ES255618A1 - Steroid compounds - Google Patents
Steroid compoundsInfo
- Publication number
- ES255618A1 ES255618A1 ES0255618A ES255618A ES255618A1 ES 255618 A1 ES255618 A1 ES 255618A1 ES 0255618 A ES0255618 A ES 0255618A ES 255618 A ES255618 A ES 255618A ES 255618 A1 ES255618 A1 ES 255618A1
- Authority
- ES
- Spain
- Prior art keywords
- keto
- acetoxy
- methyl
- pregnene
- cadmium
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
Abstract
The invention comprises 17a -bromo-9(11)-pregnene compounds of the general formulae <FORM:0936806/IV(a)/1> <FORM:0936806/IV(a)/2> wherein R represents a hydrogen atom or an acyl group, R1 represents a hydrogen or bromine atom, R11 represents a C1-5 alkyl group, and R0 represents a keto or b -hydroxy group the preparation thereof by contacting the corresponding steroids of the general formulae <FORM:0936806/IV(a)/3> <FORM:0936806/IV(a)/4> wherein R, R11 and R0 have the above significance, with bromine this process may be extended by dehydrobrominating the resulting bromo substituted steroids to form steroids of the general formulae <FORM:0936806/IV(a)/5> <FORM:0936806/IV(a)/6> wherein R, R11 and R0 have the above significance. The above processes may be modified in that the steroids of the first two formulae above wherein R1 represents hydrogen and R, R11 and R0 have the above significance are prepared by brominating the corresponding 17(20)-unsaturated 20-enol derivatives of the steroids of the second two formulae above, for example, the 20-enol acylates thereof or the 20-zinc, cadmium or magnesium enolates thereof. In the case of the 17a -monobromo-compounds the dehydrobrominating step may be carried out with a tertiary amine such as pyridine, dimethylformamide or lithium chloride in an N,N-dilower-alkylamide. In the case of the 17a ,21-dibromo-compounds, the dehydrobrominating step may be carried out with an alkali metal iodide. 3a -Acetoxy- 11b -hydroxy- 16a -methyl-pregnane is prepared by treating 3a -acetoxy-11,20-diketo-D 16-pregnene with a reagent obtained by reacting cadmium chloride with methyl magnesium bromide in the presence of cuprous chloride and treating the reaction product with hydrochloric acid to form 3a -acetoxy- 11,20-diketo- 16a -methylpregnane, forming the corresponding 20-semicarbazone, reducing the semicarbazone with sodium borohydride to form 3a ,11b -dihydroxy-16a -methyl-20-ketone-pregnane, and acylating this compound. 3a -Acetoxy-16a -methyl- 20-keto-9(11)-pregnene is prepared by brominating 3a ,11b -dihydroxy-20-keto-pregnane or the corresponding 3-acetate in the presence of a strong acid catalyst to form 17a ,21-dibromo-3a -hydroxy-20-keto-9(11)-pregnene or the corresponding 3-acetate, treating this compound with sodium iodide to form 17a -bromo-3a -hydroxy-20-keto-9(11)-pregnene or the corresponding 3-acetate, dehydrobrominating this compound with pyridine to form 3a -hydroxy-20-keto-9(11), 16-pregnadiene or the corresponding 3-acetate, treating the 3a -acetoxy-20-keto-9(11), 16-pregnadiene with a reagent obtained by reacting cadmium chloride and methyl magnesium iodide in the presence of cuprous chloride and decomposing the reaction product. 3a ,20-Diacetoxy-11-keto- 16a -methyl-17(20)-pregnene is prepared by reacting 3a -acetoxy-11,20-diketo-16-pregnene with dimethyl cadmium to form the 20-cadmium enol derivative of 3a -acetoxy-11-keto-16a -methyl-17(20)-pregnene and refluxing this compound with acetic anhydride. 3a ,20- Diacetoxy- 16a -methyl- 9(11),17(20)-pregnadiene is prepared by reacting 3a -acetoxy- 16a -methyl -20-keto-9(11)- pregnene with acetic anhydride in the presence of 2,4-dinitrobenzenesulphonic acid. 20-Cadmium enol derivative of 3a -acetoxy-16a -methyl-9(11),17(20)-pregnadiene is prepared by reacting 3a -acetoxy-20-keto-9(11),16-pregnadiene with the product obtained by reacting cadmium chloride and methyl magnesium iodide in the presence of cuprous chloride.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US790041A US3083215A (en) | 1959-01-30 | 1959-01-30 | Process for preparing 16-alkyl-delta9,11-pregnenes |
US790042A US3013034A (en) | 1959-01-30 | 1959-01-30 | Process for the preparation of 16-alkyl-11-oxygenated-16-pregnenes |
Publications (1)
Publication Number | Publication Date |
---|---|
ES255618A1 true ES255618A1 (en) | 1960-06-01 |
Family
ID=27120989
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES0255618A Expired ES255618A1 (en) | 1959-01-30 | 1960-01-30 | Steroid compounds |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE587066A (en) |
CH (1) | CH387030A (en) |
ES (1) | ES255618A1 (en) |
GB (1) | GB936806A (en) |
-
1960
- 1960-01-18 GB GB173260A patent/GB936806A/en not_active Expired
- 1960-01-28 BE BE587066A patent/BE587066A/en unknown
- 1960-01-30 CH CH102860A patent/CH387030A/en unknown
- 1960-01-30 ES ES0255618A patent/ES255618A1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE587066A (en) | 1960-07-28 |
GB936806A (en) | 1963-09-11 |
CH387030A (en) | 1965-01-31 |
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