http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IE-37048-L
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0e77f06144be4708a6ae75bd9fee56a4 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J7-0055 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J41-0055 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J71-001 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J9-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J71-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J7-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J41-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-575 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-57 |
| filingDate | 1972-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1973-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | IE-37048-L |
| titleOfInvention | 21-alkylated- 3, 20-diketo-delta 4-steroids. |
| abstract | 1416427 21-Alkylpregnanes AKZO NV 5 Jan 1973 [12 Jan 1972] 1534/72 Heading C2U The invention comprises compounds of formula wherein X is H or halo; Y is H 2 , oxo, H(OH), H(OAcyl) or H(halo); R 1 is H, Me or halo; R 2 is C 1-4 alkyl; R 3 is H or R 2 ; R 4 is H (except when Y is H 2 ), OAcyl, OAlkyl or Me; R 5 is H or C 1-4 alkyl, at least one of R 4 and R 5 being alkyl; and the 1,4- and 6,7-bonds are each saturated or unsaturated. Compounds I are prepared by 21-mono- or di-alkylation of compounds of formula (wherein A is a protected hydroxyl or oxo radical; B is H or a protected hydroxyl group; R<SP>1</SP> 4 is R 4 or OH; and R 7 is H, halo or C 1-4 alkyl) or, in Ex. 19, the 16α,17α-dimethylpregna - 1,4 - diene - 3,20 - dione, and where appropriate converting the alkylated product (which may or may not itself be a compound I) into a compound I by one or more appropriate reactions selected from: (i) elimination of 11α- mesyloxy to give #<SP>9(11)</SP>; (ii) conversion of #<SP>9(11)</SP> into 9α-halo-11#-OH or 9α,11#-dihalo, optionally via 9#,11#-epoxy intermediates; (iii) hydrolysis of protected hydroxy groups at position 3 or 11; (iv) hydrolysis of a protected oxo group at position 3 (with concurrent rearrangement of any #<SP>5</SP> or #<SP>3,5</SP> to #<SP>4</SP>); (v) acylation of 11-OH; (vi) oxidation of 3- or 11-OH to oxo; (vii) #<SP>1</SP>, #<SP>4</SP> and/or #<SP>6</SP>-dehydrogenation using microorganisms, quinones, selenium dioxide or halogenation and dehydrohalogenation; (viii) 11- microbial hydroxylation; (ix) reduction of 9α-Br to H; (x) acid or base-induced epimerization of a 6-substituent from # to α; (xi) 3-hydroxy (or acyloxy) - #<SP>5</SP>#3 - hydroxy (or acyloxy) - 5α,6α- epoxy#3 - hydroxy (or acyloxy) - 5a - hydroxy- 6# - fluoro (or methyl)#3 - oxo - 5α - OH - 6#- fluoro (or methyl)##<SP>4</SP> - 3 - oxo - 6# - fluoro (or methyl). The aforesaid 21-alkylation may be effected (a) by a Mannich reaction to introduce a 21 - (substituted aminomethyl) group which is quaternized and then reacted with a base to give a 21-methylene group which is either reduced to 21-methyl or converted by a Grignard reaction to another 21-alkyl group, or (b) by enolizing the 20-oxo group with trityllithium, a lithium dialkylamide, a Grignard reagent, or an alkali metal or amide thereof in liquid ammonia, followed by reaction with an alkyl halide. Method (b) may yield a mono- or di-alkylated product depending on the reactants and reaction conditions, and may additionally alkylate any 3- or 17-OH group in the starting material or convert an 11#-acetoxy group into a propionyloxy or isobutyryloxy group. 3 - Ethoxy - 16α,17α - dimethylpregna - 3,5- dien-20-one is prepared by enol-esterification of the corresponding #<SP>4</SP>-3,20-dione (Ex. 17). Antiinflammatory compositions for topical, rectal and parenteral administration comprise a compound I and a carrier.n[GB1416427A] |
| priorityDate | 1972-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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