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US5061806A Expired / Lapsed US ⏱️ 0.0 years remaining

Phosphinic acid derivatives

Assignee: Merck and Co Inc
•
Filing: 1990-05-24
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Granted: 1991-10-29
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Expires: 2010-05-24
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Abstract

Abstract New phosphonic acid derivatives are described which display antibacterial activity.

Inventors

  • 👤 Yoshiharu Morita
  • 👤 Yasuo Hoshide
  • 👤 Haruyuki Chaki
  • 👤 Junko Takashima
  • 👤 Arthur A. Patchett

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 16:11
CPC Classifications
C; C07; C07F; C07F9/00; C07F9/02; C07F9/547; C07F9/655; C07F9/65515; A; A61; A61P; A61P31/00; A61P31/04; C07F9/28; C07F9/38; C07F9/40; C07F9/4003; C07F9/4006; C07F9/4071; C07F9/4075

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 210 words
A compound represented by the general formula (I) ##STR12## where A 1 is a hydrogen atom, an amino acid having a protecting group for amino groups or carboxyl groups, (which residue is obtained by removing, from an amino acid or amino acid having a protecting group, the hydroxyl group of the terminal carboxyl group), or a protecting group for the amino group; X is (a) a hydroxyl group, (b) ##STR13## wherein R 1 is an alkyl group, or (c) -NHA 2 wherein A 2 is a hydrogen atom, an amino acid, an amino acid having a protecting group for amino groups of carboxyl groups, (which residue is obtained by removing, from an amino acid or amino acid having a protecting group, the hydroxyl group of the terminal carboxyl group), or a protecting group for the amino group; and Y is (a) -CH 2 OH (b) ##STR14## wherein R 2 is an alkyl group, or (c) ##STR15## wherein B is a hydroxyl group, an amino acid, an amino acid having a protecting group for amino groups or carboxyl groups, (which residue is obtained by removing, from an amino acid amino acid having a protecting group, the hydrogen atom of the terminal amino group), or a protecting group for the carboxyl group.
Claim 2
Dependent Claim 210 words
A compound represented by the general formula (I) ##STR12## where A 1 is a hydrogen atom, an amino acid having a protecting group for amino groups or carboxyl groups, (which residue is obtained by removing, from an amino acid or amino acid having a protecting group, the hydroxyl group of the terminal carboxyl group), or a protecting group for the amino group; X is (a) a hydroxyl group, (b) ##STR13## wherein R 1 is an alkyl group, or (c) -NHA 2 wherein A 2 is a hydrogen atom, an amino acid, an amino acid having a protecting group for amino groups of carboxyl groups, (which residue is obtained by removing, from an amino acid or amino acid having a protecting group, the hydroxyl group of the terminal carboxyl group), or a protecting group for the amino group; and Y is (a) -CH 2 OH (b) ##STR14## wherein R 2 is an alkyl group, or (c) ##STR15## wherein B is a hydroxyl group, an amino acid, an amino acid having a protecting group for amino groups or carboxyl groups, (which residue is obtained by removing, from an amino acid amino acid having a protecting group, the hydrogen atom of the terminal amino group), or a protecting group for the carboxyl group.
Claim 3
Dependent Claim 204 words
The compound according to claim 1, wherein A 1 is a hydrogen atom; a residue of amino acid of glycine, alanine, valine, norvaline, leucine, isoleucine, serine, threonine, phenylalanine, tyrosine, tryptophan, histidine, aspartic acid, asparagine, glutamic acid, glutamine, lysine, arginine, cysteine, methionine or proline, optionally having a protecting group for carboxyl group selected from C 1 -C 5 lower alkoxy, and aryloxy; an aralkyloxycarbonyl lower alkyloxycarbonyl group, or trityl group, X is (a) -OH, (b) ##STR16## wherein R 1 is C 1 -C 30 alkyl group, or (c) -NHA 2 , A 2 is the same as the definition of A 1 mentioned above, but, A 1 and A 2 are independent of each other; and Y is (a) -CH 2 OH, (b) ##STR17## R 2 is C 1 -C 30 alkyl group, or (c) ##STR18## B is -OH, a residue of amino acid of glycine, alanine, valine, norvaline, leucine, isoleucine, serine, threonine, phenylalanine, tyrosine, tryptophan, histidine, aspartic acid, asparagine, glutamic acid, glutamine, lysine, arginine, cysteine or methionine, optionally having a protecting group for carboxyl group selected from C 1 -C 5 lower alkoxy group and aryloxy or a protecting group for the carboxyl group selected from C 1 -C 5 lower alkoxy, and aryloxy.
Claim 4
Dependent Claim 203 words
The compound according to claim 1, wherein A 1 is a hydrogen atom; a residue of amino acid of glycine, alanine, valine, norvaline, leucine, isoleucine, serine, cysteine or methionine, optionally having a protecting group for carboxyl group selected from C 1 -C 5 lower alkoxy, methoxymethyloxy, acetoxymethyloxy, pivaloyloxyme-thyloxy, benzyloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, phthlidyloxy and aryloxy carbobenzoxy, p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, p-chlorobenzyloxycarbonyl, p-bromobenzyloxycarbonyl, p-methylbenzyloxycarbonyl, tertbutoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, or trityl group; X is (a) -OH, (b) ##STR19## R 1 is C 1 -C 30 alkyl group, or (c) -NHA 2 , A 2 is the same as the definition of A 1 mentioned above, but A 1 and A 2 are independent of each other; and Y is (a) -CH 2 OH, (b) -CH 2 DC(O)R 2 , R 2 is C 1 -C 30 alkyl group, or (c) ##STR20## B is -OH, a residue of amino acid of glycine, alanine, valine, norvaline, leucine, isoleucine, serine, cysteine, or methionine optionally having a protecting group for carboxyl group selected from C 1 -C 5 lower alkoxy group, methoxymethyloxy, acetoxymethyloxy, pivaloyloxymethyloxy, benzyloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, phthlidyloxy and aryloxy, or a protecting group for the carboxyl group selected from C 1 -C 5 lower alkoxy, methoxymethyloxy, acetoxymethyloxy, pivaloyloxymethyloxy, benzyloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, phthlidyloxy oraryloxy.
Claim 5
Dependent Claim 197 words
The compound according to claim 1, wherein A 1 is a hydrogen atom; a residue of amino acid of glycine, alanine, valine, norvaline, leucine, isoleucine, serine, cysteine or methionine, optionally having a protecting group for carboxyl group selected from methoxy, ethoxy, propoxy, tert-butoxy, methoxymethyloxy, acetoxymethyloxy, pivaloyloxymethyloxy, benzyloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, phthlidyloxy, phenyloxy and indanyloxy carbobenzoxy, p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, p-chlorobenzyloxycarbonyl, p-bromobenzyloxycarbonyl, p-methylbenzyloxycarbonyl, tert-butoxycarbonyl, 2,2,2-trichloroethoxycarbonyl or trityl group; X is (a) -OH, (b) ##STR21## R 1 is C 1 -C 30 alkyl group, or (c) NHA 2 , A 2 is the same as the definition of A 1 mentioned above, but A 1 and A 2 are independent of each other; and Y is (a) -CH 2 OH, (b) ##STR22## R 2 is C 1 -C 30 alkyl group, or (c) ##STR23## B is OH, a residue of amino acid of glycine alanine, valine, norvaline, leucine, isoleucine, serine, cysteine, or methionine, optionally having a protecting group for the carboxyl group selected from methoxy, ethoxy, propoxy, tert-butoxy, methoxymethyloxy, acetoxymethyloxy, pivaloyloxymethyloxy, benzyloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, phthalidyloxy, phenyloxy and indanyloxy or a protecting group for the carboxyl group selected from methoxy, ethoxy, propoxy, tert-butoxy, methoxymethyloxy, acetoxymethyloxy, pivaloyloxymethyloxy, benzyloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, phthalidyloxy, phenyloxy and indanyloxy.
Claim 6
Dependent Claim 61 words
The compound according to claim 1, wherein A 1 is a hydrogen atom, L-alanyl or carbobenzoxy, X is (a) -OH, (b) palmitoyloxy, or (c) -NHA 2 , A 2 is a hydrogen atom, L-alanyl optionally having tert butoxycarbonyl; carbobenzoxy, or tert-butoxycarbonyl; and Y is (a) CH 2 OH, (b) palmitoyloxymethyl, or (c) ##STR24## B is -OH, carboxyethylamino, tert-butoxycarbonylethylamino, p-nitrobenzy-loxy, or tert-butoxy.
Claim 7
Dependent Claim 11 words
The compound according to claim 1, selected from: 2,3-Dihydroxypropyl (lRS)-1-aminoethylphos-phonate hydrochloride;
Claim 8
Dependent Claim 23 words
3-Dihydroxypropyl (lRS)-1-(L-alanylamino)-ethylphosphonate hydrochloride; 2,3-Dipalmitoyloxypropyl (lRS)-1-carbobenzoxyaminoethylphosphonate; 2,3-Dipalmitoyloxypropyl (lRS)-1-aminoethylphosphonate; (2R)-2-Carbobenzoxyamino-2-(p-nitrobenzyloxycarbonyl)-ethyl (lRS)-1-carbobenzoxyaminoethylphosphonate; (2R)-2-Amino-2-carboxyethyl (lRS)-1-aminoethyl-phosphonate monohydrochloride; (2S)-2-(tert-Butoxycarbonylamino)-2-, (lS)-1-tert-butoxycarbonylethylaminocarbonyl]ethyl (lRS)-1-carbobenzoxyaminoethylphosphonate; (2S) 2-Amino-2 [(lS)-1-carboxyethylaminocarbonylethyl](lRS)-1-aminoethylphosphonate monohydrobromide; (2S)-2-(tert-Butoxycarbonyl-L-alanylamino)-2-tert-butoxycarbonyl)ethyl (lRS)-1-carbobenzoxyaminoethylphosphonate; (2S)-2-(1-alanylamino)-2-carboxylethyl-(lRS)-1-aminoethylphosphonate monohydrobromide.
Claim 9
Dependent Claim 23 words
3-Dihydroxypropyl (lRS)-1-(L-alanylamino)-ethylphosphonate hydrochloride; 2,3-Dipalmitoyloxypropyl (lRS)-1-carbobenzoxyaminoethylphosphonate; 2,3-Dipalmitoyloxypropyl (lRS)-1-aminoethylphosphonate; (2R)-2-Carbobenzoxyamino-2-(p-nitrobenzyloxycarbonyl)-ethyl (lRS)-1-carbobenzoxyaminoethylphosphonate; (2R)-2-Amino-2-carboxyethyl (lRS)-1-aminoethyl-phosphonate monohydrochloride; (2S)-2-(tert-Butoxycarbonylamino)-2-, (lS)-1-tert-butoxycarbonylethylaminocarbonyl]ethyl (lRS)-1-carbobenzoxyaminoethylphosphonate; (2S) 2-Amino-2 [(lS)-1-carboxyethylaminocarbonylethyl](lRS)-1-aminoethylphosphonate monohydrobromide; (2S)-2-(tert-Butoxycarbonyl-L-alanylamino)-2-tert-butoxycarbonyl)ethyl (lRS)-1-carbobenzoxyaminoethylphosphonate; (2S)-2-(1-alanylamino)-2-carboxylethyl-(lRS)-1-aminoethylphosphonate monohydrobromide.

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Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-10-28 1995-04-29 1995-10-29 $2000.00 Window Closed / Lapsed
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