SE305209B - - Google Patents

Info

Publication number
SE305209B
SE305209B SE1514/62A SE151462A SE305209B SE 305209 B SE305209 B SE 305209B SE 1514/62 A SE1514/62 A SE 1514/62A SE 151462 A SE151462 A SE 151462A SE 305209 B SE305209 B SE 305209B
Authority
SE
Sweden
Prior art keywords
acid
chloride
ethinylcarbonyl
acyloxyacetyl
derivative
Prior art date
Application number
SE1514/62A
Inventor
S Gottfried
L Baxendale
Original Assignee
Biorex Laboratories Ltd
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 Biorex Laboratories Ltd filed Critical Biorex Laboratories Ltd
Publication of SE305209B publication Critical patent/SE305209B/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C61/00Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C61/16Unsaturated compounds
    • C07C61/28Unsaturated compounds polycyclic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients

Abstract

The invention comprises glycyrrhetinic acid derivatives of the general formula <FORM:0887011/IV (b)/1> in which A and B and/or C and D can together represent a further bond and X is hydroxy, ethinyl or acyloxymethyl and in which rings Y and Z are cis- or trans-relationship, together with their preparation by brominating the corresponding 3,11-diketo-18a - or 18b -olean-12-ene 20-carboxylic acid to give the corresponding 2-bromo or 2,12,13-tribromo compound, dehydrobrominating to the corresponding 1,12-diene or 1,12,18-triene, and then, if desired, forming the acid chloride and converting it into the corresponding ethinylcarbonyl or acyloxyacetyl derivative. The latter steps are carried out by treatment with thionyl chloride or oxalyl chloride to form the acid chloride, followed by reaction with sodium acetylide to form the ethinylcarbonyl derivatives, or with diazomethane followed by acid treatment of the resulting diazoketone to give the acyloxyacetyl derivative. Detailed examples are given. Specifications 798,655, 843,132, 843,133 and 843,137 are referred to.
SE1514/62A 1959-07-24 1962-02-12 SE305209B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB25564/59A GB887011A (en) 1959-07-24 1959-07-24 Glycyrrhetinic acid derivatives

Publications (1)

Publication Number Publication Date
SE305209B true SE305209B (en) 1968-10-21

Family

ID=10229734

Family Applications (2)

Application Number Title Priority Date Filing Date
SE01476/67A SE329845B (en) 1959-07-24 1960-07-25
SE1514/62A SE305209B (en) 1959-07-24 1962-02-12

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SE01476/67A SE329845B (en) 1959-07-24 1960-07-25

Country Status (4)

Country Link
ES (2) ES259842A1 (en)
FR (1) FR727M (en)
GB (1) GB887011A (en)
SE (2) SE329845B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008000068A1 (en) * 2006-06-27 2008-01-03 Wellington Laboratories Inc. Method for preparing 2-iodo triterpenoid compounds

Also Published As

Publication number Publication date
GB887011A (en) 1962-01-10
ES259842A1 (en) 1961-02-01
ES259841A1 (en) 1960-11-01
FR727M (en) 1961-08-07
SE329845B (en) 1970-10-26

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