Substance P is a naturally occurring undecapeptide belonging to the tachykinin family of peptides, members of which exert prompt stimulatory action on smooth muscle tissue. Substance P is a pharmaceutical active neuropeptide that in produced in mammals and possesses a characteristic amino acid sequence that is described in U. S. Patent No. 4,680, 283. A variety of substance P antagonists can be prepared from the title compound. For example United States Patent No. 5,323, 929 describes Substance P antagonists of formula 2 where Rl is a substituted or unsubstituted aryl, heteroaryl, or cycloalkyl group.

These antagonists can be prepared by reduction of 2-phenyl-3- aminopyridine followed by the reductive amination of the resulting 2-phenyl-3 aminopiperidine using the appropriate aldehyde of formula RICH2CHO. Alternatively, these substance P antagonists can be obtained by reacting 2-phenyl-3-aminopyridine with a compound of the formula RtCH2X where X is a leaving group to produce the pyridine

analog of the substance antagonist. The pyridine analog is then reduced to obtain the final product.

Additional substance P antagonists that can be prepared from 2-phenyl-3- amino piperidine are described in United States Patent No. 5,773, 450, and PCT Applications WO 97/08144 and WO 01/77100. Methods employing 2-phenyl-3-amino piperidine to make substance P are also described in United States Patent No. 5,232, 929.

The conventional method employed to prepare 2-phenyl-3-amino piperidine is described by Miller and Farrell, (Tetrahedron Letters, 1998, 39, 6441-6444), is sensitive to air and results in a relatively low yield. In many cases, a late stage resolution has to be undertaken to obtain the active isomer, as for example see Eur. Pat. Appl 1095939. The cis configuration of the amino and phenyl substituents is accessible by catalytic hydrogenation of the appropriately substituted pyridine compound as described in WO 92/17449, WO 93/01170 and United States Patent 5,686, 615. However, this method provides the racemic material which then has to be resolved as described in WO 94/27966.

A racemic analog of the desired amine has been prepared by a nitroaldol reaction followed by conversion of the trans-nitro compound to the cis amino compound by a Nef reaction followed by reduction of the oxime (see WO 93/01170 and Tetrahedron Letters, 1993, 34, 5831 ; a related reaction is given in Synthesis 1976,615 and Journal of Prak Chemistry 1975, 317, 919).

A synthesis of 2 has been described from (S)-N, N-dibenzyl-O-tert- butyldimethylserinol (Tetrahedron Letters, 1999, 40, 5071) but the sequence involves nine steps. The key cyclization involves a displacement reaction. Phenylglycine methyl ester has also been used as the starting material to prepare an analogue of 2 (Synthesis, 1997,475), with a 4-isopropyl substituent. In this case, the carboxylic acid provides an alcohol which is then substituted for the 3-amino group. A 4-substituent is necessary as the key cyclization step is an ene reaction.

Alkylation of (4R)-4-phenyl-2-azetidinone with 1-bromo-3-chloropropane followed by hydrolysis of the lactam and cyclization resulted in formation of a cis- piperidine derivative, but then a four step sequence was required to stereoselectively convert the carbomethoxy group to amino (see WO 93/01170 and Journal of Medicinal Chemistry 1992, 35, 4911).

Ornithine has been used to prepare piperidinones where homologation was performed with the lithium enolate of ethyl acetate. Removal of the protecting Cbz group by hydrogenolysis and in situ reduction of the imine led to the trans-product as summarized in Scheme 1 (Tetrahedron Letters 1993, 34, 3593 and 1992, 32, 1089 ; Journal of Medicinal Chemistry, 1997, 40, 3402).

SCHEME 1 Reduction of the azide group in (S)-5-azido-2-hydroxy-1-phenyl-1- pentanone resulted in formation of a 4: 1 mixture of the cis/trans 3-hydroxy-2- phenylpiperidine (Heterocycles 1999, 51, 1067).

The present invention relates to a simpler process for the preparation of (S, S)-cis-2-phenyl-3-tert-butoxycarbonylamino piperidine (1) and (S, S)-cis-2-phenyl-3- tert-butoxycarbonylaminopiperidines (1A), which is outlined hereinbelow in Scheme II.

The invention relates to a process starting from the chiral material, L-ornithine (3) or a salt thereof. This amino acid, used preferably as a salt, especially as its hydrochloride salt (4) is selectively protected on the side chain amine on the 5-carbon and on the a-carbon, the two protecting groups being different and capable of being removed under different conditions. Preferably, the amine on the 5 carbon is protected by an amine protecting group that can be removed by hydrogenolysis such as benzyloxycarbonyl or dithiasuccinoyl and the like. It is preferred that the protecting group of the amine on the 6 carbon is protected with a benzyloxycarbonyl (Cbz) group in the presence of copper sulfate to complex the 2-amino carboxylate functionality. Following the hydrolysis of the copper complex to give 5, the amine of the a-carbon is protected with a second protecting group known in the art such as, for example, tert-butoxycarbonyl (Boc) group, to afford the differentially diprotected amino compound 6. The carboxylic acid of 6 is then transformed into the N-methoxy-N-methyl amide 7 commonly referred to as a Weinreb

amide. Treatment of intermediate 7 with phenyl magnesium halide, e. g. , chloride provides 8. Hydrogenation to remove the Cbz group permits internal cyclization to form the imine, reduction of the intermediate cyclic imine provides the desired compound 1 in excellent overall yield with no resolution required since the L-ornithine is chiral.

Excellent diastereoselectivity for the required cis-stereochemistry is also observed. 0 HO NH2 ÑH2 3 ornithine 0 0 1. CuS045H20 HO NH2-HCI HO NHCbz 2. IfCO3, CbzCl NH2 3. Na2EDTA NH2 4 5 Boc20 HO NHCbz NaOH- NHBoc 6 0 1. i-BuOCOCI, NMM \ N-NHCbz 2. Me (MeO) NH-HCI 7 0 PhMgCI Ph NHCbz THE' NHBoc 8 H2., vNHBoc, \ NHZ Pu-C Ph Ph H 1 SCHEME II

For those skilled in the art, there are many possible variations in the step sequence and protection group choice. The example that follows herein is intended as an illustration of a certain preferred embodiment of the invention, and no limitation of the invention is implied.

The invention is the synthesis of (S, S)-cis-2-phenyl-3-aminopiperidine (1) as a single optical isomer from the readily available, natural amino acid L-ornithine (2).

The preferred process is described herein.

In one aspect of the above-described method, the invention involves the following steps of : Step one: Reaction of L-ornithine or salt thereof e. g. , hydrochloride salt 4 with a protecting group. It is preferred that the L-ornithine or salt thereof, is reacted with copper sulfate pentahydrate under conditions effective to form a complex between the metal ion and the a-amino carboxylic acid moiety. This is followed by the reaction with Cbz chloride in the presence of a base to protect the 5-amino group.

Ethylenediaminetetraacetic acid (EDTA) disodium salt is used to de-complex the copper and provide compound 5 in 85-97% yield. Suitable bases include, but are not limited to, triethylamine, diisopropylethylamine, 2,6-lutidine, N, N, N', N'-tetramethylethylene- diamine, potassium carbonate, sodium carbonate, lithium carbonate, sodium hydroxide and potassium hydroxide. Potassium carbonate is the preferred base for this reaction.

Solvents for these reactions include alcoholic solvents, water, or a mixture of alcoholic solvents and water. The preferred solvent for this reaction is water. The product 5 is isolated as a solid, and it was used without any further purification.

Step two of this scheme involves the protection of the second amino group of the isolated intermediate 5 from step 1, using art recognized amine protecting groups.

Preferably, intermediate 5 is reacted with a base and di-t-butyl dicarbonate (Boc anhydride) to form intermediate 6. Suitable bases for this reaction include, but are not limited to, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium hydroxide, sodium hydroxide, potassium fluoride, and barium hydroxide. Solvents for these reactions include alcoholic solvents, water, or a mixture of alcoholic solvents and water. In one embodiment of step 2, the reaction is carried out in aqueous sodium hydroxide solution with di-t-butyl dicarbonate and 6 is isolated by extraction with ethyl acetate. A slight excess of Boc anhydride relative to intermediate 5 was found to be

advantageous for high yield; preferably it is present between 1.2 and 3.0 equivalents per each equivalent of intermediate 5. The preferred amount of Boc anhydride is 2 equivalents relative to intermediate 5.

Step three of this scheme involves the formation of the Weinreb amide 7.

The intermediate 6 from the previous reaction is treated with an agent to make the aryl group on intermediate 6 more active, such as a group converting the acid to an acid <BR> <BR> halide, e. g. , acid chloride or an ester orz other group which is capable of reacting with an amide (activating agent), followed by the addition of N-methoxy-N-methyl-amine hydrochloride with the appropriate base and in an appropriate solvent. Appropriate solvents for the reaction could be any homogenate hydrocarbons such as methylene chloride, dichlorobenzene, chlorobenzene, dichloroethane, or other inert solvents such as THF or toluene, and the like. Suitable bases include, but are not limited to, triethylamine, diisopropylethylamine, 2, 6-lutidine, N, N, N', N-tetramethylethylenediamine, potassium carbonate, sodium hydroxide, potassium hydroxide, and N-methylmorpholine. The carboxylic acid activating agents can be an alkyl chloroformate such as methyl or ethyl or isobutyl chloroformate. Those skilled in the art will appreciate that other activation agents such as acid chlorides or carbodiimides could also be employed.

For example, one embodiment of step 3 is carried out in methylene chloride as a solvent and N-methylmorpholine as a base and isobutyl chloroformate as the activating agent. The reaction is preferably started at-20° but is typically run at room temperature. The product 7 is isolated by extractive work up with suitable solvents, most preferably ethyl acetate.

Step four is displacement of this newly generated Weinreb amide 7 with <BR> <BR> phenylmagnesium halide, e. g. , chloride. The reaction is run under anhydrous conditions and an inert atmosphere. It is run in a suitable solvent for these types of reactions, which includes but is not limited to THF, methyl-THF, diethyl ether, diisopropyl ether, methyl- tert-butyl ether and toluene. Phenyl magnesium chloride was used, however, phenyl magnesium bromide or iodide can be used also.

To effect addition of the phenyl group to the Weinreb amide 7, it is preferred that at least three equivalents of the Grignard reagent are required as the substrate contains two acidic N-H groups. From 3-6 equivalents of the Grignard reagent is more preferred. In this embodiment, the more preferred amount is 4.0-4. 5 equivalents.

Addition of a solution of phenylmagnesium halide, e. g., phenylmagnesium chloride, to a solution of the amide 7 results in cyclization involving the 6-carbamate group and formation of the corresponding lactam in a major reaction pathway. The preferred mode of addition is an"inverse"addition where a solution of the amide 7 is added to excess Grignard reagent.

The addition of the Weinreb amide to the phenylmagnesium chloride is controlled in order to maintain an internal temperature between-20° and +5°C. The reaction is quenched with ice and acid and the product 8 is extracted and isolated in the usual fashion.

Although a variety of inert solvents can be used in the transformation of 7 to 8, the reaction conditions have to be carefully controlled. When the amide 7 was added as a solution in 1,2-dimethoxyethane, then a substantial amount of over addition, that is formation of the diphenylcarbinol, was observed. In this embodiment, THF is the preferred solvent for the Grignard addition step.

Step five involves the hydrogenation of this intermediate 8 to remove the Cbz protecting group followed by the immediate cyclization and reduction to form the product 1. This reaction is run in an appropriate solvent which includes but is not limited to alcohol solvents such as methanol, ethanol and isopropanol or inert solvents such as THF, methyl-THF, ethyl acetate, diisopropyl ether, methyl-tert-butyl ether, toluene, methylene chloride, and mixtures thereof. The preferred catalyst for this transformation is palladium on carbon; the preferred hydrogen pressure is between 50 and 200 psi, most preferably 150 psi. The catalyst loading is anywhere between 1-10 mole percent but preferably 5 mole percent. The preferred solvent is methanol.

Finally, the remaining protecting group is removed by techniques known in the art to afford a compound of Formula I. Although alternative methods could be used to deprotect the 8-amino group, hydrogenolysis allows the imine 9, which formed by the cyclization of the free 8-amino group when it has been unmasked and the carbonyl moiety, to be reduced under the same reaction conditions. Those skilled in the art appreciate that deprotection, cyclization to the imine and subsequent reduction might be accomplished as separate, discrete steps and that alternative reagents, such as sodium cyanoborohydride for the imine reduction, could be employed. Compared to related processes, as described above, the formation of the cis isomer as the major product is a novel outcome. When the 2-substituent is not phenyl, the analogous reaction provides the trans-product where the substituents are in equatorial dispositions. When a 2-aryl substituent is present, the conjugation of the imine allows enough face selectivity to be exerted by the bulky 3-nitrogen group so that reduction occurs from the least hindered face to give the cis-product.

The above-described process of the present invention achieves a significant advantage over previous approaches as resolution is avoided by the use of L- ornithine, a cheap, readily available member of the chiral pool. Formation of the diastereoisomers and enantiomer of the desired product 1 is minimized. Access to 1 by a

simple process allows access to a wide range of Substance P antagonists in optically pure form.

The examples that follow are intended as illustrations of certain preferred embodiments of the invention, and no limitation of the invention is implied.

EXAMPLES (a) 6-N-Cbz L-Ornithine 5 To a flask under air was added L-ornithine'HCI (4) (16.9g ; 100mmol) and 0. 5N NaOH (200mL; 1 OOmmol). To the resultant clear, colorless solution was added CuS045H2O (12. 5g ; 50. Ommol). After stirring for 15 min, K2C03 (13.8g ; 100mmol) was added followed by of Cbz-Cl (19mL ; 128mmol). After stirring for 3 h, the purple precipitate was collected and rinsed with MeOH (2 x 50mL). The purple precipitate was added to a solution containing of EDTA (14.6g ; 50. Ommol) in 0.25N NaOH (400mL ; 100mmol). The resultant slurry was heated to 95°C with vigorous stirring for 1 h then cooled to room temperature. The precipitate was collected and rinsed with H20 (2 x 100mL). After air-drying overnight, 22.6g (85% yield; typical yield is between 85-90%) of a pale blue solid as 5 was obtained and used without further purification.

(b) oc-N-Boc o-N-Cbz L-ornithine 6 To a flask under air was added 5 (22.6g ; 85. 0mmol) and 0. 5N NaOH (170mL ; 85mmol). A homogeneous solution was obtained after stirring for-5 min. To this solution was added MeOH (170mL) and Boc20 (37. 1g ; 170mmol). After stirring for 2 h, the white precipitate was filtered off and discarded and the solution was rotatory evaporated to remove MeOH. The resultant aqueous solution was washed with EtOAc (2 x 250mL). The pH of the aqueous solution was adjusted to-2 with conc. HCl then extracted with EtOAc (3 x 200mL). The organic phase was combined and washed with sat. NaCl (200mL). Heptane (100mL) was added to the organic phase. The organic solvent was removed via vacuum to give 21.3 g of the acid 6 (68% yield ; typical yield is between 68-85%) as a thick viscous oil and which was used without further purification.

'H-NMR (300 MHz, d6-DMSO) 5 7.23-7. 34 (m, 5H, Cru5), 7.16 (m, 1H, NHCO2R), 6.96 (d, 1H, J=8.0, NHCO2R), 4.97 (s, 2H, PhCH2), 3.81 (m, 1H, a-H), 2.95 (m, 2H, RCHNHCbz), 1.63 (m, 1H), 1.43-1. 53 (m, 3H), 1.41 (s, 9H, C (CH3) 3).

(c) Weinreb amide 7

To a flask under a nitrogen atmosphere was added the acid 6 (21. 3g ; 58. 2mmol) and CH2Clz (200mL). The reaction mixture was cooled using a salt/ice bath.

To the chilled reaction mixture was added N-methylmorpholine (NMM) (13. 3mL; 121mmol). After 15 min, i-BuOCOCI (8. 0mL ; 61. 5mmol) was added dropwise over 15 min, maintaining the internal temperature below-10°C, then the reaction mixture was maintained at-10°C for an additional 30 min. Me (OMe) NH*HCl (7.85g ; 80. 4mmol) was added. The reaction was allowed to warm to room temperature over 1 h and kept there for 3 h. The reaction mixture was poured into EtOAc (500mL) and washed successively with 2N HC1 (2 x 150mL), sat. NaHCO3 (2 x 150mL) and sat. NaCl (15mL). Heptane (200mL) was added and the solvent removal by a rotatory evaporator at 50°C, to give the Weinreb amide 7 (22.2 g; 93% yield; typical yield is between 79-93%) as a viscous oil.

'H-NMR (300 MHz, d6-DMSO) 5 7.24-7. 55 (m, 5H, Cru5), 7.16 (m, 1H, NHCO2R), 6.91 (d, 1H, J=8.0, NHCO2R), 4.97 (s, 2H, Ph2), 4.32 (m, 1H, a-H), 3.57 (s, 3H), 3.03 (s, 3H), 2.94 (m, 2H, RCH2NHCbz), 1.38-1. 48 (m, 4H), 1.33 (s, 9H, C (CH3) 3) (d) 5- (Benzoylcarbonylamino)-2S- (tert-butoxycarbonylamino)-l- phenylpentan-1-one 8 To a flask fitted with an addition funnel under a nitrogen atmosphere was placed 2M PhMgCl in THF (75mL 150mol) and anhydrous THF (50mL). The solution was cooled to 0°C by an ice bath. To the addition funnel was added the Weinreb amide 7 (11. 1 g ; 27. lmmol) in anhydrous THF (75mL). The THF solution of 7 was added dropwise to the Grignard solution over-30 min, maintaining the internal temperature between 3-4°C. After an additional 30 min, the reaction mixture was added to a slurry of ice (150g) and of 2N HC1 (150mL). The mixture was stirred for-5 minutes and then poured into i-PrOAc (600mL). The organic phase was washed with sat. NaCl (200mL).

The solvent was removed and the residue passed through silica gel using 1: 3 EtOAc/heptane. Following solvent strip, a viscous oil (8.52g) was obtained which was slurried in i-PrOAc (9mL) and heptane (8 lmL), heated to 90°C and then cooled to room temperature overnight with stirring. The white precipitate was collected, rinsed with heptane (2 x 20mL) and air dried to give the phenyl ketone 8 (7.72g ; 67% yield; typical yield is between 48-67%; >99% ee). DSC indicates that the enantiopure phenyl ketone 8 has a m. p. of 86°C.

'H-NMR (300 MHz, d6-DMSO) 5 7.95 (d, 2H, J=7.2, Ar-H), 7.62 (m, 1H, Ar-H), 7.52 (m, 2H, Ar-H), 7.24-7. 35 (m, 7H, C6H5), 5.00 (s, 2H, PhCH2), 4.93 (m, 1H, a-H), 3.00 (m, 2H, RCH2NHCbz), 1.68 (m, 1H), 1.52-1. 56 (m, 3H), 1.35 (s, 9H, C (C).

(e) (S, S)-Cis-2-Phenyl-3- (tert-butoxycarbonylamino) piperidine 1 To a 300-mL Parr reactor was added the phenyl ketone 8 (4.26g ; lO. Ommol), anhydrous MeOH (50mL) and 50% wet Englehard EscatlO 5% Pd/C (420mg; O. lOmmol ; 1 mol%). The glass liner was loaded into the reactor and stirred at 300 rpm. under150 psig of H2 at room temperature for 16 hours. The catalyst was filtered off and rinsed with MeOH (2x 50mL). The solvent was stripped by a rotatory evaporator and the crude product was passed through a plug of silica gel using 500mL of 5: 35: 60 NEt3/EtOAc/heptane. After solvent removal, 2.00 g (72% yield) of analytically pure 1 was obtained as a white solid.

'H-NMR (400 MHz, C6D6) 8 7.02-71. 8 (m, 5H, C6H5), 5.46 (d, 1H, J=8.9, NHBoc), 4.15 (m, 1H, CHNHBoc), 3.46 (d, 1H, J=2.0, CHPh), 2.68 (ddd, 1H, J=8.8, 2.0, 2.0), 2.27 (ddd, 1H, J=11. 3,11. 0,3. 0), 2.12 (m, 1H), 1.43-1. 62 (m, 3H), 1.37 (s, 9H, C (CH3) 3), 1.18 (m, 1H). A 20 mg sample was derivatized with (S)- (+)-l- (l-naphthyl) ethyl isocyanate for hplc analysis that showed the cis/trans ratio as 46: 1 (97.9 : 2.1) and the cis diastereoisomer to have an optical purity of 93% ee.