MEDROXYPROGESTERONE Property

Melting point:

204-206°C

alpha 

D25 +75° (in chloroform)

Boiling point:

419.57°C (rough estimate)

Density 

1.0906 (rough estimate)

refractive index 

1.5000 (estimate)

storage temp. 

Sealed in dry,Room Temperature

solubility 

Chloroform (Slightly), Methanol (Slightly)

pka

13.03±0.70(Predicted)

color 

White

Merck 

13,5817

BRN 

2510965

CAS DataBase Reference

520-85-4(CAS DataBase Reference)

EPA Substance Registry System

Medroxyprogesterone (520-85-4)

Safety

Hazard Codes 

Xn

Risk Statements 

48-63-68

Safety Statements 

22-24/25

WGK Germany 

3

RTECS 

TU5300000

HS Code 

29372390

Hazardous Substances Data

520-85-4(Hazardous Substances Data)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H361Suspected of damaging fertility or the unborn child

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

MEDROXYPROGESTERONE Chemical Properties,Usage,Production

Chemical Properties

MEDROXYPROGESTERONE is White Solid

Originator

Provera,Upjohn,US,1959

Uses

An orally active progestogen used in hormone replacement therepy (HRT), in the past has been used as a component of oral contraceptives.SMedroxyprogesterone Acetate USP Related Compound B.

Uses

MEDROXYPROGESTERONE is an orally active progestogen used in hormone replacement therepy (HRT), in the past has been used as a component of oral contraceptives.

Definition

ChEBI: A 3-oxo Delta4-steroid that is pregn-4-ene-3,20-dione substituted by an alpha-hydroxy group at position 17 and a methyl group at position 6.

Manufacturing Process

Preparation of 17α-Hydroxyprogesterone 3,20-Bis-(Ethylene Ketal): A solution was prepared containing 50.0 g of 17α-hydroxyprogesterone in 1,000 ml of benzene, 100 ml of ethylene glycol and 2.5 g of p-toluenesulfonic acid monohydrate. This mixture was refluxed for a period of 17 hours using a calcium carbide water-trap to remove the water formed in the reaction. After this period of reflux 6.5 ml of pyridine was added to the solution, and the mixture cooled to room temperature.
The lower glycol layer was separated and washed with benzene. The benzene layer and the benzene washings were combined and the combined solution was divided into two equal portions, one of which was used for the isolation of 17α-hydroxyprogesterone 3,20-bis-(ethylene ketal) as follows. The benzene solution was washed with 5% sodium carbonate solution, water and saturated sodium chloride solution. After being dried over anhydrous magnesium sulfate the solution was concentrated to dryness at reduced pressure, The residue was recrystallized by taking up in hot methylene chloride, adding acetone and boiling to remove the methylene chloride until a final volume of about 200 ml was reached.
The solution was then refrigerated overnight and 17.8 g of crystals were removed by filtration. A second crop was obtained yielding 3.7 g of compound. The total yield of 17α-hydroxyprogesterone 3,20-bis-(ethylene ketal) was 20.3 g (64.3% of theory). Recrystallization of the crude 17αhydroxyprogesterone 3,20-bis-(ethylene ketal) from methanol gave the pure bisketal of MP 209° to 211°C.
Preparation of 5α,6α-Oxido-17α-Hydroxyallopregnane-3,20-dione 3,20-Bis- (Ethylene Ketal): A solution was prepared by heating 19.96 g (0.0477 mol) of 17α-hydroxyprogesterone 3,20-bis-(ethylene ketal) and 500 ml of benzene. After the solution was effected the flask was cooled to 5°C and a mixture of 3.68 g (0.0449 mol) of sodium acetate and 174 ml of 40% peracetic acid was added with stirring. The reaction mixture was stirred in the ice bath for 3 hours. The lower peracid layer was separated, diluted with water and extracted twice with benzene.
The upper layer was neutralized by the addition of cold 10% sodium hydroxide solution while stirring in an ice bath. The rate of addition of the sodium hydroxide was regulated to keep the temperature below 10°C. The benzene extracts from the peracid layer were combined and washed with cold 10% sodium hydroxide solution and with saturated sodium chloride solution. All the aqueous layers were washed again with the same portion of benzene. The combined benzene layers were dried over anhydrous magnesium sulfate and concentrated to dryness at reduced pressure.
The residue was recrystallized from acetone using methylene chloride to aid in solution. The crystalline material was removed by filtration and was recrystallized from methylene chloride-acetone to yield a total of 8 g of 5α,6αoxido-17α-hydroxyallopregnane-3,20-dione 3,20-bis-(ethylene ketal) of MP 211° to 215°C. For analytical purposes, another recrystallization from methylene chloride-acetone gave pure 5α,6α-oxido-17α-hydroxyallopregnane3,20-dione 3,20-bis-(ethylene ketal) of MP 216° to 218.5°C.
Preparation of 5α,17α-Dihydroxy-6β-Methylallopregnane-3,20-dione 3,20-bis- (Ethylene Ketal): To a solution of 91.6 g of 5α,6α-oxido-17αhydroxyallopregnane-3,20-dione 3,20-bis-(ethylene ketal) in 3,500 ml of freshly distilled tetrahydrofuran was added 1,170 ml of commercial 3 molar methyl magnesium bromide in ether solution. The reaction mixture was boiled to remove 1,800 ml of solvent by distillation and thereafter 1,000 ml of freshly distilled tetrahydrofuran was added.
Boiling was continued under reflux for a period of 16 hours. The solution was then concentrated to about one-half its original volume by distillation and was poured slowly with vigorous stirring into a large volume of ice water containing 340 g of ammonium chloride. The aqueous solution was saturated with sodium chloride and extracted with benzene. The benzene extract was washed with saturated brine, and both aqueous layers were washed again with the same portions of benzene.
The combined benzene layers were dried over anhydrous sodium carbonate and the solvent was removed at reduced pressure to give 90.5 g of crude crystalline 5α,17α-dihydroxy-6β-methylallopregnane-3,20-dione 3,20-bis- (ethylene ketal). Half of the residue, 45.2 g, was recrystallized from acetone and some methylene chloride to give 34.4 g of 5α,17α-dihydroxy-6βmethylallopregnane-3,20-dione 3,20-bis-(ethylene ketal). A sample recrystallized from acetone and methylene chloride for analysis melted at 160° to 163°C.
Preparation of 5α,17α-Dihydroxy-6β-Methylallopregnane-3,20-dione: A solution was prepared containing 38.9 g of 5α,7α-dihydroxy-6βmethylallopregnane-3,20-dione 3,20-bis-(ethylene ketal) in 389 ml of boiling acetone. Thereto was added 39 ml of 1 N sulfuric acid in portions under swirling and seeding with product. Boiling was continued for a period of 2 minutes and the mixture was allowed to stand at room temperature. Thereafter the mixture was diluted with 1,500 ml of water, chilled and filtered.
The precipitate was washed with water, dilute ammonium hydroxide and water, and dried in a vacuum oven overnight. The yield was 31.2 g which was recrystallized by dissolving in 1,200 ml of dimethylformamide, heating to 150°C, cooling slightly, and adding 12 ml of hot water. The recrystallized 5α,17α-dihydroxy-6β-methylallopregnane-3,20-dione thus obtained was 28.75 g of MP 270° to 275.5°C. After an additional recrystallization from aqueous dimethylformamide, the MP was 274° to 279°C.
Preparation of 6α-Methyl-17α-Hydroxyprogesterone: A suspension was made by introducing 2 g of 5α,17α-dihydroxy-6β-methylallopregnane-3,20-dione into 200 ml of chloroform. The suspension was chilled in an ice bath with stirring, and thereupon hydrogen chloride was bubbled through the reaction mixture for 80 minutes with continuous cooling and stirring. After bubbling in nitrogen for a period of 15 minutes the solution was washed with water, 1 N sodium bicarbonate solution and again with water.
The aqueous layers were rewashed with one portion of chloroform, and the washings combined with the remainder of the chloroform solution. After drying over anhydrous magnesium sulfate, the chloroform solution was concentrated to dryness, then taken up in a small volume of methylene chloride, treated with Magnesol anhydrous magnesium silicate and filtered. Acetone was added to the solution and the solution was boiled to remove the methylene chloride. After the solution was concentrated to a volume of about 15 ml it was chilled and the crystals were collected through filtration. The 1.37 g of crystals so obtained were recrystallized from acetone to give pure 6α-methyl-17α-hydroxyprogesterone of MP 220° to 223.5°C.
Preparation of 6α-Methyl-17-Hydroxyprogesterone 17-Acetate: 1 g of 6αmethyl-17α-hydroxyprogesterone was dissolved in a mixture of 10 ml of acetic acid and 2 ml of acetic anhydride by heating. After solution was effected the mixture was cooled to 15°C, and 0.3 g of p-toluenesulfonic acid was added. After allowing the mixture to stand for a period of 2.5 hours at room temperature, the pink solution was poured into ice water to give an amorphous solid which was recovered by filtration.
The precipitate was washed carefully with water and was then dissolved in 10 ml of methanol and 1.5 ml of methylene chloride. The solution was concentrated to 10 ml, diluted with 0.5 ml of 10% sodium hydroxide, boiled for one minute and cooled. The product, which crystallized on cooling, was recrystallized to give flakes of 6α-methyl-17α-hydroxyprogesterone 17- acetate, having a MP 205° to 209°C, according to US Patent 3,147,290.

brand name

Amen (Amarin); Curretab (Solvay Pharmaceuticals); Cycrin (ESI); Provera (Pharmacia & Upjohn).

Therapeutic Function

Progestin

Purification Methods

If it contains the epi-isomer (TLC), then dissolve it in CHCl3, bubble dry HCl gas to epimerise it, evaporate and recrystallise it from chloroform. The UV has max at 241nm ( 16,150) in EtOH. The 17-acetate [71-58-9] crystallises from MeOH with m 207-208o and [] D 25 +61o (CHCl3). Its UV has max at 240nm ( 15,950) in EtOH. [Babcock et al. J Am Chem Soc 80 2904 1958, Beilstein 8 IV 2212.]