Basic .alpha.-aminoalkylphosphonate derivatives

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to a novel class of peptidyl derivatives of aromatic diesters of .alpha.-aminoalkylphosphonic acids useful for selectively inhibiting elastase, selectively inhibiting chymotrypsin-like enzymes and selectively inhibiting trypsin-like enzymes. The diesters of .alpha.-aminoalkylphosphonic acids are analogues of natural .alpha.-amino acids. This invention is also relates to a method for controlling tumor invasion, treating inflammation and controlling blood coagulation in patients using the novel compounds of the present invention. We have found that peptidyl derivatives of aromatic diesters of aminoalkylphosphonic acids are potent inhibitors of chymotrypsin-like enzymes, elastases, blood coagulation enzymes, tryptases, kallikreins, and therefore they are useful as anti-tumor, anti-inflammatory and anticoagulant agents.
2. Description of the Related Art
Serine proteases play critical roles in several physiological processes such as digestion, blood coagulation, complement activation, fibrinolysis, and reproduction. Serine proteases are not only a physiological necessity, but also a potential hazard if they are not controlled. Blood coagulation serine proteases are responsible for vascular clotting, cerebral infarction and coronary infarction. Chymotrypsin-like enzymes and plasmin are involved in tumor invasion, tissue remodeling, and clot dissociation. Uncontrolled proteolysis by other serine proteases such as elastase may cause pancreatitis, emphysema, rheumatoid arthritis, intimation and adult respiratory distress syndrome. Accordingly, specific and selective inhibitors of these proteases should be potent anticoagulants, anti-inflammatory agents and anti-tumor agents useful in the treatment of protease-related diseases (Powers and Harper, in Proteinase Inhibitors, Barrett and Salvesen, eds., Elsevier, 1986, pp. 55-152; Tryggvason, Hoyhtya and Salo, Biochem. Biophys. Acta, 1987, 907, 191-217, incorporated herein by reference). In vitro proteolysis by trypsin, chymotrypsin or the elastase family is a serious problem in the production, purification, isolation, transport or storage of peptides and proteins.
BRIEF SUMMARY OF THE INVENTION
It is an object of this invention to define a novel group of specific inhibitors for trypsin, elastase, chymotrypsin and other serine proteases. Inhibitors are compounds that can reduce or eliminate the catalytic activity of the enzyme. Trypsin and trypsin-like enzymes normally cleave peptide bonds in proteins and peptides where the amino acid residue on the carbonyl side of the split bond (P.sub.1 residue) is Lys or Arg. Elastase and elastase-like enzymes cleave peptide bonds where the P.sub.1 amino acid is Ala, Vat, Ser, Leu and other similar amino acids. Chymotrypsin and chymotrypsin-like enzymes hydrolyze peptide bonds where the P.sub.1 amino acid is Trp, Tyr, Phe, Met, Leu or other amino acid residue which contain an aromatic or large alkyl side chain. All of the above enzymes have extensive secondary specificity and recognize amino acid residues removed from the P1 residue.
It is a further object of this invention to define new protease inhibitors, especially inhibitors for chymotrypsin and chymotrypsin-like enzymes, elastase inhibitors, blood coagulation enzyme inhibitors and tryptase inhibitors. These inhibitors are useful for controlling tumor invasion, blood coagulation and various inflammatory conditions mediated by serine proteases. The inhibitors of this invention would be useful for treating diseases such as vascular clotting, intimations, tumor invasion, pancreatitis, emphysema or infantile and adult respiratory distress syndrome. The inhibitors of this invention would also be useful for controlling hormone processing by serine proteases and for treating diseases related to tryptases such as inflammation and skin blistering.
It is yet another object of this invention to define a novel group of specific inhibitors useful in vitro for inhibiting trypsin, elastase, chymotrypsin and other serine proteases of similar specificity. Such inhibitors could be used to identify new proteolytic enzymes encountered in research. They could also be used in research and industrially to prevent undesired proteolysis that occurs during the production, isolation, purification, transport and storage of valuable peptides and proteins. Such proteolysis often destroys or alters the activity and/or function of the peptides and proteins. Uses would include the addition of the inhibitors to antibodies, enzymes, plasma proteins, tissue extracts or other proteins and peptides which are widely sold for use in clinical analyses, biomedical research, and for many other reasons.
These and other objects are accomplished by the present invention which defines novel peptidyl derivative of aryl diesters of .alpha.-aminoalkylphosphonic acids. These phosphonate derivatives are potent inhibitors of serine proteases including chymotrypsin-like enzymes, trypsin-like enzymes, elastase-like enzymes, and other enzymes with other substrate specificities. The phosophonates are stable in buffer or plamsa, and inhibit the serine proteases to give stable inhibited enzyme derivatives. The phosphonates can be used both in vitro and in vivo.

DETAILED DESCRIPTION OF THE INVENTION
Peptidyl derivatives of aryl diesters of .alpha.-aminoalkylphosphonic acids have be found to be excellent inhibitors of several serine proteases including bovine thrombin, human factor XIIa, human factor Xa, human plasma kallikrein, bovine trypsin, rat skin tryptase, human leukocyte elastase, porcine pancreatic elastase, bovine chymotrypsin, human leukocyte cathepsin G and rat mast cell protease II. The diesters of .alpha.-aminoalkylphosphonic acids are analogues of natural a-amino acids and are designated by the generally accepted three letter abbreviations for the amino acid followed by the superscript P. For example diphenyl .alpha.-(N-benzyloxycarbonylamino)ethylphosphonate which is related to alanine is abbreviated as Cbz-Ala.sup.P (OPh).sub.2. ##STR1##
Peptidyl derivatives of aryl diesters of .alpha.-aminoalkylphosphonic acids inhibit serine proteases by reaction with the active site serine to form "phosphonylated" enzymes, which due to similarity of phosphorus atom to the tetrahedral intermediate formed during peptide hydrolysis, show remarkable stability. The enzyme catalytic apparatus is required to activate the phosphorus atom for nucleophilic substitution and reaction with enzyme. The activation is mainly due to precise interaction with the S.sub.1 pocket of various serine proteases. The following figure shows the reaction course of a phosophonate with a serine protease. The phosphonate first binds to the enzyme (below left) and then reacts to form a covalent bond with the active site serine residue (below right). Slow aging can take place with loss of the phenoxy group (below center). ##STR2##
Peptides with a C-terminal phosphonate residue which is an analog of valine �e.g. Val.sup.P (OPh).sub.2 ! are potent and specific irreversible inhibitors of elastase and elastase-like enzymes. The peptides with C-terminal phosphonate residues related to phenylalanine, other aromatic amino acids or amino acids with long aliphatic side chains are potent and specific inhibitors of chymotrypsin and chymotrypsin-like enzymes. The peptides with C-terminal phosphonate residues related to ornithine, lysine, arginine or containing a C-terminal diphenyl ester of .alpha.-amino-.alpha.-(4-amidinophenyl)methanephosphonate �(4-AmPhGly).sup.P (OPh).sub.2 ! or .alpha.-amino-.alpha.-(4-amidinophenylmethyl)methanephosphonate �(4-AmPhe).sup.P (OPh).sub.2 ! are specific and potent inhibitors of trypsin and trypsin-like enzymes. ##STR3##
Additional specificity as well as increased activation toward reaction with the enzyme can be introduced into the inhibitor molecule by variation of the amino acid sequence in the peptide portion of the structure. In fact there is a good agreement between the sequence of enzyme substrates such as a peptidyl p-nitroanilides and the sequence of an effective peptidyl phosphonate inhibitor. The best inhibitors have the sequence of the best peptidyl p-nitroanilide substrate for a particular enzyme. For example, the best inhibitor for chymotrypsin and chymotrypsin-like enzymes is Suc-Val-Pro-Phe.sup.P (OPh).sub.2 which has an amino acid sequence that is analogous to Suc-Val-Pro-Phe-NA, an excellent substrate for these enzymes. With human leukocyte elastase, the two best inhibitors �MeO-Suc-Ala-Ala-Pro-Val.sup.P (OPh).sub.2 and Boc-Val-Pro-Val.sup.P (OPh).sub.2 ! have an amino acid sequence similar to MeO-Suc-Ala-Ala-Pro-Val-NA and Boc-Val-Pro-Val-NA, two excellent substrates for this enzyme. For bovine thrombin, the best phosphonate inhibitor is diphenyl Boc-D-Phe-Pro-amino(4-amidinophenyl)methanephosphonate hydrochloride, which corresponds to Boc-D-Phe-Pro-Arg-NA, which is excellent substrate for thrombin, and D-Phe-Pro-Arg-H which is an excellent peptide aldehyde inhibitor of thrombin and an anticoagulant (Bajusz, S., Szell, E., Bagdy, D., Barabas, E., Horvath, G., Dioszegi, M., Fittier, Z., Szabo, G., Juhasz, A., Tomori, E., and Szilagyi, G., J. Med. Chem. 33, 1729-1735 (1990) incorporated by reference). Since good substrate sequences are known in the literature for other serine proteases, it is possible to predict the structure of additional excellent phosphonate inhibitors for these enzymes �Mammalian Proteases, A Glossary and Bibliography, Vol. 1 Endopeptidases, Academic Press, Barrett, A. J., and McDonald, J. K. eds, pp. 1-416, 1980; Mammalian Proteases, A Glossary and Bibliography, Vol. 2 Exopeptidases, Academic Press, Barrett, A. J., and McDonald, J. K. eds, pp. 1-357, 1986; Lottenberg, R., Christensen, U., Jackson, C. M., and Coleman, P. L., Methods in Enzymology 80, 341-361 (1981) the preceding articles are incorporated herein by reference!. It is also possible to design good phosophonate inhibitors for serine proteases based on on the peptide sequences found in other potent reversible and irreversible inhibitors for those same serine proteases reported in the literature �Powers and Harper, in Proteinase Inhibitors, Barrett and Salvesen, eds., Elsevier, 1986, pp. 55-152; Trainor, D. A., Trends in Pharm. Sci. 8, 303-307 (1987) the preceding articles are incorporated herein by reference!.
Examples of phosphonate inhibitors for various enzymes are given below:
__________________________________________________________________________Cbz--Gly--Leu--Phe.sup.P (OZ).sub.2 for cathepsin G and RMCP IIMeO--Suc--Ala--Ala--Pro--Met.sup.P (OZ).sub.2 for Cathepsin GSuc--Pro--Leu--Phe.sup.P (OZ).sub.2 and Boc--Ala--Ala--Phe.sup.P (OZ).sub.2 for RMCP IBoc--Gly--Leu--Phe.sup.P (OZ).sub.2, Suc--Phe--Leu--Phe.sup.P (OZ).sub.2 for human and dog skin chymaseBoc--Ala--Ala--Glu.sup.P (OZ).sub.2 for S. aureus V-8 proteaseCbz--Gly--Gly--Pro.sup.P (OZ).sub.2 for human prolyl endopeptidaseAla--Pro.sup.P (OZ).sub.2 for DPP IVSuc--Ala--Ala--Pro--Val.sup.P (OZ).sub.2 for PPESuc--Lys(Cbz)--Val--Pro--Val.sup.P (OZ).sub.2, for human leukocyte (neutrophil) elastaseadamantyl-SO.sub.2 --Lys(COCH.sub.2 CH.sub.2 CO.sub.2 H)--Ala--Val.sup.P(OZ).sub.2,adamantyl-CH.sub.2 CH.sub.2 OCO--Glu(O-t-Bu)--Pro--Val.sup.P (OZ).sub.2,adamantyl-SO.sub.2 --Lys(CO--C.sub.6 H.sub.4 CO.sub.2 H)--Ala--Val.sup.P(OZ).sub.2Suc--Ala--Ala--Pro--Leu.sup.P (OZ).sub.2 for elastolytic proteinase from " Schistosoma mansoni"Glu--Phe--X and Dns--Ala--Phe--X for plasminD--Val--Gly--X and Dns--Glu--Gly--X for factor XaCbz--Phe--X and CBz--Trp--X for porcine pancreatic and human plasma killikreinsCbz--Lys--X for human skin tryptaseCbz--Gly--X for human lung tryptaseCbz--Ile--Ala--Gly--X for factors IXa, Xa, XIa, XIIa and bovine plasma kallikreinGlu--Gly--X for urokinaseDns--Phe--Pro--X for plasminogen activatorDns--Ile--Pro--X for activated protein CCbz--Trp--X for bovine factor IXaCbz--Gly--X for bovine factor Xa and XIaCbz--Phe--X for bovine factor XIIaCbz--Phe--Gly--X for trypein__________________________________________________________________________
where Z represents an aryl group, a substituted aryl group or a highly fluorinated alkyl group and X represents Arg.sup.P (OZ).sub.2, Orn.sup.P (OZ).sub.2, Lys.sup.P (OZ).sub.2, an aryl diester of .alpha.-amino-.alpha.-(4-amidinophenyl)methanephosphonate �abbreviated NH.sub.2 -CH(AmPh)PO(OZ).sub.2 or 4-AmPhGly.sup.P (OZ).sub.2 !, or .alpha.-amino-.alpha.-(4-amidinophenylmethyl)methanephosphonate �abbreviated NH.sub.2 -CH(AmPhCH.sub.2)PO(OZ).sub.2 or 4-AmPhe.sup.P (OZ).sub.2 !.
The inhibitory potency of peptidyl derivatives of aryl diesters of .alpha.-aminoalkylphosphonic acids is also determined by the electronic property of the Z group. More electron withdrawing groups such as nitro, cyano, halogen, etc. on the aryl ring can make the phosphorus atom in the inhibitor more electrophilic and accelerate reaction with the active site serine of the serine protease. Reactivity toward serine proteases can also be obtained by using derivatives where the Z groups are highly fluorinated alkyl groups. However increased reactivity can also result in low chemical stability and in extreme cases, compounds may be too hydrolytically unstable for practical purposes if the Z group is too electronegative. Phosphonates where the Z group is not sufficiently electron withdrawing will be chemically very stable and will react very slowly with serine proteases or not at all. Such non-reactive inhibitors would include derivatives where Z is simple alkyl groups (e.g. peptidyl derivatives of alkyl diesters of .alpha.-aminoalkylphosphonic acids). Thus the phosphonate ester groups (Z) should represent a balance between these two competing factors and we find that diphenyl esters (Z=Ph) are one way to obtain a balance between increased reactivity and stability in solution.
Diphenyl esters of .alpha.-aminoalkylphosphonate can be synthesized by a previously described method (Oleksyszyn et al., 1979, Synthesis, 985 incorporated by reference). Di(substituted phenyl)esters of .alpha.-aminoalkylphosphonate can also be prepared by the same procedure using tris(substituted phenyl) phosphite instead of triphenyl phosphite. Perfluoroalkyl diesters can be synthesized by a method involving transesterification (Szewczyk et at., Synthesis, 1982, 409-414 incorporated by reference). Alternatively, the synthesis of diesters of .alpha.-aminoalkylphosphonic acids and their peptides can be performed by esterification of the phosphonic acid moiety as described previously (Bartlett et al., Bioorg. Chem., 1986, 14, 356-377 incorporated by reference).
The synthesis of AmPhe.sup.P (OPh).sub.2 derivatives is illustrated in the following figure. ##STR4##
Peptide derivatives of 4-amidinophenylglycine phosphonate diphenyl ester were prepared using the reactions outline in scheme shown above. The parent compound Z-(4-AmPhGly).sup.P (OPh).sub.2 was prepared by .alpha.-amidoalkylation of triphenyl phosphite with 4-cyanobenzaldehyde and benzyl carbamate (60.degree.-90.degree. C., AcOH, 2 h) to give Z-(4-CN-PhGly).sup.P (OPh).sub.2 (70%) which was converted to the iminoester (dry HCl in CHCl.sub.3 /ethanol) and then to the amidine derivative Z-(4-AmPhGly).sup.P (OPh).sub.2 (dry NH.sub.3 in methanol, 70-80%). Hydrogenolysis of Z-(4-AmPhGly).sup.P (OPh).sub.2 gave H-(4-AmPhGly).sup.P (OPh).sub.2 (60-80%) which was then coupled respectively with Z-Pro-OH, Boc-D-Phe-Pro-OH, and 2-NpSO.sub.2 -Gly-OH using CDI to give Z-Pro-(4-AmPhGly).sup.P (OPh).sub.2, Boc-D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2 (29%) and 2-NpSO.sub.2 -Gly-(4-AmPhGly).sup.P (OPh).sub.2 (30%). Deblocking gave D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2 (24%). The 4-amidinophenylalanine phosphonate diphenyl ester derivative Z-(4-AmPhe).sup.P (OPh).sub.2 was synthesized from 4-cyanophenylacetaldehyde using the same reaction scheme with slightly modified conditions (.alpha.-amidoalkylation, 25-35%; amidination sequence, 50-70%). Hydrogenolysis produced H-(4-AmPhe).sup.P (OPh).sub.2 (85-90%) which was coupled with Boc-D-Phe-Pro-OH to give Boc-D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2 (59%). Z-Pro-(4-AmPhe).sup.P (OPh).sub.2 was obtained as a transesterification product during the amidination of Z-Pro-(4-CN-Phe).sup.P (OPh).sub.2 (50%). Deblocking of with dry HCl/CHCl.sub.3 produced D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2 (80%).
The diphenyl phosphonate moiety is very resistent to chemical hydrolysis and at pH 7.5 we did not observe any hydrolysis after several days (monitored by .sup.31 P NMR). Furthermore, they show excellent stability in human plasma. For example Suc-Val-Pro-Phe.sup.P (OPh).sub.2 has a hydrolysis half-time in human plasma of about 20 hrs. These experiments demonstrate that the phosphonate inhibitors are remarkably stable in buffer and plasma. Thus they can be used under a variety of conditions. Phosphonates have the additional advantage of being very stable in plasma and will have a high effectiveness in vivo due to their long lifetimes. Additionally, the inhibitor-enzyme complex is very stable and the enzyme did not regain any activity after several hours in the case of chymotrypsin and after several days no recovery of activity was observed in the the cases of elastases and trypsin. These experiments show that it is possible to decrease or eliminate the enzyme activity and biological function of serine proteases for extended time periods.
Either racemic mixtures of the diphenyl .alpha.-aminoalkylphosphonate residue or pure diastereomers can be used in the inhibitor structures. The racemic compounds are more easily synthesized and are obtained from less expensive starting materials. The pure optically active .alpha.-aminoalkylphosphonate derivatives required in the synthesis are more difficult to synthesize (Kafarski et at., Can. J. Chem. 1983, 61, 2425) and require more expensive starting materials. In the case of the peptidyl phosphonate inhibitors which are mixtures of two diastereomers, only one will usually react with the enzymes. The pure diastereomers will possess higher inhibition rates and could be used at lower concentrations.
Peptidyl derivatives of aryl diesters of .alpha.-aminoalkylphosphonates may be used in vivo to treat diseases resulting from abnormal or uncontrolled blood coagulation or diseases caused by uncontrolled proteolysis by elastase, chymotrypsin, trypsin and related serine proteases. These inhibitors may be used in vitro to prevent proteolysis which occurs in the process of the production, isolation, purification, storage or transport of peptides and proteins.
The novel peptidyl derivatives of aryl diesters .alpha.-aminoalkylphosphonates of the present invention have the following structural formula: ##STR5## or a pharmaceutically acceptable salt, wherein:
R is selected from the group consisting of phenyl substituted with B, benzyl substituted with B on the phenyl ring, and C.sub.1-6 alkyl substituted with B,
B is selected from the group consisting of amidino �--C(.dbd.NH)NH.sub.2 !, guanidino --NH--C(.dbd.NH)NH.sub.2 !, isothiureido �--S--C(.dbd.NH)NH.sub.2 !, and amino,
Z and Z.sup.1 are the same or different and are selected from the group consisting of C.sub.1-6 perfluoroalkyl, phenyl, phenyl substituted with J, phenyl disubstituted with J, and phenyl trisubstituted with J,
J is selected from the group consisting of halogen, C.sub.1-6 alkyl, C.sub.1-6 perfluoroalkyl, C.sub.1-6 alkoxy, NO.sub.2, CN, OH, CO.sub.2 H, amino, C.sub.1-6 alkylamino, C.sub.2-12 dialkylamino, C.sub.1-6 acyl, C.sub.1-6 alkoxy--CO--, and C.sub.1-6 alkyl--S--,
AA.sup.4, AA.sup.3, and AA.sup.2 are the same or different and are selected from the group consisting of
(a) a single bond, and
(b) a blocked or unblocked amino acid residue with the L or D configuration at the .alpha.-carbon selected from the group consisting of alanine, valine, leucine, isoleucine, proline, methionine, methionine sulfoxide, phenylalanine, tryptophan, serine, threonine, cysteine, tyrosine, asparagine, glutamine, aspartic acid, glutamic acid, lysine, arginine, histidine, phenylglycine, norleucine, norvaline, alpha-aminobutyric acid, citrulline, hydroxyproline, ornithine, and homoarginine, and
(c) glycine, sarcosine, epsilon-aminocaproic acid, and beta-alanine,
X is selected from the group consisting of H, NH.sub.2 --CO--, NH.sub.2 --CS--, NH.sub.2 --SO.sub.2 --, Y--NH--CO--, Y--NH--CS--, Y--NH--SO.sub.2 --, Y--CS--, Y--SO.sub.2 --, Y--O--CO--, Y--CO--, and Y--CO--,
Y is selected from the group consisting of C.sub.1-6 alkyl, C.sub.1-6 fluoroalkyl, C.sub.1-6 alkyl substituted with K, C.sub.1-6 fluoroalkyl substituted with K, 9-fluorenylmethyl, phenyl, phenyl substituted with J, phenyl disubstituted with J, phenyl trisubstituted with J, naphthyl, naphthyl substituted with J, naphthyl disubstituted with J, naphthyl trisubstituted with J, C.sub.1-6 alkyl with an attached phenyl group, C.sub.1-6 alkyl with two attached phenyl groups, C.sub.1-6 alkyl with an attached phenyl group substituted with J, and C.sub.1-6 alkyl with two attached phenyl groups substituted with J, and
K is selected from the group consisting of halogen, COOH, OH, CN, NO.sub.2, NH.sub.2, C.sub.1-6 alkoxy, C.sub.1-6 alkylamine, C.sub.1-6 dialkylamine, C.sub.1-6 alkyl--O--CO--, C.sub.1-6 alkyl--O--CO--NH, and C.sub.1-6 alkyl--S--.
The blocking groups which may be present on --HN--CH(R)--P(O)-- or on the amino acid AA.sup.4, AA.sup.3, and AA.sup.2 are those well known in the art of peptide synthesis. For example, a listing of suitable peptide blocking groups is found in Gross et al., eds. The Peptides, Vol. 3 (Academic Press, New York, 1981). The particular choice of the blocking group used in the compounds of the invention depends on several factors, including the blocking group's affect on enzyme specificity, its affect on phosphonate solubility, and its utility during synthesis. Suitable blocking groups include but are not limited to carboberizyloxy (Cbz), benzoyl, t-butyloxycarbonyl (Boc), glutaryl, p-tolylsulfonyl (Tos), methoxysuccinyl (MeO-Suc), and succinyl.
The --HN--CH(R)--P(O)-- residue is derived from a blocked or unblocked alpha amino acid residue --HN--CH(R)--CO-- whose alpha carbonyl group has been replaced by a P(O) group. The R group is the side chain of the alpha amino acid. The alpha amino acid residue is derived from natural alpha amino acids such as those listed in the IUPAC-IUB Joint Commision on Biochemical Nomenclature report on the Nomenclature and Symbolism for Amino Acids and Peptides (J. Biol Chem., 260, 14-42 (1985) incorporated by reference). The choice of the particular amino acid residue used in the design of the phosphonate inhibitor will depend on the enzyme targeted for inhibition. For example, with chymotrypsin-like enzymes which prefer Trp, Tyr, or Phe at the P.sub.1 position of their substrates, -Trp.sup.P -, Tyr.sup.P -, and Phe.sup.P -residues would be suitable phosphonate residues to incorporate into the P.sub.1 position of an inhibitor. With elastase-like enzymes which prefer Vat, Ser, or Ala at the P.sub.1 position of their substrates, -Val.sup.P -, Ser.sup.P -, and Ala.sup.P -residues would be suitable phosphonate residues to incorporate in the P.sub.1 position of an inhibitor. Likewise with trypsin-like enzyme -Lys.sup.P - or -Arg.sup.P -residues would be suitable. Unnatural blocked or unblocked alpha amino acid residues can also be used in the design of phosphonate inhibitors. If the target serine protease will hydrolyze a substrate containing the unnatural amino acid residue at the P.sub.1 position or if an inhibitor structure contains the unnatural amino acid residue as the P.sub.1 residue, then this residue can be used in the design of a phosphonate inhibitor. For example, chymotrypsin hydrolyzes para-fluorophenylalanine containing substrates and thus the --HN--CH(CH.sub.2 C.sub.6 H.sub.4 F)-P(O)-- and --HN-- would be suitable for incoroporating into a chymotrypsin inhibitor. Likewise, trypsin will hydrolyze substrates with aminoethylcysteine residues and cathespin G will hydrolyze aminopropylcysteine residues and thus --HN--CH(CH.sub.2 SCH.sub.2 CH.sub.2 NH.sub.2)-P(O)-- and --HN--CH(CH.sub.2 SCH.sub.2 CH.sub.2 CH.sub.2 NH.sub.2)-P(O)-- would respectively be suitable residues to incorporate into inhibitors for trypsin and cathepsin G. One skilled in the art of designing inhibitors for proteolytic enzyme can list many other unnatural amino acid residues which could be used in the design of suitable inhibitors.
Other aryl diesters of .alpha.-aminoalkylphosphonic acids have been prepared earlier for other purposes (illustrative examples: Oleksyszyn, J. et al., Synthesis, 1979, 985-986.; Vo-Quang, Y. et al., J. Med. Chem. 1986, 43, 579-581.; Kafarski, P. et al., Tetrahedron, 1987, 43, 799-803.; Szewczyk, J. et al., Synthesis, 1982, 409-414; the preceding articles are incorporated herein by reference).
A few other derivatives of .alpha.-aminoalkylphosphonic acids have been prepared recently for inhibition of serine proteases, but they are not peptidyl derivatives or are peptidyl derivatives with the phosphonic acid moiety inside the peptide chain (Bartlett et al., Bioorg. Chem., 1986, 14, 356-377.; Lamden et al., Biochem. Biophys. Res. Commun., 1983, 112, 1085-1090; the preceding articles are incorporated herein by reference). We have published some of our work in a paper "Irreversible Inhibition of Serine Proteases by Peptidyl Derivatives of .alpha.-Aminoalkylphosphonate Diphenyl Esters", Oleksyszyn and Powers, Biochem. Biophys. Res. Commun. 161, 143-149 (May 30, 1989 issue). Subsequently, Fastrez et al., Tetrahedron Lett., 1989, 30, 6861-6864 reported phosphonate inhibitors similar to those which we reported and which we describe in this specification (both the preceding articles are incorporated herein by reference). Two peptidyl phosphonate derivatives, Cbz-Phe-Pro-Phe.sup.P (OPh).sub.2 and MeO-Suc-Ala-Ala-Pro-Val.sup.P (OPh).sub.2 were reported by us earlier (Powers, J. C. and Oleksyszyn, J., abstract to the FASEB meeting, May 1988, Las Vegas). It is not obvious from the abstract that peptide phosphonate derivatives could be designed based on the peptide inhibitors and peptide substrates for many serine proteases, and would be inhibitors for many serine proteases. In particular, in this invention we now find that Cbz-Phe-Pro-Phe.sup.P (OPh).sub.2 is a potent inhibitor of cathepsin G and rat mast cell protease II (two other serine proteases). Many other examples are given in the tables. It is not obvious from the abstract that the stereochemistry of the phosphonate will affect the inhibitory potency. Thus, MeO-Suc-Ala-Ala-Pro-Val.sup.P (OPh).sub.2 obtained by a better synthetic route is a better inhibitor of human leukocyte elastase and porcine pancreatic elastase due to the presence of a higher concentrations of the reactive stereoisomer. It is not obvious from the abstract that many different amino acid residues can be used in the design of phosphonate inhibitors. It is not obvious from the abstract that phosphonates can be designed for all serine proteases using peptides of varying length and with varying amino acid residues. It is not obvious from the abstract how to design phosphonates for elastase, chymotrypsin or any serine protease from peptide inhibitor and peptide substrate sequences.
The following compounds are representative of but do not limit the invention:
Diphenyl amino(4-amidinophenyl)methane-phosphonate dihydrochloride �abbreviated NH.sub.2 -CH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 or (4-AmPhGly).sup.P (OPh).sub.2 !
Diphenyl N-benzyloxycarbonylamino(4-amidinophenyl)methanephosphonate hydrochloride �abbreviated Cbz-NH-CH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2, or Cbz-(4-AmPhGly).sup.P (OPh).sub.2 !
Diphenyl N-(N-benzyloxycarbonylprolyl)amino(4-amidinophenyl)methanephosphonate hydrochloride �abbreviated Cbz-NH-Pro-NHCH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 or Cbz-Pro-(4-AmPhGly).sup.P (OPh).sub.2 !
Diphenyl N-(D-Phe-Pro)amino(4-amidinophenyl)methanephosphonate dihydrochloride �abbreviated D-Phe-Pro-NHCH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 or D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2 !
Diphenyl N-(Boc-D-Phe-Pro)amino(4-amidinophenyl)methanephosphonate hydrochloride �abbreviated Boc-D-Phe-Pro-NHCH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 or Boc-D-Phe-L-Pro-(4-AmPhGly).sup.P (OPh).sub.2 !
Diphenyl N-(N-.beta.-napthylsulfonylglycyl)amino(4-amidinophenyl)methanephosphonate hydrochloride �abbreviated naphthylsulfonyl-Gly-NHCH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 or 2-NpSO.sub.2 -Gly-(4-AmPhGly).sup.P (OPh).sub.2 !
Cbz-Ala.sup.P (OCH.sub.2 CF.sub.3).sub.2
Cbz-Phe.sup.P (OCH.sub.2 CF.sub.3).sub.2
Cbz-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2
Cbz-Met.sup.P (OPh).sub.2
Cbz-Met(O).sup.P (OPh).sub.2
Met.sup.P (OPh).sub.2.HBr
Cbz-NHCH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2
Benzoyl-NHCH(4-NH.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2
Cbz-NHCH(4-CN-C.sub.6 H.sub.4)PO(OPh).sub.2
NH.sub.2 CH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2
Cbz-NHCH(CH.sub.2 .dbd.CH--)PO(OPh).sub.2
Cbz-NHCH(4-CO.sub.2 H-C.sub.6 H.sub.4)PO(OPh).sub.2
Cbz-NHCH(3-CH.sub.3 -C.sub.6 H.sub.4)PO(OPh).sub.2
CF.sub.3 CF.sub.2 CF.sub.2 CO-Ala.sup.P (OPh).sub.2
Pro.sup.P (OPh).sub.2.HCl
(m-Tos-Phe)-C.sub.6 H.sub.4 CO-Val.sup.P (OPh).sub.2
Cbz-Ala-Ala.sup.P (OPh).sub.2
Cbz-Ala-Phe.sup.P (OPh).sub.2
Cbz-Ala-Val.sup.P (OPh).sub.2
Cbz-Pro-Val.sup.P (OPh).sub.2
Cbz-Pro-Phe.sup.P (OPh).sub.2
Cbz-Phe-Phe.sup.P (OPh).sub.2
Cbz-Leu-Phe.sup.P (OPh).sub.2
Cbz-Val-Phe.sup.P (OPh).sub.2
Cbz-Val-Val.sup.P (OPh).sub.2
Cbz-Pro-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2
Cbz-Pro-Phe.sup.P (OCH.sub.2 CF.sub.3).sub.2
Cbz-Pro-Val.sup.P (OEt).sub.2
Boc-Pro-Phe.sup.P (OPh).sub.2
Boc-Pro-Val.sup.P (OPh).sub.2
Boc-Pro-Nva.sup.P (OPh).sub.2
Ala-Ala.sup.P (OPh).sub.2.HBr
Ala-Pro.sup.P (OPh).sub.2.HCl
Phe-Ala.sup.P (OPh).sub.2.CF.sub.3 COOH
Cbz-Ala-Ala-Val.sup.P (OPh).sub.2
Cbz-Phe-Pro-Phe.sup.P (OPh).sub.2
Cbz-Val-Val-Val.sup.P (OPh).sub.2
Cbz-Phe-Pro-Phe.sup.P (OPh).sub.2
Suc-Phe-Pro-Phe.sup.P (OPh).sub.2
Suc-Val-Pro-Phe.sup.P (OPh).sub.2
Boc-Val-Pro-Val.sup.P (OPh).sub.2
Boc-Ala-Pro-Val.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Pro-Met.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Pro-Met(O).sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Ala-Val.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Ala-Nva.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Ala-Phe.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Pro-Val.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Pro-Phe.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Pro-Leu.sup.P (OPh).sub.2
MeO-Suc-Ala-Ala-Pro-Nva.sup.P (OPh).sub.2
Cbz-(4-CN-Phe).sup.P (OPh).sub.2
4-CN-Phe.sup.P (OPh).sub.2.HBr
Cbz-(4-AmPhe).sup.P (OPh).sub.2
(4-AmPhe).sup.P (OPh).sub.2.2HCl
Cbz-Pro-(4-CN-Phe).sup.P (OPh).sub.2
Cbz-Pro-(4-AmPhe).sup.P (OEt).sub.2
Boc-D-Phe-Pro-(4-CN-Phe).sup.P (OPh).sub.2
Boc-D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2
D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2
Boc-Phe-Phe-(4-AmPhGly).sup.P (OPh).sub.2
Cbz-Thr-(4-AmPhGly).sup.P (OPh).sub.2
Boc-Leu-Thr-(4-AmPhGly).sup.P (OPh).sub.2
(4-AmPhGly).sup.P (OPh-4-Cl).sub.2, and
Z-(4-AmPhGly).sup.P (OPh-4-Cl).sub.2.
It has been found that compounds of the present invention have anticoagulant activity as shown in Table I, Table II, and Table V by effective inhibition of the proteolytic function of blood coagulation enzymes in Hepes buffer and in pig plasma. It has also been found that compounds of the present invention have anti-tumor activity as shown in Table I, Table II, Table III, and Table IV by effective inhibition of the proteolytic function of trypsin-like, elastase-like and chymotrypsin-like enzymes. Compounds of the present invention have anti-inflammatory activity and are effective in the prevention and inhibition of edema and granuloma tissue formation as shown in Table III by effective inhibition of the proteolytic function of human leukocyte elastase.
Inactivation rates of serine proteases by aryl diesters of peptidyl derivatives of .alpha.-aminoalkylphosphonates were measured by the incubation method. An aliquot of inhibitor (25 or 50 .mu.l) in Me.sub.2 SO was added to a buffered enzyme solution (0.01-2.3 .mu.M) to initiate the inactivation. Aliquots (50 .mu.l) were withdrawn at various intervals and the residual enzymatic activity was measured. Me.sub.2 SO concentration in the reaction mixture was 8-12% (v/v). A 0.1M HEPES, 0.01M CaCl.sub.2, pH 7.5 buffer was utilized for trypsin and trypsin-like enzymes. A 0.1M HEPES, 0.5M NaCl, pH 7.5, was utilized for the other serine proteases. The inhibitor concentrations are shown in the Tables I, II, III, and IV. Peptide thioesters or peptide nitroanilides with the appropriate sequences were used as substrates for various serine proteases. All peptide thioesters hydrolysis rates were measured with the assay mixture containing 4,4'-dithiodipyridine �.epsilon..sub.324 =19800 M.sup.-1 cm.sup.1 ; Grasetti & Murray, Arch. Biochem. Biophys. 1967, 119, 41-48!. Peptide 4-nitroanilide hydrolysis was measured at 410 nm �.epsilon..sub.410 =8800 M.sup.-1 cm.sup.-1 ; Erlanger et al., Arch. Biochem. Biophys. 1961, 95, 271-278!. First order inactivation rate constants (k.sub.obs) were obtained from plots of ln v.sub.t /v.sub.o vs time, and the correlation coefficients were greater then 0.98.
Table V shows the prothrombin time of pig plasma measured in the presence of various inhibitors. Diphenyl N-benzyloxycarbonylamino(4-amidinophenyl)methanephosphonate hydrochloride can prolong the clotting time from 17.7 to 25.2 sec. Compounds Cbz-(4-AmPhGly).sup.P (OPh).sub.2, Boc-D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2, D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2, and D-Phe-Pro-(4-AmPhe)P(OPh).sub.2 were tested in human plasma with the prothrombin (PT) and activated partial thromboplastin time (APTT) coagulant assays and the PT was prolonged from 14.6 see to 17.0, 19.8, 29.3, and 28.0 sec in the presence of 125 .mu.M of Cbz-(4-AmPhGly).sup.P (OPh).sub.2, D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2, D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2, and 63 .mu.M of Boc-D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2, respectively. At the same inhibitor concentrations, the APTT was prolonged from 34.0 sec to 61.2, 73.0 106, and >140 sec, respectively for Cbz-(4-AmPhGly).sup.P (OPh).sub.2, D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2, D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2, and Boc-D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2. Both compounds Boc-D-Phe-Pro-(4-AmPhGly).sup.P (OPh).sub.2 and D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2 prolonged the PT ca. 2 fold and prolonged the APTT ca. 3-4 fold although their thrombin inhibition rates differed by over 200 fold.
Anticoagulants can prolong the clotting time of human plasma and play important roles in the treatment of blood coagulation related diseases such as vascular clotting, cerebral infarction and coronary infarction (Williams et al., Hematology, 3rd ed. McGraw Hill, 1983 and Ingram et al., Bleeding Disorders, 2nd ed. Blackwell Scientific Publications, 1985). These two books are incorporated herein by reference. The presence of certain inhibitors of this invention in the human plasma would prolong the prothrombin time, thus these inhibitors would act as anticoagulant in vivo. Currently, there are a few anticoagulant drugs in use clinically, and the inhibitors described in this invention can be used as anticoagulants in the treatment of animals.
It is known that the in vitro activity of elastase inhibitors correlates with their in vivo activity in animal models of emphysema and inflammation (Otterness et al., editor, Advances in Inflammation Research, Vol 11, Raven Press 1986, and this book is incorporated herein by reference). Thus the novel inhibitors listed in Table III will be useful for the treatment of emphysema and intimation. Elastase inhibitors have been used orally, by injection or by instillation in the lungs in animal studies �Powers, Am. Rev. Respir. Dis., 127, 54-58 (1983); Powers and Bengali, Am. Rev. Respir. Dis. 134, 1097-1100 (1986) and these two articles are incorporated herein by reference!. The inhibitors described above can be used by any of these routes.
The activity of some proteases correlate directly with the invasiveness of tumor cells �Nakajima, M. et al., Science, 1983, 220, 611-613; Sloane, B. F. et al., Cancer Res. 1982, 42, 980-987 and these two articles are incorporated herein by reference!. The tumor invasion can be stopped by treatment with inhibitors of serine proteases �Tryggvason, K. et al., Biochem. Biophys. Acta, 1987, 907, 191-217, and this article is incorporated herein by reference!. Thus the novel inhibitors showed in Table I, Table II, Table III, and Table IV will be useful for treatment of tumors.
For treatment of blood coagulation-related diseases, tumor invasion or inflammation, the compounds of the present invention may be administered orally, topically or parenterally. The term parenteral as used includes subcutaneous injection, intravenous, intramuscular, intrasternal injection or infusion techniques. The pharmaceutical compositions containing the active ingredient may be in the form suitable for oral use, for example as tablets, troches, lozenges, aqueous or oily suspension, dispersible powders or granules, emulsions, hard or soft capsules or syrups or elixirs. Dosage levels of the order to 0.2 mg to 140 mg per kilogram of body weight per day are useful in the treatment of above-indicated conditions (10 mg to 7 gms per patient per day). The amount of active ingredient that may be combined with carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
To use the above inhibitors in vitro, they are dissolved in an organic solvent such as dimethylsulfoxide or ethanol, and are added to an aqueous solution containing serine proteases. The final concentration of organic solvent should be less than 25%. The inhibitors may also be added as solids or in suspension. The serine protease inhibitors of this invention would be useful in a variety of experimental procedures where proteolysis is a significant problem. Inclusion of these inhibitors in radioimmunoassay experiments would result in higher sensitivity. The use of these inhibitors in plasma fractionation procedures would result in higher yields of valuable plasma proteins and would make purification of the proteins easier. The inhibitors disclosed here could be used in cloning experiments utilizing bacterial cultures, yeast, and cell lines. The purified cloned product would be obtained in higher yield.
TABLE I__________________________________________________________________________Rates of Inhibition of Trypsin-like Serine Protease by PeptidylDerivatives of Diphenyl .alpha.-Amino-(4-Amidinophenyl)methanephosphonate.sup.a. k.sub.obsd /�I!(M.sup.-1 s.sup.-1) bovine bovine human human plasma rat skinInhibitor trypsin.sup.b thrombin factor XIIa kallikrein tryptase.sup.c__________________________________________________________________________Cbz--NH--CH(Am--C.sub.6 H.sub.4)PO(OPh).sub.2 2,000 170 20 18,000 94Cbz--Pro--NH--CH(Am--C.sub.6 H.sub.4)PO(OPh).sub.2 100 70 2.6 59 .sup. NI.sup.dD-Phe--Pro--NH--CH(Am--C.sub.6 H.sub.4)PO(OPh).sub.2 110 730 2.8 250 NIBoc--D-Phe--Pro--NH--CH(Am--C.sub.6 H.sub.4)PO(OPh).sub.2 2,200 12,300 52 60 NINaphthylsulfonyl-Gly--NH--CH(Am--C.sub.6 H.sub.4)PO(OPh).sub.2 470 170 25 960 16__________________________________________________________________________ .sup.a Enzyme (0.06-2.3 .mu.M) was incubated with inhibitor (1.66-106 .mu.M) in 0.25-0.6 ml of 0.1 M Hepes, 0.01 M CaCl.sub.2, pH 7.5, 8-12% Me.sub.2 SO at 25.degree. C. Aliquots (50-150 .mu.L) were withdrawn at various intervals and the residual enzymatic activity measured as previously described. Residual activity was measured with ZArg--SBzl (80 .mu.M). The k.sub.obsd values were calculated from plots of 1n v/v.sub.o vs time. .sup.b Residual activity of trypsin was assayed with Z--Phe--Gly--Arg--NA (122 .mu.M). .sup.c Rat skin tryptase was assayed in 25 mM NaH.sub.2 PO.sub.4, 1 mM EDTA, 0.5 M NaCl, pH 7.5 buffer. .sup.d NI, less than 5% of inhibition was obtained after 30 min.
TABLE II__________________________________________________________________________Rates of Inhibition of Thrombin and Other Trypsin-like Serine Proteasesby Peptide Phosphonate Derivativesof 4-Aminodininophenylglycine and 4-Amidinophenylalanine.sup.a k.sub.obsd �I!(M.sup.-1 s.sup.-1) human bovine human human plasma bovineInhibitor thrombin thrombin factor XIIa kallikrein trypsin__________________________________________________________________________Cbz-(4-AmPhGly).sup.P (OPh).sub.2 80 170 20 18,000 2,000Cbz--Pro-(4-AmPhGly).sup.P (OPh).sub.2 20 70 2.6 60 100Boc--D-Phe--Pro-(4-AmPhGly).sup.P (OPh).sub.2 11,000 12,000 52 160 2,200D-Phe--Pro-(4-AmPhGly).sup.P (OPh).sub.2 700 730 2.8 250 1102-NpSO.sub.2 --Gly-(4-AmPhGly).sup.P (OPh).sub.2 170 25 960 470Cbz-(4-AmPhe).sup.P (OPh).sub.2 0.2 24H-(4-AmPhe).sup.P (OPh).sub.2 2.2 32Cbz--Pro-(4-AmPhe).sup.P (OEt).sub.2 NI NIBoc--D-Phe--Pro-(4-AmPhe).sup.P (OPh).sub.2 0.7 130D-Phe--Pro-(4-AmPhe).sup.P (OPh).sub.2 54 50__________________________________________________________________________ .sup.a Enzyme (0.03-2.3 .mu.M) was incubated with the inhibitor (1.7-420 .mu.M) in 0.3-0.6 mL of 0.1 M Hepes, 0.01 M CaCl.sub.2 (0.5 M NaCl for human thrombin), pH 7.5, 8-12% Me.sub.2 SO at 25.degree. C. Aliquots (25-150 .mu.L) were withdrawn at various intervals and the residual enzymatic activity were measured. Residual activity of trypsin and other coagulation enzymes were assayed with ZPhe--Gly--Arg--NA (100-120 .mu.M) and ZArg--SBzl (80#.mu.M), respectively. The k.sub.obs values were calculated from pseudo firstorder plots.
TABLE III__________________________________________________________________________Rate Constants for Inactivation of Serine Protease by Peptides withC-Terminal ArylDiesters of .alpha.-Aminoalkylphosphonates.sup.a. Chymotrypsin.sup.b PPE.sup.c HLE.sup.d �I! k.sub.obsd /�I! �I! k.sub.obsd /�I! �I! k.sub.obsd /�I!Inactivator (.mu.M) (M.sup.-1 s.sup.-1) (.mu.M) (M.sup.-1 s.sup.-1) (.mu.M) (M.sup.-1 s.sup.-1)__________________________________________________________________________Cbz--Pro--Val.sup.P (OPh).sub.2 8.2 NI 10 20 5.3 130Cbz--Pro--Phe.sup.P (OPh).sub.2 8.2 230 8.2 NI.sup.e 4.3 20%fCbz--Ala--Ala--Val.sup.P (OPh).sub.2 8.2 NI 24.3 340 13.5 1300MeO--Suc--Ala--Ala--Pro--Nva.sup.P (OPh).sub.2 8.2 50 8.6 4200 95 380MeO--Suc--Ala--Ala--Ala--Val.sup.P (OPh).sub.2 90.1 15 9.1 2800 5 1500MeO--Suc--Ala--Ala--Ala--Phe.sup.P (OPh).sub.2 5.3 12,000 105 NI 58 NIMeO--Suc--Ala--Ala--Pro--Val.sup.P (OPh).sub.2 180 21 9 9,100 4.9 10,100MeO--Suc--Ala--Ala--Pro--Leu.sup.P (OPh).sub.2 26 1,500 26 740 14.4 140MeO--Suc--Ala--Ala--Pro--Phe.sup.P (OPh).sub.2 11 11,000 100 NI 50 NIMeO--Suc--Ala--Ala--Pro--Met.sup.P (OPh).sub.2 30 570 30 44 76 53Boc--Val--Pro--Val.sup.P (OPh).sub.2 8.2 NI 8.7 11,000 4.5 27,000Cbz--Phe--Pro--Phe.sup.P (OPh).sub.2 4.6 17,000 92 NI 8.2 NISuc--Val--Pro--Phe.sup.P (OPh).sub.2 5.5 44,000 8.2 NI 4.1 NICbz--Phe.sup.P (OPh).sub.2 55 21Cbz--Val.sup.P (4-F--C.sub.6 H.sub.4 O).sub.2 230 0.7 30 77Cbz--Pro--Val.sup.P( 4-F--C.sub.6 H.sub.4 O).sub.2 150 13.8 150 36__________________________________________________________________________ .sup.a Conditions were as follows: 0.1 M Hepes, 0.5 M NaCl, pH 7.5 at 25.degree. C. Rate constants were obtained as described before. .sup.b Enzyme concentration 1.6 .mu.M. .sup.c Enzyme concentration 1.8 .mu.M. .sup.d Enzyme concentration 0.32 .mu.M. .sup.e NI, less than 5% of inhibition was obtained after 1 hr. .sup.f 20% of inhibition was obtained initially and the inhibition was no time dependent.
TABLE IV__________________________________________________________________________Rate Constants (k.sub.obsd /�I!) for Inactivation of Cathespin G, and RatMast Cell Protease II by PeptidylDerivatives of Diphenyl .alpha.-(N-Benzyloxycarbonyl)-2-phenylethylphosphonate.sup.a. Cathespin G.sup.b RMCP II.sup.cInactivator �I! (.mu.M) k.sub.obsd /�I! (M.sup.-1 s.sup.-1) �I! (.mu.M) k.sub.obsd /�I! (M.sup.-1 s.sup.-1)__________________________________________________________________________Cbz--Phe.sup.P (OPh).sub.2 82 76 82 89MeO--Sec--Ala--Ala--Ala--Phe.sup.P (OPh).sub.2 13.6 370 170 6.8MeO--Suc--Ala--Ala--Pro--Phe.sup.P (OPh).sub.2 13.1 440 130 39Cbz--Phe--Pro--Phe.sup.P (OPh).sub.2 5.1 5,100 5.1 32Suc--Val--Pro--Phe.sup.P (OPh).sub.2 8.4 36,000 3 15,000__________________________________________________________________________ .sup.a Inactivation rates were messured by incubation method in 0.1 M Hepes, 0.5 M NaCl, pH 7.5 buffer, containing 9% Me.sub.2 SO and at 25.degree. C. Enzyme concentration were: cathespin G, 1.6 .mu.M; RMCP II, 38 nM. .sup.b Cathespin G was assayed with Suc--Val--Pro--Phe--Na (0.5 mM). .sup.c RMCP II was assayed with Suc--Ala--Ala--Pro--Phe--SBzl (88 .mu.M) in the presence od 4,4dithiopyridine (0.33 mM).
TABLE V______________________________________Effect of Peptidyl Derivatives of Diaryl Esters of.alpha.-Aminoalkylphosphonates on PT and APTT in Pig Plasma.sup.a. �I! PT APTTCompounds (.mu.M) (sec) (sec)______________________________________Control 0 18.6 17.7Cbz-NH--CH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 32 21.3 25.2Boc-D-Phe--Pro--NH--CH(Am- 16 18.8 18.8C.sub.6 H.sub.4)PO(OPh).sub.2D-Phe--Pro--NH--CH(Am-C.sub.6 H.sub.4)PO(OPh).sub.2 32 19.1 19.7______________________________________ .sup.a Average of two trials
TABLE VI______________________________________Half-Lives for Dephosphonylation of Serine ProteasesInactivated by Diphenyl .alpha.-Aminoalkylphosphonates Derivatives.sup.a. t.sub.1/2 (Hrs) Chymo-Inactivator trypsin PPE HLE______________________________________Cbz-Val.sup.P (OPh).sub.2 -- <48 <48Cbz-Pro--Val.sup.P (OPh).sub.2 -- <48 <48Cbz-Ala--Ala--Val.sup.P (OPh).sub.2 -- -- <48MeO--Suc--Ala--Ala--Pro--Val.sup.P (OPh).sub.2 -- <48 <48Cbz-Phe.sup.P (OPh).sub.2 10.sup.b -- --MeO--Suc--Ala--Ala--Pro--Phe.sup.P (OPh).sub.2 16 -- --Cbz--Phe--Pro--Phe.sup.P (OPh).sub.2 26 -- --MeO--Suc--Ala--Ala--Ala--Phe.sup.P (OPh).sub.2 10 -- --Suc--Val--Pro--Phe.sup.P (OPh).sub.2 7.5 -- --______________________________________ .sup.a Enzylme activity was measured after removal of excess of inhibitor as described previously. .sup.b About 50% of reactivation was obtained after 10 hrs, but no furthe progress observed even after 48 hrs.
The following examples are given to illustrate the invention and are not intended to limit it in any manner.
General Synthesis Procedures
Benzyl carbamate, triphenyl phosphite, 4-cyanobenzaldehyde, 1,1'-carbonyldiimidazole (CDI), 1,3-dicyclohexylcarbodiimide (DCC), and all common chemicals were obtained from the Aldrich Co., Milwaukee, Wis. Blocked amino acid derivatives were obtained from Aldrich or Bachem Bioscience Inc., Philadelphia, Pa. The NMR spectra were recorded on a Varian Gemini 300 MHz instrument. .sup.31 P NMR spectra were obtained at 161.895 MHz using broad band .sup.1 H decoupling on a Varian XL-400 instrument; chemical shifts were reported relative to 85% phosphoric acid (sealed capillary) at 0.000 ppm with positive values downfield. Elemental analyses were performed by Atlantic Microlabs of Atlanta, Ga.
EXAMPLE 1
Diphenyl N-benzyloxycarbonylamino(4-cyanophenyl)methanephosphonate �Cbz-(4-CN-PhGly).sup.P (OPh).sub.2 ! was obtained from 9.75 g of 4-cyanobenzaldehyde, 7.65 g of benzyl carbamate and 13.5 ml of triphenyl phosphite in 20 ml of glacial acetic acid, according to the synthetic procedure described earlier (Oleksyszyn J., Subotkowska L., Mastalerz P., Synthesis, 1979, 985). Yield 70%; top. 135.degree.-138.degree. C.; Anal. Calcd. for C.sub.28 H.sub.23 O.sub.5 N.sub.2 P.1/2 H.sub.2 O: C, 66.27; H, 4.73; N, 5.52. Found: C, 66.03; H, 4.51; N, 5.49.
Cbz-NHCH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2 and Cbz-NHCH(3-Me-C.sub.6 H.sub.4)PO(OPh).sub.2 with m.p. of 151.degree.-153.degree. C. and 127.degree.-129.degree. C. respectively were obtained by the same procedure using the corresponding benzaldehyde.
Diphenyl N-benzyloxyearbonylamino(4-amidinophenyl)-methanephosphonate hydrochloride �Cbz-(4-AmPhGly).sup.P (OPh).sub.2 !. A solution of 7 g diphenyl N-benzyloxycarbonylamino(4-cyanophenyl)-methanephosphonate in 150 ml of dry chloroform and 15 ml of absolute ethanol was saturated with dry HCl at 0.degree. C. The mixture was kept in the refrigerator until TLC (thin layer chromatography) showed the absence of starting material (about 24 hrs). An excess of pentane was added and the precipitated solid was removed by filtration and dried using a vacuum line. The solid was dissolved in 200 ml of dry methanol and gaseous dry ammonia was passed through the solution (one equivalent is required) for about 20 min. Methanol and excess ammonia was removed quickly on a rotary evaporator. A 100 ml portion of fresh methanol was added and solution was heated at 50.degree. C. for about 8 hrs until the TLC shows the absence of imino ether. The solvent was evaporated and the resulting oil was dissolved in chloroform. Addition of ether caused the oil to solidify. After filtration the resulting solid was again dissolved in chloroform, the solution was filtered and the solid was precipitated by addition of ether. In several experiments, the yields were 70-80%; mp. 154.degree.-158.degree. C. (decomp); .sup.31 P NMR 14.87 ppm. Anal. Calcd. for C.sub.28 H.sub.27 O.sub.5 N.sub.3 ClP.0.3 NH.sub.4 Cl.H.sub.2 O: C, 57.41; H, 5.16; N, 7.52; Cl, 7.31. Found: C, 57.75; H, 5.00; N, 8.86; Cl, 7.43
An improved amidination procedure was also developed subsequently and should be used in future syntheses. The imino ester is dissolved in a fleshly prepared solution of ammonia (1.5 eq.) in methanol, ammonium chloride (1 eq.) is added, and the mixture is then stirred at r.t. for 1 day.
EXAMPLE 2
Cbz-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2. Tris(4-fluorophenyl) phosphite was prepared by a previously described method (Walsh, J. Am. Chem. Soc. 1959, 81, 3023-3031). Cbz-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2 was obtained from 6.8 ml of isobutyraldehyde (0.075 mole), 7.65 g benzyl carbamate (0.05 mole) and 18.2 g of tris(4-fluorophenyl) phosphite in 10 ml of glacial acetic acid as described in example 1, mp. 94.degree.-96.degree. C. Anal. Calcd. for C.sub.24 H.sub.24 NO.sub.5 PF.sub.2 : C, 60.63; H, 5.05; N, 2.95. Found C, 60.84; H, 5.11; N, 2.90.
Cbz-Ala.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala.sup.P (3,4-dichloro-C.sub.6 H.sub.3 O).sub.2, Cbz-Ala.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Cbz-Val.sup.P (4-Me-C .sub.6 H.sub.4 O).sub.2, Cbz-Val.sup.P (3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2, Cbz-Phe.sup.P (4-F-C.sub.6 H.sub.3 O).sub.2, Cbz-Phe.sup.P (3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2 can be prepared by the same procedure using the corresponding tris(substituted-phenyl) phosphite and the corresponding aldehyde.
In general, Cbz--NH--CH(R)--P(O)(OZ)(OZ.sup.1) can be prepared by reaction of R--CHO with P(OZ)(OZ.sup.1)(OZ.sup.2).
EXAMPLE 3
Diphenyl amino(4-amidinophenyl)methanephosphonate dihydrochloride �(4-AmPhGly).sup.P (OPh).sub.2 !. A sample of 1.8 g of diphenyl N-benzyloxycarbonylamino(4-amidinophenyl)methanephosphonate hydrochloride was dissolved in 150 ml of 2N HCl methanol solution and after addition of 5% Pd/C catalyst, the solution was stirred under an atmosphere of hydrogen until the theoretical amount of hydrogen was consumed. The catalyst was removed by filtration and after evaporation of the methanol, the residue was crystallized from ethanol-ether. In several experiments, the yields were 60-80%; mp. 213.degree.-215.degree. C.; Anal. Calcd. for C.sub.20 H.sub.22 N.sub.3 ClP.1/2 H.sub.2 O: C,51.85; H, 4.97; N, 9.08; Cl, 15.34. Found: C, 51.73; H, 5.02; N, 9.10; Cl, 15.36.
Ala.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2.HCl, Val.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2.HCl, Phe.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2.HCl can be prepared by the same procedure.
In general, NH.sub.2 --CH(R)--P(O)(OZ)(OZ.sup.1) hydrochloride can be prepared from Cbz--NH--CH(R)--P(O)(OZ)(OZ.sup.1) using the same procedure. This intermediate can then be used to prepare a great variety of derivatives by reaction with acylating agents, carbamylating agents, sulfonylating agents, chloroformates, or by coupling with a variety of peptides and blocked peptides using standing peptide coupling reactions, many of which are illustrated in the following examples.
Diphenyl N-(N-benzyloxycarbonylprolyl)amino(4-amidinophenyl)methanephosphonate hydrochloride �Cbz-Pro-(4-AmPhGly).sup.P (OPh).sub.2 !. To 0.5 g (2 mmol) of N-benzyloxycarbonylproline in 3 ml of DMF at 0.degree. C., 0.45 g (2.77 mmol) of CDI was added and the reaction mixture was stirred at 0.degree. C. for 1 hr. Then 0.9 g (2 mmol) of diphenyl amino(4-amidinophenyl)methanephosphonate hydrochloride was added. After stirring by 18 hrs at 0.degree.-5.degree. C., 10 ml of water was added. The oil which precipitated was washed with water and solidified by washing with a cold 0.1N solution of HCl. One gram of compound was obtained which was used without purification in the next step. .sup.31 P NMR 12.31, 12.62 (free base) and 15.11, 15.41 ppm (hydrochloride). After addition of one drop concentrated HCl to the NMR tube, 14.22, 14.54 ppm (ratio 1:1).
Benzoyl-Ala-Val.sup.P (OPh).sub.2, Formyl-Ala-Val.sup.P (OPh).sub.2, Fmoc-Ala-Val.sup.P (OPh).sub.2 �Fmoc, 9-fluorenylmethyloxycarbonyl!, PhNHCO-Ala-Val.sup.P (OPh).sub.2, PhNHCS-Ala-Val.sup.P (OPh).sub.2, Dansyl-Ala-Val.sup.P (OPh).sub.2, Tosyl-Ala-Val.sup.P (OPh).sub.2, Trityl-Ala-Val.sup.P (OPh).sub.2, Phthaloyl-Ala-Val.sup.P (OPh).sub.2, Cbz-Pro-Ala.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Cbz-Pro-Val.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2, Cbz-Pro-Val.sup.P (3-Cl-C.sub.6 H.sub.4 O).sub.2, Cbz-Pro-Phe.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, Cbz-Pro-Phe.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala-Val.sup.P (3-Me-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala-Phe.sup.P (3,4-dichloro-C.sub.6 H.sub.3 O).sub.2 can prepared by the same procedure by coupling with the appropriate blocked amino acid or amino acid derivative.
EXAMPLE 4
Diphenyl N-(D-Phe-Pro)amino(4-amidinophenyl)-methanephosphonate dihydrochloride. One gram of derivative obtained in the previous experiment was hydrogenated in 1N solution of HCl in methanol with 0.1 g 5% Pd/C, until the theoretical amount of hydrogen was consumed. After filtration of the catalyst and evaporation of the solvent, the resulting oil was dried using a vacuum line. A 0.9 g (1.64 mmol) sample of the product dihydrochloride was added to a solution of 0.43 g (1.64 mmol) of Boc-D-Phe and 0.34 g (2 mmol) of DCI in 2 ml dry DMF, which was allowed to react for 1 hrs at 0.degree. C. After 24 hrs 10 ml of water was added and the oil which precipitated was decanted. After washing with 0.1N HCl, the oil which solidified was separated by filtration and dried using a vacuum line. The dry solid was dissolved in 1N HCl solution in methanol and solution was stirred by 1 hr. Solvent was removed on a rotary evaporator and the oil was dried using a vacuum line by several hours to give 0.3 g of product. Yield 24%; mp. 220.degree.-224.degree. C.; .sup.31 P NMR, 16.95, 17.25, 17,60 ppm (stereoisomers and conformers). Anal. Calcd. for C.sub.34 H.sub.38 O.sub.5 N.sub.2 ClP.5H.sub.2 O: C, 51.78; H, 6.09; N, 8.88; Cl, 9.00; Found; C, 51.21; H, 5.95; N, 9.04; Cl, 8.97.
EXAMPLE 5
Diphenyl N-(Boc-D-Phe-Pro)amino(4-amidinophenyl)-methanephosphonate hydrochloride �Boc-D-Phe-L-Pro-(4-AmPhGly).sup.P (OPh).sub.2 !. Boc-D-Phe-OH (2.66 g, 10 mole) and L-Pro-OBzl (2.42 g) were coupled using DCC, and Boc-D-Phe-Pro-OBzl was obtained in 83% yield; .sup.1 H NMR (CDCl.sub.3) .delta.7.34 (s, 5H), 7.23 (m, 5H), 5.4 (d, 1H), 5.15 (q, 2H), 4.65 (m, 1H), 4.35 (m, 1H), 3.5 (m, 1H), 3.1-2.9 (m, 2H), 2.6 (m, 1H), 2.-1.7 (m, 4H), 1.43 (s, 9H).
Hydrogenolysis was performed in methanol with 5% water using 5% Pd/C as a catalyst. The product Boc-D-Phe-Pro-OH was obtained as a whim solid and recrystallized from aqueous methanol, yield 85%, mp 173.degree.-174.degree. C.; .sup.1 H NMR (DMSO) .delta.7.3-7.15 (m, 5H), 7.0 (d, 1H), 4.45(m, 1H), 4.10 (m, 1H), 3.6-2.7 (m, 4H), 2.2-1.6 (m, 4H), 1.30 (s, 9H); MS (FAB.sup.+) m/e 363 (M+1); �.alpha.!.sup.20.sub.D =-91.5.degree. (0.14 g/mL in methanol). Anal. (C.sub.19 H.sub.26 N.sub.2 O.sub.5) C, H, N.
To 0.36 g (1.0 mmol) of Boc-D-Phe-Pro-OH in 2 ml of dry DMF at 0.degree. C., 0.17 g (1.05 mmol) of CDI was added. After stirring for 1 hr at 0.degree. C., 0.45 g (1.0 mmol) of dihydrochloride of diphenyl amino(4-amidinophenyl)methanephosphonate was added and the solution was stirred for48 hrs at 0.degree. C. Water (10 ml) was added and the oil which precipitated out was decanted and washed with distilled water. The oil was dissolved in chloroform and the solution was washed with 4% NaHCO.sub.3, water, and 0.05N HCl. After drying over MgSO.sub.4, the solvent was removed and the resulting oil was dried on a vacuum line for a few hours to give 0.22 g of product. Yield 29%; mp. 185.degree.-190.degree. C.; .sup.31 p NMR, 12.42, 12.66, 12.79 ppm (stereoisomers and conformers) (free base); 15.12, 15.38, 15.58 (hydrochloride). Anal. Calcd. for C.sub.39 H.sub.45 O.sub.7 N.sub.5 ClP.1/2H.sub.2 O: C, 60.75; H, 5.97; N, 9.08; Cl, 4.60. Found: C, 60.98; H, 6.48; N, 8.26; Cl., 4.26.
Tosyl-D-Phe-Pro-Arg.sup.P (OPh).sub.2, Cbz-D-Phe-Pro-Arg.sup.P (OPh).sub.2, Boc-D-Phe-Pro-Arg.sup.P (OPh).sub.2, Boc-D-Phe-Pro-Orn.sup.P (OPh).sub.2, Boc-D-Phe-Pro-Arg.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Boc-D-Phe-Pro-Arg.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2, Boc-D-Phe-Pro-Arg.sup.P (3,4-dichloro-C.sub.6 H.sub.3 O).sub.2, Boc-D-Phe-Pro-Arg.sup.P (3-Cl-C.sub.6 H.sub.4 O).sub.2 can be prepared by the same procedure by coupling with the appropriate blocked peptide or peptide derivative.
EXAMPLE 6
Diphenyl N-(N-.beta.-naphylsulfonylglycyl)amino(4-amidinophenyl)methanephosphonate hydrochloride �2-NpSO.sub.2 -Gly-(4-AmPhGly).sup.P (OPh).sub.2 !. Using the same procedure as example 5, 0.3 g (1.13 mmol) of .beta.-naphylsulfonylglycine, 0.2 g (1.23 mmol) of CDI and 0.45 g (1.0 mmol) of diphenyl amino(4-amidinophenyl)methanephosphonate dihydrochloride (obtained in Example 3) were reacted and 0.21 g of product was obtained. Yield 30%; mp. 205.degree.-210.degree. C. (decomp); .sup.31 P NMR, 11.76 ppm (free base), 14.74 ppm (hydrochloride). Anal. Calcd. for C.sub.32 H.sub.30 O.sub.6 N.sub.4 ClPS.H.sub.2 O: C, 56.24; H, 4.69; N, 8.20; S, 4.69. Found: C, 56.87; H, 4.43; N, 8.79; S, 5.06.
EXAMPLE 7
Cbz-Met.sup.P (OPh).sub.2. This compound was synthesized by the method described in example 1: yield 36%; m.p. 93.degree.-95.degree. C.; one spot on TLC, R.sub.f =0.73; .sup.31 P NMR 19.68 ppm. Anal. Calcd. for C.sub.24 H.sub.26 O.sub.5 NSP: C, 61.15; H, 5.52; N, 2.97; S, 6.79. Found: C, 61.06; H, 5.60; N, 2.91; S, 6.88.
Cbz-Met.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, Cbz-Met.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2, Cbz-Met.sup.P (3-Me-C.sub.6 H.sub.4 O).sub.2, Cbz-Met.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Cbz-Met.sup.P (3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2 can be prepared by the same procedure using corresponding tris(substitutedphenyl) phosphite.
MeO-Suc-Ala-Ala-Pro-Met.sup.P (OPh).sub.2. The reaction of MeO-Suc-Ala-Ala-Pro-OH (0.64 g, 1.73 mmol), H.sub.2 N-CH(CH.sub.2 CH.sub.2 SCH.sub.3)P(O)(OPh).sub.2. HBr (0.85 g, 2 mmol), obtained from Cbz-Met.sup.P (OPh).sub.2, N-methylmorpholine (0.2 ml, 2 mmol) and DCC (0.34 g, 1.73 mmol) under an atmosphere of nitrogen gave 0.5 g (42%) of product as whim solid. A 0.2 g sample was purified on preparative TLC under an atmosphere of nitrogen to give product as a white solid: top. 41.degree.-43.degree. C.; one spot on TLC, R.sub.f =0.6; .sup.31 P NMR 19.50, 19.36 ppm, ratio 1:1.32. Anal. Calcd. for C.sub.32 H.sub.43 O.sub.9 N.sub.4 PS.THF; C, 56.69; H, 6.69; N, 7.35; S, 4.20. Found: C, 57.37; H, 6.77; N, 7.76; S, 4.49.
MeO-Suc-Ala-Ala-Pro-Met.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, MeO-Suc-Ala-Ala-Pro-Met.sup.P (3-Me-C.sub.6 H.sub.4 O).sub.2, MeO-Suc-Ala-Ala-Pro-Met.sup.P (3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2 can be prepared by the same procedure.
EXAMPLE 8
Cbz-Ala-Ala-Val.sup.P (OPh).sub.2. Cbz-Ala-Ala-OH (0.294 g, 1 mmol) was dissolved in 10 ml of dry THF and cooled to 0.degree. C. Diphenyl .alpha.-amino-2-methylpropylphosphonate, (0.305 g, 1 mmol) and DCC (0.203 g, 1 mmol) were added to this solution. After stirring for 8 hrs at 0.degree. C. and overnight at room temperature, the solution was worked-up as described above. Recrystallization from chloroform-pentane gave 0.182 g (31%) of crude product. A sample (0.1 g) was purified on preparative thin layer chromatography using chloroform-methanol (9:1) as eluent. The product was recrystallized from ethanol-pentane to give a white solid: top. 93.degree.-97.degree. C.; one spot on TLC, R.sub.f =0.71; .sup.31 P NMR 19.44, 19.31 ppm, ratio 1:1.11. Anal. Calcd. for C.sub.30 H.sub.36 O.sub.7 N.sub.3 P.EtOH; C, 61.19; H, 6.69; N, 6.69.
Cbz-Ala-Ala-Val.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala-Ala-Val.sup.P (4-OMe-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala-Ala-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Cbz-Ala-Ala-Phe.sup.P (3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2, Cbz-Ala-Ala-Nva.sup.P (3,4-dichloro-C.sub.6 H.sub.3 O).sub.2, Cbz-Ala-Ala-Met.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, Acetyl-Ala-Ala-Val.sup.P (Oph).sub.2, CF.sub.3 -CO-Ala-Ala-Val.sup.P (OPh).sub.2, Dansyl-Ala-Ala-Val.sup.P (OPh).sub.2, Tosyl-Ala-Ala-Val.sup.P (Oph).sub.2, Fmoc-Ala-Ala-Val.sup.P (OPh).sub.2, PhNHCO-Ala-Ala-Val.sup.P (OPh).sub.2 can be prepared by the same procedure by coupling with the appropriate blocked peptide or peptide derivative.
EXAMPLE 9
MeO-Suc-Ala-Ala-Ala-Nva.sup.P (OPh).sub.2. The reaction of 0.345 g (1 mmol) of MeO-Suc-Ala-Ala-Ala-OH and 0.305 g (1 mmol) of diphenyl .alpha.-aminobutylphosphonate gave 0.35 g (55.3%) of product as a white solid. A 0.1 g sample was purified on preparative TLC as described above to give the product as white solid: mp. 215.degree.-218.degree. C.; one spot on TLC, R.sub.f =0.73; .sup.31 P NMR 20.02 ppm. Anal. Calcd. for C.sub.30 H.sub.41 O.sub.9 N.sub.4 P: C, 56.96; H, 6.49; N, 8.86. Found: C, 56.72; H, 6.58; N, 8.80.
Acetyl-Ala-Ala-Ala-Nva.sup.P (OPh).sub.2, Boc-Ala-Ala-Ala-Nva.sup.P (OPh).sub.2, MeO-Suc-Ala-Ala-Ala-Nva.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, MeO-Suc-Ala-Ala-Ala-Nva.sup.P(3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2, MeO-Suc-Ala-Ala-Ala-Nva.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, MeO-Suc-Ala-Ala-Ala-Nva.sup.P (3-Cl-C.sub.6 H.sub.4 O).sub.2 can be prepared by the same procedure using the corresponding tripeptide and diester of .alpha.-aminobutylphosphonate.
EXAMPLE 10
MeO-Suc-Ala-Ala-Ala-Val.sup.P (OPh).sub.2. The reaction of MeO-Suc-Ala-Ala-Ala-OH (0.345 g, 1 mmol) and diphenyl .alpha.-amino-2-methylpropylphosphonate (0.305 g, 1 mmol) gave 0.3 g (47.5%) of product as white solid. A 0.1 g sample was purified on preparative TLC as described above to give the product as a white solid, which was then recrystallized from ethanol-hexane: mp. 197.degree.-200.degree. C.; one spot on TLC, R.sub.f =0.63; .sup.31 P NMR 19.40, 19.24 ppm, ratio 1:0.72. Anal. Calcd. for C.sub.30 H.sub.41 O.sub.9 N.sub.4 P.0.25 Hexane: C, 57.60; H, 6.85; N, 8.61. Found: C, 57.58; H, 6.62; N, 8.36.
Cbz-Ala-Ala-Ala-Val.sup.P (OPh).sub.2, MeO-Suc-AIa-Ala-Ala-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, CH.sub.3 NHCO-Ala-Ala-Ala-Val.sup.P (OPh).sub.2, PhNHCS-Ala-Ala-Ala-Val.sup.P (OPh).sub.2, MeO-Suc-Ala-Ala-Ala-Val.sup.P (3-Cl-C.sub.6 H.sub.4 O).sub.2, PhNHCO-Ala-Ala-Ala-Val.sup.P (3,4-dimethyl-C.sub.6 H.sub.3 O).sub.2, MeO-Suc-Ala-Ala-Ala-Val.sup.P (4-MeO-C.sub.6 H.sub.4 O).sub.2 can be prepared by the same procedure using the corresponding tripeptide and diester of .alpha.-amino-2-methylpropylphosphonate.
EXAMPLE 11
MeO-Suc-Ala-Ala-Ala-Phe.sup.P (OPh).sub.2. The reaction of MeO-Suc-Ala-Ala-Ala-OH (0.345 g, 1 mmol) and diphenyl .alpha.-amino-2-phenyl-ethylphosphonate (0.353 g, 1 mmol) gave 0.35 g (49.1%) of the product which was purified on the preparative TLC, as described above. Recrystallization from methanol gave a white solid: top. 207.degree.-210.degree. C.; one spot on TLC, R.sub.f =0.69; .sup.31 P NMR 19.06, 19.01 ppm, ratio 1:0.87. Anal. Calcd. for C.sub.34 H.sub.41 O.sub.9 N.sub.4 P.MeOH: C, 58.98; H, 6.32; N, 7.86. Found: C, 58.66; H, 6.08; N, 7.96.
MeO-Suc-Ala-Ala-Ala-Phe.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, MeO-Suc-Ala-Ala-Ala-Phe.sup.P (4-MeO-C.sub.6 H.sub.4 O).sub.2 can be prepared by the same procedure.
EXAMPLE 12
MeO-Suc-Ala-Ala-Pro-Val.sup.P (OPh).sub.2. MeO-Suc-Ala-Ala-Pro-OH (0.37 g, 1 mmol) was dissolved in 20 ml of dry TI-IF and cooled to 0.degree. C. Diphenyl .alpha.-amino-2-methylpropylphosphonate (0.305 g, 1 mmol) and DCC (0.203 g, 1 mmol) were added to this solution. After stirring for 6 hrs at 0.degree. C. and overnight at room temperature, the solution was filtered and 100 ml of ethyl acetate was added. The solution was then washed with 10% citric acid, 4% sodium bicarbonate and water successively. After drying over magnesium sulfate, the solution was filtered, evaporated and the residue was dissolved in 10 ml of THF. Trace of DCU was removed by filtration and after addition of 3 ml of hexane, the solution was allowed to crystallized. After a few days the product was removed by filtration and recrystallized from THF-hexane to give 0.2 g (30%) of a white solid, mp. 83.degree.-86.degree. C.; one spot on TLC, R.sub.f =0.74; .sup.31 P NMR 19.78, 19.60 ppm, ratio 1:2.12. Anal. Calcd. for C.sub.32 H.sub.43 O.sub.9 P.hexane: C, 61.30; H, 7.66; N, 7.53. Found: C, 61.04; H, 7.58; N, 7.69.
PhNHCO-Ala-Ala-Pro-Val.sup.P (3-Cl-C.sub.6 H.sub.4 O).sub.2, PhNHCS-Ala-Ala-Pro-Val.sup.P (4-Cl-C.sub.6 H.sub.4 O) .sub.2 MeO-Suc-Ala-Ala-Pro-Val.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2 can be prepared by the same procedure.
EXAMPLE 13
MeO-Suc-Ala-Ala-Pro-Leu.sup.P (OPh).sub.2. The reaction of MeO-Suc-Ala-Ala-Pro-OH (0.37 g, 1 mmol) and diphenyl .alpha.-amino-3-methylbutylphosphonate (0.32 g, 1 mmol) gave 0.38 g (50.1%) of product as white solid: mp. 60.degree.-64.degree. C.; one spot on TLC, R.sub.f =0.67; .sup.31 P NMR 20.71, 20.54 ppm, ratio 1:1.33. Anal. Calcd. for C.sub.33 H.sub.45 O.sub.9 N.sub.4 P.hexane: C, 61.74; H, 7.78; N, 7.38. Found: C, 61.04; H, 7.53; N, 7.59.
EXAMPLE 14
MeO-Suc-Ala-Ala-Pro-Phe.sup.P (OPh).sub.2. The reaction of MeO-Suc-Ala-Ala-Pro-OH (0.37 g, 1 mmol) and diphenyl .alpha.-amino-2-phenylethylphosphonate (0.35 g, 1 mmol) gave 0.4 g (50.5%) of product as a white solid: top. 53.degree.-56.degree. C.; one spot on TLC, R.sub.f =0.7; .sup.31 P NMR 19.41, 19.10 ppm, ratio 1:2.47. Anal. Calcd. for C.sub.36 H.sub.43 O.sub.9 N.sub.4 P.hexane: C, 63.62; H, 7.19; N, 7.07. Found: C, 63.42; H, 7.19; N, 7.57.
EXAMPLE 15
Cbz-Pro-Val.sup.P (OPh).sub.2. Cbz-Pro-OH (0.97 g, 4 mmol) was dissolved in 40 ml of dry THF and cooled to 0.degree. C. Diphenyl .alpha.-amino-2-methylpropylphosphonate (1.2 g, 4 mmol) and DCC (0.81 g, 4 mmol) were added to this solution. After stirring for 6 hrs at 0.degree. C. and overnight at room temperature, the DCU was removed by filtration and 50 ml of ethyl acetate was added. The solution was washed successively twice each time with 10% citric acid, water, 4% sodium bicarbonate and water. After drying over MgSO.sub.4, the mixture was filtered, evaporated and residue was dissolved in 10 ml of methylene chloride. A trace of DCU was removed by filtration and after addition of 30 ml of pentane, the solution was allowed to crystallize. After a few days the product was filtered and recrystallized from methylene chloride-hexane to give 1.4 g (65%) of a white solid: mp. 123.degree.-127.degree. C.; one spot on TLC, R.sub.f =0.74; .sup.31 P NMR 19.52(broad), 19.51(broad) ppm. Anal. Calcd. for C.sub.29 H.sub.33 O.sub.6 N.sub.2 P: C, 64.87; H, 6.15; N, 5.22. Found: C, 64.58; H, 6.23; N, 5.34.
Boc-Val-Pro-Val.sup.P (OPh).sub.2. A solution 0.536 g (1 mmol) of Cbz-Pro-Val.sup.P (OPh).sub.2 in 50 ml of methanol with 0.1 g 5% Pd/C was stirred under atmosphere of hydrogen at room temperature for 2 hrs and filtered through celite. After addition of of Boc-Val-OH (0.217 g, 1 mmol) to the filtrate, the solvent was removed in vacuo. The residue was dissolved in 20 ml of dry THF and 0.2 g of DCC (1 mmol) was added. The solution was kept at 0.degree. C. for 6 hrs and overnight at room temperature. DCU was removed by filtration and the organic layer was washed with water, twice with 4% NaHCO.sub.3, water, twice with 10% citric acid and water. After drying over sodium sulfate, the solvent was evaporated and the resulting oil was dried at low pressure for a few hours to give 0.45 g (72%) of a whim hydroscopic solid: mp. 62.degree.-66.degree. C.; one spot on TLC, R.sub.f =0.78; .sup.31 P NMR 19.64 ppm. Anal. Calcd. for C.sub.31 H.sub.44 O.sub.7 N.sub.3 P.H.sub.2 O: C, 60.10; H, 7.43. Found: C, 60.26; H, 7.49.
Boc-Val-Pro-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, PhNHCS-Val-Pro-Val.sup.P (3-Cl-C.sub.6 H.sub.4 O).sub.2, .epsilon.-Cbz-.alpha.-Cbz-Orn-Val-Pro-Val.sup.P (4-F-C.sub.6 H.sub.4 O).sub.2, Boc-Val-Pro-Val.sup.P (4-MeO-C.sub.6 H.sub.4 O).sub.2, Tosyl-Val-Pro-Val.sup.P (OPh).sub.2 can be prepared by the same procedure.
EXAMPLE 16
Cbz-Pro-Phe.sup.P (OPh).sub.2. The reaction of Cbz-Pro-OH (0.75 g, 3 mmol), diphenyl .alpha.-amino-2-phenylethylphosphonates (1.05 g, 3 mmol) and DCC (0.61 g, 3 mmol) gave 0.93 g (53%) of product as white solid: mp. 81.degree.-84.degree. C.; one spot on TLC, R.sub.f =0.74; .sup.31 P NMR 19.54, 19.48, 19,27 and 19.22 ppm (diastereomers and conformers), ratio of diastereomers 1:1. Anal. Calcd. for C.sub.33 H.sub.33 O.sub.6 N.sub.2 P: C, 67.81; H, 5.65; N, 4.79. Found: C, 67.56; H, 5.79; N, 4.72.
Cbz-Phe-Pro-Phe.sup.P (OPh).sub.2. The reaction of Cbz-Phe-OH(0.3 g, 1 mmol) with the hydrogenolysis product of Cbz-Pro-Phe.sup.P (OPh).sub.2 (0.58 g, 1 mmol) and DCC (0.2 g, 1 mmol), gave 0.4 g (54%) of a hydroscopic semi-solid product after a standard work-up. A 0.2 g sample was purified on preparative TLC to give the product as a hydroscopic semi-solid: one spot on TLC, R.sub.f =0.76; .sup.31 P NMR 19.67, 19.57, 19.32, 19.19 and 19.07 ppm (diastereomers and conformers); ratio, 1.0:0.34:0.82:0.73:0.92. Anal. Calcd. for C.sub.42 H.sub.42 O.sub.7 N.sub.3 P.2H.sub.2 O: C, 65.71; H, 5.99; N, 5.47. Found: C, 65.62; H, 6.12; N, 5.27.
EXAMPLE 17
Suc-Val-Pro-Phe.sup.P (OPh).sub.2. The reaction of Cbz-Val-OH (0.25 g, 1 mmol), DCC (0.2 g, 1 mmol) and the product of hydrogenolysis of Cbz-Pro-Phe.sup.P (OPh).sub.2 (0.584 g, 1 mmol) gave an oil which was dissolved in 30 ml of ethyl acetate. To this solution, 0.1 g (1 mmol) of succinic anhydride and 0.1 g of 5% Pd/C were added and mixture was stirred under atmosphere of hydrogen until the TLC showed only one new spot. Catalyst was removed by filtration and organic layer was washed several times with water. After drying, the organic solvent was removed to give 0.45 g (65%) of product as a hydroscopic solid: mp. 50.degree.-53.degree. C.; one spot on TLC, R.sub.f =0.4; .sup.31 P NMR 19.75, 19.23 ppm, ratio 1:1. Anal. Calcd. for C.sub.34 H.sub.40 O.sub.3 N.sub.3 P.2H.sub.2 O: C, 59.56; H, 6.42. Found: C, 59.59; H, 6.42.
Suc-Val-Pro-Phe.sup.P (4-MeS-C.sub.6 H.sub.4 O).sub.2, Suc-Val-Pro-Phe.sup.P (4-Cl-C.sub.6 H.sub.4 O).sub.2, Suc-Phe-Pro-Phe.sup.P (OPh).sub.2, Suc-Val-Pro-Phe.sup.P (3-F-C.sub.6 H.sub.4 O).sub.2, Suc-Val-Pro-Phe.sup.P (3,4,5-trichloro-C.sub.6 H.sub.2 O).sub.2, Suc-Val-Pro-Phe.sup.P (2,3,4-fluoro-C.sub.6 H.sub.2 O).sub.2, Suc-Val-Pro-Phe.sup.P (4-Me-C.sub.6 H.sub.4 O).sub.2, Acetyl-Val-Pro-Phe.sup.P (OPh).sub.2, CF.sub.3 -CO-Val-Pro-Phe.sup.P (OPh).sub.2 can be prepared by the same procedure.
EXAMPLE 18
Cbz-Ala.sup.P (OCH.sub.2 CF.sub.3).sub.2. This compound was obtained by a previously described method involving transesterification (Szewczyk et al., Synthesis, 1982, 409-414). 10 ml of trifluoroethanol and 0.46 g of Na (0.02 mole) were mixed first, then 4.11 g of Cbz-AlaP(OPh).sub.2 was added, and the mixture was stirred overnight. 3 ml of AcOH was added and the solvent was everaporated. The residue was dissolved in CHCl.sub.3 and washed with water, 2N NaOH and water, and dried over MgSO.sub.4. The solvent was evaporated and the oil was obtained, mass spectrum m/e=423 (M.sup.+).
Cbz-Phe.sup.P (OCH.sub.2 CF.sub.3).sub.2 was prepared by the same procedure, mp 85.degree.-87.degree. C., mass spectrum m/e=499 (M.sup.+). Cbz-Val.sup.P (OCH.sub.2 CH.sub.3).sub.2 was also prepared by the same procedure using ethanol instead of trifuoroethanol.
EXAMPLE 19
Benzoyl-NHCH(4-NH.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2. NH.sub.2 CH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2.HBr was obtained by deblocking Cbz-NHCH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2 with 30% of HBr/HOAc, mp. 198.degree.-200.degree. C. The reaction of NH.sub.2 CH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2.HBr and benzoyl chloride in the presence of N-methylmorpholine gave benzoyl-NHCH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2, mp. 157.degree.-159.degree. C., mass spectrum m/e=489 (M.sup.+ +1). Anal. Calc. for C.sub.26 H.sub.21 N.sub.2 O.sub.6 P: C, 63.88; H, 4.30; N, 5.73. Found: C, 64.05; H, 4.25; N, 5.69. Hydrogenolysis of benzoyl-NHCH(4-NO.sub.2 -C.sub.6 H.sub.4)PO(OPh).sub.2 in the presence of Pd/C catalyst gave the final product, mp. 156.degree.-158.degree. C., mass spectrum m/e=458 (M.sup.+). Anal. Calc. for C.sub.26 H.sub.23 N.sub.2 O.sub.4 P: C, 68.12; H, 5.02; N, 6.11. Found: C, 66.87; H, 5.15; N, 5.01.
EXAMPLE 20
4-Cyanophenylacetaldehyde. This compound was prepared from 4-cyanobenzaldehyde using a modification of a procedure previously used in the multi-step synthesis of 2-phenylpropanal �Allen, C. F. H.; van Allan, J. Org. Syn. Coll. Vol 3, 733-734 (1955)!.
Ethyl 3-(4-cyanophenyl)-2,3-epoxypropionate. Ethyl chloroacetate (6.2 g, 50 mmole) and 4-cyanobenzaldehyde (6.6 g, 50 mmole) were dissolved in 100 mL dry benzene. Freshly prepared sodium ethoxide solution in absolute ethanol (1.3 g sodium in 25 mL ethanol) was added and the mixture was stirred at r.t. for 20 h. Water (100 mL) was added with stirring and after several minutes the organic layer was separated, washed with water, dried (MgSO.sub.4), filtered, and evaporated to give the desired epoxy product as a yellow oil, yield 70-80%; .sup.1 H NMR (CDCl.sub.3) .delta.7.68 (d, 2H), 7.43 (d, 2H), 4.30 (m, 2H), 4.16 (d, 1H), 3.48, (d, 1H), 1.34 (t, 3H).
Sodium 3-(4-cyanophenyl)-2,3-epoxypropionate. Ethyl 3-(4-cyanophenyl)-2,3-epoxypropionate (10.9 g, 50 mmole) was dissolved in 50 mL absolute ethanol and cooled with an ice bath. A freshly prepared sodium ethoxide solution (1.2 g sodium in 25 mL ethanol) was added dropwise during a 10 min period. Dropwise addition of 1 g of water to the stirred mixture caused separation of the sodium salt of the epoxy compound. The mixture was stirred for 3 h, the salt was collected by filtration, washed with 50 mL ethanol and ether several times, and dried, yield 75.degree.-85%; .sup.1 H NMR (D.sub.2 O) .delta.7.58 (d, 2H), 7.33 (d, 2H), 3.93 (d, 1H), 3.39 (d, 1H).
A 1N HCl solution (50 mL, 50 mmole) was added to the sodium salt of the epoxy compound (10.6 g, 50 mmol) dissolved in 50 mL water. This resulted in the separation of an oil which solidifed after a short time. This material was refluxed with 100 mL toluene for 2.5 h to affect decarboxylation. The organic layer was separated, washed with water, dried (Na.sub.2 SO.sub.4), filtered, and evaporated to give 4-cyanophenylacetaldehyde as a yellow brownish oil which solidified after several hours, yield 35-45%. This product is unstable and was used immediately for next step, otherwise polymerization occurs. A sample of the crude product was purified by recrystallization from ether-hexane to give white crystals, mp 63.degree.-65.degree. C.; NMR (CDCl.sub.3) .delta.9.81 (s, 1H), 7.65, (d, 2H), 7.35 (d, 2H), 3.84 (s, 2H); MS m/e 146 (M+1). Anal. (C.sub.9 H.sub.7 NO.0.5H.sub.2 O) C, H, N.
Diphenyl 1-(N-Benzyloxycarbonylamino)-2-(4-cyanophenyl)ethanephosphonate �Cbz-(4-CN-Phe).sup.P (OPh).sub.2 !. This compound was synthesized from crude 4-cyanophenylacetaldehyde, benzyl carbamate, and triphenylphosphite using a modification of the previously described amidoalkylation procedure..sup.9 Benzyl carbamate (6.1 g, 40 mmole) and 4-cyanophenylacetaldehyde (4.7 g, 32 mmole) were dissolved in 50 mL toluene and refluxed for 1 h. The toluene was evaporated, glacial acetic acid (10 mL) and triphenyl phosphite (8.5 mL, 32 mmole) were added to the residue, and the mixture was heated at 80 .degree. C. for 2 h. The volatile materials were removed by evaporation in vacuo and the resulting oil was dissolved in 50 mL methanol. The solution was refrigerated overnight and the white precipitate was filtered, dried, and recrystallized from 50 mL hot methanol. The undissolved product was discarded, and the filtrate was cooled down to give white crystals, yield 25-35%; mp 136.degree.-137.degree. C.; .sup.1 H NMR (DMSO) .delta.8.20 (d, 1H), 7.75 (d, 2H), 7.54 (d, 2H), 7.35 (m, 5H), 7.3-7.1 (m, 10H), 4.95 (q, 2H), 4.60 (m, 1H), 3.4-3.0 (m, 2H); MS (FAB.sup.+) m/e 513 (m+1). Anal. (C.sub.29 H.sub.25 N.sub.2 O.sub.5 P) C, H, N.
Diphenyl 1-Amino-2-(4-cyanophenyl)ethanephosphonate Hydrobromide �4-CN-Phe.sup.P (OPh).sub.2.HBr!. Cbz-(4-CNPhe).sup.P (OPh).sub.2 (0.57 g, 1.1 mmole) was mixed with 1.0 mL 30% HBr in acetic acid. The mixture was protected against moisture and kept at r.t. for 1 h. Addition of 50 mL dry ether and stirring for several hours resulted in formation of a yellow brownish solid which was filtered, washed with ether, and dried to give the product (0.48 g, 95%); mp 197.degree.-199.degree. C.; .sup.1 H NMR (DMSO) .delta.9.0 (b, 3H), 7.85 (d, 2H), 7.65 (d, 2H), 7.4-7.0 (m, 10H), 4.7 (m, 1H), 3.4 (m, 2H); MS (FAB.sup.+) m/e 379 (M-Br).
Diphenyl 1-(N-Benzyloxycarbonylamino)-2-(4-amidinophenyl)ethanephosphonate �Cbz-(4-AmPhe).sup.P (OPh).sub.2 !. Cbz-(4-CNPhe).sup.P (OPh).sub.2 (1.03 g, 2.0 mmole) was dissolved in a mixture of methanol and chloroform (1:1, 20 mL). The solution was cooled to 0.degree. C., saturated with dry HCl, the solution was kept at 5.degree. C. for 48 h, and then the solvent was evaporated at r.t. in vacuo. The resulting semisolid was treated with 50 mL dry ether, filtered, washed with dry ether, and dissolved in 10 mL methanol containing 51 mg (3.0 mmole) ammonia. Ammonium chloride (107 mg, 2.0 mmole) was added, the mixture was stirred at r.t. for 1 day, the solvent was removed at r.t. in vacuo and the resulting semisolid was dissolved in 50 mL chloroform, filtered, and the filtrate was evaporated to give the crude product. The crude product was treated with 50 mL dry ether, stirred, and the undissolved solid collected, washed with ether and dried to give the amidine product as a yellow powder, yield 50-70%; mp>140 (dec); .sup.1 H NMR (DMSO) .delta.9.4-9.2 (d, 4H), 8.25 (d, 1H), 7.8 (d, 2H) 7.6 (d, 2H), 7.38 (m, 5H), 7.3-7.1 (m, 10H), 4.95 (q, 2H), 4.6 (m, 1H), 3.4-3.1 (m, 2H); MS (FAB.sup.+) m/e 530 (M-Cl). Anal. (C.sub.29 H.sub.29 N.sub.3 O.sub.5 ClP) C, H, N.
EXAMPLE 21
Diphenyl 1-Amino-2-(4-amidinophenyl)ethanephosphonate �(4-AmPhe).sup.P (OPh).sub.2.2HCl!. The amidine Cbz-(4-AmPhe).sup.P (OPh).sub.2 (1.0 g, 1.76 mmole) was dissolved in 150 mL methanol containing 2 mmole HCl, a catalyst (0.5 g of 5% Pd/C) was added, and the mixture was hydrogenated. After hydrogenolysis, the catalyst was removed by fitration and the filtrate was evaporated to give a near whim crystalline product, yield 85-90%; mp>180 (dec.); .sup.1 H NMR (DMSO) .delta.9.5-9.3 (d, 4H), 9.2-9.0 (m, 3H), 7.9-7.1 (m, 14H), 4.55 (m, 1H), 3.2-3.5 (m, 2H); MS (FAB.sup.+) m/e 396 (M+1-2HCl). Anal. (C.sub.21 H.sub.24 N.sub.3 O.sub.3 Cl.sub.2 P) C, H, N.
EXAMPLE 22
Diphenyl 1-(N-Benzyloxycarbonyl-L-prolyl)amino-2-(4-cyanophenyl)ethanephosphonate �Cbz-Pro-(4-CN-Phe).sup.P (OPh).sub.2 !. To a cooled solution of the phosphonate 4-CN-Phe.sup.P (OPh).sub.2.HBr (0.41 g, 0.9 mmole) and Cbz-Pro-OH (0.25 g, 1.0 mmole) in 20 mL CH.sub.2 Cl.sub.2 was added 0.14 mL Methyl amine. After stirring for 10 min, DCC (0.21 g, 1.0 mmole) was added and the mixture was stirred at 0.degree. C. for 2 h and at r.t. for 24 h. During this period, dicyclohexylurea (DCU) formed, was removed by filtration and the filtrate was evaporated. The residue was dissolved in 50 mL ethyl acetate, filtered, the filtrate was washed with 50 mL 1N HCl, water, 6% NaHCO.sub.3, and water. The organic layer was dried, filtered, and evaporated to give crude product which was then recrystallized from ether to give white crystals, yield 52% (0.29 g); mp 131.degree.-132.degree. C.; .sup.1 H NMR (DMSO) .delta.8.75(m, 1H), 7.8-7.2(m, 19H), 5.06 (m, 2H), 4.95 (m, 1H), 4.6 (q, 1H), 4.2 (m, 1H), 3.5-3.1 (m, 3H), 2.0-1.4 (m, 4H); MS (FAB.sup.+) m/e 610 (M+1). Anal. (C.sub.34 H.sub.32 N.sub.3 O.sub.6 P) C, H, N.
EXAMPLE 23
Diethyl 1-(N-benzyloxycarbonyl-L-prolyl)amino-2-(4-amidinophenyl)ethanephosphonate �Cbz-Pro-(4-AmPhe).sup.P (OEt).sub.2, 10!. This compound was obtained during the amidination procedure of dipeptide Cbz-Pro-(4-CN-Phe).sup.P (OPh).sub.2 when ethanol was used instead of methanol. Transesterification occurred and the phenyl groups were replaced by ethyl groups, yield 50% (0.11 g); mp>130.degree. C. (dec); .sup.1 H NMR (DMSO) .delta.9.4-9.2 (m, 4H), 8.4 (m, 1H), 7.8-7.1 (m, 9H), 5.0 (s, 2H), 4.5 (m, 1H), 4.2 (m, 1H), 4.0 (m, 4H), 3.5-2.9 (m, 4H), 2.1-1.4 (m, 4H), 1.25 (m, 6H); MS (FAB.sup.+) m/e 531 (M-Cl). Anal. (C.sub.26 H.sub.36 N.sub.4 O.sub.6 ClP) C, H, N.
EXAMPLE 24
Diphenyl 1-(N-t-Butyloxycarbonyl-D-phenylalanyl-L-prolyl)amino-2-(4-cyanophenyl)ethanephosphonate �Boc-D-Phe-Pro-(4-CN-Phe).sup.P (OPh).sub.2 !. The phosphonate 4-CN-Phe.sup.P (OPh).sub.2. HBr (0.46 g, 1 mmole) was coupled with Boc-D-Phe-Pro-OH (0.36 g, 1.0 mmole) using DCC. The product was obtained as a glass-like solid, yield 86% (0.62 g); mp 85.degree.-90.degree. C.; .sup.1 H NMR (DMSO) .delta.8.25 (2d, 1H), 7.8-7.0 (m, 19H), 4.8 (m, 1H), 4.4 (m, 1H), 4.3 (m, 1H), 4.2 (m, 1H), 3.5-2.8 (m, 4H), 2.0-1.4 (m, 4H), 1.3 (m, 9H); MS (FAB.sup.+) m/e 723 (M+1). Anal. (C.sub.40 H.sub.43 N.sub.4 O.sub.7 P.0.25 H.sub.2 O) C,H,N.
EXAMPLE 24
Diphenyl 1-�(N-t-Butyloxycarbonyl-D-phenylalanyl-L-prolyl)amino!-2-(4-amidinophenyl)ethanephosphonate �Boc-D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2 !. CDI (0.13 g, 0.8 mmole) was added to Boc-D-Phe-Pro-OH (0.24 g, 0.67 mmole) in 2 mL DMF. A solution of amidinc (4-AmPhe).sup.P (OPh).sub.2.2HCl (0.31 g, 0.67 mmole) in 2 mL DMF was added to a cooled solution (0.degree. C.) of the peptide and the mixture was incubated at 0.degree. C. for 2 h and r.t. for 48 h. DMF was removed in vacuo and the residue oil was dissolved in 100 mL CHCl.sub.3, filtered, and the organic layer was washed subsequently with 50 mL 0.05M HCl, 10% KCl, 6% NaHCO.sub.3, and water. The organic layer was dried, filtered, and evaporated to give a crystalline product which was then dried in vacuo, yield 59% (0.31 g); mp 145.degree.-155.degree. C. (dec.); .sup.1 H NMR (DMSO) .delta.10.1-9.7 (m, H), 9.4-9.0 (m, 3H), 8.0-7.0 (m, 19H), 6.75 (m, 1H), 4.9-4.0 (m, 3H), 3.5-2.6 (m, 6H), 2.0-1.4 (m, 4H), 1.3 (s, 9H); MS (FAB.sup.+) m/e 740 (M-Cl). Anal. (C.sub.40 H.sub.46 N.sub.5 O.sub.7 P.0.3HCl.1.5H.sub.2 O) C, H, N.
EXAMPLE 25
Diphenyl 1-(N-(D-Phenylalanyl-L-prolyl)amino-2-(4-amidinophenyl)ethanephosphonate Dihydrochloride �D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2 !. Boc-D-Phe-Pro-(4-AmPhe).sup.P (OPh).sub.2 (0.11 g) was dissolved in 2 mL CHCl.sub.3 and the solution was saturated with dry HCl. An oily precipitate formed and the mixture was kept at r.t. for 2 h before evaporating to dryness to obtain the crystalline product, yield 80% (0.08 g); mp >165.degree. C. (dec); .sup.1 H NMR (DMSO) a 9.4-9.2 (d, 4H), 8.5 (m, 3H), 8.2 (m, 1H), 7.9-7.0(m, 19H), 4.8-3.9 (m, 3H), 3.5-2.8 (m, 6H), 2.0-1.1 (m, 4H); MS (FAB.sup.+) m/e 640 (M+1-2Cl). Exact mass calcd. for C.sub.35 H.sub.39 N.sub.5 O.sub.5 P (M+1-2HCl) 640.2689. Found: 640.2786.
EXAMPLE 26
Boc-Phe-Phe-(4-AmPhGly).sup.P (OPh).sub.2. To a THF solution (5 ml) of Boc-Phe-Phe-OH (0.21 g, 0.5 mmol) was added successively N-methylmorpholine (55 .mu.l, 0.5 mmol) and isobutyl chloroformate (65 .mu.l, 0.5 mmol) at -15.degree. C. After stirring for 2 min and addition of cold THF solution (1 ml) of triethylamine (70 .mu.l, 0.5 mmol), the mixture was added to a DMF solution (1 ml) of (4-AmPhGly).sup.P (OPh).sub.2.2HCl (0.23 g, 0.5 mmol) at -15.degree. C. After stirring at -15.degree. C. for 1 hr and at 0.degree.-5.degree. C. for 12 hr, the reaction mixture was concentrated in vacuo. The residue was triturated with ether and was purified by chromatography (silica gel, CHCl.sub.3 /CH.sub.3 OH, 14:1) and solidified from ether to give the final product (80 mg, 20% yield) as a white powder; mp 149.degree.-170.degree. C., R.sub.f =0.45 (CHCl.sub.3 /CH.sub.3 OH/CH.sub.3 CO.sub.2 H, 80:10:5), Anal. Calcd. for C.sub.43 H.sub.47 O.sub.7 N.sub.5 Cl.H.sub.2 O: C, 62.2; H, 5.95; N, 8.43. Found: C, 62.3; H, 6.01; N, 8.45.
It is obvious that those skilled in the art may make modifications to the invention without departing from the spirit of the invention or the scope of the subjoined claims and their equivalents.

Basic .alpha.-aminoalkylphosphonate derivatives

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Fastrez, Tetrahedr Lett 30, 6861, 1989.
Oleksyszyn Bioch Biophys Res Comm 161, 143, 1989.