The present invention relates" to the separation of enantiomers, i.e., those isomers in which the arrangement of atoms or groups is such that the two c molecules are not superimposable. The invention more particularly relates to a high performance chiral selector useful, for example, as a chiral stationary phase (CSP) in liquid chromatographic separation of enantiomers. _ _Q Stereoisomers are those molecules which differ from each other only in the way their atoms are oriented in space. Stereoisomers are generally classified as diastereomers or enantiomers; the latter embracing those which are mirror-images of each other, the former being

- _j c those which are not. The particular arrangement of atoms that characterize a particular stereσisomer is known as its optical configuration, specified by known sequencing rules as, for example, either + or - (also D or L) and/or R or S.

2 _Q Though differing only in orientation, the practical effects of stereoisomerism are important. For example, the biological and pharmaceutical activities of many compounds are strongly influenced by the particular configuration involved. Indeed, many compounds are only

_?l ~ of widespread utility when employed in a given stereoisomeric form.

Living organisms usually produce only one enantiomer of a pair. Thus only (-)-2-methyl-l-butanol is formed in yeast fermentation of starches; only (+)-

„ _n lactic acid is formed in the contraction of muscle; fruit juices contain only (-)-malic acid, and only (-)-

35

1 quinine is obtained from the cinchona tree. In biological systems, stereochemical specificity is the rule rather than the exception, since the catalytic enzymes, which are so important in such systems, are

5 optically active. For example, the sugar (+)-glucose plays an important role in animal metabolism and is the basic raw material in the fermentation industry; however, its optical counterpart, or antipode, (-)- glucose, is neither metabolized by animals nor fermented

10 by yeasts. Other examples in this regard include the mold Penicilliu glaucum, which will only consume the (+)-enantiomer of the enantio eric mixture of tartaric acid, leaving the (-)-enantio er intact. Also, only one stereoisomer of chloromycetin is an antibiotic; and (+)- _. 5 ephedrine not only does not have any drug activity, but it interferes with the drug activity of its antipode. Finally, in the world of essences, the enantiomer (-)- carvone provides oil of spearmint with its distinctive odor, while its optical counterpart (+)-carvone provides

20 the essence of caraway.

Accordingly, it is desirable and oftentimes essential to separate stereoisomers in order to obtain the useful version of a compound that is optically active. 5 Separation in this regard is generally not a problem when diastereomers are involved: diastereomers have different physical properties, such as melting points, boiling points, solubilities in a given solvent, densities, refractive indices etc. Hence, diastereomers are normally separated from one another by conventional

35

methods, such as fractional distillation, fractional crystallization or chromatography.

Enantiomers, on the other hand, present a special problem because their physical properties are identical. Thus they cannot as a rule —and especially so when in the form of a racemic mixture-- be separated by ordinary methods: not by fractional distillation, because their boiling points are identical; not by conventional crystallization because (unless the solvent is optically active) their solubilities are identical; not by conventional chromatography because (unless the adsorbent is optically active) they are held equally onto the adsorbent. The problem of separating enantiomers is further exacerbated by the fact that conventional synthetic techniques almost always produce a mixture of enantiomers. When a mixture comprises equal amounts of enantiomers having opposite optical configurations, it is called a racemate; separation of a racemate into its respective enantiomers is generally known as a resolution, and is a process of considerable importance.

Various techniques for separating enantiomers are known. Most, however, are directed to small, analytical quantities, meaning that other drawbacks aside, when 5 applied to preparative scale amounts (the milligram to kilogram range) a loss of resolution occurs. Hand separation, the oldest method of resolution, is not only impractical but can almost never be used since racemates seldom form mixtures of crystals recognizable as mirror _Q images.

5

Another method, known as indirect separation, involves the conversion of a mixture ^" of enantiomers —the racemate— into a mixture of diastereomers. The conversion is accomplished by reacting the enantiomers with an optically pure derivatizing agent. The resultant diastereomers are then separated from one another by taking advantage of their different physical properties. Once separated by, for example, fractional crystallization, or more commonly, chromatography, the diastereomers are re-converted back into the corresponding enantiomers, which are now optically pure. Though achieving the requisite separation, the indirect method suffers in that it is time consuming and can require large quantities of optically pure derivatizing agent which can be expensive and is oftentimes not recoverable. Moreover, the de-derivatizing step may itself result in racemization thus defeating the purpose of the separation earlier achieved.

A more current method that avoids some of the drawbacks attendant the indirect method is known as the direct method of separation. The direct method, much like the indirect method, involves the formation of a diastereomeric species. However, unlike the indirect method, this species is transient, with the stability of 5 one species differing from the other.

In one application of the direct method, as disclosed, e.g., in copending and commonly assigned U.S. Patent Application Serial No. 528,007, filed May 23, 1990, now U.S. Patent No. 5,080,795 the contents of _Q which are incorporated herein by reference, enantiomers of compounds such as amino acids, amino esters,

5

alcohols, amines, sulfonic acid or derivatives thereof are separated by means of a liquid membrane that contains a chiral carrier, such as the derivatized amino acid (S)-N-(l-naphthyl)leucine octadecyl ester. The chiral carrier is capable of forming a stable complex with one of the enantiomeric configurations. The liquid membrane is located on one side of a semi-permeable barrier and the mixture of enantiomers is located on the other side of the barrier. The liquid membrane containing the chiral carrier impregnates the semi- permeable barrier under conditions effective to permit or cause a stable complex between the chiral carrier and one of the enantiomeric configurations to form in the barrier. The liquid membrane containing the stable complex is passed to a second location where the conditions are effective to dissociate the stable complex, thus allowing the recovery of the complex- forming enantiomer to take place. In one embodiment of this application, a hollow membrane fiber membrane is employed as the semi-permeable barrier.

In another, more common application of the direct method, the mixture of enantiomers is allowed to interact with a chiral stationary phase as resides, e.g., in a chromatographic column. The enantiomer that interacts more strongly with the chiral stationary phase will have a longer residence time in the column; hence, a separation of enantiomers will occur. Further, when the mode of interaction with the chiral stationary phase can be characterized, the elution order can be _Q predicted.

5

1 Examples of chiral stationary phases include those based upon (L)-N-(3,5-dinitrobenzoyl)leucine, which is useful in separating enantiomers of N-aryl derivatized amino acids and esters, and those based upon

5 (D-N-(l-naphthyl)leucine which has been effectively used to separate N-(3,5-dinitrobenzoyl) derivatized amino compounds. High performance liquid chromatographic (HPLC) columns packed with silica-bonded CSP\'s of a variety of π-electron acceptors and π- 0 electron donors —including derivatives of phenylglycine, leucine, naphthylalanine and naphthylleucine are commercially available from Regis Chemical Company, Morton Grove, Illinois.

Other examples of chiral stationary phases used

15 in the direct separation of enantiomers include, e.g., that based upon N-(3,5-dinitrobenzoyl)-α-amino-2,2- dimethγl-4-pentenyl phosphonate, as particularly described in copending and commonly assigned U.S. Patent Application Serial No. 761,212, filed on September 17,

20 1991, which is useful in separating enantiomers of β- amino alcohol compounds, such as β-blockers; and that based upon 4-(3,5-dinitrobenzoyl)amino-3-(undec-10- enyl)-l,2,3,4-tetrahydrophrenanthrene, as particular described in copending and commonly assigned U.S. Patent

2 Application Serial No. 763,043, filed September 20,

1991, which is useful in separating enantiomers of non- steroidal anti-inflammatory agents, such as naprσxen.

While these efforts indicate that there is a wide variety of useful chiral selectors available, there _Q nevertheless continues to be a pressing need for chiral selectors having analytical and, importantly.

35

preparative scale applicability over a broad range of enantiomeric compounds, especially chiral selectors that evince decreased retention and increased selectivity so as to provide improved qualitative separations of these compounds.

The present invention is directed to a high performance chiral selector that represents an improvement in the art of enantiomeric separation. The chiral selector of the present invention is designed to eliminate adsorption sites that are superfluous to the chiral recognition process, thus affording increased enantioselectivity and when employed in a liquid chromatographic column, decreased retention.

The chiral selector of the present invention is a compound having the formula:

O 0

Ar-(C II)„-(NH)„-(CR-.R ₂ )-CII-N-R ₃

I

R. wherein

Ar is a monocyclic or ortho-fused polyσyclic aromatic moiety having up to 10 ring carbon atoms, either of which may be unsubstituted or substituted with one or more C _α to C _e alkyl, C^ to C ₆ alkoxy, nitro (N0 ₂ ), N(R ₅ )a, CN, COOR ₆ , S0 ₃ H and COR _v groups wherein R _s , R ₆ and R-7 are each independently hydrogen or C _x to C ₆ alkyl;

Ε. and R ₂ are each independently hydrogen, C to C ₆ alkyl or phenyl;

R ₃ and R ₄ are each independently C _α to C _{1 Z} alkyl or C_, to C ₁₂ alkenyl; and

m and n are each independently 0 or 1, said compound being an R or an S enantiomer or a mixture of R and S enantiomers.

In one embodiment of the subject invention, the chiral selector is employed in a process of separating enantiomers of compounds wherein said compounds have first and second optical configuration, which comprises contacting a mixture of said enantiomers with the chiral selector described above, said selector being an R or S enantiomer, under conditions effective to form a complex between an enantiomer of said compound having said first optical configuration and said chiral selector, and recovering the non-complexed enantiomer of said compound having said second optical configuration. Examples of compounds whose enantiomers may be separated by the process of the present invention include alkyl carbameate derivatives of leucine 3,5-dimethylanilide; amides of 3,5-dinitrobenzoyl leucine; arylacetic acid compounds, including naproxen; β-amino alcohol compounds, including those known as β-blockers; and dinitrobenzoyl derivatives of various simple amines or -amino esters, among other compounds to which the present invention has applicability.

The present invention is also directed to an apparatus employing the chiral selector for purposes of enantiomeric separation or recognition. Apparatuses in this regard include, e.g., liquid chromatographic columns, such as high performance liquid chromatographic (HPLC) columns, enantioselective membrane transport _Q devices and liquid-liquid partitionum equipment, such as countercurrent chromatographic devices.

5

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a graph showing the normal phase separation of the enantiomers of a series of alkyl carbameate derivatives of leucine 3,5-dimethylanilide using a preferred chiral selector of the present invention as compared to a commercially available chiral selector.

Figure 2 is a graph showing the reverse phase separation of the enantiomers of a series of alkyl carbameate derivatives of leucine 3,5-dimethylanilide using a preferred chiral selector of the present invention as compared to a commercially available chiral selector.

Figure 3 is a graph showing the normal phase separation of the enantiomers of a series of alkyl carbameate derivatives of leucine 3,5-dimethylanilide and the influence thereon of tether length, number of tethers and the presence of a monofunctional silane linkage using several analogs of a preferred chiral selector of the present invention employed as a chiral stationary phase in a liquid chromatographic column. Figure 4 is a graph showing the reverse phase separation of the enantiomers of a series of alkyl carbameate derivatives of leucine 3 ,5-dimethylanilide and the influence thereon of tether length, number of tethers and the presence of a monofunctional silane linkage using several analogs of a preferred chiral selector of the present invention employed as a chiral stationary phase in a liguid chromatographic columns. The present invention relates to a high _Q performance chiral selector that exhibits improved

5

SUBSTITUTE SHEET

enantioselectivity over a broad spectrum of enantiomeric compounds.

In one aspect of the invention, the instant chiral selector is designed to eliminate adsorption sites that are either non-essential to the chiral recognition process or that are detrimental to the same. For example, in chromatographic applications known heretofore, a chiral selector is tethered to a support such as silica by means of an amide linkage that is derived from a primary amine. The resultant amide hydrogen in the connecting tether has now been found to be a potential interaction site which, under normal circumstances, plays no significant role in the chiral recognition process; it does, however, contribute to overall retention.

The chiral selector of the invention eliminates the presence of an amide hydrogen in the first instance, and thus eliminates the potential for any superfluous interaction caused by such a hydrogen. The chiral selector of the invention provides an amide linkage to a secondary, rather than a primary amine. By replacing the amide hydrogen with, e.g., an alkyl group, to thus generate a secondary amine the chiral selector of the invention, and chiral stationary phases (CSP\'s) made therefrom, generally show decreased retention and increased enantioselectivity in the separation of enantiomers.

The chiral selector of the invention is a compound having the formula:

0 0

Ar-(C II) _m -(NH)_,-(CR R ₂ ) ^• -CII-N-R ₃

I

R ₄

_ wherein 5

Ar is a monocyclic or ortho-fused polycyclic aromatic moiety having up to 10 ring carbon atoms, either of which may be unsubstituted or substituted with one or more C to C ₆ alkyl, C_. to C _β alkoxy, nitro

(N0 ₂ ), N(R ₅ ) ₃ , CN, COOR _e , S0 ₃ H and C0R-. groups wherein 0

R ₅ , R ₆ and R ₇ are each independently hydrogen or C _x to

C _G alkyl.

A preferred monocyclic aromatic moiety is phenyl; preferred ortho-fused polycyclic aromatic moieties include α-naphthyl and β-naphthyl. Preferred 5 substituents, when present, include one or more of C _x to C _e alkyl, preferably methyl; C-. to C ₆ alkoxy, preferably methoxy; and N0 ₂ .

As employed herein, the C_. to C _G alkyl groups may be in the normal or branched configuration and include, 0 e.g., methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, amyl, pentyl, hexyl and the like. The preferred Ci to C _e alkyl is C _x to C ₃ ; most preferred is methyl, C _x .

As employed herein, the C to C ₆ alkoxy groups 5 may be in the normal or branched configuration and include, e.g., methoxy, ethoxy, propoxy, butoxy, pentoxy, hexoxy and the like. The preferred C _x to C _e alkoxy has 3 carbon atoms. The most preferred alkoxy is methoxy. 0

5

Examples of preferred substituted aromatic moieties include 3,5-dinitrophenyl, 6-methoxy-3-naphthyl and 6,7-dimethyl-α-naphthyl.

In the chiral selector having the formula described above, R _x and R ₂ are each independently hydrogen, C _x to C ₆ alkyl, aryl, aralkyl or alkaryl.

As employed herein, the aryl groups are aromatic rings containing 6 to 10 ring carbon atoms. Preferred aryl groups include monocyclic or ortho-fused polycyclic aromatics, such as phenyl, α-naphthyl and β-naphthyl.

The aralkyl groups contain up to 16 carbon atoms with each aryl group containing from 6 to 10 carbon atoms, and each alkyl group containing up to 6 carbon atoms which may be in the branched or normal configuration. Preferably, each aryl group contains up to 6 carbon atoms and each alkyl group contains 1 to 3 carbon atoms. A particularly preferred aralkyl in benzyl.

The alkaryl groups contain up to 16 carbon atoms with each alkyl group containing up to 6 carbon atoms which may be in the normal or branched configuration, and each aryl group containing from 6 to 10 carbon atoms. Preferably, each alkyl group contains 1 to 3 carbon atoms and each aryl group contains up to 6 carbon atoms. A particularly preferred alkaryl is tolyl.

In preferred embodiments, R _x is hydrogen and R ₂ is C _x to C _e alkyl or aryl. Examples of particularly preferred C _x to C _e alkyls in this embodiment include methyl and isobutyl. A particularly preferred aryl in _Q this embodiment is phenyl.

5

R ₃ and R ₄ are each independently C _x to C _X2 alkyl or C ₂ to C _X2 alkenyl. The C _x to C _X2 alkyl groups may be in the normal or branched configuration and include, e.g., methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butγl, amyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl and the like. The C ₂ to C _X2 alkenyl groups may be in the normal or branched configuration. Preferable C ₂ to C _x2 alkenyls include ethenyl, 2- propenyl, 3-butenyl, 4-pentenyl, 5-hexenyl, 6-heptenyl, 7-octenyl, 8-nonenyl, 9-decenyl and 10-undecenyl.

The subscripts m and n in the formula defined above are each independently 0 or 1; preferably, m and n are each 1 when Ar is a monocyclic aromatic moiety, and m is 0 when Ar is a ortho-fused polycyclic aromatic moiety.

In a first embodiment of the present invention, Ar is phenyl substituted with one or more N0 ₂ groups, R _x is hydrogen and m and n are each 1. In one aspect of this first embodiment R ₃ and R_» are each independently C _x to C ₃ alkyl or C ₂ to C _β alkenyl. In a preferred configuration of this aspect of the first embodiment, denoted hereinafter as CS-4, Ar is 3,5-dinitrophenyl, R ₂ is isobutyl, R ₃ is 2-propenyl and R is methyl. The structure of CS-4 is shown below:

CS-4

In a second preferred configuration of this one aspect, denoted hereinafter as CS-4A, ^" Ar is 3,5- dinitrophenyl, R ₂ is phenyl, R ₃ is 2-propenyl and R ₄ is methyl. The structure of CS-4A is shown below, with phenyl denoted as Ph.

In a second embodiment of the present invention, Ar is unsubstituted α-naphthyl or B-naphthyl, R _x is hydrogen, m is 0 and n is 1. In one aspect of this second embodiment, R ₃ is C ₂ to C _X2 alkenyl and R ₄ is C _x to C ₃ alkyl. In a preferred configuration of this aspect of the second embodiment, denoted hereinafter as CS-9, Ar is unsubstituted β-naphthyl, R ₂ is methyl, R ₃ is 10-undecenyl and R ₄ is methyl. The structure of CS-9 is shown below.

In a second preferred configuration of this _Q aspect of the second embodiment, denoted hereinafter as CS-9A, Ar is unsubstituted β-naphthyl, R ₂ is isobutyl.

5

R ₃ is 10-undecenyl and R ₄ is methyl. The structure of CS-9A is shown below.

In a third embodiment of the present invention, Ar is α-naphthyl or B-naphthyl substituted with one or more lower alkoxy groups, R _α is hydrogen, and and n are each 0. In one aspect of this third embodiment, R _; is C ₂ to C _x2 alkenyl and R_, is C _x to C ₉ alkyl. In a preferred configuration of this aspect of the third embodiment, denoted hereinafter as CS-11, Ar is 7- methoxy-3-naphthyl, R ₂ is methyl, R ₃ is 2-propenyl and R ₄ is methyl. The structure of CS-11 is shown below.

In a second preferred configuration of this aspect of the third embodiment, denoted hereinafter as CS-12, Ar is a 7-methoxy-3-naphthyl, R ₂ is methyl, R ₃ is 10-undecenyl, and R ₄ is n-octyl. The structure of CS-12 is shown below.

CS-12

In a fourth embodiment of the present invention, Ar is phenyl substituted with one or more N0 ₂ groups, R ₂ is hydrogen and m and n are each 1. In one aspect of this fourth embodiment, denoted hereinafter as CS-7, Ar is 3,5-dinitrophenyl, R ₂ is isobutyl and R ₃ and R ₄ are each 2-propenyl. The structure of CS-7 is shown below.

In a second aspect of this fourth embodiment, denoted hereinafter as CS-7A, Ar is 3,5-dinitrophenyl, R ₂ is phenyl and R ₃ and R ₄ are each propenyl. The structure of CS-7 is shown below.

5

In a fifth embodiment of the present invention,

Ar is unsubstituted α-naphthyl or B-naphthyl, R _x is hydrogen, m is 0 and n is 1. In one aspect of this fifth embodiment, R ₃ and R ₄ are each C ₂ to C _e alkenyl. _Q In a preferred configuration of this aspect of the fifth embodiment, denoted hereinafter as CS-7B, Ar is

5

unsubstituted α-naphthyl, R ₂ is methyl and R ₃ and R ₄ are each 2-propenyl. The structure of CS-7B is shown below.

CS-7B

In a second preferred configuration of the fifth embodiment, denoted hereinafter as CS-7C, Ar is unsubstituted α-naphthyl, R ₂ is isobutyl and R ₃ and R ₄ are each 2-propenyl. The structure of CS-7C is shown below.

5 CS-7C

In a sixth embodiment of the present invention, Ar is phenyl substituted with one or more N0 ₂ groups, R _x is hydrogen and m and n are each 1. In one aspect of _Q this sixth embodiment R ₃ is C _v to C _x2 alkenyl and R ₄ is C _x to C _a alkyl. In a preferred configuration of this

5

aspect of the sixth embodiment, denoted hereinafter as CS-6, Ar is 3,5-dinitrophenyl, R ₂ is isobutyl, R ₃ is 10- undecenyl and R ₄ is methyl. The structure of CS-6 is shown below.

CS- 6

The chiral selectors of the present invention that are embodied above may be prepared by conventional chemical preparative techniques, as will be exemplified for CS-4, CS-6, CS-7, CS-9 and CS-11. One of skill in the art will readily appreciate the modifications necessary to prepare other chiral selectors within the scope of the chemical formula employed herein.

Enantiomeric separation using the chiral selector °f the invention may be achieved in a variety of techniques known in the art. In one embodiment in this regard, the chiral selector may form the active portion of the stationary phase in an HPLC column using techniques known in the art, such as hydrosilation followed by immobilization on a support effective for use in chromatographic separation. Supports useful in this regard include, e.g., silica and alumina.

Since the chiral selector of the invention is optically active, it is necessary to separate the chiral selector so that either the R or the S enantiomer of the chiral selector is employed as part of the stationary

phase in the column, the choice depending upon which of the enantiomers to be separated is to be preferentially bound to the chiral selector. In this embodiment, R ₃ must be alkenyl so as to permit the chiral selector to be immobilized on a support which is suitable for use in chromatographic applications. In one configuration, the chiral selector is immobilized by covalently bonding it to silanized silica.

Although a stationary phase formed using the chiral selector of the present invention may be prepared from multifunctional, e.g., trifunctional, silane precursors, it is preferred that the stationary phase be prepared using monofunctional silane precursors. The preference for using monofunctional silane precursors is because stationary phases derived from multifunctional silanes are, at least theoretically, more heterogenous than those derived from multifunctional silanes. This increased heterogeneous character is manifested by the fact that the bonding of a multifunctional silane, such ^{as a} trifunctional silane, to the silica surface can occur through one, two or three Si-O-Si linkages; additionally, polymerization of multifunctional silanes at the silica gel surface may occur. In contrast, a monofunctional silane can be bound to silica in only one manner; further, they are less reactive and can be easily purified chrσmatographically and readily characterized.

Thus in one aspect, the present invention relates to the utilization of the chiral selector of the invention in an HPLC stationary phase where said chiral selector is linked to the support material, such as

silica, through either a multifunctional or a monofunctional linkage, the monofunctional linkage is preferred. In another aspect, the present invention relates to an improvement to chromatographic columns of the type known heretofore; the improvement comprising the use of a monofunctional silane linkage to connect the active portions of the stationary phases employed in these columns, to a support material such as silica. A particular class of chromatographic columns to which this improvement especially relates are those of the type containing a derivative of a 3,5-dinitrobenzoyl amino acid or a derivative of a naphthyl amino acid. Examples of columns in this type that are those commercially available from Regis Chemical Company, Morton Grove, Illinois, and include columns whose stationary phases incorporate as an active part, 3,5- dinitrobenzoyl leucine; 3,5-dinitrobenzoyl phenylglycine; naphthylalanine; and naphthylleucine. The monofunctional linkage contemplated by the present invention, with silica (denoted herein as Si0 ₂ ) as the support, has the formula:

wherein R _β and R ₉ are each independently hydrogen or C _x to C _β alkyl, preferably methyl. Thus in the practice of the present invention, when R ₃ is alkenyl and R ₄ is alkyl or hydrogen, the terminal end of R ₃ , whereat the double bond is preferably located when R ₃ is alkenyl, attaches to the silicon of the above formula; when R ₃

and R ₄ are both alkenyl, than the monofunctional silane linkage contemplated by the invention has the formula:

wherein R _xo , ur Rι ₂ and R ₁₃ are each independently hydrogen or C _α to C _β alkyl; preferably methyl. In this embodiment, the terminal ends of R ₃ and R ₄ , whereat the double bonds are preferably located, will attach to the respective silicons of the above formula.

In another embodiment, the chiral selector of the invention may be utilized to effect separations employing semi-permeable membranes wherein the chiral selector forms part of a mobile phase. Such techniques include the use of semi-permeable membranes that are in the form of hollow fiber membranes. In this embodiment of the invention, it is preferred that R ₃ and R ₄ are alkyl, preferably a C _x to C ₆ alkyl. This is because it o is preferable that the terminal ends of R ₃ and R ₄ are each hydrogen so to minimize covalent bonding by the chiral selector. In one particularly useful embodiment in this regard, the chiral selector forms part of a liquid membrane passing on one side of a semi-permeable barrier with the enantiomers to be separated passing on the other side of the barrier. The pores of the barrier become impregnated with the liquid membrane containing the chiral selector. One of the enantiomers complexes with the chiral selector, passes through the barrier _Q into the moving liquid membrane and is conducted to a second location where disassociation takes place. This

5

technique is generally disclosed in commonly assigned U.S. Patent Application Serial No. 528,007, filed May 23, 1990, now U.S. Patent No. 5,080,795 the contents of which are incorporated herein by reference. The following examples are given to illustrate the scope of the invention. These examples are given for illustrative purposes, only, and the scope of the present invention should not be limited thereto.

EXAMPLES

A series of experiments was conducted to examine the performance of stationary phases formed in accordance with the present invention. Specifically, the chiral stationary bases formed in this regard utilized the chiral selector of the present invention wherein non-specific adsorption sites were eliminated. Multifunctional linkages to silica, as well as monofunctional linkages prepared in accordance with the present invention, were also evaluated in these experiments.

The chiral stationary phases that were evaluated in these experiments are shown in Table 1, below. As used herein, "Et" denotes "-C ₂ H ₅ " and "Me" denotes

" -CH ₃ " .

TABLE 1

SUBSTITUTE SHEET

Of the chiral stationary phases shown in Table 1, CSP-2, CSP-4, CSP-6, CSP-7, CSP-9, CSP-11 and CSP-12 were formed utilizing various embodiments of the chiral selector of the present invention. CSP-2 and CSP-11 were secured to a silica support using a conventional multifunctional linkage. CSP-4, CSP-6, CSP-9 and CSP-12 were secured to a silica support using a monofunctional linkage as contemplated by the present invention; CSP-7 was secured by both arms, R ₃ and R ₄ to a silica support using a monofunctional linkage in accordance with the present invention. CSP-3 was formed using a known chiral selector as an active portion; CSP-3 was, however, secured to a silica support using a monofunctional linkage of the type contemplated by the invention.

CSP-1, CSP-5 and CSP-8 were chiral stationary phases conventionally known and commercially available from Regis Chemical Company, Morton Grove, Illinois

MATERIALS AND APPARATUS ^In all ^of the following examples, the reagents used were of pharmaceutical or reagent grade and were used without further purification. Solvents used were HPLC grade or were distilled prior to use. Chromatographic analysis was performed using an Altex Model 100A pump, a Rheodyne Model 7125 injector with a 20 μL sample loop, a Linear UVIS 200 variable wavelength absorbance monitor, set at 254 nm, and a Hewlett-Packard HP 3394A integrating recorder. All chromatographic experiments were carried out at a nominal flow rate of 2.00 mL/min. unless otherwise indicated. In the normal phase mode, column void time was measured by injection

of tri-t-butyl benzene, a presumed unretained solute, as described by Pirkle, et al. in J. Liq. Chro atogr. , 14, 1, 1991, the contents of which are incorporated herein by reference. Solvents used were HPLC grade or were distilled prior to use. All ¹ H NMR spectra were recorded on a Varian XL 200 FT NMR spectrometer. ~E NMR chemical shifts are reported in ppm (δ) relative to tetramethylsilane. Dimethylchlorosilane, 3- aminopropyltriethoxysilane, and N-methyl-3- ammopropyltriethoxysilane, were obtained from Petrarch Systems, Inc., Bristol, PA. CSP-8 and Rexchrom 5μ, 100A silica gel were obtained from Regis Chemical Company, Morton Grove, Illinois. PREPARATION OF CSP-1 The synthetic route for the preparation of CSP-1, which may also be commercially obtained from Regis Chemical Corporation, Morton Grove, Illinois, is shown in Table 2, below.

TABLE 2

Synthetic route for preparation of CSP-1.

Preparation of 3,5-dinitrobenzoyl-(S)-leucine, (Table 2, Compound 14): (S)-Leucine (10 g) was suspended in 150 mL dry tetrahydrofuran and chilled in an ice bath while stirring under a nitrogen atmosphere. 3,5-Dinitrobenzoyl chloride (Table 2, Compound J3, 21 g) and propylene oxide (6.6 g) were added; the resulting

heterogeneous mixture became clear after several minutes. The mixture was allowed to ^\' stir for 5h, and was evaporated under reduced pressure to afford an oil which crystallized upon addition of 100 L of cold dichloromethane. Filtration and drying of the resulting crystals afforded 3,5-dinitrobenzoyl-(S)-leucine, 3^4, as a white solid (20.64 g, 83% yield). ^~ U NMR (200 MHz, d ₆ DMS0) δ: 0.95 (m,6H), 1.75 (M,3H), 4.25 (m,lH), 9.00 (t,lH), 9.17 (d,2H), 9.41 (d,lH). Preparation of 3-aminopropyl silica: Silica gel (5.0 g, Regis Rexchrom 5μ/100A) was placed in a 100 mL round bottom flask fitted with a boiling stick, Dean- Stark trap, and condenser. Benzene (50 mL) was added, and the mixture was heated at reflux for several hours. Dimethylformamide (1 mL) was then added to the benzene slurry, and the sample was evaporated to near dryness on a rotary evaporator. A dichloromethane solution of 3- aminopropyltriethoxysilane (1.0 g) was then added, and the resulting slurry was sonicated for several minutes, then evaporated to near dryness. The sample was again slurried in dichloromethane, sonicated, and evaporated to near dryness; this sequence was repeated several times to insure complete coverage of the silica gel. The nearly dry silica gel. - silane mixture was then heated with rocking on a Kύgelrohr distillation apparatus (120°C, 1 torr, 18h) . The silica gel was then slurried in ethanol, filtered through a fine sintered glass funnel, and washed repeatedly with methanol. The washed silica gel was then slurried in methanol and packed into a 4.6 mm I.D. x 25 cm length stainless steel HPLC column using an air driven Haskell pump operating

at about 9000 psi. Recovered excess stationary phase from the column packer was dried thoroughly under high vacuum; elemental analysis indicated a loading of 4.0 x 10 ^~4 moles of aminσpropyl groups per gram of stationary phase.

Preparation of the Stationary Phase, CSP-1: Acid, 1_4, (2.0 g) was suspended in 100 mL of dry tetrahydrofuran and stirred at 0°C. l-ethoxycarbonyl-2- ethoxy-1-quinolinecarboxylate (EEDQ, 2.0 g) was added, and the resulting mixture was stirred for 45 min. The mixture of activated acid thus obtained was pumped through a column containing the 3-aminopropyl silica, as prepared above, which had been equilibrated with tetrahydrofuran. The column was then sequentially eluted with methanol and then 20% 2-propanol in hexane. PREPARATION OF CSP-2

CSP-2, which contained a methyl group in place of the amide hydrogen of CSP-1, was formed using as an active portion, a chiral selector of the present invention. The active portion was secured to silica via a conventional multifunctional linkage. The synthetic route for the preparation of CSP-2 in this regard is shown in Table 3, below.

TABLE 3

Synthetic route for preparation of CSP-2

Preparation of N methyl 3-amiήopropyl silica: The preparation of N-methyl-3-aminopropyl silica followed the procedure reported for the preparation of 3-aminopropyl silica in CSP-1 supra except that N-methyl 3-ammopropyltriethoxysilane was used. Combustion analysis of residual silica removed from the column packer revealed a loading of 4.0 x 10 ^~4 moles of aminosilane per gram of stationary phase. Preparation of the Stationary Phase, CSP-2:

Preparation of the stationary phase, CSP-2, followed the procedure for the preparation of the stationary phase step in the preparation of CSP-1, supra. PREPARATION OF CSP-3 CSP-3 contained the commercially available chiral selector portion of CSP-1; however, CSP-3 was immobilized to silica by way of a monofunctional linkage in accordance with the present invention. The synthetic route for the preparation of CSP-3, the monofunctional silane analog of CSP-1 is shown in Table 4, below.

TABLE 4

Synthetic route for preparation of CSP-3 Preparation of the Allylamide (Table 4, Compound 17) : 3,5-dinitrobenzσyl-(S)-leucine, prepared as described in the procedure for CSP-1 supra, (5.0 g) was suspended in 100 mL of dry tetrahydrofuran and stirred at 0°C. l-Ethoxycarbonyl-2-ethoxy-l-quinoline-

carboxylate (EEDQ, 3.8 g) was added, and the resulting mixture was stirred for 45 min. Allylamine (0.88 g) was then added slowly via syringe, and the resulting solution was allowed to gradually warm to room temperature while stirring under a nitrogen atmosphere. After 8h the mixture was concentrate in vacuo, then purified by flash chromatography on silica using 2.5% methanol in dichloromethane to afford the allylamide, 17 (2.91 g, 52% yield). ^~ E NMR (200 MHz, CDC1 ₃ ) 6: 1.00 (m,6H), 1.90 (m,3H), 3.95 (m,2H), 4.79 (m,lH), 5.18 (m,2H), 5.81 (m,lH), 6.61 (t,lH), 8.76 (d,lH), 8.92 (s,2H), 9.08 (s,lH).

Preparation of the Organosilane (Table 4, Compound 18) : Allylamide prepared in the manner described above for Compound 17, Table 4, (3.82 g) was dissolved in 15 mL dichloromethane and 15 mL dimethylchlorosilane. Chloroplatinic acid (20 mg) dissolved in a minimum amount of 2-propanol was added, and the resulting mixture was refluxed with stirring under a nitrogen atmosphere. Progress of the reaction was monitored by disappearance of starting material in quenched reaction aliquots (quenching solution was composed of 5 mL of absolute ethanol, 5 mL triethylamine and 5 mL diethyl ether). The assay procedure consisted of removing several drops of reaction mixture, evaporating to dryness under high vacuum to remove excess dimethylchlorosilane and adding several drops of quenching solution. The mixture was then heated for several minutes on an oil bath, diluted with dichloromethane, and examined by TLC. After about 2h, TLC analysis of quenched reaction aliquots indicated

complete consumption of starting material. Residual dimethylchlorosilane was removed by three successive additions and evaporations of small portions of dichloromethane. The quenching solution was then added, and the resulting mixture was refluxed for 30 min. under a nitrogen atmosphere. The mixture was filtered to remove triethylamine hydrochloride and evaporated to afford the crude ethoxyorganσsilane which was purified by flash chromatography on silica using 10% acetonitrile in dichloromethane to afford the organosilane, 33, (3.97 g, 81% yield) as a tan powder. ¹ H NMR (200 MHz, CDC1 ₃ ) δ: 0.16 (s,6H), 0.61 (t,2H), 1.00 (m,6H), 1.21 (t,3H), 1.70 (m,5H), 3.30 (m,2H), 3.70 (q,2H), 4.62 (m,lH), 6.40 (t,lH), 8.20 (d,lH), 8.92 (d,2H), 9.14 (t,lH). Preparation of the Stationary Phase, CSP-3:

Silica gel (3.0 g, Regis Rexchrom, 5μ, lOOA) was placed in a 100 mL round bottom flask fitted with a boiling stick, Dean-Stark trap, and condenser. Benzene (35 mL) was added, and the mixture was heated at reflux for several hours. Dimethylformamide (1 mL) was then added to the benzene slurry, and the sample was evaporated to near dryness on a rotary evaporator. A dichloromethane solution of the organosilane 33 (0.77 g) was then added, and the resulting slurry was sonicated for several minutes, then evaporated to near dryness. The sample was again slurried in dichloromethane, sonicated, and evaporated to near dryness, this sequence being repeated several times to insure complete coverage of the silica gel. The nearly dry silica gel - silane mixture was then heated with rocking on a Kϋgelrohr distillation apparatus (120°C, 1 torr, 18h) . The silica gel was then

slurried in ethanol, filtered through a fine sintered glass funnel, and washed repeatedly with ethanol and then methanol. (Analysis of the ethanol washes by chiral HPLC revealed that the unbonded silane had undergone no decomposition or racemization during the course of the bonding reaction) . The washed silica gel was then slurried in methanol and packed into a 4.0 mm I.D. x 14.5 cm length stainless steel HPLC column using an air driven Haskell pump operating at about 9000 psi. Recovered excess stationary phase from the column packer was dried thoroughly under high vacuum; elemental analysis (C 5.46%) indicated a loading of 2.5 x 10"" ⁴ moles of selector per gram of stationary phase. Residual silanols on the chromatographic support were "endcapped" by passing a solution of 1 mL hexamethyldisilazane dissolved in 50 mL dichloromethane through the dichloromethane equilibrated column at a flow rate of 1 mL/min. The column was then sequentially eluted with dichloromethane, methanol and 20% 2-propanol in hexane.

PREPARATION OF CSP-4

The synthetic route for the preparation of CSP-4, which contained as an active portion, a chiral selector of the present invention, is shown in Table 5, below.

TABLE 5

Synthetic route for preparation of CSP-4

Preparation of the CS-4: 3,5-dinitrobenzoyl-(S)- leucine, prepared as described in the procedure for CSP- 1 supra (4.50 g) was dissolved in 100 mL dry tetrahydro- furan and stirred at 0°C under a nitrogen atmosphere. EEDQ (3.42 g) was added and the resulting solution was stirred for lh. N-Methyl allylamine (0.98 g) was added, and the reaction mixture was gradually allowed to warm to room temperature while stirring for 8h. The reaction mixture was then evaporated to dryness and purified by flash chromatography on silica using 4% acetonitrile in dichloromethane to afford CS-4 (2.72 g, 52% yield) as a white solid. ~E NMR (200 MHz, CDC1 ₃ ) δ: 1.02 (m,6H), 1.85 (m,3H), 3.06 (s) and 3.16 (s) (3H), 3.91 (dd) and 4.35 (dd) (2H), 4.11 (d,lH), 5.20 (m,2H), 5.85 (m,lH), 8.72 (bs,lH), 8.89 (m,2H), 9.11 (m,lH).

Preparation of the Organosilane (Table 5, Compound 20) : CS-4 (1.70 g) was converted to the corresponding organosilane, 2___\, using the hydrosilation procedure reported for the preparation of the organosilane, 18, in CSP-3 supra. Purification by flash chromatography on silica gel using 10% acetonitrile in dichloromethane afforded the organosilane 0 as a foam (790 mg, 36% yield). ^X H NMR (200 MHz, CDC1 ₃ ) δ: 0.18 (m,6H), 0.60 (m,2H), 1.01 (m,6H), 1.21 (m,3H), 1.55 (m,2H), 1.82 (m,3H), 3.07 (s) and 3.19 (s) (3H), 3.42 ( ) and 3.70 (m) (2H), 3.65 (m,2H), 5.15 (m,lH), 8.81 (m,2H), 9.01 (m,lH), 9.07 (m,lH).

Preparation of Stationary Phase, CSP-4: Bonding of the organosilane 2__Q (790 mg) to silica gel to afford CSP-4 followed the procedure reported for the

preparation of the stationary phase CSP-3 supra. Stationary phase removed from the column packer indicated (C 4.58%) a loading of 2.0 x 10" ^Λ moles of selector per gram of stationary phase. PREPARATION OF CSP-5

The synthetic route for the preparation of CSP-5, which may be commercially obtained from Regis Chemical Company, Morton Grove, Illinois, is shown in Table 6, below. TABLE 6

CSI\' J

Synthetic route for preparation of CSP-5 Preparation of amide 21 (Table 6): 10-undecen-l- oy chloride (50 g) was placed in a round bottom flask with 300 mL dichloromethane. Concentrated ammonium hydroxide solution (65 L) was then added, and the resulting solution was stirred vigorously for 2h. The two phase mixture was then separated using a separatory funnel. The organic layer was washed with water and then brine, then dried over anhydrous magnesium sulfate. Evaporation afforded amide 21 which was used without further purification or characterization, Preparation of amine 22 (Table 6): Amide 21 (6.2 g) was dissolved in 120 mL dry THF. LiAlH ₄ (2.0 g) was

SUBSTITUTESHEET

then added and the resulting mixture was refluxed for 2h under a nitrogen atmosphere. Excess LiAlH ₄ was then carefully quenched by addition of 200 mL of water. The resulting solution was extracted three times with 50 mL diethyl ether, the combined ether extracts were washed with brine, then dried over anhydrous magnesium sulfate. Evaporation of the ether layer afforded crude amine 2 which was used without further purification of characterization. Preparation of amide 23 (Table 6): 3,5- dinitrobenzoyl-(S)-leucine, prepared as described in the procedure for CSP-1 supra (5.0 g) was dissolved in 100 mL tetrahydrofuran and chilled with stirring on an ice bath. EEDQ (3.8 g) was added and the mixture was stirred under a nitrogen atmosphere for 45 min. Amine 22 (2.6 g) was then added via syringe and the resulting mixture was allowed to gradually warm to room temperature while stirring for 8h. The reaction mixture was then evaporated to dryness and purified by flash chromatography on silica using 2.5% methanol in dichloromethane to afford amide 2 . (4.5 g, 62% yield) as a white solid. -H NMR (200 MHz, CDC1 ₃ ) δ: 0.99 (m,6H), 1.30 (bs, 12H), 1.51 (m,2H), 1.80 (m,3H), 2.03 (m,2H), 3.19 (m,lH), 3.39 (m,lH), 4.64 (m,lH), 4.95 (m,2H), 5.81 (m,lH), 6.22 (m,2H), 8.42 (d,lH), 8.91 (s,2H), 9.12 (s,lH).

Preparation of the Organosilane 24 (Table 6): Amide 22_ (4.50 g) was converted to the corresponding organosilane 2Λ using the hydrosilylation procedure reported in the preparation of the organosilane 18 described in the procedure for CSP-3. Purification by

flash chromatography on silica gel using 5% acetonitrile in dichloromethane afforded the organosilane 24 (1.90 g, 35% yield) as a yellow waxy solid. ^•1 H NMR (200 MHz, CDC1 ₃ ) δ: 0.08 (s,6H), 0.58 ( ,211) , 0.99 (m,6H) _f 1.20 (t,3H), 1.30 (m,16H), 1.50 (m,2H), 1.75 (m,3H), 3.19 (m,lH), 3.39 (m,lH), 3.65 (q,2H), 4.64 (m,lH), 6.28 (bs,lH), 8.49 (bs,lH) _r 8.95 (. ^** ..2H), 9.10 (s,lH).

Preparation of the Stationary Phase CSP-5: Bonding of the organosilane 2 (1.90 g) to silica gel to afford CSP-5 followed the procedure reported for the preparation of the stationary phase CSP-3 supra. Stationary phase removed from the column packer indicated (c 5.89 ) a loadinq of 1.9 x lO ^-*1 moles of selector per gram of stationary phase. PREPARATION OF CSP-6

The synthetic route for the preparation of CSP-6, using a chiral selector, CS-6, of the present invention is shown in Table 7, below.

TABLE 7

csr*

Synthetic route for preparation of CSP-6

Preparation of amide 25 (Tab!? T± Λ ide 25 was prepared using a procedure analogous a the preparation

SUBSTITUTE SHEET

of amide 21 described in the procedure for CSP-5 supra, except that a 30% aqueous solution of methylamine was used in place of a concentrated ammonium hydroxide solution. Preparation of amine 26 (Table 7): Reduction of amide 2__ to afford amine 2jj followed the procedure described for the preparation of amine 22 as described for CSP-5 supra♦ A small amount of amine was purified by vacuum distillation with the product being obtained as a clear liquid 91° - 95°C at 0.1 torr.

Preparation of CS-6: 3,5-dinitrobenzoyl-(S)-leu¬ cine, prepared as described in the procedure for CSP-1 supra, (5.0 g) was dissolved in 100 mL tetrahydrofuran and chilled with stirring on an ice bath. EEDQ (3.8 g) was added and the mixture was stirred under a nitrogen atmosphere for 45 min. Amine 2jj (2.6 g) was added via syringe and the resulting mixture was allowed to gradually warm to room temperature while stirring for 8h. The reaction mixture was evaporated to dryness and purified by flash chromatography on silica using 2.5% methanol in dichloromethane to afford CS-6 (3.66 g, 49% yield) as a yellow oil. ^~ U NMR (200 MHz, CDC1 ₃ ) δ: 1.00 (m,6H), 1.30 (m,14H), 1.82 (m,3H), 2.03 (m,2H), 3.09 (s) and 3.19 (s) (3H), 3.81 (m,lH), 4.16 (m,lH), 4.98 (m,2H), 5.18 (m,lH), 5.80 (m,lH), 8.81 (d,lH), 8.86 (d,lH), 9.07 (m,lH).

Preparation of the Organosilane 28 (Table 7): CS-6 (3.00 g) was converted to the corresponding organosilane 2_B using the hydrosilylation procedure reported for the preparation of the organosilane 18 in CSP-3 supra. Purification by flash chromatography on

silica gel using 5% acetonitrile in dichloromethane afforded the organosilane 2 (0.68 g, ^\' 35% yield). ~H NMR (200 MHz, CDC1 ₃ ) δ: 0.10 (s,6H), 0.57 (m,2H), 0.99 (m,6H), 1.19 (t,3H), 1.30 (m,18H), 1.65 (m,3H), 2.99 (s) and 3.12 (s) (3H), 3.21 (m,2H), 3.68 (q,2H), 5.18 (m,lH), 7.73 (m,lH), 8.94 (m,2H), 9.16 (m,lH).

Preparation of Stationary Phase CSP-6: Bonding of the organosilane 8 (0.68 g) to silica gel to afford CSP-6 followed the procedure reported for the preparation of the stationary phase CSP-3 supra. Stationary phase removed from the column packer indicated (C 5.85%) a loading of 1.8 x 10 ^~4 moles of selector per gram of stationary phase. PREPARATION OF CSP-7 The synthetic route for the preparation of CSP-7, using a chiral selector, CS-7, of the present invention, both arms of which were immobilized to a silica support using a monofunctional linkage as contemplated by the present invention, is shown in Table 8, below. TABLE 8

Synthetic route for preparation of CSP-7: Preparation of CS-7: 3,5-dinitrobenzoyl-(S)-leu- cine, prepared as described in the procedure for CSP-1 supra (3.15 g) was dissolved in 100 mL of dry

tetrahydrofuran and chilled with stirring on an ice bath. EEDQ (2.39 g) was added and the mixture was stirred under a nitrogen atmosphere for 45 in. Diallylamine (0.94 g) was then added via syringe and the resulting mixture was allowed to gradually warm to room temperature while stirring for 8h. The reaction mixture was evaporated to dryness and purified by flash chromatography on silica using 1.5% methanol in dichloromethane to afford CS-7 (1.40 g, 36% yield) as a yellowish solid. -U NMR (200 MHz, CDC1 ₃ ) 6: 1.00 (m,6H), 1.85 (m,3H), 3.80 (m,lH), 4.03 (m,2H), 4.51 (m,lH), 5.12 (m,4H), 5.90 (m,2H), 8.90 (d,2H), 8.96 (d,2H), 9.10 (t,lH).

Preparation of the Organosilane 30 (Table 8): CS-7 (1.40 g) was converted to the corresponding organosilane 3_0 using the hydrosilylation procedure reported for the preparation of the organosilane 18 in CSP-3 supra♦ Purification by flash chromatography on silica gel using 5% acetonitrile in dichloromethane afforded the organosilane ^0 (1.32 g, 62% yield). ~E NMR (200 MHz, CDC1 ₃ ) δ: 0.10 (s,12H), 0.60 (m,4H), 0.99 (m,6H), 1.20 (m,6H), 1.42 (m,2H), 1.60 (m,2H), 1.80 (m,3H), 3.01 (m,lH), 3.30 (m,lH), 3.39 (m,lH), 3.70 (m,4H), 3.83 (m,lH), 5.15 (t,lH), 8.68 (d,lH), 8.82 (s,2H), 9.06 (s,lH).

Preparation of Stationary Phase CSP-7: Bonding of the organosilane 2 (0.60 g) to silica gel to afford CSP-7 followed the procedure reported for the preparation of stationary phase CSP-3 supra. Stationary phase removed from the column packer indicated (C 5.06%)

a loading of 1.8 x 10 ^~4 moles of selector per gram of stationary phase. PREPARATION OF CSP-9

The synthetic route for the preparation of CSP-9, using a chiral selector, CS-9, of the present invention is shown in Table 9, below.

TABLE 9

f ^* -(2-nFiplιlhyl)alιιnlne

Synthetic route for preparation of CSP-9 Preparation of Active Ester 31 (Table 9) : Race ic N-(2-naphthyl)alanine (17.1 g) was prepared according to the method described by Pirkle, et al. in J. Org. Chem. , 51, 102 (1986), the contents of which are incorporated herein by reference, and was placed in a round bottom flask fitted with a magnetic stirrer and a nitrogen inlet. Dimethylformamide (300 L) , N- hydrσxysuccinimide (9.15 g) and dicyclohexylcarbodiimide (18.0 g) were added and the reaction mixture was stirred for 8h at room temperature. Stirring was then discontinued, and precipitated dicyclσhexylurea (DCU) was allowed to aggregate. The reaction mixture was filtered and evaporated to dryness under reduced

SUBSTITUTE SHEET

pressure. The resulting red oily solid was purified by flash chromatography on silica to afford active ester 3_1 (21.0 g, 85% yield) as a pale yellow powder. ^X E NMR (200 MHz, CDC1 ₃ ) δ: 1.78 (d,3H), 2.77 (s,4H), 4.21 (d,lH), 4.59 (m,lH), 6.92 (m,2H), 7.23 (m,2H), 7.38 (m,lH), 6.78 (m,lH), 6.92 (m,lH), 7.20 (m,lH), 7.33 (m,lH), 7.65 (m,3H).

Preparation of CS-9: Racemic active ester 3L (3.0 g) was dissolved in 50 mL dimethylformamide and stirred at room temperature under a nitrogen atmosphere. Amine 2β , prepared as described int he procedure for CSP-6 supra (1.76 g) was added slowly via syringe and the resulting solution was stirred for lOh, then evaporated to dryness under reduced pressure. The crude product was purified by flash chromatography on silica using 10% acetonitrile in dichloromethane to afford CS-9 as a pale yellow solid (3.05 g, 84% yield). ~E NMR (200 MHz, CDC1 ₃ ) δ: 1.21 (bs,14H), 1.39 (d,3H), 2.00 (m,2H), 2.96 (s) and 3.06 (s) (3H), 3.40 (m,2H), 4.55 (1,1H), 4.96 (m,2H), 5.80 (m,lH), 6.78 (m,lH), 6.94 (m,lH), 7.20 (m,lH), 7.36 (m,lH), 7.69 (m,4H).

Chromatographic Resolution of the Enantiomers of CS-9: The enantiomers of CS-9 were preparatively resolved on a 2.5 cm I.D. x 90 cm length column containing (S) CSP 1 using a 2:1:7 mixture of 2- propanol/dichloromethane/hexane as mobile phase. The second eluting (S) enantiomer of CS-9 was obtained as a pale yellow solid (1.27 g, 85% recovery) which showed no traces of the minor enantiomer by HPLC analysis. Preparation of the (S)-Organosilane 33 (Table 9): The (S) enantiomer of CS-9 (0.98 g) was converted to the

corresponding organosilane 3J3 using the hydrosilylation procedure reported for the preparation of the organosilane 18 in CSP-3 supra. Purification by flash chromatography on silica gel using 20% acetonitrile in dichloromethane afford the (S) organosilane, 33 _^ . H NMR (200 MHz, CDC1 ₃ ) δ: 0.11 (s,6H), 0.58 (t,2H), 0.99 (t,3H), 1.26 (m,18H), 1.40 (d,3H), 2.96 (s) and 3.10 (s) (3H), 3.40 (m,2H), 3.66 (q,2H), 4.60 (m,lH), 6.76 (m,lH), 6.90 (m,2H), 7.16 (m,lH), 7.35 (m,lH), 7.69 (m,3H).

Preparation of Stationary Phase CSP-9: Bonding of the (S)-organosilane 3J3 to silica gel to afford CSP-9 followed the procedure reported for the preparation of stationary phase CSP-3 supra. Stationary phase removed from the column packer indicated (C 7.75%) a loading of 2.5 x 10 ^~4 moles of selector per gram of stationary phase.

Chromatographic Evaluation A homologous series of carbameate derivatives of amino acids were employed as analytes to evaluate the chromatographic performance of CSP\'s 1-7.

The analytes were derived from n-alkyl carbamate derivatives of the 3,5-dimethylanilide of leucine shown in Table 10, below.

TABLE 10

Leucine 3,5 Dimethylanilide Alkyl Carbamate Series, n = 1, 2, 4, 6, 8, 10, 12, 14.

The performance of CSP-1 and CSP-2 in chromatographically separating the enantiomers of the alkyl carbamate analytes of Table 10 is shown in Figure 1. As seen in Figure 1, the chromatographic separation faction, α, is greater on CSP-2 which utilized a chiral selector of the present invention, rather than the commercially available CSP-2; this was true even though CSP-2 was immobilized to silica via a multifunctional linkage. Further, CSP-2 was found to afford reduced retention and improved bandshapes for the separations shown in Figure 1.

A reversed-phase chromatographic analysis of leucine 3,5-dimethylanilide alkyl carbamate series of Table 10 was performed on CSP-1 and CSP-2; the results are shown in Figure 2. As seen from Figure 2, CSP-2, which utilizes, as an active portion, a chiral selector of the present invention, evinced superior chromatographic separation factors ,α, relative to commercially available CSP-1. Normal phase separation of the enantiomers of the leucine 3,5-dimethγlanilide alkyl carbamate series of

Table 10 was performed on CSP-3 and CSP-4, to compare the effect of a monofunctional linkage as contemplated by the present invention on a stationary phase that employs as an active portion a commercially available chiral selector (CSP-3), and on a chiral stationary phase formed from a chiral selector of the invention (CSP-4). The results are shown in Figure 3. As seen in Figure 3, the separation factor, α, afforded by CSP-4 was superior to that of CSP-3. Moreover, a comparison of the normal phase separation obtained by CSP-3, which used a conventional chiral selector but employed a monofunctional linkage of the present invention, to CSP- 1, as shown in Figure 1, which employed the same chiral selector as CSP-3 but which utilized the conventional multifunctional linkage, showed that the separation achieved by CSP-3 was greater than that of CSP-1.

Normal phase separation of the enantiomers of the leucine 3,5-dimethylanilide alkyl carbamate series of Table 10 was performed on CSP-5 and CSP-6 to investigate the effect of tether length on chromatographic behavior when a monofunctional linkage of the type contemplated by the present invention is used. CSP-5 employed the same commercially available chiral selector portion as CSP-1 and CSP-3, only CSP-5 was. immobilized to silica by way of an eleven carbon tether through a monofunctional linkage; CSP-6 utilized both a chiral selector and monofunctional linkage of the present invention, as well as an eleven carbon tether to silica. The results are shown in Figure 3. As shown in Figure 3, CSP-6 afforded greater separation than did CSP-5. Also as can be seen from Figure 3, CSP-3, which was analogous to CSP-5 but

for the fact that CSP-3 employed a three carbon tether as opposed to the eleven carbon tether of CSP-5, showed greater separation than CSP-5 which indicated that shorter tethers are preferable in the practice of the present invention.

Normal phase separation of the enantiomers of the leucine 3,5-dimethylanilide alkyl carbamate series of Table 10 was also performed on CSP-7, which utilized a chiral selector of the present invention which was immobilized to silica by two arms, each via monofunctional linkages of the invention. The results are shown in Figure 3. As can be seen in Figure 3, CSP- 7 showed superior separation, as compared with CSP-3 and CSP-5, each of which employed a conventional chiral selector portion. CSP-7 showed superior separation even though CSP-3 and CSP-5 both utilized a monofunctional linkage as contemplated by the invention.

A reversed-phase chromatographic analysis of the leucine 3,5-dimethylanilide alkyl carbamate series of Table 10 was performed with CSP-3, CSP-4, CSP-5, CSP-6 and CSP-7. The results are shown in Figure . As seen from Figure 4, the data obtained for the reversed phase separation using these CSP\'s are similar to that obtained for the normal phase separation shown in Figure 3. The performance of CSP-6, which contained an eleven carbon linkage to the silica support, was, however, no longer comparable to that of the other N-methylated CSP\'s, namely CSP-4 and CSP-7. The diminished separation factors observed for CSP-6 in this regard are believed to be a result of non-specific hydrophobic adsorption arising from the long chain of CSP-6, which result is

supported by the relatively long retention times observed for CSP-6.

Chromatographic separation of enantiomers of various 3,5-dinitrobenzoyl leucine amides was also conducted using the N-(2-naphthyl)alanine chiral stationary phase, CSP-8, as commercially available from Regis Chemical Company, Morton Grove, Illinois, and compared to the separation achieved using CSP-9, which utilized as an active portion, a chiral selector of the present invention, and which was immobilized to silica via a monofunctional linkage of the invention. The 3,5- dinitrobenzoyl leucine amides that were used and the results obtain are shown in Table 11, below.

TABLE 11

Separation of the enantiomers of three 3,5- dinitrobenzoyl leucine amides on CSP-8 and CSP-9. Conditions: flow rate = 2.0 mL/min. ; mobile phase = 20% 2-propanol in hexane.

As seen from Table 11, CSP-9 which utilized as an active portion a chiral selector of the present invention achieved superior separations in all cases than did CSP-8. In addition to showing increased enantioselectivity, CSP-9 may also show enhanced stability, especially in reversed-phase application; this is because amide linkages, as present in CSP-9, are known to be more stable toward hydrolytic cleavage than ester linkages, as present in CSP-8. Chromatographic separation of various 3,5- dinitrobenzoyl β-amino esters was conducted on CSP-11 and CSP-12 both formed in accordance with the present invention. The esters used and the conditions employed, are shown in Table 12, below. TABLE 12

CSP 11 CSP 12

Separation of the enantiomers of some 3,5-DNB β-amino esters on three naproxen-derived CSP\'s. Conditions: flow rate = 2.0 mL/min; mobile phase = 20% 2-propanol in hexane.

As seen from Table 12, excellent separation of these ester analytes was achieved with both CSP-11 and CSP-12 each of which employed as an active portion a chiral selector of the present invention, with CSP-12 further employing a monofunctional silane linkage as contemplated by the invention.