ES259869A1 - Intermediates for 18-o-alkyl-reserpic acid esters and related compounds - Google Patents

Intermediates for 18-o-alkyl-reserpic acid esters and related compounds

Info

Publication number
ES259869A1
ES259869A1 ES0259869A ES259869A ES259869A1 ES 259869 A1 ES259869 A1 ES 259869A1 ES 0259869 A ES0259869 A ES 0259869A ES 259869 A ES259869 A ES 259869A ES 259869 A1 ES259869 A1 ES 259869A1
Authority
ES
Spain
Prior art keywords
lower alkyl
meal
radical
corn
etherified
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
ES0259869A
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.)
Novartis AG
Original Assignee
Ciba Geigy AG
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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of ES259869A1 publication Critical patent/ES259869A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D459/00Heterocyclic compounds containing benz [g] indolo [2, 3-a] quinolizine ring systems, e.g. yohimbine; 16, 18-lactones thereof, e.g. reserpic acid lactone
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K20/00Accessory food factors for animal feeding-stuffs
    • A23K20/10Organic substances
    • A23K20/116Heterocyclic compounds
    • A23K20/137Heterocyclic compounds containing two hetero atoms, of which at least one is nitrogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Food Science & Technology (AREA)
  • Zoology (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Husbandry (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Fodder In General (AREA)

Abstract

The invention comprises 17-lower alkoxy-18-hydroxy-3-epialloyohimbane-16-carboxylic acid esters etherified in 18-position with an alcohol of aliphatic character and with the nucleus of formula <FORM:0885981/IV (b)/1> in which the substituents at 16-, 17- and 18-have the same configuration as in d- or l-reserpine, their N-oxides and salts of these compounds, with the proviso that in reserpic acid esters etherified in the 18-position the ether radical bound to the 18-carbon atom and the alcohol radical of the ester contain together more than two carbon atoms, and a process for their preparation by reacting the corresponding 18-hydroxy compound or an N-oxide or salt thereof with a diazo compound of aliphatic character in the presence of a strong inorganic Lewis acid, and, if necessary, converting a resulting tertiary amine into an N-oxide, a resulting base into a salt, an N-oxide into the corresponding amine, or a salt into the corresponding base. The preferred compounds are of the general formula <FORM:0885981/IV (b)/2> in which R1 is an unsubstituted or substituted lower alkyl group, R2 is lower alkyl, R3 is an unsubstituted or substituted hydrocarbon radical of aliphatic character, R4 and R5 each are hydrogen or halo atoms or lower aliphatic hydrocarbon radicals, etherified or esterified hydroxyl groups, etherified mercapto, nitro, or amino groups, halo-lower alkyl radicals, or together (in adjacent positions) from a cyclic substituent, e.g. methylene-dioxy, R6 in one of positions 5 or 6 stands for hydrogen or an alkyl radical, and salts of these compounds. Specific examples of the R3 radical are lower alkyl, lower alkenyl, cycloalkyl, cycloalkenyl, cycloalkyl-lower alkyl, aryl-lower alkyl, aryl-lower alkenyl, in which the lower alkyl groups may be further substituted by alkoxy, mercapto, amino, acyl groups or halogen atoms and the aryl radicals may be further substituted by lower alkyl, lower alkoxy, lower alkenyloxy, halogen, lower alkoxy carbonyloxy, halogen lower alkyl, nitro or amino groups. Detailed examples are given and many compounds are also tabulated. n-Propyl reserpate is prepared by treating reserpic acid with n-diazopropane. Isopropyl, isobutyl and n-hexyl reserpates are likewise prepared from the appropriate diazo alkanes.ALSO:In preparing feeds, for poultry and other animals, containing corn meal, fat, mineral salts such as manganese sulphate, di-calcium carbonate and iodized salt, fish meal, soybean meal, corn gluten meal, corn distillers' solubles and vitamins &c., a portion of the corn meal previously blended with the pre-heated, liquefied fat is added to the remainder of the corn meal in a blending machine, thereafter the mineral salts, fish meal, soybean meal, corn gluten meal and corn distillers' solubles are added in turn and after a uniform mixture has been obtained, vitamins A and D, calcium pantothenate, choline chloride, riboflavin, Vitamin B12 and methionine are added in that order butylated hydroxy toluene is added and mixing is continued until a uniform product is obtained. The feed may include also dehydrated alfalfa meal. The relative proportions of the ingredients are disclosed.ALSO:Pharmaceutical compositions having a hypotensive action comprise 17-lower alkoxy-18-hydroxy - 3 - epi - alloyohimbane - 16 - carboxylic esters etherified in 18-position with an alcohol of aliphatic character and with a nucleus of the formula <FORM:0885981/VI/1> (in which the substituents in 16-, 17- and 18-position have the same configuration as in d- or l-reserpine, their N-oxides and salts of these compounds, with the proviso that in the reserpic esters etherified at C18 the ether radical bound to the 18-O-atom and the alcohol radical of the ester group together contain more than two carbon atoms) together with a pharmaceutical carrier suitable for oral or parenteral use. The compositions may take the form of tablets, solutions or elixirs. Examples detail the formulation of ethyl 18-O-methyl reserpate in tablets. Specified salts are hydrohalides, sulphates, phosphates, acetates, propionates, glycollates, lactates, pyruvates, oxalates, malonates, succinates, maleates, fumarates, malates, tartrates, citrates, ascorbates, citraconates, mono- and dihydroxymaleates, benzoates, phenylacetates, 4-aminobenzoates, 4 - hydroxybenzoates, anthranilates, cinnamates, mandelates, salicylates, 4 - aminosalicylates, 2 - phenoxybenzoates, 2 - acetoxybenzoates and methane-, ethane, 2 - hydroxyethane - and p - toluene-sulphonates.
ES0259869A 1959-07-29 1960-07-26 Intermediates for 18-o-alkyl-reserpic acid esters and related compounds Expired ES259869A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US83018759A 1959-07-29 1959-07-29
US83735759A 1959-09-01 1959-09-01
US37097A US3119819A (en) 1959-07-29 1960-06-20 Intermediates for 18-o-alkyl-reserpic acid esters and related compounds

Publications (1)

Publication Number Publication Date
ES259869A1 true ES259869A1 (en) 1961-03-16

Family

ID=27365147

Family Applications (2)

Application Number Title Priority Date Filing Date
ES0259869A Expired ES259869A1 (en) 1959-07-29 1960-07-26 Intermediates for 18-o-alkyl-reserpic acid esters and related compounds
ES0259870A Expired ES259870A1 (en) 1959-07-29 1960-07-26 Intermediates for 18-o-alkyl-reserpic acid esters and related compounds

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES0259870A Expired ES259870A1 (en) 1959-07-29 1960-07-26 Intermediates for 18-o-alkyl-reserpic acid esters and related compounds

Country Status (8)

Country Link
US (1) US3119819A (en)
AT (1) AT241693B (en)
CH (12) CH411918A (en)
DE (1) DE1197737B (en)
ES (2) ES259869A1 (en)
FI (1) FI40249B (en)
GB (1) GB885981A (en)
SE (1) SE314883B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0126300B1 (en) * 1992-12-28 1997-12-26 나이토 하루오 Heterocyclic carbonic acid derivatives which bind to retinoid receptors
EP2386565A3 (en) * 1999-01-12 2013-11-20 Cambridge Enterprise Ltd. Compounds and methods to inhibit or augment an inflammatory response

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1045772B (en) * 1956-04-24 1958-12-04 Ciba Geigy Growth-accelerating feed

Also Published As

Publication number Publication date
CH414656A (en) 1966-06-15
SE314883B (en) 1969-09-15
CH388324A (en) 1965-02-28
US3119819A (en) 1964-01-28
CH387054A (en) 1965-01-31
CH413850A (en) 1966-05-31
CH410967A (en) 1966-04-15
CH388325A (en) 1965-02-28
GB885981A (en) 1962-01-03
FI40249B (en) 1968-07-31
CH411918A (en) 1966-04-30
ES259870A1 (en) 1961-03-16
CH392540A (en) 1965-05-31
AT241693B (en) 1965-08-10
DE1197737B (en) 1965-07-29
CH410971A (en) 1966-04-15
CH411917A (en) 1966-04-30
CH414660A (en) 1966-06-15
CH392539A (en) 1965-05-31

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