Patent US4299583A successfully refreshed from Google Patents.
Patent US5359115A successfully refreshed from Google Patents.
US5359115A
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Methods for the synthesis of phosphonate esters
Assignee: Affymax Technologies NV
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Filing: 1992-09-11
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Granted: 1994-10-25
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Expires: 2012-09-11
Abstract
Abstract Phosphonate esters can be synthesized in high yields by condensations of alcohols with methyl phosphonates followed by selective demethylation. The reaction is general, relatively insensitive to steric constraints of hindered phosphonic acids, and can also be carried out on a solid support to synthesize large collections of compounds to screen for pharmacological activity.
Inventors
- 👤 David A. Campbell
- 👤 Jeffrey W. Jacobs
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-02 14:20
CPC Classifications
C; C07; C07F; C07F9/00; C07F9/02; C07F9/28; C07F9/38; C07F9/40; C07H; C07H19/00; C07H19/02; C07H19/04; C07H19/06; C07H19/10; C07K; C07K16/00; C07K16/44; C07K5/00; C07K5/04; C07K5/06; C07K5/06191
Claims Analysis
Total Claims: 13
Claim 1
Independent Claim
171 words
A method for preparing a desired phosphonic acid monoester from a first phosphonic acid monoester, said first phosphonic acid monoester having the structure: ##STR7## wherein: R 1 is selected from the group consisting of alkyl, aryl, substituted alkyl, substituted aryl, heteroaryl, alkylaryl, and aminoalkyl; and R 2 is selected from the group consisting of methyl, ethyl, benzyl, and substituted benzyl; by treating said first phosphonic acid monoester with: a dialkylazodicarboxylate; triphenylphosphine; and a secondary alcohol having the structure R 3 OH, wherein the R 3 is selected from the group consisting of alkyl, substituted alkyl, and aminoalkyl, provided that R 3 is chosen such that R 2 and R 3 are not identical and R 2 can be selectively hydrolyzed without hydrolyzing R 3 and wherein said alcohol is covalently linked to a solid support; in an aprotic solvent to yield a phosphonate diester having the structure: ##STR8## and further treating said phosphonate diester to hydrolyze selectively said R 2 to yield said desired phosphonic acid monoester having the structure: ##STR9##
Claim 2
Independent Claim
171 words
A method for preparing a desired phosphonic acid monoester from a first phosphonic acid monoester, said first phosphonic acid monoester having the structure: ##STR7## wherein: R 1 is selected from the group consisting of alkyl, aryl, substituted alkyl, substituted aryl, heteroaryl, alkylaryl, and aminoalkyl; and R 2 is selected from the group consisting of methyl, ethyl, benzyl, and substituted benzyl; by treating said first phosphonic acid monoester with: a dialkylazodicarboxylate; triphenylphosphine; and a secondary alcohol having the structure R 3 OH, wherein the R 3 is selected from the group consisting of alkyl, substituted alkyl, and aminoalkyl, provided that R 3 is chosen such that R 2 and R 3 are not identical and R 2 can be selectively hydrolyzed without hydrolyzing R 3 and wherein said alcohol is covalently linked to a solid support; in an aprotic solvent to yield a phosphonate diester having the structure: ##STR8## and further treating said phosphonate diester to hydrolyze selectively said R 2 to yield said desired phosphonic acid monoester having the structure: ##STR9##
Claim 3
Dependent Claim
45 words
The method of claim 1, wherein said desired phosphonic acid monoester is selected from the group consisting of ethyl benzylphosphonate, isopropyl benzylphosphonate, methyl (D)-2-O-benzylphosphoryl-3-phenylpropionate, methyl (D)-2-O-benzylphosphoryl-2-phenylacetate, ethyl t-butylphosphonate, isopropyl t-butylphosphonate, methyl (D)-2-O-t-butylphosphoryl-3-phenylpropionate, methyl 2-O-(1-N-(benzyloxycarbonyl)amoinomethylphosphoryl)acetate, methyl (D)-2-O-(1-(N-(benzyloxycarbonyl)amino)methylphosphoryl)-3-phenylpropionate, methyl (D)-2-O-(1-(N-(benzyloxycarbonyl)amino)methylphosphoryl)-3-methylbutyrate, methyl 2-O-((R,S)-1-(N-(benzyloxycarbonyl)amino)-2-methylpropylphosphoryl)acetate, methyl (D)-2-O-((R,S)-1-(N-(benzyloxycarbonyl)amino)-2-methylpropylphosphoryl)-3-phenylpropionate, and methyl (D)-2-O-((R,S)-1-(N-(benzyloxycarbonyl)amino)-2-methylpropylphosphoryl)-3-methylbutyrate.
Claim 4
Dependent Claim
50 words
The method of claim 1, wherein said first phosphonic acid monoester is selected from the group consisting of methyl benzylphosphonate, methyl t-butyl-phosphonate, methyl N-CBz-aminomethylphosphonate, and methyl N-CBz-valinylphosphonate and said alcohol is selected front the group consisting of ethanol, isopropanol, methyl 3-(L)-phenyl-lactic acid, methyl S-mandelate, (S)-mandelate, methyl glycolate, and methyl 2-hydroxy-isovalerate.
Claim 5
Dependent Claim
14 words
The method of claim 1, wherein said first phosphonic acid monoester is an alpha-aminoalkylphosphonate.
Claim 6
Dependent Claim
13 words
The method of claim 1, wherein said solid support is a glass slide.
Claim 7
Dependent Claim
13 words
The method of claim 1, wherein said solid support is bead or particle.
Claim 8
Dependent Claim
67 words
The method of claim 1, wherein said solid support is prepared by treating a solid support to which an amino acid or peptide is covalently linked so as to have an amine group of said amino acid on a surface of said support with a hydroxy acid to couple said hydroxy acid to said amine group and to yield a hydroxyl moiety covalently linked to said support.
Claim 9
Dependent Claim
70 words
The method of claim 7, wherein, after said hydroxy acid is coupled to said amine group, said support is treated with (a) an alpha-aminoalkylphosphonate with the following structure: ##STR10## wherein R 4 is an alpha-aminoalkyl group, and R 2 is selected from the group consisting of methyl, ethyl, benzyl, and substituted benzyl; (b) a dialkylazodicarboxylate; and (c) a triphenylphosphine, to couple said alpha-aminoalkylphosphonate to said hydroxy groups on said surface.
Claim 10
Dependent Claim
17 words
The method of claim 8, further comprising the step of selective hydrolysis of the R 2 group.
Claim 11
Dependent Claim
21 words
The method of claim 9, further comprising the step of coupling an amino acid to the amino group of said alpha-aminoalkylphosphonate.
Claim 12
Independent Claim
144 words
A method for preparing a peptidylphosphonate, comprising: forming an aminoalkylphosphonate having the structure: ##STR11## wherein: R 1 is aminoalkyl; and R 2 is selected from the group consisting of methyl, ethyl, benzyl, and substituted benzyl; by treating said phosphonate with: a dialkylazodicarboxylate; triphenylphosphine; and a compound having the structure R 3 CH(OH)R 4 , wherein R 3 and R 4 are selected independently from the group consisting of alkyl, aryl, substituted alkyl, substituted aryl, carboxyl, amido, and aminoalkyl and wherein the compound having the structure R 3 CH(OH)R 4 is covalently linked to a solid support; in an aprotic solvent to yield a phosphonate diester with a structure: ##STR12## further treating said phosphonate diester to hydrolyze selectively said R 2 to yield a compound having the structure: ##STR13## and coupling an amino acid to an amino group of R 1 to yield a peptidylphosphonate.
Claim 13
Independent Claim
144 words
A method for preparing a peptidylphosphonate, comprising: forming an aminoalkylphosphonate having the structure: ##STR11## wherein: R 1 is aminoalkyl; and R 2 is selected from the group consisting of methyl, ethyl, benzyl, and substituted benzyl; by treating said phosphonate with: a dialkylazodicarboxylate; triphenylphosphine; and a compound having the structure R 3 CH(OH)R 4 , wherein R 3 and R 4 are selected independently from the group consisting of alkyl, aryl, substituted alkyl, substituted aryl, carboxyl, amido, and aminoalkyl and wherein the compound having the structure R 3 CH(OH)R 4 is covalently linked to a solid support; in an aprotic solvent to yield a phosphonate diester with a structure: ##STR12## further treating said phosphonate diester to hydrolyze selectively said R 2 to yield a compound having the structure: ##STR13## and coupling an amino acid to an amino group of R 1 to yield a peptidylphosphonate.
References Cited (Backward Citations)
US5143854A
Cited
US5183810A
Cited
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