AU711936B2 - Stereoselective deoxygenation reaction - Google Patents

Description

WO 98/06700 PCT/US97/14045 -1- TITLE OF THE INVENTION STEREOSELECTIVE DEOXYGENATION REACTION BACKGROUND OF THE INVENTION The present invention relates to novel key intermediates in the synthesis of an endothelin antagonist and the method for preparing these key intermediates of formula I.

Two endothelin receptor subtypes ETA and ETB are known so far. The compounds of the present invention possess high affinity to at least one of two receptor subtypes, responsible for the dilation of smooth muscle, such as blood vessels or in the trachea. The endothelin antagonist compounds of the present invention provide a new therapeutic potential, particularly for the treatment of hypertension, pulmonary hypertension, Raynaud's disease, acute renal failure, myocardial infarction, angina pectoris, cerebral infarction, cerebral vasospasm, arteriosclerosis, asthma, gastric ulcer, diabetes, restenosis, prostatauxe endotoxin shock, endotoxin-induced multiple organ failure or disseminated intravascular coagulation, and/or cyclosporin-induced renal failure or hypertension.

Endothelin is a polypeptide composed of amino acids, and it is produced by vascular endothelial cells of human or pig. Endothelin has a potent vasoconstrictor effect and a sustained and potent pressor action (Nature, 332, 411-415 (1988)).

Three endothelin isopeptides (endothelin-1, endothelin-2 and endothelin-3), which resemble one another in structure, exist in the bodies of animals including human, and these peptides have vasoconstriction and pressor effects (Proc. Natl. Acad, Sci, USA, 86, 2863-2867 (1989)).

As reported, the endothelin levels are clearly elevated in the blood of patients with essential hypertension, acute myocardial infarction, pulmonary hypertension, Raynaud's disease, diabetes or atherosclerosis, or in the washing fluids of the respiratory tract or the blood of patients with asthmaticus as compared with normal levels (Japan, J. Hypertension, 12, 79, (1989), J. Vascular medicine Biology, WO 98/06700 PCT/US97/14045 -2- 2, 207 (1990), Diabetologia, 33, 306-310 (1990), J. Am. Med.

Association, 264, 2868 (1990), and The Lancet, ii, 747-748 (1989) and ii, 1144-1147 (1990)).

Further, an increased sensitivity of the cerebral blood vessel to endothelin in an experimental model of cerebral vasospasm (Japan. Soc. Cereb. Blood Flow Metabol., 1, 73 (1989)), an improved renal function by the endothelin antibody in an acute renal failure model Clin, invest., 83, 1762-1767 (1989), and inhibition of gastric ulcer development with an endothelin antibody in a gastric ulcer model (Extract of Japanese Society of Experimental Gastric Ulcer, (1991)) have been reported. Therefore, endothelin is assumed to be one of the mediators causing acute renal failure or cerebral vasospasm following subarachnoid hemorrhage.

Further, endothelin is secreted not only by endothelial cells but also by tracheal epithelial cells or by kidney cells (FEBS Letters, 255, 129-132 (1989), and FEBS Letters, 249, 42-46 (1989)).

Endothelin was also found to control the release of physiologically active endogenous substances such as renin, atrial natriuretic peptide, endothelium-derived relaxing factor (EDRF), thromboxane A2, prostacyclin, noradrenaline, angiotensin II and substance P (Biochem. Biophys, Res. Commun., 157, 1164-1168 (1988); Biochem. Biophys, Res. Commun., 155, 20 167-172 (1989); Proc. Natl. Acad. Sci. USA, 85 1 9797-9800 (1989); J. Cardiovasc.

Pharmacol., 13, S89-S92 (1989); Japan. J. Hypertension, 12, 76 (1989) and Neuroscience Letters, 102, 179-184 (1989)). Further, endothelin causes contraction of the smooth muscle of gastrointestinal tract and the uterine smooth muscle (FEBS Letters, 247, 337-340 (1989); Eur. J.

Pharmacol., 154, 227-228 (1988); and Biochem. Biophys Res.

Commun., 159, 317-323 (1989)). Further, endothelin was found to promote proliferation of rat vascular smooth muscle cells, suggesting a possible relevance to the arterial hypertrophy (Atherosclerosis, 78, 225- 228 (1989)). Furthermore, since the endothelin receptors are present in a high density not only in the peripheral tissues but also in the central nervous system, and the cerebral administration of endothelin induces a WO 98/06700 PCT/US97/14045 -3behavioral change in animals, endothelin is likely to play an important role for controlling nervous functions (Neuroscience Letters, 97, 276- 279 (1989)). Particularly, endothelin is suggested to be one of mediators for pain (Life Sciences, 49, PL61-PL65 (1991)).

Internal hyperplastic response was induced by rat carotid artery balloon endothelial denudation. Endothelin causes a significant worsening of the internal hyperplasia Cardiovasc. Pharmacol., 22 355 359 371 373(1993)). These data support a role of endothelin in the phathogenesis of vascular restenosis. Recently, it has been reported that both ETA and ETB receptors exist in the human prostate and endothelin produces a potent contraction of it. These results suggest the possibility that endothelin is involved in the pathophysiology of benign prostatic hyperplasia Urology, 151, 763 766(1994), Molecular Pharmocol., 45, 306 311(1994)).

On the other hand, endotoxin is one of potential candidates to promote the release of endothelin. Remarkable elevation of the endothelin levels in the blood or in the culture supernatant of endothelial cells was observed when endotoxin was exogenously administered to animals or added to the culture endothelial cells, respectively. These findings suggest that endothelin is an important mediator for endotoxininduced diseases (Biochem. Biophys. Commun., 161, 1220-1227 (1989); and Acta Physiol. Scand., 137, 317-318 (1989)).

Further, it was reported that cyclosporin remarkably increased endothelin secretion in the renal cell culture (LLC-PKL cells) (Eur. J. Pharmacol., 180, 191-192 (1990)). Further, dosing of cyclosporin to rats reduced the glomerular filtration rate and increased the blood pressure in association with a remarkable increase in the circulating endothelin level. This cyclosporin-induced renal failure can be suppressed by the administration of endothelin antibody (Kidney Int., 37, 1487-1491 (1990)). Thus, it is assumed that endothelin is significantly involved in the pathogenesis of the cyclosporin-induced diseases.

WO 98/06700 PCT/US97/14045 -4- Such various effects of endothelin are caused by the binding of endothelin to endothelin receptors widely distributed in many tissues (Am. J. Physiol., 256, R856-R866 (1989)).

It is known that vasoconstriction by the endothelins is caused via at least two subtypes of endothelin receptors Cardiovasc.

Pharmacol., 17(Suppl.7), S119-SI21 (1991)). One of the endothelin receptors is ETA receptor Selective to ET-1 rather than ET-3, and the other is ETB receptor equally active to ET-1 and ET-3. These receptor proteins are reported to be different from each other (Nature, 348, 730- 735 (1990)).

These two subtypes of endothelin receptors are differently distributed in tissues. It is known that the ETA receptor is present mainly in cardiovascular tissues, whereas the ETB receptor is widely distributed in various tissues such as brain, kidney, lung, heart and vascular tissues.

Substances which specifically inhibit the binding of endothelin to the endothelin receptors are believed to antagonize various pharmacological activities of endothelin and to be useful as a drug in a wide field. Since the action of the endothelins is caused via not only the ETA receptor but also the ETB receptor, novel non-peptidic substances with ET receptor antagonistic activity to either receptor subtype are desired to block activities of the endothelins effectively in various diseases.

Endothelin is an endogenous substance which directly or indirectly (by controlling liberation of various endogenous substances) induces sustained contraction or relaxation of vascular or non-vascular smooth muscles, and its excess production or excess secretion is believed to be one of pathogeneses for hypertension, pulmonary hypertension, Raynaud's disease, bronchial asthma, gastric ulcer, diabetes, arteriosclerosis, restenosis, acute renal failure, myocardial infarction, angina pectoris, cerebral vasospasm and cerebral infarction. Further, it is suggested that endothelin serves as an important mediator involved in diseases such as restenosis, prostatauxe, endotoxin shock, endotoxininduced multiple organ failure or disseminated intravascular WO 98/06700 PCT/US97/14045 coagulation, and cyclosporin-induced renal failure or hypertension.

Two endothelin receptors ETA and ETB are known so far. An antagonistic agent against the ETB receptor as well as the ETA receptor is useful as a drug. In the field of anti-endothelin agents, some nonpeptidic compounds possessing antagonistic activity against endothelin receptors were already disclosed in patents (for example, EP 0526708 Al, WO 93/08799 Al). Accordingly, it is an object of the present invention to provide a novel therapeutics for the treatment of the abovementioned various diseases by an invention of a novel and potent nonpeptidic antagonist against either ETA or ETB receptor.

In order to accomplish the above object, the present inventors have developed an aldol reaction which enables them to prepare the compound of Formula I,

R

3 b

OH

A

COR

2

R

1 and use this key intermediate in a stereoselective deoxygenation reaction, also developed by the inventors, to prepare endothelin antagonists of the following structure:

R

3 b

R

2 A I

R'

wherein

A

represents: 5- or 6-membered heterocyclyl, 5- or 6membered carbocyclyl, and aryl; WO 98/06700 PCT/US97/14045 -6-

R

3 b is aryl, or heteroaryl;

R

1 is C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, aryl, or heteroaryl;

R

2 is OR 4 and N(R 5 )2;

R

4 is C1-C8 alkyl; and

R

5 is: H, C1-C8 alkyl, or aryl.

SUMMARY OF THE INVENTION This invention relates to a key intermediate in the synthesis of an endothelin antagonist, the synthesis of this key intermediate and the synthesis of an endothelin antagonist using this intermediate in a stereoselective deoxygenation reaction.

The instant invention relates to a compound of formula I:

R

3 b

OH

A I COR 2

R

1 wherein Aj represents: a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 or 3 heteroatoms selected from O, N and S, the heterocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 WO 98/06700 PCT/US97/14045 -7alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, CI-C8 alkyl, C2-C alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, c) aryl, wherein aryl is as defined below, C1-C8 alkoxy, C -C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3,

N(R

5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 and when two substituents are located on adjacent carbons they can join to form a 5- or 6membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, C02R 6 Br, Cl, F, I, CF3, N(R 7 )2, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0 to WO 98/06700 PCT/US97/14045 -8-

R

1 is: a) C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from O, N and S which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2,

R

2 is OR 4 or N(R 5 )2;

R

3 a is: a) -CO-C1-C8 alkyl, b) -CO-aryl, or c) -CO-heteroaryl;

R

3 b is: a) C1-C8 alkyl, b) aryl, or c) heteroaryl;

R

4 is CI-C8 alkyl; and

R

5 is: H, C1-C8 alkyl, or aryl.

Also within the scope of the instant invention is a process for the preparation of a compound of formula I: WO 98/06700 PCT/US97/14045 wherein the substituents are as defined above comprising reacting a R3a R2

A

O

R

1 in the presence of a strong base and an aprotic solvent at a temperature range of -78 0 C to about Also within the scope of the instant invention is a process for the preparation of a compound of formula II: R3b R 2

A

O

R

1

II

wherein the substituents are as defined above, comprising reacting a compound of formula I

R

3 b

COH

A I VCOR 2 WO 98/06700 PCT/US97/14045 with a reducing agent and an acid in a solvent at a temperature range of about -78 0 C to about 100°C.

DETAILED DESCRIPTION OF THE INVENTION The instant invention relates to a compound of formula I:

R

3 b

OH

A

COR

2

R

1 wherein

A

represents: a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 or 3 heteroatoms selected from O, N and S, the heterocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, c) aryl, wherein aryl is as defined below, WO 98/06700 PCT/US97/14045 11 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3,

N(R

5 C1-C8 alkoxy, Cl-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 and when two substituents are located on adjacent carbons they can join to form a 5- or 6membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, C02R 6 Br, Cl, F, I, CF3, N(R 7 )2, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0 to

R

1 is: a) C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from O, N and S which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 WO 98/06700 PCT/US97/14045 12alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2,

R

2 is OR 4 or N(R 5 )2;

R

3 b is: a) C1-C8 alkyl, b) aryl, or c) heteroaryl;

R

4 is C1-C8 alkyl; and

R

5 is: H, C1-C8 alkyl, or aryl.

An embodiment of the invention is a process for the preparation of a compound of formula I:

R

3 b

-COR

2 wherein represents: a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 4 3 heteroatoms selected from O, N and S, the heterocyclyl i unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 WO 98/06700 PCT/US97/14045 13 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, c) aryl, wherein aryl is as defined below, C1-C8 alkoxy, C1-C8 alkyl, C2-C alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3,

N(R

5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 and when two substituents are located on adjacent carbons they can join to form a 5- or 6membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, C02R 6 Br, Cl, F, I, CF3, N(R 7 )2, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0 to -1 1 WO 98/06700 WO 9806700PCTIUS97/14045 14 RI is: a) CI-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from 0, N and S which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, 1, CF3, N(R 5 C1-C8 alkoxy, Cl-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2,

R

2 is OR 4 or N(R 5 )2;

R

3 a is: a) -CO-CI-C8 alkyl, b) -CO-aryl, or c) -CO-heteroaryl;

R

3 b is: a) C1-C8 alkyl, b) aryl, or c) heteroaryl;

R

4 is Cl-C8 alkyl; and

R

5 is: H, C1-C8 alkyl, or aryl, comprising reacting a

//R

3 W R 2 WO 98/06700 PCT/US97/14045 in the presence of a strong base and an aprotic solvent at a temperature range of -78 0 C to about The process as recited above, wherein the strong base is selected from the group consisting of: LDA, LiHMDS, KHMDS, NaHMDS, KOtBu, and sodium t-amylate, in about 2 to about 6 equivalents; the aprotic solvent is selected from the group consisting of tetrahydrofuran, diethyl ether, MTBE (methyl t-butyl ether), benzene, toluene, pentane, hexane, dioxane and a mixture of said solvents; and the temperature range is about -78 0 C to about 25°C, and preferably about -50°C to about 25 0

C.

The process conditions for the process recited above are wherein the strong base is LiHMDS, KHMDS, or NaHMDS, preferably in about 3 to about 4 equivalents, the aprotic solvent is tetrahydrofuran and the temperature range is preferably about 0°C to about A second embodiment of the invention is a process for the preparation of a compound of formula II:

R

3 b

R

2

A

R

1

II

wherein Al represents: a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 or 3 heteroatoms selected from O, N and S, the heterocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 WO 98/06700 PCT/US97/14045 16alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, c) aryl, wherein aryl is as defined below, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3,

N(R

5 Cl-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 and when two substituents are located on adjacent carbons they can join to form a 5- or 6membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, C02R 6 Br, Cl, F, I, CF3, N(R 7 )2, C1-C8 alkoxy, Cl-C8 alkyl, C2-CS alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2,

R

1 is: WO 98/06700 PCT/US97/14045 17a) C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from O, N and S which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0to

R

2 is OR 4 or N(R 5 )2;

R

3 b is: a) C1-C8 alkyl, b) aryl, or c) heteroaryl;

R

4 is C1-C8 alkyl; and

R

5 is: H, C1-C8 alkyl, or aryl, comprising reacting a compound of formula I WO 98/06700 PCT/US97/14045 -18with a reducing agent and optionally an acid in a solvent at a temperature range of about -78°C to about 100 0

C.

The process as recited above, wherein the reducing agent is selected from the group consisting of: a hydride, a borane, C5-C6 cycloalkene with a transition metal catalyst and H2 with a transition metal catalyst. The reducing agents useful in this process in about 2 to about 20 equivalents and preferably about 2 to about 5 equivalents are: hydrides, such as R3SiH, R2SiH2, wherein R is C1-C8 alkyl or aryl, and NaBH4, boranes, such as BH3*NHMe2, BH3*SMe2, BH3*pyridine, and BH3-THF, C5-C6 cycloalkene with a transition metal catalyst, such as cyclohexene or cyclohexadiene with Pd/C, Pt-C, Rh/Al and Raney Ni, H2 with a transition metal catalyst, such as Pd-C, Pt-C, Rh/Al and Raney Ni, or SmI2.

The process as recited above, wherein the acid is a Lewis acid, when the reducing agent is a hydride, a borane or C5-C6 cycloalkene with a transition metal catalyst, a protic acid, when the reducing agent is H2 with a transition metal catalyst, or no acid, when the reducing agent is SmI2. The Lewis acids in about 2 to about equivalents, such as TiCl4, BF3, BC13, SnC14, A1C13, and TiCl2(OiPr)2 are useful in this process. Protic acids, such as trifluoroacetic acid, HC1, and H2S04 are useful in this process.

The process as recited above, wherein the solvent is an aprotic solvent, when the acid is a Lewis acid and the reducing agent is a hydride, a borane or C5-C6 cycloalkene with a transition metal catalyst, a protic solvent, when the acid is a protic acid and the reducing agent is H2 with a transition metal catalyst, or a solvent system consisting of an aprotic solvent and a protic solvent when the reducing agent is Sml2.

Aprotic solvents such as tetrahydrofuran, diethyl ether, MTBE (methyl t-butyl ether), dioxane, CH2C12, CHC13, nitromethane, toluene, and dichlorobenzene, and protic solvents such as ethanol, methanol or isopropanol, are solvents within the scope of the invention.

The process as recited above, wherein temperature range is about -78 0 C to about 20 0 C and preferably about -20 0 C to about when the acid is a Lewis acid and the reducing agent is a hydride or a WO 98/06700 PCT/US97/14045 19borane, about 0°C to about 100 0 C and preferably about 0°C to about when the acid is a Lewis acid or a protic acid and the reducing agent is a C5-C6 cycloalkene with a transition metal catalyst or H2 with a transition metal catalyst, or about 0°C to about 30'C, when the reducing agent is SmI2.

The preferred conditions for the process recited above are wherein the hydride is R3SiH, the Lewis acid is TiC14, the aprotic solvent is nitromethane and the temperature range is about -5°C to about The process as recited above for the preparation of a compound of formula: 0 OHOBu Bu N O

OTBS

OMe comprising reacting a ketone of formula: WO 98/06700 PCTIUS97/14045 20 0 o 'o N COBu -rOTBS Me OMe in tetrahydrofuran with about 3 to about 5 equivalents of lithium bis(trimethylsilyl)amide at about -50°C to about The process as recited above, for the preparation of the compound of formula:

O

OMe comprising reacting the tertiary alcohol WO 98/06700 PTU9/44 PCTfUS97/14045 21 0 OHOBu Bu N 0

OTBS

Me OMe in nitromethane with Et3SiH and TiC14 at about -5'C to about The process as recited above, for the preparation of the compound of formula: 0 OiPr Bu N 0 OBn OMe comprising reacting the tertiary alcohol WO 98/06700 PCTIUS97/14045 -22- 0 OH OH OiPr

I--

Bu N 0 -OBn OMe in a solution of isopropyl alcohol and tetrahydrofuran with SmI2 at about 10° The process as recited above, for the preparation of the compound of formula: Bu OiPr

-H

Bu N 0 0

OH

comprising reacting the tertiary alcohol WO 98/06700 PCT/US97/1404S -23 0 OiPr Bu N OHO 0

OH

OMe in a solution of isopropyl alcohol and tetrahydrofuran with Sml2 at about 10° 30 0

C.

It is further understood that the substituents recited above would include the definitions recited below.

The alkyl substituents recited above denote straight and branched chain hydrocarbons of the length specified such as methyl, ethyl, isopropyl, isobutyl, tert-butyl, neopentyl, isopentyl, etc.

The alkenyl-substituents denote alkyl groups as described above which are modified so that each contains a carbon to carbon double bond such as vinyl, allyl and 2-butenyl.

The alkynyl-substituents denote alkyl groups as described above which are modified so that each contains a carbon to carbon triple bond such as ethynyl,and propynyl.

Cycloalkyl denotes rings composed of 3 to 8 methylene groups, each of which may be substituted or unsubstituted with other hydrocarbon substituents, and include for example cyclopropyl, cyclopentyl, cyclohexyl and 4-methylcyclohexyl.

The alkoxy substituent represents an alkyl group as described above attached through an oxygen bridge.

Additionally, it is understood that the terms alkyl, alkenyl, akynyl, cycloalkyl and alkoxy can be substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, WO 98/06700 WO 9806700PCTJUS9714045 24 F, 1, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2.

The heteroaryl substituent represents an carbazolyl, furanyl, thienyl, pyrrolyl, isothiazolyl, imidazolyl, isoxazolyl, thiazolyl, oxazolyl, pyrazolyl, pyrazinyl, pyridyl, pyrimidyl, purinyl.

The heterocyclyl substituent represents a pyridyl, pyrimidyl, thienyl, furanyl, oxazolidinyl, oxazolyl, thiazolyl, isothiazolyl, pyrazolyl, triazolyl, imidazolyl, imidazoldinyl, thiazolidilnyl, isoxazolyl, oxadiazolyl, thiadiazolyl, morpholinyl, piperidinyl, piperazinyl, pyrrolyl, or pyrrolidinyl.

The a,fp-unsaturated ester or amide 2 R 3 A

I

0 can generally be prepared in two steps: 1) a coupling reaction at the one position of Ring A 2 R 3 a A z 1 z0 wherein Z is a leaving such as Br, Cl, 1, OTriflyl, OTosyl or OMesyl and R 2 is OR 4 or N(R 5 and 2) the conversion of the aldehyde (R 3 a= CHO) to the desired

R

6 chiral auxiliary wherein R 3 represents V\ R9 X and Y are independently: 0, S, or NR 5

R

4 is ClI-C8 alkyl; R 5 is: H, Ci-C8 alkyl, or aryl; and R 6

R

7

R

8 and WO 98/06700 PCT/US97/14045 R9 are independently: H, Cl-C8 alkyl, and aryl, such that either R 6 and R 7 are not the same and/or R 8 and R 9 are not the same, or R 6 and R 8 or R 7 and R 9 can join to form a or 6-membered ring, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1- C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 )2.

Commercially available pyridone 1 is alkylated via its dianion with propyl bromide, and the product is then converted into the bromopyridine 3a using a brominating agent such as PBr3. The nitrile 3a is then reduced to the aldehyde 3 using diisobutyl aluminum hydride (DIBAL). The aldehyde then undergoes a Heck reaction with t-butyl acrylate using NaOAc, (allyl)2PdCl2, tri-o-tolylphosphine, toluene, reflux to provide the unsaturated ester 4a in high yield. The unsaturated ester 4a is then reacted with a chiral auxiliary to give the acceptor 5a. Examples of chiral auxiliaries useful in this method are the enantiomers of pseudoephedrine, ephedrine, 1N,2N-dimethyldiaminocyclohexane, diphenylprolinol, N-methylaminoindanol, and 1N,2N-diethyldiaminocyclohexane.

WO 98/06700 WO 9806700PCTIUS97/14045 26 SCHEME 1

~CN

Me' N0

H

CN

C

3

H

7 Br Bu"(Nl0

H

PBr 3 'CN

CHO

DIBAL IH 2 Oz-CHC0 2

BU

t Bu Br BuN" Br 6 R 7 I" OBut hiral Buf)- N auxiliary 4a 0 5a 0 Commericially available acid 10 is reduced with BH3-SMe2, to the alcohol 11, which is then converted into the bromidel3, via the mesylate 12 using mesyl chloride, triethylamine followed by the addition of NaBr and dimethyl acetamide (DMAC).

WO 98/06700 PCT/US97/14045 -27- SCHEME 2

OH

OMe OMe OMs OMe OMe Commercial available 1,2-amino indanol is acylated (propionyl choride, K2C03) to give amide 8, which is then converted into the acetonide 9 (2-methoxypropene, pyridinium p-toluene-sulfonate (PPTS)). Acetonide 9 is then alkylated with the bromide 13, (LiHMDS) to give 14, which is then hydrolyzed MeOH) to give a mixture of acid and methyl ester 15. Reduction (LAH) of the ester/acid mixture provided the alcohol 16 in high yield and optical purity. Protection of the alcohol 16 (TBSC1, imidazole) provided bromide 17, the precursor to organolithium 17a.

WO 98/06700 WO 9806700PCT/TJS97/14045 28 SCHEME 3 0=

NH

2 NH CCOH

OH

0= 13, LiHMDS THF, MeOH OH/Me Br LAH -sOH OMe OMe 99.5 %ee

'OTBS

OMe 17 bMe 17a Organolithium reagent 17a was reacted with the acceptor (-78 0 C to -50 0 Workup (acetic acid-THF-water) to remove the

M

WO 98/06700 PCT/US97/14045 -29chiral auxiliary affords aldehyde 6a in high yield and good selectivity (Scheme 4).

SCHEME 4

R

6

R

7

H

X R 8

O

S Y 1)17a OBut NBu N Bu N OBut 2) H Bu 0

OTBS

OMe 6a Attempts were made to close the five membered ring via intramolecular alkylation chemistry (Scheme Thus the aldehyde 6a was converted into a 1:1 mixture of chlorides 25 (Grignard addition, then MsC1) which were then reacted with LDA (-78 0 C) to give cleanly a 60:40 mixture of 21c and 21a.

WO 98/06700 PCTIUS97/14045 30 SCHEME .OBu t

OTBS

OMe

OTBS

OTBS

OBu t

OTBS

21 c OMe 21a The low stereoselectivity of this alkylation reaction prompted us to develop an alternative ring closure strategy, involving an aldol and stereoselective de-oxygenation sequence (Scheme 6 and Scheme The aldehyde 6a was converted into the keto ester 19 in two steps involving Grignard addition to give the alcohol 18, followed by oxidation with TPAP. Finally, transesterification of the t-butyl ester (n-BuOH, Ti(OBu)4) provides the n-butyl ester 19 quantitatively (Scheme 6).

WO 98/06700 PCTIUS97/14045 -31 SCHEME 6 BrMg- BrMg OMe 6a [ox] 2) BuOH .OBu

OTBS

OMe 19 19 undergoes an aldol reaction (LiHMDS, THF, 25°C) to provide two tertiary alcohols 20 which were de-oxygenated cleanly to give the desired heterocycle 21 in excellent yield (75% for three steps). The selectivity in this reaction was estimated by 1 H NMR to be >90% de (Scheme The de-oxygenation step can be carried out using a reducing agent including but not limited to trialkylsilyl hydride or samarian iodide, using an acid with the hydride reducing agent. This I WO 98/06700 PCT/US97/14045 -32aldol reaction and de-oxygenation sequence can be carried out with a variety of ketones, such as -COaryl and -COheteraryl.

SCHEME 7

O\

0O aldol rxn

OTBS

OMe 19 OMe i

OH

OMe 21 Oxidation of the side chain hydroxyl 21 to the carboxylic acid 22 was effected using standard conditions (cat RuCl3-NalO4, CH3CN, or two steps involving i) Sulfur trioxide pyridine complex- WO 98/06700 PCTIUS97/14045 -33 dimethyl sulfoxide, ii) sodium chlorite-tert butanol). Subsequent hydrolysis (NaOH-MeOH) of 22 provided the target compound 23 cleanly. The 1 H and 13 C NMR spectrum of this material was identical with that of the authentic target compound (Scheme 8).

SCHEME 8 OMe 21 OMe

OH

Scheme 9 describes the preparation of the isopropyl ester analog of compound 23 described in Scheme 8. Unsaturated oxazoline 25 was prepared via the Horner-Emmons reaction of phosphonate 24 with the bromopyridine aldehyde 3. Conjugate addition of the lithium anion of 4-bromo-1,2-(methylenedioxy)benzene to 25 produced the desired adduct 26 with in high diastereomeric excess.

WO 98/06700 PCT/US97/14045 -34- Hydrolysis of oxazoline 26 was accomplished by refluxing in isopropyl alcohol with concentrated sulfuric acid to yield the isopropyl ester (not shown in scheme).

Subsequent carbonylation of the isopropyl ester using catalytic palladium in methanol produced diester 27. Inverse addition of the lithium anion of 17 to methyl ester 27 at 78° C generated the desired ketoester 28. Compound 28 was then treated with aqueous HF to remove the silyl protecting group. The deprotected alcohol was then cyclized with sodium t-amylate to form the aldol adduct 29. Finally, aldol adduct 29 was oxidized to the carboxylic acid, and then stereoselectively deoxygenated by the action of SmI 2 to produce 30 as a single diastereomer.

WO 98/06700 WO 9806700PCTIUJS97/14045 35 SCHEME 9 OMe (EtO) 2 P' 0 24 1. nBuLi 2.

CHO

BuN- Br 3 -OMe Ila /SMe -OMe Se

I~

Br::

O

nBuLi, THF 1. H 2 S0 4

IPA

2. Pd(OAc) 2

DPPF,

NaHCO 3 MeOH OiPr OMe 17 nBuLi, THE WO 98/06700 WO 9806700PCTIUS97/14045 36 SCHEME 9 (continued) 1. HF, AcON 2. NaOt-C 5

H

12

THF

OTBS

OMe 28 or l.iOx] 2. SMI 2

THE

'OH

0 WO 98/06700 PCT/US97/14045 37- The instant invention can be understood further by the following examples, which do not constitute a limitation of the invention. Note that the reference numbers utilized in the examples below do not necessarily correspond with the reference numbers utilized in the Schemes.

EXAMPLE 1 X CN Me N O

H

1 Preparation of 1 Compound 1 is a commericially available starting material, for example, see Aldrich Chemical Company, Milwaukee, WI, USA 53201.

EXAMPLE 2 C N CN Me N O Bu N 0 H

H

1 2 Preparation of 2 Diisopropyl amine (MW 101.19, d 0.772, 2.1 equ, 20.54 mL) in 200 mL THF. Cool to -50 0 C and add n-BuLi (1.6 M in hexanes, 2.05 equ, 96 mL), allowing solution to warm to -20°C. Age 0-3 0 C for min, then cool to -30 0 C and add 1 (MW 134.14, 75 mmol, 10.0 g).

Age 0°C to 43 0 C for 2 h. Cool to -50 0 C and add bromopropane (MW 123.00, d 1.354, 1.0 equ, 6.8 mL). Warm to 25 0 C over 30 min, and age WO 98/06700 PCT/US97/14045 38min. Add NH4C1 and CH2C12. Dry organic (magnesium sulfate) then evaporate in vacuo to afford 61% of 2.

EXAMPLE 3 S CN

CHO

Bu N 0 Bu N Br

H

2 3 Preparation of 3 Mix 2 (MW 176.22, 46 mmol) and PBr3 (MW 270.70, d 2.880, 2.5 equ, 10.8 mL) and age at 160 0 C. After 2 h, cool to 25 0 C and add some CH2C12. Slowly quench by adding water. Separate layers and wash aqueous two times with CH2C12. Combine organic layers and dry (magnesium sulfate). Concentrate and isolate solid by silica gel chromatography (90:10 hexanes:ethyl acetate) in 60% yield (MW 239.12, 6.60 g).

Dissolve product of bromination reaction (MW 239.12, 27.6 mmol, 6.60 g) in 66 mL toluene and cool to -42 0 C. Slowly add DIBAL (1.5 M in toluene, 2 equ, 37 mL) and age 1 h at -42 0 C. Add HC1 (2 N, 10 equ, 134 mL) and stir vigorously for 30 min. Dilute with ethyl acetate, separate layers, and wash aqueous with ethyl acetate.

Combine organic layers, dry (magnesium sulfate), and concentrate in vacuo to afford 90% (MW 242.11, 6.01 g) of 3.

WO 98/06700 PCT/US97/14045 -39- EXAMPLE 4a uCHO CHO Br B"Nu Bu N Br Bu N 3 4a O Preparation of 4a Dissolve 3 (MW 242.11, 24.8 mmol, 6.01 g) in 75 mL toluene. Add sodium acetate (MW 82, 3 equ, 6.13 t-butyl acrylate (MW 128.17, d 0.875, 2.5 equ, 9.08 mL), P(o-tolyl)3 (MW 304.38, mol 755 mg) and allyl palladium chloride dimer (MW 365.85, 5 mol 455 mg). Age at reflux for 24 h. Cool, filter and evaporate in vacuo. Isolate 4a (MW 289.37) by silica gel chromatography (92:8 hexanes:ethyl acetate) in 80% yield (5.74 g).

EXAMPLE 4b CHO CHO SBrr N(Me) 2 Bu N'Br Bu N

N

3 4b Preparation of 4b Dissolve 3 (MW 242.11, 24.8 mmol, 6.01 g) in 75 mL toluene. Add sodium acetate (MW 82, 3 equ, 6.13 g), dimethylacrylamide (MW 99.13, d 0.962, 1 equ, 2.55 mL), PPh3 (MW 262.29, 10 mol 653 mg) and allyl palladium chloride dimer (MW 365.85, 5 mol 455 mg). Age at 140 0 C in sealed tube for 24 h. Cool, filter and evaporate in vacuo. Isolate 4b (MW 260.34) by silica gel chromatography (80:20 hexanes:ethyl acetate) in 70% yield (4.52 g).

1 WO 98/06700 PCT/US97/14045 40 EXAMPLE

.CHO

0 O'Bu- Bu N O4a 4a

M

e j

N.

Me O'Bu Bu N 0

O

5a Preparation of Dissolve 4a (MW 289.37, 19.8 mmol, 5.74 g) in 53 mL CH2C12. Add (1R,2R)-N,N-dimethylcyclohexanediamine (MW 142.24, 1 equ, 2.83 g) and sieves (powdered, 1 wt equ, 5.74 g) and age 25 0 C for 8 h. Filter and concentrate filtrate in vacuo to afford 5a (MW 413.60, 8.19 g) in quantitative yield.

EXAMPLE

.CHO

N'N

I M N(Me), Bu Me BuN--N

N(

.N(Me) 2 0 4b Preparation of Dissolve 4b (MW 260.34, 17.4 mmol, 4.53 g) in 40 mL CH2C12. Add (1R,2R)-N,N-dimethylcyclohexanediamine (MW 142.24, 1 equ, 2.47 g) and sieves (powdered, 1 wt equ, 4.53 g) and age 25 0 C for 8 h. Filter and concentrate filtrate in vacuo to afford 5b (MW 384.57, 6.69 g) in quantitative yield.

WO 98/06700 PCTJUS97/14045 -41 EXAMPLE Me N" ,,ph S CHO 0 B O'Bu dB OtBu Bu N Bu N O O 4a Preparation of Dissolve 4a (MW 289.37, 19.8 mmol, 5.74 g) in 53 mL toluene. Add (S,S)-pseudoephedrine (MW 165.24, 1.1 equ, 3.60 g) and 4 drops of concentrated HC1. Reflux with a Dean-Stark trap for 2h.

Wash with saturated aqueous NaHCO3 and extract with ethyl acetate.

Dry organic layer with MgSO4, then filter and concentrate filtrate in vacuo to afford 5c (MW 4436.59, 8.64 g) in quantitative yield.

1 H NMR (CDC13) 8.23 J=11.78, 1 7.88 J=7.33, 1 7.39 5 7.16 J=7.33, 1 7.02 J=11.78, 1 5.31 1 H), 4.80 J=9.18, 1 2.80 J=5.79, 2 2.59 1 2.19 3 H), 1.72 2 1.56 9 1.39 2 1.27 J=4.83, 3 0.94 J=6.76, 3 H).

EXAMPLE Me I N(Me) 2 N N(Me), Bu N Bu N 0 0 4b Preparation of WO 98/06700 PCT/US97/14045 -42- Dissolve 4b (MW 260.34, 117.4 mmol, 5.74 g) in 53 mL toluene. Add (S,S)-pseudoephedrine (MW 165.24, 1.1 equ, 3.16 g) and 4 drops of concentrated HC1. Reflux with a Dean-Stark trap for 2h.

Wash with saturated aqueous NaHCO3 and extract with ethyl acetate.

Dry organic layer with MgSO4, then filter and concentrate filtrate in vacuo to afford EXAMPLE 6a

OTBS

OMe 17

CHO

OTBS

OMe 6a 6a Preparation of 6a Dissolve 17 (see Example 17, MW 373.41, 2 equ, 14.79 g) in 85 mL THF. Cool to -78 0 C and add t-BuLi (1.7 M in pentane, 4 equ, 46.6 mL), maintaining temperature below -70°C. Age 15 min, then slowly add solution of 5c (MW 436.59, 19.8 mmol, 8.64 g) in 65 mL THF. Age 1 h at -78°C, then cannula into cold aq NH4Cl (100 mL).

Add ethyl acetate and separate layers. Wash aqueous with ethyl acetate.

Combine organic layers and wash with brine, then dry (magnesium WO 98/06700 PCTIUS97/14045 -43sulfate) and evaporate in vacuo. 1 H NMR provides de data. Add THF mL), acetic acid (AcOH) (30 mL) and water (10 mL). Age 5 h at Separate layers and wash aqueous two times with ethyl acetate.

Combine organic layers, wash with brine, dry (magnesium sulfate), and evaporate in vacuo. 6a (MW 583.89) is isolated in 85% yield (9.83 g) by silica gel chromatography (92:8 hexanes:ethyl acetate).

1 H NMR (C6D6) 10.5 1 7.72 J=7.85, 1 7.30 (d, J=8.64, 1 6.83 J=8.05, 1 6.59 (dd, J=8.65, 2.61, 1 6.56 J=7.99, 1 5.92 1 3.85 (dd, J=16.32, 10.77, 1 3.48 2 3.32 3 3.01 (dd, J=14.11, 6.77, 1 2.87 (dd, J=16.30, 3.91, 1 2.79 (dd, J=13.25, 6.21, 1 2.68 J=7.66, 2 H), 2.10 1 1.72 2 1.30 9 1.25 2 1.01 9 H), 0.95 J=6.42, 3 0.94 J=8.40, 3 0.10 J=5.83, 6 H).

EXAMPLE 6b Br Me

OTBS

N'Me OMe 17 N(Me)21 Bu N O0

CHO

Bu N(Me) 2 Bu N-

OTBS

I i OTBS OMe 6b WO 98/06700 PCT/US97/14045 -44- Preparation of 6b Dissolve 17 (see Example 17, MW 373.41, 2 equ, 12.99 g) in 70 mL THF. Cool to -78 0 C and add t-BuLi (1.7 M in pentane, 4 equ, 40.9 mL), maintaining temperature below -70 0 C. Age 15 min, then slowly add solution of 5b (MW 384.57, 17.4 mmol, 6.69 g) in 55 mL THF. Age 1 h at -78 0 C, then cannula into cold aq NH4Cl (100 mL).

Add ethyl acetate and separate layers. Wash aqueous with ethyl acetate.

Combine organic layers and wash with brine, then dry (magnesium sulfate) and evaporate in vacuo. 1H NMR provides de data. Add THF (55 mL), AcOH (20 mL) and water (8 mL). Age 5 h at 25 0 C. Separate layers and wash aqueous two times with ethyl acetate. Combine organic layers, wash with brine, dry (magnesium sulfate), and evaporate in vacuo. 6b (MW 678.99) is isolated in 75% yield (8.86 g) by silica gel chromatography (70:30 hexanes:ethyl acetate).

1 H NMR (CDC13) 10.30 1 7.99 J=4.74, 1 7.11 (d, J=3.19, 1 6.89 J=8.61, 1 6.78 J=2.76, 1 6.59 (t, J=2.78, 1 5.70 J=2.86, 1 3.87 (dd, J=11.18, 4.29, 1 3.74 3 3.58 2 3.11 3 3.25 (dd, J=14.35, 6.25, 1 H), 2.88 3 2.84 2H), 2.68 (dd, J=14.35, 8.30, 1 2.47 (dd, J=9.02, 2.89, 1 2.09 1 1.75 2 1.39 2 0.99 (t, J=3.49, 3 0.92 9 0.92 J=7.15, 6 0.08 J=1.91, 6 H).

13 C NMR (CDC13) 190.5, 171.6, 165.9, 163.7, 157.9, 139.3, 137.2, 135.5, 130.0, 127.1, 120.8, 115.5, 111.7, 67.8, 55.11, 39.7, 38.9, 38.4, 37.2, 36.8, 36.0, 35.4, 26.0 (3 22.3, 18.4, 17.3, 14.7, -5.3 (2 C).

WO 98/06700 PCT/US97/14045 EXAMPLE 7 NHa

OH

7 Preparation of 7 Compound 7 is a commericially available starting material, for example, see DSM Andeno, Grubbenvorsterweg 8, P.O. Box 81, 5900 AB Venlo,The Netherlands.

EXAMPLE 8

O

NH

2

HN

OH

OH

7 8 Preparation of 8 Na2CO3 (MW 105.99, 1.5 equ, 8.8 g) dissolved in 82 mL water. Add a solution of (1R,2S) aminoindanol 7 (MW 149.19, 55.0 mmol, 8.2 g) in 160 mL CH2C12. Cool to -5 0 C and add propionyl chloride (MW 92.53, d 1.065, 1.3 equ, 6.2 mL). Warm to 25°C and age 1 h. Separate layers and dry organic (magnesium sulfate). Concentrate in vacuo to afford 8 (MW 205.26, 10 g) in 89% isolated yield.

WO 98/06700 PCT/US97/14045 -46- EXAMPLE 9 0 0 HN

N

OH

O

8 9 Preparation of 9 To a solution of 8 (MW 205.26, 49.3 mmol, 10 g) in 200 mL THF, add pyridinium p-toluenesulfonate (PPTS) (MW 251.31, 0.16 equ, 2g) then methoxypropene (MW 72.11, d 0.753, 2.2 equ, 10.4 mL).

Age 2 h at 38 0 C, then add aqueous sodium bicarbonate and ethyl acetate.

The organic layer was dried (magnesium sulfate). After concentration in vacuo, 9 (MW 245.32, 12.09 g) was formed in quantitative yield.

EXAMPLE Br o

OH

OMe Preparation of Compound 10 is a commericially available starting material, for example, see Lancaster Synthesis, P.O. Box 1000, Windham, NH 03087-9977 or Ryan Scientific, Inc., P.O. Box 845, Isle of Palms, SC 29451-0845.

WO 98/06700 PCT/US97/14045 -47- EXAMPLE 11 Br O Br OH OH OMe OMe 11 Preparation of 11 (MW 231.05, 130 mmol, 30.0 g) in 300 mL CH2C12 at 0°C. Add BH3-SMe2 (3 equ, 25.2 mL) and age for 2 h at Quench into aqueous 2 N HCI and separate layers. Dry organic (magnesium sulfate) and concentrate in vacuo to obtain 94% yield of 11 (MW 217.06, 25.5 g).

EXAMPLE 12 Br Br fOH \Y OMs OMe OMe 11 12 Preparation of 12 Dissolve 11 (MW 217.06, 47.2 mmol, 10.24 g) in 55 mL CH2C12 and cool to -20 0 C. Add DIEA (MW 129.25, d 0.742, 1.3 equ, 10.69 mL) then methane sulfonyl chloride (MsCI) (MW 114.55, d 1.480, 1.2 equ, 4.38 mL). Age -5°C to 0°C for 1 h then quench into mL water. Extract with CH2C12 then wash with 1N H2S04 (40 mL), then brine. Dry organic layers (magnesium sulfate) and concentrate in vacuo to afford 12 (MW 295.15, 13.23 g) in 95% yield.

WO 98/06700 PCT/US97/14045 -48- EXAMPLE 13 OMe OMe 12 13 Preparation of 13 12 (MW 295.15, 44.8 mmol, 13.23 g) in 44 mL dimethylacetamide (DMAC). Add NaBr (MW 102.90, 2 equ, 9.22 g) and age lh. Add 88 mL water and collect solid by filtration. Wash cake with water and dry by suction. Quantitative yield of 13 (MW 279.96, 12.54 g) is obtained.

EXAMPLE 14 0

N.

OMe 13 Preparation of 14 9 (MW 245.32, 1.1 equ, 89.1 g) in 1 L THF, cooled to 0 C. Add lithium bis(trimethylsilyl)amide (LiHMDS) (1.0 M in THF, equ, 545 mL) and age 1.5 h, warming to -30 0 C. Add 13 (MW 279.96, 327 mmol, 91.3 g) in 300 mL THF, and age -35°C for 1 h.

Warm to -10 0 C over 1 h, then quench into aqueous NH4C1. Separate WO 98/06700 PCT/US97/14045 -49layers and extract with ethyl acetate. Dry organic and concentrate in vacuo to afford crude 14 (MW 444.37).

EXAMPLE Preparation of 14 in 1 L MeOH and cooled to 10°C. Bubble in HC1 gas for 1 h until reaction is complete. 2 L H20 added and the product was filtered. The cake was washed with H20 and dried to give the product hydroxyamide, which was then dissolved in 1 L MeOH and 1.5 L 6N HCI and refluxed overnight. The mixture was cooled to 25 0 C and extracted with CH2C12 to give, after concentration, compounds 15 g, 64% from bromide 13).

EXAMPLE 16 OH/Me

'OH

OMe Preparation of 16 (mixture of acid and ester, 26.88 mmol) in 150 mL THF at -78 0 C. Add lithium aluminum hydride (LiAlH4) (1 M in THF, WO 98/06700 PCT/US97/14045 50 2 equ, 53.76 mL) over 30 min. Warm to 25 0 C over 1 h, then quench into aqueous NH4C1. Add ethyl acetate, extract ethyl acetate. Wash organics with brine, dry (magnesium sulfate), and concentrate in vacuo to afford 95% yield of 16 (MW 259.14, 6.62 g).

EXAMPLE 17 Br Br OH

OTBS

OMe OMe 16 OMe 17 Preparation of 17 16 (MW 259.14, 25.54 mmol, 6.62 g) in 35 mL CH2C12 and cool to 0°C. Add imidazole (MW 68.08, 2.5 equ, 4.35 g) and then tert-butyldimethylsilyl chloride (TBSC1) (MW 150.73, 1 equ, 3.85 g).

Age 1 h at 25°C then quench with aqueous NaHCO3 and add ethyl acetate. Extract with ethyl acetate, then dry organic layer (magnesium sulfate) and concentrate in vacuo to afford a quantitative yield of 17 (MW 373.41, 9.54 g).

IH NMR (CDC13) 7.41 J=8.74, 1H), 6.77 J=3.04, 1H), 6.63 (dd, J=8.73, 3.06, 1H), 3.78 3 3.50 J=5.75, 2 2.89 (dd, J=13.31, 6.15, 1 2.45 (dd, J=13.30, 8.26, 1 2.03 1 0.94 9 0.92 J=5.01, 3 0.07 6 H).

13 C NMR (CDCl3) 159.1, 141.6, 133.2, 117.0, 115.4, 113.2, 67.4, 55.4, 39.7, 36.3, 26.0 18.4, 16.5, -5.3 (2C).

WO 98/06700 PCT/US97/14045 -51 EXAMPLE 18 Ar 0 6a

OTBS

Ar represents: OMe Preparation of 18 Prepare 0.5 M Grignard solution from 4-bromo-1,2- (methylenedioxy)benzene (MW 201.01, 42.1 mmol, 8.46 g) and Mg (MW 24.31, 1.5 equ, 1.54 g) in 84 mL THF. Dissolve 6a (MW 583.89, 16.8 mmol, 9.83 g) in 80 mL THF and cool to -78 0 C. Slowly add Grignard solution (2.5 equ, 0.5 M, 84 mL) and age 30 min. Quench into aqueous NH4C1 and add ethyl acetate. Wash organic with brine, dry (magnesium sulfate) and evaporate in vacuo. Carry crude into oxidation.

WO 98/06700 PCT/US97/14045 -52- EXAMPLE 19 0-\ 0O OH BuOnBu Bu N Bu N Ar 0 Ar 0 19 18 Preparation of 19 Crude 18 (MW 706.01, 16.8 mmol) in 150 mL ACN. Add NMO (MW 117.15, 3 equ, 5.90 sieves (powdered, 3 wt equ, 35.6 g), and TPAP (MW 351.43, 10 mol 590 mg) and age 25 0 C for 2 h.

Concentrate to remove ACN, then elute through silica gel pad with ethyl acetate. Concentrate in vacuo, then chromatograph (90:10 hexanes:ethyl acetate) to isolate the oxidation product (85% yield over two steps).

Dissolve in 100 mL n-BuOH and add Ti(OBu)4 (MW 340.366, 5 equ, 28.59 Reflux for 48 h, then quench into water and add ethyl acetate. Filter through celite, separate the layers, and wash the organic with brine. Dry (magnesium sulfate) and evaporate in vacuo to afford 81% yield (over three steps) of 19 (MW 703.99, 9.58 g).

WO 98/06700 PCT/US97/14045 -53- EXAMPLE

OO

1 9 Ar 0 Ar Preparation of Dissolve 19 (MW 703.99, 13.6 mmol, 9.58 g) in 75 mL THF and cool to -50 0 C. Slowly add LiHMDS (1.0 M in THF, 5 equ, 68.0 mL) and age 25°C for 16 h. Quench into aqueous NH4Cl and add ethyl acetate. Wash organic with brine, dry (magnesium sulfate) and evaporate in vacuo to afford 20 (MW 703.99).

EXAMPLE 21

.OH

.OnBu WO 98/06700 PCT/US97/14045 -54- Preparation of 21 Dissolve 20 (MW 703.99, 13.6 mmol) in 125 ml nitromethane and add Et3SiH (MW 116.28, d 0.728, 10 equ, 21.7 mL).

Cool to 0°C and slowly add TiCl4 (1.0 M in CH2C12, 4 equ, 54.4 mL) and age 1 h at 0°C. Quench into 2N HCI and dilute with ethyl acetate.

Wash aqueous with ethyl acetate, then combine organics and wash with brine. Dry (magnesium sulfate) and evaporate in vacuo. Isolate by silica gel chromatography (75:25 hexanes:ethyl acetate) to afford a yield (over two steps) of 21 (MW 573.73, 5.85 g).

1 H NMR (CDC13) 7.20 J=7.80, 1 6.95 J=7.83, 1 6.88 J=8.37, 1 6.76 5 5.95 2 5.04 J=9.86, 1 H), 4.53 J=9.67, 1 4.02 2 3.78 3 3.55 1 3.45 1 3.34 J=9.82, 1 2.66 2 2.58 2 2.14 1 1.56 2 1.44 2 1.28 2 1.11 2 1.01 (d, J=6.77, 3 0.86 J=7.26, 3 0.81 J=7.37, 3 H).

13 C NMR (CDC13) 174.1, 164.3, 162.8, 157.8, 148.1, 146.8, 141.6, 136.3, 135.0, 133.1, 132.4, 129.6, 121.8, 121.2, 115.5, 112.3, 108.4, 101.1, 67.4, 64.8, 63.6, 60.4, 55.1, 51.5, 38.8, 37.6, 37.4, 32.3, 30.6, 22.3, 18.9, 18.0, 14.2, 14.0, 13.6.

EXAMPLE 22 Br Br OH OBn OMe OMe 16 22 Preparation of 22 To a suspension of 60% NaH (1.25 equ, 7.71g) in THF (450 ml) and DMF (10 ml) was added dropwise a solution of 16 (MW 259.14, 154 mmol, 40.0 g) (Compound 16 was prepared according to the procedure of described in Example 16) in THF (200 ml) below WO 98/06700 PCT/US97/14045 Benzylchloride (MW 126.59, 1.1 equ, 21.4 g) was added to the mixture and the mixture was refluxed for 4 h, cooled to room temperature, poured into ice water (500 ml), and extracted with ethyl acetate (1 The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with dil. HC1, sat. aqueous NaHCO3, water then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. 22 (MW 349.27) was isolated in 98% yield (52.8g) by silica gel chromatography (heptane-ethyl acetate gradient).

1 H NMR (CDC13): 0.96 J=6.60, 3H), 2.20 1H), 2.70 2H), 3.37 2H), 3.73 3H), 4.52 2H), 6.63 (dd, J=2.97, 8.91, 1H), 6.75 J=2.97, 1H), 7.37 5H), 7.41 J=8.91, 1H).

EXAMPLE 23 OM SMe 0 N (EtO)2P

O

27 Preparation of 27 SMe

HO

NH-HCI SMe Et H2N H N 23

OH

24 Step A: Preparation of 100 g (0.81 mols) of ethylacetimidate hydrochloride, 23 and 173 g (0.81 mols) of (S,S)-thiomicamine, 24 were combined in 1 L of CH2C12 and stirred at room temperature overnight. The reaction was then quenched with water and extracted with CH2C12. The organic WO 98/06700 PCT/US97/14045 -56phase was dried over MgSO4, filtered, and concentrated under reduced pressure. Recrystallization was accomplished using 700 mL of hot acetonitrile. Crystallization began at about 40° C. The solution was cooled to room temperature (about 20° C) then cooled to 15" C. The resulting crystals were collected by vaccum filtration and air-dried over night to afford 134.5 g of the product, compound HO MeO N SMe SMe N Niy- 0o o 26 Step B: Preparation of 26 51.1 g (215 mmol) of compound 25 from Example 23, Step A were dissolved in 1L of THF and cooled to 0° C. 24.7 g (224 mmol) of sodium t-pentoxide was then added. The mixture was aged at 0 5° C for about 30 mins. 13.9 mL (224 mmol) of Mel were then added dropwise and the solution allowed to warm to room temperature.

After 4 hours, the reaction was quenched with water and extracted with ethylacetate. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure to yield 54.04 g (100%) of crude product, 26.

MeO MeO N SMe SMe N 0 N -0 (EtO) 2

P

WO 98/06700 PCTIUS97/14045 -57- Step C: Preparation of 27 132 mL (946 mmol) of diisopropylamine were dissolved in 200 mL THF and cooled to 21° C. 420 mL (946 mmol) of nBuLi (2.25 M in hexanes) were then added. The mixture was aged at -30 to -45° C for about 40 minutes. The mixture was then cooled to -78° C and 108 g (430 mmol) of the product, 26 from Example 23, Step B in 200 mL of THF were added dropwise while maintaining an internal temperature of about -70° C. After an additional 40 minutes, 66.5 mL (460.1 mmol) of diethylchlorophosphate were added neat. The solution was then allowed to warm to -10° C, quenched with water, and extracted with ethylacetate. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to yield 166.11 g of the crude product, 27.

EXAMPLE 24 MeO SMe o

CHO

0 N" (EtO) 2 P Bu N Br 27 -OMe I /SMe

I-I

Bu N Br 28 Preparation of 28 83.3 g (215 mmol) of the product, compound 27 from Example 23, Step C were dissolved in 1L THF and cooled to -15" C.

90.3 mL (226 mmol) of nBuLi (2.5 M in hexanes) were then added dropwise while maintaining an internal temperature under 0" C. After minutes, 41.6 g (172 mmol) of 2-bromo-6-butyl-3-pyridinecarboxaldehyde in 70 mL of THF were added dropwise while WO 98/06700 PCT/US97/14045 -58maintaining an internal temperature between C and 0° C. After minutes at about C, approximately 13% of the phosphonate ester still remained unreacted. Another 6.7 g (28 mmol) of the aldehyde was then added in THF at 0° C. After another 20 minutes, 4 to 5% of the phosphonate ester remained. An additional 0.27 g (1.12 mmols) of the aldehyde were added. After 30 minutes, the reaction was quenched with water and extracted with ethylacetate. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to yield the crude product, 28.

EXAMPLE N SMe Bu N Br 28

O-\

OMe SN ,r SMe Bu N Br 29 Preparation of 29 107.6 mL (893 mmol) of 4-bromo-1,2-(methylenedioxy)benzene were dissolved in 2L THF and cooled to -78° C. 357 mL (893 mmol) of nBuLi (2.5 M in hexanes) were then added dropwise while maintaining an internal temperature below -72" C. 202 g (425 mmol) of the product from Example 24 in 300 mL THF were added dropwise while maintaining an internal temperature below -70' C. After minutes, the reaction was quenched with methanol at -70" C and allowed to warm to -10° C. Saturated aqueous NaHCO3 was added and the WO 98/06700 PCT/US97/14045 -59phases separated. The aqueous layer was filtered through celite and extracted with ethylacetate. The ethylacetate layer was then dried over MgSO4, filtered, and concentrated under reduced pressure to afford 320 g of the crude product, 29.

1H NMR 6 (ppm) 0.92 (3H, 1.35 1.68 2.46 (3H,s); 2.75 centered at 3.05 (2H,dd,dd); centered at 3.4 (2H,dd,dd); 3.34 3.96 4.87 (1H, 5.18 5.92 6.71- 6.79 (3H, aromatic multiplet); 6.81-6.88 (2H, aromatic multiplet); 7.09- 7.18 (3H, aromatic multiplet), 7.64 (1H,d).

EXAMPLE 26 0-\ 0 0 OMe N SMe 0 OiPr Bu N Br 29 Bu N Br 29 Preparation of To a solution of 47.6 g (79.6 mmol) of 29, the product from Example 25 in 200 mL of isopropanol was added 44 mL of concentrated H2S04 (18 The mixture was then heated to reflux.

After 2.5 hours, the mixture was cooled to room temperature and diluted with water. The mixture was then extracted with ethylacetate and washed with a saturated aqueous solution of NaHCO3. The organic phase was concentrated under reduced pressure and the residue dissolved in tert-buytl methyl ether. The ethereal solution was washed with IN aqueous HC1 and with a saturated aqueous solution of NaHCO3.

The organic layer was then dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography using a solvent gradient of 10:1 011 01111 WO 98/06700 PCT/US97/14045 hexane/ethylacetate to 5:1 hexane/ethylacetate to afford 25.15 g of product, 1H NMR 5( ppm) 0.91 3H, triplet); 1.07 (3H, 1.13 1.35 (2H, 1.65 2.71 2.93 4.7-4.96 (2H, overlapping multiplets); 5.96 6.72 (3H, aromatic multiplet); 7.05 7.43 (1H,d).

EXAMPLE 27 o-\ O O 0 0 OiPr fOiPr Bu N Br Bu N C02Me 31 Preparation of 31 To a solution of 2 g (3.9 mmol) of 30, the product from Example 26, 66 mg (0.12 mmol) of DPPF bis(diphenylphosphino)-ferrocene) and 67 mg (8 mmol) of NaHCO3 in mL of methanol was added 27 mg (0.12 mmol) of palladium diacetate. The mixture was heated at 70° C under 40 psi of carbon monoxide for 12 hours. The mixture was then cooled, concentrated under reduced pressure, and partitioned between ethylacetate and water.

The aqueous layer was extracted with ethylacetate and the combined organic layers were dried over MgSO4. The organic solvent was removed under reduced pressure to afford 1.56 g of the crude product, 31.

'H NMR 8 (CDC13, ppm): 0.9(3H,t); 1.06(6H,d); 1.37(2H,m); 1.66(2H,m); 2.78(2H,m); 2.93(2H,m); 3.94(3H,s); 4.89(1H,m); 5.13(1H,t); 5.88(2H,s); 6.67-6.75(3H, aromatic multiplet); 7.2(1H,d); 7.56(1H,d).

WO 98/06700 PCT/US97/14045 -61 EXAMPLE 28 0\ Br SOBn 0- C00Pr N CO 2 Me OMe 22

CO

2 iPr 31 B u N* O OBn OMe 32 Preparation of 32 To a cold solution of 22 (see Example 22, MW 349.27, 1.3 equ, 63.76 g) in THF (450 ml) was added n-BuLi (1.7M in hexane, 1.3 equ, 110 ml), maintaining temperature below -70 0 C, and the mixture was stirred at -78 0 C for 10 min. The mixture was added to a solution of 31 (MW 427.50, 0.14 mol, 60.0 g) in THF (450 ml) through cannula below -70°C. The mixture was stirred at -78 0 C for 30 min, quenched with water (450 ml), and extracted with ethyl acetate (900 ml). The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. 32 (MW 665.82) was isolated in 84% yield (78.4 g) by silica gel chromatography (heptane- ethyl acetate gradient).

1H NMR (CDC13): 0.87 J=7.26, 3H), 1.04 J=6.93, 3H), 1.05 (d, J=6.27,6H), 1.26 2H), 1.62 2H), 2.29 1H), 2.71 J=7.59, 2H), 2.92 (J=6.26, 2H), 3.03 2H), 3.45 2H), 3.80 3H), 4.52 2H), 4.66 J=7.26, 1H), 4.85 1H), 5.82 2H), 6.56 4H), WO 98/06700 PCTIUS97/14045 -62- 6.78 1H), 7.02 J=8.91, 1H), 7.14 J=8.25, 1H), 7.35 7.56 J=8.25, 1H).

EXAMPLE 29 0- O- O O ,i C 0 2'Pr r'C 2 r _COi 2 iPr B u Bu NO OBn OBn OMe OMe 32 33 Preparation of 33 To a solution of 32 (MW 665.82, 110 mmol, 73.06 g) in THF (750 ml) was added sodium tert-pentoxide (MW 110.14, 3 equ, 36.35g) at -40 0 C. The mixture was allowed to warm to OC, stirred at OC for 1.5 h, poured into water (1 and extracted with ethyl acetate (1 The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. 33 (MW 665.82) was isolated in 66% yield (48.1 g) by silica gel chromatography (heptane- ethyl acetate gradient).

1H NMR (CDC13, ppm): 0.80 J=5.94, 3H), 0.87 J=7.26, 3H), 1.03 J=6.27, 3H), 1.13 J=6.27, 3H), 1.30 2H), 1.60 2H), 2.14 2H), 2.27 1H), 2.71 2H), 3.08 2H), 3.37 1H), 3.48 J=8.91, 1H), 3.80 3H), 4.37 and 4,44 (ABq, J=11.5, 2H), 4.91 J=8.91, 1H), 4.99 1H), 5.92 2H), 6.65 J=7.92, 1H), 6.76 4H), 7,05 J=7.92, 1H), 7.28 6H), 7.71 J=8.54, 1H).

WO 98/06700 PCT/US97/14045 -63- EXAMPLE

O-\

O 0 Bu

CO

2 iPr I

CO

2 iPr Bu- O Bu-"WO OBn OBn OMe OMe 33 34 Method A: Preparation of 34 To a predegassed solution of 33 (MW 665.82, 22.8 mmol, 15.2 g) and isopropyl alcohol (5 equ, 8.7 ml) in THF (100 ml) was added SmI2 (0.1 M in THF, 4.8 equ, 1.1 L) under argon atmosphere at room temperature. The mixture was stirred at the same temperature over night, concentrated in vacuo, poured into 0.5N HCI (250 ml), and extracted with ethyl acetate (250 ml). The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water, sat. aqueous NaHCO3, 5% Na2SO3, water then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. 34 (MW 649.83) was isolated in quantitative yield (15.1 g) by silica gel chromatography (heptane- ethyl acetate gradient).

1 H NMR (CDC13, ppm): 0.84 J=7.26, 3H), 1.04 J=6.93, 3H), 1.08 J=6.27, 3H), 1.11 J=6.27, 3H), 1.26 2H), 1.56 2H), 2.20 1H), 2.65 2H), 2.72 2H), 3.18 J=9.74, 1H), 3.38 2H), 3.75 3H), 4.48 J=8.90 IH), 4.49 2H), 4.96 2H), 5.95 2H), 6.73 5H), 6.91 J=7.91, 1H), 7.15 J=7.92, 1H), 7.30 6H).

WO 98/06700 WO 9806700PCT/US97/14045 64 EXAMPLE 31 o 0 C0 2 iPr 'N 2 iPr Bu ~Bu

N-

OBn

OH

OMe OMe 34 Preparation of To a solution of 34 (MW 649.83, 18.5 mmol, 12.0 g) in THF (60 ml) and isopropyl alcohol (60 ml) was added 10% Pd-C (10.5 and the mixture was hydrogenated under H2 (3.5 kg/cm2) at 60 0

C

for 4 h. The catalyst was removed by filtration, and the filtrate was evaporated in vacuc to give 35 (MW 559.70) in 83% yield (8.62 g).

IH NMR (CDC 13, ppm): 0.86 J=7,26, 3H), 1.01 J=6.60, 3H), 1. 10 J=6.27, 3H), 1. 13 J=6.27, 3H), 1.26 (in, 2H), 1.56 (mn, 2H), 2.13 (mn, 1H), 2.65 (in, 2H), 2.78 (in, 2H), 3.28 J=9.73, 1H), 3.50 (in, 2H), 3.78 3H), 4.51 J=9.57, 4.98 (in, 1H), 5.04 (d, J=10.2, IH), 5.97 2H), 6.73 (mn, 5H), 6,86 J=8.25, 1H), 6.95 (d, J=7.92, 1H), 7.20 J=7.92, 1H).

WO 98/06700 PCT/US97/14045 EXAMPLE 32 0 0 Bu N 2 CPr B 0 2

H

OH YCO,H OMe OMe 36 Preparation of 36 To a solution of 35 (NW 559.70, 15.4 mmol, 8.62 g) and TEA (5.7 equ, 12.3 ml) in DMSO (25 ml) was added S03-PY (MW 159.16, 2.9 equ, 7.05 g) at room temperature. The mixture was stirred for 15 min, poured into water (1 and extracted with ethyl acetate (200 ml x 3 times). The combined organic layers were washed with 10% citric acid then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo to give 9.6 g of crude aldehyde.

To a solution of the crude aldehyde and 2-methyl-2-butene ml) in tertbutanol (60 ml) was added a solution of NaCIO2 (22.1 mmol, 2.00 g) in 0.5M (I)H 3.3) KH2PO4-H3P0 4 buffer (60 ml) at room temperature. The mixture was stirred for 45 min and extracted with ethyl acetate (200 ml). The organic layer was washed with citric acid, water then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo to give crude mono carboxylic acid.

To a solution of the crude mono carboxylic acid in methanol (40 ml) and dioxane (20 ml) was added 4N NaOH (148 mmol, 37 ml), and the mixture was stirred at 60°C for 1 h. After cooling, the mixture was diluted with water (50 ml), adjusted to pH 8 with 6N HC1, and washed with ethyl acetate (100 ml). The aqueous layer was WO 98/06700 PCT/US97/14045 -66acidified to pH 3 with HCI aq, and extracted with ethyl acetate (100 ml x 3 times). The combined organic layers were washed with water then brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. 36 (MW 531.60) was isolated in 48% yield (3.90 g) by silica gel chromatography (CH2Cl2-ethyl acetate gradient).

1 H NMR (CDC13, ppm): 0.84 J=7.26, 3H), 1.26 2H), 1.32 (d, J=6.60, 3H),1.49 2H), 2.67 3H), 3.14 2H), 3.59 J=9.57, 1H), 3.75 3H), 4.58 J=9.57, 1H), 4.99 J=9.56, 1H), 6.00 (s, 2H), 6.70 J=2.97, IH), 6.78 1H), 6.83 3H), 6.94 J=8.90, 1H), 7.06 J=7.91, 1H), 7.33 J=7.91, 1H).

EXAMPLE 33 0-\ 0 Br _I OTBS C0 2 iPr BoM OMe 17 Bu N C0 2 Me O 31

.CO

2 iPr Bu N 0

OTB

1 s OMe WO 98/06700 PCT/US97/14045 -67- Preparation of 37 To a solution of 2.62 g (7.02 mmol) of the arylbromide 17, Example 17 in 15 mL THF was added 3.3 mL (7.1 mmol) of nBuLi (2.15 M in hexanes) while maintaining an internal temperature below C. After 10 minutes, the solution was transferred via cooled cannula (dry ice) to a solution of the diester, 31 produced in Example 27 in 35 mL of THF. The solution was observed to turn a green-black color. The mixture was stirred for an additional 0.5 hours and then quenched with aqueous NaHCO3. The aqueous layer was extracted with ethylacetate (2X) and the combined organic layers dried over MgSO4.

Column chromatography using a 6:1 hexane/ethylacetate solvent system afforded 2.0 g of product 37 as a yellow oil.

1H NMR 6 (CDC13, ppm): 0.08(6H,s); 0.88(3H,t); 0.92(9H,s); 0.98(3H,d); 1.05(6H,d); 1.32(2H,m); 1.62(2H,m); 2.11(1H,dd); 2.72(2H,m); 2.93(2H,m); 3.12(1H,dd); 3.51(1H,dd); 3.62(IH,dd); 3.83(3H,s); 4.66(1H,t); 4.87(lH,m); 5.82(2H,m); 6.5-6.63(4H, aromatic multiplets); 6.81(1H,m); 7.02(1H,d); 7.13(1H,d); 7.58(1H,d).

EXAMPLE 34 0

O

COiPr

CO

2 iPr Bu N O Bu NZ

O

OTBS

OH

OMe OMe 37 38 Preparation of 38 WO 98/06700 PCT/US97/14045 -68- To a solution of 0.8 g (1.16 mmol) of the silyl ether, 37 from Example 33 in 20 mL acetonitrile at room temperature was added mL og aqueous HF. After 10 minutes, the reaction was quenched with aqueous NaHCO3 and extracted with ethylacetate The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to afford 0.66 g of the desilylated product, 38 as a yellow foam.

1H NMR (CDC13, ppm, 300 MHz): 5 0.8 3H), 0.95 3H), 1.00 (m, 6H), 1.25 3H), 1.55 2H), 2.00 1H), 2.77 3H), 2.90 (m, 1H), 3.16 1H), 3.40 2H), 3.75 3H), 4.55 1H), 4.81 (m, 1H), 5.76 2H), 6.50 4H), 6.74 (bs, 1H), 6.89 1H), 7.43 (d, 1H), 7.85 1H).

EXAMPLE

O-\

O0 O 0 C02iPr Bu N Bu OHC02Pr

OHH

OMe 38 39 O Me Preparation of 39 0.21 g (0.37 mmol) of compound 38, from Example 34 were dissolved in 5 mL THF and cooled to -10° C. 0.12 g (1.1 mmol) of sodium t-pentoxide were then added as a solid and the reaction allowed to warm to room temperature. The reaction was subsequently quenched with IN aqueous HC1 and extracted with ethyl acetate (2X).

WO 98/06700 PCT/US97/14045 -69- The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to afford 0.21 g (100%) of the crude cyclized product, 39.

1 H NMR 8 (CDC13, ppm, 300 MHz): 0.8 2H), 0.89 3H), 1.03 (d, 3H), 1.17 6H), 1.32 2H), 1.61 2H), 2.11 1H), 2.29 (m, IH), 2.82 2H), 3.15 1H), 3.30 1H), 3.49 1H), 3.78 (t, 3H), 5.11 2H), 5.93 2H), 6.78 6H), 7.25 1H), 7.58 (d, 1H).

EXAMPLE 36 0 Bu 0 2 Pr I CO 2 iPr Bu OH Bu,(i-OH Bu N ZOH OH 'H OMe OMe 39 Preparation of To a solution of dihydroxy ester (4.2 39 in acetone ml) at -15 °C was added Jones reagent (8.4 ml) over a period of Ih.

The reaction was aged 0.5 h, warmed to 0 oC and quenched with water.

The phases were separated and the aqueous phase was extracted with MTBE (2x10 ml). The organic phase was concentrated to a tan solid and the crude material was carried directly to the deoxygenation reaction.

1 H NMR 8 (CDC13, ppm, 300 MHz): 0.85 3H), 1.08 9H), 1.39 2H), 1.52 2H), 2.54 1H), 2.69 2H), 3.65 2H), 3.73 -0 WO 98/06700 PCT/US97/14045 3H), 4.83 1H), 5.02 1H), 5.97 2H), 6.75 6H), 7.10 (d, 1H), 7.43 1H).

EXAMPLE 37 '0 2 iPr OMe

OH

OMe Preparation of 41 To a solution of 1.0 g (1.7 mmol) of compound 40, from Example 36 in 10 mL of tetrahydrofuran (THF) was added 51 mL (5.1 mmol) of SmI2 (0.1 M in THF) at room temperature. After minutes, the reaction was quenched with 1N aqueous HC1 and extracted with ethyl acetate twice. The organic layers were dried over MgSO4, filtered and concentrated under reduced pressure to afford 0.98 g (100%) of the crude product 41 as a single diastereomer by 1 H NMR.

'H NMR 8 (CDC13, ppm, 300 MHz): 0.85 3H), 1.05 3H), 1.13 2H), 1.15 3H), 1.3 3H), 1.5 2H), 2.65 2H), 2.95 (m, 2H), 3.35 (dd, 1H), 3.52 1H), 3.72 3H), 4.55 1H), 5.00 (d, WO 98/06700 PCTIUS97/14045 71 1H), 5.90 2H), 6.75 (in, 5H), 6.95 1H), 7.08 1H), 7.37 (d, 1H).

Claims (18)

1. A compound of Formula I: R 3 b ROH A COR 2 R 1 wherein Al represents: a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 or 3 heteroatoms selected from O, N and S, the heterocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, c) aryl, wherein aryl is as defined below, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting WO 98/06700 PCT/US97/14045 -73 of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 Cl-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 and when two substituents are located on adjacent carbons they can join to form a 5- or 6- membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, C02R 6 Br, Cl, F, I, CF3, N(R 7 )2, C1-C8 alkoxy, C1-Cg alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-Cg cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0 to R 1 is: a) C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from O, N and S which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, WO 98/06700 PCTIUS97/14045 -74- R 2 is OR 4 or N(R 5 )2; R 3 b is: a) C1-C8 alkyl, b) aryl, or c) heteroaryl; A 5 R 4 is C1-C8 alkyl; and R 5 is: H, C1-C8 alkyl, or aryl.

2. A process for the preparation of a compound of formula I: COR 2 wherein represents: a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 or 3 heteroatoms selected from O, N and S, the heterocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, WO 98/06700 PCT/US97/14045 b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, S 5 CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, c) aryl, wherein aryl is as defined below, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, Cl-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R 5 and when two substituents are located on adjacent carbons they can join to form a 5- or 6- membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, CO2R 6 Br, Cl, F, I, CF3, N(R 7 )2, C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0 to S; WO 98/06700 PCTIUS97/14045 76 RI is: a) C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-Cg cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from 0, N and S which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, 1, CF3, N(R 5 ClI-C8 alkoxy, C1I-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, R 2 is OR 4 or N(R 5 )2; R 3 a is: a) -CO-C1I-C8 alkyl, b) -CO-aryl, or c) -CO-heteroaryl; R 3 b is: a) C1I-C8 alkyl, b) aryl, or c) heteroaryl; R 4 is C I-C8 alkyl; and R 5 is: H, C1I-C8 alkyl, or aryl, comprising reacting a WO 98/06700 PCT/US97/14045 -77- in the presence of a strong base and an aprotic solvent at a temperature range of -78°C to about

3. The process as recited in Claim 2, wherein the strong base is selected from the group consisting of: LDA, LiHMDS, KHMDS, NaHMDS, KOtBu, and sodium t-amylate.

4. The process as recited in Claim 3, wherein the aprotic solvent is selected from the group consisting of tetrahydrofuran, diethyl ether, methyl t-butyl ether, benzene, toluene, pentane, hexane, dioxane and a mixture of said solvents. The process as recited in Claim 4, wherein the temperature range is about -50°C to about

6. The process as recited in Claim 5, wherein the strong base is LiHMDS, KHMDS, or NaHMDS, the aprotic solvent is tetrahydrofuran and the temperature range is about -0°C to about

7. A process for the preparation of a compound of formula II: R 3 b A R2 R' II wherein represents: 0 -1 M -1 WO 98/06700 PCT/US97/14045 -78- a) 5- or 6-membered heterocyclyl containing one, two or three double bonds, but at least one double bond and 1, 2 or 3 heteroatoms selected from O, N and S, the heterocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, b) 5- or 6-membered carbocyclyl containing one or two double bonds, but at least one double bond, the carbocyclyl is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, c) aryl, wherein aryl is as defined below, CI-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, are unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, C1, F, I, CF3, N(R 5 C1-C8 alkoxy, C3-C cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R5)2, aryl is defined as phenyl or naphthyl, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, CO2R 4 Br, Cl, F, I, CF3, N(R 5 C1-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, CO(CH2)nCH2N(R5)2, and when two substituents are located on adjacent carbons they can join to form a 5- or 6- membered ring with one, two or three heteroatoms selected from O, N, and S, which is unsubstituted or substituted with with one, two or three substituents selected from the group consisting of: H, OH, CO2R 6 Br, Cl, F, I, CF3, N(R 7 )2, WO 98/06700 WO 9806700PCTIUS97/14045 79 Cl-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, n is 0to R 1 is: a) C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, b) aryl, or c) heteroaryl; heteroaryl is defined as a 5- or 6-membered aromatic ring containing 1, 2 or 3 heteroatoms selected from 0, N and S, which is unsubstituted or substituted with one, two or three substituents selected from the group consisting of: OH, C02R 4 Br, Cl, F, I, CF3, N(R 5 Cl-C8 alkoxy, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, or C3-C8 cycloalkyl, CO(CH2)nCH3, and CO(CH2)nCH2N(R 5 )2, R 2 is OR 4 or N(R 5 )2; R 3 b is: a) C I-C8 alkyl, b) aryl, or c) heteroaryl; R 4 is Cl-C8 alkyl; and R 5 is: H, Cl-C8 alkyl, or aryl, comprising reacting a compound of formula I WO 98/06700 PCT/US97/14045 R 3 b OH A r COR 2 R 1 with a reducing agent and optionally an acid in a solvent at a temperature range of about -78 0 C to about 100C.

8. The process as recited in Claim 7, wherein the reducing agent is selected from the group consisting of: a hydride, a borane, a C5-C6 cycloalkene with a transition metal catalyst, H2 with a transition metal catalyst and SmI2.

9. The process as recited in Claim 8, wherein the acid is a Lewis acid, when the reducing agent is a hydride, a borane or a C5-C6 cycloalkene with a transition metal catalyst; a protic acid, when the reducing agent is H2 with a transition metal catalyst; or is absent when the reducing agent is SmI2. The process as recited in Claim 9, wherein the solvent is an aprotic solvent, when the acid is a Lewis acid and the reducing agent is a hydride, a borane or a C5-C6 cycloalkene with a transition metal catalyst; a protic solvent, when the acid is a protic acid and the reducing agent is H2 with a transition metal catalyst; or a solvent system consisting a protic solvent in combination with aprotic solvent.

11. The process as recited in Claim 10, wherein the temperature range is about -78°C to about 20 0 C, when the acid is a Lewis acid and the reducing agent is a hydride or a borane.

12. The process as recited in Claim 10, wherein the temperature range is about 0°C to 100 0 C, when the acid is a Lewis acid WO 98/06700 PCT/US97/14045 -81 or a protic acid and the reducing agent is a C5-C6 cycloalkene with a transition metal catalyst or H2 with a transition metal catalyst.

13. The process as recited in Claim 10, wherein the temperature range is about 0°C to 30 0 C, when the reducing agent is SmI2.

14. The process as recited in Claim 11, wherein the aprotic solvent selected from the group consisting of: tetrahydrofuran, diethyl ether, methyl t-butyl ether, dioxane, CH2C12, CHC13, nitromethane, toluene, and dichlorobenzene. The process as recited in Claim 12, wherein the protic solvent selected from the group consisting of: ethanol, methanol, and isopropanol.

16. The process as recited in Claim 13, wherein the solvent system consists of a protic solvent selected from the group consisting of methanol, ethanol or isopropanol and an aprotic solvent selected from the group consisting of: tetrahydrofuran, diethyl ether, methyl t-butyl ether or dioxane.

17. The process as recited in Claim 13, wherein the Lewis acid is selected from the group consisting of: TiC14, BF3, BCl3, SnCl4, A1C13, and TiC12(OiPr)2.

18. The process as recited in Claim 15, wherein the temperature range is about -20°C to about 10°C, when the reducing agent is a hydride or a borane.

19. The process as recited in Claim 13, wherein the protic acid is selected from the group consisting of: trifluoroacetic acid, HC1, and H2S04. WO 98/06700 PCT/US97/14045

82- The process as recited in Claim 16, wherein the hydride is selected from the group consisting of: R3SiH, R2SiH2, wherein R is C1-C8 alkyl or aryl, and NaBH4. 21. The process as recited in Claim 16, wherein the borane is selected from the group consisting of: BH3-NHMe2, BH3*SMe2, BH3*pyridine, and BH3-THF. 22. The process as recited in Claim 15, wherein the reducing agent is a C5-C6 cycloalkene with a transition metal catalyst selected from cyclohexene or cyclohexadiene with Pd/C, Pt-C, Rh/Al or Raney Ni. 23. The process as recited in Claim 20, wherein the temperature range is about 0°C to about 24. The process as recited in Claim 18, wherein the H2/transition metal catalyst is selected from the group consisting of: Pd-C, Pt-C, Rh/Al and Raney Ni. The process as recited in Claim 22, wherein the temperature range is about 0°C to about 40 0 C. 26. The process as recited in Claim 18, wherein the hydride is R3SiH, the Lewis acid is TiC14 the aprotic solvent is nitromethane and the temperature range is about -5 0 C to about WO 98/06700 PCT/US97/14045 -83- 27. A process for the preparation of a compound of formula: OTBS OMe comprising reacting a ketone of formula: O OMe in tetrahydrofuran with about 3 to about 5 equivalents of lithium bis(trimethylsilyl)amide at about -50°C to about WO 98/06700 PCT/US97/14045 -84- 28. A process for the preparation of a compound of formula: OMe comprising reacting the tertiary alcohol OTBS in nitromethane with Et3SiH and TiC14 at about -5 0 C to about WO 98/06700 PCT/US97/14045 29. A process for the preparation of a compound of formula: comprising reacting the tertiary alcohol OTBS OMe in a solution of isopropyl alcohol and tetrahydrofuran with SmI2 at about 10° 30 0 C. WO 98/06700 PCT/US97/14045

86- formula: A process for the preparation of a compound of 0-\ C0 OiPr Bu N 00O OH OMe comprising reacting the tertiary alcohol 0-\ 0 Bu N OH O OH OMe in a solution of isopropyl alcohol and tetrahydrofuran with SmI2 at about 100 31. An intermediate in the synthesis of an endothelin antagonist, substantially as hereinbefore described with reference to any one of the examples. 32. A process for the preparation of an intermediate in the synthesis of an endothelin antagonist, substantially as hereinbefore described with reference to any one of the examples. 33. A process for the preparation of an endothelin antagonist, substantially as hereinbefore described with reference to any one of the examples. 34. An endothelin antagonist prepared by the process of any one of claims 7 to or 33. Dated 15 April 1999 MERCK CO., INC. BANYU PHARMACEUTICAL CO. Patent Attorneys for the Applicant/Nominated Person SPRUSON&FERGUSON *0 0 00 *0 *0 0 00 0 i 1 i -i,2 [N:/Iibc]00334:BAV