES (1) ES545116A0 (en)
FI (1) FI852750L (en)
GR (1) GR851723B (en)
HU (1) HU191694B (en)
IL (1) IL75775A0 (en)
NO (1) NO852795L (en)
NZ (1) NZ212713A (en)
PL (1) PL254496A1 (en)
PT (1) PT80799B (en)
SU (1) SU1428200A3 (en)
YU (1) YU115385A (en)
ZA (1) ZA855245B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU191938B (en) * 1984-07-11 1987-04-28 Andras Vedres Process for production of new derivatives of 9 and 11 nitro-apovincamin acid
HU191693B (en) * 1984-07-11 1987-03-30 Richter Gedeon Vegyeszet Process for production of derivatives of 9-or-11 substituated apovincamin acid
FR2623501B1 (en) * 1987-11-19 1990-03-16 Roussel Uclaf NOVEL SUBSTITUTED DERIVATIVES OF 20.21-DINOREBURNAMENINE, THEIR PREPARATION PROCESS AND THE NOVEL INTERMEDIATES THUS OBTAINED, THEIR APPLICATION AS DRUGS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
CA2238488A1 (en) * 1994-07-07 1997-06-05 Hiroyoshi Hidaka Apovincaminic acid derivatives and drugs containing the same
BR112017016819B1 (en) * 2015-02-04 2022-12-13 Harbin Pharmaceutical Group Co., Ltd. General Pharmaceutical Factory DIAZA-BENZOFLUORANTHRENE COMPOUNDS

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU191938B (en) * 1984-07-11 1987-04-28 Andras Vedres Process for production of new derivatives of 9 and 11 nitro-apovincamin acid

Also Published As

Publication number Publication date
AU4477085A (en) 1986-01-16
NZ212713A (en) 1988-03-30
DK317985A (en) 1986-01-12
KR860001111A (en) 1986-02-22
NO852795L (en) 1986-01-13
IL75775A0 (en) 1985-11-29
PT80799B (en) 1987-01-12
DK317985D0 (en) 1985-07-11
YU115385A (en) 1988-04-30
DD235646A5 (en) 1986-05-14
HU191694B (en) 1987-03-30
SU1428200A3 (en) 1988-09-30
ES545116A0 (en) 1986-01-01
CS255889B2 (en) 1988-03-15
HUT38101A (en) 1986-04-28
ZA855245B (en) 1986-02-26
FI852750L (en) 1986-01-12
GR851723B (en) 1986-02-28
AU577393B2 (en) 1988-09-22
JPS6150981A (en) 1986-03-13
PT80799A (en) 1985-08-01
PL254496A1 (en) 1988-07-21
FI852750A0 (en) 1985-07-11

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