Longer-acting progestin prodrug contraceptives

Abstract

Described herein are progestin compounds that have extended release rates and that can be used without an estrogen to produce a contraceptive state.

Claims

1. A compound having structural formula IIIA or IIIB: ##STR00067## where, R.sub.1, R.sub.2 combine together to form a fused 3 to 7 membered ring with up to two heteroatoms, or each R.sub.1, R.sub.2, is, independently H, alkyl, cycloalkyl, phenyl, aryl, heteroaryl, acyl, cyano, halogen, OH, alkoxy, alkyl-sulfonyl or sulfonamide.

2. The compound of claim 1, wherein: R.sub.1, R.sub.2 are, independently, H, alkyl, phenyl, aryl, halogen, alkoxy, alkyl-sulfonyl or sulfonamide.

3. The compound of claim 1, wherein: R.sub.1, R.sub.2 are, independently, H, alkyl, phenyl, or halogen.

4. The compound of claim 1, wherein the compound has the structure: ##STR00068##

5. The compound of claim 1, wherein the compound has the structure: ##STR00069##

6. The compound of claim 1, wherein the compound has the structure: ##STR00070##

7. The compound of claim 1, wherein the compound has the structure: ##STR00071##

8. A compound having structural formula IVA or IVB: ##STR00072## where, hAr is pyridine, pyrimidine, pyrazine, isoxazole, or oxazole; R.sub.1, R.sub.2 combine together to form a fused 3 to 7 membered ring with up to two heteroatoms, or each R.sub.1, R.sub.2, is, independently H, alkyl, cycloalkyl, phenyl, aryl, heteroaryl, acyl, cyano, halogen, OH, alkoxy, alkyl-sulfonyl or sulfonamide.

9. The compound of claim 8, wherein: R.sub.1, R.sub.2 are, independently, H, alkyl, or phenyl.

10. The compound of claim 8, wherein the compound has the structure: ##STR00073##

11. The compound of claim 8, wherein the compound has the structure: ##STR00074##

12. A method of producing a contraceptive state in a subject comprising administering an effective amount of a compound, as described in claim 1, to the subject.

13. The method of claim 12, wherein the compound is administered by subcutaneous injection.

14. The method of claim 12, wherein the biological effect lasts for at least 6 months.

Description

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(1) It is to be understood the present invention is not limited to particular devices or methods, which may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting. As used in this specification and the appended claims, the singular forms a, an, and the include singular and plural referents unless the content clearly dictates otherwise. Furthermore, the word may is used throughout this application in a permissive sense (i.e., having the potential to, being able to), not in a mandatory sense (i.e., must). The term include, and derivations thereof, mean including, but not limited to. The term coupled means directly or indirectly connected.

(2) The term alkyl as used herein generally refers to a radical substituent containing the monovalent group C.sub.nH.sub.2n, where n is an integer greater than zero. In some embodiments n is 1 to 12, in other embodiments n is 1 to 6. The term alkyl includes a branched or unbranched monovalent hydrocarbon radical. Examples of alkyl radicals include, but are not limited to: methyl, ethyl, propyl, isopropyl, butyl, iso-butyl, sec-butyl, pentyl, 3-pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl. When the alkyl group has from 1-6 carbon atoms, it is referred to as a lower alkyl. Suitable lower alkyl radicals include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, 2-propenyl (or allyl), n-butyl, t-butyl, and i-butyl (or 2-methylpropyl).

(3) The term cycloalkyl as used herein generally refers to a radical substituent containing the monovalent group C.sub.nH.sub.2n-1, where n is an integer greater than zero and wherein the carbons C.sub.1 and C.sub.n are coupled to each other to form a ring. In some embodiments n is 3 to 8. Examples of cycloalkyl radicals include, but are not limited to: cyclopropyl (n=3), cyclobutyl (n=4), cyclopentyl (n=5), cyclohexyl (n=6), cycloheptyl (n=7), and cyclooctyl (n=8).

(4) The term alkoxy generally refers to an OR group, where R is a lower alkyl, substituted lower alkyl, aryl, substituted aryl, aralkyl or substituted aralkyl. Suitable alkoxy radicals include, but are not limited to, methoxy, ethoxy, phenoxy, t-butoxy, methoxyethoxy, and methoxymethoxy.

(5) The term alkyl-sulfonyl refers to the group SO.sub.2-alkyl, where alkyl is as defined above. Preferably alkyl is C.sub.1-C.sub.6 alkyl.

(6) The term sulfonamide refers to the group SO.sub.2NRR, where R and R are each, independently, alkyl or phenyl. Preferably, R and R are C.sub.1-C.sub.6 alkyl.

(7) Aromatic heterocyclic compounds are also referred to as heteroaryls. Heteroaryls may include rings such as thiophene, pyridine, isoxazole, phthalimide, pyrazole, indole, furan, pyrimidine, pyrazine or oxazole or benzo-fused analogs of these rings. In some embodiments, a heteroaryl is a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic ring which is either saturated or unsaturated, and which consists of carbon atoms and from 1 to 4 heteroatoms (e.g., N, O, and S) and wherein the nitrogen and sulfur heteroatoms may optionally be oxidized, and the nitrogen may optionally be quaternized, and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. In some embodiments, heterocycles may include cyclic rings including boron atoms. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom that results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. Examples of such heterocycles include, but are not limited to, 1H-indazole, 2-pyrrolidonyl, 2H,6H-1,5,2-dithiazinyl, 2H-pyrrolyl, 3H-indolyl, 4-piperidonyl, 4aH-carbazole, 4H-quinolizinyl, 6H-1,2,5-thiadiazinyl, acridinyl, azocinyl, benzofuranyl, benzothiophenyl, carbazole, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, indolinyl, indolizinyl, indolyl, isobenzofuranyl, isochromanyl, isoindolinyl, isoindolyl, isoquinolinyl (benzimidazolyl), isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxazolidinyl, oxazolyl, phenanthridinyl, phenanthrolinyl, phenarsazinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, pyrrolyl, quinazolinyl, quinolinyl, quinoxalinyl, quinuclidinyl, carbolinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrazolyl, thianthrenyl, thiazolyl, thienyl, thiophenyl, triazinyl, xanthenyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.

(8) In the first embodiment ester derivatives are being described that have the following general formula I:

(9) ##STR00003## Where: progestin is levonorgestrel or etonogestrel; Z is C, NH, N-alkyl, O, or S; A, M, Q X, and Y are each, independently, C or N; R.sub.1, R.sub.2 can combine together to form a fused cycloalkyl ring or a fused 3 to 7 membered ring with up to two heteroatoms, or each R.sub.1, R.sub.2, can independently, be H, alkyl, cycloalkyl, phenyl, aryl, heteroaryl, acyl, cyano, halogen, OH, alkoxy, alkyl-sulfonyl or sulfonamide.

(10) In another embodiment ester derivatives are being described that have the following general formula II:

(11) ##STR00004## Where: progestin is levonorgestrel or etonogestrel; Z is C, NH, N-alkyl, O, or S; M, Q, X, Y are each, independently, C, N, O or S; R.sub.1, R.sub.2 can combine together to form a fused cycloalkyl ring or a fused 3 to 7 membered ring with up to two heteroatoms, or each R.sub.1, R.sub.2, can independently, be H, alkyl, cycloalkyl, phenyl, aryl, heteroaryl, acyl, cyano, halogen, OH, alkoxy, alkyl-sulfonyl or sulfonamide.

(12) In a preferred embodiment, a compound has the structural formula I:

(13) ##STR00005## where, progestin is levonorgestrel or etonogestrel; and R.sub.1, R.sub.2 combine together to form a fused 3 to 7 membered ring with up to two heteroatoms, or each R.sub.1, R.sub.2, is, independently H, alkyl, cycloalkyl, phenyl, aryl, heteroaryl, acyl, cyano, halogen, OH, alkoxy, alkyl-sulfonyl or sulfonamide.

(14) In another preferred embodiment, a compound has structural formula II:

(15) ##STR00006## where, progestin is levonorgestrel or etonogestrel; hAr is pyridine, pyrimidine, pyrazine or oxazole; and R.sub.1, R.sub.2 combine together to form a fused 3 to 7 membered ring with up to two heteroatoms, or each R.sub.1, R.sub.2, is, independently H, alkyl, cycloalkyl, phenyl, aryl, heteroaryl, acyl, cyano, halogen, OH, alkoxy, alkyl-sulfonyl or sulfonamide.

(16) In an embodiment, a method of producing a contraceptive state in a subject comprises administering an effective amount of a compound, as described herein, to the subject. The compound may be administered by subcutaneous injection. Preferably, the compound has a biological effect lasts for at least 6 months.

(17) In an embodiment, the 17-hydroxy function of levonorgestrel or etononorgestrel derivatives are esterified to form esters of phenoxy acetic acid.

EXPERIMENTAL

Synthesis

(18) In one embodiment, the compounds described herein may be synthesized according to the general Scheme 1 below.

(19) ##STR00007##

(20) In Scheme 1, X is a labile group conducive to acylation. Y is also a labile group. In some embodiments, X is a halogen or OC(O)CH.sub.2Y to form an anhydride. Y is a group suitable for nucleophilic substitution such as a halide or alkoxy group. In a preferred embodiment, Y is a halogen (Cl or Br). The group Z represents the substituent (V) or (VI), where R.sub.1 and R.sub.2 are as defined above for compounds (I) and (II).

(21) ##STR00008##

(22) A specific example of a compound made using the procedure of Scheme 1 is shown below in Scheme 2.

(23) ##STR00009##

(24) In one embodiment, the compounds described herein may be synthesized according to the general Scheme 3 below.

(25) ##STR00010##

(26) In Scheme 3, a Steglich esterification is used to form an ester between the progestin alcohol and the acetic acid portion of the prodrug component. The reaction uses a carbodiimide and a base. Suitable carbodimides include, but are not limited to, dicyclohexylcarbodiimide and diisopropylcarbodiimide. Any suitable base can be used. Preferably the base is a pyridine base such as dimethylaminopyridine (DMAP). The group Z represents the substituent (V) or (VI), where R.sub.1 and R.sub.2 are as defined above for compounds (I) and (II).

(27) A specific example of a compound made using the procedure of Scheme 2 is shown below in Scheme 4.

(28) ##STR00011##

(29) In some embodiments, when a Steglich esterification is used, a protecting groups may be used on the some of the pendant side chains. When the prodrug component includes a sulfonamide side chain a

(30) ##STR00012##

(31) ##STR00013##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (3-sulfamoylphenoxy)acetate (General Method #1)

(32) To an oven-dried round bottom flask was added 3 (973 mg, 2.5 mmol), 3-hydroxybenzenesulfonamide (from PCT Int. Appl., 2004066963, 516 mg, 3.0 mmol), and 4A molecular sieve. Anhydrous DMF was added (5 ml) and then cesium carbonate (814 mg, 2.5 mmol). The mixture was allowed to stir for 24 hours, after which time an additional 0.5 equivalent of base and 0.3 equivalent of phenol was added to fully convert the starting material by allowing to stir an additional 16 hours. The mixture was then diluted with ice-cold saturated sodium bicarbonate and the resulting solids collected by vacuum filtration, washed with water and allowed to air-dry. The product was isolated by subjecting the crude solid to flash chromatography using a 2 to 10% gradient of acetone in DCM to afford 4. 1H NMR (300 MHz, DMSO-d6) 7.52-7.31 (m, 4H), 7.13 (ddd, J=7.8, 2.4, 0.9 Hz, 1H), 5.73 (s, 1H), 4.83 (s, 2H), 3.65 (s, 1H).

(33) ##STR00014##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (3-methylphenoxy)acetate (General Method #2)

(34) To a round bottom flask was added 1 (1.41 g, 4.5 mmol), (3-methylphenoxy)acetic acid (3.0 g, 18.1 mmol), and DMAP (550 mg, 4.5 mmol) in DCM (30 mL) at ambient temperature. Once a homogenous solution was observed, DIC was added (2.8 ml, 18.1 mmol). The mixture was allowed to stir overnight. The next morning the mixture was filtered, and the filtrate was rotovaped onto silica gel and subjected to flash chromatography. The resultant foam was then crystallized from methanol and DCM yielding 1.08 g of white crystal 5 (73%). 1H NMR (300 MHz, CDCl3) 7.17 (t, J=7.5 Hz, 1H), 6.81 (d, J=7.2 Hz, 1H), 6.73-6.67 (m, 2H), 5.84 (s, 1H), 4.59 (s, 2H), 2.66 (s, 1H), 2.33 (s, 3H).

(35) ##STR00015##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (2-chloro-4-sulfamoylphenoxy)acetate (General Method #3)

(36) ##STR00016##

Formation of (4-{bis[(2,4-dimethoxyphenyl)methyl]sulfamoyl}-2-chlorophenoxy)acetic acid 8

(37) 2-Chlorophenoxyacetic acid (2.31 g, 12. 4 mmol) was dissolved in methanol, and 3 ml of acetyl chloride was added dropwise. The mixture was allowed to stir overnight, then the methanol was removed under vacuum, and the residue dissolved in DCM and washed with saturated sodium bicarbonate. The material was then used in the next step, which involved treating with 8.0 ml (0.124 mol) of chlorosulfonic acid which was added dropwise to the neat ester at 0 C., and then allowed to stir overnight while gradually warming to room temperature. The homogenous mixture was then diluted with DCM and then poured onto ice. The resulting layers were separated, and the aqueous extracted with DCM. The combined organics were washed with brine, dried over sodium sulfate, the solution was filtered and then concentrated to give 3.2 g (86%) of purplish crystalline solid [2-chloro-4-(chlorosulfonyl)phenoxy]acetic acid, methyl ester 6. .sup.1H NMR (300 MHz, CDCl.sub.3) 8.10 (d, J=2.7 Hz, 1H), 7.91 (dd, J=9.0, 2.4 Hz, 1H), 6.95 (d, J=9.0 Hz, 1H), 4.87 (s, 2H), 3.86 (s, 3H). This material was then placed in a round bottom flask, suspended in DCM (20 ml) and chilled to 0 C. 3.37 g (10.7 mmol) of Bis(2,4-Dimethoxybenzyl)amine (prepared as described in Organic and Biomolecular Chemistry, 10(37), 7610-7617, 2012) and TEA (3.0 ml, 21.4 mmol) were dissolved in DCM (30 ml) and added dropwise to the halide solution. The mixture was then allowed to gradually warm to room temperature while stirring overnight. The next day the mixture was evaporated onto silica and subjected to flash chromatography using a 0 to 10% gradient of EtOAc in DCM to obtain 5.79 g (93%) of the intermediate methyl (4-{bis[(2,4-dimethoxyphenyl)methyl]sulfamoyl}-2-chlorophenoxy)acetate 7 as a semi-crystalline solid .sup.1H NMR (300 MHz, CDCl.sub.3) 7.54 (d, J=2.1 Hz, 1H), 7.47 (dd, J=8.7 Hz, 1H), 7.19 (d, J=8.4 Hz, 2H), 6.71 (d, J=8.7 Hz, 1H), 6.42 (dd, J=8.4, 2.4 Hz, 2H), 6.29 (d, J=2.1 Hz, 2H), 4.76 (s, 2H), 4.39 (s, 4H), 3.84 (s, 3H), 3.80 (s, 6H), 3.65 (s, 6H). The methyl ester was saponified by treating with 10 ml of 5M LiOHH.sub.2O in 100 ml THF to afford acid 8 (5.65 g, 99%).

(38) A round bottom flask was charged with 1 (780 mg, 2.5 mmol), 8 (5.6 g, 10 mmol), and DMAP (305 mg, 2.5 mmol). The solids were dissolved in DCM (30 ml) and then DIC was added (1.5 ml, 10 mmol), and the mixture was allowed to stir overnight. Next day, HPLC analysis indicated about 85% conversion of starting material. The mixture was filtered, loaded onto silica gel and subjected to flash chromatography using 2-5% gradient of acetone in DCM, and then 40% acetone in hexanes. The material was then dissolved in DCM (10 ml) and chilled to 0 C. 5 ml (65 mmol) of TFA was added. The mixture was allowed to stir for one hour, then the volatiles removed under vacuum and the residue washed with saturated sodium bicarbonate and the resulting solids collected by vacuum filtration. After drying, the solids were subjected to flash chromatography using 10% acetone in DCM, to furnish 754 mg of product 9 (54%, 2 steps)1H NMR (300 MHz, DMSO-d6) 7.85 (d, J=2.4 Hz, 1H), 7.71 (dd, J=8.7, 2.1 Hz, 1H), 7.38 (s, 2H), 7.19 (d, J=8.7 Hz, 1H), 5.73 (s, 1H), 5.02 (dd, J=16.8, 5.1 Hz, 2H), 3.68 (s, 1H).

(39) ##STR00017##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl phenoxyacetate 10

(40) Prepared in accordance with general method #2.sup.1H NMR (, CDCl3 300 MHz): 7.29 (dt, 2H, ArH, J=6.6, 0.9 Hz), 7.00 (dt, 1H, ArH, J=7.0, 0.9 Hz), 6.89 (d, 2H, ArH, J=8.1, 0.9 Hz), 5.84 (s, 1H), 4.61 (s, 2H), 2.82 (m, 2H), 2.65 (s, 1H) 0.99 (t, 3H, CH3, J=7.2 Hz).

(41) ##STR00018##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl 3-phenylpropanoate 11

(42) Prepared in accordance with general method #21H NMR (, CDCl3 300 MHz): 7.24 (m, 5H, ArH), 5.83 (s, 1H), 2.95 (t, 2H, J=7.9 Hz), 2.60 (s, 1H) 0.99 (t, 3H, CH3, J=7.3 Hz).

(43) ##STR00019##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (2-chlorophenoxy)acetate 12

(44) Prepared in accordance with general method #2.sup.1H NMR (300 MHz, CDCl3) 7.39 (dd, J=7.8, 1.5 Hz, 1H), 7.25-7.17 (m, 1H), 6.96 (td, J=7.8, 1.5 Hz, 1H), 6.84 (dd, J=8.4, 0.9 Hz, 1H), 5.84 (s, 1H), 4.70 (s, 2H), 2.66 (s, 1H).

(45) ##STR00020##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (4-methoxyphenoxy)acetate 13

(46) Prepared in accordance with general method #2(300 MHz, CDCl3) 6.84 (s, 4H), 5.84 (s, 1H), 4.56 (s, 2H), 3.78 (s, 3H), 2.66 (s, 1H).

(47) ##STR00021##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl [(pyridin-3-yl)oxy]acetate 14

(48) Prepared in accordance with general method #2.sup.1H NMR (300 MHz, CDCl3) 8.33-8.27 (m, 2H), 7.30-7.18 (m, 2H), 5.85 (s, 1H), 4.66 (s, 2H), 2.68 (1H).

(49) ##STR00022##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl [(2H-1,3-benzodioxol-5-yl)oxy]acetate 15

(50) Prepared in accordance with general method #1. 1H NMR (, CDCl3 300 MHz): 6.69 (d, 1H, ArH, J=7.8 Hz), 6.51 (d, 1H, ArH, J=2.7 Hz), 6.29 (dd, 1H, ArH, J=2.7, 8.7 Hz), 5.93 (s, 2H), 5.84 (s, 1H), 4.52 (s, 2H), 2.82 (m, 1H), 2.65 (s, 1H) 1.00 (t, 3H, CH3, J=7.0 Hz).

(51) ##STR00023##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl [4-(methanesulfonyl)phenoxy]acetate 16

(52) Prepared in accordance with general method #1. 1H NMR (, CDCl3 300 MHz): 7.88 (dd, 2H, ArH, J=2.1, 6.9 Hz), 7.01 (dd, 2H, ArH, J=2.1, 6.9 Hz), 5.84 (s, 1H), 4.69 (s, 3H), 3.03 (s, 2H), 2.80 (m, 1H), 2.68 (s, 1H) 0.97 (m, 3H, CH3).

(53) ##STR00024##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl anilinoacetate 17

(54) N-Boc-phenylglycine was prepared as described in PCT Int. App., 2007026920 and then used in accordance with general method #2. The Boc group was removed using TFA in DCM. .sup.1H NMR (300 MHz, CDCl3) 7.19 (td, J=7.5, 2.1 Hz, 2H), 6.76 (t, J=7.5 Hz, 1H), 6.61 (dd, J=8.7, 1.2 Hz, 2H), 5.84 (s, 1H), 4.28 (bs, 1H), 3.89 (d, J=3.6 Hz, 2H), 2.65 (1H).

(55) ##STR00025##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (phenyl sulfanyl)acetate 18

(56) Prepared in accordance with general method #2, with the exception being that anaerobic reaction conditions were carefully employed. .sup.1H NMR (300 MHz, CDCl3) 7.45-7.40 (m, 2H), 7.34-7.20 (m, 3H), 5.84 (s, 1H), 3.61 (s, 2H), 2.60 (1H).

(57) ##STR00026##

(13S,17R)-13-ethyl-17-ethynyl-11-methylidene-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl phenoxyacetate 19

(58) Prepared in accordance with general method #2. 1H NMR (, CDCl3 300 MHz): 7.29 (dt, 2H, ArH, J=7.5, 0.6 Hz), 6.99 (t, 1H, ArH, J=7.5 Hz), 6.88 (d, 2H, ArH, J=7.8 Hz), 5.88 (s, 1H), 5.05 (s, 1H), 4.84 (s, 1H), 4.60 (s, 2H), 2.84 (m, 2H), 2.68 (s, 1H) 1.02 (t, 3H, CH3, J=7.2 Hz).

(59) ##STR00027##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl [(5-methyl-1,2-oxazol-3-yl)oxy]acetate 20

(60) Prepared in accordance with general method #1. 1H NMR (, CDCl3 300 MHz): 5.83 (s, 1H), 5.70 (d, 1H, J=0.6 Hz), 4.76 (s, 2H), 2.84 (m, 1H), 2.65 (s, 1H), 2.33 (t, 3H, CH3, J=0.6 Hz), 0.98 (t, 3H, CH3, J=7.3 Hz).

(61) ##STR00028##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl [([1,1-biphenyl]-4-yl)oxy]acetate 21

(62) Prepared in accordance with general method #1. .sup.1H NMR (300 MHz, CDCl3) 7.60-7.49 (m, 3H), 7.47-7.37 (m, 2H), 7.35-7.26 (m, 2H), 6.99-6.94 (m, 2H), 5.83 (s, 1H), 4.65 (s, 2H), 2.67 (s, 1H).

(63) ##STR00029##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (4-cyanophenoxy)acetate 22

(64) Prepared in accordance with method #2. 1H NMR (, CDCl3 300 MHz): 7.99 (dd, 2H, ArH, J=2.1, 9.6 Hz), 6.93 (dd, 2H, ArH, J=2.1, 9.0 Hz), 5.82 (s, 1H), 4.65 (s, 2H), 2.79 (m, 1H), 2.66 (s, 1H) 0.95 (t, 3H, CH3, J=7.2 Hz).

(65) ##STR00030##

(13S,17R)-13-ethyl-17-ethynyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl (2-fluorophenoxy)acetate 23

(66) Prepared in accordance with method #2. .sup.1H NMR (, CDCl3 300 MHz): 6.98 (m, 4H, ArH), 5.82 (s, 1H), 4.66 (s, 2H), 2.81 (m, 1H), 2.64 (s, 1H) 0.94 (t, 3H, CH3, J=7.3 Hz).

LIST OF ABBREVIATIONS

(67) AcClacetyl chloride Boctertiary butyl carbamate DCMdichloromethane DICN,N-diisopropylcarbodiimide DMAPN,N-dimethyl-4-aminopyridine DMFN,N-dimethylformamide DMSOdimethyl sulfoxide EtOAcethyl acetate HPLChigh pressure liquid chromatography MHzmegahertz NMRnuclear magnetic resonance TEAtriethylamine TFAtrifluoroacetic acid THFtetrahydrofuran
Experimental Test Formulations:

(68) TABLE-US-00001 Formulation Vehicle Component Amount Vendor Benzyl alcohol 1 g Sigma Aldrich Methyl cellulose 1 g Sigma Life Science Sodium phosphate dibasic 0.752 g Fluka Analytical dehydrate Sodium phosphate 2.99 g Sigma Life Science monobasic dihydrate Water 200 mL Deionized *All solids added to water and mixed under stirring for 24 hours at ambient temperature Mill: Fritsch pulverisette 23 Serial Number: 23.1000/00703

(69) Original Formulation:

(70) A stainless steel grinding bowl with a lid and seal along with three 10 mm stainless steel balls were used to formulate suspensions for injection. The compounds were weighed and added to the grinding bowl and steel balls. 1.5 mL of formulation vehicle was added to the grinding bowl, via pipette. The milling conditions used as listed: 20 minutes, 20 Hz. After milling, the suspension was transferred to a volumetric flask. Formulation vehicle was used to dilute the milled suspension to produce the desired injection dose.

(71) Experimental Biology Testing:

(72) Protocol: Testing Long Term Injectable Contraceptive

(73) Adult female rats (180-200 g body weight) were used for the study (adapted over 1 week before starting the study).

(74) For each compound, two doses were tested (2 and 4 mg/rat).

(75) Experimental Procedure:

(76) Long acting properties of each preparation had been determined in an estrous suppression assay using virgin, mature (180-200 g) cycling rats of Sprague-Dawley strain. Upon receipt the animals were smeared daily (procedure described as below) for cyclicity and those who were showing two consecutive cycles were used for the study. Each animal was injected subcutaneously (s.c) with 0.5 ml of the test preparation (in the vehicle as described above) on the same day regardless of the stage of the cycle. Each compound was initially tested in 6 rats. Everyday excluding weekend, smears were taken starting on the day after injection and continued until such time that cornification of vaginal epithelium was observed and cycling was re-established (Bialy G, Blye R P, Enever R P, Naqvi R H, Lindberg M C. Long-acting contraceptive agents: structure activity relationships in a series of norethisterone and levonorgestrel esters. Steroids 1983, v 41, p 361).

(77) Cycle Control was Detected By Vaginal Smear as Below:

(78) Epithelium and lamina propria of the vagina undergo characteristic changes during the cycle. This cyclical changes was used in rodents to stage cycle diagnosis (1). During the cycle, it comes to a complete replacement of the epithelium. In order to determine the stage of the cycle, vaginal solution/mucus was collected as follows. The rat was fixed with one hand. With the other hand, a small moistened cotton swab (2-3 mm diameter) was inserted into the vagina and removed by gently rotating cell material. This was done with caution, since excessive irritation could induce a pseudopregnancy stage in animals. A drop of water on a slide was applied and dabbed the cotton swab in it. The smear was assessed under the microscope (Nikon Eclipse Ti, Magnification: 100.25) (Nelson J F, Felicio L S, Randall P K, Sims C, Finch C E. A longitudinal study of estrous cyclicity in aging C57BL/6J mice: I. Cycle frequency, length and vaginal cytology. Biol Reprod. 1982 September; 27(2):327-39).

(79) Evaluation of Vaginal Smears in Rats:

(80) Diestrous (Stage 1)

(81) The smear of diestrous is characterized by some neutrophils and a few small degenerated, irregularly shaped epithelial cells.

(82) Proestrous (Stage 2)

(83) The microscopic image of the smear contains a moderate number of epithelial cells with large nuclei, which are usually visible as cell clusters.

(84) Estrous (Stage 3)

(85) The lamina propria leukocytes migrate into the epithelium. The smear is characterized by many big horny epithelial cells.

(86) Metestrous (Stage 4)

(87) In metestrous stage, masses of polymorphonuclear cells with some cornified epithelial cells in the smear will become visible.

(88) TABLE-US-00002 TABLE 1 Classification of the cycle stages (as per Nelson et al., 1982, (2)) is depicted in the table below: Epithelial cells Horny Cycle stages Leukocytes with nucleus epithelial cells Mucus consistency Prooestrus /+ +/++ /+ Slightly viscous Often Regularly degenerates shaped Oestrus ++/+++ Slighly viscous to Relatively small tough cells Metoestrus ++/+++ +/++ +/++ Tough Irregularly shaped with vacuoles Dioestrus +/+++ + Thin Often irregularly shaped with vacuoles

(89) TABLE-US-00003 TABLE 2 Anti-ovulatory activities of prodrug progestins in female rat model. Rat Anti-ovulatory Activity Compound Days +/ 2 Code Chemical Structure 2 mg 4 mg MPA 22 40 EC213 TMG 19 EC600 LB 33 EC601 10 34 EC624 20.5 EC625 43 69 EC626 20 EC627 6 EC628 36 EC629 0 44.8 EC630 46.5 EC631 33.5 EC632 8.5 EC633 16.3 EC634 30 EC635 13 EC636 13 EC638 8 EC639 31 EC640 0 31 EC641 23 EC642 41 EC643 3 EC644 20 EC645 31 EC646 13 EC647 20 EC648 18 EC649 18.5 EC650 0 18.5 EC651 52 EC652 27 EC653 15 EC654 8 EC655 37 EC658 29