US 5,360,928 AGrant
Synthesis and Use of Amino Acid Fluorides as Peptide Coupling Reagents
Issue Date:1994-11-01
•58 Claims
Abstract
A compound of the formula ##STR1## or the acid fluoride salts thereof wherein BLK is an N-amino protecting group or hydrogen AA is an amino acid residue and X is H or a protecting group useful as a coupling agent in peptide synthesis.
Metadata
Assignee
- Research Corporation Technologies, Inc.
Inventors
- Louis A. Carpino
- Dean Sadat-Aalaee
Application Information
Application Number:US 4261216
Filing Date:1989-10-23
Priority Date:1989-10-23
Art Unit:181
Classifications
IPC:
C07C22900
Field of Search:
562560530548552553;840;849;8451;155;161;30334;335;337;338333.5;492;530144
Patent Drawings
This patent does not have any drawings.
Description
BACKGROUND OF THE DISCLOSURE
1. Field of the Invention
The present invention relates to novel amino acid fluorides and protected amino acid fluorides and their use in synthetic biochemistry, including peptide syntheses. More particularly, this invention is directed to the N-protected amino acid fluorides, and free amino acid fluorides and the hydrogen fluoride salts thereof, the side chain of which may be unprotected or protected with a blocking group and their use thereof in peptide synthesis.
2. Background of the Prior Art
As more and more polypeptides become of medicinal importance, there is an increasing incentive to improve the methods by which they may be synthesized. In recent years, peptides which have been found to be of possible pharmacological importance include those active against various diseases, such as cancers, diabetes, and plant toxins, etc. Others have shown specific activity as growth promoters or suppressants, antibiotics, insecticides, contraceptives, anti-hypertensives, sleep-inducers, anti-depressants, analgesics, etc. The list is long and varied.
Currently, syntheses of peptides in solution by classic or various repetitive methods or on a solid support (Merrifield) are popular techniques. Solution methods have the advantages of being easily monitored and allowing purification of intermediates, if necessary, at any stage. A major drawback is the relative slow pace of the synthesis with each step being carried out manually.
The major advantage of the Merrifield Method is its easy automation so that unattended, computer-controlled machine syntheses is possible. Unfortunately, this method suffers from an inherent deficiency due to the insoluble nature of the support on which the synthesis proceeds. Unless each acylation step occurs with 100% efficiency, mixtures will inevitably be built up on the polymer. The longer the chain, the greater will be the contamination due to undesired side reactions. Products produced in such reactions remain to contaminate the desired product when at the end of the cycle it is removed from the polymeric matrix. The properties of these peptides will not differ sufficiently for peptides of greater than about 30-40 residues to make efficient separation feasible.
For very long segments (50 or more amino acids), therefore, current methods are not satisfactory. Often mixtures are obtained of such forbidding complexity that it may be difficult or impossible to isolate the desired peptide.
The problems enumerated hereinabove could be eliminated if the proper derivatives of the underlying amino acids and the proper reaction conditions could be found.
For example, FMOC, (N.alpha.-(9-fluorenylmethyl)oxycarbonyl), protected amino acid chlorides, which are described by Carpino, et al. in J. Org. Chem. 51, 3732 (1986) have been used as acylating agent for stepwise peptide syntheses for both solution and solid phase techniques.
However, the amino acid chlorides have major drawbacks associated therewith. First, the acid chlorides react with trace amounts of water, such as moisture in the air, to give the corresponding amino acid. Therefore, they are not so stable, and as such, they are not a prime candidate for long term storage. Consequently, an objective was to find an amino acid derivative which was stable to moisture.
Moreover, another problem associated with amino acid chlorides is that it has not been possible to date to synthesize amino acid chlorides in which the protecting groups on the side chains of the amino acids can be removed under extremely mild conditions. As one skilled in the art is well aware, many of the amino acids have functional groups on the side chains which can interfere with peptide formation unless otherwise protected. In peptide synthesis, only the mildest conditions should be used to remove these protecting groups. For example, one of the easiest protecting groups to remove from the side chains containing amino, hydroxyl or carboxyl functions, such as lysine, tyrosine, threonine, serine, aspartic acid, glutamic acid and the like, is t-butyl or t-butyl containing moieties. For example, trifluoracetic acid can easily remove the t-butyl group from a serine side chain; on the other hand, a benzyl protecting group on the side chain can not be removed by said treatment but instead requires a more potent acid such as HF or trifluoromethanesulfonic acid. Therefore, the conditions for removing the benzyl group from the side chain are much harsher relative to the t-butyl groups. Furthermore, the mild catalytic hydrogenolysis of benzyl groups is not generally applicable to long chain peptides or resin attached peptides.
Although benzyl groups on the side chains of N-protected amino acid chloricles, can be prepared, such as FMOC-cysteine-S-benzyl chloride, FMOC-lysine- -carbobenzoxy chloride, FMOC-tyrosine-O-benzyl chloride, FMOC-serine-O-benzyl chloride and FMOC aspartic acid -benzyl ester, these molecules suffer from the disadvantages described hereinabove. Consequently, an investigation was commenced to determine if t-butyl or "t-butyl like" containing groups can be used to protect the side chain of amino acid chlorides. Unfortunately, efforts in this area were unsuccessful. None of the above compounds could be synthesized if the t-butyl group Was used in place of the benzyl substitution.
This was not unusual since it is well known that t-butyl-based protecting groups are readily deblocked by hydrogen chloride which is an inevitable by-product of acid chloride formation and/or long term storage (hydrolysis by trace amounts of water). For example, in the case of the FMOC-tyrosine derivative 1, the acid chloride could be obtained, but after several days it was noted to lose the t-butyl group slowly. ##STR2##
Furthermore, compound 1 as well as the analogous serine and threonine derivatives could be obtained only as oils which could not be crystallized and were therefore difficult, if not impossible, to purify.
In the case of the FMOC aspartic acid derivative 4, treatment with thionyl chloride gave only the aspartic acid anhydride 6, presumably via the unstable acid chloride 5 which undergoes intramolecular loss of t-butyl chloride. ##STR3## Lysine derivative 7 could not be converted to an acid chloride because of the marked sensitivity of the BOC function. ##STR4## Similar problems arise in the cases of Arg, His, Asn, Gln, and Trp. The net result of these problems is that only about one half of the commonly occurring amino acids can be converted to stable amino acid chlorides.
Therefore, a search was undertaken to find an amino acid candidate for use in peptide synthesis which is inexpensive, stable to moisture, and which shows great potential for long-term storage. Moreover, it was hoped that a candidate could be found where the protecting groups on the amino acid side chain could be removed under milder conditions then those used to remove the benzyl group. Preferably, it was hoped that a t-butyl containing group or a group as easily removable as t-butyl could be placed on the side chain of these amino acid candidates.
The present invention circumvents the difficulties experienced with respect to the acid chlorides and accomplishes the goals described hereinabove. The compounds of the present invention are effective in coupling with amino acids or peptides to form new peptide bonds. Moreover, the compounds of the present invention are more stable to moisture then the acid chlorides and therefore can be used for long term storage. Furthermore, t-butyl containing protecting groups and other protecting groups can be placed on the side chains of these amino acid compounds and removed under milder conditions than those required for the removal of benzyl groups. Finally, the compounds of the present invention are potent acylating agents in peptide bond formation.
These compounds are, much to our surprise, the corresponding amino acid fluorides.
SUMMARY OF THE INVENTION
The present invention is directed to an amino acid of the formula: ##STR5## or the hydrogen fluoride salts thereof wherein BLK is hydrogen or an N-amino protecting group;
AA is an amino acid residue; and
X is - or a protecting group.
The present invention is also directed to a method for preparing a peptide which comprises reacting the amino acid fluoride described hereinabove with an amino acid or peptide having a free amino group and removing the protecting groups therefrom.
DETAILED DESCRIPTION OF THE INVENTION:
As used herein, the term "amino acid" refers to an organic acid containing both a basic amino group (NH.sub.2) and an acidic carboxyl group (COOH). Therefore, said molecule is amphoteric and exists in aqueous solution as dipole ions. (See, "The Condensed Chemical Dictionary", 10th ed. edited by Gessner G. Hawly, Van Nostrand Reinhold Company, London, Eng. p.48 (1981)). The preferred amino acids are the .alpha.-amino acids. They include but are not limited to the 25 amino acids that have been established as protein constituents. They must contain at least one carboxyl group and one primary or secondary amino group on the amino acid molecule. They include such proteinogenic amino acids as alanine, valine, leucine, isoleucine, norleucine, proline, hydroxyproline, phenylalanine, tryptophan, methionine, glycine, serine, threonine, cysteine, cystine, tyrosine, asparagine, glutamine, aspartic acid, glutamic acid, lysine, hydroxylysine, ornithine, arginine, histidine, penicillamine and the like.
An "amino acid residue", as defined herein, is an amino acid minus an amine hydrogen on the amino end of the molecule and the OH group on the carboxy end of the molecule (i.e., it includes the acyl group ##STR6## on the carboxy end of the molecule). Therefore, unless designated to the contrary, the group "AA" signifies an amino acid residue. For example, the amino acid residues of various amino acids are represented below:
Therefore, the symbol "AA-F" refers to an amino acid fluoride, i.e., a compound having a fluoro group attached to the acyl group ##STR27## of the amino acid. When BLK is hydrogen, then the structure becomes the amino acid fluoride of an amino acid having a free amino group. However, in view of the synthesis of the amino acid fluoride described hereinbelow, the free amino acid fluoride may be isolated as the hydrogen fluoride salt thereof.
It will be apparent to one skilled in the art, shown by exemplification in the table hereinabove that in the course of protein synthesis, it may be necessary to protect certain side chains of the amino acids to prevent unwanted side reactions. For example, it may be necessary to protect the hydroxyl group on the side chain of tyrosine, serine, or threonine in order to prevent these groups from interfering with the desired reactions. This is a common problem in peptide synthesis and many procedures are available for protecting the functional groups on the side chains of the amino acids. Such procedures for protecting various functional groups are known to one skilled in the art and are described in the treatise entitled "The PEPTIDES", Vol. 2, Edited by E. Gross and J. Meienhoffer, Academic Press, NY, New York, pp. 166-251 (1980), and the book entitled "Reagents for Organic Synthesis", by T. W. Green, John Wiley and Sons, New York, 1981, the contents of both being incorporated herein by reference.
For example, when the functional side chain contains an hydroxy group, such as threonine or serine, it can be protected by such groups as methyl, methoxymethyl(MOM), 2-methoxyethoxymethyl(MEM), tetrahydropyranyl, .beta.-trimethylsilylethyl, 4-methoxytetrahydropryanyl, 1-ethoxyethyl, t-butyl, p-methoxybenzyl, p-halobenzyl, o-nitrobenzyl, p-nitrobenzyl, o-chlorobenzyl, adamantyl, diphenylmethyl, triphenylmethyl, cyclohexyl, cyclopentyl, 1-benzyloxycarbonyl, tri-substituted silyl, wherein the substituents are independently aryl, alkyl or aralkyl, 2,2,2-trifluoroethyl, and the like. The preferred groups for the protection of the hydroxyl side chain are adamantyl, t-butyl, 4-methoxybenzyl, cyclopentyl and cyclohexyl.
When the side chain contains a phenol, such as in tyrosine, it may be protected by such groups as methyl, methoxymethyl(MOM), methoxyethoxymethyl(MEM), -trimethylsilylethyl, methylthiomethyl, tetrahydropyranyl, isopropyl, cyclohexyl, cyclopentyl, t-butyl, adamantyl, 4-methoxysilyl, o-nitrobenzyl, 2,4-dinitrophenyl, m-bromobenzyl, 2,6-dichlorobenzyl, trisubstituted-silyl wherein the substituents are independently alkyl, aryl or aralkyl, ethoxycarbonyl, carbamoyl and the like. The most preferred protecting groups are adamantyl, 4-methoxybenzyl, t-butyl, cyclopentyl, and cyclohexyl. An especially preferred protecting group is t-butyl.
A carboxy side chain, such as that found in aspartic acid or glutamic acid, can be protected by the following groups: 1-or 2-adamantyl, methoxymethyl, methythiomethyl, t-butyl, methyl, ethyl, phenyl, tetrahydropyranyl, cyclopentyl, cyclohexyl, cycloheptyl, 4-picolyl, trisubstituted-silyl wherein the substituents are independently alkyl, aryl or aralykl, N-piperidinyl, N-succinimidoyl, .beta.-trimethylsilylethyl, 4-methoxybenzyl, benzyl, p-bromobenzyl, p-chlorobenzyl, p-nitrobenzyl, phenacyl, N-phthalimidoyl, 4-alkyl-5-oxo-1,3-oxazolidinyl, trisubstituted-stannyl wherein the substituents are independently alkyl, aryl or aralkyl, and the like. The most preferred protecting group is t-butyl.
If the functional group on the side chain is mercapto, e.g., cysteine, such groups as triphenylmethyl, benzyl, 4-methylbenzyl, 3,4-dimethylbenzyl, 4-methoxybenzyl, .beta.-trimethylsilylethyl, p-nitrobenzyl, 4-picolyl, diphenylmethyl, triphenylmethyl, bis(4-methoxyphenyl)methyl, diphenyl-4-pyridylmethyl, 2,4-dinitrophenyl, t-butyl, t-butylthio, adamantyl, isobutoxymethyl, benzylthiomethyl, thiazolidinyl, acetamidomethyl, benzamidomethyl, 2-nitro-1-phenylethyl, 2,2-bis (carboethoxy) ethyl, 9-fluorenemethyl, acetyl, benzoyl, and the like can be used to protect said group. In this case, it is preferred that the protecting groups are t-butyl, t-butylthio, 4-methoxybenzyl, and triphenylmethyl.
If the side chain contains an amino group, such as the .epsilon.-amino group of lysine and ornithine, the following groups may be used: 9-fluorenylmethyloxycarbonyl, 9-(2-sulfo) fluorenylmethyloxycarbonyl, .beta.-trimethylsilylethyloxycarbonyl, 2-furanylmethyloxycarbonyl, adamantyloxycarbonyl, carbobenzoxy, t-butyloxycarbonyl, t-amyloxycarbonyl, cyclobutyloxycarbonyl, 1-methylcyclobutyloxycarbonyl, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl, 1-methylcyclohexyloxycarbonyl, isobornyloxycarbonyl, CBZ, p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, chlorobenzyloxycarbonyl, isonicotinyloxycarbonyl, p-toluenesulfonylamidocarbonyl, methylsulfonylethyloxycarbonyl, .beta.,.beta.,.beta.-trichloroethyloxycarbonyl, dithiasuccinoyl, phthaloyl, 4,5-diphenyl-4-oxazoline-2-one, piperidino oxycarbonyl trifluoroacetyl, chloroacetyl, p-toluenesulfonyl and the like. Preferred groups for the protection of this amino side chain are carbobenzoxycarbonyl, t-butyloxycarbonyl, and adamantyloxycarbonyl.
If the amino acid has an imidazole group, such as in histidine, the following groups may be used to protect the side chain: benzyloxymethyl, piperdinylcarbonyl, phenacyl, pivaloyloxymethyl, 1-(alkoxycarbonylamino)- 2,2,2-trifluoroethyl, 1-trifluoromethyl-1-(p-chlorophenoxymethoxy) -2,2,2-trifluoroethyl, 2,4-dinitrophenyl, toluenesulfonyl, FMOC, triphenylmethyl, t-butyloxycarbonyl, t-butyloxymethyl and the like. The preferred groups are FMOC, t-butyloxycarbonyl, triphenylmethyl, and t-butyloxymethyl.
When the amino acid has a guanidine side chain, such as in arginine, the following protecting groups can be used to protect the .omega. nitrogen on the guanidine moiety: methoxytrimethylbenzenzenesulfonyl, pentamethylchromanesulfonyl, mesitylenesulfonyl, toluenesulfonyl, 2,4,6-trimethylbenzenesulfonyl, trimethoxybenzensulfonyl, bisadamantyloxylcarbonyl, nitro, tosyl, and the like. The preferred protecting groups are methoxytrimethylsulfonyl, pentaamethylchromanesulfonyl, bisadamantyloxycarbonyl, and mesitylenesulfonyl.
For side chains containing an amide group such as in glutamine and asparagine, the following groups can be used to protect the side chain: dimethoxybenzyhydryl, 9-xanthenyl, 2,4,6-trimethoxybenzyl, and the like.
As used herein, the term "alkyl", when used alone or in combination with other groups refers to a carbon chain containing from 1 to 6 carbon atoms. They may be straight chains or branched and include such groups as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, t-butyl, n-pentyl, amyl, n-hexyl and the like. The preferred alkyl group contains from 1-3 carbon atoms. The term aryl as used herein refers to an aromatic ring system containing from 6-10 ring carbon atoms and up to a total of 15 carbon atoms. It includes such groups as phenyl, .alpha.-naphthyl, .beta.-naphthyl, and the like. The preferred group is phenyl.
Aralkyl groups are aryl groups attached to the main chain through an alkylene bridge. Such groups include benzyl, phenethyl and the like. The preferred aralkyl group is benzyl.
The aryl and aralkyl groups herein may be unsubstituted or may be substituted with an electron donating groups in situations wherein the protecting group is cleaved by acid. An electron donating group as defined herein shall be interpreted as a group that will release or donate electrons more than hydrogen would if it occupied the same position in the molecule. See, J. Marsh, Advance Organic Chemistry, 2nd Ed., McGraw Hill, Inc. (1977). These types of groups are well known in the art. Examples of electron donating groups include alkyl, lower alkoxy, aralkoxy; and the like. These electron donating groups, e.g., alkoxy, may be present on the aryl moiety of the following groups: DMB, TMB, Mtr, Pmc, Bz, Trt, CBZ and the like.
The protecting groups described hereinabove are well known to one skilled in the art. They can be removed under very mild acidic or basic conditions. The preferred protecting groups are those which can be cleaved by acid or base under conditions which are milder than those used to cleave the benzyl group. These include groups which can be cleaved by trifluoroacetic acid at room temperature within one to four hours. The especially preferred protecting groups are groups which can be cleaved by trifluoroacetic acid at room temperature within 1-2 hours.
These protecting groups include such groups as tetrahydropyranyl,.beta.-trimethylsilylethyl, 1-ethoxyethyl, t-butyl, p-methoxybenzyl, 1-adamantyl, diphenylmethyl, triphenylmethyl, trialkylsilyl, (e.g. trimethylsilyl, triethylsilyl, and the like) trialkylstannyl, (e.g. trimethylstannyl, triethylstannyl, and the like), bis (4-methoxyphenyl)methyl, 2-furanylmethyloxycarbonyl, t-amyloxycarbonyl, 1-methylcyclohexyloxycarbonyl, isobornyloxy carbonyl, methoxytrimethylbenzenesulfonyl, pentamethylchromanesulfonyl, 2,4,6-trimethoxybenzyl, 9-xantheneyl and the like.
However, not all of the amino acids have side-chain functional groups. For example, many amino acids have hydrogen, alkyl or aralkyl side chains. These include glycine, alanine, valine leucine, norleucine, phenylalanine, isoleucine and the like. Therefore, these amino acids do not require protecting groups thereon.
To differentiate between those amino acids having protecting groups and those not having protecting groups thereon, the term ##STR28## is used. As used herein, if no protecting group is present on the amino acid side chain, such as, e.g., in alanine, (which doesn't have a functional group and therefore no blocking group is required) "X" is -. Moreover, if the amino acid side chain has a functional group, such as in tyrosine, but is unprotected, then this also is indicated by X being defined as -. In other words, in both instances, when X is -, the side group is unprotected.
Although the term functional group is understood by one skilled in the art, it is defined as a group which could react with the reactants used or products formed under peptide forming condition if not protected by a blocking group. These functional groups include amino, carboxy, hydroxy, guanidino, imidazole, amino and the like.
On the other hand, if X is a blocking group, then this signifies that the functional group on the side chain is protected. For example, if AA is serine and X is t-butyl, then the residue ##STR29## These protecting groups include the protecting groups described hereinabove.
Abbreviations have been used in the specification and claims with respect to these blocking groups and are listed hereinbelow:
The term amino acid protecting group, as used herein, refers to blocking groups which are known in the art and which have been utilized to block the amino (NH.sub.2) group of the amino acid. Blocking groups such as 9-lower alkyl-9-fluorenyloxycarbonyl,2-chloro-1-indanylmethoxycarbonyl (CLIMOC) and benz [f] indene-3-methyloxycarbonyl (BIMOC) and dbd-TMOC are discussed in U. S. Pat. Nos. 3,835,175, 4,508,657, 3,839,396, 4,581,167, 4,394,519, 4,460,501 and 4,108,846, and the contents thereof are incorporated herein by reference as is fully set forth herein. Moreover, other amino protecting groups such as 2-(t-butyl sulfonyl)-2-propenyloxycarbonyl (Bspoc) and benzothiophene sulfone-2-methyloxycarbonyl (Bsmoc) are discussed in copending application, U. S. patent application Ser. No. 364,662 and the subject matter therein is incorporated herein by reference. Other amino protecting groups are described in an article entitled "Solid Phase Peptide Synthesis" by G. Barany and R. B. Merifield in Peptides, Vol. 2, edited by E. Gross and J. Meienhoffer, Academic Presser, New York, N.Y., pp. 100-118 ( 1980 ) , the contents of which are incorporated herein by reference. These N-amino protecting groups include such groups as the FMOC, Bspoc, Bsmoc, t-butyloxycarbonyl (BOC), t-amyloxycarbonyl (Aoc), .beta.-trimethyl-ethyloxycarbonyl (TEOC), adamantyloxycarbonyl (Adoc), 1-methyl-cyclobutyloxycarbonyl (Mcb), 2- (p-biphenylyl) propyl-2-oxycarbonyl (Bpoc), 2-(p-phenylazophenyl) propyl-2-oxycarbonyl (Azoc), 2,2-dimethyl-3,5-dimethyloxybenzyloxycarbonyl (Ddz), 2-phenylpropyl-2-oxycarbonyl (Poc), benzyloxycarbonyl (Cbz), p-toluenesulfonyl aminocarbonyl (Tac) o-nitrophenylsulfenyl (Nps), dithiasuccinoyl (Dts), phthaloyl, piperidinooxycarbonyl, formyl, trifluoroacetyl and the like.
These protecting groups can be placed into four categories:
1) a base labile N.alpha.-amino acid protecting group such as FMOC, and the like.
2) protecting groups removed by acid, such as Boc, TEOC, Aoc, Adoc, Mcb, Bpoc, Azoc, Ddz, Poc, Cbz, 2-furanmethyloxycarbonyl (Foc), p-methoxybenzyloxycarbonyl (Moz), Nps, and the like.
3) protecting groups removed by hydrogenation such as Dts, Cbz.
4) protecting groups removed by nucleophiles, such as Bspoc, Bsmoc and Nps and the like.
5) protecting groups derived from carboxylic acids, such as formyl, acetyl, trifluoroacetyl and the like, which are removed by acid, base or nucleophiles.
As defined herein, a nucleophile is an electron-rich atom, i.e., an atom which can donate an electron pair, which tends to attack a carbon nucleus but does not act as a Bronsted Lowry base. For example, a nucleophile, as defined herein, includes those molecules which are used for nucleophilic addition across a double bond and behaves in a manner similar to that described in the schemes herein below.
The general mechanism for cleavage of Bspoc and Bsmoc groups are similar in that the nucleophile is believed to react through a Michael-type addition across a double bond. Although the following schemes are shown for Bspoc, it is also illustrative of Bsmoc: ##STR30## The nucleophile is believed to attack at the terminal carbon atoms of the propenyl group (Michael acceptor) forming a zwitterion which can eliminate the OCOAA(X)OH anion and H.sup.+ to form an alkene-amine and the amide (8) after protonation. Loss of CO.sub.2 will furnish the free amino acid.
The nucleophiles which will function in concert with this invention must have an active hydrogen atom, i.e., a hydrogen atom attached to the nucleophilic atom.
It is preferred that the nucleophile is a simple amine. It is especially preferred that the simple amine is a primary or secondary amine of the formula HNR.sub.5 R.sub.6 wherein R.sub.5 and R.sub.6 are independently hydrogen, lower alkyl or substituted lower alkyl, the lower alkyl being substituted with OH, CH.sub.3, or CH.sub.2 CH.sub.3 or R.sub.5 and R.sub.6 taken together form a mono or bicyclic ring containing from 4 to 10 ring carbon atoms and 1 or 2 heteroatoms selected from the group consisting of nitrogen, sulfur or oxygen.
Typical examples of useful amines include ethanolamine, morpholine, piperidine, diethylamine, 2,6-dimethylpiperidine, piperazine, diethylamine, ethylamine and the like.
An organo mercaptan can also be used as a nucleophile, e.g., alkyl mercaptans, cycloalkyl mercaptans, aryl mercaptan or aralkyl mercaptans. The most preferred mercaptan is benzyl mercaptan.
The nucleophile can be added as a free compound or as an insoluble reagent attached to a solid support i.e., polystyrene or silica dioxide. These are represented by the formula:
wherein p is an organic polymer as defined hereinabove or a silica gel polymer; alk is a chemical bond, alkyl or aroyl chain having from about one to about ten carbon atoms and Nu--H is a nucleophile as defined hereinabove.
A preferred insoluble reagent is the silica based piperazine reagent 9: ##STR31##
Another useful nucleophile is benzylmercaptan as shown in the following scheme. ##STR32## In this scheme the thio-group reacts in a Michael fashion to remove the Bspoc protecting group.
The amino acid fluorides of the present invention can be prepared by art recognized techniques. More specifically, it can be prepared by reacting an N-protected amino acid with the reagent cyannuric fluoride according to the following equation: ##STR33## wherein BLK is an amino protecting group as defined herein and X is defined herein. It is preferred that BLK is the FMOC CLIMOC, BIMOC, DBD--TMOC, Bspoc, Bsmoc, or related base sensitive group. This reaction can be run at temperatures as low as 0.degree. and up to the refluxing temperature of the solvent, but it is preferred that reaction is run at room temperature. It also can be run in an inert solvent such as pyridine/CH.sub.2 Cl.sub.2 and the like.
The cyanuric fluoride can be prepared from the corresponding chloride in the presence of potassium fluoride at elevated temperatures ranging from 150.degree. to 250.degree. C., according to the following equation: ##STR34##
Other fluorinating agents well known in the art, such as thionyl fluoride, 2,4,6-trinitrofluorobenzene, N-methyl-2-fluoropyridinium salts, and the like may be used in place of KF to effect the formation of cyanuric fluoride.
The amino acid fluorides of the present invention are useful in peptide bond formation. The scope is quite broad, as the amino acid fluorides of the present invention can be coupled with an amino acid, a dipeptide, tripeptide, or higher peptide, having a free terminal amino group. As used herein, the term first amino acid is meant to include amino acids as well as dipeptides, and the higher peptides.
The synthesis of peptides according to the present invention requires the following steps:
1) protection of the carboxyl group on a first amino acid.
2) formation of the amino acid fluorides of the present invention in accordance with the procedure herein.
3) formation of the peptide bond by coupling the amino acid fluoride with the first amino acid.
4) removal of the protecting groups.
A variety of carboxy protecting groups known in the art may be employed. Examples of many of these possible groups may be found in "Protective Groups in Organic Synthesis", by T. W. Green, John Wiley & Sons, 1981, the contents of which is incorporated herein by reference.
The following sequence is illustrative of the coupling of an amino acid fluoride of the present invention with an amino acid having a free amino group: ##STR35##
In the above scheme, BLK is as defined hereinabove, X.sub.1, X.sub.2 and X.sub.3 are independently defined as X hereinabove, and P is a carboxy protecting group, e.g., methyl ester, t-butylester, .beta.-trimethylsilylethyl ester, benzyl ester and the like.
As shown by the above scheme, the N.alpha.-amino protected amino acid fluoride is reacted with a second amino acid in which the carboxy group is protected. A peptide is formed between the first amino acid and the second amino acid. The peptide chain can be increased by removing the alpha amino protecting group by techniques known to one skilled in the art, and then reacting the corresponding di-peptide with another N .alpha.-amino protected amino acid fluoride to form the corresponding tri-peptide. The N .alpha.-amino protecting group of the tri-peptide is removed and the above cycle is repeated until the desired peptide has been obtained.
The coupling of the N-.alpha. protected amino acid fluoride with the carboxy protected amino acid by the normal two phase techniques takes place without racemization.
The present invention can readily be utilized in solid phase peptide synthesis. Solid phase peptide synthesis is based on the stepwise assembly of a peptide chain while it is attached at one end to a solid support or solid phase peptide resin. Two methods are generally well known in the art.
One, the Merrifield method, employs a solid support for attachment of the amino acid or peptide residues. This method employs N-protected amino acids as building blocks which are added to an amino acid or peptide residue attached to the solid support at the acyl (acid) end of the molecule. After the peptide bond has been formed, the protected group is removed and the cycle repeated. When a peptide having the desired sequence has been synthesized, it is then removed from the support.
The second method, the inverse Merrifield method, employs reagents attached to solid supports in a series of columns. The amino acid or peptide residue is passed through these columns in a series to form the desired amino acid sequence.
These methods are well known in the art as discussed in U.S. Pat. Nos. 4,108,846, 3,839,396, 3,835,175, 4,508,657, 4,623,484, 4,575,541, 4,581,167, 4,394,519 as well as in Advances in Enzymology, 32, 221 (1969) and in PEPTIDES, VOL, 2, edited by Erhard Gross and Johannes Meienhoffer, Academic Press, New York, N.Y. pp. 3-255 (1980) and are incorporated herein by reference and is fully set forth herein.
The amino acid fluorides of the present invention can exist in various stereoisomeric forms, viz., the D or L stereoisomers. Moreover, the amino acid fluorides may be present in mixture of the D and L forms such as in racemic mixtures. All of these forms are contemplated to be within the scope of the present invention. It is preferred that the stereoisomer of the amino acid fluorides of the present invention exist in the L form.
EXAMPLES
The invention will now be illustrated by examples. The examples are not intended to be limiting of the scope of the present invention. In conjunction with the general and detailed descriptions above, the examples provide further understanding of the present invention.
I Preparative Examples: Preparation of Cyanuric Fluoride
A 250 mL three necked round bottomed flask equipped with a thermometer, stirring bar, distilling apparatus and powder dropping funnel was charged with oven-dried sodium fluoride (53 g, 1.25 mole) and tetramethylene sulfone (sulfolane, TMS) (145 g, 115 mL, 1.20 mole, d=1.26). To the suspension was added cyanuric chloride (62 g. 0.33 mole) in small portions by use of the powder dropping funnel over a 10-min period. The reaction mixture was gradually heated to 250.degree. C. by means of a heating mantle. The product distilled from the flask as formed and was collected in glass traps cooled in a Dry Ice-acetone bath. Collection of the distillate (29 mL) continued until distillation stopped (bp 72.degree.-78.degree. C.). Redistillation gave 24 mL (86.19 g, 86.2% d=1.6 g/mL) of the fluoride as a clear colorless liquid, bp 72.degree.-73.degree.C., lit bp 74.degree. C.
II General Procedure for Preparation of N-(9-Fluorenyl-Methoxycarbonyl) Amino Acid Fluorides
A solution (or suspension) of FMOC-amino acid (1 mmole) in dry CH.sub.2 Cl.sub.2 (5 mL) was kept under nitrogen and treated with cyanuric fluoride (1.08 g, 8 mmol, 700 uL, d=1.6) and pyridine (81 uL, 1 mmole). A clear solution was obtained which was refluxed (or stirred at room temperature) for 45-120 min. Completion of reaction was checked by TLC. During the reaction a white precipitate separated. The mixture was extracted with ice-water (2.times.15 mL) which caused the precipitate to dissolve. The organic layer was dried over MgSO.sub.4. Filtration and solvent removal gave a residue (solid or oil) which was crystallized from CH.sub.2 Cl.sub.2 /hexane or Et.sub.2 O/hexane to give the corresponding FMOC-N-protected amino acid fluoride as a white crystalline solid. The crude and recrystallized acid fluorides were analyzed by HPLC following the same technique described for the corresponding chlorides except that it was necessary to wait for 15-300 min following addition of the fluoride to dry methanol in order to allow time for complete conversion to the methyl ester. For example, a mixture initially analyzing for 93.45% FMOC-Gly-F (as methyl ester) came to complete conversion after 50 min with a measured content of 98.89% FMOC-Gly-OMe and 1.00% FMOC-Gly-OH. In case of FMOC-Val-F, initially analyzing for 82.70% FMOC-Val-F (as methyl ester) complete conversion occurred after 5 hours with a measured content of 98.19% FMOC-Val-OMe and 0.94% FMOC-Val-OH. Fischer esterification of the free acid in the methanolic HF solution did not occur. For example, a mixture initially containing 52.27% of FMOC-Gly-OH showed no significant change after 15 hours (52.19% acid) and the same results were observed in case of FMOC-Val-OH.
Example 1
N-(9-Fluorenylmethoxycarbonyl) glycine Fluoride
The reaction was used in accordance with the procedure described above.
Reaction was completed after 2 hours of reflux, the fluoride being obtained in 80.5% yield as pale yellow needles, mp 140.1.degree. C., (98.9% pure according to HPLC analysis);
IR (KBr) 3337 (NH), 1843 (COF), 1680 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.4.1-4.3 (m, 3, CHCH.sub.2), 4.5 (d, 2, NCH.sub.2 CO) , 5.3 (bs, 1, NH), 7.15-7.8 (m, 8, aryl) . Anal. Calcd for C.sub.17 H.sub.14 FNO.sub.3 : C, 68.22; H, 4.71; N, 4.67. Found: C, 68.25, H, 4.63; N, 4.79.
Example 2
N-(9-Fluorenylmethoxycarbonyl)alanine Fluoride
The reaction was run in accordance with the procedure described hereinabove.
Reaction was complete after 2 hours of reflux, the fluoride being obtained in 75.4% yield as a white solid, mp 111.degree.-2.degree.C., (98.66% pure according to HPLC analysis); [.alpha.]D.sup.23 +3.6.degree. (c 0.5, EtOAc); IR (KBr) 3326 (NH), 1845 (COF), 1690 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.1.6 (d, 3, CH.sub.3), 4.2 (t,1, CHCH.sub.2), 4.5 (m, 3, CH.sub.2 O, NCHCO), 5.2 (d, 1, NH), 7.2-7.8 (m, 8, aryl) .
Anal. Calcd for C.sub.18 H.sub.16 FNO.sub.3 : C, 69.00; H, 5.14; N, 4.47. Found: C, 69.16; H, 5.30; N, 4.30.
Example 3
N-(9-Fluorenylmethoxycarbonyl)valine Fluoride
The reaction was run in accordance with the procedure described hereinabove.
Reaction was complete after 2 hours of reflux, the fluoride being obtained in a yield of 70.2% as a white solid, mp 113.degree.-4.degree. C., (98.62% pure according to HPLC analysis); [.alpha.]D.sup.24 +10.7.degree. (c 1, CH.sub.2 Cl.sub.2); IR (KBr) 3312 (NH), 1843 (COF), 1688 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.1.0 (d, 6, CH.sub.3), 2.3 (m, 1, CHCH.sub.2), 4.2 (t, 1, CHCH.sub.3), 4.5 (m, 3, CH.sub.2 O, NCHCO), 5.15 (d, 1, NH), 7.2-7.8 (m, 8, aryl) .
Anal. Calcd for C.sub.20 H.sub.20 FNO.sub.3 : C, 70.36; H, 5.90; N, 4.10. Found: C, 70.27; H, 5.92; N, 4.19.
Example 4
N-(9-Fluorenylmethoxycarbonyl)leucine Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was complete after 1 hour of reflux, the fluoride being obtained in a yield of 75.2% as a white solid, mp 95.5.degree.-6.5.degree.C., (98.58% pure according to HPLC analysis); [.alpha.]D.sup.23 -5.8.degree.(c 1, EtOAc); IR (KBr) 3336 (NH), 1838 (COF), 1699 (OCON) cm.sup.-1 ; .sup.1 NMR (CDCl.sub.3) .delta.1.00 (d, 6CH.sub.3), 1.6-1.8 (m, 3, CH.sub.2 CH), 4.2 (t, 1, CHCH.sub.2 O), 4.5 (m, 3, CH.sub.2 O, NCHCO), 5.1 (d, 1, NH), 7.2-7.8 (m, 8, aryl) .
Anal. Calcd for C.sub.21 H.sub.22 FNO.sub.3 : C, 70.96; H, 6.23; H, 3.94. Found: C, 70.70; H, 6.48; N, 4.15.
Example 5
N-(9-Fluorenylmethoxycarbonyl) isoleucine Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was complete after 1.5 hours of reflux, the fluoride being obtained in a yield of 73.3% as a white solid, mp 115.degree.-6.degree. C., (97.13%) pure according to HPLC analysis); [.alpha.]D.sup.23 +15.6.degree. (c 0.5, EtOAc); IR (KBr) 3304 (NH), 1840 (COF), 1696 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.1.00 (m, 6, CH(Me) CH.sub.2 Me), 1.1-1.6 (m, 2, CHCH.sub.2 CH.sub.3), 2.00 (m, 1, CH), 4.2 (t, 1, CHCH.sub.2 O), 4.5 (m, 3, CH.sub.2 O, NCHCO), 5.2 (d, 1, NH), 7.2-7.8 (m, 8, aryl).
Analy. Calcd for C.sub.21 H.sub.22 FNO.sub.3 : C, 70.96; H, 6.23; N, 3.94. Found: C, 68.30; H, 6.06; N, 3.87.
Example 6
N-(9-Fluorenylmethoxycarbonyl)proline Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was complete after 12 hours of stirring at room temperature, the fluoride being obtained in a yield of 78.2% as a white solid mp, 88.degree.-9.degree. C.; [.alpha.]D.sup.30 -28.6.degree. (c 0.5, EtOAc).
Anal. Calcd for C.sub.20 H.sub.18 FNO.sub.3 : C, 70.78; H, 5.34; N, 4.12. Found: C, 70.86; H, 5.43, N, 4.21.
Example 7
N-(9-Fluorenylmethoxycarbonyl)phenylalanine Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was complete after 1 hour of reflux, the fluoride being obtained in a yield of 63.9% as white crystals, mp 118.degree.-20.degree. C., (99.3% pure according to HPLC analysis); [.alpha.]D.sup.23 +35.5.degree. (c 1, CH.sub.2 Cl.sub.2); IR (KBr) 3318 (NH), 1843 (COF), 1700 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.3.2 (d, 2, CH.sub.2 C.sub.6 H.sub.5), 4.2 (t, 1, CHCH.sub.2 O), 4.45 (m, 2, CH.sub.2 O), 4.85 (m, 1, NCHCO), 5.1 (d, 1, NH), 7.1-7.8 (m, 13 aryl).
Anal. Calcd for C.sub.24 H.sub.20 FNO.sub.3 : C, 74.03; H, 5.14; N, 3.59; F, 4.88. Found: C, 74.03; H, 5.13; N, 3.69; F, 4.68.
Example 8
N-(9-Fluorenylmethoxycarbonyl) tryptophan Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was complete after 1 hour of stirring at room temperature, the fluoride being obtained in a yield of 70.7% as a white solid, mp 125.degree.-8.degree. C. (dec.) (98.2% pure according to HPLC analysis); [.alpha.]D.sup.24 -5.2.degree. (c 1, EtOAc); IR (KRr) 3390 and 3360 (NH), 1845 (COF), 1697 (OCON) cm.sup.-1, .sup.1 H NMR (CDCl.sub.3) .delta.3.4 (d, 2, CH.sub.2 CHCO), 4.2 (t, 1, CHCH.sub.2 O), 4.4 (d, 2, CHCH.sub.2 O), 4.9 (m, 1, NCHCO), 5.3 (d, 1, NH), 7.0-8.2 (m, 14, NH+aryl) .
Anal. Calcd for C.sub.33 H.sub.31 FNO.sub.3 : C, 72.88; H, 4.94; N, 6.53. Found: C, 72.83, H, 5.01; N, 6.43.
Example 9
N-(9-Fluorenylmethoxycarbonyl)-O-(t-Butyl) serine Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was completed after 1 hour of stirring at room temperature, the fluoride being obtained in a yield of 72.7% as white crystals, mp 89.degree.-91.degree. C., (98.26% pure according to HPLC analysis); [.alpha.]D.sup.26 +28.8.degree. (c 0.5, EtOAc); IR (KBr) 3444 (NH), 1868 (COF), 1733 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.1.2 (s, 9, CMe.sub.3), 3.6 (q, 1, CHHOCMe.sub.3), 3.9 (q, 1, CHHOCMe.sub.3), 4.22 (t, 1, CHCH.sub.2 OCO), 4.45 (m, 2, CH.sub.2 OCO), 4.7 (m, 1, NCHCO), 5.65 (d, 1, NH), 7.25-7.8 (m, 8, aryl).
Anal. Calcd for C.sub.22 H.sub.24 FNO.sub.4 : C, 68.55; H, 6.27; N, 3.63. Found: C, 68.49; N, 6.32; N, 3.67.
Example 10
N-(9-Fluorenylmethoxycarbonyl)-O-(t-Butyl )threonine Fluoride
The reaction was run in accordance with the procedure described hereinabove:
Reaction was complete after 11/2 hours of stirring at room temperature, the fluoride being obtained in a yield of 72.6% as white crystals, mp 53.degree.-5.degree.C., (98.03% pure according to HPLC analysis); [.alpha.]D.sup.27 +12.3.degree. (c 0.4 EtOAc); IR (KBr) 3320 (NH), 1857 (COF), 1726 (OCON) cm.sup.-1 ; .sup.1 H NMR (CDCl.sub.3) .delta.1.15 (s, 9, CMe.sub.3), 1.3 (d, 3, CH.sub.3), 4.3-4.5 (m, 5, CHCH.sub.2 OCO, NCH(CHO--)CO), 5.6 (d, 1, NH), 7.2-7.8 (m, 8, aryl) .
Anal. Calcd for C.sub.23 H.sub.26 FNO.sub.4 : C, 69.15; H, 6.56; N, 3.50. Found: C, 69.11; H, 6.83; N, 4.00.
Example 11
N .alpha.-(9-Fluorenylmethoxycarbonyl)-N .epsilon.-(t--Butyloxycarbonyl)-lysine Fluoride
The reaction was run in accordance with the procedure described above.
Reaction was completed after 1 hour of stirring at room temperature, the fluoride being obtained in a yield of 65.9% as white crystals, mp 128.degree.-30.degree. C. (99.5% pure according to HPLC analysis); [.alpha.]D.sup.23 -2.2.degree. (c 0.5, CH.sub.2 Cl.sub.2); IR (KBr) 2254 (NH), 1854 and 1836 (COF), 1693 (OCON) cm.sup.-1 ; .sup.1 H (CDCl.sub.3) 1.4 (s, 9, CMe.sub.3), 1.5-2 (m, 6, CH.sub.2 --CH.sub.2--CH.sub.2), 3.15 (m, 2, CH.sub.2 NH), 4.2 (t, 1, CHCH.sub.2 O), 4.4-4.6 (m, 4, CH.sub.2 O, NCHCO, CH.sub.2 NH), 5.7 (d, 1, NH), 7.2-7.8 (m, 8, aryl).
Anal. Calcd For C.sub.26 H.sub.31 FN.sub.2 O.sub.5 : C, 66.36; H, 6.64; H, 5.95. Found: C, 66.16; H, 6.50; N, 5.92.
Example 12
N-(9-Fluorenylmethoxycarbonyl)aspartic Acid Fluoride-.beta.-(t-Butyl) Ester
The reaction was run in accordance with the procedure described above.
Reaction was complete after 30 minutes of stirring at room temperature, the fluoride being obtained in a yield of 67.8% as white crystals, mp 74.degree.-5.degree. C., (97.97% pure according to HPLC analysis); [.alpha.]D.sup.23 +4.00.degree. (c 0.5, EtOAc); IR (KBr) 3320 (NH), 1856 (COF), 1725 (COO ), 1695 (OCON) cm.sup.-1, .sup.1 H NMR (CDCl.sub.3) .delta.1.45 (s, 9, CMe.sub.3), 2.9 (dq, 2, CH.sub.2 COO), 4.3 (t, 1, CHCH.sub.2 OCO), 4.5 (m, 2, CHCH.sub.2 O), 4.85 (m, 1, HCHCO), 5.85 (d, 1, NH), 7.2-7.8 (m, 8, aryl).
Anal. Calcd for C.sub.23 H.sub.24 FNO.sub.5 : C, 66.81; H, 5.85; N, 3.38. Found: C, 67.03; H, 5.95; N, 3.70.
The results of the above synthesis are summarized in the Table hereinbelow:
These results indicate that cyanuric fluoride is suitable not only for the preparation of simple FMOC-amino acid fluorides but also for those containing t-BOC, t-Bu or CBZ-groups on the side chain. The amino acid fluorides described hereinabove were obtained in crystalline formed.
The use of amino acid fluorides of the present invention being used as peptide coupling agents is illustrated hereinbelow.
In the following example, the FMOC amine acids were utilized:
Example 13
Use of FMOC-AA-F in Peptide Synthesis
I General Method for Executing Rapid FMOC/4-AMP or FMOC/TAEA Peptide Synthesis. Five millimeters of a 0.1M solution of the C-terminal starting amino acid ester, 5 mL of CHCl.sub.3 containing 0.75 mmol of the appropriate ##STR36## (wherein Y is halo, i.e., chloro or fluoro) and 5 mL of 5% Na.sub.2 CO.sub.3 solution were combined and the two phase mixture stirred vigorously for 10 minutes. The organic phase was separated and treated with 5 mL of 4-AMP or TAEA. After 30 minutes 40 mL of CHCl.sub.3 was added and the organic phase washed with five 25-mL portions of 10% phosphate buffer of pH 5.5. Alternatively two 25-mL portions of saturated NaCl solution was used to remove excess 4-AMP or TAEA prior to extractions with the phosphate buffer. The organic phase was concentrated in vacuo to a volume of 5 mL on a rotary evaporator and the resulting CHCl.sub.3 solution used analogously for treatment with the next FMOC amino acid halide. II Preparation of FMOC-Val-Asp(CMe.sub.3)-Val-Leu-Leu-Ser(CMe).sub.3 -Tyr(CMe.sub.3)-OCMe.sub.3. The general procedure described above was followed beginning with 330 mg (1 mmol) of H-Tyr-(CMe.sub.3)-OCMe.sub.3 HCl, 462 mg (1.2 mmol) of FMOC-Ser-(CMe.sub.3)-F, 10 mL of methylene dichloride and 10 mL of 5% sodium carbonate solution. The mixture was stirred for 15 minutes, the organic layer separated and treated with 7.5 mL of TAEA for 30 minutes. The solution was washed with three 10-mL portions of satd sodium chloride solution and three 15-mL portions of phosphate buffer (pH 5.5). The organic layer was then treated in the same way in sequence with the remaining FMOC amino acid halides (FMOC-Leu-Cl twice, FMOC-Val-Cl, FMOC-Asp(CMe.sub.3)-F and FMOC-Val-Cl a second time). Evaporation of the organic layer was followed by column chromatography to give the protected heptapeptide, mp 249.degree.-251.degree. C., in 50-60% yield MSFAB: 1255 (M+1); calculated 1253.8 (M).
Example 14
Coupling of FMOC-Phe-F with H-Leu-OMe. Five millimeters of a 0.1M solution of H-Leu-OMe in CHCl.sub.3 was treated with 5 mL of CHCl.sub.3 containing 0.6 mmol of FMOC-Phe-F (mp 118.degree.-120.degree. ) and 5 mL of 5% Na.sub.2 CO.sub.3 solution. The two-phase mixture was stirred vigorously for 10 minutes, the layers separated and the organic layer dried over MgSO.sub.4 and evaporated with a rotary evaporator. Without purification the crude residue (90%) was examined by HPLC analysis which showed no evidence for the DL-diastereomer (0.1%). The two diastereomers are readily separated with a mobile phase consisting of 1% isopropyl alcohol in hexane (retention times: LL, 13.26 minutes; DL-17.13 minutes at flow rate 1.5 mL/minutes) using a Waters Radial Pak normal silica gel column 10 u, Z-module fitting.
Example 15
CBZ-alanine Fluoride
CBZ-Ala (1 mmole) in dry CH.sub.2 Cl.sub.2 is kept under nitrogen and treated with cyannuric fluoride (8 mmol) and pyridine (1 mmole) to form the corresponding CBZ-Ala-F.
Example 16
N-formyl-O-(t-butyl) serine Fluoride
N-formyl serine (1 mmole) in dry CH.sub.2 Cl.sub.2 under nitrogen is treated with cyannuric fluoride (8 mmol) and pyridine (1 mmol) to form the above-identified product.
Example 17
2-(t-butylsulfonyl)-2-propenyloxycarbonyl-1-phenylalanine Fluoride
A. t-Butyl Allyl Sulfide.
To a solution of 350 mL of anhydrous ethanol maintained under nitrogen was slowly added 22.99 g (1 mol) of sodium spheres. The sodium dissolved within 90 minutes, and to the resulting sodium ethoxide solution was added 90.19 g (1 mol) of t-butyl mercaptan with mechanical stirring. Allyl bromide (120.98 g; 1 mol) was then added dropwise to the mechanically stirred sodium t-butyl thiolate solution. After the addition was complete, the mixture was refluxed for 10 minutes, the solution allowed to cool, the precipitated sodium bromide filtered, and the ethanol removed by distillation at atmospheric pressure. The residue was diluted with 200 mL of water, and the layers separated. The aqueous layer was extracted with five 40-mL portions of ether. The combined organic layers were extracted with 150 mL of water, the organic layer dried over MgSO.sub.4, filtered, and the solvent removed in vacuo from a water bath at 45.degree. C. to give a yellow liquid. Distillation through a 0.8.times.15-cm fractionating column gave 56.16 g (45%) of the sulfide as a colorless liquid, bp 139.degree.-141.degree. C.
B. 1,3-Dibromo-2-(t-butylsulfonyl) Propane.
To a stirred solution of 17.37 g (0.13 mol) of t-butyl allyl sulfide in 133 mL of CCl.sub.4 at -24.degree. C. (CCl.sub.4 /dry ice) was added dropwise a solution of 21.33 g (0.13 mol) of Br.sub.2 in 67 mL of CCl.sub.4. A yellow solid precipitated during the addition. The mixture was warmed to room temperature and stirred for 10 minutes following complete solution of the yellow solid. The resulting solution was poured into a mixture of 55.50 g (0.27 mol) of 85% m-chloroperbenzoic acid in 490 mL of CH.sub.2 Cl.sub.2 kept at -24.degree. C., and the mixture stirred for 30 minutes at this temperature. The cooling bath was then removed and the mixture stirred at room temperature overnight. The precipitated m-chlorobenzoic acid was filtered and the filtrate washed with three 200-mL portions of saturated NaHCO.sub.3, followed by 200 mL of water. The organic layer was dried over MgSO.sub.4, filtered, and the solvent removed in vacuo from a water bath at 45.degree. C. The crude product was recrystallized from 20% EtOAc/Skelly B to give 32.02 g (75%) of the dibromide, mp 139.degree.-140.degree. C.
C. 2-(t-Butylsulfonyl)-2-propenyl Bromide.
A mixture of 16.78 g (0.052 mol) of 1,3-dibromo-2-(t-butylsulfonyl) propane and 14 mL (0.12 mol) of 2,6lutidine in 55 mL of CH.sub.2 Cl.sub.2 was refluxed for 75 minutes. The solution was allowed to cool to room temperature and extracted with three 80-mL portions of 5% HCl followed by 80 mL of water. The organic layer was dried over MgSO.sub.4, filtered, and the solvent removed in vacuo from a water bath at 45.degree. C. to give 11.46 g (91%) of the allyl bromide as a white solid, mp 40.5.degree.-42.0.degree. C., which was used without further purification.
D. 2-(t-Butylsulfonyl-2-propenyl Alcohol.
A mixture of 8.55 g (35.3 mmol) of 2-(t-butylsulfonyl)-2-propenyl bromide and 5.31 g (78.1 mmol) of sodium formate in 150 ml of methanol was refluxed overnight. The solution was allowed to cool and concentrated to 50 mL with the aid of a water aspirator, resulting in the precipitation of excess sodium formate. The residue was diluted with 150 mL of water and extracted with five 50-mL portions of CH.sub.2 Cl.sub.2. The organic layer was dried over MgSO.sub.4, filtered, and the solvent removed in vacuo from a water bath at 45.degree. C. The crude product was recrystallized from 15% EtOAc/Skelly F to give 4.30 g (68%) of the alcohol as a colorless solid, mp 53.5.degree.-54.5.degree. C.
E. 2-(t-Butylsulfonyl)-2-propenyl Chloroformate.
To a solution of 6.67 g (37.4 mmol) of 2-(t-butylsulfonyl)-2-propenyl alcohol in 27 mL of dry THF at 0.degree. C. was added in one portion 27 mL of phosgene. The solution was stirred for 1 hour at 0.degree. C. and allowed to stand at room temperature overnight. Excess phosgene and solvent were removed under reduced pressure. The crude product was recrystallized from 25% ether/Skelly B to give 8.23 g (91%) of the chloroformate as a colorless solid, mp 56.5-57.7.
F. 2-(t-Butylsulfonyl)-2-propenyloxycarbonyl-L-phenylalanine.
A solution of 4.57 g (19.0 mmol) of 2-(t-butylsulfonyl)-2-propenyl chloroformate and 5.64 g (18.6 mmol) of t-butyl L-phenylalaninate hydrophosphite in 90 mL of CH.sub.2 Cl.sub.2 was stirred in the presence of 165 mL of 5% NaHCO.sub.3 at room temperature for 2 hours. The aqueous phase was separated, and the organic phase washed with three 75-mL portions of 5% HCl. The organic phase was dried over MgSO.sub.4, filtered, and the solvent removed in vacuo from a water bath at 45.degree. C. The resulting oil was dissolved in 36 mL of 50% CH.sub.2 Cl.sub.2 trifluoro/acetic acid, and the solution stirred at room temperature for two hours. Excess trifluoracetic acid and solvent were removed in vacuo from a water bath at 150.degree. C. The resulting oil was crystallized from ether/Skelly F to give approximately 6.25g (91%) of the colorless acid, mp 88.0.degree.-89.5.degree. C.
G. 2-(t-butylsulfonyl)-2propenyloxycarbonyl-L-phenylalanine fluoride.
The product formed hereinabove in Example 17 F (1 mmol) is placed in dry CH.sub.2 Cl.sub.2 under nitrogen and treated with cyannuric fluoride (8 mmol) and pyridine (1 mmol) to form the above-identified product.
Example 18
BOC-Phe-F.
BOC-Phe (1 mmole) in dry CH.sub.2 Cl.sub.2 under nitrogen is treated with cyannuric fluoride (8 mmol) and pyridine (1 mmole) to form the above-identified product.
Example 19
Coupling of Bspoc-Phe-F with H-Leu-OMe
Five millimeter of 0.1M solution of H-Leu-OMe in CHCl.sub.3 was treated with 5 ml of CHCl.sub.3 containing 0.6 mmol of Bspoc-phe-F and 5 ml of 5% Na.sub.2 CO.sub.3 solution. The two phase mixture is stirred vigorously for 10 minutes, the layers separated and the organic layer dried over MgSO.sub.4 and evaporated to afford the coupled depeptide. Bspoc-Phe-Leu-OMe
Example 20
BIMOC-Phe-F
A. 1-Bromo-2-bromomethylnaphthalene.
To a solution of 103 g of 1-bromo-2-methylnaphthalene (bp 98.degree.-120.degree./0.5 mm, prepared in 90% yield by the method of Adams and Binder in JACS, 63, 2771(1941) and 82 g or N-bromosuccinimide in 1030 mL of CCl.sub.4 was added 0.54 g of dibenzoyl peroxide. The reaction mixture was refluxed with stirring for 3 h. After another 0.54 g of dibenzoyl peroxide was added, the mixture was refluxed for 3 hours. The solution was allowed to stand at room temperature overnight, and the resulting suspension was brought to the boiling point and filtered while hot. Concentration of the filtrate gave 139 g (99.4%) of the bromide as a light yellow solid, mp 104.degree.-107.degree. C., which was recrystallized from CCl.sub.4 to give 128 g (91.6%) of pure 1-bromo-2-bromomethylnaphthalene as colorless crystals, mp 106.5.degree.-107.5.degree. C.
B. Diethyl 2-(1-Bromo-2-naphthylmethyl)malonate.
To a solution of NaOEt prepared from 9.66 g of sodium and 210 mL of dry EtOH was added 63.76 mL of diethyl malonate and the reaction mixture refluxed for 2 h. To the resulting yellow solution was added in small portions 126 g of 1-bromo-2-bromomethylnaphthalene and the reaction mixture refluxed for 16 h. Distillation of ethanol from an oil bath (100.degree.-110.degree. C.) through a simple Claisen head gave a yellow suspension, to which was added 350 mL of CH.sub.2 Cl.sub.2 and 350 mL of H.sub.2 O. The aqueous layer was extracted twice with 120-mL portions of CH.sub.2 Cl.sub.2, and the combined organic layer was washed three times with 100-mL portion of H.sub.2 O, dried (MgSO.sub.4) and evaporated to give 152 g (95.6%) of the ester as a yellow solid, mp 60.degree.-65.degree. C. Recrystallization from acetic acid gave 137 g (86.2%) of the pure diester as a colorless solid, mp 77.degree.-79.degree. C.
C. .beta.-(1-Bromo-2-naphthyl)propionic Acid.
To a solution of 160 g of the product formed in B hereinabove in 239 mL of methanol was added 538 mL of 5N NaOH solution. The mixture was refluxed for 135 min, and cooled by means of an ice bath to 0.degree. C. To the reaction mixture was added 320 mL of ice water, and the resulting precipitate was collected by filtration and washed several times with small portions of ice water. To the ice-cold, stirred filtrate was added dropwise 5N HCl solution until the solution was weakly acidic. The precipitate was filtered and washed several times with small portions of water. Drying gave 86 g (63.1%) of crude diacid as a light yellow solid, mp 154.degree.-157.degree. C. Recrystallization from water gave 80 g (58.7%) of pure diacid as colorless crystals, mp 157.degree.-159.degree. C. A suspension of 47.5 g of the crude malonic acid in 968 mL of 6N HCl solution was refluxed for 16 h. The mixture was cooled by means of an ice bath to 0.degree. C., treated with 650 mL of CH.sub.2 Cl.sub.2, and stirred for 15 min. The aqueous layer was extracted twice with 100-mL portions of water, dried (MgSO.sub.4), and evaporated to give 30.3 g (74%) of yellow solid, mp 116.degree.-119.degree. C., which was recrystallized from alcohol to give 28 g (68%) of the acid as colorless crystals, mp 123.degree.-124.degree. C.
D. .beta.-(1-Bromo-2-naphthyl)propionyl chloride.
To a solution of 40.16 g of the product formed in C hereinabove in 802 mL of CH.sub.2 Cl.sub.2 was added 19.3 mL of thionyl chloride. The mixture was refluxed for 4 h, cooled to room temperature, and the solvent evaporated from a water bath (40.degree.-50.degree. C.) with a rotary evaporator (10 mm) to give a red-brown residue. In order to remove traces of thionyl chloride, small portions of CH.sub.2 Cl.sub.2 were added and the solution reevaporated three times. Eventually the crude acid chloride was obtained as a red-brown oil. The crude product was used immediately for the next step without further purification.
E. 4-Bromobenz[f]indan-1-one.
To an ice cold, stirred solution of the above crude .beta.-(1-bromo-2-naphthyl)propionyl chloride in 802 mL of dry CH.sub.2 Cl.sub.2 was added 26.11 g of anhydrous AlCl.sub.3 carefully. The reaction mixture was refluxed for 2 h, cooled to room temperature and treated carefully while stirring with 900 mL of ice-water followed by 75 mL of conc. HCl. The brown precipitate was filtered and washed five times with small portions of CH.sub.2 Cl.sub.2. The aqueous layer was separated and extracted twice with 100-mL portions of CH.sub.2 Cl.sub.2. The combined CH.sub.2 Cl.sub.2 extracts were washed three times with small portions of H.sub.2 O, dried (MgSO.sub.4) and evaporated from a water bath (50.degree.-60.degree. C.) with a rotary evaporator (7 mm) to give 30.1 g (80.1%) of the crude ketone as a yellow solid, mp 146.degree.-149.degree. C., which could be recrystallized from acetic acid to give 28.5 g (76%) of the pure ketone as colorless crystals, mp 149.degree.-151.degree. C.
F. Benz[f]indan-1-ol.
To an ice-cold solution of 22 g of the product formed in E hereinabove in 150 mL of dry THF was added carefully in small portions 16.1 g of LiAlH.sub.4. Subsequently, another 270 mL of dry THF was added to the suspension and the mixture was refluxed for 8 days. The reaction mixture was cooled to 0.degree. C. by means of an ice-bath and treated dropwise with 50 mL of ice-water followed by 1080 mL of 10% H.sub.2 SO.sub.4 solution. The mixture was extracted three times with 100-mL portions of ether and the combined ether extracts washed three times with 150-mL portions of H.sub.2 O, dried (MgSO.sub.4), and evaporated from a water bath (60.degree.-70.degree. C.) with a rotary evaporator (10 mm) to give 9.2 g (59.3%) of the crude alcohol as a light yellow solid, mp 135.degree.-139.degree. C. Recrystallization from benzene (45 mL) gave 8.6 g (55.4 %) of pure alcohol as colorless crystals, mp 139.degree.-141.degree. C.
G. Benz[f]indene.
A solution of 8.6 g of benz[f]indan-1-ol in 250 mL of 10% H.sub.2 SO.sub.4 was refluxed for 24 h. After cooling to room temperature the reaction mixture was extracted with three 150-mL portions of a mixture of benzene and hexane (1:2). The extracts were washed three times with 100-mL portions of water, dried (MgSO.sub.4), and evaporated to give 7.6 g (98%) of a colorless solid, mp 160.degree.-163.degree. C. Recrystallization from 340 mL of 95% ethanol gave 6.6 g (85%) of the hydrocarbon as colorless crystals: mp 163.degree.-164.degree. C.
H. Benz[f]indene-1-methanol.
A 1.0M solution of n-butyllithium (44 mL, 44 mmoles) was added dropwise under a nitrogen atmosphere to a stirred solution of 5 g (30.12 mmoles) of benz[f]indene in 140 mL of anhydrous ether and 20 mL of anhydrous THF cooled by means of a Dry Ice-acetone bath to -70.degree. C. The temperature of the reaction mixture was not allowed to exceed -50.degree. C. Benzindenyl lithium soon started to precipitate as small red crystals. After completion of the addition (about 2 hours), the reaction mixture was stirred at -70.degree. C. for another 45 minutes before introduction of formaldehyde. Paraformaldehyde, 13.5 g. dried overnight in vacuum over phosphorus pentoxide, was stirred and heated in a dry flask placed in an oil bath at 175.degree.-195.degree. C. The formaldehyde gas was led through a 7-mm glass tube into the benz[f]indenyl lithium solution (held below -50.degree. C.) by a stream of dry nitrogen. The temperature was not allowed to exceed -50.degree. C. After completion of the addition, 280 mL of 10% HCl solution was slowly poured into the stirred reaction mixture. The mixture was stirred for 15 minutes at room temperature. After the ether layer was separated, the aqueous solution was extracted twice with 50-mL portions of ether and the combined ether solution was washed with small portions of water until neutral. The ether solution was dried (MgSO.sub.4) and evaporated to give a light brown oil (6 g). Storage in the freezer gave a soft yellow solid which was purified by chromatography (100 g of silica gel, 1:1 ethyl acetate/hexane) to give 3.5 g (59%) of the alcohol as a yellow solid. The NMR showed the solid to be a mixture of benz[f]indene-1-methanol (95%) and benz[f]indene-3-methanol. Several recrystallizations from ligroin (bp 88.degree.-89.degree. C.) gave 3.0 g (50.6%) of pure, colorless benz[f]indene-1-methanol: mp 115.degree.-116.degree. C.
M. The BIMOC-Phe (1 mmole) formed in L hereinabove in dry CH.sub.2 Cl is kept under nitrogen and treated with Cyannuric fluoride (8 mmol) and pyridine (1 mmol) to form the corresponding BIMOC-Phe-F.
Example 21
Benz [e] indene-3-methyloxycarbonyl-phenylalanine acid fluoride
A. Benz [e]-indene-3-methanol
1-Keto-4,5-benzindane-3-carboxylic acid, [which was prepared in accordance with the procedure described by T. N. Poltabiraman and W. B. Lawson in J.Biol. Chem, 247, 302a (1972) the contents of which are incorporated herein by reference] is reduced by sodium borohydride to form the corresponding 3-carboxylic acid-1-ol. Dehydration with sulfuric acid give the corresponding unsaturated acid. The unsaturated acid was then reduced by LiAlH.sub.4 to form the 3-methanol derivative: ##STR37## B. N-[Benz[e] indene-3-methyloxycarbony] phenylalanine.
This product is prepared from the product of A hereinabove by following the procedure described in Ex. 20 I-L hereinabove
C. N-[Benz[e] indene 1-methoxycarbonyl] phenylalanine acid fluoride
The product B formed hereinabove (1 mmol) in dry Ch.sub.2 Cl.sub.2 is kept under nitrogen and treated with cyannuric fluoride (8 mmol) and pyridine (1 mmol) to form the above product.
Example 22
Benz [e] indene-1-methyloxy carbonylphenylalanine acid fluoride
A. Benz [e]-indene-1-methanol
3-Keto-4,5-benzindan-1-carboxylic acid, which was prepared in accordance with the procedure described by T. N. Paltabiraman and W. B. Lawson, in J. Biol. Chem. 242, 3029(1941) is reduced to the corresponding 1-carboxylic acid-3-ol- by NaBH.sub.4. Dehydration with H.sub.2 SO.sub.4 gave the unsaturated acid which was then reduced to benz (e)-indene-1-methanol by means of LiAlH.sub.4. ##STR38## B. N-(Benz[e]indene-1-methyloxycarbonyl) phenylalanine
This product is prepared from the product of A hereinabove by following the procedure described in Ex. 20 I-L hereinabove
C. N-[Benz(e)indene-1-methoxyoxy carbonyl]phenylalanine acid fluoride.
The product B formed hereinabove (1 mmol) in dry CH.sub.2 Cl.sub.2 is kept under nitrogen and treated with cyannuric fluoride (8 mmol) and pyridine (1 mmol) to form the above product.
Example 23
N-[Benz(e) indene 1-methoxy carbonyl]phenylalanine acid fluoride and N[Benz(e) indene 3-methoxy carbonyl]phenylalanine acid fluoride
2(.beta.)-naphthylpropronic acid is treated with thionyl chloride and cyclized in the presence of aluminum chloride to form the corresponding ketone. Reduction of the ketone with sodium borohydride, followed by dehydration with sulfuric acid gives the benz[e] indene. Formylation with ethyl formate and sodium hydride followed by treatment with sodium borohydride gave a mixture of the Benz[e] indene-3-methanol and Benz[e]-indene-1-methanol. The two alcohols are separated by chromatography.
Following the procedures in Examples 22 B-C and 23 B-C, the above-identified products are prepared.
It is to be noted from the preparations hereinabove that Benz[e]indene 1-methoxycarbonyl and the benz[e]indene-3-methoxy carbonyl can be used to protect the N .alpha.-amino group of an amino acid.
These groups are formed from the corresponding alcohol, as described in Ex. 21-23. The alcohols are then used as starting materials to form the corresponding chloroformates and azidoformates, as described in Ex. 20. The azidoformate can then be reacted with an amino acid in accordance with the procedure described in Ex. 20-L to form the corresponding N .alpha.-protected amino acid. This then is treated with cyannuric fluoride to form the corresponding amino acid fluoride.
The above preferred embodiments and examples are given to illustrate the scope and spirit of the present invention. These embodiments and examples will make apparent, to those skilled in the art, other embodiments and examples. These other embodiments and examples are within the contemplation of the present invention. Therefore, the present invention should be limited only by the appended claims.
Claims
What is claimed is:
1. A compound of the formula: ##STR39## or the acid fluoride salts thereof wherein BLK is an acid labile N-.alpha.-amino protecting group capable of being cleaved by trifluoroacetic acid, a base labile N-.alpha.-amino protecting group, an N-.alpha.-amino acid protecting group removable by hydrogenation, a nucleophile labile N-.alpha.-amino acid protecting group or N-.alpha.-amino protecting group derived from a carboxylic acid; AA is an alpha amino acid residue and X is - or a protecting group on the side chain of AA.
2. The compound according to claim 1 having the formula: ##STR40## or the acid fluoride salts thereof wherein BLK is Cbz, Bspoc, Bsmoc, FMOC, BOC, CLIMOC, BIMOC, Dbd-TMOC, AOC, ADOC, Mcb, Bpoc, Ddz, HCO, TFA, TEOC, Moz, Tac, benz[e]indene-1-methoxy carbonyl, Benz-indene-3-methoxy carbonyl, piperdine-oxycarbonyl, phthaloyl, Azoc, Poc, Foc, Nps, Dts, formyl, acetyl, or trifluoracetyl, AA is an alpha amino acid residue and X is - or a protecting group on the side chain of AA.
3. The compound according to claim 1 wherein AA is glycine, alanine, leucine, isoleucine, proline, hydroxyproline, phenylalanine, tyrosine, methionine, norleucine, serine, threonine, cystine, cysteine, tyrosine, aspartic acid, glutamic acid, asparagine, glutamine, lysine, arginine, hyroxylysine, ornithine, histidine or tryptophan and X is -.
4. The compound according to claim 1 wherein ##STR41##
5. The compound according to claim 1 wherein the side chain of the AA is hydroxy lower alkyl, carboxy lower alkyl, mercapto lower alkyl, hydroxy aryl or hydroxy benzyl and X is t-butyl.
6. The D or L stereoisomer of the compound of claim 1 or mixtures thereof.
7. The hydrogen fluoride salt of the compound of claim 1.
8. The compound according to claim 2 wherein AA is glycine, alanine, leucine, isoleucine, proline, hydroxyproline, phenylalanine, tyrosine, methionine, norleucine, serine, threonine, cysteine, cystine, tyrosine, aspartic acid, glutamic acid, asparagine, glutamine, lysine, hydroxylysine, ornothine arginine, histidine or tryptophan and X is -.
9. The compound according to claim 2 wherein ##STR42##
10. The compound according to claim 2 wherein the side chain of AA is hydroxy lower alkyl, carboxy lower alkyl, mercapto lower alkyl, hydroxyaryl or hydroxybenzyl, and X is t-butyl.
11. The compound according to claim 1 which is ##STR43## FMOC-Gly-F, FMOC-Ala-F, FMOC-Val-F, FMOC-Leu-F, FMOC-Ile-F or FMOC-Phe-F.
12. The D or L stereoisomer of the compound of claim 2 or mixtures thereof.
13. The compound according to claim 1 which is N-(fluorenylmethoxycarbonyl)-N.epsilon.-(t-butyloxycarbonyl)-lysine fluoride.
14. The compound according to claim 1 wherein BLK is CLIMOC, BIMOC, dbd-TMOC, Bspoc, Bsmoc, BOC, Aoc, TEOC, Adoc, Mcb, Bpoc, Azoc, DdZ, Poc, Cbz, Tac, Nps, Dts, phthalyl, piperidino-oxycarbonyl, formyl, trifluoroacetyl, Foc, Moz or Acetyl.
15. The compound according to claim 1 wherein BLK is FMOC, Bspoc, Bsmoc, BOC, BIMOC, CLIMOC, dbd-TMOC or CbZ.
16. The compound according to claim 1 wherein BLK is FMOC.
17. The compound according to claim 2 wherein BLK is Bspoc, Bsmoc, FMOC, TEOC, Cbz, Bpoc, BOC, formyl, Moz or trifluoracetyl.
18. The compound according to claim 1 wherein BLK is FMOC, Cbz or BOC.
19. The compound according to claim 1 wherein AA is glycine, alanine, leucine, isoleucine, proline, hydroxyproline, phenylalanine, methionine, nor-leucine, serine, cysteine, tyrosine, aspartic acid, glutamic acid, asparagine, glutamine, lysine, arginine, hydroxylysine, ornithine or tryptophan.
20. The compound according to claim 2 wherein AA is glycine, alanine, leucine, isoleucine, proline, hydroxy proline, phenylalanine, methionine, nor-leucine, serine, cysteine, tyrosine, aspartic acid, glutamic acid, asparagine, glutamine, lysine, arginine, hydroxylysine, ornithine or tryptophan.
21. The compound according to claim 1 wherein AA is serine, threonine, tyrosine, aspartic acid, glutamic acid or cysteine, and X is t-butyl.
22. The compound according to claim 2 wherein AA is serine, threonine, tyrosine, aspartic acid, glutamic acid or cysteine, and X is t-butyl.
23. The compound according to claim 1 wherein X is a protecting group.
24. The compound according to claim 2 wherein X is a protecting group.
25. The compound according to claim 1 wherein X is a protecting group and AA is threonine, serine, tyrosine, aspartic acid, glutamic acid, cysteine, lysine, ornithine, histidine, arginine or glutamine.
26. The compound according to claim 2 wherein X is a protecting group and AA is threonine, serine, tyrosine, aspartic acid, glutamic acid, cysteine, lysine, ornithine, histidine, arginine or glutamine.
27. The compound according to claim 1 wherein AA is glycine, alanine, valine, leucine, norleucine, phenylalanine, or isoleucine and X is -.
28. The compound according to claim 2 wherein AA is glycine, alanine, valine, leucine, norleucine, phenylalanine, or isoleucine and X is -.
29. The compound according to claim 1 wherein AA is serine or threonine and X is methyl, MOM, MEM, tetrahydropyranyl, .beta.-trimethylsilylethyl, 4-methoxytetrahydropyranyl, 1-ethoxyethyl, t-butyl, p-methoxybenzyl, p-halobenzyl, o-nitrobenzyl, p-nitrobenzyl, o-chlorobenzyl, adamantyl, diphenylmethyl, triphenylmethyl, cyclohexyl, cyclopentyl or benzyloxycarbonyl.
30. The compound according to claim 2 wherein AA is serine or threonine and X is methyl, MOM, MEM, tetrahydropyranyl, .beta.-trimethylsilylethyl, 4-methoxytetrahydropyranyl, 1-ethoxyethyl, t-butyl, p-methoxybenzyl, p-halobenzyl, o-nitrobenzyl, p-nitrobenzyl, o-chlorobenzyl, adamantyl, diphenylmethyl, triphenylmethyl, cyclohexyl, cyclopentyl or benzyloxycarbonyl.
31. The compound according to claim 29 wherein X is adamantyl, t-butyl, 4-methoxybenzyl, cyclopentyl or cyclohexyl.
32. The compound according to claim 30 wherein X is adamantyl, t-butyl, 4-methoxybenzyl, cyclopentyl or cyclohexyl.
33. The compound according to claim 1 wherein AA is tyrosine and X is methyl, MOM, MEM, trimethylsilylethyl, methylthiomethyl, tetrahydropyranyl, isopropyl, cyclohexyl, cyclopentyl, t-butyl, adamantyl, 4-methoxysilyl, o-nitrobenzyl, 2,4-dinitrophenyl, m-bromobenzyl, or 2,6-dichlorobenzyl.
34. The compound according to claim 2 wherein AA is tyrosine and X is methyl, MOM, MEM, trimethylsilylethyl, methylthiomethyl, tetrahydropyranyl, isopropyl, cyclohexyl, cyclopentyl, t-butyl, adamantyl, 4-methoxysilyl, o-nitrobenzyl, 2,4-dinitrophenyl, m-bromobenzyl, or 2,6-dichlorobenzyl.
35. The compound according to claim 33 wherein X is adamantyl, 4-methoxybenzyl, t-butyl, cyclopentyl or cyclohexyl.
36. The compound according to claim 34 wherein X is adamantyl, 4-methoxybenzyl, t-butyl, cyclopentyl or cyclohexyl.
37. The compound according to claim 1 wherein AA is aspartic acid or glutamic acid and X is adamantyl, methoxymethyl, methylthiomethyl, t-butyl, methyl, ethyl, phenyl, tetrahydropyranyl, cyclopentyl, cyclohexyl, cycloheptyl, 4-picolyl, N-piperidinyl, N-succinimidoyl, .beta.-trimethylsilylethyl, 4-methoxybenzyl, benzyl, p-bromobenzyl, p-chlorobenzyl, p-nitrobenzyl, phenacyl, N-phthalimidoyl or 4-loweralkyl-5-oxo-1,3,ozazolidinyl.
38. The compound according to claim 2 wherein AA is aspartic acid or glutamic acid and X is adamantyl, methoxymethyl, methylthiomethyl, t-butyl, methyl, ethyl, phenyl, tetrahydropyranyl, cyclopentyl, cyclohexyl, cycloheptyl, 4picolyl, N-piperidinyl, N-succinimidoyl, .beta.-trimethylsilylethyl, 4-methoxybenzyl, benzyl, p-bromobenzyl, p-chlorobenzyl, p-nitrobenzyl, phenacyl, N-phthalimidoyl or 4loweralkyl-5-oxo-1,3,ozazolidinyl.
39. The compound according to claim 37 wherein X is t.-butyl.
40. The compound according to claim 38 wherein X is t-butyl.
41. The compound according to claim 1 wherein AA is cysteine and X is triphenylmethyl, benzyl, 4-methylbenzyl, 3,4-dimethylbenzyl, 4-methoxybenzyl, .beta.-trimethylsilyethyl, p-nitrobenzyl, 4-picolyl , diphenylmethyl, triphenylmethyl, bis(4-methoxyphenyl)methyl, diphenyl-4-pyridylmethyl, 2,4-dinitrophenyl, t-butyl, t-butylthio, adamantyl, isobutoxymethyl, benzylthiomethyl, thiazolidinyl, acetamidomethyl, benzamidomethyl, 2-nitro-1-phenylethyl, 2,2-bis(carboethoxy)ethyl, 9-fluorenemethyl, acetyl or benzoyl.
42. The compound according to claim 2 wherein AA is cysteine and X is triphenylmethyl, benzyl, 4-methylbenzyl, 3,4-dimethylbenzyl, 4-methoxybenzyl, .beta.-trimethylsilyethyl, p-nitrobenzyl, 4-picolyl, diphenylmethyl, triphenylmethyl, bis(4-methoxyphenyl)methyl, diphenyl-4-pyridylmethyl, 2,4-dinitrophenyl, t-butyl, t-butylthio, adamantyl, isobutoxymethyl, benzylthiomethyl, thiazolidinyl, acetamidomethyl, benzamidomethyl, 2-nitro-1-phenylethyl, 2,2-bis(carboethoxy)ethyl, 9-fluorenemethyl, acetyl or benzoyl.
43. The compound according to claim 41 Wherein X is butyl, t-butylthio, 4-methoxybenzyl or triphenylmethyl.
44. The compound according to claim 42 wherein X is butyl, t-butylthio, 4-methoxybenzyl or triphenylmethyl.
45. The compound according to claim 1 wherein AA is lysine or ornithine and X is 9-fluoroenylmethyloxycarbonyl, 9-(2-sulfo)fluorenylmethyloxycarbonyl, .beta.-trimethylsilylethyloxycarbonyl, 2-furanylmnethyloxycarbonyl, adamantyloxycarbonyl, carbobenzoxy, t-butyloxycarbonyl, t-amyloxycarbonyl, cylcobutyloxy carbonyl, 1-methylcyclobutyloxycarbonyl, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl, 1-methylcyclohexyoxycarbonyl, isobornyloxycarbonyl, CBZ, p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, chlorobenzyloxycarbonyl, isonicotinyloxycarbonyl, p-toluenesulfonylamidocarbonyl, methylsulfonylethyloxycarbonyl, .beta.,.beta., .beta.-trichloroethyloxycarbonyl, dithiasuccinoyl, phthaloyl, piperidinooxycarbonyl, trifluoroacetyl, chloroacetyl or p-toluenesulfonyl.
46. The compound according to claim 43 wherein AA is lysine or ornithine and X is 9-fluoroenylmethyloxycarbonyl, 9-(2-sulfo)fluorenylmethyloxycarbonyl, .beta.-trimethylsilylethyloxycarbonyl, 2-furanylmethyloxycarbonyl, adamantyloxycarbonyl, carbobenzoxy, t-butyloxycarbonyl, t-amyloxycarbonyl, cylcobutyloxy carbonyl, 1-methylcyclobutyloxycarbonyl, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl, 1-methylcyclohexyoxycarbonyl, isobornyloxycarbonyl, CBZ, p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, chlorobenzyloxycarbonyl, isonicotinyloxycarbonyl, p-toluenesulfonylamidocarbonyl, methylsulfonylethyloxycarbonyl, .beta.,.beta.,.beta.-trichloroethyloxycarbonyl, thiasuccinoyl, phthaloyl, piperidinooxycarbonyl, trifluoroacetyl, chloroacetyl or p-toluenesulfonyl.
47. The compound according to claim 45 wherein X is Cbz, t-butyloxycarbonyl or adamantyloxycarbonyl.
48. The compound according to claim 46 wherein X is Cbz, t-butyloxycarbonyl or adamantyloxycarbonyl.
49. The compound according to claim 1 wherein AA is histidine and X is benzyloxymethyl, piperidinylcarbonyl, phenacyl, pivaloyloxymethyl, 1-(lower alkoxycarbonylamino)-2,2,2-trifluoroethyl, 1 trifluoromethyl-1-(p-chlorophenoxymethoxy)-2,2,2-trifluoroethyl, 2,4-dinitrophenyl, toluenesulfonyl, FMOC, triphenylmethyl, t-butyloxycarbonyl or t-butyloxymethyl.
50. The compound according to claim 2 wherein AA is histidine and X is benzyloxymethyl, piperidinylcarbonyl, phenacyl, pivaloyloxymethyl, 1-(lower alkoxycarbonylamino)-2,2,2-trifluoroethyl, 1-trifluoromethyl-1-(p-chlorophenoxymethoxy)-2,2,2-trifluoroethyl, 2,4-dinitrophenyl, toluenesulfonyl, FMOC, triphenylmethyl, t-butyloxycarbonyl or t-butyloxymethyl.
51. The compound according to claim 49 wherein X is FMOC, t-butyloxycarbonyl, triphenylmethyl or t-butyloxymethyl.
52. The compound according to claim 50 wherein X is FMOC, t-butyloxycarbonyl, triphenylmethyl or t-butyloxymethyl.
53. The compound according to claim 1 wherein AA is arginine and X is methoxytrimethylbenzenesulfonyl, pentamethylchromanesulfonyl, mesitylenesulfonyl, toluenesulfonyl, 2,4,6-trimethylbenzenesulfonyl, trimethoxybenzenesulfonyl, bisadamantyloxycarbonyl, nitro or tosyl.
54. The compound according to claim 2 wherein AA is arginine and X is methoxytrimethylbenzenesulfonyl, pentamethylchromanesulfonyl, mesitylenesulfonyl, toluenesulfonyl, 2,4,6-trimethylbenzenesulfonyl, trimethoxybenzenesulfonyl, bisadamantyloxycarbonyl, nitro or tosyl.
55. The compound according to claim 53 wherein X is methoxytrimethylsulfonyl, pentamethylchromanesulfonyl, bisadamantyloxycarbonyl or mesitylenesulfonyl.
56. The compound according to claim 54 wherein X is methoxytrimethylsulfonyl, pentamethylchromanesulfonyl, bisadamantyloxycarbonyl or mesitylenesulfonyl.
57. The compound according to claim 1 wherein AA is asparagine or glutamine and X is dimethoxybenzylhydryl, 9-xanthenyl, or 2,4,6-trimethoxybenzyl
58. The compound according to claim 2 wherein AA is asparagine or glutamine and X is dimethoxybenzylhydryl, 9-xanthenyl, or 2,4,6-trimethoxybenzyl.
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