1,2,3,4-tetrahydro-2-thioxo-quinolinyl and 1,2,3,4-tetrahydro-2-oxo-quinolinyl derivatives as progesterone receptor modulators

Description

BACKGROUND OF THE INVENTION

This invention relates to compounds which are agonists and antagonists of the progesterone receptor, their preparation and utility.

Intracellular receptors (IR) form a class of structurally related gene regulators known as “ligand dependent transcription factors” (R. M. Evans,

Science,

240, 889, 1988). The steroid receptor family is a subset of the IR family, including progesterone receptor (PR), estrogen receptor (ER), androgen receptor (AR), glucocorticoid receptor (GR), and mineralocorticoid receptor (MR).

The natural hormone, or ligand, for the PR is the steroid progesterone, but synthetic compounds, such as medroxyprogesterone acetate or levonorgestrel, have been made which also serve as ligands. Once a ligand is present in the fluid surrounding a cell, it passes through the membrane via passive diffusion, and binds to the IR to create a receptor/ligand complex. This complex binds to specific gene promoters present in the cell's DNA. Once bound to the DNA the complex modulates the production of mRNA and protein encoded by that gene.

A compound that binds to an IR and mimics the action of the natural hormone is termed an agonist, whilst a compound which inhibits the effect of the hormone is an antagonist.

PR agonists (natural and synthetic) are known to play an important role in the health of women. PR agonists are used in birth control formulations, typically in the presence of an ER agonist. ER agonists are used to treat the symptoms of menopause, but have been associated with a proliferative effect on the uterus that can lead to an increased risk of uterine cancers. Co-administration of a PR agonist reduces or ablates that risk.

PR antagonists may also be used in contraception. In this context they may be administered alone (Ulmann, et al,

Ann. N.Y. Acad. Sci.,

261, 248, 1995), in combination with a PR agonist (Kekkonen, et al,

Fertility and Sterility,

60, 610, 1993) or in combination with a partial ER antagonist such as tamoxifen (WO 96/19997 A1 Jul. 4, 1996).

PR antagonists may also be useful for the treatment of hormone dependent breast cancers (Horwitz, et al, Horm. Cancer, 283, pub: Birkhaeuser, Boston, Mass., ed. Vedeckis) as well as uterine and ovarian cancers. PR antagonists may also be useful for the treatment of non-malignant chronic conditions such as fibroids (Murphy, et al,

J. Clin. Endo. Metab.,

76, 513, 1993) and endometriosis (Kettel, et al,

Fertility and Sterility,

56, 402, 1991).

PR antagonists may also be useful in hormone replacement therapy for post menopausal patients in combination with a partial ER antagonist such as tamoxifen (U.S. Pat. No. 5,719,136).

PR antagonists, such as mifepristone and onapristone, have been shown to be effective in a model of hormone dependent prostate cancer, which may indicate their utility in the treatment of this condition in men (Michna, et al,

Ann. N. Y Acad. Sci.,

761, 224, 1995).

Jones, et al, (U.S. Pat. No. 5,688,810) describe the PR antagonist dihydroquinoline 1.

Jones, et al, described the enol ether 2 (U.S. Pat. No. 5,693,646) as a PR ligand.

Jones, et al, described compound 3 (U.S. Pat. No. 5,696,127) as a PR ligand.

Zhi, et al, described lactones 4, 5 and 6 as PR antagonists (J. Med. Chem., 41, 291, 1998).

Zhi, et al, described the ether 7 as a PR antagonist (J. Med. Chem., 41, 291, 1998).

Combs, et al, disclosed the amide 8 as a ligand for the PR (J. Med. Chem., 38, 4880, 1995).

Perlman, et. al., described the vitamin D analog 9 as a PR ligand (

Tet. Letters,

35, 2295, 1994).

Hamann, et al, described the PR antagonist 10 (

Ann. NY. Acad. Sci.,

761, 383, 1995).

Chen, et al, described the PR antagonist 11 (Chen, et al, POI-37, 16

th

Int. Cong. Het. Chem, Montana, 1997).

Kurihari, et. al., described the PR ligand 12 (

J. Antibiotics,

50, 360, 1997).

A number of publications reported the synthesis and utilities of benzodiazinones and benzoxazines. However, none of examples in this literature contained substituents necessary for the compounds to be active as progesterone receptor modulators. Included in this literature is the patent by Kubla et al. (U.S. Pat. No. 4,666,913) which claimed that the compound such as A and B could be used as cardiotonic agents. Ning et al. reported the synthesis of quinazolinones such as C.

Other prior art close to this invention is the literature which disclosed the benzoxazines. Among these publications, Gromachevskaya et al. (Chem. Heterocycl. Compd. (N.Y.), 33(10), 1209-1214 (1998)) studied the bromination process of certain benzoxazines such as compound D. Kobzina et al. (U.S. Pat. No. 3,917,592) claimed that compounds such as E can be used as a herbicidal agent.

Pflegel et al. (Pharmazie, 37(10), 714-717(1982)) disclosed quinazolin-2-thiones such as compound F in their study of polarography of heterocyclics. No activity of the compound F was mentioned.

DESCRIPTION OF THE INVENTION

The compounds of this invention have been shown to act as competitive inhibitors of progesterone binding to the PR and act as agonists and/or antagonists in functional models, either/or in-vitro and in-vivo. These compounds may be used for contraception, in the treatment of fibroids, endometriosis, breast, uterine, ovarian and prostate cancer, and post menopausal hormone replacement therapy.

The compounds in the present invention contain a pendent aromatic substituent. The aromatic substituents proved to be critical for the resultant compounds being active as progesterone receptor modulators and have broad structural diversity which may consists of aryl, substituted aryl, heteroaryl or substituted heteroaryl group.

This invention provides compounds of Formula I having the structure:

wherein:

R

1

, R

2

are independent substituents selected from the group which includes H, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, C

2

to C

6

alkenyl, substituted C

2

to C

6

alkenyl, C

2

to C

6

alkynyl, substituted C

2

to C

6

alkynyl, C

3

to C

8

cycloalkyl, substituted C

3

to C

8

cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, COR

A

, or NR

B

COR

A

;

or R

1

and R

2

are fused to form:

a) an optionally substituted 3 to 8 membered spirocyclic alkyl ring;

b) an optionally substituted 3 to 8 membered spirocyclic alkenyl; or

c) an optionally substituted 3 to 8 membered heterocyclic ring containing one to three heteroatoms from the group including O, S and N; the spirocyclic rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from fluorine, C

1

to C

6

alkyl, C

1

to C

6

alkoxy, C

1

to C

6

thioalkyl, —CF

3

, —OH, —CN, NH

2

, —NH(C

1

to C

6

alkyl), or —N(C

1

to C

6

alkyl)

2

;

R

A

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, aryl, substituted aryl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, substituted C

1

to C

3

aminoalkyl,

R

B

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl,

R

3

is H, OH, NH

2

, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, C

3

to C

6

alkenyl, substituted C

1

to C

6

alkenyl, alkynyl, or substituted alkynyl, COR

C

,

R

C

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, aryl, substituted aryl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, substituted C

1

to C

3

aminoalkyl,

R

4

is H, halogen, CN, NO

2

, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, alkynyl, or substituted alkynyl, C

1

to C

6

alkoxy, substituted C

1

to C

6

alkoxy, amino, C

1

to C

6

aminoalkyl, substituted C

1

to C

6

aminoalkyl,

R

5

is a trisubstituted benzene ring containing the substituents X, Y and Z as shown below,

X is taken from the group including halogen, CN, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, alkynyl, or substituted alkynyl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

thioalkoxy, substituted C

1

to C

3

thioalkoxy, amino, C

1

to C

3

aminoalkyl, substituted C

1

to C

3

aminoalkyl, NO

2

, C

1

to C

3

perfluoroalkyl, 5 or 6 membered heterocyclic ring containing 1 to 3 heteroatoms, COR

D

, OCOR

D

, or NR

E

COR

D

;

R

D

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, aryl, substituted aryl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, or substituted C

1

to C

3

aminoalkyl;

R

E

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl;

Y and Z are independent substituents taken from the group including H, halogen, CN, NO

2

, amino, aminoalkyl, C

1

to C

3

alkoxy, C

1

to C

3

alkyl, or C

1

to C

3

thioalkoxy; or

R

5

is a five or six membered ring with 1, 2, or 3 heteroatoms from the group including O, S, SO, SO

2

or NR

6

and containing one or two independent substituents from the group including H, halogen, CN, NO

2

, amino, and C

1

to C

3

alkyl, C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, COR

F

, or NR

G

COR

F

;

R

F

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl aryl, substituted aryl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, or substituted C

1

to C

3

aminoalkyl;

R

G

is H, C

1

to C

3

alkyl, or substituted C

1

to C

3

alkyl;

R

6

is H or C

1

to C

3

alkyl;

G

1

is O, NR

7

, or CR

7

R

8

;

G

2

is CO, CS, or CR

7

R

8

;

provided that when G

1

is O, G

2

is CR

7

R

8

, and G

1

and G

2

cannot both be CR

7

R

8

;

R

7

and R

8

are independent substituents selected from H or an optionally substituted alkyl, aryl, or heterocyclic moiety;

or pharmaceutically acceptable salt thereof.

Preferred compounds are those of Formula I

wherein:

R

1

is H, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, C

3

to C

8

cycloalkyl, substituted C

3

to C

8

cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, COR

A

, or NR

B

COR

A

;

R

2

is H, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, C

2

to C

6

alkenyl, substituted C

2

to C

6

alkenyl, C

3

to C

8

cycloalkyl, substituted C

3

to C

8

cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, COR

A

, or NR

B

COR

A

; or

R

1

and R

2

are fused to form an optionally substituted 3 to 8 membered spirocyclic alkyl, alkenyl or heterocyclic ring containing one to three heteroatoms from the group including O, S and N, as described above;

R

A

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, aryl, substituted aryl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, or substituted C

1

to C

3

aminoalkyl;

R

B

is H, C

1

to C

3

alkyl, or substituted C

1

to C

3

alkyl,

R

3

is H, OH, NH

2

, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, C

3

to C

6

alkenyl, substituted C

1

to C

6

alkenyl, alkynyl, or substituted alkynyl, COR

C

;

R

C

is H, C

1

to C

4

alkyl, substituted C

1

to C

4

alkyl, aryl, substituted aryl, C

1

to C

4

alkoxy, substituted C

1

to C

4

alkoxy, C

1

to C

4

aminoalkyl, or substituted C

1

to C

4

aminoalkyl;

R

4

is H, halogen, CN, NO

2

, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, C

1

to C

6

alkoxy, substituted C

1

to C

6

alkoxy, amino, C

1

to C

6

aminoalkyl, substituted C

1

to C

6

aminoalkyl,

R

5

is a trisubstituted benzene ring containing the substituents X, Y and Z as shown below:

X is selected from halogen, CN, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

thioalkoxy, substituted C

1

to C

3

thioalkoxy, amino, C

1

to C

3

aminoalkyl, substituted C

1

to C

3

aminoalkyl, NO

2

, C

1

to C

3

perfluoroalkyl, 5 membered heterocyclic ring containing 1 to 3 heteroatoms, COR

D

, OCOR

D

, or NR

E

COR

D

;

R

D

is H, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, aryl, substituted aryl, C

1

to C

3

alkoxy, substituted C

1

to C

3

alkoxy, C

1

to C

3

aminoalkyl, or substituted C

1

to C

3

aminoalkyl;

R

E

is H, C

1

to C

3

alkyl, or substituted C

1

to C

3

alkyl;

Y and Z are independent substituents taken from the group including H, halogen, CN, NO

2

, C

1

to C

3

alkoxy, C

1

to C

3

alkyl, or C

1

to C

3

thioalkoxy; or

R

5

is a five or six membered ring with 1, 2, or 3 heteroatoms from the group including O, S, SO, SO

2

or NR

6

and containing one or two independent substituents from the group including H, halogen, CN, NO

2

, amino, and C

1

to C

3

alkyl, C

1

to C

3

alkoxy.

R

6

is H, or C

1

to C

3

alkyl.

G

1

is O, NR

7

, or CR

7

R

8

G

2

is CO, CS, or CR

7

R

8

, with the proviso that when G

1

is O, G

2

is CR

7

R

8

, and G

1

and G

2

cannot both be CR

7

R

8

;

wherein R

7

and R

8

are independent substituent selected from H, alkyl, substituted alkyl, aryl, substituted aryl, heterocyclic, or substituted heterocyclic

or a pharmaceutically acceptable salt thereof.

Still, more preferred compounds are those of Formula I

wherein:

R

1

═R

2

and are selected from C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl, or spirocyclic alkyl constructed by fusing R

1

and R

2

to form a 3 to 6 membered spirocyclic ring;

R

3

is H, OH, NH

2

, C

1

to C

6

alkyl, substituted C

1

to C

6

alkyl, —COH, —CO(C

1

to C

4

alkyl) or —CO(C

1

to C

4

alkoxy);

R

4

is H, halogen, NO

2

, C

1

to C

3

alkyl, substituted C

1

to C

3

alkyl,

R

5

is a disubstituted benzene ring containing the substituents X, and Y as shown below

X is taken from the group including halogen, CN, C

1

to C

3

alkoxy, C

1

to C

3

alkyl, NO

2

, C

1

to C

3

perfluoroalkyl, 5 membered heterocyclic ring containing 1 to 3 heteroatoms, C

1

to C

3

thioalkoxy,

Y is a substituent on the 4′ or 5′ position from the group including H, halogen, CN, NO

2

, C

1

to C

3

alkoxy, C

1

to C

4

alkyl, C to C

3

thioalkoxy or

R

5

is a five membered ring with the structure shown below

U is O, S, or NR

6

,

R

6

is H, or C

1

to C

3

alkyl, C

1

to C

4

CO

2

alkyl,

X′ is from the group including halogen, CN, NO

2

, C

1

to C

3

alkyl and C

1

to C

3

alkoxy;

Y′ is from the group including H and C

1

to C

4

alkyl or

R

5

is a six membered ring with the structure shown

X

1

is N or

X

2

is halogen, CN, alkoxy, or NO

2

,

G

1

is O, NR

7

, or CR

7

R

8

G

2

is CO, CS, or CR

7

R

8

provided that when G

1

is O, G

2

is CR

7

R

8

, and G

1

and G

2

cannot both be CR

7

R

8

;

wherein R

7

and R

8

are independent substituents selected from H, alkyl, substituted alkyl, aryl, substituted aryl, heterocyclic, or substituted heterocyclic;

or pharmaceutically acceptable salt thereof.

Still, even more preferred compounds are those of Formula I

wherein:

R

1

═R

2

and are selected from the group which includes CH

3

and spirocyclic alkyl constructed by fusing R

1

and R

2

to form a 6 membered spirocyclic ring,

R

3

is H, OH, NH

2

, CH

3

, substituted methyl, COR

C

,

R

C

is H, C

1

to C

3

alkyl, C

1

to C

4

alkoxy,

R

4

is H, halogen, C

1

to C

3

alkyl,

R

5

is a disubstituted benzene ring containing the substituents X, and Y as shown below

X is taken from the group including halogen, CN, methoxy, NO

2

, 2-thiazole,

Y is a substituent on the 4′ or 5′ position from the group including H and F, or

R

5

is a five membered ring with the structure shown below

U is O, S, or NH,

X′ is from the group including halogen, CN, NO

2

,

Y′ is from the group including H and C

1

to C

4

alkyl

G

1

is O, NR

7

, or CR

7

R

8

G

2

is CO, CS, or CR

7

R

8

provided that when G

1

is O, G

2

is CR

7

R

8

, and G

1

and G

2

cannot both be CR

7

R

8

;

R

7

and R

8

are independent substituent selected from H, alkyl, substituted alkyl, aryl, substituted aryl, heterocyclic, or substituted heterocyclic;

and pharmaceutically acceptable salts thereof.

The compounds of this invention may contain an asymmetric carbon atom and some of the compounds of this invention may contain one or more asymmetric centers and may thus give rise to optical isomers and diastereomers. While shown without respect to stereochemistry in Formula I, the present invention includes such optical isomers and diastereomers; as well as the racemic and resolved, enantiomerically pure R and S stereoisomers; as well as other mixtures of the R and S stereoisomers and pharmaceutically acceptable salts thereof It will be understood by one skilled in the art that the number of substituents listed for spirocyclic or heterospirocyclic rings formed by fusing R

1

and R

2

will be determined by the size of the spirocyclic ring.

The term “alkyl” is used herein to refer to both straight- and branched-chain saturated aliphatic hydrocarbon groups having one to eight carbon atoms; “alkenyl” is intended to include both straight- and branched-chain alkyl group with at least one carbon—carbon double bond and two to eight carbon atoms; “alkynyl” group is intended to cover both straight- and branched-chain alkyl groups with at least one carbon—carbon triple bond and two to eight carbon atoms.

The terms “substituted alkyl”, “substituted alkenyl”, and “substituted alkynyl” refer to alkyl, alkenyl, and alkynyl as just described having one or more substituents from the group including halogen, CN, OH, NO

2

, amino, aryl, heterocyclic, substituted aryl, substituted heterocyclic, alkoxy, aryloxy, substituted alkyloxy, alkylcarbonyl, alkylcarboxy, alkylamino, arylthio. These substituents may be attached to any carbon of an alkyl, alkenyl, or alkynyl group provided that the attachment constitutes a stable chemical moiety.

The term “aryl” is used herein to refer to an aromatic system which may be a single ring or multiple aromatic rings fused or linked together as such that at least one part of the fused or linked rings forms the conjugated aromatic system. The aryl groups include but are not limited to phenyl, naphthyl, biphenyl, anthryl, tetrahydronaphthyl, or phenanthryl.

The term “substituted aryl” refers to an aryl as just defined having one to four substituents from the group including halogen, CN, OH, NO

2

, amino, alkyl, cycloalkyl, alkenyl, alkynyl, alkoxy, aryloxy, substituted alkyloxy, alkylcarbonyl, alkylcarboxy, alkylamino, or arylthio.

The term “heterocyclic” is used herein to describe a stable 4- to 7-membered monocyclic or a stable multicyclic heterocyclic ring which is saturated, partially unsaturated, or unsaturated, and which consists of carbon atoms and from one to four heteroatoms selected from the group including N, O and S atoms. The N and S atoms may be oxidized. The heterocyclic ring also includes any multicyclic ring in which any of above defined heterocyclic rings is fused to an aryl ring. The heterocyclic ring may be attached at any heteroatom or carbon atom provided the resultant structure is chemically stable. Such heterocyclic groups include, for example, tetrahydrofuran, piperidinyl, piperazinyl, 2-oxopiperidinyl, azepinyl, pyrrolidinyl, imidazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, isoxazolyl, morpholinyl, indolyl, quinolinyl, thienyl, furyl, benzofuranyl, benzothienyl, thiamorpholinyl, thiamorpholinyl sulfoxide, and isoquinolinyl.

The term “substituted heterocyclic” is used herein to describe the heterocyclic just defined having one to four substituents selected from the group which includes halogen, CN, OH, NO

2

, amino, alkyl, substituted alkyl, cycloalkyl, alkenyl, substituted alkenyl, alkynyl, alkoxy, aryloxy, substituted alkyloxy, alkylcarbonyl, alkylcarboxy, alkylamino, or arylthio. The term “alkoxy” refers to the OR group, where R is alkyl or substituted alkyl. The term “aryloxy” is used herein to indicate the OR group, where R is aryl or substituted aryl. The term “alkylcarbonyl” refers to the RCO group, where R is alkyl or substituted alkyl. The term “alkylcarboxy” refers to the COOR group, where R is alkyl or substituted alkyl. The term “aminoalkyl” refers to both secondary and tertiary amines wherein the alkyl or substituted alkyl groups, containing one to eight carbon atoms, which may be either same or different and the point of attachment is on the nitrogen atom The term “halogen” refers to Cl, Br, F, and I element.

The compounds of this invention can be prepared following the Schemes illustrated below:

As demonstrated in Scheme I, the compounds of this invention are generally prepared by employing the suitable coupling reaction as a key step. An appropriately substituted ortho-amino benzoic acid or its derivatives such as ethyl ester (X=Br, I, Cl, or a latent coupling precursor such as alkoxy group which can be converted into OTf group suitable in the coupling reaction) was treated with a suitable organo metallic reagent, e.g. Grignard reagent, in appropriate nonprotic solvents which include but are not limited to THF or ether to give ortho-amino carbinol 2 under an inert atmosphere such as argon or nitrogen at −78° C. to room temperature. The arylation of amino carbinol 2 to yield 3 can be effected by various coupling reactions including Suzuki, Stille reactions. These reactions are commonly performed in the presence of a transition metallic catalyst, e.g., palladium or nickel complex often with phosphino ligands, e.g., Ph

3

P, dppf, dppe or a catalyst such as palladium acetate. Under this catalytic condition, an appropriately substituted nucleophilic reagent, e.g., aryl boronic acid, arylstannane, or aryl zinc compound, is coupled with amino carbinol 2 to give 3. If a base is needed in the reaction, the commonly used bases include but are not limited to sodium bicarbonate, sodium carbonate, potassium phosphate, barium carbonate, cesium fluoride, or potassium acetate. The most commonly used solvents in these reactions include benzene, DMF, isopropanol, ethanol, DME, ether, acetone, or a mixture of above solvent and water. The coupling reaction is generally executed under an inert atmosphere such as nitrogen or argon at temperatures ranging from room temperature to 95° C. The compounds of this invention 4 can be effected by treatment of amino carbinol 3 with an appropriate ketone in the presence of an suitable acid catalyst such as p-toluenesulfonic acid in a suitable solvent such as toluene, benzene under an inert atmosphere such as argon or nitrogen at room temperature to reflux.

Scheme II describes the procedure to prepare benzoxazines bearing two different substituents at position-4. The Weinreb amide 6 can be prepared from an appropriately substituted isatoic anhydride 5 when treated with N-, O-dimethylhydroxyl-amine hydrochloride salt in a protic solvent such as ethanol, or isopropanol at reflux under an inert atmosphere such as argon or nitrogen. Coupling of amide 6 with an aryl electrophile such as aryl boronic acid or arylstannane to give 7 can be effected by employing a typical coupling reaction such as Suzuki, Stille coupling procedure in a similar fashion as described for the preparation of compound 3. Treatment of Weinreb amide 7 with organo metallic compounds, e.g., alkyllithium, alkynyllithium, aryllithium, or their Grignard counterpart in a nonprotic solvent such as THF or ether under an inert atmosphere such as argon or nitrogen at −78° to room temperature affords amino ketone 8. Conversion of ketone 8 to carbinol 9 can be effected by treatment of 8 with an organo metallic reagent such as alkyl alkynyl, or aryl Grignard reagent in a nonprotic solvent such as THF or ether under an inert atmosphere such as argon or nitrogen at −78° C. to room temperature. Conversion of ketone 8 to carbinol 9 can also be effected by reduction of ketone group of 8 to the carbinol moiety of 9 using an appropriate reducing reagent such as lithium aluminum hydride, sodium borohydride in a suitable solvent such as THF, ether, or anhydrous alcohol under an inert atmosphere in the temperature ranging from 0° C. to the boiling point of the solvent. Further conversion of 9 to the compounds of this invention can be effected as described in scheme I for the preparation of compound 4.

Alternatively, ortho-amino ketone 8 can be prepared by treatment of ortho-amino benzonitrile 11 with an organo metallic compound such as organo lithium reagent or Grignard reagent in a suitable solvent such as THF or ether under an inert atmosphere such as argon or nitrogen at temperatures ranging from −78° C. to room temperature as illustrated in Scheme III. Benzonitrile 11 can be readily prepared from an appropriately substituted benzonitrile such as bromobenzonitrile 10 using a suitable coupling reaction such as Stille or Suzuki protocol carried out in a similar fashion as described for the preparation of the Weinreb amide 7.

Scheme IV illustrates the synthesis of 3,4-dihydroquinazolin-2-ones. The substituted 2-aminobenzonitrile 11 is treated with an organo metallic compound such as an organo lithium or Grignard reagent in a nonprotic solvent such as THF or ether under an inert atmosphere such argon or nitrogen at −78° C. to room temperature to produce an imino intermediate which is reacted with a suitable carbonate such as diethyl carbonate or dimethyl carbonate in situ at 0° C. to 60° C. to give quinazolin-2-ones 12. Protection of quinazolin-2-ones 12 with a suitable protective group such as a para-methoxybenzyl moiety can be effected by treating 12 with a suitable base such as potassium hydride, potassium t-butoxide, or sodium hydride followed by addition of a protective reagent such as para-methoxybenzyl chloride in an appropriate solvent such as DMF, or a mixture of solvents such as THF and DMF under an inert atmosphere such as nitrogen or argon at 0° C. to room temperature. The Michael addition of a suitable organo metallic compound such as organo lithium or Grignard reagent to the protected quinazolin-2-ones 12 to give 13 can be accomplished in the presence of a suitable Lewis acid such as magnesium triflate in a nonprotic solvent such as THF or ether under an inert atmosphere such as argon or nitrogen at 0° C. to room temperature.

Removal of the protective group can be effected by treating 13 with a suitable deprotecting reagent, e.g. for the para-methoxybenzyl protective group it can be removed by treatment of 13 with protic acid such as TFA or with Ceric ammonium nitrate in a suitable solvent such as methylene chloride at 0° C. to room temperature under an inert atmosphere such as argon or nitrogen. Prior to the removal of protective group, the alkylation of 3-nitrogen can be achieved by treating 13 with an appropriate base such as sodium hydride, potassium hydride, or potassium t-butoxide in a suitable solvent such as DMF followed by quenching the reaction solution with an organo iodide or an organo triflate such as iodomethane under an inert atmosphere such as argon or nitrogen at 0° C. to room temperature. The compounds of the present invention 14 can be prepared when the protective group is removed with a suitable reagent, e.g. for the para-methoxybenzyl protective group it can be removed by treatment of 13 with protic acid such as TFA or with Ceric ammonium nitrate in a suitable solvent such as methylene chloride at 0° C. to room temperature under an inert atmosphere such as argon or nitrogen.

The conversion of compounds 14 to 3,4-dihydroquinazolin-2-thiones 15 can be accomplished by treatment of 14 with a suitable sulfur reagent such as Lawesson's reagent in a nonprotic solvent such as o-xylene, chlorobenzene, or toluene under an inert atmosphere such as argon or nitrogen at reflux.

As illustrated in scheme V, the compounds 14 or 15 can be further derivatized at position-1 via numerous approaches leading to a variety of the novel derivatives including 1-alkyl, substituted 1-alkyl, 1-carbonyl, substituted 1-carbonyl, 1-carboxy, substituted 1-carboxy derivatives. For example, alkyl or substituted alkyl derivatives 16 or 17 can be formed by treatment of carbamate 14 or 15 with a suitable base such as sodium hydride in a suitable solvent such as DMF under an inert atmosphere such as argon or nitrogen followed by addition of an appropriate electrophile such as alkyl or substituted alkyl bromide, iodide, or triflate. Such transformation of 14, 15, 16, or 17 at position-1 can also be effected using biphasic condition as indicated in scheme V in which alkylation is executed using a biphasic catalyst such as tributylammonium bromide in a suitable solvent such as acetonitrile. A further example of such modification in position-1 includes but is not limited to the one depicted in scheme V in that heating of 14 or 15 with triethyl orthoformate affords 1-substituted derivatives of compound 14 or 15.

The acylation or carboxylation of the compound 14 or 15 at position-1 to give compound 18 or 19 can be readily effected by treatment of 14 or 15 with a suitable acylating or carboxylating reagent such as di-t-butyl dicarbonate in the presence of a suitable basic catalyst such as DMAP in a suitable solvent such as acetonitrile under an inert atmosphere such as argon or nitrogen. The amination of position-1 of compound 14 or 15 to give compounds 20 and 21 can be furnished using a suitable aminating reagent such as chloroamine in the presence of a suitable base such as sodium hydride in a suitable solvent such as THF or diethyl ether following the literature procedure (Metlesics et al.

J. Org. Chem.

30, 1311 (1965)).

According to scheme VI an appropriate aniline such as 4-bromoaniline 22, is reacted in the presence of a base in a suitable nonprotic solvent with an acryloyl chloride 23 to form the amide 24. The base is preferably a strong base such as sodium hydride or sodium or potassium hexamethyldisilylamide, utilizing THF as the solvent under an inert atmosphere (nitrogen or argon) from 0° C. up to the reflux temperature of the solvent.

Reaction of the amide 24 under strongly acidic conditions, sulfuric acid, borontrifluoride etherate, or preferably aluminum chloride either as a melt, or in an inert solvent (dichlorobenzenes) under an inert atmosphere (nitrogen or argon) from 0° C. up to the reflux temperature of the solvent then provides the cyclic amide 25. Subsequent reaction of compound 25 with an aryl or heteroaryl boronic acid, boronic acid anhydride or trialkyl stannane then provides access to the desired biaryl compound 26. The reaction can be carried out in a solvent such as acetone, ethanol, benzene, toluene or THF, under an inert atmosphere (nitrogen or argon) from 0° C. up to the reflux temperature of the solvent, in the presence of a palladium catalyst such as tetrakis(triphenylphosphine) palladium (0) or palladium acetate and may require an additive such as sodium carbonate, cesium fluoride or potassium phosphate.

The conversion of compounds 26 to thioamide 27 can be accomplished by treatment of 26 with a suitable sulfur reagent such as Lawesson's reagent in a nonprotic solvent such as o-xylene, chlorobenzene, or toluene under an inert atmosphere such as argon or nitrogen at reflux.

According to scheme VII, an appropriate cyclic amide such as 25, is allowed to react with NaH in THF to form the anion species and then a benzyl halide is added to convert the starting material to the N-protected amide product, 28. Reaction of 28 with an aryl boronic acid in the presence of a palladium catalyst such as tetrakis(triphenylphosphine)palladium (0) or palladium acetate permits a coupling of the two aromatic species to yield 29. The reaction is normally carried out under biphasic conditions. That is, water is often employed along with an appropriate organic solvent, such as toluene or DMF. The palladium catalyst is typically added last and the reaction mixture is refluxed in the presence of an inert gas such as nitrogen. The product is treated with a Grignard Reagent, an alkyl magnesium halide, in THF followed by the addition of ammonium chloride solution to afford the enamine derivative 30. The reduction of the double bond in 30 and removal of the protecting group can be accomplished in a single step by catalytic reduction in a Parr Hydrogenation Apparatus using palladium on charcoal to form the target compound 31.

3-Fluoro-5-(2,4,4-trimethyl-1,2,3,4-hydro-qinolinyl)-benzonitrile (compound 35) can be prepared by Scheme VIII, a process similar to Scheme VII. According to scheme VIII, compound 28 is allowed to react with a Grignard reagent, an alkyl magnesium halide, in THF followed by the addition of ammonium chloride solution to afford the enamine derivative 32. Reduction of the double bond with sodium cyanoborohydride affords the reduced derivative 33. Removal of the protecting group with a strong acid such as triflic or sulfuric acid affords the deprotected compound 34 which can then be coupled with a suitably substituted phenylboronic acid in the presence of a palladium catalyst such as tetrakis(triphenylphosphine)palladium (0) or palladium acetate permits a coupling of the two aromatic species to yield 35. The reaction is normally carried out under biphasic conditions. That is, water is often employed along with an appropriate organic solvent, such as toluene or DMF.

The compounds of the present invention can be used in the form of salts derived from pharmaceutically or physiologically acceptable acids or bases. These salts include, but are not limited to, the following salts with inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid and, as the case may be, such organic acids as acetic acid, oxalic acid, succinic acid, and maleic acid. Other salts include salts with alkali metals or alkaline earth metals, such as sodium, potassium, calcium or magnesium in the form of esters, carbamates and other conventional “pro-drug” forms, which, when administered in such form, convert to the active moiety in vivo.

This invention includes pharmaceutical compositions and treatments which comprise administering to a mammal a pharmaceutically effective amount of one or more compounds as described above wherein G

2

is C═O as antagonists of the progesterone receptor. The invention further provides comparable methods and compositions which utilize one or more compounds herein wherein G

2

is C═S as agonists of the progesterone receptor. Moreover the invention further provides comparable methods and compositions which utilize one or more compounds herein wherein G

1

=O and G

2

=CR

7

CR

8

are agonists of the progesterone receptor and when G

1

=CR

7

CR

8

and G

2

=CR

7

CR

8

are agonists of the progesterone receptor.

The progesterone receptor antagonists of this invention, used alone or in combination, can be utilized in methods of contraception and the treatment and/or prevention of benign and malignant neoplastic disease. Specific uses of the compounds and pharmaceutical compositions of invention include the treatment and/or prevention of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy; carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors. Additional uses of the present progesterone receptor antagonists include the synchronization of the estrus in livestock. When used in contraception the progesterone receptor antagonists of the current invention may be used either alone in a continuous administration of between 1 and 500 mg per day, or alternatively used in a different regimen which would entail 2-4 days of treatment with the progesterone receptor antagonist after 21 days of a progestin, in this regimen between 0.1 and 500 mg daily doses of the progestin (e.g. levonorgestrel, trimegestone, gestodene, norethistrone acetate, norgestimate or cyproterone acetate) would be followed by between 0.1 and 500 mg daily doses of the progesterone receptor antagonists of the current invention.

The progesterone receptor antagonists of this invention, used alone or in combination, can also be utilized in methods of treatment and/or prevention of benign and malignant neoplastic disease. Specific uses of the compounds and pharmaceutical compositions of invention include the treatment and/or prevention of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy; carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors. Additional uses of the present progesterone receptor antagonists include the synchronization of the estrus in livestock.

The progesterone receptor agonists of this invention, used alone or in combination, can be utilized in methods of contraception and the treatment and/or prevention of dysfunctional bleeding, uterine leiomyomata, endometriosis; polycystic ovary syndrome, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate. Additional uses of the invention include stimulation of food intake.

When used in contraception the progesterone receptor agonists of the current invention are preferably used in combination or sequentially with an estrogen agonist (e.g. ethinyl estradiol). The preferred dose of the progesterone receptor agonist is between 0.01 and 500 mg per day.

When the compounds are employed for the above utilities, they may be combined with one or more pharmaceutically acceptable carriers or excipients, for example, solvents, diluents and the like, and may be administered orally in such forms as tablets, capsules, dispersible powders, granules, or suspensions containing, for example, from about 0.05 to 5% of suspending agent, syrups containing, for example, from about 10 to 50% of sugar, and elixirs containing, for example, from about 20 to 50% ethanol, and the like, or parenterally in the form of sterile injectable solutions or suspensions containing from about 0.05 to 5% suspending agent in an isotonic medium. Such pharmaceutical preparations may contain, for example, from about 25 to about 90% of the active ingredient in combination with the carrier, more usually between about 5% and 60% by weight.

The effective dosage of active ingredient employed may vary depending on the particular compound employed, the mode of administration and the severity of the condition being treated. However, in general, satisfactory results are obtained when the compounds of the invention are administered at a daily dosage of from about 0.5 to about 500 mg/kg of animal body weight, preferably given in divided doses two to four times a day, or in a sustained release form For most large mammals, the total daily dosage is from about 1 to 100 mg, preferably from about 2 to 80 mg. Dosage forms suitable for internal use comprise from about 0.5 to 500 mg of the active compound in intimate admixture with a solid or liquid pharmaceutically acceptable carrier. This dosage regimen may be adjusted to provide the optimal therapeutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation.

These active compounds may be administered orally as well as by intravenous, intramuscular, or subcutaneous routes. Solid carriers include starch, lactose, dicalcium phosphate, microcrystalline cellulose, sucrose and kaolin, while liquid carriers include sterile water, polyethylene glycols, non-ionic surfactants and edible oils such as corn, peanut and sesame oils, as are appropriate to the nature of the active ingredient and the particular form of administration desired. Adjuvants customarily employed in the preparation of pharmaceutical compositions may be advantageously included, such as flavoring agents, coloring agents, preserving agents, and antioxidants, for example, vitamin E, ascorbic acid, BHT and BHA.

The preferred pharmaceutical compositions from the standpoint of ease of preparation and administration are solid compositions, particularly tablets and hard-filled or liquid-filled capsules. Oral administration of the compounds is preferred.

These active compounds may also be administered parenterally or intraperitoneally. Solutions or suspensions of these active compounds as a free base or pharmacologically acceptable salt can be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid, polyethylene glycols and mixtures thereof in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases, the form must be sterile and must be fluid to the extent that easy syringe ability exits. It must be stable under conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacterial and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol (e.g., glycerol, propylene glycol and liquid polyethylene glycol), suitable mixtures thereof, and vegetable oil.

The following non-limiting examples illustrate preparation of compounds of the invention.

EXAMPLE 1

1-(4-Amino-3′-chloro-biphenyl-3-yl)-ethanone

A mixture of 2-amino-5-bromo-N-methoxy-N-methylbenzamide (7.78 g, 30 mmol), 3-chlorophenyl boronic acid (5.63 g, 36 mmol), tetrakis(triphenylphosphine)palladium (0) (1.73 g, 1.5 mmol), and sodium carbonate (7.63 g, 72 mmol) in a mixture of DME and water (150 mL/30 mL) was degassed to remove the oxygen and was then heated at 85° C. under nitrogen for 3 hours. The reaction mixture was cooled to room temperature and treated with brine (30 mL) and ethyl acetate (100 mL). The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×40 mL). The combined organic layers were washed with brine and dried with MgSO

4

. After removal of solvent, the residue was purified by a flash chromatography (silica gel, hexane:ethyl acetate/1:1) to give 5-(3-chlorophenyl)-N-methoxy-N-methylbenzamide as a brown oil (5 g, 57%). To a solution of this benzamide (5 g, 17.2 mmol) in anhydrous THF was added in a dropwise fashion a solution of methyllithium in ether (1.4M, 28.6 mL, 40 mL) at −78° C. under nitrogen. After stirring for 30 minutes, the reaction mixture was treated with a saturated aqueous ammonium chloride solution (50 mL) at −78° C. Ethyl acetate (100 mL) was added, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3×20 mL). The combined organic layers were washed (brine) and dried (MgSO

4

). After removal of solvent, the residue was purified by a flash chromatography (silica gel, hexane:ethyl acetate/2:1) to afford 1-(4-amino-3 ′-chloro-biphenyl-3-yl)-ethanone as yellow solid (2 g, 47%): mp 89-90° C.;

1

H-NMR (CDCl

3

) δ 7.89 (d, 1H, J=2.0 Hz), 7.51 (m, 2H), 7.25-7.40 (i, 3H), 6.73 (d, 1H, J=8.6 Hz), 6.38 (br, 2H), 2.65 (s, 3H); MS (EI) m/z 268([M+Na]

+

, 60%); Anal. Calc. For C

14

H

12

ClNO: C, 68.44, H, 4.92, N, 5.70. Found: C, 68.40, H, 4.89, N, 5.61.

EXAMPLE 2

1-(4-Amino-3′-chloro-biphenyl-3-yl)-dimethyl-methanol

To a solution of 1-(4-amino-3′-chloro-biphenyl-3-yl)-ethanone (.55 g, 2.2 mmol) in anhydrous THF under nitrogen was added a solution of methyl magnesium bromide (3.0 M in diethyl ether, 1 mL, 3 mmol) at 0° C. The mixture was slowly warmed to room temperature and kept stirring under nitrogen for 18 hours. The mixture was treated with 10 mL of saturated ammonium chloride aqueous solution and ethyl acetate (50 mL) was added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3×5 mL). The combined organic layers were washed with brine (20 mL) and dried (MgSO

4

). After removal of the solvent, the residue was purified by a flash chromatography (silica gel, hexane:ethyl acetate/2:1) to afford the title compound as an off-white solid: 186-188° C. (HCl salt). Anal. Calc. For C

15

H

17

Cl

2

NO: C, 60.42, H, 5.75, N, 4.7. Found: C, 60.51, H, 5.62, N, 4.56.

EXAMPLE 3

6-(3-Chloro-phenyl)-2,4,4-trimethyl-2-trifluoromethyl-1,4-dihydro-2H-benzo[d][1,3]oxazine

A mixture of (4-amino-3-chloro-biphenyl-3-yl)-dimethyl-methanol (0.25 g, 0.95 mmol), trifluoromethylacetone (0.16 g, 1.43 mmol), and p-toluenesulfonic acid (0.01 g, 0.05 mmol) in dry toluene (5 mL) was stirred under a blanket of nitrogen for 48 hours. Upon completion of the reaction, the toluene was removed and the residue purified via flash chromatography (silica gel, 10% ethyl acetate/hexane) to give 6-(3-chloro-phenyl)-2,4,4-trimethyl-2-trifluoromethyl-1,4-dihydro-2H-benzo [d][1,3]-oxazine (0.22 g, 65%) as a clear oil. The oil was dissolved in ether at −78° C. and then treated with a solution of

1

N HCl in ether to give the hydrochloride salt of the title compound as a white solid:

1

H-NMR (DMSO-d

6

) δ 7.67 (bs, 1H), 7.58 (d, 1H, J=7.88 Hz), 7.42 (m, 3H), 7.32 (d, 1H, J=7.96 Hz), 6.84 (d, 1H, J=8.03 Hz), 1.52 (s, 3H), 1.5 (s, 6H); MS (APCI) m/z 354 ([M−H]

−

, 100%); Anal. Calc. For C

18

H

17

ClF

3

NO: C, 55.12; H, 4.62; N, 3.57. Found: C, 54.97; H, 4.59; N, 3.41.

EXAMPLE 4

6-(3-Chloro-phenyl)-2,2,4,4-tetramethyl-1,4-dihydro-2H-benzo[d][1,3]oxazine

A mixture of (4-amino-3-chloro-biphenyl-3-yl)-dimethyl-methanol (0.46 g, 1.8 mmol), acetone (0.16 g, 2.7 mmol), and p-toluenesulfonic acid (0.017 g, 0.09 mmol) in dry toluene (6 mL) was heated at 33° C. under a blanket of nitrogen overnight. Upon completion of the reaction, the toluene was removed and the compound purified via a flash chromatography (silica gel, 15% ethyl acetate/hexane) to give 6-(3-chloro-phenyl)-2,2,4,4-tetramethyl-1,4-dihydro-2H-benzo[d][1,3]oxazine (0.36 g, 68%) as a yellow oil. The oil was dissolved in ether at −78° C. and then treated with a solution of 1N HCl in ether to give the hydrochloride salt of the title compound as a yellow solid:

1

H-NMR (DMSO-d

6

) δ 7.70 (bs, 1H), 7.61 (d, 1H, J=7.82 Hz), 7.52 (bs, 1H), 7.44 (m, 2H), 7.33 (d, 1H, J=8.21 Hz), 6.87 (d, 1H, J=7.85 Hz), 1.5 (s, 6H), 1.4 (s, 6H); MS (ESI) m/z 302 ([M+H]

+

, 100%); Anal. Calc. For C

18

H

20

ClNO: C, 63.91; H, 6.26; N, 4.14. Found: C, 64.08; H, 6.43; N, 4.14.

EXAMPLE 5

6-(3-Nitro-phenyl)-2,2,4,-trimethyl-1,4-dihydro-2H-benzo [d][1,3]oxazine

Prepared from 1-(4-amino-3′-nitro-biphenyl-3-yl)-ethanol and acetone in the same fashion as that of Example 4. Yellow solid: mp 188-189° C.; Anal. Calc. For C

17

H

18

N

2

O

3

.0.35H

2

O: C, 67.02; H, 6.19; N, 9.20. Found: C, 66.7; H, 5.89; N, 9.03.

EXAMPLE 6

4-Amino-3′-chloro-biphenyl-3-carbonitile

A mixture of 2-amino-5-bromobenzonitrile (log, 50 mmol), 3-chlorophenyl boronic acid (9.5 g, 60 mmol), tetrakis(triphenylphosphine)-palladium (0) (3.5 g, 3 mmol), and sodium carbonate (13 g, 120 mmol) in a mixture of DME and water (100 mL/25 mL) was degassed to remove the oxygen and then heated to 85° C. under a blanket of nitrogen for 5 hours. The reaction mixture was cooled to ambient temperature and quenched with a saturated aqueous ammonium chloride solution (80 mL). Ethyl acetate (200 mL) was added, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3×40 mL). The combined organic layers were washed with brine and dried with MgSO

4

. The solvent was removed in vacuo and the residue was purified by a silica gel flash chromatography (hexane:ethyl acetate/4:1) to afford 4-amino-3′-chloro-biphenyl-3-carbonitrile as an off-white solid (8 g, 87%): mp 118-119° C.;

1

H-NMR (DMSO-d

6

)δ 7.80 (d, 1H, J=2.3 Hz), 7.65-7.72 (m, 2H), 7.57 (d, 1H, J=8.0 Hz), 7.42 (t, 1H, J=7.9 Hz), 7.31 (m, 1H), 6.87 (d, 1H, J=8.7 Hz), 6.29 (br, 2H); Anal. Calc. For C

13

H

9

ClN

2

: C, 68.28, H, 3.97, N, 12.25. Found: C, 67.68, H, 4.06, N, 11.89.

EXAMPLE 7

6-(3-Chlorophenyl)-4-cyclopropyl-1H-quinazolin-2-one

Prepared using a similar procedure as described in the literature (Tucker et al.

J. Med. Chem.,

1994, 37, 2437-2444). To a solution of cyclopropylmagnesium bromide prepared from magnesium (0.9 g, 37 mmol) and cyclopropyl bromide (3.2 mL, 40 mmol) in anhydrous THF was added at 50° C. under nitrogen a solution of 4-amino-3′-chloro-biphenyl-3-carbonitrile (2.3 g, 10 mmol) in anhydrous THF. After addition, the reaction mixture was kept at 50° C. for 30 minutes under nitrogen and treated with dimethyl carbonate in a dropwise manner. The reaction solution was stirred at 50° C. under nitrogen for 30 minutes and cooled to ambient temperature. A saturated aqueous ammonium chloride solution (30 mL) was added followed by addition of ethyl acetate (80 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3×40 mL). The combined organic layers were washed with brine and dried with MgSO

4

. After removal of the solvent, the residue was purified by a flash chromatography (silica gel, methylene chloride: methanol/25:1) to give 6-(3-chlorophenyl)-4-cyclopropyl-1H-quinazolin-2-one as a yellowish solid (0.55 g, 18%): mp 189-190° C.;

1

H-NMR (DMSO-d

6

) δ 11.71 (s, 1H, D

2

O exchangeable), 8.56 (d, 1H, J=1.3 Hz), 8.09 (dd, 1H, J=8.6, 1.6 Hz), 7.92 (s, 1H), 7.77 (d, 1H, J=7.7 Hz), 7.52 (t, 1H, J=7.9 Hz), 7.45 (d, 1H, J=8.1 Hz), 7.36 (d, 1H, J=8.6 Hz), 3.15 (m, 1H), 1.20 (m, 4H); MS (CI) m/z 297 ([M+H]

+

, 100%); Anal. Calc. For C

17

H

13

ClN

2

O: C, 69.98, H, 4.49, N, 9.23. Found: C, 67.98, H, 4.46, N, 9.10.

EXAMPLE 8

6-(3-Chlorophenyl)-4-cyclopropyl-1-(4-methoxybenzyl)-1H-quinazolin-2-one

To a suspension of 6-(3-chlorophenyl)-4-cyclopropyl-1H-quinazolin-2-one (0.5 g, 1.68 mmol) in anhydrous DMF was added potassium hexamethylsilyl amide (0.45 g, 2.1 mmol) at ambient temperature under nitrogen. The reaction mixture was stirred at ambient temperature for 30 minutes, treated with p-methoxy benzyl chloride (0.35 mL, 2.5 mmol), and heated at 55° C. for 5 hours. The mixture was then cooled to room temperature and quenched with a saturated aqueous ammonium chloride solution (10 mL). Methylene chloride (50 mL) was added and organic layer was separated. The aqueous layer was extracted with methylene chloride (2×20 mL) and the combined organic layers were washed with brine and dried (MgSO

4

). After removal of solvent, the residue was separated on a flash chromatography (silica gel, hexane:ethyl acetate/1:1) to afford 6-(3-chlorophenyl)-4-cyclopropyl-1-(4-methoxybenzyl)-1H-quinazolin-2-one as an off-white solid: mp 173-174° C.;

1

H-NMR (DMSO-d

6

) δ 8.65 (d, 1H, J=1.8 Hz), 8.10 (dd, 1H, J=8.9, 1.8 Hz), 7.93 (d, 1H, J=1.6 Hz), 7.79 (d, 1H, J=7.6 Hz), 7.53 (d, 2H, J=8.4 Hz), 7.46 (t, 1H, J=8.1 Hz), 7.21 (d, 2H, J=8.6 Hz), 6.88 (d, 2H, J=8.6 Hz), 5.41 (s, 2H), 3.73 (s, 3H), 3.18 (m, 1H), 1.18-1.27 (m, 4H); MS (CI) m/z 417([M+H]

+

, 100%); Anal. Calc. For C

25

H

21

ClN

2

O

2

: C, 72.02, H, 5.08, N, 6.72. Found: C, 71.88, H, 4.91, N, 6.70.

6-(3-Chlorophenyl)-4-cyclopropyl-2-(4-methoxybenzyloxy)quinazoline was obtained as a side product, off-white solid: mp 158-159° C.;

1

H-NMR (DMSO-d

6

) δ 8.75 (d, 1H, J=1.7 Hz), 8.26 (dd, 1H, J=8.8, 1.8 Hz), 8.01 (s, 1H), 7.84 (m, 2H), 7.56 (t, 1H, J=7.9 Hz), 7.45 (m, 3H), 6.96 (d, 2H, J=8.6 Hz), 5.38 (s, 2H), 3.75 (s, 3H), 3.24 (m, 1H), 1.25 (rm, 4H); MS (CI) m/z 417([M+H]

+

, 100%); Anal. Calc. For C

25

H

21

ClN

2

O

2

: C, 72.02, H, 5.08, N, 6.72. Found: C, 72.19, H, 4.91, N, 6.65.

EXAMPLE 9

6-(3-Chlorophenyl)-4-cyclopropyl-4-methyl-3,4-dihydro-1H-quinazolin-2-one

To a solution of 6-(3-chlorophenyl)-4-cyclopropyl-1-(4-methoxybenzyl)-1H-quinazolin-2-one (0.25 g, 0.6 mmol) in anhydrous ether was added, at ambient temperature under nitrogen, magnesium triflate (0.78 g, 2.4 mmol). The mixture was stirred for 30 minutes and treated with a solution of methylmagnesium bromide in ether (3.0 M, 1.0 mL, 3.0 mmol). The reaction mixture was kept at room temperature under nitrogen for 3 hours and quenched with a mixture of a saturated aqueous ammonium chloride solution (10 mL) and 1N aqueous HCl solution (5 mL). The mixture was stirred at room temperature for 20 minutes and ethyl acetate (40 mL) was added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine and dried (MgSO

4

). The solvent was removed and a half portion of the residue was dissolved in TFA (3 mL) and was stirred under nitrogen at room temperature for 72 hours. The solution was poured onto ice-water and the white precipitate obtained was collected on a filter. The solid was washed with water and then purified by a flash chromatography (methylene chloride:methanol/25:1, silica gel) to give 6-(3-chlorophenyl)-4-cyclopropyl-4-methyl-3,4-dihydro-1H-quinazolin-2-one as off-white solid (40 mg, 43%): mp 125-127° C.;

1

H-NMR (DMSO-d

6

) δ 9.21 (s, 1H), 7.71 (s, 1H), 7.61 (d, 1H, J=7.8 Hz), 7.55 (d, 1H, J=1.6 Hz), 7.47 (dd, 1H, J=8.3, 1.8 Hz), 7.45 (t, 1H, J=7.8 Hz), 7.36 (d, 1H, J=8.1 Hz), 6.84 (d, 1H, J=8.2 Hz), 6.79 (s, 1H), 1.54 (s, 3H), 1.11 (m, 1H), 0.42 (m, 1H), 0.15-0.20 (i, 3H); MS (ESI) m/z 313([M+H]

+

, 100%).

EXAMPLE 10

6-(3-Chlorophenyl)-4-cyclopropyl-3,4-dimethyl-3,4-dihydro-1H-quinazolin-2-one

To a solution of half of the crude addition product from Example 9 in anhydrous DMF (5 mL) was added under nitrogen at room temperature sodium hydride (25 mg, 0.63 mmol). The mixture was stirred at ambient temperature for 30 minutes and treated with methyl iodide (0.5 mL, excess). After stirring for 3.5 hours, a mixture of saturated aqueous ammonium chloride and 1N HCl aqueous solution (10 mL/5 mL) was added to the reaction mixture. Ethyl acetate (30 mL) was added and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (3×10 mL) and the combined organic layers were washed with brine and dried (MgSO

4

). The solvent was removed and residue was dissolved in a mixture of methylene chloride and TFA (2 mL/2 mL). After stirring for 3 hours, the solution was poured onto ice-water and neutralized by addition of a saturated aqueous sodium bicarbonate solution. The ethyl acetate (30 mL) was added and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine and dried (MgSO

4

). The solvent was removed in vacuo and the residue was purified by a flash chromatography (silica gel, hexane:ethyl acetate/1:1) to afford 6-(3-chlorophenyl)-4-cyclopropyl-3,4-dimethyl-3,4-dihydro-1H-quinazolin-2-one as a white solid (11 mg, 11% for three steps): mp 193-194° C.;

1

H-NMR (DMSO-d

6

) δ 9.51 (s, 1H), 7.68 (s, 1H), 7.59 (d, 1H, J=8.0 Hz), 7.57 (d, 1H, J=1.6 Hz), 7.51 (dd, 1H, J=8.3, 1.7 Hz), 7.46 (t, 1H, J=7.8 Hz), 7.35 (d, 1H, J=8.1 Hz), 6.87 (d, 1H, J=8.3 Hz), 3.02 (s, 3H), 1.51 (s, 3H), 1.25 (m, 1H), 0.32-0.51 (i, 3H), 0.25 (m, 1H); MS (CI) m/z 327 ([M+H]

+

, 100%). Anal. Calc. For C

19

H

19

ClN

2

O.0.3H

2

O: C, 68.69, H, 5.95, N, 8.43. Found: C, 68.69, H, 5.70, N, 8.18.

EXAMPLE 11

6-(3-Chloro-phenyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one

Sodium hydride (1.16 g, ca 29 mmol, 60% in oil) was washed with hexane (×3) then placed in anhydrous THF (50 mL) under nitrogen. To this slurry was then added dropwise a solution of 4-bromoaniline (5.0 g, 29 mmol) in dry THF (100 mn). After 0.5 h, the mixture was cooled to 0° C. and treated with a solution of 3,3-dimethylacryloyl chloride in anhydrous THF (30 ml). After 4 h, the mixture was quenched with saturated aqueous ammonium chloride solution, and extracted with diethyl ether. The organic layer was washed with water, brine, dried (Na

2

SO

4

) and evaporated. The residue was then crystallized from EtOAc/hexane to afford N-(3,3′-dimethylacryoloyl)-4-bromoaniline (3.36 g, 13.22 mmol, 46%) as a white solid:

1

H NMR (CDCl

3

) δ 7.42 (s, 4H), 7.06 (s, 1H), 5.68 (s, 1H), 2.21 (s, 3H), 1.09 (s, 3H); MS (EI) m/z 253 [M

+

].

N-(3,3′-Dimethylacryoloyl)-4-bromoaniline (4.0 g, 15.38 mmol) was heated under nitrogen to ca. 130-140° C. causing the solid to melt. Aluminum chloride (3.07 g, 23 mmol) was added and heating continued. After 1 h, the mixture was cooled and quenched carefully with water and then extracted with dichloromethane (3×60 mL). The combined organic layers were washed with water, dried (MgSO

4

) and evaporated. The residue was then subjected to column chromatography (SiO

2

, EtOAc/hexane gradient elution) to afford 6-bromo-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (1.69 g, 6.6 mmol, 47%/O) as a white solid:

1

H-NMR (CDCl

3

) δ 8.82 (s, 1H), 7.39 (d, 1H, J=2 Hz), 7.29 (dd, 1H, J=8.3, 2.0 Hz), 6.71 (d, 1H, J=8.0 Hz), 2.47 (s, 2H), 1.32 (s, 6H).

To a solution of the last cited compound (0.5 g, 1.96 mmol) in dimethoxyethane (15 mL) was added tetrakis(triphenylphosphine)palladium (0) (0.11 g, 0.09 mmol) under nitrogen. After 15 min., 3-chlorophenylboronic acid (0.6 g, 3.9 mmol) was added followed by potassium carbonate (1.62 g, 11.7 mmol) in water (7.5 mL). After 1.5 h at reflux, the mixture was cooled, filtered, and extracted with EtOAc. The organic layer was washed with water, dried (MgSO

4

) and evaporated. The residue was then subjected to column chromatography (SiO

2

, EtOAc:hexane/3:1) and crystallized from dichloromethane/hexane to afford 6-(3-chloro-phenyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (0.21 g, 0.73 mmol, 37%) as a white solid; mp. 211-215° C.;

1

H-NMR (CDCl

3

) δ 8.48 (s, 1H), 7.53 (s, 1H), 7.47 (d, 1H, J=2.0 Hz), 7.44-7.29 (m, 4H), 6.87 (1H, d, J=2.0 Hz), 2.54 (s, 2H), 1.39 (s, 6H); MS ((−)ES) m/z 284 [M−H]

−

.

EXAMPLE 12

Pharmacology

The compounds of this invention were tested in the relevant assay as described below and their potency are in the range of 0.01 nM to 5 μM in the in vitro assays and 0.001 to 300 mg/kg in the in vivo assays. The selected examples are listed below

TABLE 1

hPR CV-1

Compound

R

1

R

2

R

3

IC

50

(nM)

1

Me

Me

Cl

10.0

2

CF

3

Me

Cl

50.0

3

Me

H

NO

2

1675

R = H, hPR CV-1, IC

50

= 1075 nM

R = Me, hPR CV-1, IC

50

= 580 nM

hPR CV-1, IC

50

= 1075 nM

A. In-vitro Biology

The in-vitro biology is determined by (1) competitive Radioligand Binding: using the A-form of the human progesterone receptor with progesterone as the radioligand; (2) co-transfection assay, which provides functional activity expressed as agonist EC50 and Antagonist IC50 values; (3) a T47D cell proliferation, which is a further functional assay which also provides agonist and antagonist data; and (4) T47D cell alkaline phosphatase assay, which is a further functional assay which also provides agonist and antagonist data.

1. hPR Binding Assay

This assay is carried out in accordance with: Pathirana, C.; Stein, R. B.; Berger, T. S.; Fenical, W.; Ianiro, T.; Mais, D. E.; Torres, A.; Glodman, M. E.,

Nonsteroidal human progesterone receptor modulators from the marine alga

cymoplia barbata, J. Steroid Biochem. Mol. Biol., 1992, 41, 733-738.

2. PRE-Luciferase Assay in CV-1 Cells

The object of this assay is to determine a compound's progestational or antiprogestational potency based on its effect on PRE-luciferase reporter activity in CV-1 cells co-transfected with human PR and PRE-luciferase plasmids. The materials methods used in the assay are as follows.

a. Medium:

The growth medium was as follows: DMEM (BioWhittaker) containing 10% (v/v) fetal bovine serum (heat inactivated), 0.1 mM MEM non-essential amino acids, 100 U/ml penicillin, 100 mg/ml streptomycin, and 2 mM GlutaMax (GIBCO, BRL). The experimental medium was as follows: DMEM (BioWhittaker), phenol red-free, containing 10% (v/v) charcoal-stripped fetal bovine serum (heat-inactivated), 0.1 mM MEM non-essential amino acids, 100 U/ml penicillin, 100 mg/ml streptomycin, and 2 mM GlutaMax (GIBCO, BRL).

b. Cell Culture Transfection, Treatment and Luciferase Assay:

Stock CV-1 cells are maintained in growth medium Co-transfection is done using 1.2×10

7

cells, 5 mg pLEM plasmid with hPR-B inserted at Sph1 and BamH1 sites, 10 mg pGL3 plasmid with two PREs upstream of the luciferase sequence, and 50 mg sonicated calf thymus DNA as carrier DNA in 250 ml. Electroporation is carried out at 260 V and 1,000 mF in a Biorad Gene Pulser II. After electroporation, cells are resuspended in growth medium and plated in 96-well plate at 40,000 cells/well in 200 μl. Following overnight incubation, the medium is changed to experimental medium. Cells are then treated with reference or test compounds in experimental medium. Compounds are tested for antiprogestational activity in the presence of 3 nM progesterone. Twenty-four hr. after treatment, the medium is discarded, cells are washed three times with D-PBS (GIBCO, BRL). Fifty μl of cell lysis buffer (Promega, Madison, Wis.) is added to each well and the plates are shaken for 15 min in a Titer Plate Shaker (Lab Line Instrument, Inc.). Luciferase activity is measured using luciferase reagents from Promega.

c. Analysis of Results:

Each treatment consists of at least 4 replicates. Log transformed data are used for analysis of variance and nonlinear dose response curve fitting for both agonist and antagonist modes. Huber weighting is used to downweight the effects of outliers. EC

50

or IC

50

values are calculated from the retransformed values. JMP software (SAS Institute, Inc.) is used for both one-way analysis of variance and non-linear response analyses.

d. Reference Compounds:

Progesterone and trimegestone are reference progestins and RU486 is the reference antiprogestin. All reference compounds are run in full dose-response curves and the EC

50

or IC

50

values are calculated.

TABLE 2

Estimated EC

50

, standard error (SE), and 95% confidence

intervals (CI) for reference progestins from three individual studies

EC50

95% CI

Compound

Exp.

(nM)

SE

lower

upper

Progesterone

1

0.616

0.026

0.509

0.746

2

0.402

0.019

0.323

0.501

3

0.486

0.028

0.371

0.637

Trimegestone

1

0.0075

0.0002

0.0066

0.0085

2

0.0081

0.0003

0.0070

0.0094

3

0.0067

0.0003

0.0055

0.0082

TABLE 3

Estimated IC

50

, standard error (SE), and 95% confident interval

(CI) for the antiprogestin, RU486 from three individual studies

IC 50

95% CI

Compound

Exp.

(nM)

SE

lower

upper

RU486

1

0.028

0.002

0.019

0.042

2

0.037

0.002

0.029

0.048

3

0.019

0.001

0.013

0.027

Progestational activity: Compounds that increase PRE-luciferase activity significantly (p<0.05) compared to vehicle control are considered active.

Antiprogestational activity: Compounds that decrease 3 nM progesterone induced PRE-luciferase activity significantly (p<0.05)

EC

50

: Concentration of a compound that gives half-maximal increase PRE-luciferase activity (default-nM) with SE.

IC

50

: Concentration of a compound that gives half-maximal decrease in 3 nM progesterone induced PRE-luciferase activity (default-nM) with SE.

3. T47D Cell Proliferation Assay

The objective of this assay is the determination of progestational and antiprogestational potency by using a cell proliferation assay in T47D cells. A compound's effect on DNA synthesis in T47D cells is measured. The materials and methods used in this assay are as follows.

a. Growth Medium:

DMEM:F12 (1:1) (GIBCO, BRL) supplemented with 10% (v/v) fetal bovine serum (not heat-inactivated), 100 U/ml penicillin, 100 mg/ml streptomycin, and 2 mM GlutaMax (GIBCO, BRL).

b. Treatment Medium:

Minimum Essential Medium (MEM) (#51200-038GIBCO, BRL) phenol red-free supplemented with 0.5% charcoal stripped fetal bovine serum, 100 U/ml penicillin, 200 mg/ml streptomycin, and 2 mM GlutaMax (GIBCO, BRL).

c. Cell Culture

Stock T47 D cells are maintained in growth medium. For BrdU incorporation assay, cells are plated in 96-well plates (Falcon, Becton Dickinson Labware) at 10,000 cells/well in growth medium After overnight incubation, the medium is changed to treatment medium and cells are cultured for an additional 24 hr before treatment. Stock compounds are dissolved in appropriate vehicle (100% ethanol or 50% ethanol/50% DMSO), subsequently diluted in treatment medium and added to the cells. Progestin and antiprogestin reference compounds are run in full dose-response curves. The final concentration of vehicle is 0.1%. In control wells, cells receive vehicle only. Antiprogestins are tested in the presence of 0.03 nM trimegestone, the reference progestin agonist. Twenty-four hours after treatment, the medium is discarded and cells are labeled with 10 mM BrdU (Amersham Life Science, Arlington Heights, Ill.) in treatment medium for 4 hr.

d. Cell Proliferation Assay

At the end of BrdU labeling, the medium is removed and BrdU incorporation is measured using a cell proliferation ELISA kit (#RPN 250, Amersham Life Science) according to manufacturer's instructions. Briefly, cells are fixed in an ethanol containing fixative for 30 min, followed by incubation in a blocking buffer for 30 min to reduce background. Peroxidase-labeled anti-BrdU antibody is added to the wells and incubated for 60 min. The cells are rinsed three times with PBS and incubated with 3,3′5,5′-tetramethylbenzidine (TMB) substrate for 10-20 min depending upon the potency of tested compounds. Then 25 μl of 1 M sulfuric acid is added to each well to stop color reaction and optical density is read in a plate reader at 450 nm within 5 min.

e. Analysis of Results:

Square root-transformed data are used for analysis of variance and nonlinear dose response curve fitting for both agonist and antagonist modes. Huber weighting is used to downweight the effects of outliers. EC

50

or IC

50

values are calculated from the retransformed values. JMP software (SAS Institute, Inc.) is used for both one-way analysis of variance and non-linear dose response analyses in both single dose and dose response studies.

f. Reference Compounds:

Trimegestone and medroxyprogesterone acetate (MPA) are reference progestins and RU486 is the reference antiprogestin. All reference compounds are run in full dose-response curves and the EC

50

or IC

50

values are calculated.

TABLE 4

Estimated EC

50

, standard error (SE), and 95%

confidence intervals (CI) for individual studies

EC

50

95% CI

Compound

Exp

(nM)

SE

lower

upper

Trimegestone

1

0.017

0.003

0.007

0.040

2

0.014

0.001

0.011

0.017

3

0.019

0.001

0.016

0.024

MPA

1

0.019

0.001

0.013

0.027

2

0.017

0.001

0.011

0.024

TABLE 5

Estimated IC

50

, standard error, and 95%

confident interval for the antiprogestin, RU486

IC

50

95% CI

Compound

Exp

(nM)

SE

lower

upper

RU486

1

0.011

0.001

0.008

0.014

2

0.016

0.001

0.014

0.020

3

0.018

0.001

0.014

0.022

EC

50

: Concentration of a compound that gives half-maximal increase in BrdU incorporation with SE; IC

50

: Concentration of a compound that gives half-maximal decrease in 0.1 trimegestone induced BrdU incorporation with SE

4. T47D Cell Alkaline Phosphatase Assay

The purpose of this assay is to identify progestins or antiprogestins by determining a compound's effect on alkaline phosphatase activity in T47D cells. The materials and methods used in this assay are as follows.

a. Culture Medium:

DMEM:F12 (1:1) (GIBCO, BRL) supplemented with 5% (v/v) charcoal stripped fetal bovine serum (not heat-inactivated), 100 U/ml penicillin, 100 μg/ml streptomycin, and 2 mM GlutaMax (GIBCO, BRL).

b. Alkaline Phosphatase Assay Buffer:

I. 0.1 M Tris-HCl, pH 9.8, containing 0.2% Triton X-100

II. 0.1 M Tris-HCl, pH 9.8 containing 4 mM p-nitrophenyl phosphate (Sigma).

c. Cell Culture and Treatment:

Frozen T47D cells were thawed in a 37° C. water bath and diluted to 280,000 cells/ml in culture medium. To each well in a 96-well plate (Falcon, Becton Dickinson Labware), 180 μl of diluted cell suspension was added. Twenty μl of reference or test compounds diluted in the culture medium was then added to each well. When testing for progestin antagonist activity, reference antiprogestins or test compounds were added in the presence of 1 nM progesterone. The cells were incubated at 37° C. in a 5% CO

2

/humidified atmosphere for 24 hr.

d. Alkaline Phosphatase Enzyme Assay:

At the end of treatment, the medium was removed from the plate and fifty μl of assay buffer I was added to each well. The plates were shaken in a titer plate shaker for 15 min, Then 150 μl of assay buffer II was added to each well. Optical density measurements were taken at 5 min intervals for 30 min at a test wavelength of 405 nM.

e. Analysis of Results:

Analysis of dose-response data For reference and test compounds, a dose response curve is generated for dose (X-axis) vs. the rate of enzyme reaction (slope) (Y-axis). Square root-transformed data are used for analysis of variance and nonlinear dose response curve fitting for both agonist and antagonist modes. Huber weighting is used to downweight the effects of outliers. EC

50

or IC

50

values are calculated from the retransformed values. JMP software (SAS Institute, Inc.) is used for both one-way analysis of variance and non-linear dose response analyses in both single dose and dose response studies.

f. Reference Compounds:

Progesterone and trimegestone are reference progestins and RU486 is the reference antiprogestin. All reference compounds are run in full dose response curves and the EC

50

or IC

50

values are calculated.

TABLE 6

Estimated EC

50

, standard error (SE), and 95% confidence intervals

(CI) for reference progestins from three independent experiments

EC50

95% CI

Compound

Exp.

(nM)

SE

lower

upper

Progesterone

1

0.839

0.030

0.706

0.996

2

0.639

0.006

0.611

0.669

3

1.286

0.029

1.158

1.429

Trimegestone

1

0.084

0.002

0.076

0.091

2

0.076

0.001

0.072

0.080

3

0.160

0.004

0.141

0.181

TABLE 7

Estimated IC

50

, standard error, and 95% confident interval for the

reference antiprogestin RU486 from three independent experiments

IC 50

95% CI

Compound

Exp

(nM)

SE

lower

upper

RU486

1

0.103

0.002

0.092

0.115

2

0.120

0.001

0.115

0.126

3

0.094

0.007

0.066

0.134

B. In-vivo Biology

The primary in-vivo assay is the rat decidualization model which may be used to determine progestational effects of both agonists and antagonists. The secondary in-vivo assay is the rat ovulation inhibition model which is under development and hence the protocol is un-available.

1. Rat Decidualization Assay

The objective of this procedure is used to evaluate the effect of progestins and antiprogestins on rat uterine decidualization and compare the relative potencies of various test compounds. The materials and methods used in this assay are as follows.

a. Methods:

Test compounds are dissolved in 100% ethanol and mixed with corn oil (vehicle). Stock solutions of the test compounds in oil (Mazola™) are then prepared by heating (˜80° C.) the mixture to evaporate ethanol. Test compounds are subsequently diluted with 100% corn oil or 10% ethanol in corn oil prior to the treatment of animals. No difference in decidual response was found when these two vehicles were compared.

b. Animals (RACUC Protocol #5002)

Ovariectomized mature female Sprague-Dawley rats (˜60-day old and 230 g) are obtained from Taconic (Taconic Farms, N.Y.) following surgery. Ovariectomy is performed at least 10 days prior to treatment to reduce circulating sex steroids. Animals are housed under 12 hr light/dark cycle and given standard rat chow and water ad libitum.

c. Treatment

Rats are weighed and randomly assigned to groups of 4 or 5 before treatment. Test compounds in 0.2 ml vehicle are administered by subcutaneous injection in the nape of the neck or by lavage using 0.5 ml. The animals are treated once daily for seven days. For testing antiprogestins, animals are given the test compounds and a EC50 dose of progesterone (5.6 mg/kg) during the first three days of treatment. Following decidual stimulation, animals continue to receive progesterone until necropsy four days later.

d. Dosing

Doses are prepared based upon mg/kg mean group body weight. In all studies, a control group receiving vehicle is included. Determination of dose-response curves is carried out using doses with half log increases (e.g. 0.1, 0.3, 1.0, 3.0 mg/kg).

e. Decidual Induction

Approximately 24 hr after the third injection, decidualization is induced in one of the uterine horns by scratching the antimesometrial luminal epithelium with a blunt 21 G needle. The contralateral horn is not scratched and serves as an unstimulated control. Approximately 24 hr following the final treatment, rats are sacrificed by CO

2

asphyxiation and body weight measured. Uteri are removed and trimmed of fat. Decidualized (D-horn) and control (C-horn) uterine horns are weighed separately.

f. Analysis of Results:

The increase in weight of the decidualized uterine horn is calculated by D-horn/C-horn and logarithmic transformation is used to maximize normality and homogeneity of variance. The Huber M-estimator is used to down weight the outlying transformed observations for both dose-response curve fitting and one-way analysis of variance. JMP software (SAS Institute, Inc.) is used for both one-way ANOVA and non-linear dose-response analyses.

g. Reference Compounds:

All progestin reference compounds were run in full dose-response curves and the EC

50

for uterine wet weight were calculated.

TABLE 8

Estimated EC

50

, standard error (SE), and

95% confidence intervals for individual studies

EC

50

95% CI

Compound

Exp

(mg/kg, s.c.)

SE

lower

upper

Progesterone

1

5.50

0.77

4.21

7.20

2

6.21

1.12

4.41

8.76

3-Ketodesogestrel

1

0.11

0.02

0.07

0.16

2

0.10

0.05

0.11

0.25

3

0.06

0.03

0.03

0.14

Levonorgestrel

1

0.08

0.03

0.04

0.16

2

0.12

0.02

0.09

0.17

3

0.09

0.02

0.06

0.13

4

0.09

0.02

0.06

0.14

MPA

1

0.42

0.03

0.29

0.60

2

0.39

0.05

0.22

0.67

3

0.39

0.04

0.25

0.61

TABLE 9

Estimated average EC

50

, standard error, and 95% confidence

intervals for dose-response curves of 3 reference compounds

EC50

95% CI

Compound

(mg/kg, s.c.)

SE

lower

upper

Progesterone

5.62

0.62

4.55

7.00

3-Ketodesogestrel

0.10

0.02

0.07

0.14

Levonorgestrel

0.10

0.01

0.08

0.12

TABLE 10

Estimated IC

50

, standard error, and 95%

confident interval for the antiprogestin, RU 486

IC

50

95% CI

Compound

Exp.

(mg/kg, p.o.)

SE

lower

upper

RU 486

1

0.21

0.07

0.05

0.96

2

0.14

0.02

0.08

0.27

Concentration: Compound concentration in assay (default-mg/kg body weight)

Route of administration: Route the compound is administered to the animals

Body weight: Mean total animal body weight (default-kg)

D-horn: Wet weight of decidualized uterine horn (default-mg)

C-horn: Wet weight of control uterine horn (default-mg)

Decidual response: [(D−C)/C]×100%

Progestational activity: Compounds that induce decidualization significantly (p<0.05) compared to vehicle control are considered active

Antiprogestational activity: Compounds that decrease EC

50

progesterone induced decidualization significantly (p<0.05)

EC

50

for uterine weight: Concentration of compound that gives half-maximal increase in decidual response (default-mg/kg)

IC

50

for uterine weight: Concentration of compound that gives half-maximal decrease in EC

50

progesterone induced decidual response (default-mg/kg)

EXAMPLE 13

5-(2,4,4-Trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)thiophene-2-carbonitile

A solution of 2-amino-5-bromobenzoic acid (10 g, 46 mmol) in dry THF (200 mL) was treated at −78° C. under nitrogen with a solution of methylmagnesium bromide in ether (3.0 M, 90 mL, 270 mmol). The reaction mixture was slowly warmed to ambient temperature, kept stirring for 48 hours under nitrogen and then poured into a cold 0.5 N aqueous hydrochloride solution (300 mL). The mixture was neutralized with aqueous 1 N sodium hydroxide solution and ethyl acetate (300 mL) was added. The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with brine and dried (MgSO

4

). After removal of solvent in vacuo, the residue was purified by a silica gel flash column chromatography (hexane:ethyl acetate/3:2) to give 2-(2-amino-5-bromophenyl)propan-2-ol as off-white solid (6 g, 57%): mp 62-63° C.;

1

H-NMR (CDCl

3

) δ 7.19 (d, 1H, J=2.3 Hz), 7.12 (dd, 1H, J=8.4, 2.3 Hz), 6.51 (d, 1H, J=8.4 Hz), 4.70 (s, 2H), 1.82 (s, 1H), 1.65 (s, 6H).

To a solution of 2-(2-amino-5-bromophenyl)propan-2-ol (27 g, 125 mmol) in anhydrous toluene was added at ambient temperature under a blanket of nitrogen acetylaldehyde (10.5 mL, 187 mmol). After 10 minutes, the mixture was passed through a pad of silica gel and filtrate was concentrated to yield 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine as off-white solid (25 g, 78%):

1

H-NMR (DMSO-d

6

) δ 7.22 (d, 1H, J=2.2 Hz), 7.08 (dd, 1H, J=8.6, 2.3 Hz), 6.51 (d, 1H, J=8.6 Hz), 6.36 (s, 1H), 4.72 (m, 1H), 1.45 (s, 3H), 1.40 (s, 3H), 1.25 (d, 3H, J=5.5 Hz).

A mixture of 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine (3.6 g, 14 mmol), bis(pinacolato)diboron (5 g, 19.7 mmol), potassium acetate (4 g, 41 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]palladium (II) chloride (1:1 complex with methylene chloride, 0.4 g, 0.5 mmol) in DMF (80 mL) was subject to a positive nitrogen flow to remove oxygen and then heated at 85° C. under a blanket of nitrogen for 18 hours. The mixture was allowed to cool to ambient temperature, treated with 5-bromo-2-thiophenecarbonitrile (4 g, 21 mmol), [1,1′-bis(diphenylphosphino)ferrocene]palladium (II) chloride (1:1 complex with methylene chloride, 0.4 g, 0.5 mmol), and aqueous sodium carbonate solution (2M, 35 mL, 70 mmol), and then heated at 85° C. under nitrogen for 3 hours. The reaction mixture was allowed to cool to ambient temperature, brine (100 mL) and ethyl acetate (150 mL) were added. The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried (MgSO

4

) and concentrated. The residue was purified by a flash silica gel column chromatography (THF:hexane/1:4) to afford the title compound as an off-white solid (1 g, 25%): mp 172-173° C.;

1

H-NMR (DMSO-d

6

) δ 7.88 (d, 1H, J=4.0 Hz), 7.47 (d, 1H, J=4.0 Hz), 7.43 (d, 1H, J=2.0 Hz), 7.32 (dd, 1H, J=8.36, 2.4 Hz), 6.77 (s, 1H), 6.60 (d, 1H, J=8.4 Hz), 4.83 (m, 1H), 1.51 (s, 3H), 1.48 (s, 3H), 1.28 (d, 3H, J 5.6 Hz); MS (ESI) m/z 283 [M−H]

−

.

EXAMPLE 14

3-Fluoro-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)benzonitrile

Prepared according to the procedure for Example 13 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 3-bomo-5-fluorobenzonitrile. A white solid: mp 163-164° C.;

1

H-NMR (DMSO-d

6

) δ 8.02 (t, 1H, J=1.5 Hz), 7.87 (dt, 1H, J=10.6, 2.2 Hz), 7.65 (m, 1H), 7.55 (d, 1H, J=2.2 Hz), 7.44 (dd, 1H, J=8.4, 2.2 Hz), 6.63 (d, 1H, J=8.4 Hz), 6.58 (s, TH), 4.82 (m, TH), 1.52 (s, 3H), 1.50 (s, 3H), 1.28 (d, 3H, J=5.1 Hz); MS (ESI) m/z 295 [M−H]

−

.

EXAMPLE 15

4-(2,4,4-Trimethyl-14-dihydro-2H-3,1-benzoxazin-6-yl)thiophene-2-carbonitile

Prepared according to the procedure for Example 13 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 4-bromo-2-thiophenecarbonitrile. An off-white solid: mp 175-176° C.;

1

H-NMR (DMSO-d

6

) δ 8.39 (d, 1H, J=1.5 Hz), 8.13 (d, 1H, J=1.5 Hz), 7.47 (d, TH, J=1.9 Hz), 7.36 (dd, TH, J=8.4, 1.9 Hz), 6.59 (d, TH, J=8.4 Hz), 6.41 (s, 1H), 4.78 (m, 1H), 1.51 (s, 3H), 1.47 (s, 3H), 1.28 (d, 3H, J 5.4 Hz); MS (ESI) m/z 285 [M+H]

+

.

EXAMPLE 16

4-Methyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)thiophene-2-carbonitrile

Prepared according to the procedure for Example 13 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 5-bromo-4-methyl-2-thiophenecarbonitrile. A yellowish solid: mp 145-146° C.;

1

H-NMR (DMSO-d

6

) δ 7.79 (s, 1H), 7.18 (d, 1H, J=2.0 Hz), 7.13 (dd, 1H, J=8.4, 2.0 Hz), 6.68 (s, 1H), 6.54 (d, 1H, J=8.3 Hz), 4.83 (m, 1H), 2.26 (s, 3H), 1.49 (s, 3H), 1.46 (s, 3H), 1.28 (d, 3H, J=5.5 Hz); MS (ESI) m/z 299 [M+H]

+

.

EXAMPLE 17

3-1(2R,4S)-2,4-Dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-5-fluorobenzonitrile

To a solution of 2-amino-4-bromobenzonitrile (5 g, 25 mmol) in anhydrous THF, was added at 0° C. under nitrogen, phenylmagnesium bromide (3 M in ether, 25 mL, 75 mmol). The mixture was allowed to warm to room temperature, stirred under nitrogen for 15 hours, and treated with 2N aqueous hydrogen chloride solution (100 mL). The aqueous solution was heated to 50° C. for 3 hours, cooled to room temperature, and neutralized with a cold saturated sodium bicarbonate solution. Ethyl acetate (100 mL) was added and the organic layer was separated and aqueous layer was extracted with ethyl acetate (3×40 mL). The combined organic layers were dried (MgSO

4

) and evaporated. The residue was purified by a flash column chromatography (silica gel, hexane:ethyl acetate/4:1) to yield (2-amino-5-bromophenyl)(phenyl)methanone as a yellow crystal (2.13 g, 31%): MS (ESI) m/z 276/278 [M+H]

+

.

To a solution of (2-amino-5-bromophenyl)(phenyl)methanone (1 g, 3.6 mmol) in anhydrous THF (15 mL) was added at room temperature under nitrogen methylmagnesium bromide (3M in ether, 3 mL, 9 mmol). After 3 hours, the mixture was treated with a saturated aqueous ammonium sulfate solution (30 mL) and ethyl acetate (50 mL). The organic layer was separated, dried (MgSO

4

), and evaporated. The residue was then dissolved in anhydrous toluene and treated at ambient temperature under nitrogen with acetylaldehyde (2 mL). After 2 minutes, the solvent was removed and residue was purified by a column chromatography (silica gel, hexane:ethyl acetate/4:1) to afford 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine as a yellowish solid (0.8 g, 70%): MS (ESI) m/z 318/320 [M+H]

+

.

A mixture of 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine (0.6 g, 1.9 mmol), 3-cyano-5-fluorobenzene boronic acid (0.45 g, 2.7 mmol), tetrakis(triphenylphosphine)palladium (0) (0.2 g, 0.17 mmol), sodium carbonate (0.6 g, 5.7 mmol) in a mixture of DME and water (20/5 mL) was subject to a positive nitrogen flow to remove oxygen and then heated to 85° C. under a blanket of nitrogen for 2 hours. The mixture was allowed to cool to ambient temperature. Brine (30 mL) and ethyl acetate (100 mL) were added. The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×30 mL). The combined organic layers were dried (MgSO

4

), and evaporated. The residue was purified by a silica gel column chromatography (hexane:ethyl acetate/4:1) to afford the title compound as off-white solid (0.09 g, 13%): mp128-129° C.;

1

H-NMR (DMSO-d

6

) δ 8.08 (s, 1H), 7.91 (dt, 1H, J=10.7, 1.9 Hz), 7.71 (d, 1H, J=2.0 Hz), 7.65 (m, 1H), 7.57 (dd, 1H, J=8.8, 2.4 Hz), 7.32-7.36 (m, 2H), 7.24-7.29 (in, 3H), 6.71 (d, 1H, J=1.6 Hz), 6.69 (d, 1H, J=8.3 Hz), 4.33 (m, 1H), 1.84 (s, 3H), 1.24 (d, 3H, J=5.5 Hz); MS (ESI) m/z 357 [M−H]

−

.

EXAMPLE 18

tert-Butyl 2-Cyano-5(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate

tert-Butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate was prepared according to the coupling procedure for Example 17 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 1-t-butoxycarbonylpyrrol-2-yl boronic acid. To a solution of tert-butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate (1 g, 2.9 mmol) in anhydrous THF (20 mL) was added at −78° C. under nitrogen chlorosulfonyl isocyanate (0.35 mL, 4.0 mmol). The mixture was kept stirring at −78° C. under nitrogen for 2 hours, treated with anhydrous DMF (5 mL), and allowed to warm to room temperature. Aqueous ammonium sulfate solution (50 mL) and ethyl acetate (100 mL) was added and organic layer was separated, dried (MgSO

4

), and evaporated. The residue was purified by a silica gel column chromatography (hexane:ethyl acetate/4:1) to afford the title compound as a white solid (0.019 g, 1.78%):

1

H-NMR (DMSO-d

6

) δ 7.48 (d, 1H, J 2.0 Hz), 7.36 (dd, 1H, J=8.3, 2.0 Hz), 7.32 (d, 1H, J=3.6 Hz), 7.14 (d, 1H, J=8.3 Hz), 6.46 (d, 1H, J=4.0 Hz), 5.35 (q, 1H, J=5.2 Hz), 1.58 (d, 3H, J=5.6 Hz), 1.56 (s, 3H), 1.51 (s, 3H), 1.38 (s, 9H); MS (ESI) m/z 366 [M−H]

−

.

EXAMPLE 19

9H-Fluoren-9-ylmethyl-6-[1-(tert-butoxycarbonyl)-5-cyano-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1(4H)-carboxylate

A mixture of tert-butyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-1-carboxylate (1.7 g, 4.96 mmol), 9-fluorenylmethyl chloroformate (1.92 g, 7.5 mL), sodium carbonate (4 g, 37 mmol) in dioxane (50 mL) and water (50 mL) was stirred at room temperature under a blanket of nitrogen for 6 hours. Ethyl acetate (100 mL) was added and organic layer was separated, dried (MgSO

4

), and evaporated. The residue was purified by a silica gel column chromatography (hexane:ethyl acetate/6:1) to afford 9H-fluoren-9-ylmethyl-6-[1-(tert-butoxycarbonyl)-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1 (4H)-carboxylate as a clean oil.

Using the procedure for Example 18, the title compound (0.8 g, 65%) was prepared from 9H-fluoren-9-ylmethyl-6-[1-(tert-butoxycarbonyl)-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1 (4H)-carboxylate (1.2 g, 2.1 mmol) and chlorosulfonyl isocyanate (0.28 mL, 3.1 mmol). A white solid: mp 135-136° C.;

1

H-NMR (DMSO-d

6

) δ 7.90 (t, 2H, J=6.7 Hz), 7.64 (d, 1H, J=7.5 Hz), 7.59 (d, 1H, J=7.1 Hz), 7.40 (td, 2H, J=7.2, 2.0 Hz), 7.31-7.34 (m, 3H), 7.29 (d, 1H, J=1.2 Hz), 7.04-7.09 (m, 2H), 6.44 (d, 1H, J=3.57 Hz), 5.30 (q, 1H, J=5.6 Hz), 4.86 (dd, 1H, J=10.7, 5.2 Hz), 4.64 (dd, 1H, J=10.8, 5.2 Hz), 4.33 (t, 1H, J=4.7 Hz). 1.50 (s, 3H), 1.30 (s, 9H), 1.20 (s, 3H), 1.03 (d, 3H, J=5.6 Hz); MS (ESI) m/z 590 [M+H]

+

.

EXAMPLE 20

5-(2,4,4-Trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-2-carbonitrile

9H-Fluoren-9-ylmethyl-6-[1-(tert-butoxycarbonyl)-5-cyano-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1(4H)-carboxylate (0.5 g, 0.84 mmol) was heated under a blanket of nitrogen at 160° C. until gas evolution ceased. After cooling to room temperature, 9H-fluoren-9-ylmethyl-6-[5-cyano-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1(4H)-carboxylate was obtained as a white solid (0.4 g, 97%).

A solution of 9H-fluoren-9-ylmethyl-6-[5-cyano-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1 (4H)-carboxylate (0.1 g, 0.2 mmol) in 20% piperidine in DMF (5 mL) was stirred at room temperature under nitrogen for 10 minutes. The mixture was poured into a saturated ammonium sulfate solution (30 mL) and extracted with diethyl ether (3×30 mL). The combined organic layers were dried (MgSO

4

) and evaporated. The residue was purified by a silica gel column chromatography (hexane:ethyl acetate/3:1) to afford the title compound as a white solid (0.03 g, 56%): mp 201-202° C.;

1

H-NMR (DMSO-d

6

) δ 12.27 (s, 1H), 7.44 (d, 1H, J=2.1 Hz), 7.32 (dd, 1H, J=8.3, 1.1 Hz), 6.92 (dd, 1H, J=4.1, 2.6 Hz), 6.57 (d, 1H, J=8.3 Hz), 6.50 (dd, 1H, J=4.2, 2.6 Hz), 6.40 (s, 1H), 4.77-4.80 (m, 1H), 1.51 (s, 3H), 1.46 (s, 3H), 1.27 (d, 3H, J=5.7 Hz); MS (ESI) m/z 266 [M−H]

−

.

EXAMPLE 21

9H-Fluoren-9-ylmethyl 6-(5-cyano-1-methyl-1H-pyrrol-2-yl)-2,4,4-trimethyl-2H-′3,1-benzoxazine-1(4H)-carboxylate

A mixture of 9H-fluoren-9-ylmethyl-6-[5-cyano-1H-pyrrol-2-yl]-2,4,4-trimethyl-2H-3,1-benzoxazine-1 (4H)-carboxylate (0.4 g, 0.8 mmol) and potassium carbonate (1.5 g) in anhydrous DMF was treated at ambient temperature under a blanket of nitrogen with iodomethane (1.5 mL, excess). The mixture was stirred for 30 minutes. A saturated ammonium sulfate solution (50 mL) and ethyl acetate (50 mL) was added. The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×5 mL). The combined organic layers were dried (MgSO

4

), evaporated to yield the title compound as a white solid (0.35 g, 87%): mp 63-64° C.;

1

H-NMR (DMSO-d

6

) δ 7.90 (m, 2H), 7.62 (d, 1H, J=7.7 Hz), 7.58 (d, 1H, J=7.7 Hz), 7.40 (m, 2H), 7.29-7.32 (m, 3H), 7.14 (dd, 1H, J=8.1, 1.9 Hz), 7.01-7.04 (m, 2H), 6.33 (d, 1H, J=4.3 Hz), 5.31 (q, 1H, J=5.8 Hz), 4.88 (dd, 1H, J=10.8, 5.0 Hz), 4.65 (dd, 1H, J=10.8, 4.6 Hz),4.34(t, 1H, J=4.6 Hz), 3.71 (s, 3H), 1.52(s, 3H), 1.21 (s, 3H), 1.06 (d, 3H, J=5.4 Hz); MS (ESI) m/z 504 [M+H]

+

.

EXAMPLE 22

1-Methyl-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-1H-pyrrole-2 carbonitrile

Prepared according to the procedure for Example 20 from 9H-fluoren-9-ylmethyl 6-(5-cyano-1-methyl-1H-pyrrol-2-yl)-2,4,4-trimethyl-2H-′3,1-benzoxazine-1(4H)-carboxylate (0.3 g, 0.6 mmol) and 20% piperidine in DMF. A white solid (0.07 g, 42%): mp 195-196° C.;

1

H-NMR (DMSO-d

6

) δ 7.16 (d, 1H, J=2.8 Hz), 7.08 (dd, 1H, J=8.1, 1.9 Hz), 6.98 (d, 1H, J=4.1 Hz), 6.63 (d, 1H, J=8.5 Hz), 6.61 (s, 1H), 6.20 (d, 1H, J=4.1 Hz), 4.79-4.81 (m, 1H), 3.67 (s, 3H), 1.49 (s, 3H), 1.45 (s, 3H), 1.27 (d, 3H, J=5.5 Hz); MS (ESI) m/z 282 [M+H]

+

.

EXAMPLE 23

5-(2-Methylspiro[4H-3,1-benzoxazine-4,1′-cyclopentane]-6-yl)-4 methyl-2-thiophenecarbonitrile

2-Methyl-6-bromospiro[4H-3,1-benzoxazine-4,1′-cyclopentane] was prepared using the same procedure as for 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine in Example 13.

The title compound was prepared according to the procedure for Example 13 from 2-methyl-6-bromospiro[4H-3,1-benzoxazine-4,1′-cyclopentane] and 5-bromo-4-methyl-2-thiophenecarbonitrile. A yellowish solid: mp 58-60° C.;

1

H-NMR (DMSO-d

6

) δ 7.79 (s, 1H), 7.16 (d, 1H, J=1.9 Hz), 7.12 (dd, 1H, J=8.4, 2.2 Hz), 6.66 (s, 1H), 6.63 (d, 1H, J=8.4 Hz), 4.75 (m, 1H), 2.26 (s, 3H), 2.14 (m, 1H), 1.87 (m, 1H), 1.4-1.7 (m, 6H), 1.32 (d, 3H, J=5.5 Hz).

EXAMPLE 24

4-(2-Methylspiro[2H-3,1-benzoxazine-4,1′-cyclopentane]-6-yl)-2-thiophenecarbonitrile

Prepared according to the procedure for Example 13 from 2-methyl-6-bromospiro[4H-3,1-benzoxazine-4,1′-cyclopentane] and 4-bromo-2-thiophenecarbonitrile. An off-white solid: mp 103-104° C.

EXAMPLE 25

5-(2-Methylspiro[2H-3,1-benzoxazine-4,1′-cyclohexane]-6-yl)-4-methyl-2-thiophenecarbonitrile

2-Methyl-6-bromospiro[2H-3,1-benzoxazine-4,1′-cyclohexane] was prepared using the same procedure as for 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine in Example 13.

The title compound was prepared according to the procedure for Example 13 from 2-methyl-6-bromospiro[4H-3,1-benzoxazine-4,1′-cyclohexane] and 5-bromo-4-methyl-2-thiophenecarbonitrile. A brown solid:

1

H-NMR (DMSO-d

6

) δ 7.78 (s, 1H), 7.17 (d, 1H, J=1.8 Hz), 7.14 (dd, 1H, J=8.4, 2.2 Hz), 6.64 (s, 1H), 6.63 (d, 1H, J=8.2 Hz), 4.74 (r, 1H), 2.26 (s, 3H), 2.14 (m, 1H), 1.87 (m, 1H), 1.4-1.7 (m, 8H), 1.31 (d, 3H, J=5.3 Hz); MS (ESI) m/z 337 [M−H]

−

.

EXAMPLE 26

4-(2-Methylspiro[2H-3,1-benzoxazine-4,1′-cyclohexane]-6-yl)2-thiophenecarbonitrile

Prepared according to the procedure for Example 13 from 2-methyl-6-bromospiro [4H-3,1-benzoxazine-4,1′-cyclohexane] and 4-bromo-2-thiophenecarbonitrile. A brown solid; mp 111-112° C.;

1

H-NMR (DMSO-d

6

) δ 8.42 (s, 1H), 8.14 (s, 11H), 7.47 (s, 1H), 7.35 (dd, 1H, J=8.3, 1.1 Hz), 6.58 (d, 1H, J=8.4 Hz), 6.38 (s, 1H), 4.72 (m, 1H), 1.92-2.16 (m, 2H), 1.35-1.75 (m, 8H), 1.31 (d, 3H, J=5.3 Hz); MS (ESI) m/z 325 [M+H]

+

.

EXAMPLE 27

6-(3-Fluorophenyl)-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine

Prepared according to the coupling procedure for Example 17 from 3-fluorophenyl boronic acid and 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine. A yellow solid: mp 139-140° C.;

1

H-NMR (CDCl

3

) δ 7.40-7.19 (m, 6H), 7.01-6.94 (m, 1H), 6.72 (d, 1H, J=8.24 Hz), 4.90 (q, 1H, J=5.48 Hz), 1.62 (s, 3H), 1.59 (s, 3H), 1.46 (d, 3H, J=5.5 Hz); MS (ES) m/z 272 ([M+H]

+

).

EXAMPLE 28

6-(3-Chlorophenyl)-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine

Prepared according to the coupling procedure for Example 17 from 3-chlorophenyl boronic acid and 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine. A orange solid: mp 144-146° C.;

1

H-NMR (CDCl

3

) δ 7.50 (t, 1H, J=1.78 Hz), 7.40 (dt, 1H, J=7.61, 1.45 Hz), 7.33 (t, 1H, J=7.76 Hz), 7.29-7.22(m, 4H) 6.72 (d, 1H, J=8.24 Hz), 4.90 (q, 1H, J=5.45 Hz), 1.62 (s, 3H), 1.59 (s, 3H), 1.46 (d, 3H, J=5.5 Hz); MS (ES) m/z 288/290 ([M+H]

+

).

EXAMPLE 29

6-(3-Chloro-4-fluorophenyl)-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine

A mixture of 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine (3.0 g, 11.7 mmol), 3-chloro-4-fluorobenzeneboronic acid (3.1 g, 17.6 mmol), tetrakis(triphenylphosphine)palladium (0) (0.67 g, 0.59 mmol), and sodium carbonate (3.72 g, 35.1 mmol) in DME (80 mL) and water (40 mL) was subject to a blanket of nitrogen flow for 15 minutes at 50° C. and then was heated at 85° C. under nitrogen for 1 hour. The reaction was cooled to room temperature and ethyl acetate (200 mL) was added. The organic layer was washed twice with aqueous ammonium chloride (50 mL) and once with brine (50 mL), dried over sodium sulfate and concentrated to a yellow solid. The solid was triturated with ether (25 mL) and hexane (25 mL), collected on a filter, and dried to give 6-(3-chloro-4-fluorophenyl)-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine (1.87 g, 35%) as a yellow solid: mp 173-175° C.;

1

H-NMR (DMSO-d

6

) δ 7.79 (dd, 1H, J=6.84, 2.14 Hz), 7.60-7.57 (m, 1H), 7.43-7.39 (m, 2H), 7.29 (dd, 1H, J=8.12, 2.14 Hz), 6.62 (d, 1H, J=8.54 Hz), 6.40 (s, 1H), 4.79 (q, 1H, J=5.55 Hz), 1.53 (s, 3H), 1.48 (s, 3H), 1.28 (d, 3H, J=5.55 Hz); MS (ES) m/z 306/308([M+H]

+

).

EXAMPLE 30

2-Fluoro-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)benzonitrile

Prepared according to the coupling procedure for Example 13 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 5-bromo-2-fluorobenzonitrile. A white solid: mp 184-186° C.;

1

H-NMR (DMSO-d

6

) δ 8.17 (dd, 1H, J=5.86, 3.42 Hz), 8.00-7.98 (m, 1H), 7.52 (t, 1H, J=9.28 Hz), 7.45 (d, 1H, J=1.95 Hz), 7.34 (dd, 1H, J=8.30, 1.95 Hz), 6.63 (d, 1H, J=8.3 Hz), 6.45 (d, 1H), 4.8 (q, 1H, J=5.37 Hz), 1.53 (s, 3H), 1.49 (s, 3H), 1.29 (d, 3H, J=5.37 Hz); MS (ES) m/z 297 ([M+H]

+

).

EXAMPLE 31

4-(2,4,4-Trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)-2-furonitrile

Prepared using the coupling procedure for Example 13 from 6-bromo-2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazine and 4-bromo-2-cyanofuran. A light brown solid: mp 116-118° C.;

1

H-NMR (DMSO-d

6

) δ 8.43 (s, 1H), 8.06 (s, 1H), 7.38 (d, 1H, J=1.98 Hz), 7.25 (dd, 1H, J=7.93, 1.98 Hz) 6.58 (d, 1H, J=7.93 Hz), 6.37 (s, 1H), 4.77 (q, 1H, J=5.55 Hz), 1.50 (s, 3H), 1.46 (s, 3H), 1.27 (d, 3H, J=5.55 Hz); MS (ES) m/z 269 ([M+H]

+

); Anal. Calc. For C

16

H

16

N

2

O

2

: C, 71.62; H, 6.01, N, 10.44. Found: C, 71.55; H, 6.26, N, 10.17.

EXAMPLE 32

3-[4,4-Dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]-5-fluorobenzonitrile

A mixture of 2-(2-amino-5-bromo-phenyl)-propan-2-ol (5 g, 21.7 mmol), trifluoroacetaldehyde methyl hemiacetal (5 mL), and magnesium sulfate (10 g) in toluene (75 mL) was heated at 80° C. under nitrogen. After disappearance of the starting material, the reaction was filtered through a pad of silica gel and the filtrate dried over sodium sulfate and concentrated to give 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine as an amorphous solid:

1

H-NMR (DMSO-d

6

) δ 7.31 (d, 1H, J=1.99 Hz), 7.19 (dd, 1H, J=8.73, 2.38 Hz), 6.88 (s 1H), 6.74 (d, 1H, J=8.33 Hz), 5.32 (m, 1H), 1.52 (s, 6H).

A mixture of 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3, 1-benzoxazine (0.5 g, 1.61 mmol), 3-cyano-5-fluorobenzeneboronic acid (0.39 g, 1.8 mmol), tetrakis(triphenylphosphine)-palladium (0) (0.2 g, 0.161 mmol), and sodium carbonate (0.5 g, 4.83 mmol) in DME (50 mL) and water (25 mL) was subject to a blanket of nitrogen flow for 15 minutes at 50° C. and then was heated at 85° C. under nitrogen for 1 hour. The reaction mixture was cooled to room temperature and ethyl acetate (200 mL) was added. The organic layer was washed twice with aqueous ammonium chloride (20 mL) and once with brine (20 mL), dried over sodium sulfate and concentrated to a yellow solid. Purification via flash column chromatography (silica gel, 5% ethyl acetate/hexane) gave 3-[4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]-5-fluorobenzonitrile (0.396 g, 73%) as a white solid: mp 102-103° C.;

1

H-NMR (DMSO-d

6

) δ 8.07 (s, 1H), 7.91 (d, 1H, J=10.7 Hz), 7.7 (d, 1H, J=10.7 Hz) 7.62 (d, 1H, J=1.98 Hz), 7.53 (dd, 1H, J=8.33, 1.98 Hz), 7.05 (s, 1H), 6.87 (d, 1H, J=8.33 Hz), 5.39-5.37 (m, 1H), 1.61 (s, 3H), 1.59 (s, 3H); MS (ES) m/z 349 ([M−H]

−

).

EXAMPLE 33

4-[4,4-Dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]thiophene-2-carbonitrile

Prepared using the coupling procedure for Example 13 starting with 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine and 4-bromo-2-thiophenecarbonitrile. A yellow solid:

1

H-NMR (DMSO-d

6

) δ 8.43 (s, 1H), 8.19 (s, 1H), 7.54 (d, 1H, J=1.98 Hz), 7.46 (dd, 1H, J=8.33, 1.98 Hz), 6.90 (s, 1H), 6.83 (d, 1H, J=8.33 Hz), 5.35 (d, 1H, J=3.57 Hz), 1.59 (s, 3H), 1.57 (s, 3H); MS (ES) m/z 337 ([M−H]

−

).

EXAMPLE 34

4-[1-Acetyl-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]thiophene-2-carbonitile

4-[4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]thiophene-2-carbonitrile (0.25 g, 0.74 mmol) was dissolved in DMF (10 mL), NaH (0.09 g, 2.22 mmol) was added and the mixture was stirred for 30 minutes prior to the addition of acetyl chloride (0.079 mL, 1.11 mmol). Upon disappearance of the starting material the reaction mixture was poured into brine (100 mL) and the product extracted with ether (150 mL), dried over sodium sulfate and concentrated. The residue was purified by a flash column chromatography (silica gel, 25% ethyl acetate/hexane) to yield 4-[1-acetyl-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]thiophene-2-carbonitrile (0.1 g, 36%) as an amorphous solid:

1

H-NMR (DMSO-d

6

) δ 8.58 (s, 1H), 8.5 (s, 1H), 7.83-7.80 (m, 2H), 7.64 (d, 1H, J=8.74 Hz), 6.42 (q, 1H, J=10 Hz), 2.24 (s, 3H), 1.73 (s, 3H), 1.42 (s, 3H).

EXAMPLE 35

(6(5-Cyanothien-3-yl)-4,4-dimethyl-2-(trifluoromethyl)-2H-3,1-benzoxazin-1(4H)-yl)methyl Pivalate

4-[4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]thiophene-2-carbonitrile (0.30 g, 0.89 mmol) was dissolved in DMF (10 mL), NaH (0.065 g, 2.7 mmol) was added and the was mixture stirred for 30 minutes prior to the addition of tert-butyl chloroacetate (0.19 mL, 1.3 mmol). Upon disappearance of the starting material the reaction mixture was poured into brine (100 mL) and the product extracted with ether (150 mL), dried over sodium sulfate and concentrated. Flash column chromatography (silica gel, 8% ethyl acetate/hexane) gave (6(5-cyanothien-3-yl)-4,4-dimethyl-2-(trifluoromethyl)-2H-3,1-benzoxazin-1(4H)-yl)methyl pivalate (0.127 g, 32%) as an amorphous solid:

1

H-NMR (CDCl

3

) δ 7.82 (s, 1H), 7.58 (s, 1H), 7.41 (dd, 1H, J=8.33, 1.98 Hz), 7.25 (d, 1H, J=1.98 Hz) 7.10 (d, 1H, J=8.33 Hz), 6.79 (d, 1H, J=8.33 Hz), 5.66 (d, 1H, J=11.9 Hz), 5.38 (d, 1H, J=11.9 Hz), 1.72 (s, 3H), 1.55 (s, 3H), 1.18 (s, 9H).

EXAMPLE 36

3-Fluoro-5-(2,2,4,4-tetramethyl-1,-dihydro-2H-3,1-benzoxazin-6-yl)benzonitrile

Prepared using the coupling procedure for Example 13 starting with 6-bromo-2,2,4,4-tetramethyl-1,4-dihydro-2H-3,1-benzoxazine and 3-bromo-5-fluorobenzonitrile. A white solid:

1

H-NMR (DMSO-d

6

) δ 8.03 (s, 1H), 7.87 (d, 1H, J=10.7 Hz), 7.65 (d, 1H, J=10.7 Hz), 7.57 (d, 1H, J=1.98 Hz) 7.45 (dd, 1H, J=8.33, 1.98 Hz), 6.65 (d, 1H, J=8.33 Hz), 6.42 (s, 1H), 1.52 (s, 6H), 1.34 (s, 6H); MS (ES) m/z 311 ([M+H]

+

).

EXAMPLE 37

4-(2,2,4,4-Tetramethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)thiophene-2-carbonitrile

Prepared using the coupling procedure for Example 13 starting with 6-bromo-2,2,4,4-tetramethyl-1,4-dihydro-2H-3,1-benzoxazine and 4-bromo-2-cyanothiophene. An amorphous orange solid:

1

H-NMR (DMSO-d

6

) δ 8.4 (d, 1H, J=1.69 Hz), 8.14 (d, 1H, J=1.69 Hz), 7.49 (d, 1H, J=2.20 Hz), 7.38 (dd, 1H, J=8.43, 2.02 Hz), 6.61 (d, 1H, J=8.43 Hz), 6.26 (s, 1H), 1.49 (s, 6H), 1.32 (s, 6H); MS (ES) m/z 299 ([M+H]

+

).

EXAMPLE 38

5-[4,4-Dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]-4-methylthiophene-2-carbonitile

Prepared according to the coupling procedure for Example 13 from 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine and 5-bromo-4-methyl-2-thiophene-carbonitrile. A yellowish solid: mp 97-98° C.;

1

H-NMR (DMSO-d

6

) δ 7.82 (s, 1H), 7.26 (d, 1H, J=1.7 Hz), 7.21 (dd, 1H, J=8.1, 2.1 Hz), 7.16 (s, 1H), 6.88 (d, 1H, J=8.1 Hz), 5.40 (m, 1H), 2.27 (s, 3H), 1.56 (s, 3H), 1.55 (s, 3H); MS (ESI) m/z 351 [M−H]

−

.

EXAMPLE 39

6-(3-Chlorophenyl)-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine

Prepared according to the coupling procedure for Example 17 from 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine and 3-chlorophenyl boronic acid. A yellowish solid: mp 108-109° C.;

1

H-NMR (DMSO-d

6

) δ 7.69 (t, 1H, J=1.7 Hz), 7.59 (d, 1H, J=7.8 Hz), 7.35-7.50 (m, 3H), 7.32 (dt, 1H, J=8.1, 1.1 Hz), 6.91 (s, 1H), 6.87 (d, 1H, J=8.4 Hz), 5.35 (m, 1H), 1.60 (s, 3H), 1.59 (s, 3H); MS (ESI) m/z 340 [M−H]

−

.

EXAMPLE 40

6-(3-Fluorophenyl)-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

Prepared by coupling 3-fluorophenylboronic acid with an equivalent amount of 6-bromo-4,4-dimethyl-3,4-dihydo-1H-quinolin-2-one using a catalytic amount of tetrakis(triphenylphosphine)palladium (0) with overnight refluxing in toluene containing an equivalent amount of potassium carbonate dissolved in water. Work up in the usual manner followed by recrystallization from ethanol gave a gray solid: mp

190-192

° C.

1

H-NMR (DMSO-d

6

) δ 10.27 (s, 1H), 7.57 (s, 1H), 7.50 (r, 4H), 7.15 (m, 1H), 6.95 (d, 1H J=8.2 Hz), 2.39 (s, 2H), 1.29 (s, 6H); MS (APCI (−)) m/z 268 [M−H]

−

Anal. Calc. For C

17

H

16

FNO 0.25H

2

O: C, 74.57, H, 6.07, N, 5.12. Found: C, 74.86, H, 5.97, N 5.06.

EXAMPLE 41

3-(4,4-Dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-5-fluorobenzonitrile

6-bromo-4,4-quinolin-2-one was allowed to couple with an equivalent of bis(pinacolato)diboron in refluxing DMF containing an equivalent of sodium carbonate dissolved in a minimal amount of water and a catalytic quantity of tetrakis(triphenylphosphine)palladium (0). After refluxing overnight an equivalent of 3-bromo-5-fluorobenzonitrile was added. Another equivalent of sodium carbonate was then added, followed by an additional amount of the same catalyst. After several hours of reflux, the reaction mixture was filtered and taken to dryness in vacuo. The residue was extracted into ethyl acetate and the solution was dried over magnesium sulfate, filtered and the filtrate was again roto-evaporated to give a solid residue. Recrystallization from ethanol afforded the title compound as a gray solid: mp 249-250° C.

1

H-NMR (DMSO-d

6

) δ 10.32(s, 1H), 8.09 (t, 1H, J=1.6 Hz), 7.93 (d, 1H, J=12.7 Hz) 7.77, (d, 1H, J=8.1 Hz), 7.70 (s, 1H), 7.61(d, 1HJ=8.9 Hz), 6.95 (d, 1H, J=8.3 Hz),2.40 (s, 2H), 1.30 (s, 6H); MS (APCI (−)) m/z 293 [M−H]

−

Anal. Calc. For C

18

H

15

FN

2

O 1.5H

2

O: C, 67.28, H, 5.65, N, 8.72. Found: C, 67.36, H, 4.90, N s8.44.

EXAMPLE 42

3-(4,4-Dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)benzonitrile

Prepared by coupling 3-cyanophenylboronic acid with an equivalent amount of 6-bromo-4,4-dimethyl-3,4-dihydo-1H-quinolin-2-one using a catalytic amount of tetrakis(triphenylphosphine)palladium (0) as a catalyst with overnight refluxing in toluene containing an equivalent amount of potassium carbonate dissolved in water in the usual manner followed by recrystallization from ethanol gave a gray solid: mp. 190-192° C.;

1

H-NMR (DMSO-d

6

) δ 10.29 (s, 1H), 8.17 (s, 1H), 8.00 (d, 1H, J=7.9 Hz), 7.77 (d, 1H, J=6.4 Hz), 7.65 (m, 2H), 7.55 (d, 1H, J=8.2 Hz), 6.97 (d, 1H, J=8.3 Hz), 2.40 (s, 2H), 1.30 (s, 6H); MS (APCI (−)) m/z 275 [M−H]

−

Anal. Calc. For C

18

H

16

N

2

O 0.25H

2

O: C, 75.77, H, 6.01, N, 9.82. Found: C, 75.45, H, 5.65, N 9.20.

EXAMPLE 43

6-(3-Chlorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-thione

Prepared by heating under reflux overnight a mixture of 6-(3-chlorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-one and an equal weight of phosphorus pentasulfide in pyridine was stirred. Removal of the pyridine in vacuo followed by treating the residue with 6N hydrochloric acid and recrystallization of the residue in ethanol gave the product as a yellow solid: mp. 197-1980 C.

1

H-NMR (DMSO-d

6

) 8 12.34 (s, 1H), 7.75 (m, 1H), 7.64 (m, 2H), 7.57 (dd, 1H J=9.3 and 2.1 Hz), 7.48 (t, 1H, J=7.7 Hz), 7.41 (m, 1H),7.20 (d, 1H, J=8.3 Hz), 3.34 (s, 2H), 1.26 (s, 6H); MS (APCI (−)) m/z 300 [M−H]

−

Anal. Calc. For C

17

H

16

CINS: C, 67.65, H, 5.34, N, 4.64. Found: C, 67.77, H, 5.57, N 4.54.

EXAMPLE 44

6-(3-Fluorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-thione

Prepared by heating under reflux overnight a mixture of 6-(3-fluororophenyl) 4,4-dimethyl-3,4-dihydroquinoline-2(1H)-one and an equal weight of phosphorus pentasulfide was stirred in pyridine. Workup as in the previous example gave a yellow solid, mp 209-211° C.

1

H-NMR (DMSO-d

6

) δ 12.34 (s, 1H), 7.65 (d, 1H J=2.2 Hz) 7.57 (dd, 1H J

1

=8.24 J

2

=2.2 Hz), 7.51(m, 3H), 7.18(m, 2H), 2.84(s, 2H), 1.26(s, 6H). MS m/z 284 [M−H]

−

Anal. Calc. For C

17

H

16

FINS: C, 71.55, H, 5.65, N, 4.91. Found: C, 71.18, H, 5.59, N4.82.

EXAMPLE 45

3-(4,4-Dimethyl-2-thioxo-1,2,3,4,-tetrahydroquinolin-6-yl)benzonitrile

Prepared by heating under reflux overnight a stirred mixture of 3-(4,4-dimethyl-2-oxo-1,2,3,4,-tetrahydroquinolin-6-yl)benzonitrile and an equal weight of phosphorus pentasulfide in pyridine and workup as in the previous example gave a yellow solid: mp 220-223° C. dec.

1

H-NMR (DMSO-d

6

) δ 12.35 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, J=6.0 Hz), 7.80 (d, 1H, J=7.9 Hz), 7.72 (s, 1H), 7.65 (m, 2H), 7.21 (d, 1H, J=8.4 Hz), 2.85 (s, 2H), 1.27 (s, 6H); MS (APCI (−)) m/z 291 [M−H]

−

Anal. Calc. For C

18

H

16

N

2

S 3H

2

O: C, 62.40, H, 6.40, N, 8.09. Found: C, 62.12, H, 4.88, N 7.77.

EXAMPLE 46

3-(4,4-Dimethyl-2-thioxo-1,2,3,4-tetrahydroquinolin-6-yl)-5-fluorobenzonitrile

Prepared by heating under reflux overnight a stirred mixture of 3-(4,4-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-5-fluorobenzonitrile and an equal weight of phosphorus pentasulfide in pyridine and workup as in the previous example gave a yellow solid: mp. 240-2420 C dec.;

1

H-NMR (DMSO-d

6

) δ 12.37 (s, 1H), 8.13 (s, 1H), 7.98 (dt, 1H, J=10.4 and 5.4 Hz), 7.81 (d, 1H, J=8.4 Hz), 7.7 (d, 1H, J=1.8 Hz), 7.68 (dd, 1H, J=8.3 and 1.9 Hz), 7.22 (d, 1H, J=8.3 Hz), 2.85 (s, 2H), 1.27 (s, 6H); MS m/z 309 [M−H]

−

Anal. Calc. For C

18

H

15

FN

2

S 0.10H

2

O: C, 69.25, H, 4.91, N, 8.97. Found: C, 69.15, H, 4.74, N 8.75.

EXAMPLE 47

6-(3-Fluoro-phenyl)-2,4,4-trimethyl-1,2,3,4-tetrahydro-quinoline

6-Bromo-1-(4-methoxy-benzyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one.

To a solution of 6-bromo-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (0.5 g, 1.97 mmol) in THF (25 mL) was added 60% NaH (0.12 g, 2.95 mmol) suspended in mineral oil. The resulting reaction mixture was stirred at room temperature for 30 min., 4-methoxybenzyl chloride (0.34 g, 2.17) added, and heated under reflux for 20 h. The reaction was cooled to room temperature then quenched slowly with water. After extraction with ethyl acetate, the organic layer was dried (MgSO

4

), evaporated and the residue purified by chromatography (SiO

2

3:7 ethyl acetate/hexane). The white crystalline product was obtained (0.35 g, 48%); mp 118-119° C.,

1

H NMR (DMSO-d

6

) δ 1.23 (s, 6H), 2.59 (s, 2H), 3.70 (s, 3H), 3.72 (s, 1H), 4.41 (d, 1H, J=5.86 Hz), 5.09 (s, 1H), 6.87 (m, 2H), 7.01 (d, 1H, J=8.78 Hz), 7.17 (d, 1H, J=8.98 Hz), 7.23 (d, 1H, J=8.79), 7.34 (dd, 1H, J=6.59 and 2.2 Hz), 7.43(d, 1H, J=2.2 Hz); MS (APCI (+)) [M+H]

+

=374/376.

6-(3-Fluoro-phenyl)-1-(4-methoxy-benzyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one.

A mixture of 6-Bromo-1-(4-methoxy-benzyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (2.9 g, 7.75 mmol) in ethylene glycol dimethyl ether (50 mL), K

2

CO

3

(1.18 g, 8.53 mmol) in H

2

O (50 mL), and a catalytic amount of tetrakistriphenylphosphine palladium was heated under reflux overnight. After cooling to room temperature, the mixture was extracted with ethyl acetate and the organic phase was washed with NaHCO

3

solution, brine, dried over MgSO

4

, concentrated, and crystallized from ethanol to obtain the product as a white crystalline material (1.8 g, 60%): mp 159-162° C.,

1

H NMR (DMSO-d

6

) δ 1.32 (s, 6H), 2.63 (s, 2H), 3.70 (s, 3H), 5.15 (s, 2H), 6.89 (d, 2H, J=11.72 Hz), 7.14 (m, 2H), 7.22 (d, 2H, J=8.8 Hz), 7.53 (m, 4H), 7.60 (d, 1H, J=2.2 Hz); MS (APCI (+)) [M+H]

+

=390.

6-Bromo-1-(4-methoxy-benzyl)-2,4,4-trimethyl-1,4-dihydro-quinoline.

To a solution of 6-(3-Fluoro-phenyl)-1-(4-methoxy-benzyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (1.16 g, 2.99 mmol) in THF (15 mL) at room temperature was added a solution of 1.4 M MeMgBr (2.6 mL, 12.56 mmol) and the resulting reaction mixture was stirred for 6 h. The solution was quenched with H

2

O, extracted with EtOAc, treated with ammonium chloride solution, washed with brine, dried over MgSO

4

, and concentrated. The product was purified by column chromatography using a 2:8 hexane/ethyl acetate mixture and used below.

To a solution of 6-(3-Fluoro-phenyl)-1-(4-methoxy-benzyl)-2,4,4-trimethyl-1,2,3,4-tetrahydroquinoline (0.15 g, 0.39 mmol) in EtOH (35 mL) was added 10%Pd/C and hydrogenated for 10 h at 40 psi. The catalyst was removed by filtration through celite and the product purified by chromatography. A reddish liquid was obtained.

1

H NMR (DMSO-d

6

) δ 1.15 (d, 3H, J=6.73 Hz), 1.21(s, 3H), 1.34(m, 4H), 1.60(dd, 1H, J.=10.1, J

2

=2.69, Hz), 3.40(m, 1H), 5.95(s, 1H), 6.55(d, 1H, J=8.08 Hz), 7.01(m, 1H), 7.21(dd, 1H, J

1

=5.78 J

2

=2.02 Hz), 7.35(m, 4H); MS (FI Pos) [M+H]

+

=270.

Still other compounds, including 5-(2,4,4-Trimethyl-1,2,3,4-tetrahydro-quinolin-6-yl)-1H-pyrrole-2-carbonitrile, 1-Methyl-5-(2,4,4-trimethyl-1,2,3,4-tetrahydro-quinolin-6-yl)-1H-pyrrole-2-carbonitrile, and 3-Fluoro-5-(2,4,4-trimethyl-1,2,3,4-tetrahydro-quinolin-6-yl)-benzonitrile may be prepared using the methods described above.

All publications cited in this specification are incorporated herein by reference herein. While the invention has been described with reference to a particularly preferred embodiment, it will be appreciated that modifications can be made without departing from the spirit of the invention. Such modifications are intended to fall within the scope of the appended claims.

Claims

1. A compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C6, alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is a substituted benzene ring of the structure: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, alkynyl, substituted alkynyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 or 6 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; RD is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RE is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, aminoalkyl, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; G1 is CR7R8; G2 is CO; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
2. The compound according to claim 1, wherein:R1 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R2 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C1 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C1 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy.
3. The compound according to claim 1 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the carbon-based 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; RR is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; X is selected from the group consisting of halogen, CN, C1 to C3 alkoxy, C1 to C1 alkyl, NO2, C1 to C3 perfluoroalkyl, 5 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, and C1 to C3 thioalkoxy; Y is on the 4′ or 5′ position and is selected from the group consisting of H, halogen, CN, NO2, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy.
4. The compound according to claim 3, wherein X is CN and Y is 5′-fluoro.
5. The compound according to claim 1, which is selected from the group consisting of 6-(3-Chloro-phenyl)-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one, 6-(3-Fluorophenyl)-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one, 3-(4,4-Dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-5-fluorobenzonitrile, and 3-(4,4-Dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)benzonitrile, or a pharmaceutically acceptable salt thereof.
6. A compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl, R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is selected from the group consisting of a), b), c), and d): a) a substituted benzene ring of the structure: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, alkynyl, substituted alkynyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 or 6 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; RD is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RE is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl, Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, aminoalkyl, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; b) a five membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, and SO2 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; c) a five membered ring having in its backbone 1, 2, or 3 NR6 heteroatoms and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; and d) a six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NR6CORF; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CS; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
7. The compound according to claim 6 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the carbon-based 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; U is O, S, or NR6; X′ is selected from the group consisting of halogen, CN, NO2, C1 to C3 alkyl and C1 to C3 alkoxy; Y′ is selected from the group consisting of H and C1 to C3 alkyl.
8. The compound according to claim 7, wherein U is S, X′ is CN and Y′ is H or —CH3.
9. The compound according to claim 6, which is selected from the group consisting of 6-(3-Chlorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-thione, 6-(3-Fluorophenyl)-4,4-dimethyl-3,4-dihydroquinoline-2(1H)-thione, 3-(4,4-Dimethyl-2-thioxo-1,2,3,4-tetrahydroquinolin-6-yl)benzonitrile, and 3-(4,4-Dimethyl-2-thioxo-1,2,3,4-tetrahydroquinolin-6-yl)-5-fluorobenzonitrile, or a pharmaceutically acceptable salt thereof.
10. The compound according to claim 6 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the carbon-based 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl, X is selected from the group consisting of halogen, CN, C1 to C3 alkoxy, C1 to C3 alkyl, NO2, C1 to C3 perfluoroalkyl, 5 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, and C1 to C3 thioalkoxy; Y is on the 4′ or 5′ position and is selected from the group consisting of H, halogen, CN, NO2, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy.
11. The compound according to claim 10, wherein X is CN and Y is 5′-fluoro.
12. The compound according to claim 6 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the carbon-based 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; X1 is CX2; X2 is halogen, CN, C1 to C3 alkoxy, or NO2.
13. The compound according to claim 6,wherein:R1 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R2 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6, alkenyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6, alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is (i), (ii), (iii), (iv): (i) the substituted benzene ring a), wherein: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; (ii) the five membered ring b) having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, and SO2 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, and C1 to C3 alkoxy; (iii) the five membered ring c) having in its backbone 1, 2, or 3 NR6 heteroatoms and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, and C1 to C3 alkoxy, or (iv) the six membered ring d) having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, and C1 to C3 alkoxy.
14. A compound of the formula: wherein:R1 is selected from the group consisting of C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; R2 is selected from the group consisting of C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, substituted or C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is a five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
15. The compound according to claim 14, whereinR1 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R2 is C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is the five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, and C1 to C3 alkoxy.
16. The compound according to claim 14 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; U is O, S, or NR6; X′ is selected from the group consisting of halogen, CN, NO2, C1 to C3 alkyl and C1 to C3 alkoxy; Y′ is selected from the group consisting of H and C1 to C3 alkyl.
17. The compound according to claim 16, wherein U is S, X′ is CN and Y′ is H or CH3.
18. The compound according to claim 14 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the carbon-based 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; X1 is CX2; X2 is halogen, CN, C1 to C3 alkoxy, or NO2.
19. A compound of the formula: wherein:R1 and R2 are independently selected from the group consisting of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, and substituted C2 to C6 alkynyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C1 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is a five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, and SO2 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
20. The compound according to claim 19 of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; U is O or S; R6 is H or C1 to C3 alkyl; X′ is selected from the group consisting of halogen, CN, NO2, C1 to C3 alkyl and C1 to C3 alkoxy; Y′ is selected from the group consisting of H and C1 to C3 alkyl.
21. The compound according to claim 20, wherein U is S, X′ is CN and Y′ is H or CH3.
22. The compound according to claim 19, wherein:R1 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R2 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is the five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, and SO2 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, and C1 to C3 alkoxy.
23. A compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C, alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA, or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring, b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is a five membered ring having in its backbone 1 NR6 heteroatom, attached through a carbon-atom of said ring, and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
24. The compound according to claim 23,wherein:R1 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; R2 is H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is the five membered ring and contains one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, and C1 to C3 alkoxy.
25. A compound of the formula: wherein:R1═R2 and are C1 to C3 alkyl or substituted C1 to C3 alkyl, or R1 and R2 are fused to form the carbon-based 3 to 6 membered saturated spirocyclic ring; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, or CORC; RC is H, C1 to C3 alkyl, or C1 to C3 alkoxy; R4 is H, halogen, NO2, C1 to C3 alkyl, or substituted C1 to C3 alkyl; X1 is N; G1 is CR7R8; and G2 is CO or CS.
26. A pharmaceutical composition comprising a compound of claim 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
27. A pharmaceutical composition comprising a compound of claim 14, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
28. A pharmaceutical composition comprising a compound of claim 23, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
29. A pharmaceutical composition comprising a compound of claim 6, or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient.
30. A pharmaceutical composition comprising a compound of claim 19, or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient.
31. A pharmaceutical composition comprising a compound of claim 25, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
32. A method of inducing contraception in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof.
33. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
34. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof.
35. A method of inducing contraception in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 14 or a pharmaceutically acceptable salt thereof.
36. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 14, or a pharmaceutically acceptable salt thereof, wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
37. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 14 or a pharmaceutically acceptable salt thereof.
38. A method of inducing contraception in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 23 or a pharmaceutically acceptable salt thereof.
39. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 23, or a pharmaceutically acceptable salt thereof, wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
40. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 23 or a pharmaceutically acceptable salt thereof.
41. A method of inducing contraception in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 6 or a pharmaceutically acceptable salt thereof.
42. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 6, or a pharmaceutically acceptable salt thereof, wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
43. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 6, or a pharmaceutically acceptable salt thereof.
44. A method of inducing contraception in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 19 or a pharmaceutically acceptable salt thereof.
45. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to mammal in need thereof a pharmaceutically effective amount of a compound of claim 19, or a pharmaceutically acceptable salt thereof, wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
46. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 19 or a pharmaceutically acceptable salt thereof.
47. A method of inducing contraception in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 25 or a pharmaceutically acceptable salt thereof.
48. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 25, or a pharmaceutically acceptable salt thereof, wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
49. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of claim 25 or a pharmaceutically acceptable salt thereof.
50. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof.
51. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of claim 14 or a pharmaceutically acceptable salt thereof.
52. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of claim 19 or a pharmaceutically acceptable salt thereof.
53. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of claim 23 or a pharmaceutically acceptable salt thereof.
54. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of claim 6 or a pharmaceutically acceptable salt thereof.
55. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of claim 25 or a pharmaceutically acceptable salt thereof.
56. A method of treating benign or malignant neoplastic disease in a mammal, the method comprising administering to a mammal in need thereof a pharmaceutically effective amount of a compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is selected from the group consisting of a) and b): a) a substituted benzene ring of the structure: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, alkynyl, substituted alkynyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 or 6 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; RD is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RE is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, aminoalkyl, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; or b) a five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; RG is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO or CS; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof; wherein the benign or malignant neoplastic disease is selected from the group consisting of uterine myometrial fibroids, endometriosis, benign prostatic hypertrophy, carcinomas and adenocarcinomas of the endometrium, ovary, breast, colon, prostate, pituitary, meningioma and other hormone-dependent tumors.
57. A method of treatment in a mammal of carcinomas or adenocarcinomas of the endometrium, ovary, breast, colon, or prostate, the method comprising administering to a mammal in need thereof a compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl, RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is selected from the group consisting of a) and b): a) a substituted benzene ring of the structure: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, alkynyl, substituted alkynyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 or 6 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; RD is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RE is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, aminoalkyl, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; or b) a five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO or CS; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
58. A method of hormone replacement therapy, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6 alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is selected from the group consisting of a) and b): a) a substituted benzene ring of the structure: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, alkynyl, substituted alkynyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 or 6 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; RD is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl, RE is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, aminoalkyl, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; or b) a five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO or CS; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.
59. A method of contraception, the method comprising administering to a female of child bearing age in need thereof a pharmaceutically effective amount of a compound of the formula: wherein:R1 and R2 are independent substituents selected from the group consisting of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, and NRBCORA; or R1 and R2 are fused to form: a) a 3 to 8 membered carbon-based saturated spirocyclic ring; b) a 3 to 8 membered carbon-based spirocyclic ring having one or more carbon—carbon double bonds; or c) a 3 to 8 membered heterocyclic ring containing in its backbone one to three heteroatoms selected from the group consisting of O, S and N; the rings of a), b) and c) being optionally substituted by from 1 to 4 groups selected from the group consisting of fluorine, C1 to C6 alkyl, C1 to C6 alkoxy, C1 to C6 thioalkoxy, CF3, OH, CN, NH2, NH(C1 to C6 alkyl), and N(C1 to C6alkyl)2; RA is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RB is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R3 is H, OH, NH2, C1 to C6 alkyl, substituted C1 to C6 alkyl, C3 to C6 alkenyl, substituted C3 to C6 alkenyl, alkynyl, substituted alkynyl, or CORC; RC is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; R4 is H, halogen, CN, NO2, C1 to C6 alkyl, substituted C1 to C6 alkyl, alkynyl, substituted alkynyl, C1 to C6 alkoxy, substituted C1 to C6 alkoxy, amino, C1 to C6 aminoalkyl, or substituted C1 to C6 aminoalkyl; R5 is selected from the group consisting of a) or b): a) a substituted benzene ring of the structure: X is selected from the group consisting of halogen, CN, C1 to C3 alkyl, substituted C1 to C3 alkyl, alkynyl, substituted alkynyl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 thioalkoxy, substituted C1 to C3 thioalkoxy, amino, C1 to C3 aminoalkyl, substituted C1 to C3 aminoalkyl, NO2, C1 to C3 perfluoroalkyl, 5 or 6 membered heterocyclic ring containing in its backbone 1 to 3 heteroatoms, CORD, OCORD, and NRECORD; RD is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RE is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; Y and Z are independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, aminoalkyl, C1 to C3 alkoxy, C1 to C3 alkyl, and C1 to C3 thioalkoxy; or b) a five or six membered ring having in its backbone 1, 2, or 3 heteroatoms selected from the group consisting of O, S, SO, SO2 and NR6 and containing one or two independent substituents selected from the group consisting of H, halogen, CN, NO2, amino, C1 to C3 alkyl, C1 to C3 alkoxy, C1 to C3 aminoalkyl, CORF, and NRGCORF; wherein said five or six membered ring b) is attached through a carbon-atom of said ring; RF is H, C1 to C3 alkyl, substituted C1 to C3 alkyl, aryl, substituted aryl, C1 to C3 alkoxy, substituted C1 to C3 alkoxy, C1 to C3 aminoalkyl, or substituted C1 to C3 aminoalkyl; RG is H, C1 to C3 alkyl, or substituted C1 to C3 alkyl; R6 is H or C1 to C3 alkyl; G1 is CR7R8; G2 is CO or CS; R7 and R8 are independently selected from the group consisting of H, alkyl, substituted alkyl, aryl, and heterocyclic; or pharmaceutically acceptable salt thereof.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 09/552,629, filed Apr. 19, 2000, now U.S. Pat. No. 6,358,948, issued Mar. 19, 2002, which claims the benefit of the priority of U.S. Patent Application No. 60/219,339, filed May 4, 1999, now abandoned.

US Referenced Citations (38)

Number	Name	Date	Kind
3526621	Bernardi et al.	Sep 1970	A
3635941	Weaver et al.	Jan 1972	A
3635964	Skorcz	Jan 1972	A
3917592	Kobzina	Nov 1975	A
4093730	Butti	Jun 1978	A
4440785	Walsh	Apr 1984	A
4666913	Kuhla	May 1987	A
4670566	Walsh	Jun 1987	A
4721721	Kuhla	Jan 1988	A
4792561	Walker et al.	Dec 1988	A
4822794	Spada	Apr 1989	A
4831027	Narr	May 1989	A
4853473	Fischer	Aug 1989	A
5007952	Kume	Apr 1991	A
5171851	Kim	Dec 1992	A
5414088	von der Saal	May 1995	A
5447928	Williams et al.	Sep 1995	A
5453516	Fischer	Sep 1995	A
5475020	Johnson	Dec 1995	A
5519021	Young et al.	May 1996	A
5521166	Grubb	May 1996	A
5681817	Hodgen	Oct 1997	A
5688808	Jones	Nov 1997	A
5688810	Jones	Nov 1997	A
5693646	Jones	Dec 1997	A
5693647	Jones	Dec 1997	A
5696127	Jones	Dec 1997	A
5696130	Jones	Dec 1997	A
5696133	Jones	Dec 1997	A
5719136	Chwalisz	Feb 1998	A
5733902	Schneider	Mar 1998	A
5808139	Pathirana	Sep 1998	A
5874430	Christ	Feb 1999	A
6077840	Kurihara	Jun 2000	A
6306851	Santilli	Oct 2001	B1
6319912	Grubb	Nov 2001	B1
6329416	Grubb	Dec 2001	B1
6339098	Collins	Jan 2002	B1

Foreign Referenced Citations (37)

Number	Date	Country
3633861	Apr 1988	DE
4330234	Mar 1995	DE
4344463	Jun 1995	DE
022317	Jan 1981	EP
208510	Jan 1987	EP
311135	Apr 1989	EP
0 166 533	Apr 1990	EP
385850	Sep 1990	EP
483077	Sep 1991	EP
454330	Oct 1991	EP
535529	Sep 1992	EP
510235	Oct 1992	EP
947507	Oct 1999	EP
978279	Feb 2000	EP
63112584	May 1988	JP
WO8603749	Jul 1986	WO
WO9104974	Apr 1991	WO
WO9106545	May 1991	WO
WO9312085	Jun 1993	WO
WO9414434	Jul 1994	WO
WO9429272	Dec 1994	WO
WO9511013	Apr 1995	WO
WO9520389	Aug 1995	WO
WO9520972	Aug 1995	WO
WO9533746	Dec 1995	WO
WO9615794	May 1996	WO
WO9619458	Jun 1996	WO
WO9619997	Jul 1996	WO
WO9713767	Apr 1997	WO
WO9749407	Dec 1997	WO
WO9814436	Apr 1998	WO
WO9827059	Jun 1998	WO
WO9855116	Dec 1998	WO
WO9910325	Mar 1999	WO
WO9911264	Mar 1999	WO
WO9915500	Apr 1999	WO
WO9944608	Sep 1999	WO

Non-Patent Literature Citations (65)

Entry
Draetta, G. and Pagano, M. in “Annual Reports in Medicinal chemistry, vol. 31”, 1996, Academic Press, San Diego, p 241-246.*
R. Evans, “The Steroid and Thyroid Hormone Receptor Superfamily”, Science, 240:889 (May 13, 1988).
A. Ulmann et al, “Clinical Uses of Mifepristone (MFP)”, Ann. N.Y. Acad. Sci., 261:248 (Jun. 12, 1995).
R. Kekkonen et al, “Sequential Regiment of the Antiprogesterone RU486 and Synthetic Progestin for Contraception”, Fertility and Sterility, 60(4):610 (Oct. 1993).
K. Horwitz et al, “Progestin, Progesterone Receptors, and Breast Cancer”, Horm. Cancer, publisher: Birkhaeuser, Boston, Mass., ed. Vedeckis, pp. 283-306 (1996). (abstract only).
A. Murphy et al, “Regression of Uterine Leiomyomata in Response to the Antiprogesterone RU486”, J. Clin. Endo. Metab., 76(2):513 (Feb., 1993).
L. Kettel et al, “Endocrine Responses to Long-Term Administration of the Antiprogesterone RU486 in Patients with Pelvic Endometriosis”, Fertility and Sterility, 56(3):402 (Sep. 1991).
H. Michna et al, “Differentiation Therapy with Progesterone Antagonists”, Ann. N.Y. Acad. Sci., 761:224 (Jun., 1995).
L. Zhi et al, “5-Aryl-1,2-Dihydrochromeno[3,4-f]quinolines: A Novel Class of Nonsteroidal Human Progesterone Receptor Agonists”, J. Med. Chem., 41(3):291 (Oct. 22, 1998).
D. Combs et al, “Nonsteroidal Progesterone Receptor Ligands. 2. High-Affinity Ligands with Selectivity for Bone Cell Progesterone Receptors”, J. Med. Chem., 38:4880 (Dec. 8, 1995).
K. Perlman et al, “20-Oxopregnacalciferols: Vitamin D Compounds that Bind the Progesterone Receptor”, Tet. Letters, 35(15)2295 (1994).
L. Hamann et al, “Synthesis and Biological Activity of Novel Nonsteroidal Progesterone Receptor Antagonists”, Ann. N.Y. Acad. Sci., 761:383 (Jun. 12, 1995).
R. Chen et al, “Synthesis and SAR of a Novel Series of Spirobenzothlzaepine Derivatives with Antiprogestin Activity”, POI-37, 16th Int. Cong. Het. Chem., Montana (1997).
B. Narr et al, “Preparation, Testing, and Formulation of Imidazobenzoxazinones as Cardiotonics”, Chemical Abstracts, 109:22973 (1988).
R. Hartmann et al, “Effects of Brofoxine, A New Anxiolytic on Experimentally Induced Conflict in Rats”, Proc. West. Pharmacol. Soc., 21:51-55 (1978).
B. Singh et al, “Novel cAMP PDE III Inhibitor” Imidazo[4,5-b]pyridin-2(3H)-ones and Thiazolo[4,5-b]pyridin-2(3H)-ones and their Analogs, J. Med. Chem., 37:248 (Jan. 21, 1994).
A. Andreani et al, “Potential Antitumor Agents XVII (1). Cytotoxic Agents from Indole Derivatives and their Intermediates”, Acta, Pharm. Nord., 2(6):407 (1990).
Sakata et al, “Silver Halide Photographic Meterials Useful for Platemaking”, Chemical Abstracts, 123:301431 (1993).
P. Pflegel et al, “Polarografie con 7-Chlor-5-phenyl-2-thioxo-1H-2,3-dihydro-1,3,4-benzotriazepinen”, Pharmazie, 37(10):714-717 (1982).
E. Barengolts et al, “Progesterone Antagonist RU486 has Bone-Sparing Effects in Ovariectomized Rats”, Bone, 17(1):21 (Jul., 1995).
E. Gromachevskaya et al, “Studies of 4H-3, 1-Benzoxazines”, Chem. Heterocycl. Cmpds., 33(10):1209-1214 (1997).
D. Chiarino et al, “2,1-Benzisothiazoline 2,2-Dioxide and Derivatives”, J. Heterocycl. Chem., 23(6):1645-1649 (Nov.-Dec., 1986).
A. Turck et al, “On the Metabolism of 3-Substituted and 3,6-Disubstituted Pyridazines”, Tetrahedron, 49(3):599-606 (1993).
V. Kumar et al, “Synthesis of 7-Azaindole and 7-Azaoxindole Derivatives through a Palladium-Catalyzed Cross-Coupling Reaction”, J. Org. Chem., 57(25):6995-6998 (1992).
P. Canonne et al, “Spirocyclization of 1-(o-Aminophenyl)cycloalkanols and 1-(2'-Amino-3'-pyridinyl)cycloalkanols”, J Heterocyclic Chem., 26:113 (Jan.-Feb., 1989).
M-C Forest et al, “A Novel Class of Cardiotonic Agents: Synthesis and Biological Evaluation of 5-Substituted 3,6-Dihydrothiadiazin-2-ones with Cyclic AMP Phosphodiesterase Inhibiting and Myofibrillar Calcium Sensitizing Properties”, J. Med. Chem., 35:163-172 (Jan., 1992).
D. Combs et al, “Heteroatom Analogues of Bemoradan: Chemistry and Cardiotonic Activity of 1,4-Benzothiazinylpyridazinones”, J. Med. Chem., 35:172-176 (Jan., 1992).
Kurihari et al., “Synthesis of (±)-PF1092A, B, C; New Nonsteroidal Progesterone Receptor Ligands”, J. Antibiotics, 50(4):360 (Apr., 1997).
A. Kende et al., “Regioselective C-3 Alkylation of Oxindole Dianion”, Synth. Commun. 12(1):1 (1982).
T. Tucker et al., “Synthesis of a Series of 4-(Arylethylnyl)-6-Chloro-4-Cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as Novel Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors”, J. Med. Chem., 37:2347-2444 (Jul. 22, 1994).
J. Edwards et al., “5-Aryl-1,2-Dihydro-5H-Chromeno[3,4-f]Quinolines as Potent, Orally Active, Nonsteroidal Progesterone Receptor Agonists: The Effect of D-Ring Substituents”, J. Med. Chem., 41:303-310 (Jan. 29, 1998).
Derwent WPI abstract, “New Imidazo-Pyridine Derivatives—Useful as Platelet Agglutination Inhibitor, Antiallergic, Antiinflammatory Sedative, Cardiac, and Cardiovascular Vasodilators”, JP 63112584.
Derwent WPI abstract, N. Brumagniez et al., “Benzimidazole and Azabenzimidazole(s)—Having Cardiotonic, Vasodialating, Anti-Hypertensive, Anti-Aggregation, and Anti-Ulcer Activity”, EP 385850.
Derwent WPI abstract, F. Arndt et al., “New Heterocycle substituted Benzo-Fused Azine and Azole Derivatives—Useful as Selective Herbicides for Pre or Post-Emergence Application”, EP 311135.
K. Horwitz et al., “Progestin Progesterone Receptors, and Breast Cancer”, “Hormones and Cancer”, publisher: Birkhaeuser, Boston, Mass., ed. Vedeckis, p. 283-306 (1996).
V. Mamaev et al., “Synthesis of 4H-Thieno [3,2-B] Pyrrol-5(6H)-One” Bulletin of the Academy of Sciences on the USSR. Division of Chemical Science, US, Consultants Bureau, New York. vol. 9, p. 1549-1553, (1996).
Derwent WPI Abstract, K. Chwalisz et al. “Female Contraceptive Method Comprises Gestation Treatment with Intermittent Progesterone Antagonist Administration.”, DE 4,330,234.
Derwent WPI Abstract, K. Chwalisz et al. “Contraceptive Pack for Implantation Inhibition—Contains Competitive Progesterone Antagonist and Gestagen for Sequential Oral Administration.”, DE 4,344,463.
K. Kolasa et al., “Preliminary Pharmacological Studies of the Central Action of Phenyl and Piperidinomethyl Derivatives of 2-Benzoxazolone”, Chemical Abstracts, vol. 99, No. 1, Abts. No. 157a (Jul. 4, 1983).
N. Meanwell et al., “Regiospecific Functionalization of 1,3-dihydro-2H-Benzimidazol-2-One and Structurally Related Cyclic Urea Derivatives”, J. Organic Chem., 60(6):1565-82 (Mar. 24, 1995).
B. Singh et al., “An Efficient and Novel Synthesis of Fused Thiazol-2(3H)-ones” Heterocycles, 36(1);133-134, p. 136, compounds 16a, 18a (Jan. 1993).
G. Vernin et al., “Etude Dans 1a Serie des Radicaux Heterocycliques. Partie XV. Decomposition aprotique de 1′ amino-6-ethyl-2-benzothiazole dans des substrats aromatiques et heteroaromatiques: preparation des mesityl-6- et furyl-6-ethyl-2-benzothiazoles, des sels quaternaires et des spiropyrannes correspondants”, Helvetica Chimica Acta, 62(1/3):21-30 (Jan. 24, 1979).
P. Zhang et al, “Cyclocarbamate Derivatives as Progesterone Receptor Modulators”, U.S. patent application No. 09/552,633, filed Apr. 19, 2000.
A. Fensome et al, “Indoline Derivatives”, U.S. patent application No. 09/522,632, filed Apr. 19, 2000.
J. Ullrich et al, “3,3-Substituted Indoline Derivatives”, U.S. patent application No. 09/552,352, filed Apr. 19, 2000.
A. Fensome et al, “Thio-Oxindole Derivatives”, U.S. patent application No. 09/552,033, filed Apr. 19, 2000.
P. Zhang et al, “Cyclothiocarbamate Derivatives as Progesterone Receptor Modulators”, U.S. patent application No. 09/552,354, filed Apr. 19, 2000.
P. Zhang et al, “Benzimidazolones and Analogues”, U.S. patent application No. 09/552,546, filed Apr. 19, 2000.
P. Zhang et al, “Cyclic Urea and Cyclic Amide Derivatives”, U.S. patent application No. 09/552,356, filed Apr. 19, 2000.
M. Collins et al, “Cyanopyrroles”, U.S. patent application No. 09/552,544, filed Apr. 19, 2000.
G. Grubb et al, “Cyclic Regimens Using Quinazolinone and Benzoxazine Derivatives”, U.S. patent application No. 09/552,357, filed Apr. 19, 2000.
G. Grubb et al, “Cyclic Regimens Using Cyclic Urea and Cyclic Amide Derivatives”, U.S. patent application No. 09/552,037, filed Apr. 19, 2000.
G. Grubb et al, “Combination Regimens Using Progesterone Receptor Modulators”, U.S. patent application No. 09/552,350, filed Apr. 19, 2000.
G. Grubb et al, “Combination Therapies Using Benzimidazolones”, U.S. patent application No. 09/552,355, filed Apr. 19, 2000.
G. Grubb et al, “Cyclic Regimens Using Cyclocarbamate and Cyclic Amide Derivatives”, U.S. patent application No. 09/552,545, filed Apr. 19, 2000.
G. Grubb et al, “Cyclic Regimens Utilizing Indoline Derivatives”, U.S. patent application No. 09/552,358, filed Apr. 19, 2000.
L. Zhi et al, “Tetracyclic Receptor Modulator Compounds and Methods”, U.S. patent application No. 09/552,353, filed Apr. 19, 2000.
A. Fensome et al, “Thio-Oxindole Derivatives”, U.S. patent application No. 10/022,467, filed Oct. 30, 2001 (division of (CZ) cited above).
A. Santilli et al, “Cyclocarbamate and Cyclic Amide Derivatives”, U.S. patent application No. 09/906,875, filed Jul. 17, 2001 (division of (BH) cited above).
A. Fensome et al, “Indoline Derivatives”, U.S. patent application No. 10/014,173, filed Dec. 11, 2001 (division of (CX) cited above).
P. Zhang et al, “Cyclic Urea and Cyclic Amide Derivatives”, U.S. patent application No. 10/050,287, filed Jan. 16, 2002 (division of (CCT) cited above).
M. Collins et al, “Cyanopyrroles”, U.S. patent application No. 10/043,513, filed Jan. 9, 2002 (division of (CCU) cited above).
G. Grubb et al, “Combination Regimens Using 3,3-Substituted Idoline Derivatives”, U.S. patent application No. 09/977,790, filed Oct. 15, 2001.
P. Zhang et al, “Benzimidazolones and Analogues”, U.S. patent application filed Feb. 12, 2002 (division of (CCS) cited above).
G. Grubb et al, “Combination Therapies Using Benzimidazolones”, U.S. patent application filed Mar. 1, 2002 (division of (CCY) cited above).

Provisional Applications (1)

	Number	Date	Country
	60/219339	May 1999	US

1,2,3,4-tetrahydro-2-thioxo-quinolinyl and 1,2,3,4-tetrahydro-2-oxo-quinolinyl derivatives as progesterone receptor modulators

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications