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1. NZ582668 - PREPARATION OF N-ALKYLATED OPIATES BY REDUCTIVE AMINATION

Note: Text based on automatic Optical Character Recognition processes. Please use the PDF version for legal matters

[ EN ]

PREPARATION OF N-ALKYLATED OPIATES BY REDUCTIVE A INATION

FIELD OF THE INVENTION

[00013 The present invention generally relates to processes for the synthesis of intermediates or end product morphinans, More specifically, the invention is directed to the synthesis of N-alkylated opiates by reductive amination using asymmetric hydrogen transfer.

BACKGROUND OF THE INVENTION

[0002] N-alkylated morphinans are important pharmaceuticals, typically used as analgesics, opiate agonists, and antagonists. With the increasing use of these agents, a practical and effective method of preparation of these compounds is vital to synthesizing diverse N-alkyl substituted morphinans.

[0003] There are three main methods for preparing N-alkylated morphinans. In a first method, the morphinan nitrogen is alkylated by a SN2 methodology using an alkyl halide (or other appropriate leaving group) in the presence of a base. Normally, mixtures of mono and dialkylated morphinans are obtained. The dialkyiated morphinan typically results from over-alkylation on the nitrogen atom. In the case of opiates having a 3-phenolic group, aikylation of the 3-phenolic group also results. Complex isolations are normally employed to separate the mono-aikylated from the higher alkylated species. Accordingly, careful reaction conditions are necessary to prepare the mono-aikylated product in sufficient yield.

[0004] A second method for synthesizing N-alkylated morphinans consists of reductive aikylation. In this type of reaction, the free base of the amine is reacted with an aldehyde forming an imine or Schiff Base. Reduction of the Schiff Base is normally accomplished by the use of a hydride transfer agent. This methodology is generally known as "reductive aikylation". Normal reducing reagents for this reaction include borohydride reagents (e.g., sodium borohydride reagents, sodium cyanoborohydride), boranes, and aluminum hydride reagents {e.g., lithium aluminum hydride). See, for example, A.F. Abdel-Magid, et ai., Reductive Amination of Aldehydes and Ketones by Using Sodium Tnacetoxyborohydride, Tet. Lett. 31 (39), pp. 5595-98 (1990). These reagents need to be used in stoichiometric quantities to achieve complete reduction. Difficulties resulting from this synthetic method include the release of boron or aluminum salts from the product. Improved procedures have utilized metal catalytic methodology to achieve this reduction. See, for example, WO 2006/035195 (N. Goodwin, et al.). Hydrogen gas in the presence of a transition metal catalyst has aiso been used to achieve this reduction.

[0005] A third method for preparation of N-alkylated morphinans consists of an acylation reduction methodology. Typically, in this synthetic process, the amine is reacted with an acyl equivalent, then reduced using boranes or main group hydride species (e.g. lithium aluminum hydride). Careful control of reaction conditions must be observed to prevent hydrolysis of the acyl equivalent.

[0006] Thus, a need remains for a quick and effective synthetic method for the preparation of N-alkylated morphinans resulting in high yields

[0006a] A reference herein to a patent document or other matter which is given as prior art is not to be taken as an admission that that document or matter was, in New Zealand, known or that the information it contains was part of the common general knowledge as at the priority date of any of the claims.

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SUMMARY OF THE INVENTION

[0007] Among the various aspects of the present invention is the provision of a process for the preparation of N-alkylated morphinans. In particular, an N-imine moiety or a hemiaminal moiety of a morphinan is reduced in the presence of a ruthenium, rhodium, or iridium asymmetric catalyst and a hydrogen source. The resulting N-alkylated morphinan may then be derivatized, if desired, in one or more additional steps to form other morphinans.

[0008] Briefly, therefore, the present invention is directed to a process for the preparation of a N-alkylated morphinan (II) having the formula


the process comprising reducing an N-imine morphinan or a hemiaminal moiety of a morphinan in the presence of a ruthenium, rhodium, or iridium asymmetric catalyst and a hydrogen source, the N-imine morphinan or the hemiaminal morphinan {I} having the formula:


Ri is hydrogen, hydrocarbyl, substituted hydrocarbyl, halo, or -ORm

R2 is hydrogen, hydrocarbyl, substituted hydrocarbyl, halo, or -OR2n

R3 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or -~OR3» ;

RG is hydrogen, hydrocarbyl, substituted hydrocarbyl, or -ORen

R? is hydrogen, hydrocarbyl, substituted hydrocarbyl, or -OR?n ;

Rs is hydrogen, hydrocarbyl, substituted hydrocarbyl, or -OF½;

Ri is hydrogen or hydroxy;

Rii i is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group; R211 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group; R311 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group; Re is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group; R711 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group; Rai 1 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group; Z, is >NCH(OH)(R9) or >N*=CH(R9);

Z2 is >NCH2(R9); and

Rg is hydrogen, acyl, hydrocarbyl, substituted hydrocarbyl, or heterocyclo.

[0008a] The present invention is also directed to a process for the preparation of a N-ai morphinan (II) having the formula


the process comprising reducing an N-imine morphinan or hemiaminal morphinan in the presence of a ruthenium, rhodium, or iridium asymmetric cataiyst and a hydrogen source, the N-imine morphinan or hemiaminal morphinan (I) having the formula;


wherein

Ri is hydrogen, hydrocarbyl, substituted hydrocarbyl, halo, or -ORm;

R2 is hydrogen, hydrocarbyl, substituted hydrocarbyl, halo, or ~OR2n;

R3 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or -OR3n ;

F¾ is hydrogen, hydrocarby!, substituted hydrocarbyl, or -ORen

R7 is hydrogen, hydrocarbyi, substituted hydrocarbyl, or -OR7n;

Re is hydrogen, hydrocarbyl, substituted hydrocarbyi, or -ORen;

Ru is hydrogen or hydroxy;

Riii is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group;

R211 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group;

R311 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group;

Ren is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group;

R711 is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group;

Ren is hydrogen, hydrocarbyl, substituted hydrocarbyl, or a hydroxy protecting group;

Zi is >NCH(OH)( 9) or >N*=CH(R9);

Z2 is >NCH2(R9); and

Rg is hydrogen, acyl, hydrocarbyl, substituted hydrocarbyl, or heterocycio.

[0009] Other aspects and features will be in part apparent and in part pointed out hereinafter.

DETAILED DESCRIPTION OF THE INVENTION

[0010] The present invention is directed to improved synthetic methods for the preparation of

N-alkylated morphinans, salts, intermediates, and analogs thereof. In one aspect of the present invention, the synthetic methods utiiize a ruthenium, rhodium, or iridium asymmetric homogeneous catalyst and a hydrogen source to reduce an N-imine moiety or a hemiaminal moiety of a morphinan (sometimes collectively referred to herein as the "N-imine/hemiaminal morphinan") to the corresponding alkyi group.

Morphinan Compounds

[0011] For purpose of discussion, the ring atoms of the morphinans of the present invention are numbered as follows. And within the core morphinan structure, there may be four chiral carbons, i.e., C-5, C-13, C-14, and C-9.


[0012] Further, for purposes of illustration, in relevant part, the N-imine and the hemiaminal moieties of the morphinans of the present invention correspond to Formulae (la) and (ib), respectively:


N-imine morphinan hemiaminal morphinan

[0013] In addition, as used herein, the symbol ">" is used in conjunction with the imine nitrogen atom and the hemiaminal nitrogen atom to represent the two covalent bonds that bind the nitrogen atom to the morphinan.

[0014] in one embodiment of the present invention, the morphinan corresponds to Formula

{la}, where Rg is hydrogen, or substituted or unsubststuted Ci-s aikyl, C^ alkenyl, aryl, heterocyclo or acyl.

Typical acyl groups include, but are not limited to, esters, amides, and carbamates. The optical activity, with respect to the rotation of polarized light, of the morphinan having Formula (la) may be (+} or (-). Furthermore, the configuration of the chiral carbons, C-5, C-13, C-14, and C-9, respectively, of the Formula (la) compound may be RRRR, RRSR, RRRS, RRSS, RSRR, RSSR, RSRS, RSSS, SRRR, SRSR, SRRS, SRSS, SSRR, SSSR, SSRS, or SSSS, provided that the C-15 and the C-16 carbons are both either on the alpha face of the molecule or the beta face of the molecule.

[0015] In one example of this embodiment, 9 is hydrogen, Ch alky!, C^ alkenyl, aryl, heterocyclo, ester, amide, or carbamate. In a more restrictive example, Rg is hydrogen, methyl, ethyl, propyl, cyclopropyl, cyciopropylmethyl, butyl, isobutyl, t-butyl, cyclobutyl, cyclobutylmethyl, methy!carbonyi, ethylcarbonyl, propylcarbonyl, cyctopropyicarbonyl, butylcarbonyi, isobutylcarbonyl, cyclobutylcarbonyl, or allyl; preferably, hydrogen, methyl, ethyl, cyclopropyl or cyclobutyl. In one preferred example, Rg is cyclopropyl. In another preferred example, R9 is cyclobutyl.

[0016] In another embodiment, the morphinan corresponds to Formula (lb) wherein Z¾ is

>NCH(OH)( Rg) where Rg is hydrogen, or substituted or unsubstituted C1-8 alkyl, C^ alkenyl, aryl, heterocyclo or acyl. Typical acyl groups include, but are not limited to, esters, amides, and carbamates. The optical activity of the morphinan having Formula (lb) may be (+) or (-). In embodiments in which Rg is hydrogen or hydroxy, the configuration of the chiral carbons, C-5, C-13, C-14, and C-9, respectively, may be RRRR, RRSR, RRRS, RRSS, RSRR, RSSR, RSRS, RSSS, SRRR, SRSR, SRRS, SRSS, SSRR, SSSR, SSRS, or SSSS, provided that the C-15 and the C-16 carbons are both either on the alpha face of the molecule or the beta face of the molecule. In embodiments in which Rg is not hydrogen or hydroxy, the carbon (C-18) attached to N-17 is also chiral, and thus, the configuration of C-5, C-13, C-14, C-9, and C-18, respectively, may be RRRRR, RRRRS, RRSRR, RRSRS, RRRSR, RRRSS, RRSSR, RRSSS, RSRRR, RSRRS, RSSRR, RSSRS, RSRSR, RSRSS, RSSSR, RSSSS,

SRRRR, SRRRS, SRSRR, SRSRS, SRRSR, SRRSS, SRSSR, SRSSS, SSRRR, SSRRS, SSSRR, SSSRS, SSRSR, SSRSS, SSSSR, or SSSSS, provided that the C-15 and the C-16 carbons are both either on the alpha face of the molecule or the beta face of the molecule.

[001 7] In one example of this embodiment, Rg is hydrogen, Ch alky!, C2-8 alkenyl, aryl, heterocyclo, ester, amide, or carbamate, In a more restrictive example, Rg is hydrogen, methyl, ethyl, propyl, cyclopropyl, cyclopropylmethyl, butyl, isobutyl, t-butyl, cyclobutyl, cyclobutylmet yl, methylcarbonyl, ethylcarbonyl, propylcarbonyl, cyclopropylcarbonyl, butylcarbonyl, isobutylcarbonyl, cyclobutylcarbonyl, or allyl; preferably, hydrogen, methyl, ethyl, cyclopropyl or cyclobutyl. In one preferred example, Rg is cyclopropyl. In another preferred example, R is cyclobutyl.

[0018] For any of the above embodiments where the N-imine/hemiaminai morphinan corresponds to Formula (I} and Zi is >NCH(OH){ Rg) or >l\ CH(Rg), R3 is typically -OR311 where R311 is hydrogen, alkyl, acyl, alkary!, aryl, or a hydroxy protecting group. In one example of this embodiment, R311 is hydrogen, CLS alkyl, aryl, C1.8 alky]-C(0}-, aryl-C(O)-, Ci-s alkyl-OC(O)-, or aryl-OC(0}-. In another example, R311 is hydrogen or Ch alky!; preferably hydrogen or methyl. In a preferred example, R311 is hydrogen.

[0019] In one embodiment in which the morphinan corresponds to Formula (I), RG is hydrogen, or substituted or unsubstituted Ci-e alkyl, C2-a alkenyl, phenyl, or -ORen. In one example of this embodiment, Re is -ORen where Ren is C1-8 alkyl, CMalkenyl, hydrogen or a hydroxy protecting group. In a more restrictive example, Ren is methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, isobutyl, t-butyl, cyclobutyl, hydrogen, or a hydroxy protecting group; preferably, methyl, ethyl, hydrogen, or a hydroxy protecting group; more preferably, hydrogen or a hydroxy protecting group.

[0020] In another embodiment in which the morphinan corresponds to Formula (I), Ri, R2,

Re, R7, and e are hydrogen. In an alternative embodiment, at least one of Ri, R2, R6, R7, and Rs is other than hydrogen; for example, R\ may be hydrocarbyl, halo, or -ORm where Rm is hydrogen, alkyl, acyl, alkaryi, aryl, or a hydroxy protecting group. In another example, R7 is a substituted hydrocarbyl group; for example, 3,3-dimethylbutan-2-ol.

[0021] When a morphinan corresponding to Formula (i) is reduced in the presence of a ruthenium, rhodium, or iridium asymmetric catalyst and a hydrogen source in accordance with the process of the present invention, the resulting morphinan corresponds to Formula (!l):


wherein Ri, R2, R3, R6, R?, Rs, nt and R1 are as previously defined for Formula (I) and I2 is >NCH2(Rg). The optical activity of the morphinan having Formula (il) may be (+) or (-), and the configuration of the chiraf carbons, C-5, C-13, C-14, and C-9, respectively, may be RRRR, RRSR, RRRS, RRSS, RSRR, RSSR, RSRS, RSSS, SRRR, SRSR, SRRS, SRSS, SSRR, SSSR, SSRS, or SSSS, provided that the C-15 and the C-16 carbons are both either on the alpha face of the molecule or the beta face of the molecule.

[0022] Exemplary morphinan (li) products include buprenorphine, 6-ketainaltrexone, nalmefene, nalbuphine, and diprenorphine:


Buprenorphine 6-Ketalnaltrexone


Nalbuphine Diprenorphine

Ruthenium, Rhodium! or iridium Asymmetric Catalysts

[0023] Generally, the ruthenium, rhodium, or iridium asymmetric catalyst of the present invention facilitate reductions of the hemiaminal (Zi = >NCH(OH)( F¾}) and/or the i ine (Zi = >N*=CH(R9}) moieties. In general, these asymmetric catalysts comprise (a) a metal source consisting of a ruthenium complex, a rhodium complex, an iridium complex, or a combination thereof and (b) one or more chiral ligands. Typically, the ratio of metal to chiral ligand is about 1 :1. In one example, the metal source is a ruthenium complex or a rhodium complex. In another example, the metal source is dichloro(arene)Ru(ll) dimer,

dichloro(pentamethylcyclopentadienyl)Rh(li) dimer, BINAP-Ru (II) diacetate, BINAP-Ru (I!) dichloride, BINAP-Ru (II) dibromide, BINAP-Ru (II) diiodide, [RuCI((R or S)BINAP)(C6H6)]CI, or

dich!oro(pentamethylcyclopentadienyl)iridium (III) dimer.

[0024] Typically, the asymmetric catalysts of the present invention comprise ruthenium, rhodium, iridium, or a combination thereof complexed with bidentate, chiral ligands using nitrogen, oxygen, or phosphorous donor atoms as more fully described in, for example, US 5,693,820 {Helmchen et al.) and R. Noyori et al., Asymmetric Catalysts by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones, Agew. Chem. Int. Ed. 2001 , 40, pp. 40-73. These catalysts are sometimes referred to as Noyori catalysts. In one example, the chiral ligand of the present asymmetric catalysts corresponds to Formulae (670), (680), (690), or (700}


670 680 690 700

wherein R^i, Rs72, Rs73, Rcsi, f½, Re92> R?oi, and R702 are independently a!kyl or aryl and wherein Rm and R&2 of Formula (690) and R701 and R702 of Formula (700), and the carbon atoms to which they are attached, may optionally form a cyclic or bicyclic compound. In the above structures, the "*" indicates a chiral carbon atom. The configuration of the chiral carbons of the asymmetric catalyst may be RR, RS, SR, or SS.

[0025] In one embodiment, the ligand corresponds to Formula (670) and Rm and Rm are each phenyl and Re i is aryl. In another example of this embodiment, Re7i is tolyl, mesityl, or naphthyi, In an alternative embodiment, the ligand corresponds to Formula (680) and Re&i is tolyl, mesityl, 2,4,6-triisopropylphenyl, or naphthyi. In another example, the ligand corresponds to Formula (690) and R691 and R692 are hydrogen thus forming the compound, aminoethanol. In an alternative example, the ligand corresponds to Formula (690) and Regi and R692 are selected to form the following compound:

In another embodiment, the ligand corresponds to Formula (700) and R701 and R702 are hydrogen thus forming the compound, ethylenediamine.

[0026] In a preferred example, the ligand is (1 S,2S)-{+)-N-4-toluenesulfony!-1 ,2-diphenylethylene-1 ,2-diamine, (1 R,2R)-(-)-N -toluenesulfonyl-1 ,2~diphenylethy!ene-1 ,2-diamine, dl-N-tosyl-1 ,2-diphenylethylenediamine, N-tosyl-1 ,2-diphenylethylenediamine, N-tosyl-1 ,2-ethylenediamine, or N-tosyl-1 ,2-diaminocyclohexane.

[0027] Examples of active ruthenium and rhodium asymmetric catalysts of the present invention include the following;


Chemical Formula: C20H29CI 2O2RUS Chemical Formula: C32H37ClN202RuS Chemical Formula: C24H35CIN2O2 Exact Mass: 498.1 Exact Mass: 650.1 Exact Mass: 552.1 Molecular Weight: 498 Moiecular Weight: 650.2 Molecular Weight: 552.1

Hydrogen Source

[0028] The hydrogen source of the present process is any hydrogen source known to those skilled in the art. Methods of hydrogenation include in situ hydrogen transfer and high-pressure hydrogenation. In one example, the hydrogen source is hydrogen gas. To accomplish the reduction using this source, however, special reactors are required. On a preparative scale, this poses safety challenges. An alternative to hydrogen gas is producing hydrogen in situ through hydrogen transfer methods. By producing the hydrogen source in situ, the pressures of standard hydrogenations (sometimes at 50 atms H2) are avoided, thereby allowing for a safer preparation environment. Further, these reactions tend to be very mild. For example, using the hydrogen transfer methodology described, functional groups such as esters, amides, ethers, alkenes, and hydroxyls remain intact throughout the process.

[0029] Generally, the hydrogen source for the process of the present invention is selected from isopropanol, formic acid, organic or inorganic salts of formic acid, or a combination thereof. In some instances, a smail amount of base may be used to activate the catalyst, For example, in isopropanol, KOH is often used as an activator, in other examples, triethylamine may be used. In one example, the hydrogen source comprises an organic or inorganic salt of formic acid, preferably, the triethylamine salt of formic acid. In a preferred example, the hydrogen source is about a 5:2 mixture of formic acid to triethylamine.

Solvent

[0030] Typically, the solvent for the process of the present invention is selected from a nitrile

(e.g., acetonitrile, propionnitrile), tetrahydrofuran (THF), an alcohol (e.g., methanol, ethanol, etc.), a halocarbon {e.g., a chloroalkyl such as dichloromethane, chloroform, 1 ,2-dichloroethane, or tetrachloroethyiene), dimethylformamide (DIV1F), dimethylacetamide (DMAc), N-methyl pyrrolidinone (NMP), an alkyl acetate (e.g., ethyl acetate or propyl acetate), toluene, water, or a combination thereof. In a more restrictive example, the solvent is acetonitrile, DMAc or a combination of acetonitrile and methanol.

[0031] Generally, the reaction of the present invention can be conducted at a temperature range from ambient temperature (~20°C) to about 120°C. in one example, the reaction is carried out at temperature range of about OX to about 80°C, preferably from about room temperature to about 40°C.

Imine/Hemiaminal Formation

[0032] Typically, the N-imine morphinan and the hemiaminal morphinan of the present invention are synthesized by reacting a nor-morphinan with an aldehyde having the formula, F¾CHO, as shown below:


where Ri, f¾ f¾, Re, 7, Re, Rg and Ru, are as previously defined for morphinans corresponding to Formula (I). Upon formation, the N-imine morphinan (!a) and the hemiaminal morphinan (lb) form an equilibrium, The aldehyde is typically introduced in an amount ranging from about 1 ,0 to about 1.25 equivalents of aldehyde per equivalent of nor-morphinan. The solvent system for this step typically comprises an organic solvent, such as methanol, acetonitrile, toluene, ethyl acetate or a combination thereof. This reaction may be carried out, for

Page I I

example, at a temperature range of about room temperature (25 °C) to about reflux. Preferably, the reaction is carried out at about room temperature (25 °C) over a period of about 1 to about 5 hours, typically about 3 hours. An azeotropic distillation step may be added to increase the reaction rate of imine formation.

Formation of the N-alkviated Morphinan

[0033] Once the formation of the N-imine morphinan (la) and the hemiaminal morphinan (lb) is complete, the synthesis of the N-alkylated morphinan (II) can occur according to the following reaction scheme:

[0034] Typically, for this type of reaction, the N-imine morphinan (la) and the hemiaminal morphinan (lb) are in equilibrium. When treated with a ruthenium, rhodium, or iridium asymmetric catalyst and a hydrogen source, as described herein, the N-imine moiety is converted to the corresponding tertiary amino group and the hydroxy group of the hemiaminal moiety is removed thereby forming the N-alkylated morphinan product (H). Without being bound to any particular theory, it is believed that the product (II) is predominantly, if not entirely, formed from the N-imine morphinan (la), it may be that the reduction of the N-imine morphinan to the product, coupled with the equilibrium formed with the hemiaminal morphinan, is the driving force behind the reaction. That is, the more N-imine morphinan is reduced to product, the more hemiaminal morphinan converts to the N-imine morphinan to maintain balance in the equilibrium. Sufficient evidence for this theory, however, is lacking. It is known, that when the mixture of N-imine and hemiaminal morphinans is reacted with a ruthenium, rhodium, or iridium asymmetric catalyst and a hydrogen source, the end product forms in high yield.

[0035] Generally, for the reduction of morphinans (ia) and (lb) to the product (l!), the substrate to solvent ratio is from about 1 :2 to about 1 :20, preferably about 1 :4 to about 1 :5. The hydrogen source can be any of those previously discussed. In one preferred example, the hydrogen source is 1 to 5 equivalents of a 2:5 mixture of triethyiamine to formic acid ( Et.3/HC02H), plus an additional equivalent to form a salt with the morphinan nitrogen, which increases solubility of the morphinan. Other salts that may be used include the methanesulfonate, acetate, and hydrochloride salt. These salts, however, may react at a slower rate. The catalyst is generally loaded at about a 1/50 to about a 1/1000 loading ratio on a molar basis. Typically, this reaction occurs in a temperature range of about room temperature to about 40°C. The more dilute the solvent, the longer the reaction time at room temperature.

[0036] In another typical example, the product {II) is further reacted to form the desired morphinan. For example, the product (II) may be reacted with an acid (e.g., formic acid) to remove a protecting group.

DEFINITIONS

[0037] The compounds described herein may have asymmetric centers. Compounds of the present invention containing an asymmetrically substituted atom may be isolated in optically active or racemic form. Cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomeric form is specifically indicated. All processes used to prepare compounds of the present invention and intermediates made therein are considered to be part of the present invention.

[0038] The term "acyl," as used herein alone or as part of another group, denotes the moiety formed by removal of the hydroxy group from the group COOH of an organic carboxylic acid, e.g., RC(O)-, wherein R is R , RiO, RiRjN-, or RiS~, Ri is hydrocarbyl, heterosubstituted hydrocarbyl, or heterocyclo, and R2 is hydrogen, hydrocarbyl or substituted hydrocarbyi.

[0039] The term "acyloxy," as used herein alone or as part of another group, denotes an acyl group as described above bonded through an oxygen linkage (O), e.g., RC(0)0- wherein R is as defined in connection with the term "acyl."

[0040] The term "alkyl" as used herein describes groups which are preferably lower aikyl containing from one to eight carbon atoms in the principal chain and up to 20 carbon atoms. They may be straight or branched chain or cyclic and include methyl, ethyl, propyl, isopropyl, butyl, hexyl and the like,

[0041] The term "alkenyl" as used herein describes groups which are preferably lower alkenyl containing from two to eight carbon atoms in the principal chain and up to 20 carbon atoms. They may be straight or branched chain or cyclic and include ethenyl, propenyl, isopropenyl, butenyl, isobutenyl, hexeny!, and the like.

[0042] The term "alkynyl" as used herein describes groups which are preferably lower alkynyl containing from two to eight carbon atoms in the principal chain and up to 20 carbon atoms. They may be straight or branched chain and include ethyny!, propynyi, butynyl, isobutynyl, hexynyl, and the like.

[0043] The term "aromatic" as used herein alone or as part of another group denotes optionally substituted homo- or heterocyclic aromatic groups. These aromatic groups are preferably monocyclic, bicyclic, or tricyclic groups containing from 6 to 14 atoms in the ring portion. The term "aromatic" encompasses the "aryl" and "heteroaryl" groups defined below.

[0044] The term "aryl" or "Ar" as used herein alone or as part of another group denote optionally substituted homocyclic aromatic groups, preferably monocyclic or bicyciic groups containing from 6 to 12 carbons in the ring portion, such as phenyl, biphenyl, naphthyl, substituted phenyl, substituted biphenyl or substituted naphthyl. Phenyl and substituted phenyl are the more preferred aryl.

[0045] The terms "halogen" or "halo" as used herein alone or as part of another group refer to chlorine, bromine, fluorine, and iodine.

[0046] The term "heteroatom" shall mean atoms other than carbon and hydrogen.

[0047] The terms "heterocycio" or "heterocyclic" as used herein alone or as part of another group denote optionally substituted, fuliy saturated or unsaturated, monocyclic or bicyciic, aromatic or non-aromatic groups having at least one heteroatom in at least one ring, and preferably 5 or 6 atoms in each ring. The heterocycio group preferably has 1 or 2 oxygen atoms and/or 1 to 4 nitrogen atoms in the ring, and is bonded to the remainder of the molecule through a carbon or heteroatom. Exemplary heterocycio groups include heteroaromatics as described below. Exemplary substituents include one or more of the following groups: hydrocarbyl, substituted hydrocarbyl, hydroxy, protected hydroxy, acyl, acyloxy, alkoxy, alkenoxy, alkynoxy, aryloxy, halogen, amido, amino, cyano, ketals, acetals, esters and ethers.

[0048] The term "heteroaryl" as used herein alone or as part of another group denote optionally substituted aromatic groups having at least one heteroatom in at least one ring, and preferably 5 or 6 atoms in each ring. The heteroaryl group preferably has 1 or 2 oxygen atoms and/or 1 to 4 nitrogen atoms in the ring, and is bonded to the remainder of the molecule through a carbon. Exemplary heteroaryls include furyi, benzofuryl, oxazolyl, isoxazolyl, oxadiazolyl, benzoxazolyl, benzoxadiazolyl, pyrrolyl, pyrazoiyl, imidazolyl, triazolyl, tetrazolyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, indolyl, isoindolyl, indolizinyi, benzimidazolyl, indazoiyi, benzotriazolyl, tetrazolopyridazinyl, carbazolyl, purinyl, quinolinyl, isoquinolinyl, imidazopyridyl and the like. Exemplary substituents include one or more of the following groups: hydrocarbyl, substituted hydrocarbyl,

hydroxy, protected hydroxy, acyl, acyloxy, alkoxy, aikenoxy, alkynoxy, aryloxy, halogen, amido, amino, cyano, ketals, acetals, esters and ethers.

[0049] The terms "hydrocarbon" and "hydrocarbyl" as used herein describe organic compounds or radicals consisting exclusively of the elements carbon and hydrogen. These moieties include alkyl, alkenyl, alkynyl, and aryi moieties. These moieties also include alkyl, alkenyl, alkynyl, and aryl moieties substituted with other aliphatic or cyclic hydrocarbon groups, such as alkaryl, alkenaryl and alkynaryi. Unless otherwise indicated, these moieties preferably comprise 1 to 20 carbon atoms.

[0050] The term "hydroxy protecting group" as used herein denote a group capable of protecting a free hydroxy group ("protected hydroxy") which, subsequent to the reaction for which protection is employed, may be removed without disturbing the remainder of the molecule. Exemplary hydroxy protecting groups include ethers (e.g., ally!, triphenylmethyl (trityl or Tr), benzyl, p-methoxybenzyl (PMB), p-methoxyphenyi (PMP)), acetals (e.g., methoxymethyl (MOM), β-methoxyethoxymethyl (MEM), tetrahydropyranyl (THP), ethoxy ethyl (EE), methylthiomethyl (MTM), 2-methoxy-2-propyl (MOP), 2-trimethylsilyle!hoxymethyl (SEM)), esters (e.g., benzoate (Bz), ally I carbonate, 2,2,2-trichloroethyl carbonate (Troc), 2-trimethylsilylethyl carbonate), silyl ethers (e.g., trimethylsilyl (TMS), Iriethylsilyl (TES), triisopropylsilyl (TIPS), triphenylsi!yl (TPS), t-butyldimethylsilyl (TBDMS), t-butyldiphenylsilyl (TBDPS) and the like. A variety of protecting groups for the hydroxy group and the synthesis thereof may be found in "Protective Groups in Organic Synthesis" by T.W. Greene and P.G.M. Wuts, John Wiley & Sons, 1999,

[0051] The "substituted hydrocarbyl" moieties described herein are hydrocarbyl moieties which are substituted with at least one atom other than carbon, including moieties in which a carbon chain atom is substituted with a hetero atom such as nitrogen, oxygen, silicon, phosphorous, boron, sulfur, or a halogen atom. These substituents include halogen, heterocyclo, alkoxy, aikenoxy, aryloxy, hydroxy, protected hydroxy, acyl, acyioxy, nitro, amino, amido, nitro, cyano, ketals, acetals, esters and ethers.

[0052] When introducing elements of the present invention or the preferred embodiments(s) thereof, the articles "a", "an", "the" and "said" are intended to mean that there are one or more of the elements. The terms "comprising", "including" and "having" are intended to be inclusive and mean that there may be additional elements other than the listed elements.

[0053] Having described the invention in detail, it will be apparent that modifications and variations are possible without departing from the scope of the invention defined in the appended claims.

EXAMPLES

[0054] The following non-limiting examples are provided to further illustrate the present invention.

Example 1 : Synthesis of Buprenorphine

[0055] The overall synthesis of buprenorphine from NOR-buprenorphine is depicted in the following reaction scheme:

[0056] NOR-Buprenorphine (3.67 g, 8.87 mmol) was added to acetonitrile (30 mL),

Cyclopropanecarboxaldehyde (1.25 g, 17.84 mmoi} was added and the slurry stirred for 1 hour at room temperature. At that time, a 5 to 2 mixture of 98% formic acid/ triethylamine [prepared by adding 98% formic acid (5.34 g, 1 16 mmol) to triethylamine (4.70 g, 46,4 mmol)] in 10 mL of acetonitrile was added. Dichloro(p-cymene)ruthenium (II) dimer (27 mg) was added followed by (1 S, 2S)-(+)-N-tosyl-diphenylethylenediamine (32 mg). The reaction was purged by nitrogen gas for 30 minutes and became homogeneous after this time. A steady flow of nitrogen was allowed to pass over the reaction. The reaction was stirred for 36 hours at room temperature. Evaporation of the mixture produced a thick oil (5.34 g}. 10 mL acetonitrile was added and stirred at room temperature for 1 hour, and a precipitate formed. The precipitate was removed by filtration and washed with 5 mL cold (5°C) acetonitrile. The precipitate was dried yielding the title product (3.66 g, 88.5% yield). HPLC analysis indicated 99.02 %

buprenorphine.

Example 2: Synthesis of Naltrexone from Noroxymorphone

[0057] The overall synthesis of naltrexone from noroxymorphone is depicted in the following reaction scheme:


Chemical Formula: C^H^ Oj Chemical Formula: CieH2 N05 Chemical Formula:

Exact Mass: 287.1 Exact Mass: 331.1 Exact Mass: 401.2 Molecular Weight: 287.3 Molecufar Weight: 331.4 Molecular Weight: 401.5


Chemica! Formula: C20H23NO,j

Exact Mass: 341.2 Chemical Formula: C22H27N0s Chemical Formula: C22H2(SN05+ Molecular Weight: 341.4 Exact Mass: 385,2 Exact Mass: 384.2

Molecular Weight: 385.5 Molecular Weight: 384.4

Naltrexone


6-ketalnoroxymorphone

[0058] Noroxymorphone (3.30 g, 11.5 mmole) was slurried with ethylene glycol (14.26 g, 230 mmol, 12.85 mL). Meihanesulfonic acid (2.21 g, 23.0 mmol, 1.49 mL) was then added dropwise. The reaction was allowed to stir overnight (16 h) at room temperature. Thers, the reaction was poured slowly into 29% NH3/ H;0 (50 mL) and stirred for 2 hours at room temperature where a white precipitate appeared. 6-Ketal Noroxymorphone (3.75g, 98.5% yield) was isolated by filtration of the reaction mixture, washing the solid with distilled water (50 mL), and drying under reduced pressure (48 h, 25°C, 1 torr). HPLC analysis indicated 99.0% 6-ketalnoroxymorphone.