CA2325523A1 - Prodrugs of phosphorous-containing pharmaceuticals - Google Patents
Prodrugs of phosphorous-containing pharmaceuticals Download PDFInfo
- Publication number
- CA2325523A1 CA2325523A1 CA002325523A CA2325523A CA2325523A1 CA 2325523 A1 CA2325523 A1 CA 2325523A1 CA 002325523 A CA002325523 A CA 002325523A CA 2325523 A CA2325523 A CA 2325523A CA 2325523 A1 CA2325523 A1 CA 2325523A1
- Authority
- CA
- Canada
- Prior art keywords
- ester
- methyl
- valyloxy
- propionyloxymethyl
- compound according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Pharmaceutical compounds with the formula: Drug-P(=O)-O-Linker(-R2')k-R2 where Drug-P(=O)-O- is the residue of a drug comprising a phosphonate, phosphinate or phosphoryl function, such as alendronate or foscarnet, R2 and R2' (if present) are independently the acyl residue of an aliphatic amino acid; Linker is an at least difunctional moiety comprising a first function ester-bonded to the phosphonate, phosphinate or phosphoryl function spaced from a second function ester-bonded to R2; and k is 1 or zero; have enhanced bioavailability or other pharmacokinetic performance relative to the parent drug.
Description
WO 99/51b13 PCT/SE99/00528 PRODRUGS OF PHOSPHOROUS-CONTAINING PHARMACEUTICALS
Technical Field This invention relates to the field of phosphorous-containing pharmaceuticals, including phosphonates, phosphinates and phosphates and in particular to prodrugs of such pharmaceuticals. The invention provides novel pharmaceutical compounds and compositions, methods for their preparation and pharmaceutical methods employing them.
to Background Art Many phosphorous-containing pharmaceuticals have not reached their full clinical potential due to difficulties in administering them, particularly via the oral route. Bis-phosphonate bone resorption agents such as alendronate, for example, have oral bioavailabilities of just a few percent and adsorption is diminished by food fruit juice 15 coffee, dairy products etc. This poor bioavailability is exacerbated by the caustic nature of the drug which leads to irritation of the gastric walls, resulting in an administration regime calling for a fasted stomach and the patient standing for half an hour after ingestion to ensure transport of the drug past the gastric region.
20 A significant amount of work has been done to attempt to solve the administration difficulties by optimising the formulation of phosphorous-containing drugs.
Merck for example describe various formulations of the bis-phosphonate alendronate, such as a pH buffered formulation in W098 14196, an effervescent formulation in 44017, the monohydrate and disodium in W096 39410, the anhydrate in W096 25 39149, a liquid formulation with complexing agent in W095 33755 and calcium salts in EP 449 405. To our knowledge, however, none of these conventional formulation approaches has produced a clinically succesful administration form.
Merck and others have also explored prodrugs of bis-phosphonate bone resorption 3o agents in an attempt to improve the clinical utility of these drugs. For example, Leiras OY's US 5,376,649 describes esters of halogenated bis-phosphonates of the clodronate type, wherein the prodrug moiety comprises an alkyl, alkenyl, alkynyl, aryl, araikyl and silyl. No improvements in bioavailability are reported.
Leo's US
Technical Field This invention relates to the field of phosphorous-containing pharmaceuticals, including phosphonates, phosphinates and phosphates and in particular to prodrugs of such pharmaceuticals. The invention provides novel pharmaceutical compounds and compositions, methods for their preparation and pharmaceutical methods employing them.
to Background Art Many phosphorous-containing pharmaceuticals have not reached their full clinical potential due to difficulties in administering them, particularly via the oral route. Bis-phosphonate bone resorption agents such as alendronate, for example, have oral bioavailabilities of just a few percent and adsorption is diminished by food fruit juice 15 coffee, dairy products etc. This poor bioavailability is exacerbated by the caustic nature of the drug which leads to irritation of the gastric walls, resulting in an administration regime calling for a fasted stomach and the patient standing for half an hour after ingestion to ensure transport of the drug past the gastric region.
20 A significant amount of work has been done to attempt to solve the administration difficulties by optimising the formulation of phosphorous-containing drugs.
Merck for example describe various formulations of the bis-phosphonate alendronate, such as a pH buffered formulation in W098 14196, an effervescent formulation in 44017, the monohydrate and disodium in W096 39410, the anhydrate in W096 25 39149, a liquid formulation with complexing agent in W095 33755 and calcium salts in EP 449 405. To our knowledge, however, none of these conventional formulation approaches has produced a clinically succesful administration form.
Merck and others have also explored prodrugs of bis-phosphonate bone resorption 3o agents in an attempt to improve the clinical utility of these drugs. For example, Leiras OY's US 5,376,649 describes esters of halogenated bis-phosphonates of the clodronate type, wherein the prodrug moiety comprises an alkyl, alkenyl, alkynyl, aryl, araikyl and silyl. No improvements in bioavailability are reported.
Leo's US
4,732,998, US 4,870,063 and W086 00902 describe prodrugs of certain non-hydroxylated bis-phosphonates. In particular the pivaloyloxymethyl and acetoxyrnethyl tetraesters are prepared (although no improvements in bioavailability are reported) and certain other esters postulated, such as the C3-C6 alkanoyloxymethyl, C4 C, 1-(alkanoyloxy)ethyl, CS-C8 1-methyl-1-(alkanoyloxy)ethyl, C4-C, 1-(alkoxycarbonyloxy)ethyl, C3-C6 alkoxycarbonyloxymethyl, CQ-C, 1-alkoxycarbonyloxy)ethyl, CS-Cg 1-methyl-1-(alkoxycarbonyloxy)ethyl, 3-phthalidyl, 4-crotonolactonyl, y-butyrolacton-4-yl, (2-oxo-1,3-dioxolen-4-yl)methyl, (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl, (5-phenyl-2-oxo-1,3-dioxolen-4-yl)methyl, dialkylaminoalkyl, acetonyl and methoxymethyl.
Merck's US 5,227,506 describes acyloxymethyl esters of a number of bis-phosphonates, notable alendronate, wherein the acyl component is C,-C,Z
alkanoyl.
As with the Leo patents above the preferred prodrug is pivaloylxoymethyl, although no bioavailability data is provided.
Other phosphorous-containing drugs where attempts to improve bioavailability shortcomings have employed prodrugs include the antiviral agent foscarnet (phosphonoformate). Astra's W098 16537 and W09825938 describe 2o monosaccharide and cyclic esters of foscarnet. Boehringer's W09722368, Hostetler's US 5,696,277 and W094/13682, UC's W096 15132 (inter alia) describe lipid or glycerol esters of foscarnet. Iyer et al, Tett. Letters 30 No 51, (1989) describe acyloxyalkyl esters, wherein the acyl component is C,-C4 alkanoyl.
Glazier's W091/19721 describes acyloxybenzyloxy esters. Walker et al, Int J
Pharmaceutics 104 (1994)157-167 describes foscarnet-tyrosine conjugates wherein the hydroxy group on the amino acid side chain is esterified to the phosphonate.
These compounds are not however orally administered prodrugs, but rather are designed to penetrate the blood brain barner following iv administration.
3o A still further group of pharmaceuticals where prodrugs have been proposed to attempt to overcome bioavailability shortcomings are the phosphonate nucleoside analogues, such as those disclosed in Gilead's W098 04569 and an extensive series of patents in the name Rega Stichting/Institute of Organic Chemistry &
Biochemistry of the Academy of Sciences of the Czech Republic including EP 481214. However, to our knowledge, the only such phosphonates to show clinical practicality are the now marketed bis-POM and bis-POC adefovir (bis-pivoxil and bis-isopropyloxycarbonyloxymethyl esters, respectively). WO 95/01363 also shows a form of phosphonate nucleoside analogue.
Monophosphate esters of monophosphorylated nucleoside analogues are desclosed in EP 763049 (glyceryl diethers), WO 95 32984 (lipid esters), US 5484911 (ether lipids)WO 98 51692 (substituted benzyl esters) WO 96 33201 (alkylthioacyl esters) Glazier's WO 91/19721 (above) and US 5 627 165 and Texas Uni's WO 90/08155 purport to provide prodrugs of diverse phosphorous-containing pharmaceuticals.
Bodor's WO 92/00988 employs a phosphonate prodrug of non-phosphorous pharmaceuticals to target compounds to the brain.
Brief Description of the Invention A first aspect of the invention provides pharmaceutical compound with the formula:
Drug-P(=O)-O-Linker (-R2')k -Rz where Drug-P(=O)-O- is the residue of a drug comprising a phosphonate, phosphinate or phosphoryl function, RZ and RZ' (if present) are independently the acyl residue of an aliphatic amino acid;
Linker is an at least difunctional moiety comprising a first function ester-bonded to the phosphonate, phosphinate or phosphoryl function spaced from a second function ester-bonded to Rz; and k is 1 or zero.
The enzymatic and/or chemical cleavage of the compounds of the present invention occurs in such a manner that the parent drug is released and the moiety or moieties split off remain non-toxic or are metabolized so that non-toxic or acceptable amounts of metabolic products are produced.The present compounds thus modify the in vivo availability of the parent compound compared to what would be the case if the parent compound was to be administered itself. For instance the prodrugs of the invention may give higher bioavailabities, varied bioavailability kinetics or bioavailabilities with a decreased interpersonal spread.
Representative phosphorous-containing drugs amenable to the prodrugs of the present invention include phosfestrol, (E)-(a,(3-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate), nucleoside analogue phosphonates, nucleotide analogue mono-, di or triphosphates, phosphonoformic acid, phosphonoacetic acid, bis phosphonate bone metabolism agents, fosinoprilate, (3-phosphonocarboxylic acid to farnesyl protein transferase inhbitors, a-phosphonosulfonate squalene synthase inhibitors, phosphonomethylamine neutral endopeptidase (24.11 ) inhibitors.
Favoured -linker (-RZ')k - R2 structures include those of the formulae:
R4~ p RaR
R2- O - ()ql ()qr-T -~ o R4L' R4R 1 I a or R2 - O - ()ql Ring - ()qr-T --~ o R4R Ilb 1$
where Rz is the acyl residue of an aliphatic amino acid, R4Land R4~' are independently H, hydroxymethyl, C,_3 alkyl, C3-Cbcycloalkyl, C,-2o C,alkyl-C,-C6cycloalkyl, phenyl or benzyl, R4R and R4R' are independently H, C,_3 alkyl or phenyl, ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
Additional -linker (-RZ')k-RZ structures and intermediates for their application, such 5 as those of the formula:
O
R2'- O
where RZ and Rz' are as described above are disclosed and claimed in our co-pending application PCT/SE99/00194, the contents of which are hereby incorporated by reference.
Further linker-RZ structures include:
R2~ O'\
such as alanyloxymethyl-, valyloxymethyl-, leucyloxymethyl- t-leucyloxymethyl-ar isoleucyloxymethyl, especially valyloxymethyl-.
Where the Drug comprises a phosphonate or phosphoryl function, or a plurality of such functions, the compound of the invention may comprise a plurality of -linker (-RZ')~ - Rz structures, preferably identical to each other for ease of synthesis.
Preferred values for R4Rand R4R' are hydrogen for ease of synthesis, although compounds wherein one of R4Rand R4R' is hydrogen and the other methyl have the advantage of releasing the innocuous biproduct ethanol upon degradation.
Representative values for R4L and R4L' include methyl, hydrogen;
hydroxymethyl, methyl; or ethyl, ethyl, respectively. A particularly preferred value is methyl, methyl.
Favoured values for ql and qr, respectively, include 1,0;
2,0;
Merck's US 5,227,506 describes acyloxymethyl esters of a number of bis-phosphonates, notable alendronate, wherein the acyl component is C,-C,Z
alkanoyl.
As with the Leo patents above the preferred prodrug is pivaloylxoymethyl, although no bioavailability data is provided.
Other phosphorous-containing drugs where attempts to improve bioavailability shortcomings have employed prodrugs include the antiviral agent foscarnet (phosphonoformate). Astra's W098 16537 and W09825938 describe 2o monosaccharide and cyclic esters of foscarnet. Boehringer's W09722368, Hostetler's US 5,696,277 and W094/13682, UC's W096 15132 (inter alia) describe lipid or glycerol esters of foscarnet. Iyer et al, Tett. Letters 30 No 51, (1989) describe acyloxyalkyl esters, wherein the acyl component is C,-C4 alkanoyl.
Glazier's W091/19721 describes acyloxybenzyloxy esters. Walker et al, Int J
Pharmaceutics 104 (1994)157-167 describes foscarnet-tyrosine conjugates wherein the hydroxy group on the amino acid side chain is esterified to the phosphonate.
These compounds are not however orally administered prodrugs, but rather are designed to penetrate the blood brain barner following iv administration.
3o A still further group of pharmaceuticals where prodrugs have been proposed to attempt to overcome bioavailability shortcomings are the phosphonate nucleoside analogues, such as those disclosed in Gilead's W098 04569 and an extensive series of patents in the name Rega Stichting/Institute of Organic Chemistry &
Biochemistry of the Academy of Sciences of the Czech Republic including EP 481214. However, to our knowledge, the only such phosphonates to show clinical practicality are the now marketed bis-POM and bis-POC adefovir (bis-pivoxil and bis-isopropyloxycarbonyloxymethyl esters, respectively). WO 95/01363 also shows a form of phosphonate nucleoside analogue.
Monophosphate esters of monophosphorylated nucleoside analogues are desclosed in EP 763049 (glyceryl diethers), WO 95 32984 (lipid esters), US 5484911 (ether lipids)WO 98 51692 (substituted benzyl esters) WO 96 33201 (alkylthioacyl esters) Glazier's WO 91/19721 (above) and US 5 627 165 and Texas Uni's WO 90/08155 purport to provide prodrugs of diverse phosphorous-containing pharmaceuticals.
Bodor's WO 92/00988 employs a phosphonate prodrug of non-phosphorous pharmaceuticals to target compounds to the brain.
Brief Description of the Invention A first aspect of the invention provides pharmaceutical compound with the formula:
Drug-P(=O)-O-Linker (-R2')k -Rz where Drug-P(=O)-O- is the residue of a drug comprising a phosphonate, phosphinate or phosphoryl function, RZ and RZ' (if present) are independently the acyl residue of an aliphatic amino acid;
Linker is an at least difunctional moiety comprising a first function ester-bonded to the phosphonate, phosphinate or phosphoryl function spaced from a second function ester-bonded to Rz; and k is 1 or zero.
The enzymatic and/or chemical cleavage of the compounds of the present invention occurs in such a manner that the parent drug is released and the moiety or moieties split off remain non-toxic or are metabolized so that non-toxic or acceptable amounts of metabolic products are produced.The present compounds thus modify the in vivo availability of the parent compound compared to what would be the case if the parent compound was to be administered itself. For instance the prodrugs of the invention may give higher bioavailabities, varied bioavailability kinetics or bioavailabilities with a decreased interpersonal spread.
Representative phosphorous-containing drugs amenable to the prodrugs of the present invention include phosfestrol, (E)-(a,(3-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate), nucleoside analogue phosphonates, nucleotide analogue mono-, di or triphosphates, phosphonoformic acid, phosphonoacetic acid, bis phosphonate bone metabolism agents, fosinoprilate, (3-phosphonocarboxylic acid to farnesyl protein transferase inhbitors, a-phosphonosulfonate squalene synthase inhibitors, phosphonomethylamine neutral endopeptidase (24.11 ) inhibitors.
Favoured -linker (-RZ')k - R2 structures include those of the formulae:
R4~ p RaR
R2- O - ()ql ()qr-T -~ o R4L' R4R 1 I a or R2 - O - ()ql Ring - ()qr-T --~ o R4R Ilb 1$
where Rz is the acyl residue of an aliphatic amino acid, R4Land R4~' are independently H, hydroxymethyl, C,_3 alkyl, C3-Cbcycloalkyl, C,-2o C,alkyl-C,-C6cycloalkyl, phenyl or benzyl, R4R and R4R' are independently H, C,_3 alkyl or phenyl, ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
Additional -linker (-RZ')k-RZ structures and intermediates for their application, such 5 as those of the formula:
O
R2'- O
where RZ and Rz' are as described above are disclosed and claimed in our co-pending application PCT/SE99/00194, the contents of which are hereby incorporated by reference.
Further linker-RZ structures include:
R2~ O'\
such as alanyloxymethyl-, valyloxymethyl-, leucyloxymethyl- t-leucyloxymethyl-ar isoleucyloxymethyl, especially valyloxymethyl-.
Where the Drug comprises a phosphonate or phosphoryl function, or a plurality of such functions, the compound of the invention may comprise a plurality of -linker (-RZ')~ - Rz structures, preferably identical to each other for ease of synthesis.
Preferred values for R4Rand R4R' are hydrogen for ease of synthesis, although compounds wherein one of R4Rand R4R' is hydrogen and the other methyl have the advantage of releasing the innocuous biproduct ethanol upon degradation.
Representative values for R4L and R4L' include methyl, hydrogen;
hydroxymethyl, methyl; or ethyl, ethyl, respectively. A particularly preferred value is methyl, methyl.
Favoured values for ql and qr, respectively, include 1,0;
2,0;
3,0; or 4,0;
particularly 1,0 when the -linker (-Rz')k-Rz structure has the formula IIa.
Alternative convenient values for ql and qr, respectively, include 1,1;
2,1;
3,1;
4,1; or l0 2,2.
Where the -linker (-RZ')k-RZ structure has the formula IIb, that is includes a -ring-moiety an alternative convenient configuration has ql and qr both 0.
The -ring- moiety in the above depicted -linker (-RZ')k-RZ structure may comprise furyl, thienyl, pyranyl, pynrolyl, pyrrolinyl, pyrrolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, imidazolyl, imidazolinyl, imidazolidinyl, pyridyl, piperidinyl, pyrazinyl, piperazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolidinyl, isoxazolyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, isothiazolidinyl, and the like or bicyclic rings especially of the above fused to a phenyl ring such as 2o indolyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzothiazolyl, benzoxazolyl, benzothienyl etc. The carbo or heterocyclic ring may be bonded via a carbon or via a hetero atom, for instance a nitrogen atom, such as N-piperidyl, N-morpholinyl etc.
The -ring- moiety is conveniently phenyl, furyl, pyridyl, cyclobutyl, cyclopentyl or cyclohexyl.
The -ring- moiety can be optionally substituted with one to three substituents such as halo, amino, mercapto, oxo, vitro, NHC,-C6 alkyl, N(C,-C6 alkyl)2, C,-C6 alkyl, C,-C6 alkenyl, C,-C6 alkynyl, C,-C6 alkanoyl, C,-C6 alkoxy, thioC,-C6 alkyl, thioC,-alkoxy, hydroxy, hydroxyC,-C6 alkyl, haloC,=C6 alkyl, aminoC,-C6 alkyl, C,-C6 alkyl, 3ti cyano, carboxyl, carbalkoxy, carboxamide, carbamoyl, sulfonylamide, benzyloxy, WO 99!51613 PCT/SE99/00528 morpholyl-C,-C6 alkyloxy, a monocyclic carbo- or heterocycle, as defined above, a optional substituent comprises an additional group RZ ( )q,-.
The aliphatic amino acid RZ is derived from D- or L- glycine, alanine, v ine, leucine, tent-leucine and isoleucine. Preferably the or each RZ is derived fro -valine to ensure nature identical breakdown products.
1o The currently prefer ed value for T is a bond.
Representative phosphorous-containing drugs incl a phosfestrol, (E)-(a,(3-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate) and ytostatic metabolites such as phosphorylated nucleoside anlaogues such FLG, cytarabin or gemcitabin.
Representative drugs comprising a ply6sphonate function include antiviral nucleoside or nucleotide analogues such as P EA, HPMPC, PMPA and the like or phosphates such as the monophosphates, ' hosphate or triphospates of those nucleoside analogues which require p sphorylation for activity, such as gemcitabine, ACV, 2o AZT, ddI, ddC, PCV, V, H2G, BVDU, FMAU, 3TC, FTC etc. Certain mixed amino acid/fatty aci acyloxyalkylphosphonates are proposed in our copending application PCT 97 001903 and it should be thus appreciated that the prodrugs of the present in ention are fatty acyl-free and/or apply the novel linkers defined herein in the nho honate nucleotide field.
Taking the phosphonate antivirals adefovir and cidovir as examples, prodrugs of the carbo- or heterocyclic group spaced by alkyl, such as C1_3 alkylaryl, etc. A
favoured optional substituent comprises an additional group R2-( )q,-.
The aliphatic anuno acid R2 is derived from D- or L- glycine, alanine, valine, leucine, tent-leucine and isoleucine. Preferably the or each R2 is derived from L-valine to ensure nature identical breakdown products.
The currently preferred value for T is a bond.
Representative phosphorous-containing drugs include phosfestrol, (E)-(a,,(3-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate) and cytostatic metabolites such as phosphorylated nucleoside anlaogues such as FLG, cytarabin or gemcitabin.
Representative drugs comprising a phosphonate function include antiviral nucleoside or nucleotide analogues such as PMEA, HPMPC, PMPA and the like or phosphates such as the monophosphates, diphosphate or triphospates of those nucleoside analogues which require phosphorylation for activity, such as gemcitabine, ACV, AZT, ddI, ddC, PCV, GCV, H2G, BVDU, FMAU, 3TC, FTC etc. Certain mixed amino acid/fatty acid acyloxyalkylphosphonates are proposed in our copending application PCT SE97 001903 (W098 21223) and it should be thus appreciated that the prodrugs of the present invention are fatty acyl-free and/or apply the novel linkers defined herein in the phosphonate nucleotide field.
Taking the phosphonate antivirals adefovir and cidovir as examples, prodrugs of the invention can be applied as shown in Formula PF2:
AMENDED SHEET
particularly 1,0 when the -linker (-Rz')k-Rz structure has the formula IIa.
Alternative convenient values for ql and qr, respectively, include 1,1;
2,1;
3,1;
4,1; or l0 2,2.
Where the -linker (-RZ')k-RZ structure has the formula IIb, that is includes a -ring-moiety an alternative convenient configuration has ql and qr both 0.
The -ring- moiety in the above depicted -linker (-RZ')k-RZ structure may comprise furyl, thienyl, pyranyl, pynrolyl, pyrrolinyl, pyrrolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, imidazolyl, imidazolinyl, imidazolidinyl, pyridyl, piperidinyl, pyrazinyl, piperazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolidinyl, isoxazolyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, isothiazolidinyl, and the like or bicyclic rings especially of the above fused to a phenyl ring such as 2o indolyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzothiazolyl, benzoxazolyl, benzothienyl etc. The carbo or heterocyclic ring may be bonded via a carbon or via a hetero atom, for instance a nitrogen atom, such as N-piperidyl, N-morpholinyl etc.
The -ring- moiety is conveniently phenyl, furyl, pyridyl, cyclobutyl, cyclopentyl or cyclohexyl.
The -ring- moiety can be optionally substituted with one to three substituents such as halo, amino, mercapto, oxo, vitro, NHC,-C6 alkyl, N(C,-C6 alkyl)2, C,-C6 alkyl, C,-C6 alkenyl, C,-C6 alkynyl, C,-C6 alkanoyl, C,-C6 alkoxy, thioC,-C6 alkyl, thioC,-alkoxy, hydroxy, hydroxyC,-C6 alkyl, haloC,=C6 alkyl, aminoC,-C6 alkyl, C,-C6 alkyl, 3ti cyano, carboxyl, carbalkoxy, carboxamide, carbamoyl, sulfonylamide, benzyloxy, WO 99!51613 PCT/SE99/00528 morpholyl-C,-C6 alkyloxy, a monocyclic carbo- or heterocycle, as defined above, a optional substituent comprises an additional group RZ ( )q,-.
The aliphatic amino acid RZ is derived from D- or L- glycine, alanine, v ine, leucine, tent-leucine and isoleucine. Preferably the or each RZ is derived fro -valine to ensure nature identical breakdown products.
1o The currently prefer ed value for T is a bond.
Representative phosphorous-containing drugs incl a phosfestrol, (E)-(a,(3-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate) and ytostatic metabolites such as phosphorylated nucleoside anlaogues such FLG, cytarabin or gemcitabin.
Representative drugs comprising a ply6sphonate function include antiviral nucleoside or nucleotide analogues such as P EA, HPMPC, PMPA and the like or phosphates such as the monophosphates, ' hosphate or triphospates of those nucleoside analogues which require p sphorylation for activity, such as gemcitabine, ACV, 2o AZT, ddI, ddC, PCV, V, H2G, BVDU, FMAU, 3TC, FTC etc. Certain mixed amino acid/fatty aci acyloxyalkylphosphonates are proposed in our copending application PCT 97 001903 and it should be thus appreciated that the prodrugs of the present in ention are fatty acyl-free and/or apply the novel linkers defined herein in the nho honate nucleotide field.
Taking the phosphonate antivirals adefovir and cidovir as examples, prodrugs of the carbo- or heterocyclic group spaced by alkyl, such as C1_3 alkylaryl, etc. A
favoured optional substituent comprises an additional group R2-( )q,-.
The aliphatic anuno acid R2 is derived from D- or L- glycine, alanine, valine, leucine, tent-leucine and isoleucine. Preferably the or each R2 is derived from L-valine to ensure nature identical breakdown products.
The currently preferred value for T is a bond.
Representative phosphorous-containing drugs include phosfestrol, (E)-(a,,(3-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate) and cytostatic metabolites such as phosphorylated nucleoside anlaogues such as FLG, cytarabin or gemcitabin.
Representative drugs comprising a phosphonate function include antiviral nucleoside or nucleotide analogues such as PMEA, HPMPC, PMPA and the like or phosphates such as the monophosphates, diphosphate or triphospates of those nucleoside analogues which require phosphorylation for activity, such as gemcitabine, ACV, AZT, ddI, ddC, PCV, GCV, H2G, BVDU, FMAU, 3TC, FTC etc. Certain mixed amino acid/fatty acid acyloxyalkylphosphonates are proposed in our copending application PCT SE97 001903 (W098 21223) and it should be thus appreciated that the prodrugs of the present invention are fatty acyl-free and/or apply the novel linkers defined herein in the phosphonate nucleotide field.
Taking the phosphonate antivirals adefovir and cidovir as examples, prodrugs of the invention can be applied as shown in Formula PF2:
AMENDED SHEET
R4~ O R4R O Base RZ-O- ()Gi 04r-T-~O O_~P~O
R RaR~ Rf3 Rf4 or O RaR O Base R2-O- ()qi -ring- ()Gr-T~-O O-P O
R4R~ Rf3 Rf4 where RZ is the acyl residue of an aliphatic amino acid, R4~and R4L' are independently H, C,_3 alkyl, hydroxymethyl, C3-6cycloalkyl, C,-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C,_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-to R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
base is a natural or unnatural nucleotide base, especially guanine, adenine or cytosine, Rf3 is H or a further structure of the formula IIa or IIb and Rf4 is H or CHZOH.
Currently favoured values in formula PF2 include: R3R and R3R' are preferably H
and/or R,L and R3L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and q1 is 0 or more preferably 1.
Thus a preferred group of phosphonate antivirals within the scope of the invention include:
R RaR~ Rf3 Rf4 or O RaR O Base R2-O- ()qi -ring- ()Gr-T~-O O-P O
R4R~ Rf3 Rf4 where RZ is the acyl residue of an aliphatic amino acid, R4~and R4L' are independently H, C,_3 alkyl, hydroxymethyl, C3-6cycloalkyl, C,-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C,_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-to R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
base is a natural or unnatural nucleotide base, especially guanine, adenine or cytosine, Rf3 is H or a further structure of the formula IIa or IIb and Rf4 is H or CHZOH.
Currently favoured values in formula PF2 include: R3R and R3R' are preferably H
and/or R,L and R3L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and q1 is 0 or more preferably 1.
Thus a preferred group of phosphonate antivirals within the scope of the invention include:
9-[2-phosphonomethoxy)ethyl]adenine, mono(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl)adenine, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono(2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono(2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono-(5-(L-vaiyloxy)-2,2-dimethylvaleryloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono [4-( L-valyloxy)-butanoyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl)adenine, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl)adenine, mono-(2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine, mono-(4-N-valyloxy)cyclohexanoyloxymethyl) ester 9-[2-phosphonomethoxy)ethyl]adenine, mono-(1-valyloxy-2-methylpropane-2-aminocarbonyloxymethyl) ester 9-[2-phosphonomethoxy)ethyl]adenine, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-3o dihydro-pyridine-3-carbonyloxymethyl) ester 9-[2-phosphonomethoxy)ethyl]adenine, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester 9-[2-phosphonomethoxy)ethyl]adenine, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester 9-[2-phosphonomethoxy)ethylJadenine, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 5 9-[2-phosphonomethoxy)ethyl]adenine, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 9-[2-phosphonomethoxy)ethylJadenine, mono-(3-(L-valyloxy)-2-methyl, 2-hydroxymethylpropionyloxymethyl) ester the corresponding bis esters and pharmaceutically acceptable salts thereof. A
further 10 preferred group comprises the corresponding derivatives of PMPA and HPMPC.
A particularly preferred group comprises.
9-[2-phosphonomethoxy)ethylJadenine di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester 9-[2-phosphonomethoxy)ethyl]adenine mono-(2-methyl-2-(D-valyloxymethyl) propionyloxyrnethyl) ester 9-[2-phosphonomethoxy)ethylJadenine di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethylJadenine mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethylJadenine di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethylJadenine mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester and especially 9-[2-phosphonomethoxy)ethyl]adenine di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester and 9-[2-phosphonomethoxy)ethyl]adenine mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester;
and the corresponding derivatives of PMPA and HPMPC.
A further convenient group comprises 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-leucyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono (2-methyl-2-(L-glycyloxymethyl) to propionyloxymethyl) ester, the con:esponding bis esters and the corresponding derivatives of PMPA and HPMPC.
A further group of useful compounds comprises:
i5 9-[2-phosphonomethoxy)ethyl]adenine mono-L-valyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine di-L-valyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-leucyloxymethyl ester, 9-[2-phosphonomethoxy}ethyl]adenine di-L-leucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-isoleucyloxymethyl ester, 2o 9-[2-phosphonomethoxy)ethyl]adenine di-L-isoleucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-t-leucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine di-L-t-leucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-alanyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine di-L-alanyloxymethyl ester, 25 and the corresponding derivatives of HPMPC and PMPA.
This aspect of the invention further provides a method for the treatment or prophylaxis of virus infections comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in need 3o thereof. Viral infections include herpesvirus infections such as HSV-1, HSV-2, VZV, CMV, HHV6, HHV8 and retroviruses such as HIV-1 and HN-2. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the preparation of a medicament for the prophylaxis or treatment of viral infections.
A further group of phosphorous containing antivirals amenable to the invention include foscarnet (phosphonoformate) and PAA (phosphonoacetate). Taking foscarnet as an example:
O O~~
HO-P-u-OH
I
O
H
it will be apparent that aside from conventional pharmaceutically acceptable esters to applied to the carboxy function, one or two -linker(-Rz')k Rz structures, preferably those of formula IIa or IIb can be applied to the phosphonate function to define compounds such as O
O O
O~O-P-~OH
l O
H
Thus a preferred group of compounds comprises foscarnet derivatives of the formula PF 1:
R4~ O R4R O O
R2-O- ()qi ()qr-T--u--O O-P-~O-Rf2 R4~ R4R
Rf1 or R4R ~ O
R2-O-Oq~ Ring-()qr-T-11-O -P-ll-O-Rf2 O
_ R4R
Rf1 where RZ is the acyl residue of an aliphatic amino acid, S R4Land R4L' are independently H, C,_3 alkyl, hydroxymethyl; C3-bcycloalkyl, C,-,alkyl-C,Cbcycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C,_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4 or -O-to R4 is H or C,_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and Rfl is H, a further ester of formula IIa or IIb and Rf2 is H, a further linker(-RZ')e-RZ ester or a conventional pharmaceutically acceptable ester, including acyloxyalkyl esters.
Currently favoured values in Formula PF1 include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rfl is a further ester it is convenient if it is identical to the other linker{RZ')k-RZ moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters or alternatively a similar structure to the linker(-RZ')k-RZ moiety as envisaged in our copending PCT/SE99/00194.
A favoured group of compounds within formula PF1 include:
phosphonoformic acid, mono(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, phosphonoformic acid, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, phosphonoformic acid, mono(2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 3o phosphonoformic acid, mono(2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, phosphonoformic acid, mono((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, phosphonoformic acid, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, phosphonoformic acid, mono-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, phosphonoformic acid, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, phosphonoformic acid, mono [4-( L-valyloxy)-butanoyloxymethyl] ester, phosphonoformic acid, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, phosphonoformic acid, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, phosphonoformic acid, mono- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxyrnethyl) ester, phosphonoformic acid, mono-(4-N-valyloxy)cyclohexanoyloxymethyl) ester to phosphonoformic acid, mono-(1-valyloxy-2-methylpropane-2-aminocarbonyloxymethyl) ester phosphonoformic acid, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester phosphonoformic acid, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyioxy methyl) 15 ester phosphonoformic acid, mono-(2-hydroxymethyl-2-rnethylpropionyloxymethyl) ester phosphonoformic acid, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester phosphonoformic acid, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 2o phosphonoformic acid, mono-(3-(L-valyloxy)-2-methyl, 2-hydroxymethyl-propionyloxymethyl) ester the corresponding bis esters, the corresponding compounds additionally bearing a conventional carboxyl ester, and pharmaceutically acceptable salts thereof.
25 An especially favoured group comprises:
phosponoformic acid di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester phosponoformic acid mono-(2-methyl-2-(D-valyloxyrnethyl) propionyloxymethyl) ester phosponoformic acid di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 30 phosponoformic acid mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, phosponoformic acid di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, phosponoformic acid mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester and especially phosponoformic acid di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester phosponoformic acid mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester;
and pharmaceutically acceptable salts and conventional pharmaceutical carboxy-esters thereof.
A further useful group of compounds comprises:
phosponofonnic acid mono-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, to phosponoformic acid mono-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyI) ester, phosponoformic acid mono-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, phosponoformic acid mono-{2-methyl-2-(L-alanyloxymethyl) propionyloxyrnethyl) 15 ester, phosponofonmic acid mono-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, and the corresponding bis esters, conventional pharmaceutically acceptable carboxy esters and pharmaceutically acceptable salts thereof.
A further group of useful compounds comprises:
phosponoformic acid mono-L-valyloxymethyl ester, phosponoformic acid di-L-valyloxymethyl ester, phosponoformic acid mono-L-leucyloxymethyl ester, 2s phosponoformic acid di-L-leucyloxymethyl ester, phosponoformic acid mono-L-isoleucyloxymethyl ester, phosponoformic acid di-L-isoleucyloxymethyl ester, phosponoformic acid mono-L-t-leucyloxymethyl ester, phosponoformic acid di-L-t-leucyloxymethyl ester, 3o phosponoformic acid mono-L-alanyloxymethyl ester, phosponoformic acid di-L-alanyloxymethyl ester, conventional pharmaceutically acceptable carboxy esters and pharmaceutically acceptable salts thereof.
further 10 preferred group comprises the corresponding derivatives of PMPA and HPMPC.
A particularly preferred group comprises.
9-[2-phosphonomethoxy)ethylJadenine di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester 9-[2-phosphonomethoxy)ethyl]adenine mono-(2-methyl-2-(D-valyloxymethyl) propionyloxyrnethyl) ester 9-[2-phosphonomethoxy)ethylJadenine di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethylJadenine mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethylJadenine di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethylJadenine mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester and especially 9-[2-phosphonomethoxy)ethyl]adenine di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester and 9-[2-phosphonomethoxy)ethyl]adenine mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester;
and the corresponding derivatives of PMPA and HPMPC.
A further convenient group comprises 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-leucyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono -(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, 9-[2-phosphonomethoxy)ethyl]adenine mono (2-methyl-2-(L-glycyloxymethyl) to propionyloxymethyl) ester, the con:esponding bis esters and the corresponding derivatives of PMPA and HPMPC.
A further group of useful compounds comprises:
i5 9-[2-phosphonomethoxy)ethyl]adenine mono-L-valyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine di-L-valyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-leucyloxymethyl ester, 9-[2-phosphonomethoxy}ethyl]adenine di-L-leucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-isoleucyloxymethyl ester, 2o 9-[2-phosphonomethoxy)ethyl]adenine di-L-isoleucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-t-leucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine di-L-t-leucyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine mono-L-alanyloxymethyl ester, 9-[2-phosphonomethoxy)ethyl]adenine di-L-alanyloxymethyl ester, 25 and the corresponding derivatives of HPMPC and PMPA.
This aspect of the invention further provides a method for the treatment or prophylaxis of virus infections comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in need 3o thereof. Viral infections include herpesvirus infections such as HSV-1, HSV-2, VZV, CMV, HHV6, HHV8 and retroviruses such as HIV-1 and HN-2. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the preparation of a medicament for the prophylaxis or treatment of viral infections.
A further group of phosphorous containing antivirals amenable to the invention include foscarnet (phosphonoformate) and PAA (phosphonoacetate). Taking foscarnet as an example:
O O~~
HO-P-u-OH
I
O
H
it will be apparent that aside from conventional pharmaceutically acceptable esters to applied to the carboxy function, one or two -linker(-Rz')k Rz structures, preferably those of formula IIa or IIb can be applied to the phosphonate function to define compounds such as O
O O
O~O-P-~OH
l O
H
Thus a preferred group of compounds comprises foscarnet derivatives of the formula PF 1:
R4~ O R4R O O
R2-O- ()qi ()qr-T--u--O O-P-~O-Rf2 R4~ R4R
Rf1 or R4R ~ O
R2-O-Oq~ Ring-()qr-T-11-O -P-ll-O-Rf2 O
_ R4R
Rf1 where RZ is the acyl residue of an aliphatic amino acid, S R4Land R4L' are independently H, C,_3 alkyl, hydroxymethyl; C3-bcycloalkyl, C,-,alkyl-C,Cbcycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C,_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4 or -O-to R4 is H or C,_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and Rfl is H, a further ester of formula IIa or IIb and Rf2 is H, a further linker(-RZ')e-RZ ester or a conventional pharmaceutically acceptable ester, including acyloxyalkyl esters.
Currently favoured values in Formula PF1 include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rfl is a further ester it is convenient if it is identical to the other linker{RZ')k-RZ moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters or alternatively a similar structure to the linker(-RZ')k-RZ moiety as envisaged in our copending PCT/SE99/00194.
A favoured group of compounds within formula PF1 include:
phosphonoformic acid, mono(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, phosphonoformic acid, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, phosphonoformic acid, mono(2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 3o phosphonoformic acid, mono(2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, phosphonoformic acid, mono((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, phosphonoformic acid, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, phosphonoformic acid, mono-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, phosphonoformic acid, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, phosphonoformic acid, mono [4-( L-valyloxy)-butanoyloxymethyl] ester, phosphonoformic acid, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, phosphonoformic acid, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, phosphonoformic acid, mono- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxyrnethyl) ester, phosphonoformic acid, mono-(4-N-valyloxy)cyclohexanoyloxymethyl) ester to phosphonoformic acid, mono-(1-valyloxy-2-methylpropane-2-aminocarbonyloxymethyl) ester phosphonoformic acid, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester phosphonoformic acid, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyioxy methyl) 15 ester phosphonoformic acid, mono-(2-hydroxymethyl-2-rnethylpropionyloxymethyl) ester phosphonoformic acid, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester phosphonoformic acid, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 2o phosphonoformic acid, mono-(3-(L-valyloxy)-2-methyl, 2-hydroxymethyl-propionyloxymethyl) ester the corresponding bis esters, the corresponding compounds additionally bearing a conventional carboxyl ester, and pharmaceutically acceptable salts thereof.
25 An especially favoured group comprises:
phosponoformic acid di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester phosponoformic acid mono-(2-methyl-2-(D-valyloxyrnethyl) propionyloxymethyl) ester phosponoformic acid di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 30 phosponoformic acid mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, phosponoformic acid di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, phosponoformic acid mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester and especially phosponoformic acid di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester phosponoformic acid mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester;
and pharmaceutically acceptable salts and conventional pharmaceutical carboxy-esters thereof.
A further useful group of compounds comprises:
phosponofonnic acid mono-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, to phosponoformic acid mono-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyI) ester, phosponoformic acid mono-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, phosponoformic acid mono-{2-methyl-2-(L-alanyloxymethyl) propionyloxyrnethyl) 15 ester, phosponofonmic acid mono-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, and the corresponding bis esters, conventional pharmaceutically acceptable carboxy esters and pharmaceutically acceptable salts thereof.
A further group of useful compounds comprises:
phosponoformic acid mono-L-valyloxymethyl ester, phosponoformic acid di-L-valyloxymethyl ester, phosponoformic acid mono-L-leucyloxymethyl ester, 2s phosponoformic acid di-L-leucyloxymethyl ester, phosponoformic acid mono-L-isoleucyloxymethyl ester, phosponoformic acid di-L-isoleucyloxymethyl ester, phosponoformic acid mono-L-t-leucyloxymethyl ester, phosponoformic acid di-L-t-leucyloxymethyl ester, 3o phosponoformic acid mono-L-alanyloxymethyl ester, phosponoformic acid di-L-alanyloxymethyl ester, conventional pharmaceutically acceptable carboxy esters and pharmaceutically acceptable salts thereof.
This aspect of the invention further provides a method for the treatment or prophylaxis of virus infections comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in need thereof. Viral infections include herpesvirus infections such as HSV-1, HSV-2, VZV, CMV, HHV6, HHV8 and retroviruses such as HIV-1 and HIV-2. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the preparation of a medicament for the prophylaxis or treatment of viral infections.
A further class of phosphonates which are amenable to the invention and which share a structural similarity with phosphonoformic acid are the (3-phosphonocarboxylic acid farnesyl protein transferase inhibitors, especially those of the of the formula PF4:
IS
R4~ O RaR O O O- Rf2 RZ.-O- ()qi ()qr-T~1I--O O-P N~
Rf3 R4~ RaR ~ O
Rf1 or O O- Rf2 R2 - O - Uqi-' Ring ~)Gr -T ~11- O
Rf3 R4R, O O
Rf1 where RF 1 is H or a further structure of formula IIa or IIb Rf2 is H or a conventional pharmaceutically acceptable ester, Rf3 is a polyunsaturated, branched C~zz alkyl, RZ is the acyl residue of an aliphatic amino acid, R4Land RdL' are independently H, C1_3 alkyl, hydroxymethyl, C3-6cycloalkyl, C1-3alkyl-ClC6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, CI_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle Currently favoured values in Formula PF4 include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rf 1 is a further ester it is convenient if it is identical to other linker-R2 moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters or alternatively a similar structure to the linker-R2 moiety as envisaged in our copending PCT/SE99/00194 (W099 41275). A convenient polyunsaturated alkyl Rf3 has the formula:
a ~~ U
where the asterisk shows the point of attachment.
Other structurally similar phosponates include a-phosphonosulphonates such as squalene synthase inhibitors of the formula PFS:
~M~NDED SH~~T
R aR O'~o' O Rf2 4L ~ R
R2-O- ()qi ()qr-T~O O-, Rf3 O
R4~ R4R
Rf1 or O
R O: S-O-Rf2 R2 - O - ()qi- Ring - ()4r -T ~ O -Rf3 O
Rf1 where RF1 is H or a further structure of formula IIa or IIb Rf2 is H or a conventional pharmaceutically acceptable ester a further structure of formula IIa or IIb Rf3 is a polyunsaturated, branched C6_zz alkyl, Rz is the acyl residue of an aliphatic amino acid, R4Land R4~' are independently H, C,_, alkyl, hydroxymethyl, C,-bcycloalkyl, C,-3alkyl-C,Cbcycloalkyl phenyl or benzyl, to R4R and R4R' are independently H, C,_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C,_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
1s Currently favoured values in Formula PFS include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rfl is a further ester it is convenient if it is identical to other linker-2o Rz moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters, or alternatively a similar structure to the linker-Rz moiety. A convenient polyunsaturated alkyl Rf3 has the formula:
where the asterisk denotes the point of attachment.
The aspects of the invention immediately above further provide respective methods for the treatment or prophylaxis of neoplasma or cholesterol disorders comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in need thereof. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the 1 o preparation of a medicament for the prophylaxis or treatment of neoplasma or cholesterol disorders.
A particularly preferred group of phosphorous containing drugs are the bisphosphonates active in bone and calcium metabolism. Favoured bis-phosphonates 15 drugs have the formula:
O,, O
HO-P P~-OH
HO OH
X
where X is H, halo, hydroxy; and Y is a) C,_,o alkyl, optionally substituted with 2o heterocycle, -NRaRe, where Ra and Rb are independently hydrogen, C,_6 alkyl or join together to form a 5 to 7 membered ring, optionally containing a further hetero atom, 25 OH, halo, -S(C,_6 alkyl), phenyl, -C,_, cycloalkyl, (optionally substituted with -NRaRb or OH);
b) C3_, cycloalkyl, optionally substituted with -1VK,Rb, OH, halo, -S(C,_6 alkyl), phenyl, morpholino or pyridyl;
c) halo;
d) piperidinyl;
e) pyrrolidinyl;
f) -S(C,_6 alkyl), optionally substitued with 5 -NRaRb, OH, halo or phenyl;
g) -S-phenyl, optionally substituted with halo, nitro, C,_6 alkyl, C,_6 alkoxy, trifluormethyl, -CONRaRe or -COOH.
1o Preferred bis-phosphonates include alendronate (X is hydroxy, Y is NHZCHZCHZCHZ-), clodronate (X is chloro, Y is chloro), etidronate (X is hydroxy, Y
is CH3-), pamidronate (X is hydroxy, Y is NH~CHZCH,-), ibandronate (X is hydroxy, Y is N (CHzCH2CHZCH2CH3)(CH3)CHzCH2-), tiludronate (X is H, Y is 4-chlorophenylthio-), risedronate (X is hydroxy, Y is 3-pyridinylmethylene-) and 15 zoledronate (X is hydroxy, Y is (2-(1H-imidazol-1-yl)methylene-) Preferred compounds within this bis-phosphonate aspect of the invention thus include those of the formula A1:
O YY O
Ra1-O-P P-O-Ra2 ~O ~ ~O\
Ra3 Ra4 2o A-1 wherein YY and XX have the following values:
NHZ(CHZ)3- OH (alendronate) NHZ(CHZ)Z- OH (pamidronate) cycloheptylamino- H (cimadronate) chloro- chloro (clodronate) pyrrolidin-1-ylCH2CH2- OH ~ (EB 1053) CH3- OH (etidronate) methylpentylaminoCHZCH2- OH (ibandronate) dimethylaminoCHZCHZ OH (olpadronate) pyridin-3-ylCH2- OH (risedronate) (4-chlorophenyl)-thio- H (tiludronate) imidazo-(1,2-a)pyridin-3-ylCHz-OH (YH 529) 1 H-imidazol-1 ylCHz- OH (zoledronate) wherein amino groups on YY can be optionally substituted with conventional pharmaceutically acceptable amide groups such as -C(=O)C,_6alkyl or an aminoacyl or peptidyl derivative, as described in WO 96/31227;
and wherein at least one of Ral-Ra4 is a structure of the formula R2-_ O - ()qi ()qr-T --~ o R4L~ RaR
or R2-O- ()ql- Ring ()qr-T --~O
where RZ is the acyl residue of an aliphatic amino acid, R4Land R4L' are independently H, C,_, alkyl, hydroxymethyl, C3-6cycloalkyl, C,-3alkyl-C,Cbcycloalkyl, phenyl or benzyl, R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, 2o T is a bond, -NR4- or -O
R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and the remainder of Ral-4 are hydrogen or conventional pharmaceutically acceptable esters. Preferably Ral and Ra2 comprise the same structure of formula IIa or IIb and Ra3 and Ra4 are H. A free amine group on YY could also be protected with the same linker (RZ')k-Rz structure, as envisaged in our copending application no PCT/SE99/00194.
In formula A-1, R4R and R4R' are preferably H and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond.
Preferably qr is 1 or more preferably 0 and ql is 0 or more preferably 1.
Representative compounds within formula A-1 thus include;
(4-amino-1-hydroxybutylidine)-bisphosphonate, di(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di (2-L-valyloxy)-DL-propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(5-(L-valyloxy)-2,2-2s dimethylvaleryloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, bis [4-(L-valyloxy)-butanoyloxymethyl] ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(4-(L-valyloxy) benzoyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, (4-amino-I-hydroxybutylidine)-bisphosphonate, di- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(4-valyloxy)cyclohexanoyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethylJ ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di- ( I -(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) (4-amino-1-hydroxybutylidine)-bisphosphonate, di-((1,3-di-(valyloxy)propyl-2-to oxycarbonyloxy methyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(2-(L-valyloxymethyl)-2-ethyl 15 butyroyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, di (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, di (3-(L-valyloxy)-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 2o 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di(2-methyl-2-(L-valyloxyrnethyl) propionyloxymethyl) ester, 1-hydroxy-2-{IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di (2-(L-valyloxy)-25 methyl-(S)-(+)-butyryloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, I-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, 30 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di (2-L-valyloxy)-DL-propionyloxymethyl) ester, 1-hydroxy-2-( 1 H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-I-yl)ethylidene-bis phosphonate, di-((2-(L-valyloxy}-ethoxycarbonyloxy) methyl) ester, 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, bis [4-(L-valyloxy)-butanoyloxymethyl] ester, I-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(4-(L-valyloxy) benzoyloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di- (2-methyl-1-(L-1o valyloxy)-2-propoxycarbonyloxymethyl) ester, I-hydroxy-2-(1H-imidazolyl-I-yl)ethylidene-bis phosphonate, di-(4-valyloxy)cyclohexanoyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl]ester 15 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di- (1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester I-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(2-hydroxymethyl-20 2-methylpropionyloxymethyl) ester 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(3-(L-valyloxy)-methyl-propionyloxymethyl) ester 25 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(3-(L-valyloxy}-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate di(2-methyl-2-(L-valyloxyrnethyl) propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di(2-methyl-2-(L-valyloxy) 3o propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di (2-L-valyloxy)-DL-propionyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-((2-(L-valyloxy)-10 ethoxycarbonyIoxy) methyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, bis [4-(L-valyloxy)-butanoyloxymethyl] ester, I-hydroxy-2-(pyrid-3-yI)ethylidene bis-phosphonate, di-(4-(L-valyloxy) benzoyloxymethyl) ester, 15 I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(4-20 valyloxy)cyclohexanoyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di- (I-(2-L-valyloxyethyl)-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester 25 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester I-hydroxy-2-(pyrid-3-y1)ethylidene bis-phosphonate, di-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(3-(L-valyloxy)-2-methyl, 2-hydroxymethylpropionyloxymethyl) ester and pharmaceutically acceptable salts thereof.
A further group of representative compounds include:
(4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-methyl-2-(L-valyloxymethyl) propionyloxyrnethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, (4-amino-i-hydroxybutylidine)-bisphosphonate, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono [4-( L-valyloxy)-butanoyloxymethyl] ester, (4-amino-l-hydroxybutylidine)-bisphosphonate, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono- (2-methyl-1-(~.-valyloxy)-propoxycarbonyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-{4-valyloxy)cyclohexanoyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester WO 99/S1b13 PCT/SE99/00528 (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(3-(L-valyloxy}-2-methyl-l0 propionyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-(3-(L-valyloxy}-2-methyl,2-hydroxymethylpropionyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono(2-methyl-2-(L-15 valyloxymethyl) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 2o 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, I-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono ((1,3-di-valyloxy}propyl-2-oxycarbonyloxy methyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono (2-L-valyloxy)-2s DL-propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(S-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-I-yl)ethylidene-bis phosphonate, mono- ((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, 30 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono [4-(L-valyloxy)-butanoyloxymethyl] ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono- (2-methyl-1-(L-valyloxy)-2-propoxycarbonylmethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(4-N-valyloxy)cyclohexanoyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester ~5 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(3-(L-20 valyloxy)-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate mono(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 25 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono((1,3-di-valyloxy)propyl-3o 2-oxycarbonyloxy methyl) ester, 1-hydroxy-2-(pyrid-3-yI)ethylidene bis-phosphonate, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono [4-( L-valyloxy)-butanoyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(3-(3,4-di-(L-valyloxy) 1o phenyl) propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(4 -valyloxy)cyclohexanoyloxymethyl) ester 15 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-((1,3-di-20 (valyloxy)propyl-2-oxycarbonyloxy methyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 25 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(3-(L-valyloxy)-2-methyl, 2-hydroxymethyl-propionyloxymethyl) ester and pharmaceutically acceptable salts thereof.
A favoured group of compounds within formula A-1 include:
alendronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 5 alendronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 10 risedronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ~s zoledronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, 2o zoledronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, pamidronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, pamidronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-valyloxy} propionyloxymethyl) ester, 25 pamidronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, pamidronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, cimadronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 3o cimadronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, cimadronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, cimadronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(D-valyloxy) propionyloxyrnethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(L-1o valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 15 [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(D-20 valyloxy) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, etidronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 25 etidronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, etidronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, etidronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, 30 olpadronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, olpadronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, olpadronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(D-valyloxy) propionyIoxymethyl) ester, olpadronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 1o ibandronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine)-bis-phosphonate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 2o [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, tiludronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-{D-valyloxymethyl) propionyloxymethyl) ester, tiludronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 3o tiludronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, tiludronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof.
A particularly favoured group of compounds of the invention comprises:
alendronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-{L-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, to [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-valyloxyrnethyl) propionyloxymethyl) ester, 15 tiludronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof, especially the alendronate, zoledronate and risedronate derivatives.
A further useful group of compounds within formula A-1 include:
alendronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-leucyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, parnidronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, ~o cimadronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxyrnethyl) ester, cimadronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, ~ 5 clodronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyioxymethyl) ester, clodronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, 20 [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrroiidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-t-2s leucyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-{2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, 3o etidronate di-(2-methyl-2-(L-isoleucyloxyrnethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, s olpadronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, I o ibandronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, 15 [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-20 (L-alanyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof, especially the alendronate, zoledronate and risedronate derivatives.
A further group of representative compounds comprises alendronate mono-L-valyloxymethyl ester, alendronate di-L-valyloxymethyl ester, alendronate mono-L-leucyloxymethyl ester, 3o alendronate di-L-leucyloxymethyl ester, alendronate mono-L-isoleucyloxymethyl ester, alendronate di-L-isoleucyloxymethyl ester, alendronate mono-L-t-leucyloxymethyl ester, alendronate di-L-t-leucyloxymethyl ester, alendronate mono-L-alanyloxymethyl ester, alendronate di-L-alanyloxymethyl ester, risedronate mono-L-valyloxyrnethyl ester, risedronate di-L-valyloxymethyl ester, risedronate mono-L-leucyloxymethyl ester, risedronate di-L-leucyloxymethyl ester, risedronate mono-L-isoleucyloxymethyl ester, 1 o risedronate di-L-isoleucyloxymethyl ester, risedronate mono-L-t-leucyloxymethyl ester, risedronate di-L-t-leucyloxymethyl ester, risedronate mono-L-alanyloxymethyl ester, risedronate di-L-alanyloxymethyl ester, zoledronate mono-L-valyloxymethyl ester, zoledronate di-L-valyloxymethyl ester, zoledronate mono-L-leucyloxymethyl ester, zoledronate di-L-leucyloxymethyl ester, zoledronate mono-L-isoleucyloxymethyl ester, 2o zoledronate di-L-isoleucyloxymethyl ester, zoledronate mono-L-t-leucyloxymethyl ester, zoledronate di-L-t-leucyloxymethyi ester, zoledronate mono-L-alanyloxymethyl ester, zoledronate di-L-alanyloxymethyl ester, and pharmaceutically acceptable salts thereof.
This aspect of the invention further provides a method for the treatment or prophylaxis of bone and calcium disorders comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in 3o need thereof. Bone and calcium disorders include osteoporosis, Paget's disease, hypercalcaemia of malignancy, tooth loss, bone loss in immunotherapy and rheumatoid arthritis, decreasing fracture, post orthopedic prosthesis and inhibiting ossification. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the preparation of a medicament for the prophylaxis or treatment of bone and calcium disorders.
A still further preferred group of prodrugs of the invention are those based on fosinoprilate having the formula PF3:
O
\ O H OH
~~~N
j~P
O O
R4R ~ R4R' O - ()qi ~)qr-T -~- O
O
R4L' or / H H
N
P
O O
R3R ~ R3R' R2 -O_ ()qi-ring- OGr-T-~-O
O
where RZ is the acyl residue of an aliphatic amino acid, 1o R4Land R4L' are independently H, C,_, alkyl, hydroxymethyl, C3-bcycloalkyl, C,-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR3- or -O-15 R3 is H or C,_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and pharmaceutically acceptable salts thereof.
In formula PF3, R4R and R4R' are preferably H and/or R4L and RqL' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond.
Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1.
Representative compounds within formula PF3 thus include (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinylJacetyl]-L-proline, (2-methyl-2-io (L-valyloxy) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, 15 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinylJacetyl]-L-proline, ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-L-valyloxy)-DL-propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (5-(L-2o valyloxy)-2,2-dimethylvaleryloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, ((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, [4-( L-valyloxy)-butanoyloxymethylJ ester, 25 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (4-(L-valyloxy) benzoyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-methyl-1-30 (L-valyloxy)-2-propoxycarbonyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline,(4-N-valyloxy)cyclohexanoyloxymethyl) ester WO 99/51613 PC'f/SE99/00528 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, [N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline,( 1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester s (4S)-4-cyclohexyl-1-[[(R}(4-phenylbutyl)phosphinyl]acetyl]-L-proline, ((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline(2-hydroxymethyl-2-methylpropionyloxymethyl) ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline(2-(L-1 o valyloxymethyl)-2-ethyl butyroyloxymethyl) ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (3-(L-valyloxy)-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 1 s and pharmaceutically acceptable salts thereof.
A favoured group of compounds within formula PF3 comprises:
(4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-valyloxymethyl) propionyloxymethyl) ester, 20 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[((R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-valyloxy) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[((R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline mono-(2-2s methyl-2-(D-valyloxy) propionyloxymethyl) ester, and especially;
(4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-valyloxyrnethyl) propionyloxymethyl) ester:
and pharmaceutically acceptable salts thereof A further group of convenient compounds comprises (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetylJ-L-proline (2-methyl-(L-isoleucyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-leucyoxymethyl) propionyloxymethyl) ester, 5 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-alanyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-10 (L-glycyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof.
A further group of useful compounds comprises:
(4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-15 valyloxymethyl ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-leucyloxymethyl ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-isoleucyloxymethyl ester, 2o (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-t-leucyloxymethyl ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-alanyloxymethyl ester, and pharmaceutically acceptable salts thereof.
This aspect of the invention further provides a method for the treatment or prophylaxis of hypertension comprising the oral administration of an effective amount of a compound defined above to a mammal (including humans) in need 3o thereof. The invention further provides the use of these compounds in medicine and their use in the preparation of a medicament for the treatment or prophylaxis of hypertension A further phosphonate compound amenable to the prodrugs of the invention are the neutral endopeptidase inhibitors such as CGS-24592 (Novartis), preferably those of the formula PF6:
I
i I
R4L O R4R O ~ Ri2 R2-O- Oqi Oqr -T -~--O p- ~p~H NH~O
R4L' R4R' ~ O O
Rf1 w or I
I~1~"
Rf2 R2-O- ()ql- Ring - ()qr -T ~-O _ ~p~H NH~O
R4R' ~ O O
Rf1 where RF1 is H or a further structure of formula IIa or IIb 1o RfZ is H or a conventional pharmaceutically acceptable ester, Rz is the acyl residue of an aliphatic amino acid, R4Land R4L' are independently H, C,_3 alkyl, hydroxymethyl, C3-bcycloalkyl, C,-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
2o and pharmaceutically acceptable salts thereof.
Currently favoured values in Formula PF6 include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rfl is a further ester it is convenient if it is identical to other linker-RZ moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters.
Compounds of the invention are typically prepared by esterifying the mother 1 o compound in which exposed functions such as the 4-amino group of alendronate or the carboxy group of foscarnet are protected with conventional amine and carboxy etc protecting groups respectively, with a structure of the formula IIa or IIb, the preparation of which are described in the abovementioned PCT/SE99/00194:
R4~ O R4R
*R2 -O- ()ql ()qr-T ---~-O halo R4~ R4R
I I a' or *R2 O- Oql Ring - ()qr-T --~1- O halo ~s Ilb' *RZ is the acyl residue of an aliphatic amino acid, N-protected with a conventional N-protecting group such as CBz, Fmoc or Boc R4Land R4L' are independently H, C,_3 alkyl, hydroxymethyl, C3-bcycloalkyl, C,-3alkyl-C,Cbcycloalkyl phenyl or benzyl, 2o R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR3- or -O-R3 is H or C,_3alkyl;
"ring" is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and halo is bromo, chloro and especially iodo. Alternatively, iodomethyl N-protected aminoacid esters are employed for linker-RZ structures of the formula:
R2~" O ~
Hydroxymethyl bearing linkers such as those within formula IIa are prepared by methoxybenzylation of the free carboxy group of a bis hydroxy compound such as glycerol or bis 2,2 hydroxymethyl propionic acid, CBz monoprotection of one of the hydroxy groups, esterification with the N-protected RZ group, debenzylation, reaction with chloroiodomethyl and iodination as shown below prior to esterificaiton to a phosphorous-containing pharmaceutical.
The mother compounds, that is the phosphorous containing drug, are all well known and readily accessible to those in the art.
In drugs comprising multiple phosphoryl/phosphonate/phosphinate functions, it is generally advantageous that an hydroxy group on each phosphorous moiety is esterified with a linker (-RZ')k-Rz structure such as those of formula IIa or IIb etc.
2o Regioselective protecting groups which bridge the phosphate groups of bis phosphonates and thus assist mono and diacylation include Si compounds such as dichlorotetraisopropyldisosiloxane or cresols.
Methodology for the derivatisation of phosphorous-containing compounds with acyloxyalkyl groups and which can be used analogously for the coupling of the -linker (-Rz')k-RZ structure is described in US patent 5 227 506, WO 94/13682, WO
94/13324, WO 98/04569, Starret et al J Med Chem 37 1857-1864 (1994) and Iyer et al Tetrahedron Lett 30 7141-7144 (1989). A number of approaches are also illustrated in the examples below. The N-protecting group on group RZ is removed by conventional methodology.
The term "N-protecting group" or "N-protected" as used herein refers to those groups intended to protect the N-terminus of an amino acid or peptide or to protect an amino group against undesirable reactions during synthetic procedures. Commonly used N-protecting groups are disclosed in Greene, "Protective Groups in Organic Synthesis"
(John Wiley & Sons, New York, 1981 ), which is hereby incorporated by reference.
N-protecting groups include acyl groups such as formyl, acetyl, propionyl, pivaloyl, t-butylacetyl, 2-chloroacetyl, 2-bromoacetyl, trifluoracetyl, trichloroacetyl, phthalyl, o-nitrophenoxyacetyl, a-chlorobutyryl, benzoyl, 4-chlorobenzoyl, 4-bromobenzoyl, 4-nitrobenzoyl, and the like; sulfonyl groups such as benzenesulfonyl, p-toluenesulfonyl, and the like, carbamate forming groups such as benzyloxycarbonyl, p-chlorobenzyloxycarbonyl, p-methoxybenzyloxycarbonyl, to p-nitrobenzyloxycarbonyl, 2-nitrobenzyloxycarbonyl, p-bromobenzyloxycarbonyl, 3,4-dimethoxybenzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 2-nitro-4,5-dimethoxybenzyloxycarbonyl, 3,4,5-trimethoxybenzyloxycarbonyl, 1-(p-biphenylyl)-1-methylethoxycarbonyl, a,a-dimethyl-3,5-dimethoxybenzyloxycarbonyl, benzhydryloxycarbonyl, t-butoxycarbonyl, 15 diisopropylmethoxycarbonyl, isopropyloxycarbonyl, ethoxycarbonyl, rnethoxycarbonyl, allyloxycarbonyl, 2,2,2-trichloroethoxycarbonyl, phenoxycarbonyl, 4-nitrophenoxycarbonyl, fluorenyl-9-methoxycarbonyl, cyclopentyloxycarbonyl, adamantyloxycarbonyl, cyclohexyloxycarbonyl, phenylthiocarbonyl, and the like; alkyl groups such as benzyl, triphenylmethyl, 2o benzyloxymethyl and the like; and silyl groups such as trimethylsilyl and the like.
Favoured N-protecting groups include formyl, acetyl, allyl, F-moc, benzoyl, pivaloyl, t-butylacetyl, phenylsulfonyl, benzyl, t-butoxycarbonyl (BOC) and benzyloxycarbonyl (Cbz).
25 Hydroxy and/or carboxy protecting groups are also extensively reviewed in Greene ibid and include ethers such as methyl, substituted methyl ethers such as methoxymethyl, methylthiomethyl, benzyloxymethyl, t-butoxymethyl, 2-methoxyethoxymethyl and the like, silyl ethers such as trimethylsilyl (TMS), t-butyldimethylsilyl (TBDMS) tribenzylsilyl, triphenylsilyl, t-butyldiphenylsilyl 3o triisopropyl silyl and the like, substituted ethyl ethers such as 1-ethoxymethyl, 1-methyl-1-methoxyethyl, t-butyl, allyl, benzyl, p-methoxybenzyl, dipehenylmethyl, triphenylmethyl and the like, aralkyl groups such as trityl, and pixyl (9-hydroxy-9-phenylxanthene derivatives, especially the chloride). Ester hydroxy protecting groups include esters such as formate, benzylformate, chloroacetate, methoxyacetate, phenoxyacetate, pivaloate, adamantoate, mesitoate, benzoate and the like.
Carbonate hydroxy protecting groups include methyl vinyl, allyl, cinnamyl, benzyl and the like.
The compounds of the invention can form salts which form an additional aspect of the invention. Appropriate pharmaceutically acceptable salts of the compounds of the invention include salts of organic acids, especially carboxylic acids, including but not limited to acetate, trifluoroacetate, lactate, gluconate, citrate, tartrate, maleate, malate, pantothenate, isethionate, adipate, alginate, aspartate, benzoate, butyrate, 1o digluconate, cyclopentanate, glucoheptanate, glycerophosphate, oxalate, heptanoate, hexanoate, fumarate, nicotinate, palmoate, pectinate, 3-phenylpropionate, picrate, pivalate, proprionate, tartrate, lactobionate, pivolate, camphorate, undecanoate and succinate, organic sulphonic acids such as methanesulphonate, ethanesulphonate, 2-hydroxyethane sulphonate, camphorsulphonate, 2-napthalenesulphonate, 1 s benzenesulphonate, p-chlorobenzenesulphonate and p-toluenesulphonate; and inorganic acids such as hydrochloride, hydrobromide, hydroiodide, sulphate, bisulphate, hemisulphate, thiocyanate, persulphate, phosphoric and sulphonic acids.
The compounds of the invention may in some cases be isolated as the hydrate.
2o While it is possible for the active agent to be administered alone, it is preferable to present it as part of a pharmaceutical formulation. Such a formulation will comprise the above defined active agent together with one or more acceptable carriers/excipients and optionally other therapeutic ingredients. The carriers) must be acceptable in the sense of being compatible with the other ingredients of the 25 formulation and not deleterious to the recipient.
The formulations include those suitable for rectal, nasal, topical (including buccal and sublingual), vaginal or parenteral (including subcutaneous, intramuscular, intravenous and intradermal) administration, but preferably the formulation is an 30 orally administered formulation. The formulations may conveniently be presented in unit dosage form, e.g. tablets and sustained release capsules, and may be prepared by any methods well known in the art of pharmacy.
Such methods include the step of bringing into association the above defined active agent with the carrier. In general, the formulations are prepared by uniformly and intimately bringing into association the active agent with liquid carriers or finely divided solid carriers or both, and then if necessary shaping the product. The invention extends to methods for preparing a pharmaceutical composition comprising bringing a compound of the invention or its pharmaceutically acceptable salt in 1o conjunction or association with a pharmaceutically acceptable carrier or vehicle. If the manufacture of pharmaceutical formulations involves intimate mixing of pharmaceutical excipients and the active ingredient in salt form, then it is often preferred to use excipients which are non-basic in nature, i.e. either acidic or neutral.
Formulations for oral administration in the present invention may be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active agent; as a powder or granules; as a solution or a suspension of the active agent in an aqueous liquid or a non-aqueous liquid; or as an oil-in-water liquid emulsion or a water in oil liquid emulsion and as a bolus etc.
With regard to compositions for oral administration {e.g. tablets and capsules), the term suitable Garner includes vehicles such as common excipients e.g. binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, polyvinylpyrrolidone (Povidone), methylcellulose, ethylcellulose, sodium carboxymethylcellulose, hydroxypropylmethylcellulose, sucrose and starch; fillers and carriers, for example corn starch, gelatin, lactose, sucrose, microcrystalline cellulose, kaolin, mannitol, dicalcium phosphate, sodium chloride and alginic acid; and lubricants such as magnesium stearate, sodium stearate and other metallic stearates, glycerol stearate stearic acid, silicone fluid, talc waxes, oils and colloidal silica.
Flavouring agents such as peppermint, oil of wintergreen, cherry flavouring or the like can also be used.
It may be desirable to add a colouring agent to make the dosage form readily identifiable. Tablets may also be coated by methods well known in the art.
A tablet may be made by compression or moulding, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing in a suitable machine the active agent in a free flowing form such as a powder or granules, optionally mixed with a binder, lubricant, inert diluent, preservative, 1o surface-active or dispersing agent. Moulded tablets may be made by moulding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent. The tablets may be optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active agent.
1s Other formulations suitable for oral administration include lozenges comprising the active agent in a flavoured base, usually sucrose and acacia or tragacanth;
pastilles comprising the active agent in an inert base such as gelatin and glycerin, or sucrose and acacia; and mouthwashes comprising the active agent in a suitable liquid Garner.
2o Detailed Description of the Invention Various aspects of the invention will now be illustrated by way of example only with reference to the following non-limiting synthesis and biological examples:
25 Preparation of intermediates Example P-I-1 N-BOC-L-isoleucine iodometh, l ester ~ O
O- _N
H I
O
a) N-BOC-L-isoleucine chloromethyl ester To a solution of N-BOC-L-isoleucine (23.1 g, 0.1 mol) in dioxane (500 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (65.6 mL, 0.1 mol). After stirring for 15 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (500 mL) and then chloroiodomethane (72.8 mL, 1 mol) was added and the solution was stirred for 6h at room temperature. The solution was to concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate ( 1:1 v/v, 400 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and then filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 1-2% MeOH in CHZCIz), to give 20.8 g ofN-BOC-L-isoleucine chloromethyl ester.
b) N-BOC-L-isoleucine iodomethyl ester.
To a solution ofN-BOC-L-isoleucine chloromethyl ester (19.6 g, 70 mmol) in acetonitrile (300 mL), was added sodium iodide (31.5 g, 210 mmol). The solution 2o was stirred for 4 h at 60 °C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CHzCl2 and washed with aqueous sodium thiosulfate (0.1 M}. The organic phase was dried (NaZS04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 2%
MeOH in CHZCIz), to give 22.6 g of N-BOC-L-isoleucine iodomethyl ester.
'H-NMR (CDC13): 6.04 (d, 1H), 5.82 (d, 1H), 4.97 (d, 1H), 4.25 (dd, 1H), 1.98-1.80 (m, 1H), 1.43 (s, 9H), 1.50-1.05 (m, 2H), 0.97-0.88 (m, 6H).
Example PI-2 2.2-dimethvl-3-lN-Boc-L-valvloxy~propionic acid iodomethyl ester O
O NH
I~0~~~
OO
a) 2,2-dimethyl-3-( N-Boc-L-valyloxy)propionic acid.
N-Boc-L-valine (I0.8g, 50 mmoie), 4-dimethylaminopyridine (610 mg, 5 mmoIe) and DCC (6.18 g, 30 mmole) were dissolved in methylene chloride (100 ml).
After stirring for 2 hour the mixture was filtered. To the filtrate were added 2,2-dimethyl-3-hydroxy-propionic acid (3.54g, 30 mmoIe) and pyridine (10 m1). After 18 hr, the reaction mixture was filtered, and the filtrate was poured into sodium hydrogen carbonate aqueous solution, the organic phase was then washed with citric acid to aqueous solution and water succesively. After evaporation the product was isolated with silica gel column chromatography to yield 4.4g.
b) 2,2-dimethyl-3-(N-Boc-L-valyloxy)propionic acid chloromethyl ester.
2,2-Dimethyl-3-(N-Boc-L-valyloxy)propionic acid (3.9 g, 12.3 mmole) was ~5 dissolved in dioxane (60 m1). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 7.78 ml, 12 mmole). The solution was dried in vacuo, and it was coevaporated with toluene for several times. The residue was dissolved in methylene chloride and then chloroiodomethane (18.9 ml, 260 mmole) was added to the solution. After 18 hr, the reaction solution was evaporated and the 20 product was isolated with silica gel column chromatography to yield 3.7 g.
c) 2,2-dimethyl-3-(N-Boc-L-valyloxy)propionic acid iodomethyl ester.
2,2-Dimethyl-3-( N-Boc-L-valyloxy)propionic acid chloromethyl ester ( 3.6 g, mmole ) was dissolved in acetonitrile (50 ml). Sodium iodide (2.1 g, 14 mmole) was 25 added to the solution. After reaction at 70° C for 2 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered.
The solution was dried and gave 4.348 of the titled product..
'H-NMR (CDCl3): 5.92 (dd, 2H) 5.10 (d, 1H) 4.24 (m, 1H) 4.15 (dd, 2H) 2.01 30 (m, 1 H) 1.44 (s, 9H) 1.25 (d, 6H) 0.91 (m, 6H ) Example P-I-3 3,3- bis fN-CBz-L-valyloxvmeth~)-propionic acid iodometh 1 ester O
N O ~ I
O
I~o O O
o ~
a) 3,3-Bis (N-CBz-L-valyloxymethyl)-propionic acid chloromethyl ester.
3,3- bis (N-CBz-L-valyloxymethyl)-propionic acid (3 g, 5 mmole) prepared according to PCT/SE99/00194) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 3.11 ml, 4.8 to mmole). The solution was dried in vacuo, and it was coevaporated with toluene several times. The residue was dissolved in methylene chloride (15 ml) and then chloroiodomethane (7.3 ml, 100 mmole) was added to the solution. The reaction solution was refluxed for 18 hr and then evaporated and the product was isolated with silica gel column chromatography. 900 mg.
b) 3,3-bis-(N-CBz-L-valyloxymethyl)propionic acid iodomethyl ester .
3,3-Bis (N-CBz-L-valyloxymethyl)-propionic acid chloromethyl ester (900 mg, 1.38 mmole) was dissolved in acetonitrile (S ml). Sodium iodide (289 mg, 1.93 mmole) was added to the solution. After reaction at 70° C for 3 hr, the reaction mixture was 2o filtered and the residue was dissolved in methylene chloride (5 ml) and refiltered.
The solution was dried and gave the titled product. 800 mg.
'H-NMR (CDC13): 7.35 (m, 10 H) 5.88 (dd, 2H) 5.25 (d, 2H) 4.29 (m, 2H) 4.18 (m, 4H) 2.56 (m, 1H) 2.42 (d, 2H) 2.16 (m, 2H) 0.93 (m 12 H) Example P-I-4 2-lN-CBz-L-valyloxylethoxycarbonyloxymethyl iodide WO 99/51613 PG"f/SE99/00528 O
O
p N"O w O~ ~O
O
2-(N-CBz-L-valyloxy)ethoxycarbonyloxymethyl chloride (1.16 g, 3 mmole) was dissolved in acetonitrile (10 ml). Sodium iodide (630 g, 4.2 mmole) was added to the solution. After reaction at 65° C for 2.5 hr, the reaction mixtwe was cooled down to room temperature and filtered and the residue was dissolved in methylene chloride (5 ml) and refiltered. The solution was dried and gave the titled product. 1.2 g.
'H-NMR (CDCl3): 7.35 (m, SH) 5.93 (dd, 2H) 5.26 (d, 1H) 5.11 (s, 2H) 4.39 (m, SH) 1 o 2.18 (m, 1 H) 0.94 (m, 6 H).
Example P-I-S
1,3-bisfN-tert-butoxvcarbonyl-L-valyloxy)-2-propyl iodomethYl carbonate O
N-Boc-Valyl -O
~--O O~I
N-Boc-Valyl -O
15 a) 1-O-(N tent-butoxycarbonyl-L-valyl)glycerol.
N tert-Butoxycarbonyl-L-valine (32.53 g, 0.150 mol), N,N'-dicyclohexyl-carbodiimide (37.85 g, 0.183 mol, and 4-dimethylaminopyridine (1.83 g, 0.015 mol) were added to glycerol (138.12 g., 1.5 mol) in 500 mL dry DMF and the mixture was stirred at rt under NZ for 3 days. The reaction mixture was filtered, concentrated under 2o vacuum, and then partitioned between 300 mL EtOAc and 150 mL HZO. The aqueous phase was reextracted with 150 mL EtOAc. The organic phases were combined and washed successively with 100 mL each of saturated aqueous NaHC03, saturated NH4Cl, and brine. Drying over anhydrous NazS04, and concentration under vacuum gave a viscous light yellow oil as crude product.
Flash 25 column chromatography on silica gel with 4/1 EtOAc - petroleum ether (BP 40-°C) gave 18.27 g (42%) of product (alternative nomenclature: 3-(N-tert-butoxycarbonyl-L-valyloxy)-1,2-propanediol). Reactions done overnight gave similar yields.
b) 1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol.
1-O-(N tert-butoxycarbonyl-L-valyl)glycerol (17.95 g. 61.6 mmol), Boc-L-valine (6.69 g, 30.8 mmol), DMAP (0.38 g, 3.1 mmol}, and DCC (7.10 g, 34.4 mmol) in 240 mL CHZCIZ and 60 mL DMF were stirred at rt under Nz for 18 h. The reaction mixture was filtered, concentrated under vacuum, and redissolved in 200 mL
EtOAc.
The organic solution was washed with 50 mL saturated NH4C1. The aqueous phase was reextracted with SO mL EtOAc. The organic phases were combined, washed successively with 50 mL saturated NaHC03 and 50 mL brine, dried over NazS04, and concentrated under vacuum. Flash column chromatography of the crude material on silica gel (eluent 2/ 1 petroleum ether - EtOAc, and then EtOAc) gave 7.41 g (49%) of the title compound (alternative nomenclature: 1,3-bis(N-tert-butoxycarbonyl-L-valyloxy)-2-propanol).
c) 2-D-chloromethoxycarbonyl-1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol Chloromethyl chloroformate (2.70 mL, 30 mmol) was added to a solution of 1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol (7.27 g, 14.8 mmol) and pyridine (7.2 mL, 89 mmol) in 60 mL dry CHZC12, in an ice bath, under N2. After stirring for 1 h 45 min, the reaction mixture was diluted with 100 mL CHZCIz and washed with 40 mL water. The aqueous phase was reextracted with 20 mL H20. The organic phases were combined, washed with 40 mL saturated NaHC03, followed by 2 x 50 mL
brine, dried over NazS04, and concentrated under vacuum. Flash column chromatography on silica gel with 2/1 hexane- EtOAc gave 8.03 g (93%) of the title compound (alternative nomenclature: 1,3-bis(N-tert-butoxycarbonyl-L-valyloxy)-propyl chloromethyl carbonate).
d) 2-O-iodomethoxycarbonyl-1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol.
3o A solution of 2-O-chloromethoxycarbonyl-1,3-di-O-(N tert-butoxycarbonyl-L-valyl)propane-1,2,3-triol (7.86 g, 13.5 mmol} and NaI (8.09 g, 54.0 mmol) in 135 mL
dry acetonitirile was refluxed at 80 °C for 4 h under N,. The reaction mixture was concentrated under vacuum, and then partitioned between 150 mL diethyl ether and SO mL HZO. The aqueous layer was reextracted with 2 x 25 mL ether. The combined organic phases were washed successively with 25 mL aqueous NazS2O3 and 50 mL
brine, dried over NazS04, and concentrated. Flash column chromatography (silica gel, 2/1 hexane-ethyl acetate gave 8.38 g (92%) title product (alternative name: 2-iodomethoxycarbonyloxy-1,3-bis-(N-tert-butoxycarbonyl-L-valyloxy)propane or 1,3-bis(N-tert-butoxycarbonyl-L-valyloxy)-2-propyl iodomethyl carbonate) as a white solid.
'H NMR (250 MHz, CDCl3) S 0.81 (d, 6H), 0.88 (m, 6H), 1.36 (s, 18H), 2.06 (m, 2H), 4.11-4.46 (m, 6H), 5.0 (br d, 2H), 5.12 (m, 1 H), 5.88 (s, 2H).
Example P-1-6 3-benzvloxvcarbon~propionic acid iodomethyl ester a) Succinic acid monobenzyl ester .
Succinic anhydride (30 g, 300 mmole) was dissolved in methylene chloride (300 ml).
To the solution were added benzyl alcohol (10.2 ml, 100 mmole), 4-dimethylaminopyridine (1.22 g, 10 mmole) and pyridine (48 ml). After 3 hours the reaction mixture was poured in to citric acid aqueous solution. The organic phase was concentrated to small volume and sodium hydrogen carbonate and water were added. Then mixture was stirred for 30 min. The aqueous phase was collected, and to it was added citric acid aqueous solution. The product precipitated out, was collected and dried. 15.3 g.
b) 3-benzyloxycarbonylpropionic acid chloromethyl ester.
Succinic acid monobenzyl ester (4.16 g, 20 mmole) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 11.6 ml, 18 mmole). The solution was dried in vacuo and coevaporated with toluene several times. The residue was dissolved in methylene chloride (60 ml) and then chloroiodomethane (14.5 ml, 200 mmole) was added to the solution. The reaction solution was stirred for 18 hr and then evaporated and the product was isolated with silica gel column chromatography. 3.64 g 'H-NMR (CDC13): 7.35 (m, SH), 5.67 (s, 2H), 5.13 (s, 2H), 2.72 (s, 4H).
c) 3-Benzyloxycarbonylpropionic acid iodomethyl ester.
3-Benzyloxycarbonylpropionic acid chloromethyl ester (2 g, 1.38 mmole) was dissolved in acetonitrile (30 ml). Sodium iodide (1.6 g, 10.9 mmole) was added to the solution. After reaction at 70° C for 3 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered. The solution was dried and gave intermediate 3-benzyloxycarbonylpropionic acid iodomethyl ester in to quantitative yield. This intermediate is bonded to an accessible function of a drug, such as a ring hydroxy or carboxy function using conventional alkylation/acylation conditions as described generally herein. Following deprotection of the terminal carboxy, a di/trifunctional linker bearing R2, such as 1,3-bis- O-(L-valyl)glycerol or iodomethyloxy-L-valyl is acylated/alkylated thereon or RZ amide bonded thereon by 15 conventional techniques as described herein, such as with DCC coupling agent.
Iodomethvl 2-methyl-2-(N-benzvloxycarbonyl-L-va~loxvmeth~l propionate 2o a) 4-Methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate.
2-(Hydroxymethyl)-2-methyl propionic acid was esterified by alkylation with 4-methoxybenzyl chloride by conventional means, namely treatment with aqueous NaOH, followed by evaporation and dissolution in an organic solvent such as DMF
to which the 4-methoxybenzyl chloride is added and the reaction warmed and 25 agitated, such as stirring at 60 C for one hour. The reaction mixture is cooled, concentrated by rotavapor and the resulting concentrated suspension partitioned between water and dichloromethane. The organic phase is evaporated and the residue subjected to silica gel column chromatography, for example with 0, 2, 4% EtOH
in dichloromethane to yield the title compound (7.10 g). Rf (2%MeOH/CHCl3) 0.40.
b) 4-Methoxybenzyl 2-(N- benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate.
SS
4-Methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate (2.50 g, 10.5 mmol), N-benzyloxy carbonyl-L-valine (2.SI g, 10 mmole), 4-dimethylaminopyridine (183 mg) and I-hydroxybenzotriazole (l.3Sg, 10 mmole) were mixed and dissolved in N,N-dimethylformamide (90 ml). Then dicyclohexyl-carbodiimide (2.47 g 12 mmol) was S added. After stirring for 3 days at room temperature the suspension was filtered and the filtrate evaporated in vacuo. The residue was partitioned between O.1M
citric acid and dichloromethane. The organic phase was then extracted with aqueous saturated NaHC03 and evaporated in vacuo. The residue was silica gel column chromatographed (0, l, 2, 3% ethanol in dichloromethane). The appropriate fractions to were pooled and evaporated in vacuo to give the title compound (2.72 g).
R~. (2%MeOH/CHC13) 0.75.
d) 2-(N- benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionic acid.
To a solution of 4-methoxybenzyl 2-(N- benzyloxycarbonyl -L-valyloxymethyl)-2-1S methyl propionate (2.72 g, 5.76 mmole), was added trifluoroacetic acid (11.5 ml) and the emerging dark red solution was stirred for 30 min at room temperature. The solution was evaporated to dryness with dioxane and toluene. The residue was silica gel column chromatographed (2, 3, 4% ethanol in dichloromethane). The appropriate fractions were pooled and evaporated in vacuo to give the title compound (1.86 g). Rf 20 (2%MeOH/CHCl3) 0.30.
'H-NMR (CDCI3): 7.32 (s, SH), 5.32 (d, 1H), 5.10 (s, 2H), 4.32 (d,d, IH), 4.21 (d,d, 2H), 2.13 (m, 1H), 1.26 (s, 3H), 1.25 (s, 3H), 0.95 (d, 3H), 0.86 (d, 3H).
25 c) Chloromethyl2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate.
2-(N- benzyloxycarbonyl -L-valyloxymethyl)-2-methyl propionic acid was esterified by conventional techniques, namely dissolution in an organic solvent such as dioxane and dropwise addition of aqueous tetrabutylammonium hydroxide, followed by 3o evaporation. The residue is dissolved in dichloromethane and then chloroiodomethane and the mixture stirrred for 6 hours at room temperature, followed by partition, shaking the filtrate with aqueous sodium thiosulphate.
O.1M, filtration and evaporation. The title compound (1.40 g) was obtained after silica gel column chromatography (0, 1, 2, 3% ethanol in dichloromethane). Rr (2%MeOH/CHC13) 0.80.
c) Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate was converted to iodide by conventional techniques, namely addition to NaI in acetonitrile, stirring and heating, for instance to 75 C for four hours. The resulting suspension is filtered and the filtrate evaporated, dissolved in organic solvent such as to toluene and shaken with aqueous sodium thiosulphate (O.1M) and evaporation to give the title compound (1.25 g) practically pure. Rf (2%MeOH/CHC13) 0.80.
'H-NMR (CDCl3): 7.35 (s, SH); 5.90 (d,d, 2H), 5.24 (d, 1H), 5.10 (s, 2H), 4.31 (d,d, 1H), 4.14 (d,d, 2H), 2.16 (m, 1H), 1.22 (s, 6H), 0.96 (d, 3H), 0.87 (d, 3H).
Example A-I-2 Iodomethvl 2-(N-benzvloxycarbonyl-L-valyloxyl-DL propionate O O~I
CBzNH
a) Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-DL-propionate.
2-(N-benzyloxycarbonyl-L-valyloxy) propionic acid (1 g) was esterified by the method described in Example A-I-I, step d. The title compound (0.76 g) was obtained after silica gel column chromatography (0, 1 % ethanol in dichloromethane).
Rf (2%MeOH/CHC13) 0.75.
b) Iodomethyl2-(N-benzyloxycarbonyl-L-valyloxy)-DL-propionate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (0.95 g) practically pure. Rf (2%MeOH/CHC13) 0.75.
'H-NMR (CDC1,): 7.33 (s, SH), 5.98 (d, 1H), 5.86 (d, 1H), 5.26 (d, 1H), 5.10 (s, 2H), 5.07 (q, 1H), 4.38 (d,d, 1H), 2.30 (m, 1H), 1.49 (d, 3H), 1.03 (d, 3H), 0.95 (d, 3H).
Example A-I-3 Iodomethvl (1,3-di-(N-benzvloxvcarbonyl~L-valyloxy,Lpr~vl carbonate O
N-CBz-Valyl -O ~
O- _O~I
N-CBz-Vatyl-O
a) Chloromethyl (1,3-di-(N-benzyloxycarbonyl)-L-valyloxy)-2-propyl carbonate.
1o To a solution of 1,3-di-((N-benzyloxycarbonyl)-L-valyloxy)propan-2-of (1.34 g, 2.4 mmole) in dichloromethane (10 ml) was added dry pyridine (1.15 ml, 14.4 mmol) and chloromethyl chloroformate (0.43 ml, 4.8 mmole) at 0°C. The reaction was then stirred for 30 min and then poured into aqueous 50% saturated sodium chloride /
O.1M citric acid solution and extracted with dichloromethane. The organic phase was evaporated and the residue silica gel column chromatographed (0, 1, 1.5%
ethanol in dichloromethane). The appropriate fractions were pooled and evaporated in vacuo to give the title compound (1.26g). Rf (2%MeOH/ CHC13) 0.85.
2o b) Preparation of iodomethyl (1,3-di-(N-benzyloxycarbonyl)-L-valyloxy)-2-propyl carbonate.
Chloromethyl (1,3-di-(N-benzyloxycarbonyl)valyloxy)-2-propyl carbonate was converted to iodide by the method described in Example A-I-l, step e) to give the title compound (1.37 g) practically pure. Rr (2%MeOH/CHC13) 0.85.
'H-NMR (CDC13): 7.34 (s, lOH), 5.93 (d, 1H), 5.89 (d, 1H), 5.21 (m, 3H), 5.11 (s, 4H), 4.50-4.17 (m, 6H), 2.12 (m, 2H), 0.97 (d, 6H), 0.88 (d, 6H).
Example A-I-4 3o Iodomethvl2-lN-benzyloxycarbonyl-L-valyloxy~isobutyrate O
CBzNH O O~I
O
a) 4-Methoxybenzyl 2-hydroxyisobutyrate.
2-hydroxy isobutyric acid (1.56 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a). The title s compound (2.65 g) was obtained after silica gel column chromatography (0, 1, 2%
ethanol in dichloromethane). Rf (2%MeOH/CHCI3) 0.45.
b) 4-Methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate.
4-methoxybenzyl 2-hydroxyisobutyrate was acylated with N-benzyloxycarbonyl-L-to valine by the method described in Example A-I-1, step b). The title compound (3.21 g) was obtained after silica gel column chromatography (0; 1, 1.5% ethanol in dichloromethane). R~ (2%MeOH/CHCl3) 0.70.
c) 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyric acid.
1 s 4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate was de-esterified by the method described in Example A-I-1 step c. The title compound (2.01 g) was obtained after silica gel column chromatography (2, 10, 20% ethanol in dichloromethane). Rf (2%MeOH/CHCI,) 0.30.
20 'H-NMR (CDCI3): 7.32 (s, SH), 5.33 (d, 1H), 5.10 (s, 2H), 4.31 (d,d, 1H), 2.22 (m, 1 H), 1.57 (s, 6H), 0.98 (d, 3H), 0.89 (d, 3H).
d) Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate.
2-(N-benzyloxycarbonyl-L-valyloxy) isobutyric acid was esterified by the method 2s described in Example A-I-1, step d. The title compound (1.90 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCI3) 0.80.
e) Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate was converted to iodide by the method described in Example A-I-l, step a to give the title compound (2.32 g) practically pure. Rf (2%MeOH/CHC13) 0.80.
'H-NMR (CDC13): 7.33 (s, SH), 5.89 (s, 2H), 5.22 (d, 1H), 5.11 (s, 2H), 4.29 (d,d, 1H), 2.21 (m, 1H), 1.55 (s; 3H), 1.53 (s, 3H), 1.00 (d, 3H), 0.93 (d, 3H).
Iodomethvl 2-lN-benzvloxvcarbonyl-L-valvloxv)-3-methyl-(S)l+ -butyrate O
CBzNH O O~I
O
io a) 4-Methoxybenzyl 2-hydroxy-3-methyl-(S)-(+)-butyrate.
2-hydroxy-3-methyl-(S)-(+)-butyric acid (1.77 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a. The title compound (3.10 g) was obtained after silica gel column chromatography (0, 1, 2%
~5 ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.50.
b) 4-Methoxybenzyl2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate.
20 4-Methoxybenzyl 2-hydroxy-3-methyl-(S)-(+)-butyrate was acylated with N-benzyloxycarbonyl-L-valine by the method described in Example A-I-1, step b.
The title compound (5.74 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCI,) 0.70.
25 c) 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyric acid.
4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate was de-esterified by the method described in Example A-I-1, step c. The title compound (3.41 g) was obtained after silica gel column chromatography (2, 10, 20%
ethanol in dichloromethane). Rr (2%MeOH/CHC13) 0.45.
WO 99/51613 PCTlSE99/00528 'H-NMR (CDC13): 7.36 (s, SH), 5.38 (d, 1H), S.I 1 (s, 4H), 4.90 (d, 1H), 4.4I
(d,d, 1H), 2.28 (m, 2H), 1.04-0.89 (m, 12H).
d) Chloromethyl2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate.
2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyric acid was esterified by the method described in Example A-I-1, step d. The title compound (2.96 g) was obtained after silica gel column chromatography (0, 1, 2% ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.85.
e) Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (3.64 g) practically pure. Rf (2%MeOH/CHC13) 0.85.
'H-NMR (CDC13): 7.36 (s, SH), 6.00 (d, 1H), 5.83 (d, 1H), 5.28 (d, 1H), 5.11 (s, 4H), 4.83 (d, 1H), 4.41 (d,d, 1H), 2.29 (m, 2H), 1.05-0.90 (m, 12H).
2o EXAMPLE A-I-6 Iodomethvl 2-(N-benzyloxycarbonvl-L-va~Ioxy)-2=phenyl-DL-acetate O
cBZNH ° o~~
I
a) 4-Methoxybenzyl 2-hydroxy-2-phenyl-DL-acetate.
DL-mandelic acid (2.28 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a. The title compound (3.69 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.55.
b) 4-Methoxybenzyl2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate.
4-Methoxybenzyl 2-hydroxy-2-phenyl-DL-acetate was acylated with N-benzyloxycarbonyl-L-valine by the method described in Example A-I-l, step b.
The title compound (6.50 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCI,) 0.75.
c) 2-{N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetic acid.
4-Methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate was to de-esterified by the method described in Example A-I-1, step c. The title compound {4.75 g) was obtained after silica gel column chromatography (2, 10, 20%
ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.40.
'H-NMR (CDC13): 7.36 (m, lOH), 5.91 (d, 1H), 5.27 (m, 1H), 5.04 (s, 2H), 4.57-4.40 (2xd,d, 1H), 2.30 (m, 1H), 1.01-0.82 (m, 6H).
d) Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate.
2-{N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetic acid was esterified by the method described in Example A-I-1, step d. The title compound (1.69 g) was obtained after silica gel column chromatography (0, 1, 2% ethanol in dichloromethane). R,. (2%MeOH/CHCl3) 0.80.
e) Iodomethyl2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate.
Chloromethyl 2-{N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (1.89 g) practically pure. R~ (2%MeOH/CHC13) 0.80.
'H-NMR {CDCl3): 7.36 (m, lOH), 5.94-5.82 (m, 3H), 5.28 (m, 1H), 5.10 (s, 2H), 4.46 (m, 1 H), 2.21 (m, 1 H), 1.08-0.8 S (m, 6H).
Example A-I-7 Iodomethvl 4-fN-benz r~loxycarbonyl-L-valvloxy) benzoate O
CBzNH ~
O ~. I O.~ I
i O
a) 4-Methoxybenzyl 4-hydroxybenzoate.
4-Hydroxybenzoic acid (1.38 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a. The title compound (2.06 g) was obtained after silica gel column chromatography (0, 1, 2, 3% ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.40.
b) 4-Methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
4-Methoxybenzyl 4-hydroxybenzoate was acylated with N-benzyloxycarbonyl-L-valine by the method described in Example A-I-1, step b. The title compound (2.71 g) was obtained after silica gel column chromatography {0, 1 % ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.70.
c) 4-(N-benzyloxycarbonyl-L-valyloxy) benzoic acid.
4-Methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate was de-esterified by the method described in Example A-I-1, step c. The title compound (1.86 g) was obtained after silica gel column chromatography (2, 10, 20% ethanol in dichioromethane). Rf (2%MeOH/CHCl3) 0.20.
'H-NMR (CDC13): 8.15 (d, 2H), 7.34 (m, SH), 7.22 {d, 2H), 5.38 (d, 1H), 5.17 (s, 2H), 4.58 (d,d, 1H), 2.34 (m, 1H), 1.12 (s, 3H), 0.96 (d, 3H).
d) Chloromethyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
4-(N-benzyloxycarbonyl-L-valyloxy) benzoic acid was esterified by the method described in Example A-I-l, step d. The title compound (0.95 g) was obtained after silica gel column chromatography (0, 1 % ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.80. -WO 99/51613 PC'T/SE99/00528 e) Iodomethyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
Chloromethyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (1.16 g) practically pure. R,. (2%MeOH/CHC13) 0.80.
'H-NMR (CDC13): 8.11 (d, 2H), 7.35 (m, SH), 7.21 (d, 2H), 6.15 (s, 2H), 5.32 (d, 1H), 5.14 (s, 2H), 4.55 (d,d, 1H), 2.34 (m, 1H), 1.10 (s, 3H), 1.03 (d, 3H).
Example A-1-8 to Iodomethyl5-(N-CBz-L-valvloxy~-2,2-dimethylvalerate O
I ~ O O. Cbz-Val a) 4-Methoxybenzyl 2,2-dimethyl-4-pentenoate To a solution of 2,2-dimethyl-4-pentenoic acid (11.5 g, 90 mmol) in DMF (250 mL) at room temperature, was added potassium tent-butoxide ( 11.1 g, 99 mmol). The 15 reaction mixture was stirred at 60 °C for lh. 4-Methoxybenzyl chloride (16.9 g, 108 mmol) was added and the reaction mixture was stirred at 60 °C for 4h.
The DMF was evaporated under vacuum, the residue was dissolved in ether (S00 mL) and washed with water (3 x 200 mL). The organic phase was dried with NazS04 and evaporated to give 21.4 g of 4-methoxybenzyl 2,2-dimethyl-4-pentenoate.
b) 4-Methoxybenzyl5-hydroxy-2,2-dimethylvalerate.
A mixture of 4-methoxybenzyl 2,2-dimethyl-4-pentenoate (9.50 g, 38 mmol) and 9-BBN (115 mL, 57 mmol, 0.5 M in THF) was stirred at 60 °C for 60 min, whereupon the reaction mixture was cooled to -5 °C. Hz0 (35 mL) was added, the reaction mixture was stirred for 5 min at -S °C, an aqueous solution of NaOH (35 mL, 3M) was added and the reaction mixture was stirred for a further 10 min at -5 °C. An aqueous solution of H202 (35 mL, 30%) was added dropwise and the temperature of the reaction mixture was allowed to assume room temperature, whereupon the reaction mixture was stirred for 30 min at room temperature. After evaporation, water (200 mL) was added and the resulting mixture was extracted with CHzCl2 (5 x mL). The combined organic layers were dried (NaZS04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1-->8% MeOH in CHzCIZ), to give 6.32 g of 4-methoxybenzyl 5-hydroxy-2,2-dimethylvalerate.
c) 4-Methoxybenzyl5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
To a mixture of DCC (9.41 g, 46 mmol), DMAP (0.586 g, 4.8 mmol) and N-CBz-L-valine (12.1 g, 48 mmol) in CHZCIz (200 mL) at 0 °C, was added dropwise a solution of 4-methoxybenzyl 5-hydroxy-2,2-dimethyl-valerate (6.40 g, 24 mmol) in CHZC12 (50 mL). After 1 h at 0 °C, the temperature of the reaction mixture was allowed to 1o assume room temperature and then the mixture was stirred for Sh at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 1-~4% MeOH in CH~CIZ), to give 8.61 g 4-methoxybenzyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
d) 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid.
To a solution of 4-methoxybenzyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate (8.24 g, 16.5 mmol) in CHZCIz (100 mL) at room temperature, was added trifluoroacetic acid (5 mL). After lh at room temperature, the reaction mixture was concentrated 2o under reduced pressure. The crude product was column chromatographed (silica gel, 3~5% MeOH in CHZC12), to give 6.00 g of 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid.
'H-NMR (CDC13): 10.94 (br s, 1H), 7.35 (s, SH), 5.45 (d, 1H), 5.11 (s, 2H), 4.30 (dd, 1 H), 4.21-4.00 (m, 2H), 2.28-2.07 (m, 1 H), 1.68-1.51 (m, 4H), 1.21 (s, 6H), 0.97 (d, 3H), 0.89 (d, 3H).
e) Chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
To a solution of 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid (5.88 g, 15.5 mmol) 3o in dioxane (100 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (10.1 g). After stirnng for S min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (11.3 mL, 155 mmol) was added and the solution was stirred for 6h at room temperature.
The solution was concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off 5 and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 1-4% MeOH in CHZCIz), to give 3.95 g of chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
l0 f) Iodomethyl5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
To a solution of chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate (3.85 g, 9 mmol) in acetonitrile (SO mL), was added sodium iodide (5.40 g, 36 mmol). The solution was stirred for 4 h at 60 °C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CHZCIz and washed with 15 aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1% MeOH in CHZC12), to give 4.26 g of iodomethyl (N-CBz-L-valyloxy)-2,2-dimethylvalerate 20 'H-NMR (CDC13): 7.34 (s, SH), 5.90 (s, 2H), 5.32 (d, 1H), 5.10 (s, 2H), 4.29 (dd, 1H), 4.18-4.02 (m, 2H), 2.26-2.08 (m, 1H), 1.65-1.50 (m, 4H), 1.17 (s, 6H), 0.97 (d, 3H), 0.89 (d, 3H).
Example A-1-9 25 2-(N-CBz-L-valyloxY)-ethyl iodomethyl carbonate O
I~O~O~O ~N-Cbz)-Val a) 2-(N-CBz-L-valyloxy)-ethanol To a mixture of DCC (11.4 g, 55 mmol), DMAP (0.611 g, 5 mmol) and ethyleneglycol (55.8 mL, 1 mol) in CH2Cl2 (300 mL) at 0 °C, was added dropwise a 3o solution ofN-CBz-L-valine (12.6 g, 50 mmol) in CHZC12 (100 mL). After lh at 0 °C, the temperature of the reaction mixture was allowed to assume room temperature and then the mixture was stirred for Sh at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 5-X10% MeOH in CHZC12), to give 12.0 g 2-(N-CBz-L-valyloxy)-ethanol.
b) 2-(N-CBz-L-valyloxy)-ethyl chloromethyl carbonate.
To a mixture of 2-(N-CBz-L-valyloxy)-ethanol (12.0 g, 40.6 mmol) and pyridine (19.7 mL, 0.24 mmol) in CHzCl2 (300 mL) at 0 °C, was added dropwise chloromethyl chloroformate (I0.5 g, 81.2 mmol). After 30 min at 0 °C, the reaction 1 o mixture was washed with H20 (200 mL). The H20 phase was washed with CI
IZCIz (100 mL) and the solvent of the combined organic phases was removed under reduced pressure. The crude product was column chromatographed (silica gel, 0.5-~ 1 % MeOH in CHZCl2), to give 8.26 g 2-(N-CBz-L-valyloxy)-ethyl chloromethyl carbonate.
1s c) 2-(N-CBz-L-valyloxy)-ethyl iodomethyl carbonate.
To a solution of 2-(N-CBz-L-valyloxy)-ethyl chloromethyl carbonate (3.88 g, 10 mmol) in acetonitrile (50 mL), was added sodium iodide (7.50 g, 50 mmol). The solution was stirred for 4 h at 60 °C. The resulting suspension was filtered and the 20 filtrate was evaporated. The residue was dissolved in CHZCIz and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure, to give 4.51 g 2-(N-CBz-L-valyloxy)-ethyl iodomethyl carbonate.
25 'H-NMR (CDCI,): 7.34 (s, SH), 5.93 (s, 2H), 5.26 (d, 1H), 5.11 (s, 2H), 4.48-4.26 (m, SH) 2.28-2.10 (m, 1H), 0.97 (d, 3H), 0.90 (d, 3H).
Example A-I-10 2,2-dimethyl-3-f N-CBz-D-vary)-propionic acid iodomethyl ester HN- _O
O
O
I~O
a) 2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid.
To a solution of 2,2-dimethyl propionic acid 4-methoxybenzyl ester (4.7 g, 20 mmole) and N-CBz-D-valine (5.5 g, 22 mmole) in dichloromethane (100 ml) were added 4-dimethyaminopyridine (305 mg, 2.5 mmole) and DCC (5.15 g, 25 mmole).
After 18 hr, the solution was washed successively with sodium bicarbonate aqueous solution, citric acid solution and water. The organic phase was dried and the residue was dissolved in dichloromethane (100 ml). To the solution was added trifluoroacetic acid ( 10 ml). After 3 hr, it was evaporated and the product was isolated with silica to gel column chromatography. 4.5 g.
'H-NMR (CDCl3): 7.36 (m, 5 H) 5.11 (s, 2H) 4.30 (m, 1H) 4.18 (dd, 2H) 2.17 (m, 1H), 1.23 (d, 6 H) 0.93 (m, 6H).
b) 2,2-dimethyl-3- ( N-CBz-D-Valyloxy )-propionic acid chloromethyl ester.
(2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid (4.5 g, 12.8 mmole) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 8.3 ml, 12.8 mmole). The solution was dried in vacuo, and it was coevaporated with toluene several times. The residue was dissolved in methylene chloride and then chloroiodomethane (18 ml, 260 mmole) was added to the solution. After 18 hr, the reaction solution was evaporated and the product was isolated with silica gel column chromatography. 3.5 g.
c) 2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid iodomethyl ester.
2,2-Dimethyl-3-(N-CBz-D-valyloxy)-propionic acid chloromethyl ester (2.4 g, 6 mmole) was dissolved in acetonitrile (30 ml). Sodium iodide (1.26 g, 8.4 mmole) was added to the solution. After reaction at 70° C for 2 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered.
3o The solution was dried and gave the titled product. 2.688.
'H-NMR (CDC13): 7.36 (m, 5 H) 5.90 (dd, 2H) 5.26 (d, 1H) 5.11 (s, 2H) 4.31 (m, 1 H) 4.15 (dd, 2H) 2.18 (m, 1 H) 1.22 (d, 6H) 0.92 (m, 6H).
WO 99/51613 PCTlSE99/00528 Example A-1-11 4-IN-CBz-L-valvlox~r) butyric acid iodomethyl ester O
p HN- _O
I/~O O
O I
a) 4-(N-CBz-L-valyloxy) butyric acid t-butyl ester.
N-CBz-L-valine (16.25 g, 65 mmole) was dissolved in DMF (40 ml). To the solution was added potassium t-butoxide (7.24 g, 65 mmole). After 10 min, 4-bromobutyric acid t-butyl ester (12 g, 53 mmole) was added. The reaction mixture was kept at 65°
C for 2.5 hr and then poured into sodium bicarbonate aqueous solution and extracted 1o with dichloromethane. The organic phase was dried and the product was isolated with silica gel column chromatography. 20.1 g.
b) 4-(N-CBz-L-valyloxy)butyric acid chloromethyl ester.
4-( N-CBz-L-valyloxy) butyric acid t-butyl ester (20 g, 50.8 mmole) was treated with t s trifluoroacetic acid (30 ml) at 0° C for 3 h and then evaporated.
The residue was coevaporated with toluene several time. The intermediate acid (2.56 g, 7.6 mmole) was dissolved in dioxane ( 10 ml) and to the solution was added tetrabutylammonium hydroxide (40 %, 4.66 ml, 7.2 mmole). The solution was dried and dissolved in dichloromethane (20 ml) and then chloroiodomethane (10 ml, 144 mmole) was added 2o to the solution. After 18 hr, the reaction solution was evaporated and the product was isolated with silica gel column chromatography. Yield 2.1 g.
c) 4-(N-CBz-L-valyloxy)butyric acid iodomethyl ester.
4-(N-CBz-L-valyloxy) butyric acid chloromethyl ester (1.54 g, 4 mmole) was 2s dissolved in acetonitrile (15 ml). Sodium iodide (840 rng, 5.6 mmole) was added to the solution. After reaction at 55° C for 3 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered. The solution was dried and gave the titled product. Yield 1.9 g.
'H-NMR (CDC13): 7.36 (m, SH) 5.90 (dd, 2 H) 5.25 (d, 1H) 5.11 (s, 2H) 4.29 (dd, 1H
4.18 (t, 2H) 2.43 (t, 2H) 2.20 (m, 1H) 2.00 (m, 2H) 0.93 (dd, 6 H).
Example A-I-12 s Iodomethvl 3-(N-benzvloxvcarbon 1-L-valvloxy -benzoate O
O
CBzNH ~ ~ 'OBI
O
a) 4-Methoxybenzyl 3-hydroxybenzoate.
To a solution of 3-hydroxybenzoic acid (6.9g, SO mmole) in DMF (100 ml) was added potassium-tert.-butoxide (6.17 g, 55 mmole) and the mixture was stirred at 1 o room temperature for one hour. 4-Methoxybenzyl chloride (9.4g, 60 mmole) was added and the mixture was stirred for 16 hours at 60°C. The mixture was evaporated under reduced pressure and ethyl acetate (250 ml) were added. The organic phase was washed five times with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography 15 with toluene/acetone. Yield: 10.5g = 81%
b) 4-Methoxybenzyl 3-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
To a cooled solution of 4-methoxybenzyl 3-hydroxybenzoate (7.7g, 29.8 mmole), dimethylaminopyridine (0.73g, 6 mmole) and N-benzyloxycarbonyl-L-valine (8.3g, 20 33 mmole) in 100 ml dichloromethane was added dicyclohexyl-carbodiimide (7.22g, 35 mmole) and the mixture was stirred for 2 days at room temperature. The mixture was cooled and the urethane was filtered. The solution was evaporated and ethyl acetate (250 ml) was added. The organic phase was washed twice with 5% acetic acid; 5% sodium hydrogencarbonate and water. The organic phase was dried with 25 sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexanelethyl acetate. Yield: 13.9g = 94%
c) 3-(N-benzyloxycarbonyl-L-valyloxy) benzoic acid.
To a solution of 4-methoxybenzyl-3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate (13.7g, 27.8 mmole) in dichloromethane (150 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred for 2 hours at room temperatwe. The solution was evaporated under reduced pressure and the product crystallized from toluene.Yield:
s 10.1 g = 87%.
'H-NMR (DMSO d-6) 1.01 (m, 6H) 2.21 (m, 1H) 4.17 (d, d, 1H) 5.08 (s, 2H) 7.28-7.96 (m, lOH) 1o d) Chloromethyl3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate.
To a solution of 3-(N-benzyloxycarbonyl-valyloxy)benzoic acid (7.42g, 20 mmole) in 1,4-dioxane (100 ml) was added a 40% solution of tetrabutylammonium hydroxide (12.97g, 20 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated 15 two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in dichloromethane (50 ml) and chloroiodomethane (35.3g, 200 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. Ethyl acetate (100 ml) was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced 2o pressure: The product was isolated by silica gel column chromatography.
Yield: 3.8g = 45%.
e) Iodomethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate.
To a solution of chloromethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate (2.Og, 25 4.76 mmole) in dry acetone (30 ml) was added sodium iodide (3.15g, 21 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate/water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure. Yield: 2.3g = 94%.
'H-NMR (CDC13) 1.02 (m, 6H) 2.38 (m, 1H) 4.56 (d, d , 1H) 5.14 (s , 2H) 5.30 (d, 1 H) 6.14 (s, 2H) 7.26-7.50 (m, 7H) 7.80(s, 1 H) 7.96 (d, 1 H) Example A-I-13 Iodomethvl3-lN-benzy_lox carbonyl-L-valyloxy)-,propionate O O
I~O- v _O NHCBz a) 3-buten-1-yl-3-(N-benzyloxycarbonyl)-propionate.
To a solution of 3-buten-1-of (2.16g, 30 mmole), N-benzyloxycarbonyl-1-valine (8.29g, 33 mmole) and 4-dimethylaminopyridine (0.37g, 3 mmole) in dichloromethane (80 ml) was added dicyclohexyl-carbodiimide (7.228, 35 mmole) and the mixture was stirred overnight at room temperature. The mixture was cooled and the urethane was filtered. The solution was evaporated under reduced to pressure and ethyl acetate (200 ml) was added. The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate.
Yield:
8.3g = 90%.
is b) 3-(N-benzyloxycarbonyl-L-valyloxy)-propanoic acid.
To a solution of 3-buten-1-yl -3-( N-benzyloxycarbonyl-L-valyloxy)-propionate (9.2g, 30 mmole) in 150 ml benzene was added tetrabutylarnmonium bromide 2o (1.628, 5 mmole) and 100 ml water. The mixture was cooled to about 5°C and potassium permanganate (14.82g, 90 mmole) was added in portions. The mixture was stirred 2 hours at room temperature, diluted with water and decoiorized by the addition of sodium bisulfate. The mixture was acidified with 2M
hydrogen chloride and extracted 3 times with ethyl acetate. The combined organic phases were 25 washed with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 5.4g = SS%.
'H-NMR (DMSO d-6) 0.90 (m, 6H) 2.5 (m, 2H) 3.88 (d, d, 1H) 4.32 (m, 2H) 5.03 30 (s, 2H) 7.36 (m, SH) 7.68 (d, 1H) c) Chloromethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-propionate.
To a solution of 3-(N-benzyloxycarbonyl-L-valyloxy)propanoic acid (5.2g, 16.08 mmole) in 1,4-dioxane (50 ml) was added a 40% solution of tetrabutylammonium hydroxide (10.43g, 16.08 mmole) and the mixture was stirred 2 hours at room s temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 40 ml dichloromethane and chloroiodomethane (28.4g. 160 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. Ethyl acetate (100 ml) was added and the organic phase to washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography. Yield:
2.2g = 35%
d) Iodomethyl3-( N-benzyloxycarbonyl-L-valyloxy)-propionate.
1s To a solution of chloromethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-propionate (2.OSg, 5.51 mmole) in dry acetone (50 ml) was added sodium iodide (4.12g, 27.5 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl acetate water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium 2o sulfate and evaporated under reduced pressure. Yield: 2.35g = 92%.
'H-NMR (CDC13) 0.94 (m, 6H) 2.17 (m, 1H) 2.68 (t, 2H) 4.40 (m, 3H) 5.12 (s, 2H) 5.91 (s, 2H) 7.26 (m, SH).
25 Example A-I-13A
1.3-bis(N tert-butoxvcarbonvl-L-valylox~r)-2~ropyl 1-iodoethyl carbonate a) 1,3-bis(N tent-butoxycarbonyl-1.-valyloxy)-2-propyl 1-chloroethyl carbonate.
To a solution of 1,3-bis(N tent-butoxycarbonyl-L-valyloxy)-2-propanol (0.545 g, 1.11 mmol) in 5 mL dry CHZCl2 were added pyridine (540 pL, 6.68 mmol), with cooling and stirring in an ice bath, followed by 1-chloroethyl chloroformate (242 pL, 2.22 mmol). After 1 h, the reaction mixture was diluted with 5 mL CHZCIz and washed with water (5 mL) and brine (5 mL). The organic phase was dried over anhydrous NazS04 and concentrated on a rotavapor, coevapoating several times with toluene. Column chromatogaphy (silica, 4/1 petroleum ether - ethyl acetate) gave the 1o chloride (596 mg, 90%) as a white solid.
b) 1,3-bis(N tert-butoxycarbonyl-L-valyloxy)-2-propyl 1-iodoethyl carbonate.
A mixture of the chloride (596 mg, 1.0 mmol) from step (a) and NaI (684 mg, 4.57 ~s mmol) in 10 ml dry MeCN was refluxed at 80 °C for 4 h. The reaction mixture was concentrated under vacuum and then partitioned between 30 mL diethyl ether and mL water. The organic phase was washed with 5% aqueous sodium thiosulfate (2 x mL), and the last aqueous layer was reextracted with ether (5 mL). The organic phases were combined, washed with brine, dried over NazS04, and concentrated.
2o Flash column chromatography (silica, 4/1 petroleum ether - ethyl acetate) gave a fraction (275 mg) containing 80% iodide, as determined from 'H NMR, and small amounts of the starting chloride and alkene from the elimination side reaction.
'H NMR (250 MHz, CDCI3) 8 0.81-0.85 (m, 6H), 0.88-0.92 (m, 6H), 1.37 (s, 18H), 25 2.05 (m, 2H), 2.17 (d, 3H, J= 6.1 Hz), 4.12-4.46 (m, 6H), 5.00 (d,. 2H, J=
8.8 Hz), 5.11 (m, 1H), 6.68 and 6.69 (2 sets of q, 1H, J= 6.1 Hz).
L~,."
Example A-I-14 3-(N benzvloxvcarbonvl-L-valvloxy)-2 2-dimethvlpropyl iod-omethvl carbonate O O
I ~'O~O
HN O
O
(a) 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethyl-1-propanol.
A mixture ofN benzyloxycarbonyl-L-valine (2.50 g, 10.0 mmol), 2,2-dimethyl-1,3-propanediol (5.30 g, 50.9 mmol), dicyclohexylcarbodiimide (2.60 g, 12.6 mmol), and 4-dimethylaminopyridine (125 mg, 1.0 mmol) in 100 mL dry CHZCl2 was stirred for 23 h. The reaction mixture was filtered and washed successively with 50 mL
each of water, saturated aqueous NH4C1, saturated aqueous NaHC03, and water. The organic io phase was dried over anhydrous NazS04 and concentrated. The title compound (2.99 g, 87%) was isolated by flash column chromatography (silica, 2/1 petroleum ether -ethyl acetate) as a white waxy solid.
(b) 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethylpropyl chloromethyl carbonate.
Chloromethyl chloroformate (1.50 mL, 16.6 mmol) was added to a solution of the alcohol (2.74 g, 8.12 mmol) from step (a) and pyridine (4.9 mL, 61 mmol) in 40 mL
dry CHZCIz, in an ice bath. After stirnng for 1 h, the mixture was diluted with CHZC12 and washed successively with water, saturated NaHC03, and brine. The organic 2o phase was dried over anhydrous NazS04 and concentrated, coevaporating several times with toluene on a rotavapor. Flash column chromatography (silica, 2/1 petroleum ether - ethyl acetate) gave 3.31 g (95%) of the title compound.
(c) 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethylpropyl iodomethyl carbonate.
A mixture of the chloride (3.14 g, 7.30 mmol) from step (b) and NaI (4.37 g, 29.2 mmol) in 73 mL dry MeCN was refluxed at 80 °C for 3 h. After removal of solvent under vacuum, the mixture was partitioned between 80 mL ethyl acetate and 40 mL
water. The organic phase was washed with 5% NazSz03, and then brine, dried over 7s anhydrous NazS04, and concentrated. Flash column chromatography (silica, petroleum ether - ethyl acetate) gave 3.68 g (97%) of the title compound.
'H NMR (250 MHz, CDCI,) 8 0.88 and 0.96 (2d, 3H each), 0.98 (s, 6H), 2.18 (m, IH), 3.94 and 4.02 (2s, 2H each), 4.32 (dd, 1H, J= 9.0, 4.7 Hz), 5.11 {s, 2H), 5.26 (d, 1H), 5.92 and 5.93 (ABq, 2H, JAB = S.lHz), 7.35 (s, SH).
Example A-I-15 1-(N benzvloxvcarbonvl-L-valvloxvl-2-methyl-2-nronvl iodomethvl carbonate O O
I/'~O~O O .,,, N~O /
O H
io (a) 1-(N benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propanol N Benzyloxycarbonyl-L-valine (2.02 g, 8.0 mmol), 4-dimethylaminopyridine (100 mg, 0.8 mmol), and ), and dicyclohexylcarbodiimide (2.04 g, 9.9 mmol, in 20 mL
CHZCIZ) were added to 2-methyl-1,2-propanediol (12.2 mmol) in 30 mL dry CHZCI2, 1s with cooling in an ice bath. DMF (S mL) was added. After stirring for 5 h at 10 °C , the reaction mixture was filtered, concentrated, and then redissolved in ethyl acetate.
The organic solution was washed with saturated NaCI, dried over anhydrous Na2S04, and concentrated. Flash column chromatography (silica, 2/1 petroleum ether -ethyl acetate) gave 2.3 g of the title compound.
(b) 1-(N benzyloxycarbonyl-I,-valyloxy)-2-methyl-2-propyl chloromethyl carbonate.
All of the alcohol from above was dissolved in 35 mL dry CHZCl2 and cooled in an ice bath. Pyridine (3.50 mL, 43.4 mmol) was added, followed by chloromethyl chloroformate (1.30 mL, 14.4 mmol). After 1 h, the ice bath was removed and stirring was continued for 2 h at ambient temperature.The mixture was diluted with CH,C12 (50 mL) and washed with water (50 mL), and then brine (2 x 25 mL).Drying over anhydrous NazS04 of the combined organic phases and concentration under vacuum, coevaporating several times with toluene, gave a yellow-brown oil that was 3o subjected to flash column chromatography (silica, 2/1 petroleum ether -ethyl acetate) to yield 2.86 g (86% from N benzyloxycarbonyl-L-valine) of the title compound.
(c) 1-(N benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propyl iodomethyl carbonate.
A mixture of the chloride (2.84 g, 6.84 mmol) from step (b) and NaI (4.15 g, 27.2 mmol) in 68 mL dry acetonitrile was refluxed at 75 °C for 4 h. After evaporation of solvent under vacuum, the residue was partitioned between ethyl acetate (80 mL) and water (40 mL), and the organic layer was washed with 5% NazSz03 (15 mL) and 1o brine (25 mL). Drying the organic phase over anhydrous Na2S04 and concentration gave a yellow oil that was subjected to flash column chromatography (silica, petroleum ether - ethyl acetate) to furnish 3.29 g (95%) of the title compound.
'H NMR (250 MHz, CDCI,) 8 0.90 and 0.94 (2d, 3H each, J= 6.8 Hz), 1.52 (s, 6H), 2.17 (m, 1H), 4.35 (m, 1H), 4.22 and 4.39 (ABq, 2H, J,,B = 11.7 Hz), 5.10 (s, 2H}, 5.30 (d, 1H), 5.86 (s, 2H), 7.34 (s, SH) Example A-I-16 Iodomethvl 3.4-di-(N-CBZ-L-valvloxv)hvdrocinnamate O O
CBz-NH O i O~I
CBz-N H
O
a) 4-Methoxybenzyl-3,4-dihydroxyhydrocinnamate.
3,4-Dihydroxycinnamic acid (6.5 g, 35.7 mmol) was dissolved in DMF (50 ml) and cooled to 0°C on an ice-bath. 4-Potassium tert-butoxide (35.7 mmol), was then added and the mixture was left for approximately 30 min at 0°C, followed by dropwise adition of 4-methoxy-benzylchloride (39 mmol) in DMF (25 ml). The mixture was allowed to reach room temperature and left over-night. The solvent was then evaporated and the crude product was purified by chromatography (ethyl acetate-hexane, 1:1) to give 6 g ofthe title compound (55%).
b) 4-Methoxybenzyl-3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate.
4-Methoxybenzyl-3,4-dihydroxyhydrocinnamate (5 g, 16.5 mmol), N,N
dimethylaminopyridine (2g, 16.5 mmol), N,N'- dicychlohexyl carbodiimide (8.5 g, 41.3 mmol) and Cbz-L-valine (10.4 g, 4I.3 mmol) were dissolved in dichloromethane (50 ml). After 4 h, the the mixture was filtered and evaporated onto silica gel and purified by chromatography (hexane-EtOAc, 5:2 -a 3:2) to give pure title product (10.1 g, 79 %).
c) 3,4-Di-(N-CBZ-L-valyloxy)hydrocinnamic acid.
4-Methoxybenzyl-3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate (10 g, 13 mmol) was dissolved in dichloromethane and 1,1,1 trifluoroacetic acid (30 ml) and left at ambient temperature for 3.5 h. Evaporation under reduced pressure and purification by chromatography (chloroform-methanol, 10:1 ) yielded 6.7 g (80%) pure title product.
'H NMR (CDC13 45 °C): 7. 24-7.0 (m, 13H), 5.65 (br s, 1H), 5.55 (hr s, 1H), 5.1 (m, 4H), 4.46 (m, 2H), 2.95 (t, 2H), 2.66 (t, 2H), 2.35 (m, 2H).
d) Chloromethyl 3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate.
3,4-Di-(N-CBZ-L-valyloxy)hydrocinnamic acid (4.2 g, 6.47 mmol) was dissolved in 2o dioxane (70 ml). Tetrabutylammonium hydroxide was added dropwise until pH=8.
The solvent was then removed under reduced pressure The solid was redissolved in dioxane (30 ml) and toluene (30 ml) and evaporated. The procedure was repeated twice (for removal of water). Dichloromethane (60 ml) and chloro-iodomethane was added in one portion and the mixture was left at ambient temperature for 6 h.
Evaporation of the solvent and purification by chromatography yielded 1.7 g title product (38%).
e) Iodomethyl 3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate.
Chloromethyl 3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate (1.9 g, 2.7 mmol) and 3o sodium iodide (2 g, 13.3 mmol) were dissolved in acetonitrile (50 ml) and heated to 65° C for 60 min. The solvent was removed under reduced pressure and the residue was taken up in dichloromethane and filtrated. Removal of the solvent and purification by chromatography (ethyl acetate-hexane, 2:5) gave pure title product ( 1.9 g, 90 %) 'H NMR (CDC13 45 °C): 7.34-7.02 (m, 13H), 5.89 {s, 2H), 5.64 (br s, 2H), 5.14-5.02 (m, 4H), 4.47 (m, 2H), 2.96 (t, 2H), 2.64 (t, 2H), 2.33 (m, 2H), 1.08-0.99 (m, 12H) Example A-I-17 3-(N-CBZ-L-valyloxYlphenvl iodomethyl carbonate O
O ~ O~O~I
CBz-NH
1o a) 3-(N-CBz-L-valyloxy)phenol.
CBz-L-valine (10 g, 40 mmol), 1,3-dihydroxybenzene (8.7g, 79 mmol) N,N'dicychlohexylcarbodiimide (10.2g, 44 mmol) and 4-dimethylaminopyridine (2.4 g, 20 mmol) were dissolved in DMF (50 ml) and left at ambient temperature overnight. The reaction mixture was filtered, the solvent removed under reduced 15 pressure and the crude product was taken up in dichloromethane and filtered.
Removal of the solvent followed by purification by chromatography (chloroform-methanol, 10:1) yielded pure title product (10.9 g, 79%).
b) (N-CBZ-L-valyloxy)phenyl chloromethyl carbonate.
20 3-(N-CBz-L-valyloxy)phenol (5.4 g, 15 7 mmol) was dissolved in dichloromethane (70 ml) and cooled in an ice-bath. Pyridine (1.2 g, 23.5 mmol was added followed by dropwise addition of 1-chloro-methylchloroformate (2.3 g, 18.8 mmol) in dichloromethane (10 ml). The mixture was left at room temperature for 4 h.
Water (25 ml) was then added and the phases were separated. The organic layer was washed 25 with 0.01 M aqueous hydrochloric acid (25 ml). Purification by chromatography (ethyl acetate-hexane, 1:1 ) gave the title compound (4.5 g, 65 %) c) 3-(N-CBZ-L-valyloxy)phenyl iodomethyl carbonate.
(N-CBZ-L-valyloxy)phenyl chloromethyl carbonate (l.Sg, 3.44 mmol) and sodium iodide (2 g, 13.3 mmol) were stirred at 60°C in acetonitrile (50 ml}
for 4.5 h.The mixture was filered, the solvent removed and the crude product was taken up in ml hexane-ethyl acetate, 1:1, and filtered through a sintered glass funnel, packed with 2 cm silica gel. Removal of the solvent yielded pure title product (1.68 g, 92%) 'H NMR (CDCl3 45 °C): 7.38-7.02 (m, 9H), 6.03 (s, 2H), 5.2 (br s, 1H), 5.14 (s, 2H), 4.48 (m, 1 H), 2.3 0 (m, 1 H), 1.09-1.01 (m, 6H) Example A-I-18 to Iodomethyl2-lN-CBZ-L-valvloxy}phenylacetate O
O O~I
O
CBz-NH
a) 4-Methoxybenzyl 2-hydroxyphenylacetate.
2-hydroxyphenylacetic acid (10 g, 66 mmol) was dissolved in N,N dimethyl-formamide (100 ml) and cooled on ice-bath. Potassium tert-butoxide (8.85 g, 78 15 mmoi) was added. The mixture was left for 30 min and allowed to reach room temperature. 4-Methoxy-benzylchloride (11.7 g, 72 mmol) in N,N dimethyl-formamide (30 ml) was then added dropwise, under nitrogen atmosphere and left over-night. The solvent was evaporated under reduced pressure and the crude mixture was dissolved in ether (100 ml) and washed with water (25 ml), brine and dried over 2o sodium sulphate. Chromatography (hexane-ethyl acetate, 2:1) followed by recrystallization (hexane-ethyl acetate) gave the title compound (7.6 g, 42%).
b) 4-Methoxybenzyl2-(N-CBz-L-valyloxy)phenylacetate.
4-Methoxybenzyl 2-hydroxyphenylacetate 3g, 11 mmol), N,N,-dichyclohexyl-25 carbodiimide (2.7 g, 13.2 mmol), dimethylaminopyridine (0.134 g, 1.1 mmol) and CBz-L-valine (3.3 g, 13.2 mmol) were dissolved in dichloromethane (50 ml).
After the weekend the solid was filtered off, the solvent removed under reduced pressure WO 99/51613 PCf/SE99/00528 and the crude product purified by chromatography (ethyl aceta~,'ne~c~ne; ~ :2) to give the title compound (5.2 g, 93%).
c) 2-(N-CBz-L-valyloxy)phenylacetic acid.
5 4-Methoxybenzyl 2-(N-CBz-L-valyloxy)phenylacetate (4.25 g, 8.4 mmol), was dissolved in dichloromethane (40 ml). Triflouroacetic acid (8 ml) was added with cooling on ice. The mixture was allowed to reach room temperature and stirred for 40 min. The solvent was removed under reduced pressure and the crude product was recrystallized twice (hexan-ethyl acetate + a small amount of dichloromethane) to 1o give the title compound (2.6 g, 80 %).
'H NMR (CDCI, 45 °C): 7.35-7.08 (m, 9H), 5.35 (br s, 1H), 5.13 (s, 2H), 4.48 (m, 1H), 3.57 (s, 2H), 2.33 (m, 1H), 1.08 (d, 3H), 1.02 (d, 3H).
15 d) Chloromethyl2-(N-CBZ-L-valyloxy)phenylacetate.
This compound was prepared in poor yield from 2-(N-CBz-L-valyloxy)phenylacetic acid (5.5 g, 14.3 mmol) by an unoptimized procedure essentially as described in Example A-I-16 d). Yield: 0.265 g 20 'H NMR (CDC13 45 °C): 7.28-7.01 (m, 9H), 5.55 (s, 2H), 5.2 (br s, 1H), 5.07 (s, 2H), 4.43 (m, 1H), 3.53 (s, 2H), 2.26 (m, 1H), 1.02 (d, 3H), 0.95 (d, 3H).
e) Iodomethyl 2-(N-CBZ-L-valyloxy)phenylacetate.
Chloromethyl 2-(N-CBZ-L-valyloxy)phenylacetate is treated with NaI and purified 25 as described in the Examples above to yield the title compound.
Example A-I-19 Iodomethyl 4-lN-CBZ-L-valyloxyxy~phenvlacetate O
O ~ O
CBz-NH
O~I
io a) 4-Methoxybenzyl 4-hydroxyphenylacetate.
Prepared from 4-hydroxyphenylacetic acid (10 g, 65.7 mmol) in 70 % yield by the same procedure as for Example A-I-18 a) above, but wherein the solvent for the recrystallization was changed to hexane-ether.
b) 4-Methoxybenzyl4-(N-CBz-L-valyloxy)phenylacetate.
Prepared from 4-methoxybenzyl 4-hydroxyphenylacetate (3 g, 11 mmol) by the same procedure as for Example A-I-18 b) in 87 % yield. Solvent for chromatography:
ethyl acetate-hexane, 1:2.
c) 4-(N-CBZ-L-valyloxy)phenylacetic acid.
Prepared in 82 % yield from 4-methoxybenzyl 4-(N-CBz-L-valyloxy)phenylacetate (1.6 g, 288 mmol) by the procedure described for Example A-I-18 c). Solvent for recrystallization: hexane-ether and a small amount of dichloromethane.
'H NMR (CDC13 45 °C): 7.36-7.27 (m, 7H), 7.02 (d, 2H), 5.25 (d, 1H), 5.14 (s, 2H), 4.52 (m, 1H), 3.64 (s, 2H), 2.3 (m, 1H), 1.08 (d, 3H), 1.02 (d, 3H).
d) Chloromethyl4-(N-CBZ-L-valyloxy)phenylacetate.
Prepared from 4-(N-CBZ-L-valyloxy)phenylacetic acid (3 g, 7.8 mmol) in 26 2o yield by the same procedure as described for Example A-I-18 d). Solvent for chromatography: hexane-ether, 3:2.
e) Iodomethyl 4-(N-CBZ-L-valyloxy)phenylacetate.
Chloromethyl 4-(N-CBZ-L-valyloxy)phenylacetate (0.83 g, 1.9 mmol) and sodium iodide (1.15 g, 7.6 mmol) were heated in acetonitril (45 ml) for 5 h. The mixture was filtrated, the solvent removed, taken up in dichloromethane and filtrated again.
Evaporation and purification by chromatography (ether-hexane, 2:3) yielded the title product (0.8 g, 80 %).
'H NMR (CDCI, 45 °C): 7.38-7.09 (m, 4H), 5.$4 (s, 1H), 5.30 (br s, 1H), 5.15 (s, 2H), 4.5 (m, 1H), 3.56 (s, 2H), 2.36 (m, 1H), 1.10 (d, 3H), 1.00 (d, 3H).
Example A-I-20 Iodometh~l 4-(2-N-benzylox~rcarbonyl-L-val ,~loxyethyl benzoate a) 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl~toluene.
To a cooled solution of 4-methylphenylethanol-2 (S.Og, 36.7 mmole), 4 dimethylaminopyridine (0.98g, 8 mmole) and N-benzyloxycarbonyl-L-valine ( 10.05g, 40 mmole) in dichloromethane ( 120 ml) was added dicyclohexyl-carbodiimide (9.1 g, 44 mmole) and the mixture was stirred overnight at room temperature. The mixture was cooled and the urethane was filtered. The solution was 1o evaporated under reduced pressure and ethyl acetate (250 ml) was added. The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 13.3g = 97%
b) 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)- benzoic acid.
To a cooled mixture of chromic anhydride (7.558, 75 mmole) in acetic acid (100 ml) was added dropwise a solution of 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)-toluene (9.3g, 25.1 mmole) in acetone (50 ml). The mixture was stirred at room temperature for 3 days and reduced to about 100 ml. 600m1 10% sodium chloride 2o solution was added and the mixture was extracted four times with ethyl acetate. The organic phase was washed with brine and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product was islolated by silica gel column chromatography with dichloromethane/methanol. Yield : 2,1 g = 21 %.
'H-NMR (CDC13) 0.79 (d, 3H) 0.90 (d, 3H) 2.08 (m,lH) 3.04 (t, 2H) 4.28 (d, d,lH) 4.39 (m, 2H) 5.11 (s, 2H) 5.26 (d, 1H) 7.34 (m, 7H) 8.04 (d, 2H) c) Chloromethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)benzoate.
To a solution of 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)benzoic acid (2.Og, 5.0 3o mmole) in 1,4-dioxane (20 ml)was added a 40% solution of tetrabutylammonium hydroxide (3.1 g, 4.75 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and coevaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in dichloromethane (10 ml) and iodochloromethane (I3.2g, 75 mmole) was added The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 50 ml ethyl acetate were added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography.Yield:
O.Sg =23%
d) Iodomethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl) benzoate.
o To a solution of chloromethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl) benzoate (O.Sg, 1.11 mmole). In dry acetone (10 ml) was added sodium iodide (0.75g, 5.0 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate/water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate is and evaporated under reduced pressure.Yield: 0.53g = 88%.
'H-NMR (CDCI,) 0.88 (d, 3H) 0.90 (d, 3H) 2.08 (m, 1H) 3.02 (t, 2H) 4.28 (d, d, 1H) 4.38 (m, 2H) 5.10 (s, 2H) 5.22 (d, 1H) 6.15 (s, 2H) 7.35(m, 7H) 7.98 (d, 2H ) 20 Example A-I-21 Iodometh,~(N-benzvloxycarbonyl-L-isoleucvloxvmethvll 2-meth~,rl,propionate.
a) 4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2s 2-methyl propionate.
To a cooled solution of 4-methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate (6.Og, 25 mmole), 4-dimethylaminopyridine (0.61 g, 5 mmole) and N-benzyloxycarbonyl-L-isoleucine (6.90g, 26 mmole) in dichloromethane (100 ml) was added dicyclohexyl-carbodiimide (6.2g, 30 mmole) and the mixture was stirred 3o overnight at room temperature.The mixture was cooled and the urethane was filtered.
The solution was evaporated and 200 ml ethyl acetate was added, The organic phase was washed twice with S% acetic acid, 5% sodium hydrogencarbonate and water.
The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone.Yield: 11.7g = 96%.
2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2-methyl) propionic acid.
To a solution of 4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl}-2-methyl propionate (ll.Og, 22.6 mmole) in 100 ml dichloromethane was added trifluoroacetic acid (15 ml) and the mixture was stirred overnight at room temperature. The solution was evaporated under reduced pressure and coevaporated two times with toluene. The residue was stirred 1 hour with 100 ml ethanol and the 1o white solid was filtered (byproduct). The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 7.4g = 89%.
'H-NMR (CDCI,) 0.90 (m, 6H) 1.26 (m, 8H) 1.88 (m, 1H) 4.12 (d, d, 2H) 4.38 (d, d, 1H) 5.10 (s, 2H) 5.32 (d, 1H) 7.28 (m, 5H) c) Chloromethyl 2-(N-benzyloxycarbonyl-L-isoleucyloxy)-2-methyl propionate.
To a solution of 2-(N-benzyloxycarbony-L-isoleucyloxymethyl)-2-methyl 2o propionic acid (7.Og, 19 mmole) in 80 ml 1,4-dioxane was added a 40%
solution of tetrabutylammonium hydroxide (12.4g, 19 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 25 ml dichloromethane and iodochloromethane (33.7g, mmole) was added . The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone.Yield: 4.2 = 54%
d) Iodomethyl2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2-methyl propionate.
To a solution of chloromethyl 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2-methyl propionate (3.Og, 7.2 mmole) in 50 ml dry acetone was added sodium iodide (4.8g, 32 mmole) and the mixture was stirred overnight at room temperature.
The mixture was evaporated under reduced pressure and extracted with ethyl actate 5 water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure. Yield: 3.3g = 90%.
'H-NMR (CDC13) 0.93 (m, 6H) 1.23 (m, 8H) 4.12 (m, 2H) 4.38 {d, d, 1H) 5.10 (s, 2H) 5.26 (d, 1H) 5.92 (m, 2H) 5.35 (m, SH) Example A-I-22 Iodometh 1~4- N-benzylox cy arbonyl-L-va~loxy)cvclohexanoate.
a) 4-Methoxybenzyl 4-hydroxycyclohexanoate.
To a solution of ethyl 4-hydroxycyclohexanoate (8.61g, 50 mmole) in 50 ml ethanol was added a solution of potassium hydroxide 85% (3.63g, 55 mmole) and the mixture was stirred for 6 hours at 70°C. The mixture was evaporated under reduced pressure, coevaporated two times with N,N-dimethylformamide and reduced to about 100 ml. 4-Methoxybenzyl chloride (9.4g, 60 mmole) was added and the mixture was 2o stirred for 18 hours at 60°C. The mixture was evaporated under reduced pressure and 250 ml ethyl acetate was added. The organic phase was washed five times with water, dried with sodiun sulfate and evaporated under reduced pressure. Yield:
13.2g =100% (crude) b) 4-methoxybenzyl4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate.
To a cooled solution of 4-methoxybenzyl 4-hydroxycyclohexanoate (7.Sg, 28 mmole), 4-dimethylaminopyridine (0.73g, 6 mmole) and N-benzyloxycarbonyl-L-valine (7.54g, 30 mmole) in dichloromethane (90 ml) was added dicylohexyl-3o carbodiimide (6.8g, 33 mmole) and the mixture was stirred for 2 days at room temperature. The mixture was cooled and the urethane was filtered. The solution was evaporated and 250 ml ethyl acetate was added.The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone.Yield :
13g = 93%
c) 4-(N-benzyloxycarbonyl-L-valyloxy) cyclohexanoic acid.
To a solution of 4-methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate (12g, 24.1 mmole} in dichloromethane (100 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred for 3 hours at room temperature. The solution was evaporated under reduced pressure and coevaporated 1o two times with toluene. The residue was stirred 1 hour with about 100 ml ethanol and the white solid was filtered (byproduct). The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography with toluene/acetone. Yield: 6.8g = 74%.
'H-NMR (CDC13) 0.91 (m, 6H) 1.52-2.54 (m, lOH) 4.28 (m, 1H) 4.82-5.08 (m, 1H) 5.11 (s, 2H) 5.28 (d, 1 H) 7.36 (m, SH) d) Chloromethyl4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate.
To a solution of 4-(N-benzyloxycarbonyl-L-valyloxy) cyclohexanoic acid (6.6g, 2o mmole) in 1,4-dioxane (70 ml) was added a 40% solution of tetrabutylammonium hydroxide {11.34g, I7.5 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 60 ml dichloromethane and iodochloromethane (30.98, 175 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 4.1g = 55%.
e) Iodomethyl 4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate.
To a solution of chloromethyl 4-{N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate (4.Og, 9.4 mmole) in dry acetone (50 ml) was added sodium iodide (6.3g, 42 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure.Yield 4.Sg = 93%.
'H-NMR (CDC13) 0.90 (m, 6H) 1.52-2.02 (m, 8H) 2.18 (m, 1H) 2.43 {m, 1H) 4.30 (m, 1H) 4.76-5.08 (m, 1H) 5.11 (s, 2H) 5.26 (d, 1H) 5.91 (d, 2H) 7.34 (m, SH) to Example A-I-23 Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxymeth~)-2-ethyl but~rrate O
O~I
N-CBz-Valy1-'O
a) 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethylbutan-1-ol.
To a cooled solution of 2-ethyl-2-hydroxymethyl-butan-1-of (33.1 g, 250 mmole), 4 dimethylaminopyridine ( 1.22g, 10 mmole) and N-benzyloxycarbonyl-L-valine (12.6g, 50 mmole) in 350 ml dichloromethane was added dropwise a solution of dicyclohexyl-carbodiimide ( 12.4g, 60 mmole) in 50 ml dichloromethane. The mixture was stirred 2 days at room temperature and cooled. The urethane was filtered 2o and the solution evaporated under reduced pressure. 350 ml ethyl acetate was added and the organic phase was washed twice with 5% acetic acid, 5%
sodium-hydrogencarbonate and water. The organic phase was dried with sodium sulfat and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 16.4g = 90%.
c) 2-(N-benzyloxycarbonyl-L-valyloxymethyl )-2-ethyl-butyric acid.
To a cooled mixture of chromic anhydride (B.Sg, 85,2 mmole) in 100 ml acetic acid was added dropwise a solution of 2-(N-benzyloxycarbonyl-L-valyoxymethyl)-2-ethyl-butan-1-of (10.4g, 28.4 mmole) in 50 ml acetone and the mixture was stirred 24 3o hours at room temperature. The mixture was added to 1000 ml 10% sodium chloride solution and extracted four times with ethyl acetate. The organic phase was washed twice with brine, dried with sodium sulfate and evaporated under reduced pressure.
The product was isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 7g = 65%.
'H-NMR (CDCI,) 0.88 (m, 12H) 1.67 (m, 4H) 2.14 (m, 1H) 4.26 (m, 3H) 5.10 (s, 2H) 5.30 (d, 2H) 7.34 (m, SH) d) Chloromethyl 2-(N-benzyoxycarbonyl-L-valyloxymethyl -2-ethyl 1o butyrate.
To a solution of 2-(N-benzyloxycarbony-L-valyloxymethyl~2-ethyl-butyric acid (7.2g,18,9 mmole) in 1,4-dioxane (80 ml) was added a 40% solution of tetrabutylammonium hydroxide (12.26g, 18.9 mmole) and the mixture was stirred hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated once with 1,4-dioxane and two times with toluene. The dried product was dissolved in 30 ml dichloromethane and iodochloromethane (49.48, 280 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate were added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced 2o pressure. The product was isolated by silica gel column chromatography.
Yield: 5.2g = 63%.
e) Iodomethyl 2-( N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyrate.
To a solution of chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyrate (S.Og, 11.7 mmole) in dry acetone (60 ml) was added sodium iodide (7.Sg, 50 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water.
The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium 3o sulfate and evaporated under reduced pressure. Yield: 5.4g = 90%.
'H-NMR (CDC13) 0.92 (m, 12H) 1.65 (m, 4H) 2.18 (m, 1H) 4.28 (m, 3H) 5.10 (s, 2H) 5.22 (d, 1 H) 5.92 (s, 2H) 7.36 (m, SH) Example A-I-24 2JN-(,iodomethoxycarbonyl -~aminol-2-meth 1-y 1-(N-benzyloxvcarbon val~yLpropane O
o NJL.o~i CBzN H o H
a) 2-(N-tert.-butyloxycarbonylamino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy}-propane.
To a cooled solution of 2-(N-(tert.-butyloxycarbonyl)-amino)-2-methylpropan-1-oI
(J. Am. Chem. Soc 113 (1991) p 8883) (4.73g, 25 mmole), 4-dirnethylamino-to pyridine (0.61g, 5 mmole) and N-benzyloxycarbonyl-L-valine (6.28g, 25 mmole) in dichloromethane (70 ml) was added dicyclohexyl-carbodiimide (6.19g, 30 mmole) and the mixture was stirred 2 days at roommtemperature. The mixture was cooled, the urethane was filtered and the solution evaporated under reduced pressure.
Ethyl acetate (200 ml) was added and the organic phase was washed twice with 5%
acetic 1s acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with,sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate.Yield: 10.28 =
96%.
b) 2-amino-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane.
2o To a solution of 2-(N-(tert.-butyloxycarbonyl)-amino-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane (lOg, 23 mmole) in dichloromethane (150 ml) was added trifluoroacetic acid (30 ml) and the mixture was stirred for 1 hour at room temperature. The solution was evaporated under reduced pressure and 10%
sodium carbonate solution was added. The product was extracted four times with 2s dichloromethane, dried with sodium sulfate and evaporated under reduced pressure.
The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 3.Og = 40% (crude) c) 2-(N-(chloromethoxycarbonyl)-amino)-2-methyl-1- (N-benzyloxycarbonyl-L-valyloxy)-propane.
To a solution of 2-amino-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane (2.9g, 9 mmole) and pyridine (2 ml) in dichloromethane (50 ml) was added 5 chloromethyl chloroformate(I.SSg, 12 mmole) and the mixture was stirred for hours at room temperature. The mixture was evaporated under reduced pressure and ethyl acetate was added. The organic phase was washed with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate.Yield: l.lg = 29%.
d) 2-(N-(iodomethoxycarbonyl)-amino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane.
To a solution of 2-(N-(chloromethoxycarbonyl)-amino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)propane (I.OSg, 2.53 mmole) in dry acetone (20 ml) was added sodium iodide (1.8g, 12 mmole) and the mixture was stirred for 36 hours at room temperature. The mixture was evaporated under reduced pressure and ethyl acetate and water were added. The organic phase was washed with 10%
sodium thiosulfate solution and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure.Yield: 1.04g = 81%.
'H-NMR (CDCI,) 0.92 (m, 6H) 1.35 (s, 6H) 2.10 (m,lH) 3.88 (m, 1H) 4.35 (m, 2H) 5.11 (s, 2H) 5.32 (d, 1H) 5.82 (s, 1H) 5.91 (s, 2H) 7.35 (m, SH) Example A-I-25 1-(2-N-CBz-L-valvlox~~)-6-oxo-1,6-dihydro~vridine-3-carboxylic acid iodometh- Iy ester O
O
O~N~
O-Cbz-Val a) 6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
To a solution of 6-hydroxynicotinic acid (4.87 g, 35 mmol) in DMF (100 mL) at room temperature, was added potassium tert-butoxide (3.93 g, 35 mmol). The reaction mixture was stirred at 60 °C for lh. 4-Methoxybenzylchloride (8.30 g, 53 mmol) was added and the reaction mixture was stirred at 60 °C for 4h.
The DMF was evaporated under vacuum, the residue was dissolved in ether (200 mL) and washed with water (3 x 100 mL). The organic phase was dried with NazS04 and evaporated to give 4.41 g of 6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl 1 o ester.
b) 1-(2-Hydroxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
To a solution of 6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl is ester (4.41 g, 17 moral) and KzC03 (2.58 g, 18.7 mmol) in DMF (100 mL) at room temperature, was added 2-bromoethanol (2.02 g, 16.2 mmol). The reaction mixture was stirred at 80 °C for 30h, whereupon the DMF was evaporated under vacuum.
The crude product was column chromatographed (silica gel, 2-~S% MeOH in CHzCl2), to give 3.91 g of 1-(2-hydroxyethyl)-6-oxo-1,6-dihydro-pyridine-3-2o carboxylic acid 4-methoxybenzyl ester.
c) 1-(2-N-CBz-L-valyloxyethyl )-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
To a mixture of DCC (5.06 g, 24.5 mmol), DMAP (318 mg, 2.6 mmol) and N-CBz-2s L-valine (6.48 g, 25.8 mmol) in CHzCIz (200 mL) at 0 °C, was added dropwise a solution of 1-(2-hydroxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4 methoxybenzyl ester (6.40 g, 24 mmol) in CHZCl2 (200 mL). After lh at 0 °C, the temperature of the reaction mixture was allowed to assume room temperature and then the mixture was stirred for Sh at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 2-~5% MeOH in CHZC12), to give 6.81 g 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
d) 1-(2-N-CBz-L-valyloxyethyl)-2-pyridone-5-carboxylic acid.
To a solution of 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-to carboxylic acid 4-methoxybenzyl ester (6.46 g, 12 mmol) in CHzCl2 (85 mL) at room temperature, was added trifluoroacetic acid (15 mL). After lh at room temperature, the reaction mixture was concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 3-~6% MeOH in CHZCIz), to give 4.91 g (2-N-CBz-L-valyloxyethyl)-2-pyridone-5-carboxylic acid.
i5 'H-NMR (CDC13): 12.15 (br s, 1H), 8.29 (d, J= 2.2 Hz, 1H), 7.93 (dd, J= 9.5, 2.2 Hz, 1 H), 7.31 (m, SH), 6.69 (d, J = 9.5 Hz, 1 H), 5.53 (d, 1 H), 5.07 (s, 2H), 4.52-4.05 (m, SH), 2.20-2.00 (m, 1H), 0.90 (d, 3H), 0.81 (d, 3H).
2o e) 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid chloromethyl ester.
To a solution of 1-(2-N-CBz-L-valyloxyethyl)-2-pyridone-S-carboxylic acid (4.91 g, 11.8 mmol) in dioxane (200 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (7.65 g). After stirring for 5 min, the solution was 25 evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (200 mL) and then chloroiodomethane (8.74 mL, 120 mmol) was added and the solution was stirred for 12h at room temperature:
The solution was concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off 30 and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 2-4% MeOH in CH,CIz), to give 1.80 g of 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid chloromethyl ester.
f) 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid iodomethyl ester To a solution of 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid chloromethyl ester (1.80 g, 3.87 mrnol) in acetonitrile (30 mL), was added sodium iodide (2.32 g, 15.5 mmol). The solution was stirred for 4 h at 60 °C.
The resulting suspension was filtered and the filtrate was evaporated. The residue to was dissolved in CHZC12 and washed with aqueous sodium thiosulfate (0.1 M).
The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1% MeOH in CHZC12), to give 2.04 g 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid iodomethyl ester.
'H-NMR (CDC13): 8.19 (d, J= 2.5 Hz, 1H), 7.79 (dd, J= 9.6, 2.5 Hz, 1H), 7.32 (m, SH), 6.52 (d, J = 9.6 Hz, 1 H), 6.04 (s, 2H), 5.3 8 (d, 1 H), 5.07 (s, 2H), 4.54-4.06 (m, SH), 2.20-2.00 (m, 1H), 0.91 (d, 3H), 0.81 (d, 3H).
2o Example A-I-26 Iodomethvl 5-ffN benzylox carbonyl-L-valvloxvlmethyl]-2-furoate O
\ !
O- 'NH O--~
/ O
O O
O
(a) 5-[(N Benzyloxycarbonyl-L-valyloxy)methyl]-2-furaldehyde.
A solution of 5-(hydroxymethyl)-2-furaldehyde (1.00 g, 7.69 mmol) in 5 mL dry CHZC12 was added to a mixture of N benzyloxycarbonyl-L-valine (2.40 g, 9.57 mmol), N,N'-dicyclohexylcarbodiimide (2.00 g, 9.69 mmol), and 4-dimethyl-aminopyridine ( 117 mg, 0.96 mmol) in 45 mL CHzCIz. After stirnng overnight, the reaction slurry was filtered, concentrated under vacuum, and subjected to flash column chromatography (silica, 2/1 petroleum ether - ethyl acetate to give the valine ester (quantitative yield).
(b) 5-[(N Benzyloxycarbonyl-L-valyloxy)methyl]-2-furoic acid A solution of NaClOz (2.8 mmol) in 3 mL water was added dropwise to a stirred solution of 5-[(N benzyloxycarbonyl-L-valyloxy)methylJ-2-furaldehyde (798 mg, 2.22 mmol) from step (a) in 3 mL MeCN, with cooling in an ice bath. After 2.5 h, the ice bath was removed, 2 mL more MeCN was added, and the two-phase liquid reaction mixture was stirred at room temperature for 25 h. The reaction mixture was io diluted with water, made basic with saturated NaHC03, and extracted with ethyl acetate (3 x SO mL). The separated aqueous solution was acidified to pH 2 with 5%
aqueous HCl and extracted with ethyl acetate (3 x 50 mL). This second ethyl acetate solution was washed with brine, dried over anhydrous Na2S04, and evaporated to dryness under vacuum to give the carboxylic acid (287 mg, 34%) which was used in the next step without further purification.
(c) Chloromethyl 5-[(N benzyloxycarbonyl-L-valyloxy)methylj-2-furoate.
Tetrabutylammonium hydroxide (40 wt. % solution in water, 0.55 mL, 0.84 mmol) was added to the carboxylic acid (286 mg, 0.76 mmol) from step (b) in 5 mL
2o dioxane. The yellow solution was concentrated under vacuum, coevaporating several times with dioxane, toluene, and, lastly, CHZC12. The residue was charged with mL dry CHZCIz and chloroiodomethane (0.55 mL, 7.55 mmol) was added. After stirring for 20.5 h, the reaction mixture was concentrated and subjected to flash column chromatography (silica, 2/1 petroleum ether - ethyl acetate) to give the chloromethyl ester (137 mg, 42%).
(d) Iodomethyl 5-[(N benzyloxycarbonyl-L-valyloxy)methyl]-2-furoate.
All of the chloromethyl ester (137 mg, 0.32 mmol) from step (c) was refluxed with NaI (195 mg, 1.3 mmol) in 3.2 mL dry MeCN at 70 °C for 4 h. The solvent was 3o removed under vacuum and the residue was subjected to flash column chromatography (silica, 3/1 petroleum ether - ethyl acetate) to give the iodomethyl ester (152 mg, 92%).
'H NMR (250 MHz, CDC13) 8 0.84 and 0.93 (2d, 3H each, J= 6.8 Hz), 2.16 (rn, 1H), 4.33 (dd, 1H, J= 9.1, 4.7 Hz), 5.09-5.21 (m, 4H), 5.36 (d, 1H, J= 9.1 Hz), 6.08 (s, 2H), 6.52 (d, 1H, J= 3.4 Hz), 7.19 (d, 1H, J= 3.5 Hz), 7.33 (s, SH).
Example A-I-27 Iodomethyl 4-(2-N-benzylox can 1-~ L-valyloxyethoxyl benzoate a) 4-Methoxybenzyl 4-(2-hydroxyethoxy)benzoate.
To a solution of 4-methoxybenzyl 4-hydroxybenzoate (7.Og, 27 mmole) in dry N,N-io dimethylformamide (50 ml) was added potassium carbonate (4.15g, 30 mmole) and 2-bromoethanol.The mixture was stirred 48 hours at 80°C, evaporated under reduced pressure and ethyl acetate and water were added. The organic phase was washed five times with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography 15 with hexane/ethyl acetate.Yield: 6.8g = 83%.
b) 4-methoxybenzyl4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)benzoate.
To a solution of 4-methoxybenzyl 4-(2-hydroxyethoxy) benzoate (6.6g, 21.8 mmole), 4-dimethylaminopyridine (0.61g, 5 mmole) and N-benzyloxycarbonyl-L-2o valine (6.3g, 25 mmole) in dichloromethane (80 ml) was added dicyclohexyl-carbodiimide (5.2g, 25 mmole) and the mixture was stirred overnight at room temperature. The mixture was cooled and the urethane was filtered.The solution was evaporated and ethyl acetate (200 ml) was added. The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic 25 phase was dried with sodium sulfate and evaporated under reduced pressure.
The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 10.6g = 90 %.
c) 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)-benzoic acid.
30 To a solution of 4-methoxybenzyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) benzoate ( 10.2g, 19.04 mmole) in dichloromethane ( 100 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred 3 hours at room temperature.
The solution was evaporated under reduced pressure and co-evaporated two times with toluene. The product was isolated by silica gel column chromatography.
Yield:
6.9g = 87%.
'H-NMR (CDCl3) 0.94 (m, 6H) 2.18 (m, 1H) 4.22- 4.68 (m, SH) 5.10 (s, 2H) 6.94 (d, 2H) 7.35 (m, SH) 8.05 (d, 2H) d) Chloromethyl 4-( 2-N-benzyloxycarbonyl-L-valyloxyethoxy) 1o benzoate.
To a solution of 4-(2- N-benzyloxycarbonyl-L-valyloxyethoxy) benzoic acid (6.7g, 16.1 mmole) in 1,4-dioxane (80 ml} was added a 40% solution of tetrabutylammonium hydroxide (9.74g, 15 mmole) and the mixturewas stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and ~5 coevaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in dichloromethane (30 ml) and iodochloromethane (42.5g, 241 mmole) was added. The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 150 ml ethyl actate were added and the organic phase washed twice with water, dried with sodium sulfate and 2o evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 1.2g = 17%
e) Iodomethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) benzoate.
To a solution of chloromethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) 25 benzoate (l.lg, 2.37 mmole) in dry acetone (40 ml) was added sodium iodide (l.Sg, 10.0 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water.
The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure.Yield: 1.3g = 98%.
'H-NMR (CDC13) 0.88 (d, 3H) 0.95 (d, 3H) 2.18 (m, 1H) 4.22 (m, 2H) 4.32 (d, d, 1H) 4.50 (m, 2H) 5.10 {s, 2H) 5.22 (d, 1H) 6.14 (s, 2H) 6.90 (d, 2H) 7.35(m, 7H) 7.98 (d, 2H) Example A-I-28 Iodomethvl 4-f 3-(Cbz-L-valyloxy)-1-propel]Ibenzoate O
O O
N-O
a) t-Butyl4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate.
t-Butyl 4-(3-hydroxy-1-propyl)benzoate (Taylor et al .l. Org. Chem. 1995, 60, 7947) (3.3 g, 14 mmol), N,N'-dicychlohexyl carbodiimide (3.3 g, 16.8 mmol), CBZ-L-valine (4.2 g, 16.8 mmol) and N,N dimethylaminopyridine (0.85 g, 7 mmol) were to dissolved in a minimum amount of dichloromethane and left at ambient temperature over-night. The slurry was then filtrated and the solvent evaporated.
Purification by chromatography (dichloromethane-ether, 20:1) gave pure title compound (7 g, %).
Z 5 b) Chloromethyl 4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate t-Butyl 4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate (6.5 g, 13.8 mmol) was dissolved in dichloromethane (50 ml). Triflouroacetic acid (10 ml) was added and the mixture was left over-night. The solvent was then removed and the crude residue co-evaporated with toluene and 1,4-dioxan and dried in vacuum over-night. The dried 2o product was dissolved in 1,4-dioxane (100 ml) and tetrabutyl ammoniumhydroxide (40 w/w % in water) was added dropwise until the pH = 7-8. The solvent was co-evaported with toluene four times, and then dissolved in dichloromethane (100 ml) followed by addition of 100 g of molecular sieve (4~) and the mixture was stirred for 30 minutes. Chloroiodomethane (15 ml) was added and the reaction mixture was 25 left for five hours. Filtration and purification by chromatography (hexane-ethyl acetate, 3:1 ) gave pure title product (3.3 g, 52 %).
c) Iodomethyl4-[3-(cbz-L-valyloxy)-1-propyl]benzoate Chloromethyl 4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate (3 g, 6.5 mmol) and sodium iodide (4.9 g, 32 mmol) were dissolved in acetonitril (SO ml) and heated to 65 C for 4 hours. The solvent was removed under reduced pressure and the residue was taken up in dichloromethane and filtrated. Removal of the solvent and purification by chromatography (dichloromethane-ether, 20:1) gave pure title product (2.4 g, 67 %).
'H NMR (CDC13 45 °C): 7.95 (d, 2H), 7.36-7.24 (m, 7H), 6.15 (s, 2H), 5.2 (br s, 1H), i o 5.12 (s, 2H), 4.330-4.20 (m, 1 H), 4.15 (t, 2H), 2.74 (t, 2H), 2.2-2.1 (m, 1 H), 1.99 (m, t 2H), 0.98 (d, 3H), 0.91 (d, 3H) Example A-I-29 Iodomethvl 4-f 3-(Cbz-L-isoleucyloxv)-1-propvl]Ibenzoate 0 o~i i O
O
a) t-Butyl4-[3-(Cbz-L-isoleucyloxy)-1-propyl]benzoate.
Prepared from t-butyl 4-(3-hydroxy-1-propyl)benzoate (3.5 g, 14.8 mmol) by the same procedure as described for Example A-I-28 to give the title compound (7 g, 97%).
b) Chloromethyl4-[3-(Cbz-L-isoleucyloxy)-1-propyl]benzoate.
Prepared from the material of step a) (6.9 g, 14.4 mmol) by the procedure described in Example A-I-28 to give the title compound (3.8 g, 55%) as a colourless oil.
c) Iodomethyl4-[3-(Cbz-L-isoleucyloxy)-1-propyl]benzoate.
Prepared from the product of step b (3.26 g, 6.8 mmol) by the same procedure as for Example A-I-28 to give pure title compound. (3.46 g, 90 %).
'H NMR (CDC13 45 °C): 7.98-7.93 {m, 2H), 7.35-7.23 (m, 7H), 6.15 (s, 2H), 5.25-5.15 (br s, 1H), 5.13 (s, 2H), 4.32 (m, 1H), 4.12 (t, 2H), 2.74 (t, 2H), 1.94 (m, 2H), 1.86 (m, 1H), 1.5-1.4 (m, 1H), 1.25-1.15 (m, 1H), 0.95-0.86 (m, 6H).
Example A-I-30 Iodomethvl 2-( N-benzylox carbonylamino-2-meth~propionvlox~
1 o methyl 1-2-methyl propionate a) 2-benzyloxycarbonylamino-2-methyl propionic acid.
To a solution of sodium carbonate (13.3g, 125 mmole) in water (100 ml) was added 2-amino-2-methylpropionic acid (S.Og, 50 mmole) and the mixture was stirred for 30 minutes. The solution was cooled to about 10°C and a 50% solution of benzyl chloroformiate (20.Sg, 60 mmole) was added dropwise. The mixture was stirred at roomtemperature overnight and acidified with 2M hydrochloric acid. The mixture was extracted two times with ethyl acetate. The organic phase was washed with water, dried with sodium sulfate and evaporated under reduced pressure. The product 2o was isolated by silica gel column chromatography with hexane/ethyl acetate.
Yield:
7.7g = 64%
b) 4-methoxybenzyl2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate.
To a cooled solution of 4-methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate (3.6g, 15 mmol), 4-dimethylaminopyridine (0.37g, 3 mmole) and 2-benzyloxycarbonylamino-2-methylpropionic acid (3.8g, 16 m-mole) in dichloromethane (60 ml) was added dicyclohexyl-carbodiimide (3.7g, 18 mmole) and the mixture was stirred overnight at room temperature.The mixture was cooled and 3o the urethane was filtered. The solution was evaporated and 150 ml ethyl acetate were added, The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene / acetone. Yield: 6,2g =91 c) 2-(benzyloxycarbonylamino-2-methylpropionyloxymethyl )-2-methylpropionic acid.
To a solution of 4-methoxybenzyl 2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2methyl propionate (6,1 g, 13,3 mmole) dichloromethane (50 ml) was added trifluoro acetic acid (10 ml) and the mixture was stirred 3 hours at room temperature. The solution was evaporated under reduced 1o pressure and coevaporated two times with toluene. The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 4.1g =
91%
'H-NMR (CDCI,) 1.22 (s, 6H) 1.52 (s, 6H) 4.13 (m, 2H) 5.07 (s, 2H) 5.44 (s, 1H) i5 7.33 (m, SH) d) Chloromethyl 2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate.
To a solution of 2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-2o methyl propionic acid (4.Og, 11.8 mmole) in 80 ml 1,4-dioxane was added a 40%
solution of tetrabutylammonium hydroxide (7.Sg, 11.5 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene.
The dried product was dissolved in 20 ml dichloromethane and iodochloromethane 25 (31.7g. 180 mmole) was added. The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate were added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 2.Og = 45%.
e) Iodomethyl 2-( N-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate.
To a solution of chloromethyl 2-(N-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate (1.9g, 4.92 mmole) in 50 ml dry acetone was added sodium iodide (3.Og, 20 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water. The organic phase was washed with a 5%
sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure.
Yield: 2,1 g.
to 'H-NMR (CDC13) 1.20 (s, 6H) 1.53 (s, 6H) 4.13 (s, 2H) 5.07 (s, 2H) 5.30 {s, 1H) 5.90 (s, 2H) 7.35 (m, SH) Example A-I-31 Iodomethvl2-methvl-2-(N-benzvlox carbonyl-L-alanyloxvmethyl)pro~ionate The title compound (alternative nomenclature 2,2-dimethyl-3-(CBz-alanyloxy)-propioic acid iodomethyl ester) is prepared in a similar manner as described in Example A-I-10 using N-CBz protected L-alanine in place of N-CBz-D-valine.
20 'H-NMR. (CDCI3): 7.33 (m, 5H), 5.91 (m, 2H), 5.11 (s, 2H), 4.38 (m, 1H), 4.14 (m, 2H), 1.40 (d, 3H), 1.21 (d, 6H).
Example A-I-32 Iodomethyl 3-(N-CBz-L-valvloxy)-2-metl~l-propionate O
N-CBz-L-Val-O O~I
a) 3-(N-CBz-L-valyloxy)-2-methyl-1-propano I .
To a mixture of DCC (16.5 g, 80 mmol), DMAP (0.977 g, 8 mmol) and N-CBz-L-3o valine {20.1 g, 80 mmol) in CHzCIz {400 mL)-at 0 °C, was added dropwise a solution of 2-methyl-1,3-propanediol (72.1 g, 800 mrnol) in CHZCIz (100 mL). After lh at 0 °C, the temperature of the reaction mixture was allowed to assume room temperature and then the mixture was stirred for 16h at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure.
The crude product was column chromatographed (silica gel, 5% MeOH in CHZCIz}, to give 20.3 g 3-(N-CBz-L-valyloxy)-2-methyl-1-propanol.
b) 3-(N-CBz-L-valyloxy)-2-methyl-propionic acid.
To a solution of Cr03 (4.29 g, 42.9 mmol) in HOAc (50 mL) at 20 °C, was added dropwise a solution of 3-(N-CBz-L-valyloxy)-2-methyl-1-propanol (4.61 g, 14.3 1 o mmol) in aceton (25 mL). After stirnng for 24h, water (300 mL) was added and the reaction mixture was extracted with CHZCIz (4x200 mL) . The combined organic layers was concentrated under reduced pressure. The residue was column chromatographed (silica gel, 5-10% MeOH in CHzCIz), to give 3.10 g of 3-(N-CBz-L-valyloxy)-2-methyl-propionic acid.
'H-NMR (CDC13): I I.54 (br s, IH), 7.33 (s, SH), 5.48 (d, 1H), S.11 (s, 2H), 4.40-4.00 (m, 3H), 2.95-2.70 (m, 1H), 2.25-2.05 (m, IH), 1.30-1.12 (m, 3H), 0.95 (d, 3H), 0.87 (d, 3H).
2o c) Chloromethyl3-(N-CBz-L-valyloxy)-2-methyl-propionate.
To a solution of 3-(N-CBz-L-valyloxy)-2-methyl-propionic acid (3.10 g, 9.2 mmol) in dioxane (100 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (5.97 g). After stirring for 5 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (6.70 mL, 92 mmol) was added and the solution was stirred for 6h at room temperature.
The solution was concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and 3o the filtered through anhydrous sodium sulfate and evaporated to dryness.
The residue was column chromatographed (silica gel, 0.5-2% MeOH in CHZC12), to give 1.90 g of chloromethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate.
d) Iodomethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate.
To a solution of chloromethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate (1.84 g, 4.77 mmol) in acetonitrile (50 mL), was added sodium iodide (2.86 g, 19.0 mmol).
The solution was stirred for 3.5 h at 60 °C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CHZC12 and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1% MeOH in CHZCIz), to give 1.78 g of iodomethyl (N-CBz-L-valyloxy)-2-methyl-propionate.
'H-NMR (CDCl3): 7.35 (s, SH), 5.90 (s, 2H), 5.25 (d, 1H), 5.10 (s, 2H), 4.36-4.18 (m, 3H), 2.94-2.73 (m, 1H), 2.26-2.08 {m, 1H), 1.28-1.18 (m, 3H), 0.96 (d, 3H), 0.87 (d, 3H).
IS
Example A-I-33 Iodometh~(N-CBz-L-t-butyl~lvcvloxy,)-2 2-dimeth~rlnropionate O O~~
CBzHN
O O
a) 4-Methoxybenzyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-2o dimethylpropionate.
To a mixture of DCC (4.95 g, 24 mmol), DMAP (293 mg, 2.4 mmol) and N-CBz-L-t-butylglycine (6.37 g, 24 mmol) in CHzCl2 (100 mL) at 0 °C, was added dropwise a solution of 4-methoxybenzyl 2,2-dimethyl-3-hydroxypropionate (2.86 g, I2 mmol) in CHzCl2 (50 mL). After lh at 0 °C, the temperature of the reaction mixture was 25 allowed to assume room temperature and then the mixture was stirred for 48h at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 1-2% MeOH in CHZC12), to give 5.60 g 4-methoxybenzyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
b) 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionic acid To a solution of 4-methoxybenzyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate (5.60 g, 11.5 mmol) in CHzCl2 (90 mL) at room temperature, was added trifluoroacetic acid (10 mL). After lh at room temperature, the reaction mixture was concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 3--~S% MeOH in CHZC12), to give 2.70 g of 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionic acid.
'H-NMR (CDCl3): 11.2 (br s, 1H), 7.34 (s, SH), 5.44 (d, 1H), 5.11 (s, 2H), 4.25-4.03 to (m, 3H), 1.32-1.22 (m, 6H), 0.97 (s, 9H).
c) Chloromethyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
To a solution of 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionic acid (2.70 g, 7.38 mmol) in dioxane (100 mL), was added dropwise a 40% aqueous solution of 15 tetrabutylammonium hydroxide (4.79 g). After stirnng for S min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (5.37 mL, 73.8 mmol) was added and the solution was stirred for 6h at room temperature.
The solution was concentrated under reduced pressure and the residue was shaken with 2o hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 0.5-1% MeOH in CH2C12), to give 2.44 g of chloromethyl 3-(N-CBz-L-t-butylglycyloxy}-2,2-dimethylpropionate.
d) Iodomethyl3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
To a solution of chloromethyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate (2.44 g, 5.90 mmol) in acetonitrile (SO mL), was added sodium iodide (3.54 g, 23.6 mmol). The solution was stirred for 3.S h at 60 °C. The resulting suspension was 3o filtered and the filtrate was evaporated. The residue was dissolved in CHZCIz and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1 % MeOH in CHzCIz), to give 2.61 g of iodomethyl (N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
'H-NMR (CDCI,): 7.32 (s, SH), 5.89-5.82 (m, 2H), 5.40 (d, 1H), 5.07 (s, 2H), 4.17 (d, 1H), 4.11 (s, 2H), 1.22-1.19 (m, 6H), 0.95 (s, 9H).
Example A-I-34 N benzyloxycarbonvl-traps-4-(N be loxycarbonvl-L-valyloxy~ L~roline iodometh, 1 ester.
O ~CBz O
O
to CBzNH O'/I
(a) N benzyloxycarbonyl-traps-4-hydroxy-L-proline p-methoxybenzyl ester.
Cesium carbonate ( 1.23 g, 3.78 mmol) was added to a stirred solution of N
benzyloxycarbonyl-traps-4-hydroxy-L-proline (2.00 g, 7.54 mmol) in 20 mL dry 15 DMF. After 15 min, p-methoxybenzyl chloride ( 1.25 mL, 9.21 mmol) was added and the mixture was stirred for 17 h. The solvent was evaporated under vacuum, and the residue was partitioned between EtOAc (100 mL) and water (50 mL).The organic phase was washed with water (2 x 25 mL), dried over anhydrous Na2S04, and concentrated. Flash column chromatography (silica gel, 2/1 EtOAc - petroleum ether) 2o gave 2.69 g (92%) of the p-methoxybenzyl ester.
(b) N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-proline p-methoxybenzyl ester.
A mixture of N benzyloxycarbonyl-traps-4-hydroxy-L-proline p-methoxybenzyl 25 ester (2.54 g, 6.59 mmol), N benzyloxycarbonyl-L-valine (1.82 g, 7.24 mmol), 4-dimethylaminopyridine (90 mg, 0.7 mmol), and dicyclohexylcarbodiimide (1.64 g, 7.95 mmol) in 26 mL dry CHZCIz was stirred overnight. The slurry was filtered, and the filtrate was concentrated under vacuum to give an oil that was subjected to flash column chromatography (silica gel, 3/1 and~then 2/1 petroleum ether - EtOAc) to 3o yield 3.70 g ( 91 %) of the title compound.
(c) N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-proline chloromethyl ester.
The p-methoxybenzyl group was removed by stirnng a solution of the compound (2.47 g, 4.0 mmol) from step (b) and 8 mL CF,COOH in 40 mL CHZCl2 for 30 min.
The reaction mixture was concentrated under vacuum, coevaporating several times with more CHzCl1 and toluene. A second sample (1.14 g, 1.84 mmol) was treated similarly. The crude products obtained from both samples were combined and subjected to flash column chromatography (silica gel, 15% methanol in CHzCh to to give 2.58 g of cream-colored solids containing N benzyloxycarbonyl-traps-4-(N
benzyloxycarbonyl-L-valyloxy)-1.-proline (TLC 15/85 MeOH/CHZCIz Rf = 0.25).
This material ( 1.14 g) was dissolved in 10 mL dioxane. Tetrabutylammonium hydroxide ( 1.15 mL of a 40 wt % solution in H20, 1.76 mmol) was added, the mixture was evaporated to dryness, and the residue was coevaporated several times 15 with toluene and, lastly, CHzCl2. The resulting. Q salt was stirred with chloroiodomethane (1.30 mL, 17.8 mmol) in dry CHZCIz (20 mL) for 20 h. The solvent was removed under vacuum, 25 mL of 2/1 petroleum ether - EtOAc was added, and the precipitates which formed were filtered. Concentration of the filtrate, followed by flash column chromatography (silica gel, 4/1 and then 2/1 petroleum 2o ether - EtOAc) gave the chloromethyl ester (580 mg) as white solids.
(d) N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-proline iodomethyl ester.
The chloromethyl ester (533 mg, 0.974 mmol) from step (c) and NaI (594 mg, 3.96 25 mmol) were refluxed in dry MeCN (10 mL) at 75 °C for 4 h. After removal of solvent under vacuum, the mixture was partitioned between 20 mL EtOAc and 10 mL water.
The organic phase was washed with S% NazSz03 and then brine, dried over anhydrous NazS04, and concentrated. Flash column chromatography (silica gel, petroleum ether - EtOAc) gave the iodomethyl ester (526 mg, 84%) as white solids.
'H NMR (2S0 MHz, CDC1,) 8 0.86 and 0.94 (2d, 3H each, J= 6.8 Hz), 2.13 (m, 2H), 2.31 (m, 1H), 3.65-3.80 (m, 2H), 4.24 (m, 1H), 4.43 (m, 1H), 5.03-5.19 (m, 4H), 5.30 (br s, 1H), 5.54 (br d, 1H), 5.70 and 5.83-5.97 (s and ABq, 2H total), 7.30-7.32 (m, 1 OH).
Prodru~~s of the invention 4-amino-1-hydroxvbutvlidene-1 1-bisphosphonic acid tri(2 meth 1 valvloxvmethyl~propionvloxvmeth 11 ester.
to a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, tri(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyl-oxymethyl) ester and 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyloxymethyl) ester.
15 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid is prepared by the methodology in Kieczykowski et al, J Org Chem 1995, 60, 8310-8312, and the 4-amino group CBz protected as shown in US 5 227 506. To a solution thereof (195 mg, 0.51 mmole) in dry N,N-dimethylformamide (2 m1), was added diisopropylethyl-amine (0.27 ml, 1.53 mmole), followed by an injection of a solution of iodomethyl 2-2o methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionate (626 mg, 1.27 mmole) in N,N-dimethylformamide (2 mI). After stirnng under argon for 2,5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (10 ml). Crystals were f Itered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate. The organic phase was filtered 25 through anhydrous sodium sulfate and evaporated. The title compounds were isolated by silica gel column chromatography (0-4, 7-8, 20-30% ethanol in dichloromethane).
Triester (70 mg). Rf ( 10%MeOH/ CHC13) 0.45. 'H-NMR (CDC13): 7.30 (m, 20H), 5.85-5.43 (m, 9H), 5.08 (m, 8H), 4.36-3.95 (m, 9H), 3.10 (m, 2H), 2.15-1.75 (m, 30 7H), 1.19 (s, 18H), 0.86 (m, 18H).3'P-NMR (CDC13+1%CD30D) (H3P04 reference):
8 23.8 (d), 11.8(d);
Diester (185 mg), R~(10%MeOH/ CHC13) 0.10 (at the center of oval spot from baseline). 'H-NMR (CDC13+1 %CD30D): 7.31 (m, 15H), 5.79-5.63 (m, 4H), 5.08 (m, 6H), 4.35-4.10 (m, 6H), 3.10 (m, 2H), 2.18-1.70 (m, 6H), 1.19 (m, 12H), 0.87 (m, 12H). 3'P-NMR (CDC13+1%CD,OD)(H3P04 reference): 8 16.6 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, tri(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester.
A solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid tri(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyloxymethyl) to Ester (203 mg, 0.136 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (8.7 ml) was hydrogenated over a Pd-black catalyst (93 mg) at 40 psi of hydrogen for 16 h. The suspension was filtered through Celite on a fine pore sized glassinter and washed with methanol/ethyl acetate (2:1 ). The filtrate was evaporated to dryness in vacuo and the title compound as the tetra acetate was obtained as a white solid after a 1 s few co-evaporations with dioxane and hexane.
3'P-NMR (CDC13+5%CD,OD)(H3P04 reference): 8 23.1 (m), 11:1 (m).
Example A-2 20 4Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid dil2 methyl 2 (L
val loxYmethyl~ronionvloxvmethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyloxymethyl) ester (130 25 mg, 0.112 mmol) was hydrogenated over Pd-black (48 mg) by the method of Example A-1 b), to give the title compound as the triacetate as a white solid (90 mg).
3'P-NMR (CDC13+5%CD30D)(H3P04 reference}: 8 16.2 (br, s).
3o Example A-3 4-Amino-1-hydroxvbutylidene-1 1-bisphOSphonic acid di(2 methyl 2 ~~L va~loxyl propionyloxymethyll ester WO 99/51613 PCT'/SE99/00528 a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxy) propionyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (306 mg, 0.80 mmole) was esterified by the method described in Example A-1-a. After silica gel column chromatography (2-4, 6-12, 15-20% ethanol in dichloromethane), the pure fractions containing the title compound were pooled together and evaporated.
The residue was then dissolved in ethyl acetate and the solution extracted twice with 1o aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. (116 mg of title compound). Rf. (20%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDC13+1%CD,OD): 7.28 (m, 15H), 5.60 (m, 4H), 5.05 (m, 6H), 4.13 (m, 15 2H), 3.09 (m, 2H), 2.19-1.72 (m, 6H), 1.49 (m, 12H), 0.89 (m, 12H). "P-NMR
(CDCl3+1 %CD30D)(H3P04 reference): 8 15.3 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester.
20 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxy) propionyloxymethyl) ester (116 mg, 0.107 mmol) was hydrogenated over Pd-black (46 mg) by the method of Example A-1-b, to give the title compound as the triacetate as a white solid (71 mg).
25 3'P-NMR (CDC13+S%CD,OD)(H3P04 reference): 8 14.9 (s).
Example A-4 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosnhonic acid di (2-~L valyloxy~ 3 methyl ~S)~+~utyr5rloxymethXl) ester.
a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-l,l-bisphosphonic acid, di (2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (383 mg, 1 mmole) was esterified by the method described in Example A-3-a to yield 184 mg of title compound. Rf (20%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDCl3+ 1 %CD30D): 7.27 (m, 15H), 5.62 (m, 4H), 5.15-4.72 (m, 8H), 4.32 (m, 2H), 3.08 (m, 2H), 2.16-1.73 (m, 6H), 0.88 (rn, 24H). "P-NMR
(CDCI,+1%CD30D)(H3P04 reference): 8 15.5 (s).
io b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di (2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester (184 mg, 0.166 mmol) was hydrogenated over Pd-black (71 mg) by the method of Example A-i5 1-b, to give the title compound as the triacetate as a white solid (95 mg).
3'P-NMR (CDC13+5%CD30D)(H3P04 reference): b 14.6 (s).
Example A-5 20 4-amino-1-hvdroxvbutvlidene-1 1-bisph~ osnhonic acid mono 2 methyl 2 (L
val~ymethyl) nropionyloxymethyl~ ester.
a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, tribenzyl mono (2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) 25 propionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-I-hydroxybutylidene-1,1-bisphosphonic acid (1.54 g, 4 mmole) in dry N,N-dimethylformamide (24 ml), heated at 50 °C, was added diisopropylethylamine (2.78 ml, 16 mmole), followed by dropwise addition of benzylbromide ( 1.9 ml, 16 mmole). After stirring under argon for 4 h, the solution 3o was concentrated on rotavapor and treated with ethyl acetate (20 ml).
Crystals were filtered off and the filtrate was extracted with brine. The organic phase was filtered through anhydrous sodium sulfate and evaporated. The 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, tribenzylester was isolated by silica geI
column chromatography (2-4, 7-10, 15-20% ethanol in dichloromethane). The pure fractions containing the pure triester were pooled together and evaporated.
The residue was then dissolved in ethyl acetate and the solution extracted three times with 2M aqueous solution of citric acid. Triester (990 mg); Rf (20%MeOH/ CHC13) 0.15 (at the center of oval spot from baseline);
3'P-NMR (CDC13) (H3P04 reference): 8 20.4(d), 13.3 (d); 'H-NMR (CDCI3): 7.35-7.10 (m, 20H), 5.20-4.91 (m, 8H), 4.60 (br, 1H), 3.00 (m, 2H), 2.12-1.75 (m, 4H).
1o b) Dried tribenzyl ester (395 mg) was dissolved in dry N,N-dimethylformamide (3 ml), followed by addition of diisopropylethylamine (99 ml) and a solution of iodornethyl 2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionate (737 mg) in N,N-dimethylformamide (1 ml). After stirring under argon for 4 h at 30 °C, the solution was concentrated to dryness on rotavapor and treated with ethyl acetate (10 ml). Crystals were filtered off and the filtrate was extracted with brine brine containing a small amount of sodium thiosulfate. The organic phase was filtered through anhydrous sodium sulfate and evaporated. The title compound (84 mg) was isolated by silica gel column chromatography (1, 2, 3% ethanol in dichloromethane). Rf (2%MeOH/ CHCI3) 0.60;
3'P-NMR (CDC13) (H3P04 reference): 8 16.4(m). 'H-NMR (CDC13): 7.28 (m, 25H), 5.22 (d, 1H), 5.62-5.53 (m, 3H), 5.07, 5.04 (2xs, lOH), 4.93 (br, 1H), 4.27 (d,d, 1H), 4.1 S (d,d, 2H), 3.11 (m, 2H), 2.13-1.77 (m, SH), 1.17 (s, 6H), 0.92 (d, 3H), 0.83 (d, 3H).
c) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid, mono (2-methyl-2-(L -valyloxymethyl) propionyloxyrnethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid tribenzyl mono (2-methyl-2-(N-benzyloxycarbonyl-L-valyloxyrnethyl) propionyloxymethyl) 3o ester (84 mg, 0.083 mmol) was hydrogenated over Pd-black (60 mg) by the method of Example A-1-b, to give the title compound as a white solid (35 mg).
3'P-NMR (CDC13+5%CD30D)(H3P04 reference): 8 14.5 (m).
Example A-6 4-amino-1-hvdroxvbutvlidene-1 1-bis~hosphonic acid di l2-l-L valyloxy) 2 phenyl DL-acetyloxvmethyll ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (192 mg, 0.5 mmole) was esterified with the corresponding iodomethyl ester by the method described in Example A-3-a to yield 72 mg of the title compound as the tri-N-CBz protected form, ready for deprotection. Rf (20%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDCl3+ 1 %CD30D): 7.44-7.10 (m, 25H), 5.94 (m, 2H), 5.59 (m, 2H), 5.18-4.85 (m, 6H), 4.36 (m, 2H), 3.00 (m, 2H), 2.12-1.63 (m, 6H), 0.95 (m, 12H).
3'P-NMR (CDC13+1%CD,OD)(H3P04 reference): 8 15.5 (s).
Example A-7 4-amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di 111 3 di valvloxy)prop,Yl 2 ox carbonyloxy methvll ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (141 mg, 0.37 mmole) was esterified from the corresponding iodomethyl ester by the method described in Example A-1-a to yield 90 mg of title compound as the tri CBz protected form, ready for deprotection. Rf (10%MeOH/CHC13) 0.20 (at the center of oval spot from baseline). (153 mg of mixture of the diester and triester).
'H-NMR (CDC13+ 1 %CD30D) of title compound: 7.29 (m, 25H), 5.65 (m, 4H), 5.14-4.85 (m, 12H), 4.45-4.05 (m, 12H), 3.11 (rn, 2H), 2.14-1.76 (m, 8H), 0.87 (m, 24H).
3'P-NMR (CDCl3+1 %CD,OD)(H3PO4 reference): 8 16.7 (s).
Example A-8 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di l2-L-valyloxYl DL
propionyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (158 mg, 0.41 mmole) was esterified from the corresponding iodomethyl ester by the method described in Example A-3-a to yield 110 mg of the title compound as the tri N-Boc protected from, ready for deprotection. Rf (20%MeOH/CHCl3) 0.15 (at the center of oval spot from baseline).
'H-NMR (CDCI,+1%CD30D): 7.29 (m, 15H), 5.65 (m, 4H), 5.15-4.95 (m, 8H), 4.33 (m, 2H), 3.09 (m, 2H), 2.22-1.74 (m, 6H), 1.52 (m, 6H), 0.92 (m, 12H). 3'P-NMR
(CDC13+1 %CD30D)(H,P04 reference): 8 16.8 (s).
Example A-9 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di l5 ~L valYloxv) 2 2 dimethvlvalervloxXlneth Il ester a) 4-Benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(S-(N-CBz-L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (575 mg, 1.50 mmol) in DMF (10 mL), was added diisopropylamine (0.78 mL, 4.5 mmol), followed by an injection of a solution of give iodomethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate (1.95 g, 3.75 mmol) in DMF (5 mL). After stirnng under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mI,). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate.
The organic phase was filtered through anhydrous sodium sulfate and evaporated.
After silica gel column (silica gel, 4-X20% MeOH in CHZCl2), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl 3o acetate phase was evaporated, to give 171 mg of 4-benzyloxy carbonylamino-1 hydroxybutylidene-1,1-bisphosphonic acid di-(5-(N-CBz-L-valyloxy)-2,2 dimethylvaleryloxymethyl) ester.
'H-NMR (CDC13): 7.30 (br s, 15H), 5.85-5.25 (m, 4H), 5.20-4.95 (m, 6H), 4.30-3.95 (m, 6H), 3.18-3.00 (m, 2H), 2.20-1.75 (m, 6H), 1.7-1.4 (m, 8H), 1.3-1.0 (s, 12H), 1.0-0.8 (m, 12H).
s "P-NMR (CDC13)(H,PO4 reference): 16.0 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester.
to A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(5-(N-CBz-L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester (171 mg, 0.147 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst (30 mg) at 40 psi of hydrogen for 6 h.
The suspension was filtered through celite and the filtrate was evaporated to dryness 15 under reduced pressure, to give 95 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester was obtained as a white solid.
'H-NMR (CDCI,): 5.75-5.30 (m, 4H), 5.20-4.95 (m, 6H), 4.20-3.80 (m, 6H), 3.00-20 2.80 (m, 2H), 2.20-1.40 (m, 14H), 1.3-1.0 (m, 12H), 1.0-0.8 (m, 12H).
3'P-NMR (CDC13+CD3pD)(H,P04 reference): 8 17.3 (br s) Example A-10 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di-((2 (L valylo~) 25 ethox carbonvloxv) methyl) ester a) 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(N-CBz-L-valyloxy)-ethoxycarbonyloxy) methyl) ester To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 3o acid (550 mg, 1.44 mmol) in DMF (10 mL), was added diisopropylamine (0.75 mL, 4.32 mmol), followed by an injection of a solution of 2-(N-CBz-L-valyloxy)-ethyl iodomethyl carbonate (1.40 g, 3.60 mmol) in DMF (5 mL). After stirnng under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mL). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate. The organic phase was filtered through anhydrous sodium sulfate and evaporated. After silica gel column (silica gel, 4-X20% MeOH in CHZC12), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 160 mg of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(N-CBz-L-valyloxy}-ethoxycarbonyloxy) methyl) ester.
'H-NMR (CDC13): 7.29 (br s, 15H), 5.90-5.30 (m, 4H), S.1 S-4.90 (m, 6H), 4.50-4.00 (m, 10H), 3.18-3.00 (m, 2H), 2.20-1.50 (m, 6H), 1.05-0.80 (m, 12H).
"P-NMR (CDCl3)(H,P04 reference): 16.5 (s}.
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester.
A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(N-CBz-L-valyloxy)-ethoxycarbonyloxy) methyl) ester (160 mg, 0.147 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was 2o hydrogenated over a Pd-black catalyst (30 mg) at 40 psi of hydrogen for 7 h. The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 100 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester was obtained as a white solid.
'H-NMR (CDC13): 5.80-5.40 (m, 4H), 4.70-4.05 (m, l OH), 4.4-4.2 (m, 4H), 3.00-2.80 (m, 2H), 2.20-1.50 (m, 6H), 1.05-0.80 (m, 12H).
3'P-NMR (CDC13+CD30D)(H3P04 reference): b 17.5 (br s).
3o Example A-11 4-Amino-1-hvdroxvbutvliden-1 1-bisphosphonic acid bis j2 2 dimethvl 3 (D
valvloxyl-~ropion~vmethyl~! ester WO 99/51613 PCT/SE99/O(lSZ8 a) 4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid bis [2,2-dimethyl-3-(N-CBZ-D-valyloxy)-propionyloxymethylJ ester To a solution of 4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid (382 mg, 1 mmole) and diisopropylethyl (0.43 ml, 2.5 mmole) in DMF (3 ml) at -40° C was added 2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid iodomethyl ester (1.23 g, 2.5 mmole) in DMF (4 ml). The reaction was kept at 0° C
for 2.5 hr and then at 4° C for 18 hr. The reaction mixture was evaporated in vacuo and ethyl acetate (20 ml) was added. The precipitate was filtered off and the organic phase was to washed with sodium bicarbonate aqueous solution and dried. The product was isolated with silica gel column chromatography. 125 mg.
'H-NMR (CDCI3): 7.31 (m, 15 H) 5.71 (m, 4 H) 5.58 (d, 2 H) 5.12 (s, 4H) 5.05 (s, 2H) 4.30 (dd, 2H) 4.12 (m, 4 H) 3.18 (m, 2H) 2.05 (m, 6 H) 0.92 (dd, I2 H).
3'P-NMR (CDC13): 15.1 b) 4-Amino-1-hydroxybutyliden-1,1-bisphosphonic acid bis [2,2-dimethyl-3-(D-valyloxy)-propionyloxymethyl] ester.
4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid bis [2,2-dimethyl-3-(N-CBZ-D-valyloxy)-propionyloxymethyl) ester (130 mg) was dissolved in a mixed solvent of EtOAc/MeOH/AcOH (6 ml/3 ml/1.5 ml). To the solution was added palladium black (60 mg). The reaction was kept under hydrogen atmosphere (40 psi) until sampling showed the complete deprotection of the benzyloxycarbonyl groups. The reaction mixture was filtered, and then dried and coevaporated with 2s toluene and methanol, giving the titled product. 102 mg.
3'P-NMR ( CDC13 + CD30D ) : 14.1 Example A-12 4-Amino-I-h~droxybutvliden-1 1-bisnhosnhonic acid bis j4 (N CBz L valvloxv) butanoyloxvmethyl]! ester a) 4-Benzyloxycarbonylamino-1-hydroxybutyliden-I,1-bisphos~t~ni~~tcitt'tiiS
[4-(N-CBz-L-valyloxy)-butanoyloxymethyl] ester.
4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid (573 mg, 1.5 mmole) was dissolved in dioxane (10 ml). To the solution was added tetrabutylammonium hydroxide (40 %, 2.43 ml, 3.75 mmole). The solution was evaporated and coevaporated with DMF several times. The residue was dissolved in DMF (5 ml). To the solution was added 4-(N-CBz-L-valyloxy) butyric acid iodomethyl ester ( 1.79 g, 3.75 mmole) in DMF (S ml) portionwise in one hour.
The reaction was kept at room temperature for 3 hr and then evaporated in vacuo.
Later, 1 o ethyl acetate (20 ml) was added. The precipitate was filtered off and the organic phase was washed with sodium bicarbonate aqueous solution and dried. The product was isolated with silica gel column chromatography. 135 mg.
'H-NMR (CDC13):7.25 (m, 15 H) 5.60 (m, 6 H ) 5.05 (m, 8H) 4.30-3.90 (m, 6 H) 3.10 (m, 2 H) 2.50-1.80 (m, 14 H) 0.85 (m, I2 H).
3'P-NMR (CDC13): 13.7.
b) 4-amino-1-hydroxybutyliden-I,I-bisphosphonic acid bis 4-(L-valyloxy)-butanoyloxymethyl] ester.
4-Benzyloxycarbonylamino-I-hydroxybutyliden-I,1-bisphosphonic acid bis [4-(N-CBz-L-valyloxy)-butanoyloxymethyl] ester (100 mg) was dissolved in a mixed solvent of EtOAc/MeOH/AcOH (6 ml/3 ml/1.5 ml). To the solution was added palladium black (80 mg). The reaction was kept under hydrogen atmosphere (40 psi) until sampling showed the complete deprotection of the benzyloxycarbonyl groups.
The reaction mixture was filtered, and then dried and coevaporated with toluene and methanol, giving the titled product. 70 mg.
3'P-NMR (CD,OD): 17.7 3o Example A-13 4-amino-1-hydroxybutvliden-1 1-bisphosphonic acid di (3 (L valyloxy) benzovlox~methyl) ester WO 99/51613 PC"f/SE99/00528 a) 4-B enzyloxycarbonylamino- I -hydroxybutyliden-1,1-bisphonic acid, di-(3-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-biphosphonic acid (0.59g, I.5 mmole) and diisopropylethyl-amine (0.64g, S mmole) in N,N-dimethylformamide (40 ml) was added dropwise a solution of iodomethyl-3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate (2.2g, 4.3 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (50 1o ml) was added and the mixture was filtered after 2 hours. The organic phase was washed twice with 5% sodium hydrogencarbonate solution and dried with sodium sulfate. The product was isolated by silica gel column chromatography.
Yield: 0.23g = 15%
'H-NMR (CDCI3 + 5% CD30D) 0.89 (m, 12H) 1.58-2.28 (m, 6H) 2.92 (m, 2H) 4.26 (m, 2H) 5.00 (m, 6H) 5.46-6.02 (m, 4H) 6.78- 7.86 (8m, 23H) 3'P-NMR (CDCl3 + 5% CD30D) 16.5 (s) b) 4-amino-1-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-(L-2o valyloxy) benzoyloxymethyl) ester.
Deprotection of the CBz groups of 4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphonic acid, di-(3-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester using mild conditions as specified in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 1981 ) yields the title compound.
Example A-14 4-Amino-1-hvdroxvbutvliden-1 1-bisnhosnhonic acid di l3 fL valvloxvl ~ropionyloxymethyl] ester 3o a) 4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-( N-benzyloxycarbonyl-L-valyloxy)-propionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutyliden-I,I-bisphosphonic acid (0.88g, 2,5 mmole) and diisopropylethyl-amine (0.78g, 6 mmole) in N,N-dimethylformamide {40 ml) was added dropwise a solution of iodomethyI-3-(N-benzyloxycarbonyl-L-valyloxy)-propionate (2.3g, 4.95 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature under argon and evaporated under reduced pressure. Ethyl acetate (50 ml) was added and the mixture was filtered after 2 hours. The organic phase was washed twice with S% sodium hydrogencarbonate solution and dried with sodium sulfate. The product was isolated by silica gel column chromatography.Yield: 0.19g = 8%
'H-NMR {CDC13 + 5% CD30D) 0.89 (m, 12H) 1.62-2.16 (m, 6H) 2.60 (m, 4H) 3.08 (m, 2H) 4.12 (m, 2H) 4.30 (m, 4H) 5.02 (m, 6H) 5.42-5.64 (m, 4H) 7.24 (m, 15H) to "P-NMR (CDC13 + 5% CD30D) 16,9 (s) b) 4-Amino-I-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-(L-valyloxy)-propionyloxymethyl) ester.
Deprotection ofthe CBz groups of4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-(N-benzyloxycarbonyl-L-valyloxy)-propionyloxyrnethyl) ester using mild conditions as specified in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 1981 ) yields the title compound.
2o Example A-15 4-amino-1-hydroxvbutvlidene-1 1-bisnhosnhonic acid di (4 lL va~lox~
benzoyloxvmethvll ester a) 4-B enzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 2s acid, di-(4-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (14I mg, 0.37 mmole) was esterified from the con esponding iodomethyl ester by the method described in Example A-3-a) to yield 55 mg of title compound. Rf (20%MeOH/CHCI,) 0.15 (at the center of oval spot from baseline).
'H-NMR (CDC13+ I %CD30D): 7.82 (m, 4H), 7.29 (m, I 5H), 6.97 (m, 4H), 5.85 (m, 4H), 5.11 (m, 6H), 4.46 (m, 2H), 3.10 (m, 2H), 2.30-1.77 (m, 6H), 1.52 (m, 6H), 0.99 (m, 12H).
3'P-NMR (CDCI,+1%CD30D)(H3P04 reference): 8 15.6(s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di-(4-(L-valyloxy) benzoyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di-(4-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester is CBz deprotected using mild conditions as prescribed in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 1981 ) to yield the title compound.
to Example A-16 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di !3 !3 4 di !L va~loxv) phenyl) propionvlox~nethyl~ ester a) 4-benzyloxycarbonylamino-1-hydroxybutylidene- l , l -bisphosphonic 15 acid, di-(3-(3,4-di(N-benzyloxycarbonyl-L-valyloxy) phenyl) propionyloxy-methyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (143 mg, 0.37 mmole) was esterified from the corresponding iodoemthyl ester by the method described in Example A-3-a) to yield 169 mg of the title compound. Rr 20 (20%MeOH/CHCI3) 0.15 (at the center of oval spot from baseline).
'H-NMR (CDCI3+ 1%CD30D): 7.40-6.85 (m, 31H), 5.62 (m, 4H), 5.02 (m, lOH), 4.43 (m, 4H), 3.10 (m, 2H), 2.84 (m, 4H), 2.61 (m, 4H), 2.35-1.73 (m, 8H), 1.52 (m, 6H), 0.99 (m, 24H). "P-NMR (CDCl3+1 %CD30D)(H3P04 reference): 8 14.3 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutyIidene-1,1-bisphosphonic acid, di-{3-(3,4-di(N-benzyloxycarbonyl-L-valyloxy) phenyl) propionyloxy- methyl) ester 3o is CBz deprotected using mild conditions as prescribed in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 198I) to yield the title compound.
Example A-17 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid tril3 lL valvloxyl 2 2 dimethvlpropoxycarbonvloxymethyl,fester a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid tri(3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethylpropoxycarbonyl oxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (174 mg, 0.45 mmol) in dry DMF (1 mL) were added diisopropylethylamine (240 p,L, 1.38 mmol), followed by 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-1o dimethylpropyl iodomethyl carbonate (592 mg, 1.14 mmol). After stirring for 5 h at ambient temperature, under nitrogen, the reaction mixture was concentrated on a rotavapor, treated with ethyl acetate (15 mL), and filtered. The organic solution was washed with 5% NazS203, followed by brine. Drying over anhydrous NazS04 and concentration gave a yellow oil that was subjected to column chromatography (silica, 15 2/1 petroleum ether - ethyl acetate, 2.5 - 20% methanol in CHZCIz) to give fine, white solids (147 mg) enriched in the triester. The solids were dissolved in ethyl acetate, washed twice with 5% aqueous EDTA-disodium salt, dried over anhydrous NazSO,, and evaporated to dryness under vacuum.
Rf (10% methanol in CHzCl2) 0.30; ' H NMR (250 MHz, CDCl3 + 1 % CD30D) 8 20 0.85-0.95 (m, 36 H), 1.70-2.20 (m, 7H), 3.10 (br s, 2H), 3.85-3.95 (br, 12 H), 4.25 (m, 3H), 5.05 (s, 8H), 5.52-6.0 (m, lOH), 7.30 (s, 20H); 3'P NMR (101 MHz, + 1% CD30D) 8 13.6 and 24.6 (2d, .I= 47 Hz). The diester was a minor component:
"p NMR 8 18.6 (s).
b) Removal of benzyloxycarbonyl protecting groups.
25 The triester (110 mg} from step (a) was hydrogenated at 40 psi over Pd black (14 mg) in 4.2 mL solvent (2/1/1 ethyl acetate - methanol - acetic acid) for 18.5 h.
The suspension was filtered through a small column of celite and washed with ethyl acetate - methanol. The filtrate was evaporated to dryness under vacuum to give white solids (97 mg). Because proton NMR showed incomplete deprotection, the material was resubmitted for hydrogenation (14 mg Pd, 10 mL solvent) overnight to give the deprotected triester (as the acetate salt, 79 mg) as shown by the disappearance of peaks for the benzyloxy group at 8 5.05 and 7.30.
"P NMR ( 1 O 1 MHz, CDC13) 8 12.5 and 24Ø
Example A-18 4-Amino-1-hvdroxvbutvlidene-1 1-bisnhosnhonic acid di j2-methyl 1 ~ valvloxvl 2-propoxycarbonYloxymethyll ester a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid to di(1-(N benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propoxycarbonyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (460 mg, 1.2 mmol) was esterified by the method described in Example A-17 a) with 1-(N
benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propyl iodomethyl carbonate (1.54 g, 3.0 15 mmol) for 2h. After column chromatography (silica, 4-20% methanol in CHZC12), the pure fractions containing the title compound were pooled together and concentrated.
The residue was dissolved in ethyl acetate, washed twice with 5% aqueous EDTA-disodium salt, and then, water, dried over NazS04, and evaporated to dryness under vacuum to give the diester as off white solids (92 mg).
20 "P NMR (101 MHz, CDC13 + 1% CD30D) 8 19.5 (s);'H NMR (250 MHz, CDCl3 +
1% CD30D) 8 0.76-1.41 (m, 24H), 1.74 (br s, 4H), 2.05 (m, 2H), 3.02 (br s, CHIN), 3.90-4.30 (m, CHZOC=O and CHa valine), 4.93-5.01 (m, 6H), 5.30-5.90 (m, OCH~O
and NHC=O), 7.22 (s, 15H).
(b ) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-1-25 (L-valyloxy)-2-propoxycarbonyloxymethyl) ester.
The benzyloxycarbonyl-protected diester (86 mg) from step (a) was hydrogenated by the method described in Example A-17 b) to give the title compound (as the acetate salt) as a white powder (72 mg).
3'P NMR (101 MHz, CDC13) b 19.2 (s).
Example A-19 4-amino-1-hydroxybutylidene-1 1-bisphosphonic acid di (2 methyl 2 (L
isoleuc~ox~!nneth~l)propion~loxvmethvll ester.
a) 4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di (2-methyl-2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)propionyl-oxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (824mg, 2.1 mmole) and diisopropylethylamine (0.8g, 6.3 mmole) in dry N,N-dimethylformamide (15 ml) was added dropwise a solution of iodomethyl 2-methyl-is 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl) propionate (3.1g, 5.21 mmole) in N,N-dimethylformamide (6 ml). The mixture was stirred 2 hours at room temperature and evaporated under reduced pressure. Ethyl acetate (70 ml) was added and after 1 hour the crystals were filtered. The organic phase was washed two times with saturated sodium hydrogencarbonate solution, dried with sodium sulfate and 2o evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol.Yield: 0.36g 'H-NMR (CDCl3) 0.86(m, 12H) 1.20 (m, 16H) 1.60-2.20 (m, 6H) 3.10 (m, 2H) 3.80-4.40 (m, 6H) 5.08 (m, 6H) 5.45 (m, 4H) 7.29 (m, 15H) 25 "P-NMR (CDCl3 +S~~o CD30D) 14.2 (s) b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di (2-methyl-2-(isoleucyloxymethyl)propionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 3o acid di (2-methyl-2-(N-benzyloxycarbonylamino-L-isoleucyloxymethyl)propionyl-oxymethyl) ester (0.195g, 0.171 mmole) in ethyl acetate (10 ml), methanol (10 ml) and acetic acid (S ml) was added palladium black (100mg). The mixture was hydrogenated overnight at 45 psi. The catalyst was filtered and washed with ethyl acetate, methanol and acetic acid. The solution was evaporated under reduced pressure and the product was dried in vacuo to yield the title compound as the triacetate salt. Yield: 150mg.
"P-NMR (CDC13 +S% CD30D) 18.1 (s) Example A-20 4-amino-1-hydroxybutvlidene-1 1-bisphosnhonic acid di (4 fL valyloxyl ~yclohexano Ioxmethyl) ester a) 4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di (4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoyloxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-biphosphonic acid (0.706g, 1.8 mmole) and diisopropylethylamine (07g, 5.4 mmole) in N,N-dimethylformamide (15 m1) was added dropwise a solution of iodomethyl 4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate (2.35g, 4.5 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature 2o under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (60 ml) was added and the solid was filtered after 2 hours. The organic phase was washed twice with saturated sodium hydrogencarbonate and brine. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The products were isolated by silica gel column chromatography with dichloromethane/
methanol. After silica gel column chromatography the fractions were dissolved in ethyl acetate and washed three times with 5% aqueous EDTA-disodium salt solution, dried with sodium sulfate, evaporated under reduced pressure and dried in vacuo to yield 298mg 'H-NMR (CDC13) 0.84 (m, 12H) 1.35-2.35 (m, 24H) 3.10 (m, 2H) 4.08 (m, 2H) 5.02 (m, 8H) 5.55 (m, 4H) 7.24 (m, 15H) 3'P-NMR (CDCI3 + S% CD30D) 15.2 (s) -WO 99/S1b13 PCT/SE99/00528 b) 4-amino-I-hydroxybutylidene-1,1-bisphosphonic acid di (4-(L-valyloxy)-cyclohexanoyloxymethyl) ester.
4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di (4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoyloxymethyl) ester is de-CBz protected using conventional conditions as exemplified above to yield the title compound.
Example A-21 4-amino-I-hydroxvbutvlidene-1 1-bisphosnhonic acid tri l4 (L valvloxy,~
to cvclohexano loxvmethvll ester The appropriate fraction of Example A-20, step a) was dissolved in ethyl acetate and washed three times with 5% aqueous EDTA-disodium salt solution, dried with sodium sulfate, evaporated under reduced pressure and dried in vacuo to yield 15 mg which is deprotected using conventional conditions as exemplified above to yiled the title compound.
'H-NMR (protected form) (CDCl3) 0.86 (m, 18H) I.3-2.5 (m, 34H) 3.10 (m, 2H) 4.22 (m, 3H) 4.55-5.10 (m, 11H) 5.50 (m, 6H) 7.28 (m, 20H) 20 "P-NMR (CDCI, + 5% CD30D) 20.8 (d) 10.0 (d) Example A-22 4amino-1-hvdroxvbutvlidene-1 1-bisph_ osnhonic acid di 11V (2 L val ~~loxv 1 1 dimethvl-ethyl)aminocarbonvloxvmethvllester.
a) 4-N-benzyloxycarbonylamino- I -hydroxybutylidene-1,1-bisphosphonic acid di [N-(2-L-valyloxy-1,1-dimethyl-ethyl)aminocarbonyloxymethyl]ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidenel,l-biphosphonic aid (O.lg, 0. mmole) and diisopropylethylamine (0.31g, 2.4 mmole) in N,N-3o dimethylformamide (5 ml) was added dropwise a solution of 2-(N-( iodomethoxy-carbonyl)-amino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane in N,N-dimethylformamide (2.5 ml). The mixture was stirred 2 hours at room temperature under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (40 ml) was added and the solid was filtered after 2 hours. The organic phase was washed twice with saturated sodium hydrogencarbonate and brine. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol acetic acid. After silica gel column chromatography the fractions were dissolved in ethyl acetate and washed three times with 5% aqueous EDTA-disodium salt solution, dried with sodium sulfate, evaporated under reduced pressure and dried in vacuo.
Yield: 165mg.
'H-NMR (CDC13) 0.80 (m, 12H) 1.20 (m, 12H) 1.88 (m, 6H) 3.00 (m, 2H) 3.64 (m, 4H) 4.20 (m, 2H) 5.00 (m, 6H) 5.50 (m, 4H) 7.26 (m, 15H) "P-NMR (CDCl3 + 5% CD30D) 14.8 (s) b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di [N-(2-L-valyloxy-1,1-dimethyl-ethyl)aminocarbonyloxymethyl] ester.
A solution of 4-N-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid di[N-(2-L-valyloxy-1,1-dimethyl-ethyl)aminocarbonyloxymethyl] ester (0.16g 0.14mmole) in ethyl acetate (Sml), methanol (10 ml) and acetic acid (5 ml) was hydrogenated with palladium black O.lg) at room temperature and 45 psi overnight .
2o The catalyst was filtered and washed with ethyl acetate and methanol. The solution was evaporated under reduced pressure and the product was dried in vacuo to yield the triacetate salt. Yield: 100mg 3'P-NMR (CDCl3 + 5% CD30D) 14.7 (s) Example A-23 4-amino-1-h~droxvbutylidene-1 1-bisphOSDhonic acid di 1 (2 L valylox~th ly-) 6 oxo-1.6-dihvd. ro-nyridine-3-carbonyloxymeth~) ester 3o a) 4-Benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (565 mg, 1.44 mmol) in DMF (10 mL), was added diisopropylamine (0.75 mL, 4.32 mmol), followed by an injection of a solution of give 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid iodomethyl ester (2.00 g, 3.60 mmol) in DMF (5 mL). After stirring under argon for 1.5 h at room temperature, the solution was concentrated and treated with ethyl acetate (100 mL).
Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate. The organic phase was filtered through anhydrous sodium sulfate and evaporated. After silica gel column (silica gel, 4-a20%
MeOH in 1o CHZCIZ), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 205 mg of benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester.
'H-NMR (CDCI3): 8.35-7.95 (m, 2H), 7.85-7.50 (m,2H), 7.26 (br s, 15H), 6.60-6.20 (m,2H), 5.90-5.35 (m, 4H), 5. i 5-4.80 (m, 6H), 4.50-4.00 (m, l OH), 3.18-3.00 (m, 2H), 2.45-1.55 (m, 6H), 1.00-0.80 (m, 12H).
3'P-NMR (CDCI,)(H3P0, reference): 16.8 (s).
b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester.
A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-l,l-bisphosphonic 2s acid di-(1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester ( 180 mg, 0. i 45 mmol) in methanol / ethyl acetate /
acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst (30 mg) at 40 psi of hydrogen for 10 h. The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 85 mg of 4-amino-1-3o hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-L-valyloxyethyl)-6-oxo-1,6 dihydro-pyridine-3-carbonyloxymethyl) ester was obtained as a white solid.
'H-NMR (CDC13): 8.65-8.20 (m, 2H), 7.95-7.65 (m, 2H), 6.65-6.30 (m, 2H), 5.90-5.35 (m, 4H), 4.70-4.00 (m, lOH), 3.18-3.00 (m, 2H), 2.45-1.55 (m, 6H), 1.00-0.80 (m, 12H).
3'P-NMR (CDC13)(H3P04 reference): 13.9 (s).
Example A 24 4-Amino-1-hydroxvbutvlidene-1 1-bisnhosphonic acid di (fl 3 di (valvloxvlnronvl 2-oxycarbonvloxy methyl) ester to a) 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di ((1,3-di-(N-benzyloxycarbonyl)valyloxy)propyl-2-oxycarbonyloxy methyl) ester.
4-benzyloxycarbonylamino-1-hydroxybutylidene-l,l-bisphosphonic acid (141 mg, 0.37 mmole) was esterified by the method described in Example A-1 a using the 1 s corresponding iodomethyl ester to give 90 mg of the title compound.
Rf (10%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDC13+ 1 %CD30D): 7.29 (m, 25H), 5.65 (m, 4H), 5.14-4.85 (m, 12H), 4.45-4.05 (m, 12H), 3.11 (m, 2H), 2.14-1.76 (m, 8H), 0.87 (m, 24H). "P-NMR
20 (CDC13+1 %CD30D)(H,P04 reference): 8 16.7 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid di ((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester.
A solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 25 acid di ((1,3-di-(N-benzyloxycarbonyl)valyloxy)propyl-2-oxycarbonyloxy methyl) ester (162 mg, 0.1 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (6 ml) was hydrogenated over a Pd-black catalyst (70 mg) at 40 psi of hydrogen for 16 h.
The suspension was filtered through Celite on a fine pore sized glass sinter and washed with methanol/ethyl acetate (2:1). The filtrate was evaporated to dryness in 3o vacuo and the title compound was obtained as the pentacetate, a white solid after a few co-evaporations with dioxane and hexane.
3'P-NMR (CDCl3+ 5%CD30D)(H3P04 reference): b 13.5 (br).
Example A 25 4-Amino-1-hvdroxvbutyliden-1 1-bisnhosphonic acid di~2 lL valvloxymethyl) 2 ethyl butvrovloxymethyl) ester a) 4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl )-butyroyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-biphosphonic acid (0.777g, 2.0 mmole) and diisopropylethylamine (0.78g, 6.0 mmole) in N,N-to dimethylformamide (15 ml) was added dropwise a solution of iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyrate (2.6g, 5 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (60 ml) was added and the solid was filtered after 2 hours. The organic phase was washed 1 s twice with saturated sodium hydrogencarbonate and brine. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The products were isolated by silica gel column chromatography with dichloromethane/methanol.
After silica gel column chromatography the~pure fractions were dissolved in ethyl acetate and washed three times with S% aqueous EDTA-disodium salt solution, dried with 2o sodium sulfate, evaporated under reduced pressure and dried in vacuo.Yield:
320mg 'H-NMR (CDC13) 0.84 (m, 24H) 1.5-2.2 (m, 14H) 3.10 (m, 2H) 4.20 (m, 2H) 5.0 (m, 6H) 5.50 (m, 4H) 7.26 (m, 15H) 3'P-NMR (CDC13 + 5% CD30D) 14.5 (s) 2s b) 4-amino-1-hydroxybutyliden-1,1-bisphosphonic acid di-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester.
A solution of4-benzyloxycarbonylamino-1-butylidene-1,1-bisphosphonic acid di-(2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester (0.195g, 0.167 mmole) in methanol (15 ml), ethyl acetate (5 ml) and acetic acid (10 3o ml) was hydrogenated with palladium black (120mg) at room temperature overnight with 45 psi. The catalyst was filtered and washed with ethyl acetate, methanol and acetic acid. The solution was evaporated under reduced pressure and solidified with ether. The product was filtered and dried in vacuo to yield the tri acetate salt.
Yield: 0.125g. "P-NMR (CDC13 + 5% CD30D) 14.9 (s) Example A 26 4-Amino-1-hvdroxybutvlidene-1 1-bisphosphonic acid bis l3 fL valvloxvl 2 methvl-propionvloxymethvl) ester a) 4-Benzyloxy carbonylamino-I-hydroxybutylidene-I,1-bisphosphonic acid bis (3-(N-CBz-L-valyloxy)-2-methyl-propionyloxymethyl) ester.
to To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (580 mg, 1.48 mmol) in DMF (10 mL), was added diisopropylamine (0.773 mL, 4.44 mmol), followed by an injection of a solution of iodomethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate ( 1.77 g, 3.70 mmol) in DMF (5 mL). After stirring under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mL). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate.
The organic phase was filtered through anhydrous sodium sulfate and evaporated.
After silica gel column (silica gel, 4-X20% MeOH in CHZCIz), the pure fractions containing the title compound were combined and evaporated. The residue was then 2o dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 189 mg of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(N-CBz-L-valyloxy)-2-methyl-propionyloxymethyl) ester.
'H-NMR (CDC13+1 %CD30D): 7.32 (br s, I SH), 5.85-5.30 (m, 4H), 5.18-4.93 (m, 6H), 4.30-3.95 (m, 6H), 3.22-3.00 (m, 2H), 2.93-2.70 (m, 2H), 2.20-1.65 (m, 6H), 1.35-1.05 (m, 6H), 1.00-0.75 (m, 12H).
3'P-NMR (CDCl3)(H3P04 reference): 15.1 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester.
A solution of4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(N-CBz-L-valyloxy)-2-methyl-propionyloxymethyl) ester (189 mg, 0.175 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst (35 mg) at 50 psi of hydrogen for 7h.
The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 110 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester as the acetate salt, a white solid.
3'P-NMR (CDCI,+CD30D)(H3P04 reference): & 14.7 (br s) Example A 27 4-Amino-1-hvdroxvbutvlidene-1 1-bisnhosphonic acid bis l3 (L t butvlQlvcvloxv) 2 2-dimethvlnronionvloxvmethvl) ester a) 4-Benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-( N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (588 mg, 1.50 mmol) in DMF (10 mL), was added diisopropylamine (0.783 mL, 4.50 mmol), followed by an injection of a solution of iodomethyl 3-(N-CBz-L-t-1o butylglycyloxy)-2,2-dimethylpropionate (1.90 g, 3.75 mmol) in DMF (5 mL).
After stirring under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mL). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate.
The organic phase was filtered through anhydrous sodium sulfate and evaporated.
After silica gel column (silica gel, 520% MeOH in CHZCIz), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 158 mg of 4-benzyloxy carbonylamino-1-2o hydroxybutylidene-1,1-bisphosphonic acid bis (3-( N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester.
'H-NMR (CDCl3+1 %CD30D): 7.26 (br s, 1 SH), 5.85-5.40 (rn, 4H), S.15-4.88 (m, 6H), 4.20-3.95 (m, 6H), 3.20-3.00 (m, 2H), 2.10-1.65 (m, 4H), 1.22-1.05 (m, 12H), 1.00-0.75 (m, 18H).
3'P-NMR (CDCI3)(H3P04 reference): 15.1 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-( L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester.
3o A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-l,l-bisphosphonic acid bis (3-( N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionyIoxymethyl) ester (158 mg, 0.139 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst {40 mg) at 50 psi of hydrogen for 16h.
The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 100 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-( L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester as a white solid.
3'P-NMR (CDCl3+CD3pD)(H3P04 reference): 8 14.6 (br s) Example A 28 4-amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di~trans 4 (L valvloxvl L
1 o prolyoxvmeth~] ester a) 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di[N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-prolyoxymethyl] ester.
15 Diisopropylethylamine (195 p,L, 1.12 mmol) was added to a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (144 mg, 0.38 mmol) in 1 mL dry DMF, followed by the dropwise addition of a solution of the iodomethyl ester (520 mg, 0.814 mmol) from step (d) in 3 mL DMF. After stirring at ambient temperature for 5.5 h, the reaction mixture was concentrated on a rotavapor, 2o treated with EtOAc (20 mL), and filtered. The precipitates were washed with 10 mL
more EtOAc. The organic solution was washed with 10 mL saturated aqueous NaHC03 containing a small amount of NazS203, followed by reextraction of the aqueous phase with 10 mL EtOAc. The organic phases were combined, washed with mL brine, dried over anhydrous NazS04, and concentrated. Flash column 25 chromatography (silica gel, 5 - 25 % MeOH in CHZClZ (20 mL) yielded a fraction that gave light yellow solids (59 mg) enriched in the diester. The solids were dissolved in 25 mL EtOAc, washed with 5% aqueous EDTA-disodium salt (2 x 2 mL), dried over anhydrous Na2S04, and evaporated to dryness under vacuum.
30 'H NMR (250 MHz, CDCI, + 1% CD30D) 8 0.81-0.97 (m, 12H), 1.60-2.50 (br, l OH), 3.09 (br s, 2H), 3.55-3.77 (m, 4H), 4.20 (br s, 2H), 4.43 (m, 2H), 4.80-5.40 (m, 12H), 5.64 (br, 4H), 7.28-7.35 (m, 25H);
3'P NMR (101 MHz, CDC13 + 1% CD30D) 8 18.3.
b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di[traps-4-(N
benzyloxycarbonyl-L-valyloxy)-L-prolyoxymethyl] ester.
The product of step a) is deCBz protected by gentle conditions as described in Greene supra to yield the title compound.
Biological Example 1 The bioavailability of prodrugs of the invention built on the bis-phosphonate alendronate was assayed in rats. The prodrugs of the invention were orally administered at a dose corresponding to 0.1 mmol/kg to triplicate rats in a propylene glycol vehicle. The mother compound was also administered IV at 1/10 of that does for the calculation of absolute oral bioavailability.
Urine was collected over 24 hours in a metabolic cage and analysed as shown in to Kline et al J Chromat. 534 (1990) 139-149, but modified as follows: 1 ml of urine is mixed with 50 p,l or 1.25 M calcium chloride and 100 p.l of 1 M sodium hydroxide.
After centrifugation, the urine was aspirated off and the pellet redissolved in 0.8 ml 0.2 M acetic acid, 0.4 ml of 0.01 M EDTA and 0.4 ml of 0.2 m sodium acetate. 1 ml of water was added and the solution loaded onto a preconditioned DEA
cartridge.
i5 The cartridge was washed with 1 ml of water and alendronate eluted with 1 ml of 1M
carbonate buffer, pH 10.4. A part of the eluent, 150 ~l was mixed with 5 p,l of 0.05 M potassium cyanide and 5 p,l of NDA solution (1 mg/ml) in methanol. 50 p,l was injected into the chromatograph.
2o Absolute bioavailability is determined as the ratio between the AUC for the mother compound administered N against the AUC for the prodrug administered orally.
Results are presented in table 1 below:
Table 1 compound absolute bioavailability (%) alendronate 2.2 Example A-2 42 Example A-11 34 Example A-3 25 Example A-S 14 Example A-4 12 Example A-18 10 Example A-10 Example A-19 g Example A-24 11 Example A-22 g Example A-23 10 Example A-12 g The compounds of the invention exhibit substantially enhanced oral bioavailability relative to the alendronate. The pivaloyloxymethyl alendronate ester presented as the preferred prodrug in US 5 227 506 provided no better bioavailability than the mother compound in this assay (results not shown).
Although the invention has been illustrated by reference to a number of examples 1 o built on the phosphorous-containing drug alendronate and employing various linkers and amino acids, it will be appreciated that the invention is not so limited to these values but extends throughout the spirit and scope of the accompanying claims.
A further class of phosphonates which are amenable to the invention and which share a structural similarity with phosphonoformic acid are the (3-phosphonocarboxylic acid farnesyl protein transferase inhibitors, especially those of the of the formula PF4:
IS
R4~ O RaR O O O- Rf2 RZ.-O- ()qi ()qr-T~1I--O O-P N~
Rf3 R4~ RaR ~ O
Rf1 or O O- Rf2 R2 - O - Uqi-' Ring ~)Gr -T ~11- O
Rf3 R4R, O O
Rf1 where RF 1 is H or a further structure of formula IIa or IIb Rf2 is H or a conventional pharmaceutically acceptable ester, Rf3 is a polyunsaturated, branched C~zz alkyl, RZ is the acyl residue of an aliphatic amino acid, R4Land RdL' are independently H, C1_3 alkyl, hydroxymethyl, C3-6cycloalkyl, C1-3alkyl-ClC6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, CI_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle Currently favoured values in Formula PF4 include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rf 1 is a further ester it is convenient if it is identical to other linker-R2 moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters or alternatively a similar structure to the linker-R2 moiety as envisaged in our copending PCT/SE99/00194 (W099 41275). A convenient polyunsaturated alkyl Rf3 has the formula:
a ~~ U
where the asterisk shows the point of attachment.
Other structurally similar phosponates include a-phosphonosulphonates such as squalene synthase inhibitors of the formula PFS:
~M~NDED SH~~T
R aR O'~o' O Rf2 4L ~ R
R2-O- ()qi ()qr-T~O O-, Rf3 O
R4~ R4R
Rf1 or O
R O: S-O-Rf2 R2 - O - ()qi- Ring - ()4r -T ~ O -Rf3 O
Rf1 where RF1 is H or a further structure of formula IIa or IIb Rf2 is H or a conventional pharmaceutically acceptable ester a further structure of formula IIa or IIb Rf3 is a polyunsaturated, branched C6_zz alkyl, Rz is the acyl residue of an aliphatic amino acid, R4Land R4~' are independently H, C,_, alkyl, hydroxymethyl, C,-bcycloalkyl, C,-3alkyl-C,Cbcycloalkyl phenyl or benzyl, to R4R and R4R' are independently H, C,_3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C,_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
1s Currently favoured values in Formula PFS include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rfl is a further ester it is convenient if it is identical to other linker-2o Rz moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters, or alternatively a similar structure to the linker-Rz moiety. A convenient polyunsaturated alkyl Rf3 has the formula:
where the asterisk denotes the point of attachment.
The aspects of the invention immediately above further provide respective methods for the treatment or prophylaxis of neoplasma or cholesterol disorders comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in need thereof. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the 1 o preparation of a medicament for the prophylaxis or treatment of neoplasma or cholesterol disorders.
A particularly preferred group of phosphorous containing drugs are the bisphosphonates active in bone and calcium metabolism. Favoured bis-phosphonates 15 drugs have the formula:
O,, O
HO-P P~-OH
HO OH
X
where X is H, halo, hydroxy; and Y is a) C,_,o alkyl, optionally substituted with 2o heterocycle, -NRaRe, where Ra and Rb are independently hydrogen, C,_6 alkyl or join together to form a 5 to 7 membered ring, optionally containing a further hetero atom, 25 OH, halo, -S(C,_6 alkyl), phenyl, -C,_, cycloalkyl, (optionally substituted with -NRaRb or OH);
b) C3_, cycloalkyl, optionally substituted with -1VK,Rb, OH, halo, -S(C,_6 alkyl), phenyl, morpholino or pyridyl;
c) halo;
d) piperidinyl;
e) pyrrolidinyl;
f) -S(C,_6 alkyl), optionally substitued with 5 -NRaRb, OH, halo or phenyl;
g) -S-phenyl, optionally substituted with halo, nitro, C,_6 alkyl, C,_6 alkoxy, trifluormethyl, -CONRaRe or -COOH.
1o Preferred bis-phosphonates include alendronate (X is hydroxy, Y is NHZCHZCHZCHZ-), clodronate (X is chloro, Y is chloro), etidronate (X is hydroxy, Y
is CH3-), pamidronate (X is hydroxy, Y is NH~CHZCH,-), ibandronate (X is hydroxy, Y is N (CHzCH2CHZCH2CH3)(CH3)CHzCH2-), tiludronate (X is H, Y is 4-chlorophenylthio-), risedronate (X is hydroxy, Y is 3-pyridinylmethylene-) and 15 zoledronate (X is hydroxy, Y is (2-(1H-imidazol-1-yl)methylene-) Preferred compounds within this bis-phosphonate aspect of the invention thus include those of the formula A1:
O YY O
Ra1-O-P P-O-Ra2 ~O ~ ~O\
Ra3 Ra4 2o A-1 wherein YY and XX have the following values:
NHZ(CHZ)3- OH (alendronate) NHZ(CHZ)Z- OH (pamidronate) cycloheptylamino- H (cimadronate) chloro- chloro (clodronate) pyrrolidin-1-ylCH2CH2- OH ~ (EB 1053) CH3- OH (etidronate) methylpentylaminoCHZCH2- OH (ibandronate) dimethylaminoCHZCHZ OH (olpadronate) pyridin-3-ylCH2- OH (risedronate) (4-chlorophenyl)-thio- H (tiludronate) imidazo-(1,2-a)pyridin-3-ylCHz-OH (YH 529) 1 H-imidazol-1 ylCHz- OH (zoledronate) wherein amino groups on YY can be optionally substituted with conventional pharmaceutically acceptable amide groups such as -C(=O)C,_6alkyl or an aminoacyl or peptidyl derivative, as described in WO 96/31227;
and wherein at least one of Ral-Ra4 is a structure of the formula R2-_ O - ()qi ()qr-T --~ o R4L~ RaR
or R2-O- ()ql- Ring ()qr-T --~O
where RZ is the acyl residue of an aliphatic amino acid, R4Land R4L' are independently H, C,_, alkyl, hydroxymethyl, C3-6cycloalkyl, C,-3alkyl-C,Cbcycloalkyl, phenyl or benzyl, R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, 2o T is a bond, -NR4- or -O
R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and the remainder of Ral-4 are hydrogen or conventional pharmaceutically acceptable esters. Preferably Ral and Ra2 comprise the same structure of formula IIa or IIb and Ra3 and Ra4 are H. A free amine group on YY could also be protected with the same linker (RZ')k-Rz structure, as envisaged in our copending application no PCT/SE99/00194.
In formula A-1, R4R and R4R' are preferably H and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond.
Preferably qr is 1 or more preferably 0 and ql is 0 or more preferably 1.
Representative compounds within formula A-1 thus include;
(4-amino-1-hydroxybutylidine)-bisphosphonate, di(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di (2-L-valyloxy)-DL-propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(5-(L-valyloxy)-2,2-2s dimethylvaleryloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, bis [4-(L-valyloxy)-butanoyloxymethyl] ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(4-(L-valyloxy) benzoyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, (4-amino-I-hydroxybutylidine)-bisphosphonate, di- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(4-valyloxy)cyclohexanoyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethylJ ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di- ( I -(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) (4-amino-1-hydroxybutylidine)-bisphosphonate, di-((1,3-di-(valyloxy)propyl-2-to oxycarbonyloxy methyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, di-(2-(L-valyloxymethyl)-2-ethyl 15 butyroyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, di (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, di (3-(L-valyloxy)-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 2o 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di(2-methyl-2-(L-valyloxyrnethyl) propionyloxymethyl) ester, 1-hydroxy-2-{IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di (2-(L-valyloxy)-25 methyl-(S)-(+)-butyryloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, I-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, 30 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di (2-L-valyloxy)-DL-propionyloxymethyl) ester, 1-hydroxy-2-( 1 H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-I-yl)ethylidene-bis phosphonate, di-((2-(L-valyloxy}-ethoxycarbonyloxy) methyl) ester, 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, bis [4-(L-valyloxy)-butanoyloxymethyl] ester, I-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(4-(L-valyloxy) benzoyloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di- (2-methyl-1-(L-1o valyloxy)-2-propoxycarbonyloxymethyl) ester, I-hydroxy-2-(1H-imidazolyl-I-yl)ethylidene-bis phosphonate, di-(4-valyloxy)cyclohexanoyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl]ester 15 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di- (1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester I-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(2-hydroxymethyl-20 2-methylpropionyloxymethyl) ester 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 1-hydroxy-2-(IH-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(3-(L-valyloxy)-methyl-propionyloxymethyl) ester 25 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, di-(3-(L-valyloxy}-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate di(2-methyl-2-(L-valyloxyrnethyl) propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di(2-methyl-2-(L-valyloxy) 3o propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di (2-L-valyloxy)-DL-propionyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-((2-(L-valyloxy)-10 ethoxycarbonyIoxy) methyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, bis [4-(L-valyloxy)-butanoyloxymethyl] ester, I-hydroxy-2-(pyrid-3-yI)ethylidene bis-phosphonate, di-(4-(L-valyloxy) benzoyloxymethyl) ester, 15 I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(4-20 valyloxy)cyclohexanoyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di- (I-(2-L-valyloxyethyl)-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester 25 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester I-hydroxy-2-(pyrid-3-y1)ethylidene bis-phosphonate, di-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester I-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, di-(3-(L-valyloxy)-2-methyl, 2-hydroxymethylpropionyloxymethyl) ester and pharmaceutically acceptable salts thereof.
A further group of representative compounds include:
(4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-methyl-2-(L-valyloxymethyl) propionyloxyrnethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, (4-amino-i-hydroxybutylidine)-bisphosphonate, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono [4-( L-valyloxy)-butanoyloxymethyl] ester, (4-amino-l-hydroxybutylidine)-bisphosphonate, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono- (2-methyl-1-(~.-valyloxy)-propoxycarbonyloxymethyl) ester, (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-{4-valyloxy)cyclohexanoyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester WO 99/S1b13 PCT/SE99/00528 (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester (4-amino-1-hydroxybutylidine)-bisphosphonate, mono-(3-(L-valyloxy}-2-methyl-l0 propionyloxymethyl) ester (4-amino-I-hydroxybutylidine)-bisphosphonate, mono-(3-(L-valyloxy}-2-methyl,2-hydroxymethylpropionyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono(2-methyl-2-(L-15 valyloxymethyl) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 2o 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, I-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono ((1,3-di-valyloxy}propyl-2-oxycarbonyloxy methyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono (2-L-valyloxy)-2s DL-propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(S-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, 1-hydroxy-2-(IH-imidazolyl-I-yl)ethylidene-bis phosphonate, mono- ((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, 30 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono [4-(L-valyloxy)-butanoyloxymethyl] ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono- (2-methyl-1-(L-valyloxy)-2-propoxycarbonylmethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(4-N-valyloxy)cyclohexanoyloxymethyl) ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester, 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester ~5 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 1-hydroxy-2-(1H-imidazolyl-1-yl)ethylidene-bis phosphonate, mono-(3-(L-20 valyloxy)-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate mono(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 25 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono((1,3-di-valyloxy)propyl-3o 2-oxycarbonyloxy methyl) ester, 1-hydroxy-2-(pyrid-3-yI)ethylidene bis-phosphonate, mono(2-L-valyloxy)-DL-propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono [4-( L-valyloxy)-butanoyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(4-(L-valyloxy) benzoyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(3-(3,4-di-(L-valyloxy) 1o phenyl) propionyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono- (2-methyl-1-(L-valyloxy)-2-propoxycarbonyloxymethyl) ester, 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(4 -valyloxy)cyclohexanoyloxymethyl) ester 15 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-[N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-((1,3-di-20 (valyloxy)propyl-2-oxycarbonyloxy methyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(2-hydroxymethyl-2-methylpropionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester 25 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 1-hydroxy-2-(pyrid-3-yl)ethylidene bis-phosphonate, mono-(3-(L-valyloxy)-2-methyl, 2-hydroxymethyl-propionyloxymethyl) ester and pharmaceutically acceptable salts thereof.
A favoured group of compounds within formula A-1 include:
alendronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 5 alendronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 10 risedronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ~s zoledronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, 2o zoledronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, pamidronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, pamidronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-valyloxy} propionyloxymethyl) ester, 25 pamidronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, pamidronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, cimadronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 3o cimadronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, cimadronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, cimadronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, clodronate mono-(2-methyl-2-(D-valyloxy) propionyloxyrnethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(L-1o valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 15 [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(D-20 valyloxy) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, etidronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, 25 etidronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, etidronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, etidronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, 30 olpadronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, olpadronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, olpadronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(D-valyloxy) propionyIoxymethyl) ester, olpadronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 1o ibandronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, ibandronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine)-bis-phosphonate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 2o [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, tiludronate mono-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-{D-valyloxymethyl) propionyloxymethyl) ester, tiludronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, 3o tiludronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, tiludronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof.
A particularly favoured group of compounds of the invention comprises:
alendronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-{L-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, to [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-valyloxyrnethyl) propionyloxymethyl) ester, 15 tiludronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof, especially the alendronate, zoledronate and risedronate derivatives.
A further useful group of compounds within formula A-1 include:
alendronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-leucyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, alendronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, parnidronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, ~o cimadronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxyrnethyl) ester, cimadronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, ~ 5 clodronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyioxymethyl) ester, clodronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, 20 [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrroiidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-t-2s leucyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-{2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, 3o etidronate di-(2-methyl-2-(L-isoleucyloxyrnethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, s olpadronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, I o ibandronate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-alanyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-isoleucyloxymethyl) propionyloxymethyl) ester, 15 [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-leucyoxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-20 (L-alanyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-glycyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof, especially the alendronate, zoledronate and risedronate derivatives.
A further group of representative compounds comprises alendronate mono-L-valyloxymethyl ester, alendronate di-L-valyloxymethyl ester, alendronate mono-L-leucyloxymethyl ester, 3o alendronate di-L-leucyloxymethyl ester, alendronate mono-L-isoleucyloxymethyl ester, alendronate di-L-isoleucyloxymethyl ester, alendronate mono-L-t-leucyloxymethyl ester, alendronate di-L-t-leucyloxymethyl ester, alendronate mono-L-alanyloxymethyl ester, alendronate di-L-alanyloxymethyl ester, risedronate mono-L-valyloxyrnethyl ester, risedronate di-L-valyloxymethyl ester, risedronate mono-L-leucyloxymethyl ester, risedronate di-L-leucyloxymethyl ester, risedronate mono-L-isoleucyloxymethyl ester, 1 o risedronate di-L-isoleucyloxymethyl ester, risedronate mono-L-t-leucyloxymethyl ester, risedronate di-L-t-leucyloxymethyl ester, risedronate mono-L-alanyloxymethyl ester, risedronate di-L-alanyloxymethyl ester, zoledronate mono-L-valyloxymethyl ester, zoledronate di-L-valyloxymethyl ester, zoledronate mono-L-leucyloxymethyl ester, zoledronate di-L-leucyloxymethyl ester, zoledronate mono-L-isoleucyloxymethyl ester, 2o zoledronate di-L-isoleucyloxymethyl ester, zoledronate mono-L-t-leucyloxymethyl ester, zoledronate di-L-t-leucyloxymethyi ester, zoledronate mono-L-alanyloxymethyl ester, zoledronate di-L-alanyloxymethyl ester, and pharmaceutically acceptable salts thereof.
This aspect of the invention further provides a method for the treatment or prophylaxis of bone and calcium disorders comprising the oral administration of an effective amount of a compound of the invention to a mammal (including humans) in 3o need thereof. Bone and calcium disorders include osteoporosis, Paget's disease, hypercalcaemia of malignancy, tooth loss, bone loss in immunotherapy and rheumatoid arthritis, decreasing fracture, post orthopedic prosthesis and inhibiting ossification. The invention further provides the use of the compounds defined above in medicine and the use of these compounds in the preparation of a medicament for the prophylaxis or treatment of bone and calcium disorders.
A still further preferred group of prodrugs of the invention are those based on fosinoprilate having the formula PF3:
O
\ O H OH
~~~N
j~P
O O
R4R ~ R4R' O - ()qi ~)qr-T -~- O
O
R4L' or / H H
N
P
O O
R3R ~ R3R' R2 -O_ ()qi-ring- OGr-T-~-O
O
where RZ is the acyl residue of an aliphatic amino acid, 1o R4Land R4L' are independently H, C,_, alkyl, hydroxymethyl, C3-bcycloalkyl, C,-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR3- or -O-15 R3 is H or C,_3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and pharmaceutically acceptable salts thereof.
In formula PF3, R4R and R4R' are preferably H and/or R4L and RqL' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond.
Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1.
Representative compounds within formula PF3 thus include (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinylJacetyl]-L-proline, (2-methyl-2-io (L-valyloxy) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-(-L-valyloxy)-2-phenyl-DL-acetyloxymethyl) ester, 15 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinylJacetyl]-L-proline, ((1,3-di-valyloxy)propyl-2-oxycarbonyloxy methyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-L-valyloxy)-DL-propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (5-(L-2o valyloxy)-2,2-dimethylvaleryloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, ((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, [4-( L-valyloxy)-butanoyloxymethylJ ester, 25 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (4-(L-valyloxy) benzoyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, (2-methyl-1-30 (L-valyloxy)-2-propoxycarbonyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline,(4-N-valyloxy)cyclohexanoyloxymethyl) ester WO 99/51613 PC'f/SE99/00528 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline, [N-(2-L-valyloxy-1,1-dimethyl-ethyl) aminocarbonyloxymethyl] ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline,( 1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester s (4S)-4-cyclohexyl-1-[[(R}(4-phenylbutyl)phosphinyl]acetyl]-L-proline, ((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline(2-hydroxymethyl-2-methylpropionyloxymethyl) ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline(2-(L-1 o valyloxymethyl)-2-ethyl butyroyloxymethyl) ester (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester 4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (3-(L-valyloxy)-2-methyl,2-hydroxymethyl-propionyloxymethyl) ester 1 s and pharmaceutically acceptable salts thereof.
A favoured group of compounds within formula PF3 comprises:
(4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-valyloxymethyl) propionyloxymethyl) ester, 20 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[((R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-valyloxy) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[((R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline mono-(2-2s methyl-2-(D-valyloxy) propionyloxymethyl) ester, and especially;
(4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-valyloxyrnethyl) propionyloxymethyl) ester:
and pharmaceutically acceptable salts thereof A further group of convenient compounds comprises (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetylJ-L-proline (2-methyl-(L-isoleucyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-leucyoxymethyl) propionyloxymethyl) ester, 5 (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-2-(L-t-leucyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-(L-alanyloxymethyl) propionyloxymethyl) ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline (2-methyl-10 (L-glycyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof.
A further group of useful compounds comprises:
(4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-15 valyloxymethyl ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-leucyloxymethyl ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-isoleucyloxymethyl ester, 2o (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-t-leucyloxymethyl ester, (4S)-4-cyclohexyl-1-[[(R)(4-phenylbutyl)phosphinyl]acetyl]-L-proline L-alanyloxymethyl ester, and pharmaceutically acceptable salts thereof.
This aspect of the invention further provides a method for the treatment or prophylaxis of hypertension comprising the oral administration of an effective amount of a compound defined above to a mammal (including humans) in need 3o thereof. The invention further provides the use of these compounds in medicine and their use in the preparation of a medicament for the treatment or prophylaxis of hypertension A further phosphonate compound amenable to the prodrugs of the invention are the neutral endopeptidase inhibitors such as CGS-24592 (Novartis), preferably those of the formula PF6:
I
i I
R4L O R4R O ~ Ri2 R2-O- Oqi Oqr -T -~--O p- ~p~H NH~O
R4L' R4R' ~ O O
Rf1 w or I
I~1~"
Rf2 R2-O- ()ql- Ring - ()qr -T ~-O _ ~p~H NH~O
R4R' ~ O O
Rf1 where RF1 is H or a further structure of formula IIa or IIb 1o RfZ is H or a conventional pharmaceutically acceptable ester, Rz is the acyl residue of an aliphatic amino acid, R4Land R4L' are independently H, C,_3 alkyl, hydroxymethyl, C3-bcycloalkyl, C,-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C,_,alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
2o and pharmaceutically acceptable salts thereof.
Currently favoured values in Formula PF6 include: R4R and R4R' are preferably H
and/or R4L and R4L' are preferably ethyl or especially methyl. T is preferably -O- or more preferably a bond. Preferably qr is 1 or more preferably 0 and ql is 0 or preferably 1. If Rfl is a further ester it is convenient if it is identical to other linker-RZ moiety. Conventional pharmaceutically acceptable esters for Rf2 include the methyl, ethyl and isopropyl esters.
Compounds of the invention are typically prepared by esterifying the mother 1 o compound in which exposed functions such as the 4-amino group of alendronate or the carboxy group of foscarnet are protected with conventional amine and carboxy etc protecting groups respectively, with a structure of the formula IIa or IIb, the preparation of which are described in the abovementioned PCT/SE99/00194:
R4~ O R4R
*R2 -O- ()ql ()qr-T ---~-O halo R4~ R4R
I I a' or *R2 O- Oql Ring - ()qr-T --~1- O halo ~s Ilb' *RZ is the acyl residue of an aliphatic amino acid, N-protected with a conventional N-protecting group such as CBz, Fmoc or Boc R4Land R4L' are independently H, C,_3 alkyl, hydroxymethyl, C3-bcycloalkyl, C,-3alkyl-C,Cbcycloalkyl phenyl or benzyl, 2o R4R and R4R' are independently H or C,_3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR3- or -O-R3 is H or C,_3alkyl;
"ring" is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and halo is bromo, chloro and especially iodo. Alternatively, iodomethyl N-protected aminoacid esters are employed for linker-RZ structures of the formula:
R2~" O ~
Hydroxymethyl bearing linkers such as those within formula IIa are prepared by methoxybenzylation of the free carboxy group of a bis hydroxy compound such as glycerol or bis 2,2 hydroxymethyl propionic acid, CBz monoprotection of one of the hydroxy groups, esterification with the N-protected RZ group, debenzylation, reaction with chloroiodomethyl and iodination as shown below prior to esterificaiton to a phosphorous-containing pharmaceutical.
The mother compounds, that is the phosphorous containing drug, are all well known and readily accessible to those in the art.
In drugs comprising multiple phosphoryl/phosphonate/phosphinate functions, it is generally advantageous that an hydroxy group on each phosphorous moiety is esterified with a linker (-RZ')k-Rz structure such as those of formula IIa or IIb etc.
2o Regioselective protecting groups which bridge the phosphate groups of bis phosphonates and thus assist mono and diacylation include Si compounds such as dichlorotetraisopropyldisosiloxane or cresols.
Methodology for the derivatisation of phosphorous-containing compounds with acyloxyalkyl groups and which can be used analogously for the coupling of the -linker (-Rz')k-RZ structure is described in US patent 5 227 506, WO 94/13682, WO
94/13324, WO 98/04569, Starret et al J Med Chem 37 1857-1864 (1994) and Iyer et al Tetrahedron Lett 30 7141-7144 (1989). A number of approaches are also illustrated in the examples below. The N-protecting group on group RZ is removed by conventional methodology.
The term "N-protecting group" or "N-protected" as used herein refers to those groups intended to protect the N-terminus of an amino acid or peptide or to protect an amino group against undesirable reactions during synthetic procedures. Commonly used N-protecting groups are disclosed in Greene, "Protective Groups in Organic Synthesis"
(John Wiley & Sons, New York, 1981 ), which is hereby incorporated by reference.
N-protecting groups include acyl groups such as formyl, acetyl, propionyl, pivaloyl, t-butylacetyl, 2-chloroacetyl, 2-bromoacetyl, trifluoracetyl, trichloroacetyl, phthalyl, o-nitrophenoxyacetyl, a-chlorobutyryl, benzoyl, 4-chlorobenzoyl, 4-bromobenzoyl, 4-nitrobenzoyl, and the like; sulfonyl groups such as benzenesulfonyl, p-toluenesulfonyl, and the like, carbamate forming groups such as benzyloxycarbonyl, p-chlorobenzyloxycarbonyl, p-methoxybenzyloxycarbonyl, to p-nitrobenzyloxycarbonyl, 2-nitrobenzyloxycarbonyl, p-bromobenzyloxycarbonyl, 3,4-dimethoxybenzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 2-nitro-4,5-dimethoxybenzyloxycarbonyl, 3,4,5-trimethoxybenzyloxycarbonyl, 1-(p-biphenylyl)-1-methylethoxycarbonyl, a,a-dimethyl-3,5-dimethoxybenzyloxycarbonyl, benzhydryloxycarbonyl, t-butoxycarbonyl, 15 diisopropylmethoxycarbonyl, isopropyloxycarbonyl, ethoxycarbonyl, rnethoxycarbonyl, allyloxycarbonyl, 2,2,2-trichloroethoxycarbonyl, phenoxycarbonyl, 4-nitrophenoxycarbonyl, fluorenyl-9-methoxycarbonyl, cyclopentyloxycarbonyl, adamantyloxycarbonyl, cyclohexyloxycarbonyl, phenylthiocarbonyl, and the like; alkyl groups such as benzyl, triphenylmethyl, 2o benzyloxymethyl and the like; and silyl groups such as trimethylsilyl and the like.
Favoured N-protecting groups include formyl, acetyl, allyl, F-moc, benzoyl, pivaloyl, t-butylacetyl, phenylsulfonyl, benzyl, t-butoxycarbonyl (BOC) and benzyloxycarbonyl (Cbz).
25 Hydroxy and/or carboxy protecting groups are also extensively reviewed in Greene ibid and include ethers such as methyl, substituted methyl ethers such as methoxymethyl, methylthiomethyl, benzyloxymethyl, t-butoxymethyl, 2-methoxyethoxymethyl and the like, silyl ethers such as trimethylsilyl (TMS), t-butyldimethylsilyl (TBDMS) tribenzylsilyl, triphenylsilyl, t-butyldiphenylsilyl 3o triisopropyl silyl and the like, substituted ethyl ethers such as 1-ethoxymethyl, 1-methyl-1-methoxyethyl, t-butyl, allyl, benzyl, p-methoxybenzyl, dipehenylmethyl, triphenylmethyl and the like, aralkyl groups such as trityl, and pixyl (9-hydroxy-9-phenylxanthene derivatives, especially the chloride). Ester hydroxy protecting groups include esters such as formate, benzylformate, chloroacetate, methoxyacetate, phenoxyacetate, pivaloate, adamantoate, mesitoate, benzoate and the like.
Carbonate hydroxy protecting groups include methyl vinyl, allyl, cinnamyl, benzyl and the like.
The compounds of the invention can form salts which form an additional aspect of the invention. Appropriate pharmaceutically acceptable salts of the compounds of the invention include salts of organic acids, especially carboxylic acids, including but not limited to acetate, trifluoroacetate, lactate, gluconate, citrate, tartrate, maleate, malate, pantothenate, isethionate, adipate, alginate, aspartate, benzoate, butyrate, 1o digluconate, cyclopentanate, glucoheptanate, glycerophosphate, oxalate, heptanoate, hexanoate, fumarate, nicotinate, palmoate, pectinate, 3-phenylpropionate, picrate, pivalate, proprionate, tartrate, lactobionate, pivolate, camphorate, undecanoate and succinate, organic sulphonic acids such as methanesulphonate, ethanesulphonate, 2-hydroxyethane sulphonate, camphorsulphonate, 2-napthalenesulphonate, 1 s benzenesulphonate, p-chlorobenzenesulphonate and p-toluenesulphonate; and inorganic acids such as hydrochloride, hydrobromide, hydroiodide, sulphate, bisulphate, hemisulphate, thiocyanate, persulphate, phosphoric and sulphonic acids.
The compounds of the invention may in some cases be isolated as the hydrate.
2o While it is possible for the active agent to be administered alone, it is preferable to present it as part of a pharmaceutical formulation. Such a formulation will comprise the above defined active agent together with one or more acceptable carriers/excipients and optionally other therapeutic ingredients. The carriers) must be acceptable in the sense of being compatible with the other ingredients of the 25 formulation and not deleterious to the recipient.
The formulations include those suitable for rectal, nasal, topical (including buccal and sublingual), vaginal or parenteral (including subcutaneous, intramuscular, intravenous and intradermal) administration, but preferably the formulation is an 30 orally administered formulation. The formulations may conveniently be presented in unit dosage form, e.g. tablets and sustained release capsules, and may be prepared by any methods well known in the art of pharmacy.
Such methods include the step of bringing into association the above defined active agent with the carrier. In general, the formulations are prepared by uniformly and intimately bringing into association the active agent with liquid carriers or finely divided solid carriers or both, and then if necessary shaping the product. The invention extends to methods for preparing a pharmaceutical composition comprising bringing a compound of the invention or its pharmaceutically acceptable salt in 1o conjunction or association with a pharmaceutically acceptable carrier or vehicle. If the manufacture of pharmaceutical formulations involves intimate mixing of pharmaceutical excipients and the active ingredient in salt form, then it is often preferred to use excipients which are non-basic in nature, i.e. either acidic or neutral.
Formulations for oral administration in the present invention may be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active agent; as a powder or granules; as a solution or a suspension of the active agent in an aqueous liquid or a non-aqueous liquid; or as an oil-in-water liquid emulsion or a water in oil liquid emulsion and as a bolus etc.
With regard to compositions for oral administration {e.g. tablets and capsules), the term suitable Garner includes vehicles such as common excipients e.g. binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, polyvinylpyrrolidone (Povidone), methylcellulose, ethylcellulose, sodium carboxymethylcellulose, hydroxypropylmethylcellulose, sucrose and starch; fillers and carriers, for example corn starch, gelatin, lactose, sucrose, microcrystalline cellulose, kaolin, mannitol, dicalcium phosphate, sodium chloride and alginic acid; and lubricants such as magnesium stearate, sodium stearate and other metallic stearates, glycerol stearate stearic acid, silicone fluid, talc waxes, oils and colloidal silica.
Flavouring agents such as peppermint, oil of wintergreen, cherry flavouring or the like can also be used.
It may be desirable to add a colouring agent to make the dosage form readily identifiable. Tablets may also be coated by methods well known in the art.
A tablet may be made by compression or moulding, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing in a suitable machine the active agent in a free flowing form such as a powder or granules, optionally mixed with a binder, lubricant, inert diluent, preservative, 1o surface-active or dispersing agent. Moulded tablets may be made by moulding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent. The tablets may be optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active agent.
1s Other formulations suitable for oral administration include lozenges comprising the active agent in a flavoured base, usually sucrose and acacia or tragacanth;
pastilles comprising the active agent in an inert base such as gelatin and glycerin, or sucrose and acacia; and mouthwashes comprising the active agent in a suitable liquid Garner.
2o Detailed Description of the Invention Various aspects of the invention will now be illustrated by way of example only with reference to the following non-limiting synthesis and biological examples:
25 Preparation of intermediates Example P-I-1 N-BOC-L-isoleucine iodometh, l ester ~ O
O- _N
H I
O
a) N-BOC-L-isoleucine chloromethyl ester To a solution of N-BOC-L-isoleucine (23.1 g, 0.1 mol) in dioxane (500 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (65.6 mL, 0.1 mol). After stirring for 15 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (500 mL) and then chloroiodomethane (72.8 mL, 1 mol) was added and the solution was stirred for 6h at room temperature. The solution was to concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate ( 1:1 v/v, 400 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and then filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 1-2% MeOH in CHZCIz), to give 20.8 g ofN-BOC-L-isoleucine chloromethyl ester.
b) N-BOC-L-isoleucine iodomethyl ester.
To a solution ofN-BOC-L-isoleucine chloromethyl ester (19.6 g, 70 mmol) in acetonitrile (300 mL), was added sodium iodide (31.5 g, 210 mmol). The solution 2o was stirred for 4 h at 60 °C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CHzCl2 and washed with aqueous sodium thiosulfate (0.1 M}. The organic phase was dried (NaZS04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 2%
MeOH in CHZCIz), to give 22.6 g of N-BOC-L-isoleucine iodomethyl ester.
'H-NMR (CDC13): 6.04 (d, 1H), 5.82 (d, 1H), 4.97 (d, 1H), 4.25 (dd, 1H), 1.98-1.80 (m, 1H), 1.43 (s, 9H), 1.50-1.05 (m, 2H), 0.97-0.88 (m, 6H).
Example PI-2 2.2-dimethvl-3-lN-Boc-L-valvloxy~propionic acid iodomethyl ester O
O NH
I~0~~~
OO
a) 2,2-dimethyl-3-( N-Boc-L-valyloxy)propionic acid.
N-Boc-L-valine (I0.8g, 50 mmoie), 4-dimethylaminopyridine (610 mg, 5 mmoIe) and DCC (6.18 g, 30 mmole) were dissolved in methylene chloride (100 ml).
After stirring for 2 hour the mixture was filtered. To the filtrate were added 2,2-dimethyl-3-hydroxy-propionic acid (3.54g, 30 mmoIe) and pyridine (10 m1). After 18 hr, the reaction mixture was filtered, and the filtrate was poured into sodium hydrogen carbonate aqueous solution, the organic phase was then washed with citric acid to aqueous solution and water succesively. After evaporation the product was isolated with silica gel column chromatography to yield 4.4g.
b) 2,2-dimethyl-3-(N-Boc-L-valyloxy)propionic acid chloromethyl ester.
2,2-Dimethyl-3-(N-Boc-L-valyloxy)propionic acid (3.9 g, 12.3 mmole) was ~5 dissolved in dioxane (60 m1). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 7.78 ml, 12 mmole). The solution was dried in vacuo, and it was coevaporated with toluene for several times. The residue was dissolved in methylene chloride and then chloroiodomethane (18.9 ml, 260 mmole) was added to the solution. After 18 hr, the reaction solution was evaporated and the 20 product was isolated with silica gel column chromatography to yield 3.7 g.
c) 2,2-dimethyl-3-(N-Boc-L-valyloxy)propionic acid iodomethyl ester.
2,2-Dimethyl-3-( N-Boc-L-valyloxy)propionic acid chloromethyl ester ( 3.6 g, mmole ) was dissolved in acetonitrile (50 ml). Sodium iodide (2.1 g, 14 mmole) was 25 added to the solution. After reaction at 70° C for 2 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered.
The solution was dried and gave 4.348 of the titled product..
'H-NMR (CDCl3): 5.92 (dd, 2H) 5.10 (d, 1H) 4.24 (m, 1H) 4.15 (dd, 2H) 2.01 30 (m, 1 H) 1.44 (s, 9H) 1.25 (d, 6H) 0.91 (m, 6H ) Example P-I-3 3,3- bis fN-CBz-L-valyloxvmeth~)-propionic acid iodometh 1 ester O
N O ~ I
O
I~o O O
o ~
a) 3,3-Bis (N-CBz-L-valyloxymethyl)-propionic acid chloromethyl ester.
3,3- bis (N-CBz-L-valyloxymethyl)-propionic acid (3 g, 5 mmole) prepared according to PCT/SE99/00194) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 3.11 ml, 4.8 to mmole). The solution was dried in vacuo, and it was coevaporated with toluene several times. The residue was dissolved in methylene chloride (15 ml) and then chloroiodomethane (7.3 ml, 100 mmole) was added to the solution. The reaction solution was refluxed for 18 hr and then evaporated and the product was isolated with silica gel column chromatography. 900 mg.
b) 3,3-bis-(N-CBz-L-valyloxymethyl)propionic acid iodomethyl ester .
3,3-Bis (N-CBz-L-valyloxymethyl)-propionic acid chloromethyl ester (900 mg, 1.38 mmole) was dissolved in acetonitrile (S ml). Sodium iodide (289 mg, 1.93 mmole) was added to the solution. After reaction at 70° C for 3 hr, the reaction mixture was 2o filtered and the residue was dissolved in methylene chloride (5 ml) and refiltered.
The solution was dried and gave the titled product. 800 mg.
'H-NMR (CDC13): 7.35 (m, 10 H) 5.88 (dd, 2H) 5.25 (d, 2H) 4.29 (m, 2H) 4.18 (m, 4H) 2.56 (m, 1H) 2.42 (d, 2H) 2.16 (m, 2H) 0.93 (m 12 H) Example P-I-4 2-lN-CBz-L-valyloxylethoxycarbonyloxymethyl iodide WO 99/51613 PG"f/SE99/00528 O
O
p N"O w O~ ~O
O
2-(N-CBz-L-valyloxy)ethoxycarbonyloxymethyl chloride (1.16 g, 3 mmole) was dissolved in acetonitrile (10 ml). Sodium iodide (630 g, 4.2 mmole) was added to the solution. After reaction at 65° C for 2.5 hr, the reaction mixtwe was cooled down to room temperature and filtered and the residue was dissolved in methylene chloride (5 ml) and refiltered. The solution was dried and gave the titled product. 1.2 g.
'H-NMR (CDCl3): 7.35 (m, SH) 5.93 (dd, 2H) 5.26 (d, 1H) 5.11 (s, 2H) 4.39 (m, SH) 1 o 2.18 (m, 1 H) 0.94 (m, 6 H).
Example P-I-S
1,3-bisfN-tert-butoxvcarbonyl-L-valyloxy)-2-propyl iodomethYl carbonate O
N-Boc-Valyl -O
~--O O~I
N-Boc-Valyl -O
15 a) 1-O-(N tent-butoxycarbonyl-L-valyl)glycerol.
N tert-Butoxycarbonyl-L-valine (32.53 g, 0.150 mol), N,N'-dicyclohexyl-carbodiimide (37.85 g, 0.183 mol, and 4-dimethylaminopyridine (1.83 g, 0.015 mol) were added to glycerol (138.12 g., 1.5 mol) in 500 mL dry DMF and the mixture was stirred at rt under NZ for 3 days. The reaction mixture was filtered, concentrated under 2o vacuum, and then partitioned between 300 mL EtOAc and 150 mL HZO. The aqueous phase was reextracted with 150 mL EtOAc. The organic phases were combined and washed successively with 100 mL each of saturated aqueous NaHC03, saturated NH4Cl, and brine. Drying over anhydrous NazS04, and concentration under vacuum gave a viscous light yellow oil as crude product.
Flash 25 column chromatography on silica gel with 4/1 EtOAc - petroleum ether (BP 40-°C) gave 18.27 g (42%) of product (alternative nomenclature: 3-(N-tert-butoxycarbonyl-L-valyloxy)-1,2-propanediol). Reactions done overnight gave similar yields.
b) 1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol.
1-O-(N tert-butoxycarbonyl-L-valyl)glycerol (17.95 g. 61.6 mmol), Boc-L-valine (6.69 g, 30.8 mmol), DMAP (0.38 g, 3.1 mmol}, and DCC (7.10 g, 34.4 mmol) in 240 mL CHZCIZ and 60 mL DMF were stirred at rt under Nz for 18 h. The reaction mixture was filtered, concentrated under vacuum, and redissolved in 200 mL
EtOAc.
The organic solution was washed with 50 mL saturated NH4C1. The aqueous phase was reextracted with SO mL EtOAc. The organic phases were combined, washed successively with 50 mL saturated NaHC03 and 50 mL brine, dried over NazS04, and concentrated under vacuum. Flash column chromatography of the crude material on silica gel (eluent 2/ 1 petroleum ether - EtOAc, and then EtOAc) gave 7.41 g (49%) of the title compound (alternative nomenclature: 1,3-bis(N-tert-butoxycarbonyl-L-valyloxy)-2-propanol).
c) 2-D-chloromethoxycarbonyl-1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol Chloromethyl chloroformate (2.70 mL, 30 mmol) was added to a solution of 1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol (7.27 g, 14.8 mmol) and pyridine (7.2 mL, 89 mmol) in 60 mL dry CHZC12, in an ice bath, under N2. After stirring for 1 h 45 min, the reaction mixture was diluted with 100 mL CHZCIz and washed with 40 mL water. The aqueous phase was reextracted with 20 mL H20. The organic phases were combined, washed with 40 mL saturated NaHC03, followed by 2 x 50 mL
brine, dried over NazS04, and concentrated under vacuum. Flash column chromatography on silica gel with 2/1 hexane- EtOAc gave 8.03 g (93%) of the title compound (alternative nomenclature: 1,3-bis(N-tert-butoxycarbonyl-L-valyloxy)-propyl chloromethyl carbonate).
d) 2-O-iodomethoxycarbonyl-1,3-di-O-(N tert-butoxycarbonyl-L-valyl)glycerol.
3o A solution of 2-O-chloromethoxycarbonyl-1,3-di-O-(N tert-butoxycarbonyl-L-valyl)propane-1,2,3-triol (7.86 g, 13.5 mmol} and NaI (8.09 g, 54.0 mmol) in 135 mL
dry acetonitirile was refluxed at 80 °C for 4 h under N,. The reaction mixture was concentrated under vacuum, and then partitioned between 150 mL diethyl ether and SO mL HZO. The aqueous layer was reextracted with 2 x 25 mL ether. The combined organic phases were washed successively with 25 mL aqueous NazS2O3 and 50 mL
brine, dried over NazS04, and concentrated. Flash column chromatography (silica gel, 2/1 hexane-ethyl acetate gave 8.38 g (92%) title product (alternative name: 2-iodomethoxycarbonyloxy-1,3-bis-(N-tert-butoxycarbonyl-L-valyloxy)propane or 1,3-bis(N-tert-butoxycarbonyl-L-valyloxy)-2-propyl iodomethyl carbonate) as a white solid.
'H NMR (250 MHz, CDCl3) S 0.81 (d, 6H), 0.88 (m, 6H), 1.36 (s, 18H), 2.06 (m, 2H), 4.11-4.46 (m, 6H), 5.0 (br d, 2H), 5.12 (m, 1 H), 5.88 (s, 2H).
Example P-1-6 3-benzvloxvcarbon~propionic acid iodomethyl ester a) Succinic acid monobenzyl ester .
Succinic anhydride (30 g, 300 mmole) was dissolved in methylene chloride (300 ml).
To the solution were added benzyl alcohol (10.2 ml, 100 mmole), 4-dimethylaminopyridine (1.22 g, 10 mmole) and pyridine (48 ml). After 3 hours the reaction mixture was poured in to citric acid aqueous solution. The organic phase was concentrated to small volume and sodium hydrogen carbonate and water were added. Then mixture was stirred for 30 min. The aqueous phase was collected, and to it was added citric acid aqueous solution. The product precipitated out, was collected and dried. 15.3 g.
b) 3-benzyloxycarbonylpropionic acid chloromethyl ester.
Succinic acid monobenzyl ester (4.16 g, 20 mmole) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 11.6 ml, 18 mmole). The solution was dried in vacuo and coevaporated with toluene several times. The residue was dissolved in methylene chloride (60 ml) and then chloroiodomethane (14.5 ml, 200 mmole) was added to the solution. The reaction solution was stirred for 18 hr and then evaporated and the product was isolated with silica gel column chromatography. 3.64 g 'H-NMR (CDC13): 7.35 (m, SH), 5.67 (s, 2H), 5.13 (s, 2H), 2.72 (s, 4H).
c) 3-Benzyloxycarbonylpropionic acid iodomethyl ester.
3-Benzyloxycarbonylpropionic acid chloromethyl ester (2 g, 1.38 mmole) was dissolved in acetonitrile (30 ml). Sodium iodide (1.6 g, 10.9 mmole) was added to the solution. After reaction at 70° C for 3 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered. The solution was dried and gave intermediate 3-benzyloxycarbonylpropionic acid iodomethyl ester in to quantitative yield. This intermediate is bonded to an accessible function of a drug, such as a ring hydroxy or carboxy function using conventional alkylation/acylation conditions as described generally herein. Following deprotection of the terminal carboxy, a di/trifunctional linker bearing R2, such as 1,3-bis- O-(L-valyl)glycerol or iodomethyloxy-L-valyl is acylated/alkylated thereon or RZ amide bonded thereon by 15 conventional techniques as described herein, such as with DCC coupling agent.
Iodomethvl 2-methyl-2-(N-benzvloxycarbonyl-L-va~loxvmeth~l propionate 2o a) 4-Methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate.
2-(Hydroxymethyl)-2-methyl propionic acid was esterified by alkylation with 4-methoxybenzyl chloride by conventional means, namely treatment with aqueous NaOH, followed by evaporation and dissolution in an organic solvent such as DMF
to which the 4-methoxybenzyl chloride is added and the reaction warmed and 25 agitated, such as stirring at 60 C for one hour. The reaction mixture is cooled, concentrated by rotavapor and the resulting concentrated suspension partitioned between water and dichloromethane. The organic phase is evaporated and the residue subjected to silica gel column chromatography, for example with 0, 2, 4% EtOH
in dichloromethane to yield the title compound (7.10 g). Rf (2%MeOH/CHCl3) 0.40.
b) 4-Methoxybenzyl 2-(N- benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate.
SS
4-Methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate (2.50 g, 10.5 mmol), N-benzyloxy carbonyl-L-valine (2.SI g, 10 mmole), 4-dimethylaminopyridine (183 mg) and I-hydroxybenzotriazole (l.3Sg, 10 mmole) were mixed and dissolved in N,N-dimethylformamide (90 ml). Then dicyclohexyl-carbodiimide (2.47 g 12 mmol) was S added. After stirring for 3 days at room temperature the suspension was filtered and the filtrate evaporated in vacuo. The residue was partitioned between O.1M
citric acid and dichloromethane. The organic phase was then extracted with aqueous saturated NaHC03 and evaporated in vacuo. The residue was silica gel column chromatographed (0, l, 2, 3% ethanol in dichloromethane). The appropriate fractions to were pooled and evaporated in vacuo to give the title compound (2.72 g).
R~. (2%MeOH/CHC13) 0.75.
d) 2-(N- benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionic acid.
To a solution of 4-methoxybenzyl 2-(N- benzyloxycarbonyl -L-valyloxymethyl)-2-1S methyl propionate (2.72 g, 5.76 mmole), was added trifluoroacetic acid (11.5 ml) and the emerging dark red solution was stirred for 30 min at room temperature. The solution was evaporated to dryness with dioxane and toluene. The residue was silica gel column chromatographed (2, 3, 4% ethanol in dichloromethane). The appropriate fractions were pooled and evaporated in vacuo to give the title compound (1.86 g). Rf 20 (2%MeOH/CHCl3) 0.30.
'H-NMR (CDCI3): 7.32 (s, SH), 5.32 (d, 1H), 5.10 (s, 2H), 4.32 (d,d, IH), 4.21 (d,d, 2H), 2.13 (m, 1H), 1.26 (s, 3H), 1.25 (s, 3H), 0.95 (d, 3H), 0.86 (d, 3H).
25 c) Chloromethyl2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate.
2-(N- benzyloxycarbonyl -L-valyloxymethyl)-2-methyl propionic acid was esterified by conventional techniques, namely dissolution in an organic solvent such as dioxane and dropwise addition of aqueous tetrabutylammonium hydroxide, followed by 3o evaporation. The residue is dissolved in dichloromethane and then chloroiodomethane and the mixture stirrred for 6 hours at room temperature, followed by partition, shaking the filtrate with aqueous sodium thiosulphate.
O.1M, filtration and evaporation. The title compound (1.40 g) was obtained after silica gel column chromatography (0, 1, 2, 3% ethanol in dichloromethane). Rr (2%MeOH/CHC13) 0.80.
c) Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate was converted to iodide by conventional techniques, namely addition to NaI in acetonitrile, stirring and heating, for instance to 75 C for four hours. The resulting suspension is filtered and the filtrate evaporated, dissolved in organic solvent such as to toluene and shaken with aqueous sodium thiosulphate (O.1M) and evaporation to give the title compound (1.25 g) practically pure. Rf (2%MeOH/CHC13) 0.80.
'H-NMR (CDCl3): 7.35 (s, SH); 5.90 (d,d, 2H), 5.24 (d, 1H), 5.10 (s, 2H), 4.31 (d,d, 1H), 4.14 (d,d, 2H), 2.16 (m, 1H), 1.22 (s, 6H), 0.96 (d, 3H), 0.87 (d, 3H).
Example A-I-2 Iodomethvl 2-(N-benzvloxycarbonyl-L-valyloxyl-DL propionate O O~I
CBzNH
a) Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-DL-propionate.
2-(N-benzyloxycarbonyl-L-valyloxy) propionic acid (1 g) was esterified by the method described in Example A-I-I, step d. The title compound (0.76 g) was obtained after silica gel column chromatography (0, 1 % ethanol in dichloromethane).
Rf (2%MeOH/CHC13) 0.75.
b) Iodomethyl2-(N-benzyloxycarbonyl-L-valyloxy)-DL-propionate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-methyl propionate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (0.95 g) practically pure. Rf (2%MeOH/CHC13) 0.75.
'H-NMR (CDC1,): 7.33 (s, SH), 5.98 (d, 1H), 5.86 (d, 1H), 5.26 (d, 1H), 5.10 (s, 2H), 5.07 (q, 1H), 4.38 (d,d, 1H), 2.30 (m, 1H), 1.49 (d, 3H), 1.03 (d, 3H), 0.95 (d, 3H).
Example A-I-3 Iodomethvl (1,3-di-(N-benzvloxvcarbonyl~L-valyloxy,Lpr~vl carbonate O
N-CBz-Valyl -O ~
O- _O~I
N-CBz-Vatyl-O
a) Chloromethyl (1,3-di-(N-benzyloxycarbonyl)-L-valyloxy)-2-propyl carbonate.
1o To a solution of 1,3-di-((N-benzyloxycarbonyl)-L-valyloxy)propan-2-of (1.34 g, 2.4 mmole) in dichloromethane (10 ml) was added dry pyridine (1.15 ml, 14.4 mmol) and chloromethyl chloroformate (0.43 ml, 4.8 mmole) at 0°C. The reaction was then stirred for 30 min and then poured into aqueous 50% saturated sodium chloride /
O.1M citric acid solution and extracted with dichloromethane. The organic phase was evaporated and the residue silica gel column chromatographed (0, 1, 1.5%
ethanol in dichloromethane). The appropriate fractions were pooled and evaporated in vacuo to give the title compound (1.26g). Rf (2%MeOH/ CHC13) 0.85.
2o b) Preparation of iodomethyl (1,3-di-(N-benzyloxycarbonyl)-L-valyloxy)-2-propyl carbonate.
Chloromethyl (1,3-di-(N-benzyloxycarbonyl)valyloxy)-2-propyl carbonate was converted to iodide by the method described in Example A-I-l, step e) to give the title compound (1.37 g) practically pure. Rr (2%MeOH/CHC13) 0.85.
'H-NMR (CDC13): 7.34 (s, lOH), 5.93 (d, 1H), 5.89 (d, 1H), 5.21 (m, 3H), 5.11 (s, 4H), 4.50-4.17 (m, 6H), 2.12 (m, 2H), 0.97 (d, 6H), 0.88 (d, 6H).
Example A-I-4 3o Iodomethvl2-lN-benzyloxycarbonyl-L-valyloxy~isobutyrate O
CBzNH O O~I
O
a) 4-Methoxybenzyl 2-hydroxyisobutyrate.
2-hydroxy isobutyric acid (1.56 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a). The title s compound (2.65 g) was obtained after silica gel column chromatography (0, 1, 2%
ethanol in dichloromethane). Rf (2%MeOH/CHCI3) 0.45.
b) 4-Methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate.
4-methoxybenzyl 2-hydroxyisobutyrate was acylated with N-benzyloxycarbonyl-L-to valine by the method described in Example A-I-1, step b). The title compound (3.21 g) was obtained after silica gel column chromatography (0; 1, 1.5% ethanol in dichloromethane). R~ (2%MeOH/CHCl3) 0.70.
c) 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyric acid.
1 s 4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate was de-esterified by the method described in Example A-I-1 step c. The title compound (2.01 g) was obtained after silica gel column chromatography (2, 10, 20% ethanol in dichloromethane). Rf (2%MeOH/CHCI,) 0.30.
20 'H-NMR (CDCI3): 7.32 (s, SH), 5.33 (d, 1H), 5.10 (s, 2H), 4.31 (d,d, 1H), 2.22 (m, 1 H), 1.57 (s, 6H), 0.98 (d, 3H), 0.89 (d, 3H).
d) Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate.
2-(N-benzyloxycarbonyl-L-valyloxy) isobutyric acid was esterified by the method 2s described in Example A-I-1, step d. The title compound (1.90 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCI3) 0.80.
e) Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy) isobutyrate was converted to iodide by the method described in Example A-I-l, step a to give the title compound (2.32 g) practically pure. Rf (2%MeOH/CHC13) 0.80.
'H-NMR (CDC13): 7.33 (s, SH), 5.89 (s, 2H), 5.22 (d, 1H), 5.11 (s, 2H), 4.29 (d,d, 1H), 2.21 (m, 1H), 1.55 (s; 3H), 1.53 (s, 3H), 1.00 (d, 3H), 0.93 (d, 3H).
Iodomethvl 2-lN-benzvloxvcarbonyl-L-valvloxv)-3-methyl-(S)l+ -butyrate O
CBzNH O O~I
O
io a) 4-Methoxybenzyl 2-hydroxy-3-methyl-(S)-(+)-butyrate.
2-hydroxy-3-methyl-(S)-(+)-butyric acid (1.77 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a. The title compound (3.10 g) was obtained after silica gel column chromatography (0, 1, 2%
~5 ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.50.
b) 4-Methoxybenzyl2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate.
20 4-Methoxybenzyl 2-hydroxy-3-methyl-(S)-(+)-butyrate was acylated with N-benzyloxycarbonyl-L-valine by the method described in Example A-I-1, step b.
The title compound (5.74 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCI,) 0.70.
25 c) 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyric acid.
4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate was de-esterified by the method described in Example A-I-1, step c. The title compound (3.41 g) was obtained after silica gel column chromatography (2, 10, 20%
ethanol in dichloromethane). Rr (2%MeOH/CHC13) 0.45.
WO 99/51613 PCTlSE99/00528 'H-NMR (CDC13): 7.36 (s, SH), 5.38 (d, 1H), S.I 1 (s, 4H), 4.90 (d, 1H), 4.4I
(d,d, 1H), 2.28 (m, 2H), 1.04-0.89 (m, 12H).
d) Chloromethyl2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate.
2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyric acid was esterified by the method described in Example A-I-1, step d. The title compound (2.96 g) was obtained after silica gel column chromatography (0, 1, 2% ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.85.
e) Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate.
Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (3.64 g) practically pure. Rf (2%MeOH/CHC13) 0.85.
'H-NMR (CDC13): 7.36 (s, SH), 6.00 (d, 1H), 5.83 (d, 1H), 5.28 (d, 1H), 5.11 (s, 4H), 4.83 (d, 1H), 4.41 (d,d, 1H), 2.29 (m, 2H), 1.05-0.90 (m, 12H).
2o EXAMPLE A-I-6 Iodomethvl 2-(N-benzyloxycarbonvl-L-va~Ioxy)-2=phenyl-DL-acetate O
cBZNH ° o~~
I
a) 4-Methoxybenzyl 2-hydroxy-2-phenyl-DL-acetate.
DL-mandelic acid (2.28 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a. The title compound (3.69 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.55.
b) 4-Methoxybenzyl2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate.
4-Methoxybenzyl 2-hydroxy-2-phenyl-DL-acetate was acylated with N-benzyloxycarbonyl-L-valine by the method described in Example A-I-l, step b.
The title compound (6.50 g) was obtained after silica gel column chromatography (0, 1, 1.5% ethanol in dichloromethane). Rf (2%MeOH/CHCI,) 0.75.
c) 2-{N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetic acid.
4-Methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate was to de-esterified by the method described in Example A-I-1, step c. The title compound {4.75 g) was obtained after silica gel column chromatography (2, 10, 20%
ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.40.
'H-NMR (CDC13): 7.36 (m, lOH), 5.91 (d, 1H), 5.27 (m, 1H), 5.04 (s, 2H), 4.57-4.40 (2xd,d, 1H), 2.30 (m, 1H), 1.01-0.82 (m, 6H).
d) Chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate.
2-{N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetic acid was esterified by the method described in Example A-I-1, step d. The title compound (1.69 g) was obtained after silica gel column chromatography (0, 1, 2% ethanol in dichloromethane). R,. (2%MeOH/CHCl3) 0.80.
e) Iodomethyl2-(N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate.
Chloromethyl 2-{N-benzyloxycarbonyl-L-valyloxy)-2-phenyl-DL-acetate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (1.89 g) practically pure. R~ (2%MeOH/CHC13) 0.80.
'H-NMR {CDCl3): 7.36 (m, lOH), 5.94-5.82 (m, 3H), 5.28 (m, 1H), 5.10 (s, 2H), 4.46 (m, 1 H), 2.21 (m, 1 H), 1.08-0.8 S (m, 6H).
Example A-I-7 Iodomethvl 4-fN-benz r~loxycarbonyl-L-valvloxy) benzoate O
CBzNH ~
O ~. I O.~ I
i O
a) 4-Methoxybenzyl 4-hydroxybenzoate.
4-Hydroxybenzoic acid (1.38 g) was esterified by alkylation with 4-methoxybenzyl chloride by the method described in Example A-I-1, step a. The title compound (2.06 g) was obtained after silica gel column chromatography (0, 1, 2, 3% ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.40.
b) 4-Methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
4-Methoxybenzyl 4-hydroxybenzoate was acylated with N-benzyloxycarbonyl-L-valine by the method described in Example A-I-1, step b. The title compound (2.71 g) was obtained after silica gel column chromatography {0, 1 % ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.70.
c) 4-(N-benzyloxycarbonyl-L-valyloxy) benzoic acid.
4-Methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate was de-esterified by the method described in Example A-I-1, step c. The title compound (1.86 g) was obtained after silica gel column chromatography (2, 10, 20% ethanol in dichioromethane). Rf (2%MeOH/CHCl3) 0.20.
'H-NMR (CDC13): 8.15 (d, 2H), 7.34 (m, SH), 7.22 {d, 2H), 5.38 (d, 1H), 5.17 (s, 2H), 4.58 (d,d, 1H), 2.34 (m, 1H), 1.12 (s, 3H), 0.96 (d, 3H).
d) Chloromethyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
4-(N-benzyloxycarbonyl-L-valyloxy) benzoic acid was esterified by the method described in Example A-I-l, step d. The title compound (0.95 g) was obtained after silica gel column chromatography (0, 1 % ethanol in dichloromethane). Rf (2%MeOH/CHC13) 0.80. -WO 99/51613 PC'T/SE99/00528 e) Iodomethyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
Chloromethyl 4-(N-benzyloxycarbonyl-L-valyloxy) benzoate was converted to iodide by the method described in Example A-I-1, step a to give the title compound (1.16 g) practically pure. R,. (2%MeOH/CHC13) 0.80.
'H-NMR (CDC13): 8.11 (d, 2H), 7.35 (m, SH), 7.21 (d, 2H), 6.15 (s, 2H), 5.32 (d, 1H), 5.14 (s, 2H), 4.55 (d,d, 1H), 2.34 (m, 1H), 1.10 (s, 3H), 1.03 (d, 3H).
Example A-1-8 to Iodomethyl5-(N-CBz-L-valvloxy~-2,2-dimethylvalerate O
I ~ O O. Cbz-Val a) 4-Methoxybenzyl 2,2-dimethyl-4-pentenoate To a solution of 2,2-dimethyl-4-pentenoic acid (11.5 g, 90 mmol) in DMF (250 mL) at room temperature, was added potassium tent-butoxide ( 11.1 g, 99 mmol). The 15 reaction mixture was stirred at 60 °C for lh. 4-Methoxybenzyl chloride (16.9 g, 108 mmol) was added and the reaction mixture was stirred at 60 °C for 4h.
The DMF was evaporated under vacuum, the residue was dissolved in ether (S00 mL) and washed with water (3 x 200 mL). The organic phase was dried with NazS04 and evaporated to give 21.4 g of 4-methoxybenzyl 2,2-dimethyl-4-pentenoate.
b) 4-Methoxybenzyl5-hydroxy-2,2-dimethylvalerate.
A mixture of 4-methoxybenzyl 2,2-dimethyl-4-pentenoate (9.50 g, 38 mmol) and 9-BBN (115 mL, 57 mmol, 0.5 M in THF) was stirred at 60 °C for 60 min, whereupon the reaction mixture was cooled to -5 °C. Hz0 (35 mL) was added, the reaction mixture was stirred for 5 min at -S °C, an aqueous solution of NaOH (35 mL, 3M) was added and the reaction mixture was stirred for a further 10 min at -5 °C. An aqueous solution of H202 (35 mL, 30%) was added dropwise and the temperature of the reaction mixture was allowed to assume room temperature, whereupon the reaction mixture was stirred for 30 min at room temperature. After evaporation, water (200 mL) was added and the resulting mixture was extracted with CHzCl2 (5 x mL). The combined organic layers were dried (NaZS04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1-->8% MeOH in CHzCIZ), to give 6.32 g of 4-methoxybenzyl 5-hydroxy-2,2-dimethylvalerate.
c) 4-Methoxybenzyl5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
To a mixture of DCC (9.41 g, 46 mmol), DMAP (0.586 g, 4.8 mmol) and N-CBz-L-valine (12.1 g, 48 mmol) in CHZCIz (200 mL) at 0 °C, was added dropwise a solution of 4-methoxybenzyl 5-hydroxy-2,2-dimethyl-valerate (6.40 g, 24 mmol) in CHZC12 (50 mL). After 1 h at 0 °C, the temperature of the reaction mixture was allowed to 1o assume room temperature and then the mixture was stirred for Sh at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 1-~4% MeOH in CH~CIZ), to give 8.61 g 4-methoxybenzyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
d) 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid.
To a solution of 4-methoxybenzyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate (8.24 g, 16.5 mmol) in CHZCIz (100 mL) at room temperature, was added trifluoroacetic acid (5 mL). After lh at room temperature, the reaction mixture was concentrated 2o under reduced pressure. The crude product was column chromatographed (silica gel, 3~5% MeOH in CHZC12), to give 6.00 g of 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid.
'H-NMR (CDC13): 10.94 (br s, 1H), 7.35 (s, SH), 5.45 (d, 1H), 5.11 (s, 2H), 4.30 (dd, 1 H), 4.21-4.00 (m, 2H), 2.28-2.07 (m, 1 H), 1.68-1.51 (m, 4H), 1.21 (s, 6H), 0.97 (d, 3H), 0.89 (d, 3H).
e) Chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
To a solution of 5-(N-CBz-L-valyloxy)-2,2-dimethylvaleric acid (5.88 g, 15.5 mmol) 3o in dioxane (100 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (10.1 g). After stirnng for S min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (11.3 mL, 155 mmol) was added and the solution was stirred for 6h at room temperature.
The solution was concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off 5 and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 1-4% MeOH in CHZCIz), to give 3.95 g of chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
l0 f) Iodomethyl5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate.
To a solution of chloromethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate (3.85 g, 9 mmol) in acetonitrile (SO mL), was added sodium iodide (5.40 g, 36 mmol). The solution was stirred for 4 h at 60 °C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CHZCIz and washed with 15 aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1% MeOH in CHZC12), to give 4.26 g of iodomethyl (N-CBz-L-valyloxy)-2,2-dimethylvalerate 20 'H-NMR (CDC13): 7.34 (s, SH), 5.90 (s, 2H), 5.32 (d, 1H), 5.10 (s, 2H), 4.29 (dd, 1H), 4.18-4.02 (m, 2H), 2.26-2.08 (m, 1H), 1.65-1.50 (m, 4H), 1.17 (s, 6H), 0.97 (d, 3H), 0.89 (d, 3H).
Example A-1-9 25 2-(N-CBz-L-valyloxY)-ethyl iodomethyl carbonate O
I~O~O~O ~N-Cbz)-Val a) 2-(N-CBz-L-valyloxy)-ethanol To a mixture of DCC (11.4 g, 55 mmol), DMAP (0.611 g, 5 mmol) and ethyleneglycol (55.8 mL, 1 mol) in CH2Cl2 (300 mL) at 0 °C, was added dropwise a 3o solution ofN-CBz-L-valine (12.6 g, 50 mmol) in CHZC12 (100 mL). After lh at 0 °C, the temperature of the reaction mixture was allowed to assume room temperature and then the mixture was stirred for Sh at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 5-X10% MeOH in CHZC12), to give 12.0 g 2-(N-CBz-L-valyloxy)-ethanol.
b) 2-(N-CBz-L-valyloxy)-ethyl chloromethyl carbonate.
To a mixture of 2-(N-CBz-L-valyloxy)-ethanol (12.0 g, 40.6 mmol) and pyridine (19.7 mL, 0.24 mmol) in CHzCl2 (300 mL) at 0 °C, was added dropwise chloromethyl chloroformate (I0.5 g, 81.2 mmol). After 30 min at 0 °C, the reaction 1 o mixture was washed with H20 (200 mL). The H20 phase was washed with CI
IZCIz (100 mL) and the solvent of the combined organic phases was removed under reduced pressure. The crude product was column chromatographed (silica gel, 0.5-~ 1 % MeOH in CHZCl2), to give 8.26 g 2-(N-CBz-L-valyloxy)-ethyl chloromethyl carbonate.
1s c) 2-(N-CBz-L-valyloxy)-ethyl iodomethyl carbonate.
To a solution of 2-(N-CBz-L-valyloxy)-ethyl chloromethyl carbonate (3.88 g, 10 mmol) in acetonitrile (50 mL), was added sodium iodide (7.50 g, 50 mmol). The solution was stirred for 4 h at 60 °C. The resulting suspension was filtered and the 20 filtrate was evaporated. The residue was dissolved in CHZCIz and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure, to give 4.51 g 2-(N-CBz-L-valyloxy)-ethyl iodomethyl carbonate.
25 'H-NMR (CDCI,): 7.34 (s, SH), 5.93 (s, 2H), 5.26 (d, 1H), 5.11 (s, 2H), 4.48-4.26 (m, SH) 2.28-2.10 (m, 1H), 0.97 (d, 3H), 0.90 (d, 3H).
Example A-I-10 2,2-dimethyl-3-f N-CBz-D-vary)-propionic acid iodomethyl ester HN- _O
O
O
I~O
a) 2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid.
To a solution of 2,2-dimethyl propionic acid 4-methoxybenzyl ester (4.7 g, 20 mmole) and N-CBz-D-valine (5.5 g, 22 mmole) in dichloromethane (100 ml) were added 4-dimethyaminopyridine (305 mg, 2.5 mmole) and DCC (5.15 g, 25 mmole).
After 18 hr, the solution was washed successively with sodium bicarbonate aqueous solution, citric acid solution and water. The organic phase was dried and the residue was dissolved in dichloromethane (100 ml). To the solution was added trifluoroacetic acid ( 10 ml). After 3 hr, it was evaporated and the product was isolated with silica to gel column chromatography. 4.5 g.
'H-NMR (CDCl3): 7.36 (m, 5 H) 5.11 (s, 2H) 4.30 (m, 1H) 4.18 (dd, 2H) 2.17 (m, 1H), 1.23 (d, 6 H) 0.93 (m, 6H).
b) 2,2-dimethyl-3- ( N-CBz-D-Valyloxy )-propionic acid chloromethyl ester.
(2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid (4.5 g, 12.8 mmole) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40 %, 8.3 ml, 12.8 mmole). The solution was dried in vacuo, and it was coevaporated with toluene several times. The residue was dissolved in methylene chloride and then chloroiodomethane (18 ml, 260 mmole) was added to the solution. After 18 hr, the reaction solution was evaporated and the product was isolated with silica gel column chromatography. 3.5 g.
c) 2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid iodomethyl ester.
2,2-Dimethyl-3-(N-CBz-D-valyloxy)-propionic acid chloromethyl ester (2.4 g, 6 mmole) was dissolved in acetonitrile (30 ml). Sodium iodide (1.26 g, 8.4 mmole) was added to the solution. After reaction at 70° C for 2 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered.
3o The solution was dried and gave the titled product. 2.688.
'H-NMR (CDC13): 7.36 (m, 5 H) 5.90 (dd, 2H) 5.26 (d, 1H) 5.11 (s, 2H) 4.31 (m, 1 H) 4.15 (dd, 2H) 2.18 (m, 1 H) 1.22 (d, 6H) 0.92 (m, 6H).
WO 99/51613 PCTlSE99/00528 Example A-1-11 4-IN-CBz-L-valvlox~r) butyric acid iodomethyl ester O
p HN- _O
I/~O O
O I
a) 4-(N-CBz-L-valyloxy) butyric acid t-butyl ester.
N-CBz-L-valine (16.25 g, 65 mmole) was dissolved in DMF (40 ml). To the solution was added potassium t-butoxide (7.24 g, 65 mmole). After 10 min, 4-bromobutyric acid t-butyl ester (12 g, 53 mmole) was added. The reaction mixture was kept at 65°
C for 2.5 hr and then poured into sodium bicarbonate aqueous solution and extracted 1o with dichloromethane. The organic phase was dried and the product was isolated with silica gel column chromatography. 20.1 g.
b) 4-(N-CBz-L-valyloxy)butyric acid chloromethyl ester.
4-( N-CBz-L-valyloxy) butyric acid t-butyl ester (20 g, 50.8 mmole) was treated with t s trifluoroacetic acid (30 ml) at 0° C for 3 h and then evaporated.
The residue was coevaporated with toluene several time. The intermediate acid (2.56 g, 7.6 mmole) was dissolved in dioxane ( 10 ml) and to the solution was added tetrabutylammonium hydroxide (40 %, 4.66 ml, 7.2 mmole). The solution was dried and dissolved in dichloromethane (20 ml) and then chloroiodomethane (10 ml, 144 mmole) was added 2o to the solution. After 18 hr, the reaction solution was evaporated and the product was isolated with silica gel column chromatography. Yield 2.1 g.
c) 4-(N-CBz-L-valyloxy)butyric acid iodomethyl ester.
4-(N-CBz-L-valyloxy) butyric acid chloromethyl ester (1.54 g, 4 mmole) was 2s dissolved in acetonitrile (15 ml). Sodium iodide (840 rng, 5.6 mmole) was added to the solution. After reaction at 55° C for 3 hr, the reaction mixture was filtered and the residue was dissolved in methylene chloride (20 ml) and refiltered. The solution was dried and gave the titled product. Yield 1.9 g.
'H-NMR (CDC13): 7.36 (m, SH) 5.90 (dd, 2 H) 5.25 (d, 1H) 5.11 (s, 2H) 4.29 (dd, 1H
4.18 (t, 2H) 2.43 (t, 2H) 2.20 (m, 1H) 2.00 (m, 2H) 0.93 (dd, 6 H).
Example A-I-12 s Iodomethvl 3-(N-benzvloxvcarbon 1-L-valvloxy -benzoate O
O
CBzNH ~ ~ 'OBI
O
a) 4-Methoxybenzyl 3-hydroxybenzoate.
To a solution of 3-hydroxybenzoic acid (6.9g, SO mmole) in DMF (100 ml) was added potassium-tert.-butoxide (6.17 g, 55 mmole) and the mixture was stirred at 1 o room temperature for one hour. 4-Methoxybenzyl chloride (9.4g, 60 mmole) was added and the mixture was stirred for 16 hours at 60°C. The mixture was evaporated under reduced pressure and ethyl acetate (250 ml) were added. The organic phase was washed five times with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography 15 with toluene/acetone. Yield: 10.5g = 81%
b) 4-Methoxybenzyl 3-(N-benzyloxycarbonyl-L-valyloxy) benzoate.
To a cooled solution of 4-methoxybenzyl 3-hydroxybenzoate (7.7g, 29.8 mmole), dimethylaminopyridine (0.73g, 6 mmole) and N-benzyloxycarbonyl-L-valine (8.3g, 20 33 mmole) in 100 ml dichloromethane was added dicyclohexyl-carbodiimide (7.22g, 35 mmole) and the mixture was stirred for 2 days at room temperature. The mixture was cooled and the urethane was filtered. The solution was evaporated and ethyl acetate (250 ml) was added. The organic phase was washed twice with 5% acetic acid; 5% sodium hydrogencarbonate and water. The organic phase was dried with 25 sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexanelethyl acetate. Yield: 13.9g = 94%
c) 3-(N-benzyloxycarbonyl-L-valyloxy) benzoic acid.
To a solution of 4-methoxybenzyl-3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate (13.7g, 27.8 mmole) in dichloromethane (150 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred for 2 hours at room temperatwe. The solution was evaporated under reduced pressure and the product crystallized from toluene.Yield:
s 10.1 g = 87%.
'H-NMR (DMSO d-6) 1.01 (m, 6H) 2.21 (m, 1H) 4.17 (d, d, 1H) 5.08 (s, 2H) 7.28-7.96 (m, lOH) 1o d) Chloromethyl3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate.
To a solution of 3-(N-benzyloxycarbonyl-valyloxy)benzoic acid (7.42g, 20 mmole) in 1,4-dioxane (100 ml) was added a 40% solution of tetrabutylammonium hydroxide (12.97g, 20 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated 15 two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in dichloromethane (50 ml) and chloroiodomethane (35.3g, 200 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. Ethyl acetate (100 ml) was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced 2o pressure: The product was isolated by silica gel column chromatography.
Yield: 3.8g = 45%.
e) Iodomethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate.
To a solution of chloromethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate (2.Og, 25 4.76 mmole) in dry acetone (30 ml) was added sodium iodide (3.15g, 21 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate/water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure. Yield: 2.3g = 94%.
'H-NMR (CDC13) 1.02 (m, 6H) 2.38 (m, 1H) 4.56 (d, d , 1H) 5.14 (s , 2H) 5.30 (d, 1 H) 6.14 (s, 2H) 7.26-7.50 (m, 7H) 7.80(s, 1 H) 7.96 (d, 1 H) Example A-I-13 Iodomethvl3-lN-benzy_lox carbonyl-L-valyloxy)-,propionate O O
I~O- v _O NHCBz a) 3-buten-1-yl-3-(N-benzyloxycarbonyl)-propionate.
To a solution of 3-buten-1-of (2.16g, 30 mmole), N-benzyloxycarbonyl-1-valine (8.29g, 33 mmole) and 4-dimethylaminopyridine (0.37g, 3 mmole) in dichloromethane (80 ml) was added dicyclohexyl-carbodiimide (7.228, 35 mmole) and the mixture was stirred overnight at room temperature. The mixture was cooled and the urethane was filtered. The solution was evaporated under reduced to pressure and ethyl acetate (200 ml) was added. The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate.
Yield:
8.3g = 90%.
is b) 3-(N-benzyloxycarbonyl-L-valyloxy)-propanoic acid.
To a solution of 3-buten-1-yl -3-( N-benzyloxycarbonyl-L-valyloxy)-propionate (9.2g, 30 mmole) in 150 ml benzene was added tetrabutylarnmonium bromide 2o (1.628, 5 mmole) and 100 ml water. The mixture was cooled to about 5°C and potassium permanganate (14.82g, 90 mmole) was added in portions. The mixture was stirred 2 hours at room temperature, diluted with water and decoiorized by the addition of sodium bisulfate. The mixture was acidified with 2M
hydrogen chloride and extracted 3 times with ethyl acetate. The combined organic phases were 25 washed with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 5.4g = SS%.
'H-NMR (DMSO d-6) 0.90 (m, 6H) 2.5 (m, 2H) 3.88 (d, d, 1H) 4.32 (m, 2H) 5.03 30 (s, 2H) 7.36 (m, SH) 7.68 (d, 1H) c) Chloromethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-propionate.
To a solution of 3-(N-benzyloxycarbonyl-L-valyloxy)propanoic acid (5.2g, 16.08 mmole) in 1,4-dioxane (50 ml) was added a 40% solution of tetrabutylammonium hydroxide (10.43g, 16.08 mmole) and the mixture was stirred 2 hours at room s temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 40 ml dichloromethane and chloroiodomethane (28.4g. 160 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. Ethyl acetate (100 ml) was added and the organic phase to washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography. Yield:
2.2g = 35%
d) Iodomethyl3-( N-benzyloxycarbonyl-L-valyloxy)-propionate.
1s To a solution of chloromethyl 3-(N-benzyloxycarbonyl-L-valyloxy)-propionate (2.OSg, 5.51 mmole) in dry acetone (50 ml) was added sodium iodide (4.12g, 27.5 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl acetate water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium 2o sulfate and evaporated under reduced pressure. Yield: 2.35g = 92%.
'H-NMR (CDC13) 0.94 (m, 6H) 2.17 (m, 1H) 2.68 (t, 2H) 4.40 (m, 3H) 5.12 (s, 2H) 5.91 (s, 2H) 7.26 (m, SH).
25 Example A-I-13A
1.3-bis(N tert-butoxvcarbonvl-L-valylox~r)-2~ropyl 1-iodoethyl carbonate a) 1,3-bis(N tent-butoxycarbonyl-1.-valyloxy)-2-propyl 1-chloroethyl carbonate.
To a solution of 1,3-bis(N tent-butoxycarbonyl-L-valyloxy)-2-propanol (0.545 g, 1.11 mmol) in 5 mL dry CHZCl2 were added pyridine (540 pL, 6.68 mmol), with cooling and stirring in an ice bath, followed by 1-chloroethyl chloroformate (242 pL, 2.22 mmol). After 1 h, the reaction mixture was diluted with 5 mL CHZCIz and washed with water (5 mL) and brine (5 mL). The organic phase was dried over anhydrous NazS04 and concentrated on a rotavapor, coevapoating several times with toluene. Column chromatogaphy (silica, 4/1 petroleum ether - ethyl acetate) gave the 1o chloride (596 mg, 90%) as a white solid.
b) 1,3-bis(N tert-butoxycarbonyl-L-valyloxy)-2-propyl 1-iodoethyl carbonate.
A mixture of the chloride (596 mg, 1.0 mmol) from step (a) and NaI (684 mg, 4.57 ~s mmol) in 10 ml dry MeCN was refluxed at 80 °C for 4 h. The reaction mixture was concentrated under vacuum and then partitioned between 30 mL diethyl ether and mL water. The organic phase was washed with 5% aqueous sodium thiosulfate (2 x mL), and the last aqueous layer was reextracted with ether (5 mL). The organic phases were combined, washed with brine, dried over NazS04, and concentrated.
2o Flash column chromatography (silica, 4/1 petroleum ether - ethyl acetate) gave a fraction (275 mg) containing 80% iodide, as determined from 'H NMR, and small amounts of the starting chloride and alkene from the elimination side reaction.
'H NMR (250 MHz, CDCI3) 8 0.81-0.85 (m, 6H), 0.88-0.92 (m, 6H), 1.37 (s, 18H), 25 2.05 (m, 2H), 2.17 (d, 3H, J= 6.1 Hz), 4.12-4.46 (m, 6H), 5.00 (d,. 2H, J=
8.8 Hz), 5.11 (m, 1H), 6.68 and 6.69 (2 sets of q, 1H, J= 6.1 Hz).
L~,."
Example A-I-14 3-(N benzvloxvcarbonvl-L-valvloxy)-2 2-dimethvlpropyl iod-omethvl carbonate O O
I ~'O~O
HN O
O
(a) 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethyl-1-propanol.
A mixture ofN benzyloxycarbonyl-L-valine (2.50 g, 10.0 mmol), 2,2-dimethyl-1,3-propanediol (5.30 g, 50.9 mmol), dicyclohexylcarbodiimide (2.60 g, 12.6 mmol), and 4-dimethylaminopyridine (125 mg, 1.0 mmol) in 100 mL dry CHZCl2 was stirred for 23 h. The reaction mixture was filtered and washed successively with 50 mL
each of water, saturated aqueous NH4C1, saturated aqueous NaHC03, and water. The organic io phase was dried over anhydrous NazS04 and concentrated. The title compound (2.99 g, 87%) was isolated by flash column chromatography (silica, 2/1 petroleum ether -ethyl acetate) as a white waxy solid.
(b) 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethylpropyl chloromethyl carbonate.
Chloromethyl chloroformate (1.50 mL, 16.6 mmol) was added to a solution of the alcohol (2.74 g, 8.12 mmol) from step (a) and pyridine (4.9 mL, 61 mmol) in 40 mL
dry CHZCIz, in an ice bath. After stirnng for 1 h, the mixture was diluted with CHZC12 and washed successively with water, saturated NaHC03, and brine. The organic 2o phase was dried over anhydrous NazS04 and concentrated, coevaporating several times with toluene on a rotavapor. Flash column chromatography (silica, 2/1 petroleum ether - ethyl acetate) gave 3.31 g (95%) of the title compound.
(c) 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethylpropyl iodomethyl carbonate.
A mixture of the chloride (3.14 g, 7.30 mmol) from step (b) and NaI (4.37 g, 29.2 mmol) in 73 mL dry MeCN was refluxed at 80 °C for 3 h. After removal of solvent under vacuum, the mixture was partitioned between 80 mL ethyl acetate and 40 mL
water. The organic phase was washed with 5% NazSz03, and then brine, dried over 7s anhydrous NazS04, and concentrated. Flash column chromatography (silica, petroleum ether - ethyl acetate) gave 3.68 g (97%) of the title compound.
'H NMR (250 MHz, CDCI,) 8 0.88 and 0.96 (2d, 3H each), 0.98 (s, 6H), 2.18 (m, IH), 3.94 and 4.02 (2s, 2H each), 4.32 (dd, 1H, J= 9.0, 4.7 Hz), 5.11 {s, 2H), 5.26 (d, 1H), 5.92 and 5.93 (ABq, 2H, JAB = S.lHz), 7.35 (s, SH).
Example A-I-15 1-(N benzvloxvcarbonvl-L-valvloxvl-2-methyl-2-nronvl iodomethvl carbonate O O
I/'~O~O O .,,, N~O /
O H
io (a) 1-(N benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propanol N Benzyloxycarbonyl-L-valine (2.02 g, 8.0 mmol), 4-dimethylaminopyridine (100 mg, 0.8 mmol), and ), and dicyclohexylcarbodiimide (2.04 g, 9.9 mmol, in 20 mL
CHZCIZ) were added to 2-methyl-1,2-propanediol (12.2 mmol) in 30 mL dry CHZCI2, 1s with cooling in an ice bath. DMF (S mL) was added. After stirring for 5 h at 10 °C , the reaction mixture was filtered, concentrated, and then redissolved in ethyl acetate.
The organic solution was washed with saturated NaCI, dried over anhydrous Na2S04, and concentrated. Flash column chromatography (silica, 2/1 petroleum ether -ethyl acetate) gave 2.3 g of the title compound.
(b) 1-(N benzyloxycarbonyl-I,-valyloxy)-2-methyl-2-propyl chloromethyl carbonate.
All of the alcohol from above was dissolved in 35 mL dry CHZCl2 and cooled in an ice bath. Pyridine (3.50 mL, 43.4 mmol) was added, followed by chloromethyl chloroformate (1.30 mL, 14.4 mmol). After 1 h, the ice bath was removed and stirring was continued for 2 h at ambient temperature.The mixture was diluted with CH,C12 (50 mL) and washed with water (50 mL), and then brine (2 x 25 mL).Drying over anhydrous NazS04 of the combined organic phases and concentration under vacuum, coevaporating several times with toluene, gave a yellow-brown oil that was 3o subjected to flash column chromatography (silica, 2/1 petroleum ether -ethyl acetate) to yield 2.86 g (86% from N benzyloxycarbonyl-L-valine) of the title compound.
(c) 1-(N benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propyl iodomethyl carbonate.
A mixture of the chloride (2.84 g, 6.84 mmol) from step (b) and NaI (4.15 g, 27.2 mmol) in 68 mL dry acetonitrile was refluxed at 75 °C for 4 h. After evaporation of solvent under vacuum, the residue was partitioned between ethyl acetate (80 mL) and water (40 mL), and the organic layer was washed with 5% NazSz03 (15 mL) and 1o brine (25 mL). Drying the organic phase over anhydrous Na2S04 and concentration gave a yellow oil that was subjected to flash column chromatography (silica, petroleum ether - ethyl acetate) to furnish 3.29 g (95%) of the title compound.
'H NMR (250 MHz, CDCI,) 8 0.90 and 0.94 (2d, 3H each, J= 6.8 Hz), 1.52 (s, 6H), 2.17 (m, 1H), 4.35 (m, 1H), 4.22 and 4.39 (ABq, 2H, J,,B = 11.7 Hz), 5.10 (s, 2H}, 5.30 (d, 1H), 5.86 (s, 2H), 7.34 (s, SH) Example A-I-16 Iodomethvl 3.4-di-(N-CBZ-L-valvloxv)hvdrocinnamate O O
CBz-NH O i O~I
CBz-N H
O
a) 4-Methoxybenzyl-3,4-dihydroxyhydrocinnamate.
3,4-Dihydroxycinnamic acid (6.5 g, 35.7 mmol) was dissolved in DMF (50 ml) and cooled to 0°C on an ice-bath. 4-Potassium tert-butoxide (35.7 mmol), was then added and the mixture was left for approximately 30 min at 0°C, followed by dropwise adition of 4-methoxy-benzylchloride (39 mmol) in DMF (25 ml). The mixture was allowed to reach room temperature and left over-night. The solvent was then evaporated and the crude product was purified by chromatography (ethyl acetate-hexane, 1:1) to give 6 g ofthe title compound (55%).
b) 4-Methoxybenzyl-3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate.
4-Methoxybenzyl-3,4-dihydroxyhydrocinnamate (5 g, 16.5 mmol), N,N
dimethylaminopyridine (2g, 16.5 mmol), N,N'- dicychlohexyl carbodiimide (8.5 g, 41.3 mmol) and Cbz-L-valine (10.4 g, 4I.3 mmol) were dissolved in dichloromethane (50 ml). After 4 h, the the mixture was filtered and evaporated onto silica gel and purified by chromatography (hexane-EtOAc, 5:2 -a 3:2) to give pure title product (10.1 g, 79 %).
c) 3,4-Di-(N-CBZ-L-valyloxy)hydrocinnamic acid.
4-Methoxybenzyl-3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate (10 g, 13 mmol) was dissolved in dichloromethane and 1,1,1 trifluoroacetic acid (30 ml) and left at ambient temperature for 3.5 h. Evaporation under reduced pressure and purification by chromatography (chloroform-methanol, 10:1 ) yielded 6.7 g (80%) pure title product.
'H NMR (CDC13 45 °C): 7. 24-7.0 (m, 13H), 5.65 (br s, 1H), 5.55 (hr s, 1H), 5.1 (m, 4H), 4.46 (m, 2H), 2.95 (t, 2H), 2.66 (t, 2H), 2.35 (m, 2H).
d) Chloromethyl 3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate.
3,4-Di-(N-CBZ-L-valyloxy)hydrocinnamic acid (4.2 g, 6.47 mmol) was dissolved in 2o dioxane (70 ml). Tetrabutylammonium hydroxide was added dropwise until pH=8.
The solvent was then removed under reduced pressure The solid was redissolved in dioxane (30 ml) and toluene (30 ml) and evaporated. The procedure was repeated twice (for removal of water). Dichloromethane (60 ml) and chloro-iodomethane was added in one portion and the mixture was left at ambient temperature for 6 h.
Evaporation of the solvent and purification by chromatography yielded 1.7 g title product (38%).
e) Iodomethyl 3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate.
Chloromethyl 3,4-di-(N-CBZ-L-valyloxy)hydrocinnamate (1.9 g, 2.7 mmol) and 3o sodium iodide (2 g, 13.3 mmol) were dissolved in acetonitrile (50 ml) and heated to 65° C for 60 min. The solvent was removed under reduced pressure and the residue was taken up in dichloromethane and filtrated. Removal of the solvent and purification by chromatography (ethyl acetate-hexane, 2:5) gave pure title product ( 1.9 g, 90 %) 'H NMR (CDC13 45 °C): 7.34-7.02 (m, 13H), 5.89 {s, 2H), 5.64 (br s, 2H), 5.14-5.02 (m, 4H), 4.47 (m, 2H), 2.96 (t, 2H), 2.64 (t, 2H), 2.33 (m, 2H), 1.08-0.99 (m, 12H) Example A-I-17 3-(N-CBZ-L-valyloxYlphenvl iodomethyl carbonate O
O ~ O~O~I
CBz-NH
1o a) 3-(N-CBz-L-valyloxy)phenol.
CBz-L-valine (10 g, 40 mmol), 1,3-dihydroxybenzene (8.7g, 79 mmol) N,N'dicychlohexylcarbodiimide (10.2g, 44 mmol) and 4-dimethylaminopyridine (2.4 g, 20 mmol) were dissolved in DMF (50 ml) and left at ambient temperature overnight. The reaction mixture was filtered, the solvent removed under reduced 15 pressure and the crude product was taken up in dichloromethane and filtered.
Removal of the solvent followed by purification by chromatography (chloroform-methanol, 10:1) yielded pure title product (10.9 g, 79%).
b) (N-CBZ-L-valyloxy)phenyl chloromethyl carbonate.
20 3-(N-CBz-L-valyloxy)phenol (5.4 g, 15 7 mmol) was dissolved in dichloromethane (70 ml) and cooled in an ice-bath. Pyridine (1.2 g, 23.5 mmol was added followed by dropwise addition of 1-chloro-methylchloroformate (2.3 g, 18.8 mmol) in dichloromethane (10 ml). The mixture was left at room temperature for 4 h.
Water (25 ml) was then added and the phases were separated. The organic layer was washed 25 with 0.01 M aqueous hydrochloric acid (25 ml). Purification by chromatography (ethyl acetate-hexane, 1:1 ) gave the title compound (4.5 g, 65 %) c) 3-(N-CBZ-L-valyloxy)phenyl iodomethyl carbonate.
(N-CBZ-L-valyloxy)phenyl chloromethyl carbonate (l.Sg, 3.44 mmol) and sodium iodide (2 g, 13.3 mmol) were stirred at 60°C in acetonitrile (50 ml}
for 4.5 h.The mixture was filered, the solvent removed and the crude product was taken up in ml hexane-ethyl acetate, 1:1, and filtered through a sintered glass funnel, packed with 2 cm silica gel. Removal of the solvent yielded pure title product (1.68 g, 92%) 'H NMR (CDCl3 45 °C): 7.38-7.02 (m, 9H), 6.03 (s, 2H), 5.2 (br s, 1H), 5.14 (s, 2H), 4.48 (m, 1 H), 2.3 0 (m, 1 H), 1.09-1.01 (m, 6H) Example A-I-18 to Iodomethyl2-lN-CBZ-L-valvloxy}phenylacetate O
O O~I
O
CBz-NH
a) 4-Methoxybenzyl 2-hydroxyphenylacetate.
2-hydroxyphenylacetic acid (10 g, 66 mmol) was dissolved in N,N dimethyl-formamide (100 ml) and cooled on ice-bath. Potassium tert-butoxide (8.85 g, 78 15 mmoi) was added. The mixture was left for 30 min and allowed to reach room temperature. 4-Methoxy-benzylchloride (11.7 g, 72 mmol) in N,N dimethyl-formamide (30 ml) was then added dropwise, under nitrogen atmosphere and left over-night. The solvent was evaporated under reduced pressure and the crude mixture was dissolved in ether (100 ml) and washed with water (25 ml), brine and dried over 2o sodium sulphate. Chromatography (hexane-ethyl acetate, 2:1) followed by recrystallization (hexane-ethyl acetate) gave the title compound (7.6 g, 42%).
b) 4-Methoxybenzyl2-(N-CBz-L-valyloxy)phenylacetate.
4-Methoxybenzyl 2-hydroxyphenylacetate 3g, 11 mmol), N,N,-dichyclohexyl-25 carbodiimide (2.7 g, 13.2 mmol), dimethylaminopyridine (0.134 g, 1.1 mmol) and CBz-L-valine (3.3 g, 13.2 mmol) were dissolved in dichloromethane (50 ml).
After the weekend the solid was filtered off, the solvent removed under reduced pressure WO 99/51613 PCf/SE99/00528 and the crude product purified by chromatography (ethyl aceta~,'ne~c~ne; ~ :2) to give the title compound (5.2 g, 93%).
c) 2-(N-CBz-L-valyloxy)phenylacetic acid.
5 4-Methoxybenzyl 2-(N-CBz-L-valyloxy)phenylacetate (4.25 g, 8.4 mmol), was dissolved in dichloromethane (40 ml). Triflouroacetic acid (8 ml) was added with cooling on ice. The mixture was allowed to reach room temperature and stirred for 40 min. The solvent was removed under reduced pressure and the crude product was recrystallized twice (hexan-ethyl acetate + a small amount of dichloromethane) to 1o give the title compound (2.6 g, 80 %).
'H NMR (CDCI, 45 °C): 7.35-7.08 (m, 9H), 5.35 (br s, 1H), 5.13 (s, 2H), 4.48 (m, 1H), 3.57 (s, 2H), 2.33 (m, 1H), 1.08 (d, 3H), 1.02 (d, 3H).
15 d) Chloromethyl2-(N-CBZ-L-valyloxy)phenylacetate.
This compound was prepared in poor yield from 2-(N-CBz-L-valyloxy)phenylacetic acid (5.5 g, 14.3 mmol) by an unoptimized procedure essentially as described in Example A-I-16 d). Yield: 0.265 g 20 'H NMR (CDC13 45 °C): 7.28-7.01 (m, 9H), 5.55 (s, 2H), 5.2 (br s, 1H), 5.07 (s, 2H), 4.43 (m, 1H), 3.53 (s, 2H), 2.26 (m, 1H), 1.02 (d, 3H), 0.95 (d, 3H).
e) Iodomethyl 2-(N-CBZ-L-valyloxy)phenylacetate.
Chloromethyl 2-(N-CBZ-L-valyloxy)phenylacetate is treated with NaI and purified 25 as described in the Examples above to yield the title compound.
Example A-I-19 Iodomethyl 4-lN-CBZ-L-valyloxyxy~phenvlacetate O
O ~ O
CBz-NH
O~I
io a) 4-Methoxybenzyl 4-hydroxyphenylacetate.
Prepared from 4-hydroxyphenylacetic acid (10 g, 65.7 mmol) in 70 % yield by the same procedure as for Example A-I-18 a) above, but wherein the solvent for the recrystallization was changed to hexane-ether.
b) 4-Methoxybenzyl4-(N-CBz-L-valyloxy)phenylacetate.
Prepared from 4-methoxybenzyl 4-hydroxyphenylacetate (3 g, 11 mmol) by the same procedure as for Example A-I-18 b) in 87 % yield. Solvent for chromatography:
ethyl acetate-hexane, 1:2.
c) 4-(N-CBZ-L-valyloxy)phenylacetic acid.
Prepared in 82 % yield from 4-methoxybenzyl 4-(N-CBz-L-valyloxy)phenylacetate (1.6 g, 288 mmol) by the procedure described for Example A-I-18 c). Solvent for recrystallization: hexane-ether and a small amount of dichloromethane.
'H NMR (CDC13 45 °C): 7.36-7.27 (m, 7H), 7.02 (d, 2H), 5.25 (d, 1H), 5.14 (s, 2H), 4.52 (m, 1H), 3.64 (s, 2H), 2.3 (m, 1H), 1.08 (d, 3H), 1.02 (d, 3H).
d) Chloromethyl4-(N-CBZ-L-valyloxy)phenylacetate.
Prepared from 4-(N-CBZ-L-valyloxy)phenylacetic acid (3 g, 7.8 mmol) in 26 2o yield by the same procedure as described for Example A-I-18 d). Solvent for chromatography: hexane-ether, 3:2.
e) Iodomethyl 4-(N-CBZ-L-valyloxy)phenylacetate.
Chloromethyl 4-(N-CBZ-L-valyloxy)phenylacetate (0.83 g, 1.9 mmol) and sodium iodide (1.15 g, 7.6 mmol) were heated in acetonitril (45 ml) for 5 h. The mixture was filtrated, the solvent removed, taken up in dichloromethane and filtrated again.
Evaporation and purification by chromatography (ether-hexane, 2:3) yielded the title product (0.8 g, 80 %).
'H NMR (CDCI, 45 °C): 7.38-7.09 (m, 4H), 5.$4 (s, 1H), 5.30 (br s, 1H), 5.15 (s, 2H), 4.5 (m, 1H), 3.56 (s, 2H), 2.36 (m, 1H), 1.10 (d, 3H), 1.00 (d, 3H).
Example A-I-20 Iodometh~l 4-(2-N-benzylox~rcarbonyl-L-val ,~loxyethyl benzoate a) 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl~toluene.
To a cooled solution of 4-methylphenylethanol-2 (S.Og, 36.7 mmole), 4 dimethylaminopyridine (0.98g, 8 mmole) and N-benzyloxycarbonyl-L-valine ( 10.05g, 40 mmole) in dichloromethane ( 120 ml) was added dicyclohexyl-carbodiimide (9.1 g, 44 mmole) and the mixture was stirred overnight at room temperature. The mixture was cooled and the urethane was filtered. The solution was 1o evaporated under reduced pressure and ethyl acetate (250 ml) was added. The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 13.3g = 97%
b) 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)- benzoic acid.
To a cooled mixture of chromic anhydride (7.558, 75 mmole) in acetic acid (100 ml) was added dropwise a solution of 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)-toluene (9.3g, 25.1 mmole) in acetone (50 ml). The mixture was stirred at room temperature for 3 days and reduced to about 100 ml. 600m1 10% sodium chloride 2o solution was added and the mixture was extracted four times with ethyl acetate. The organic phase was washed with brine and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product was islolated by silica gel column chromatography with dichloromethane/methanol. Yield : 2,1 g = 21 %.
'H-NMR (CDC13) 0.79 (d, 3H) 0.90 (d, 3H) 2.08 (m,lH) 3.04 (t, 2H) 4.28 (d, d,lH) 4.39 (m, 2H) 5.11 (s, 2H) 5.26 (d, 1H) 7.34 (m, 7H) 8.04 (d, 2H) c) Chloromethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)benzoate.
To a solution of 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl)benzoic acid (2.Og, 5.0 3o mmole) in 1,4-dioxane (20 ml)was added a 40% solution of tetrabutylammonium hydroxide (3.1 g, 4.75 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and coevaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in dichloromethane (10 ml) and iodochloromethane (I3.2g, 75 mmole) was added The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 50 ml ethyl acetate were added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography.Yield:
O.Sg =23%
d) Iodomethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl) benzoate.
o To a solution of chloromethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethyl) benzoate (O.Sg, 1.11 mmole). In dry acetone (10 ml) was added sodium iodide (0.75g, 5.0 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate/water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate is and evaporated under reduced pressure.Yield: 0.53g = 88%.
'H-NMR (CDCI,) 0.88 (d, 3H) 0.90 (d, 3H) 2.08 (m, 1H) 3.02 (t, 2H) 4.28 (d, d, 1H) 4.38 (m, 2H) 5.10 (s, 2H) 5.22 (d, 1H) 6.15 (s, 2H) 7.35(m, 7H) 7.98 (d, 2H ) 20 Example A-I-21 Iodometh,~(N-benzvloxycarbonyl-L-isoleucvloxvmethvll 2-meth~,rl,propionate.
a) 4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2s 2-methyl propionate.
To a cooled solution of 4-methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate (6.Og, 25 mmole), 4-dimethylaminopyridine (0.61 g, 5 mmole) and N-benzyloxycarbonyl-L-isoleucine (6.90g, 26 mmole) in dichloromethane (100 ml) was added dicyclohexyl-carbodiimide (6.2g, 30 mmole) and the mixture was stirred 3o overnight at room temperature.The mixture was cooled and the urethane was filtered.
The solution was evaporated and 200 ml ethyl acetate was added, The organic phase was washed twice with S% acetic acid, 5% sodium hydrogencarbonate and water.
The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone.Yield: 11.7g = 96%.
2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2-methyl) propionic acid.
To a solution of 4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl}-2-methyl propionate (ll.Og, 22.6 mmole) in 100 ml dichloromethane was added trifluoroacetic acid (15 ml) and the mixture was stirred overnight at room temperature. The solution was evaporated under reduced pressure and coevaporated two times with toluene. The residue was stirred 1 hour with 100 ml ethanol and the 1o white solid was filtered (byproduct). The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 7.4g = 89%.
'H-NMR (CDCI,) 0.90 (m, 6H) 1.26 (m, 8H) 1.88 (m, 1H) 4.12 (d, d, 2H) 4.38 (d, d, 1H) 5.10 (s, 2H) 5.32 (d, 1H) 7.28 (m, 5H) c) Chloromethyl 2-(N-benzyloxycarbonyl-L-isoleucyloxy)-2-methyl propionate.
To a solution of 2-(N-benzyloxycarbony-L-isoleucyloxymethyl)-2-methyl 2o propionic acid (7.Og, 19 mmole) in 80 ml 1,4-dioxane was added a 40%
solution of tetrabutylammonium hydroxide (12.4g, 19 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 25 ml dichloromethane and iodochloromethane (33.7g, mmole) was added . The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone.Yield: 4.2 = 54%
d) Iodomethyl2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2-methyl propionate.
To a solution of chloromethyl 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)-2-methyl propionate (3.Og, 7.2 mmole) in 50 ml dry acetone was added sodium iodide (4.8g, 32 mmole) and the mixture was stirred overnight at room temperature.
The mixture was evaporated under reduced pressure and extracted with ethyl actate 5 water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure. Yield: 3.3g = 90%.
'H-NMR (CDC13) 0.93 (m, 6H) 1.23 (m, 8H) 4.12 (m, 2H) 4.38 {d, d, 1H) 5.10 (s, 2H) 5.26 (d, 1H) 5.92 (m, 2H) 5.35 (m, SH) Example A-I-22 Iodometh 1~4- N-benzylox cy arbonyl-L-va~loxy)cvclohexanoate.
a) 4-Methoxybenzyl 4-hydroxycyclohexanoate.
To a solution of ethyl 4-hydroxycyclohexanoate (8.61g, 50 mmole) in 50 ml ethanol was added a solution of potassium hydroxide 85% (3.63g, 55 mmole) and the mixture was stirred for 6 hours at 70°C. The mixture was evaporated under reduced pressure, coevaporated two times with N,N-dimethylformamide and reduced to about 100 ml. 4-Methoxybenzyl chloride (9.4g, 60 mmole) was added and the mixture was 2o stirred for 18 hours at 60°C. The mixture was evaporated under reduced pressure and 250 ml ethyl acetate was added. The organic phase was washed five times with water, dried with sodiun sulfate and evaporated under reduced pressure. Yield:
13.2g =100% (crude) b) 4-methoxybenzyl4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate.
To a cooled solution of 4-methoxybenzyl 4-hydroxycyclohexanoate (7.Sg, 28 mmole), 4-dimethylaminopyridine (0.73g, 6 mmole) and N-benzyloxycarbonyl-L-valine (7.54g, 30 mmole) in dichloromethane (90 ml) was added dicylohexyl-3o carbodiimide (6.8g, 33 mmole) and the mixture was stirred for 2 days at room temperature. The mixture was cooled and the urethane was filtered. The solution was evaporated and 250 ml ethyl acetate was added.The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone.Yield :
13g = 93%
c) 4-(N-benzyloxycarbonyl-L-valyloxy) cyclohexanoic acid.
To a solution of 4-methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate (12g, 24.1 mmole} in dichloromethane (100 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred for 3 hours at room temperature. The solution was evaporated under reduced pressure and coevaporated 1o two times with toluene. The residue was stirred 1 hour with about 100 ml ethanol and the white solid was filtered (byproduct). The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography with toluene/acetone. Yield: 6.8g = 74%.
'H-NMR (CDC13) 0.91 (m, 6H) 1.52-2.54 (m, lOH) 4.28 (m, 1H) 4.82-5.08 (m, 1H) 5.11 (s, 2H) 5.28 (d, 1 H) 7.36 (m, SH) d) Chloromethyl4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate.
To a solution of 4-(N-benzyloxycarbonyl-L-valyloxy) cyclohexanoic acid (6.6g, 2o mmole) in 1,4-dioxane (70 ml) was added a 40% solution of tetrabutylammonium hydroxide {11.34g, I7.5 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 60 ml dichloromethane and iodochloromethane (30.98, 175 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 4.1g = 55%.
e) Iodomethyl 4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate.
To a solution of chloromethyl 4-{N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate (4.Og, 9.4 mmole) in dry acetone (50 ml) was added sodium iodide (6.3g, 42 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water. The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure.Yield 4.Sg = 93%.
'H-NMR (CDC13) 0.90 (m, 6H) 1.52-2.02 (m, 8H) 2.18 (m, 1H) 2.43 {m, 1H) 4.30 (m, 1H) 4.76-5.08 (m, 1H) 5.11 (s, 2H) 5.26 (d, 1H) 5.91 (d, 2H) 7.34 (m, SH) to Example A-I-23 Iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxymeth~)-2-ethyl but~rrate O
O~I
N-CBz-Valy1-'O
a) 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethylbutan-1-ol.
To a cooled solution of 2-ethyl-2-hydroxymethyl-butan-1-of (33.1 g, 250 mmole), 4 dimethylaminopyridine ( 1.22g, 10 mmole) and N-benzyloxycarbonyl-L-valine (12.6g, 50 mmole) in 350 ml dichloromethane was added dropwise a solution of dicyclohexyl-carbodiimide ( 12.4g, 60 mmole) in 50 ml dichloromethane. The mixture was stirred 2 days at room temperature and cooled. The urethane was filtered 2o and the solution evaporated under reduced pressure. 350 ml ethyl acetate was added and the organic phase was washed twice with 5% acetic acid, 5%
sodium-hydrogencarbonate and water. The organic phase was dried with sodium sulfat and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 16.4g = 90%.
c) 2-(N-benzyloxycarbonyl-L-valyloxymethyl )-2-ethyl-butyric acid.
To a cooled mixture of chromic anhydride (B.Sg, 85,2 mmole) in 100 ml acetic acid was added dropwise a solution of 2-(N-benzyloxycarbonyl-L-valyoxymethyl)-2-ethyl-butan-1-of (10.4g, 28.4 mmole) in 50 ml acetone and the mixture was stirred 24 3o hours at room temperature. The mixture was added to 1000 ml 10% sodium chloride solution and extracted four times with ethyl acetate. The organic phase was washed twice with brine, dried with sodium sulfate and evaporated under reduced pressure.
The product was isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 7g = 65%.
'H-NMR (CDCI,) 0.88 (m, 12H) 1.67 (m, 4H) 2.14 (m, 1H) 4.26 (m, 3H) 5.10 (s, 2H) 5.30 (d, 2H) 7.34 (m, SH) d) Chloromethyl 2-(N-benzyoxycarbonyl-L-valyloxymethyl -2-ethyl 1o butyrate.
To a solution of 2-(N-benzyloxycarbony-L-valyloxymethyl~2-ethyl-butyric acid (7.2g,18,9 mmole) in 1,4-dioxane (80 ml) was added a 40% solution of tetrabutylammonium hydroxide (12.26g, 18.9 mmole) and the mixture was stirred hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated once with 1,4-dioxane and two times with toluene. The dried product was dissolved in 30 ml dichloromethane and iodochloromethane (49.48, 280 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate were added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced 2o pressure. The product was isolated by silica gel column chromatography.
Yield: 5.2g = 63%.
e) Iodomethyl 2-( N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyrate.
To a solution of chloromethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyrate (S.Og, 11.7 mmole) in dry acetone (60 ml) was added sodium iodide (7.Sg, 50 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water.
The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium 3o sulfate and evaporated under reduced pressure. Yield: 5.4g = 90%.
'H-NMR (CDC13) 0.92 (m, 12H) 1.65 (m, 4H) 2.18 (m, 1H) 4.28 (m, 3H) 5.10 (s, 2H) 5.22 (d, 1 H) 5.92 (s, 2H) 7.36 (m, SH) Example A-I-24 2JN-(,iodomethoxycarbonyl -~aminol-2-meth 1-y 1-(N-benzyloxvcarbon val~yLpropane O
o NJL.o~i CBzN H o H
a) 2-(N-tert.-butyloxycarbonylamino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy}-propane.
To a cooled solution of 2-(N-(tert.-butyloxycarbonyl)-amino)-2-methylpropan-1-oI
(J. Am. Chem. Soc 113 (1991) p 8883) (4.73g, 25 mmole), 4-dirnethylamino-to pyridine (0.61g, 5 mmole) and N-benzyloxycarbonyl-L-valine (6.28g, 25 mmole) in dichloromethane (70 ml) was added dicyclohexyl-carbodiimide (6.19g, 30 mmole) and the mixture was stirred 2 days at roommtemperature. The mixture was cooled, the urethane was filtered and the solution evaporated under reduced pressure.
Ethyl acetate (200 ml) was added and the organic phase was washed twice with 5%
acetic 1s acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with,sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate.Yield: 10.28 =
96%.
b) 2-amino-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane.
2o To a solution of 2-(N-(tert.-butyloxycarbonyl)-amino-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane (lOg, 23 mmole) in dichloromethane (150 ml) was added trifluoroacetic acid (30 ml) and the mixture was stirred for 1 hour at room temperature. The solution was evaporated under reduced pressure and 10%
sodium carbonate solution was added. The product was extracted four times with 2s dichloromethane, dried with sodium sulfate and evaporated under reduced pressure.
The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 3.Og = 40% (crude) c) 2-(N-(chloromethoxycarbonyl)-amino)-2-methyl-1- (N-benzyloxycarbonyl-L-valyloxy)-propane.
To a solution of 2-amino-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane (2.9g, 9 mmole) and pyridine (2 ml) in dichloromethane (50 ml) was added 5 chloromethyl chloroformate(I.SSg, 12 mmole) and the mixture was stirred for hours at room temperature. The mixture was evaporated under reduced pressure and ethyl acetate was added. The organic phase was washed with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate.Yield: l.lg = 29%.
d) 2-(N-(iodomethoxycarbonyl)-amino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane.
To a solution of 2-(N-(chloromethoxycarbonyl)-amino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)propane (I.OSg, 2.53 mmole) in dry acetone (20 ml) was added sodium iodide (1.8g, 12 mmole) and the mixture was stirred for 36 hours at room temperature. The mixture was evaporated under reduced pressure and ethyl acetate and water were added. The organic phase was washed with 10%
sodium thiosulfate solution and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure.Yield: 1.04g = 81%.
'H-NMR (CDCI,) 0.92 (m, 6H) 1.35 (s, 6H) 2.10 (m,lH) 3.88 (m, 1H) 4.35 (m, 2H) 5.11 (s, 2H) 5.32 (d, 1H) 5.82 (s, 1H) 5.91 (s, 2H) 7.35 (m, SH) Example A-I-25 1-(2-N-CBz-L-valvlox~~)-6-oxo-1,6-dihydro~vridine-3-carboxylic acid iodometh- Iy ester O
O
O~N~
O-Cbz-Val a) 6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
To a solution of 6-hydroxynicotinic acid (4.87 g, 35 mmol) in DMF (100 mL) at room temperature, was added potassium tert-butoxide (3.93 g, 35 mmol). The reaction mixture was stirred at 60 °C for lh. 4-Methoxybenzylchloride (8.30 g, 53 mmol) was added and the reaction mixture was stirred at 60 °C for 4h.
The DMF was evaporated under vacuum, the residue was dissolved in ether (200 mL) and washed with water (3 x 100 mL). The organic phase was dried with NazS04 and evaporated to give 4.41 g of 6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl 1 o ester.
b) 1-(2-Hydroxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
To a solution of 6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl is ester (4.41 g, 17 moral) and KzC03 (2.58 g, 18.7 mmol) in DMF (100 mL) at room temperature, was added 2-bromoethanol (2.02 g, 16.2 mmol). The reaction mixture was stirred at 80 °C for 30h, whereupon the DMF was evaporated under vacuum.
The crude product was column chromatographed (silica gel, 2-~S% MeOH in CHzCl2), to give 3.91 g of 1-(2-hydroxyethyl)-6-oxo-1,6-dihydro-pyridine-3-2o carboxylic acid 4-methoxybenzyl ester.
c) 1-(2-N-CBz-L-valyloxyethyl )-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
To a mixture of DCC (5.06 g, 24.5 mmol), DMAP (318 mg, 2.6 mmol) and N-CBz-2s L-valine (6.48 g, 25.8 mmol) in CHzCIz (200 mL) at 0 °C, was added dropwise a solution of 1-(2-hydroxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4 methoxybenzyl ester (6.40 g, 24 mmol) in CHZCl2 (200 mL). After lh at 0 °C, the temperature of the reaction mixture was allowed to assume room temperature and then the mixture was stirred for Sh at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 2-~5% MeOH in CHZC12), to give 6.81 g 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 4-methoxybenzyl ester.
d) 1-(2-N-CBz-L-valyloxyethyl)-2-pyridone-5-carboxylic acid.
To a solution of 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-to carboxylic acid 4-methoxybenzyl ester (6.46 g, 12 mmol) in CHzCl2 (85 mL) at room temperature, was added trifluoroacetic acid (15 mL). After lh at room temperature, the reaction mixture was concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 3-~6% MeOH in CHZCIz), to give 4.91 g (2-N-CBz-L-valyloxyethyl)-2-pyridone-5-carboxylic acid.
i5 'H-NMR (CDC13): 12.15 (br s, 1H), 8.29 (d, J= 2.2 Hz, 1H), 7.93 (dd, J= 9.5, 2.2 Hz, 1 H), 7.31 (m, SH), 6.69 (d, J = 9.5 Hz, 1 H), 5.53 (d, 1 H), 5.07 (s, 2H), 4.52-4.05 (m, SH), 2.20-2.00 (m, 1H), 0.90 (d, 3H), 0.81 (d, 3H).
2o e) 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid chloromethyl ester.
To a solution of 1-(2-N-CBz-L-valyloxyethyl)-2-pyridone-S-carboxylic acid (4.91 g, 11.8 mmol) in dioxane (200 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (7.65 g). After stirring for 5 min, the solution was 25 evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (200 mL) and then chloroiodomethane (8.74 mL, 120 mmol) was added and the solution was stirred for 12h at room temperature:
The solution was concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off 30 and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 2-4% MeOH in CH,CIz), to give 1.80 g of 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid chloromethyl ester.
f) 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid iodomethyl ester To a solution of 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid chloromethyl ester (1.80 g, 3.87 mrnol) in acetonitrile (30 mL), was added sodium iodide (2.32 g, 15.5 mmol). The solution was stirred for 4 h at 60 °C.
The resulting suspension was filtered and the filtrate was evaporated. The residue to was dissolved in CHZC12 and washed with aqueous sodium thiosulfate (0.1 M).
The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1% MeOH in CHZC12), to give 2.04 g 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid iodomethyl ester.
'H-NMR (CDC13): 8.19 (d, J= 2.5 Hz, 1H), 7.79 (dd, J= 9.6, 2.5 Hz, 1H), 7.32 (m, SH), 6.52 (d, J = 9.6 Hz, 1 H), 6.04 (s, 2H), 5.3 8 (d, 1 H), 5.07 (s, 2H), 4.54-4.06 (m, SH), 2.20-2.00 (m, 1H), 0.91 (d, 3H), 0.81 (d, 3H).
2o Example A-I-26 Iodomethvl 5-ffN benzylox carbonyl-L-valvloxvlmethyl]-2-furoate O
\ !
O- 'NH O--~
/ O
O O
O
(a) 5-[(N Benzyloxycarbonyl-L-valyloxy)methyl]-2-furaldehyde.
A solution of 5-(hydroxymethyl)-2-furaldehyde (1.00 g, 7.69 mmol) in 5 mL dry CHZC12 was added to a mixture of N benzyloxycarbonyl-L-valine (2.40 g, 9.57 mmol), N,N'-dicyclohexylcarbodiimide (2.00 g, 9.69 mmol), and 4-dimethyl-aminopyridine ( 117 mg, 0.96 mmol) in 45 mL CHzCIz. After stirnng overnight, the reaction slurry was filtered, concentrated under vacuum, and subjected to flash column chromatography (silica, 2/1 petroleum ether - ethyl acetate to give the valine ester (quantitative yield).
(b) 5-[(N Benzyloxycarbonyl-L-valyloxy)methyl]-2-furoic acid A solution of NaClOz (2.8 mmol) in 3 mL water was added dropwise to a stirred solution of 5-[(N benzyloxycarbonyl-L-valyloxy)methylJ-2-furaldehyde (798 mg, 2.22 mmol) from step (a) in 3 mL MeCN, with cooling in an ice bath. After 2.5 h, the ice bath was removed, 2 mL more MeCN was added, and the two-phase liquid reaction mixture was stirred at room temperature for 25 h. The reaction mixture was io diluted with water, made basic with saturated NaHC03, and extracted with ethyl acetate (3 x SO mL). The separated aqueous solution was acidified to pH 2 with 5%
aqueous HCl and extracted with ethyl acetate (3 x 50 mL). This second ethyl acetate solution was washed with brine, dried over anhydrous Na2S04, and evaporated to dryness under vacuum to give the carboxylic acid (287 mg, 34%) which was used in the next step without further purification.
(c) Chloromethyl 5-[(N benzyloxycarbonyl-L-valyloxy)methylj-2-furoate.
Tetrabutylammonium hydroxide (40 wt. % solution in water, 0.55 mL, 0.84 mmol) was added to the carboxylic acid (286 mg, 0.76 mmol) from step (b) in 5 mL
2o dioxane. The yellow solution was concentrated under vacuum, coevaporating several times with dioxane, toluene, and, lastly, CHZC12. The residue was charged with mL dry CHZCIz and chloroiodomethane (0.55 mL, 7.55 mmol) was added. After stirring for 20.5 h, the reaction mixture was concentrated and subjected to flash column chromatography (silica, 2/1 petroleum ether - ethyl acetate) to give the chloromethyl ester (137 mg, 42%).
(d) Iodomethyl 5-[(N benzyloxycarbonyl-L-valyloxy)methyl]-2-furoate.
All of the chloromethyl ester (137 mg, 0.32 mmol) from step (c) was refluxed with NaI (195 mg, 1.3 mmol) in 3.2 mL dry MeCN at 70 °C for 4 h. The solvent was 3o removed under vacuum and the residue was subjected to flash column chromatography (silica, 3/1 petroleum ether - ethyl acetate) to give the iodomethyl ester (152 mg, 92%).
'H NMR (250 MHz, CDC13) 8 0.84 and 0.93 (2d, 3H each, J= 6.8 Hz), 2.16 (rn, 1H), 4.33 (dd, 1H, J= 9.1, 4.7 Hz), 5.09-5.21 (m, 4H), 5.36 (d, 1H, J= 9.1 Hz), 6.08 (s, 2H), 6.52 (d, 1H, J= 3.4 Hz), 7.19 (d, 1H, J= 3.5 Hz), 7.33 (s, SH).
Example A-I-27 Iodomethyl 4-(2-N-benzylox can 1-~ L-valyloxyethoxyl benzoate a) 4-Methoxybenzyl 4-(2-hydroxyethoxy)benzoate.
To a solution of 4-methoxybenzyl 4-hydroxybenzoate (7.Og, 27 mmole) in dry N,N-io dimethylformamide (50 ml) was added potassium carbonate (4.15g, 30 mmole) and 2-bromoethanol.The mixture was stirred 48 hours at 80°C, evaporated under reduced pressure and ethyl acetate and water were added. The organic phase was washed five times with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography 15 with hexane/ethyl acetate.Yield: 6.8g = 83%.
b) 4-methoxybenzyl4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)benzoate.
To a solution of 4-methoxybenzyl 4-(2-hydroxyethoxy) benzoate (6.6g, 21.8 mmole), 4-dimethylaminopyridine (0.61g, 5 mmole) and N-benzyloxycarbonyl-L-2o valine (6.3g, 25 mmole) in dichloromethane (80 ml) was added dicyclohexyl-carbodiimide (5.2g, 25 mmole) and the mixture was stirred overnight at room temperature. The mixture was cooled and the urethane was filtered.The solution was evaporated and ethyl acetate (200 ml) was added. The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic 25 phase was dried with sodium sulfate and evaporated under reduced pressure.
The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 10.6g = 90 %.
c) 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy)-benzoic acid.
30 To a solution of 4-methoxybenzyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) benzoate ( 10.2g, 19.04 mmole) in dichloromethane ( 100 ml) was added trifluoroacetic acid (20 ml) and the mixture was stirred 3 hours at room temperature.
The solution was evaporated under reduced pressure and co-evaporated two times with toluene. The product was isolated by silica gel column chromatography.
Yield:
6.9g = 87%.
'H-NMR (CDCl3) 0.94 (m, 6H) 2.18 (m, 1H) 4.22- 4.68 (m, SH) 5.10 (s, 2H) 6.94 (d, 2H) 7.35 (m, SH) 8.05 (d, 2H) d) Chloromethyl 4-( 2-N-benzyloxycarbonyl-L-valyloxyethoxy) 1o benzoate.
To a solution of 4-(2- N-benzyloxycarbonyl-L-valyloxyethoxy) benzoic acid (6.7g, 16.1 mmole) in 1,4-dioxane (80 ml} was added a 40% solution of tetrabutylammonium hydroxide (9.74g, 15 mmole) and the mixturewas stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and ~5 coevaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in dichloromethane (30 ml) and iodochloromethane (42.5g, 241 mmole) was added. The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 150 ml ethyl actate were added and the organic phase washed twice with water, dried with sodium sulfate and 2o evaporated under reduced pressure. The product was isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 1.2g = 17%
e) Iodomethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) benzoate.
To a solution of chloromethyl 4-(2-N-benzyloxycarbonyl-L-valyloxyethoxy) 25 benzoate (l.lg, 2.37 mmole) in dry acetone (40 ml) was added sodium iodide (l.Sg, 10.0 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water.
The organic phase was washed with a 5% sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure.Yield: 1.3g = 98%.
'H-NMR (CDC13) 0.88 (d, 3H) 0.95 (d, 3H) 2.18 (m, 1H) 4.22 (m, 2H) 4.32 (d, d, 1H) 4.50 (m, 2H) 5.10 {s, 2H) 5.22 (d, 1H) 6.14 (s, 2H) 6.90 (d, 2H) 7.35(m, 7H) 7.98 (d, 2H) Example A-I-28 Iodomethvl 4-f 3-(Cbz-L-valyloxy)-1-propel]Ibenzoate O
O O
N-O
a) t-Butyl4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate.
t-Butyl 4-(3-hydroxy-1-propyl)benzoate (Taylor et al .l. Org. Chem. 1995, 60, 7947) (3.3 g, 14 mmol), N,N'-dicychlohexyl carbodiimide (3.3 g, 16.8 mmol), CBZ-L-valine (4.2 g, 16.8 mmol) and N,N dimethylaminopyridine (0.85 g, 7 mmol) were to dissolved in a minimum amount of dichloromethane and left at ambient temperature over-night. The slurry was then filtrated and the solvent evaporated.
Purification by chromatography (dichloromethane-ether, 20:1) gave pure title compound (7 g, %).
Z 5 b) Chloromethyl 4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate t-Butyl 4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate (6.5 g, 13.8 mmol) was dissolved in dichloromethane (50 ml). Triflouroacetic acid (10 ml) was added and the mixture was left over-night. The solvent was then removed and the crude residue co-evaporated with toluene and 1,4-dioxan and dried in vacuum over-night. The dried 2o product was dissolved in 1,4-dioxane (100 ml) and tetrabutyl ammoniumhydroxide (40 w/w % in water) was added dropwise until the pH = 7-8. The solvent was co-evaported with toluene four times, and then dissolved in dichloromethane (100 ml) followed by addition of 100 g of molecular sieve (4~) and the mixture was stirred for 30 minutes. Chloroiodomethane (15 ml) was added and the reaction mixture was 25 left for five hours. Filtration and purification by chromatography (hexane-ethyl acetate, 3:1 ) gave pure title product (3.3 g, 52 %).
c) Iodomethyl4-[3-(cbz-L-valyloxy)-1-propyl]benzoate Chloromethyl 4-[3-(Cbz-L-valyloxy)-1-propyl]benzoate (3 g, 6.5 mmol) and sodium iodide (4.9 g, 32 mmol) were dissolved in acetonitril (SO ml) and heated to 65 C for 4 hours. The solvent was removed under reduced pressure and the residue was taken up in dichloromethane and filtrated. Removal of the solvent and purification by chromatography (dichloromethane-ether, 20:1) gave pure title product (2.4 g, 67 %).
'H NMR (CDC13 45 °C): 7.95 (d, 2H), 7.36-7.24 (m, 7H), 6.15 (s, 2H), 5.2 (br s, 1H), i o 5.12 (s, 2H), 4.330-4.20 (m, 1 H), 4.15 (t, 2H), 2.74 (t, 2H), 2.2-2.1 (m, 1 H), 1.99 (m, t 2H), 0.98 (d, 3H), 0.91 (d, 3H) Example A-I-29 Iodomethvl 4-f 3-(Cbz-L-isoleucyloxv)-1-propvl]Ibenzoate 0 o~i i O
O
a) t-Butyl4-[3-(Cbz-L-isoleucyloxy)-1-propyl]benzoate.
Prepared from t-butyl 4-(3-hydroxy-1-propyl)benzoate (3.5 g, 14.8 mmol) by the same procedure as described for Example A-I-28 to give the title compound (7 g, 97%).
b) Chloromethyl4-[3-(Cbz-L-isoleucyloxy)-1-propyl]benzoate.
Prepared from the material of step a) (6.9 g, 14.4 mmol) by the procedure described in Example A-I-28 to give the title compound (3.8 g, 55%) as a colourless oil.
c) Iodomethyl4-[3-(Cbz-L-isoleucyloxy)-1-propyl]benzoate.
Prepared from the product of step b (3.26 g, 6.8 mmol) by the same procedure as for Example A-I-28 to give pure title compound. (3.46 g, 90 %).
'H NMR (CDC13 45 °C): 7.98-7.93 {m, 2H), 7.35-7.23 (m, 7H), 6.15 (s, 2H), 5.25-5.15 (br s, 1H), 5.13 (s, 2H), 4.32 (m, 1H), 4.12 (t, 2H), 2.74 (t, 2H), 1.94 (m, 2H), 1.86 (m, 1H), 1.5-1.4 (m, 1H), 1.25-1.15 (m, 1H), 0.95-0.86 (m, 6H).
Example A-I-30 Iodomethvl 2-( N-benzylox carbonylamino-2-meth~propionvlox~
1 o methyl 1-2-methyl propionate a) 2-benzyloxycarbonylamino-2-methyl propionic acid.
To a solution of sodium carbonate (13.3g, 125 mmole) in water (100 ml) was added 2-amino-2-methylpropionic acid (S.Og, 50 mmole) and the mixture was stirred for 30 minutes. The solution was cooled to about 10°C and a 50% solution of benzyl chloroformiate (20.Sg, 60 mmole) was added dropwise. The mixture was stirred at roomtemperature overnight and acidified with 2M hydrochloric acid. The mixture was extracted two times with ethyl acetate. The organic phase was washed with water, dried with sodium sulfate and evaporated under reduced pressure. The product 2o was isolated by silica gel column chromatography with hexane/ethyl acetate.
Yield:
7.7g = 64%
b) 4-methoxybenzyl2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate.
To a cooled solution of 4-methoxybenzyl 2-(hydroxymethyl)-2-methyl propionate (3.6g, 15 mmol), 4-dimethylaminopyridine (0.37g, 3 mmole) and 2-benzyloxycarbonylamino-2-methylpropionic acid (3.8g, 16 m-mole) in dichloromethane (60 ml) was added dicyclohexyl-carbodiimide (3.7g, 18 mmole) and the mixture was stirred overnight at room temperature.The mixture was cooled and 3o the urethane was filtered. The solution was evaporated and 150 ml ethyl acetate were added, The organic phase was washed twice with 5% acetic acid, 5% sodium hydrogencarbonate and water. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene / acetone. Yield: 6,2g =91 c) 2-(benzyloxycarbonylamino-2-methylpropionyloxymethyl )-2-methylpropionic acid.
To a solution of 4-methoxybenzyl 2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2methyl propionate (6,1 g, 13,3 mmole) dichloromethane (50 ml) was added trifluoro acetic acid (10 ml) and the mixture was stirred 3 hours at room temperature. The solution was evaporated under reduced 1o pressure and coevaporated two times with toluene. The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 4.1g =
91%
'H-NMR (CDCI,) 1.22 (s, 6H) 1.52 (s, 6H) 4.13 (m, 2H) 5.07 (s, 2H) 5.44 (s, 1H) i5 7.33 (m, SH) d) Chloromethyl 2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate.
To a solution of 2-(2-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-2o methyl propionic acid (4.Og, 11.8 mmole) in 80 ml 1,4-dioxane was added a 40%
solution of tetrabutylammonium hydroxide (7.Sg, 11.5 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene.
The dried product was dissolved in 20 ml dichloromethane and iodochloromethane 25 (31.7g. 180 mmole) was added. The solution was stirred overnight at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate were added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with toluene/acetone. Yield: 2.Og = 45%.
e) Iodomethyl 2-( N-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate.
To a solution of chloromethyl 2-(N-benzyloxycarbonylamino-2-methylpropionyloxymethyl)-2-methyl propionate (1.9g, 4.92 mmole) in 50 ml dry acetone was added sodium iodide (3.Og, 20 mmole) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and extracted with ethyl actate water. The organic phase was washed with a 5%
sodium thiosulfate solution, dried with sodium sulfate and evaporated under reduced pressure.
Yield: 2,1 g.
to 'H-NMR (CDC13) 1.20 (s, 6H) 1.53 (s, 6H) 4.13 (s, 2H) 5.07 (s, 2H) 5.30 {s, 1H) 5.90 (s, 2H) 7.35 (m, SH) Example A-I-31 Iodomethvl2-methvl-2-(N-benzvlox carbonyl-L-alanyloxvmethyl)pro~ionate The title compound (alternative nomenclature 2,2-dimethyl-3-(CBz-alanyloxy)-propioic acid iodomethyl ester) is prepared in a similar manner as described in Example A-I-10 using N-CBz protected L-alanine in place of N-CBz-D-valine.
20 'H-NMR. (CDCI3): 7.33 (m, 5H), 5.91 (m, 2H), 5.11 (s, 2H), 4.38 (m, 1H), 4.14 (m, 2H), 1.40 (d, 3H), 1.21 (d, 6H).
Example A-I-32 Iodomethyl 3-(N-CBz-L-valvloxy)-2-metl~l-propionate O
N-CBz-L-Val-O O~I
a) 3-(N-CBz-L-valyloxy)-2-methyl-1-propano I .
To a mixture of DCC (16.5 g, 80 mmol), DMAP (0.977 g, 8 mmol) and N-CBz-L-3o valine {20.1 g, 80 mmol) in CHzCIz {400 mL)-at 0 °C, was added dropwise a solution of 2-methyl-1,3-propanediol (72.1 g, 800 mrnol) in CHZCIz (100 mL). After lh at 0 °C, the temperature of the reaction mixture was allowed to assume room temperature and then the mixture was stirred for 16h at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure.
The crude product was column chromatographed (silica gel, 5% MeOH in CHZCIz}, to give 20.3 g 3-(N-CBz-L-valyloxy)-2-methyl-1-propanol.
b) 3-(N-CBz-L-valyloxy)-2-methyl-propionic acid.
To a solution of Cr03 (4.29 g, 42.9 mmol) in HOAc (50 mL) at 20 °C, was added dropwise a solution of 3-(N-CBz-L-valyloxy)-2-methyl-1-propanol (4.61 g, 14.3 1 o mmol) in aceton (25 mL). After stirnng for 24h, water (300 mL) was added and the reaction mixture was extracted with CHZCIz (4x200 mL) . The combined organic layers was concentrated under reduced pressure. The residue was column chromatographed (silica gel, 5-10% MeOH in CHzCIz), to give 3.10 g of 3-(N-CBz-L-valyloxy)-2-methyl-propionic acid.
'H-NMR (CDC13): I I.54 (br s, IH), 7.33 (s, SH), 5.48 (d, 1H), S.11 (s, 2H), 4.40-4.00 (m, 3H), 2.95-2.70 (m, 1H), 2.25-2.05 (m, IH), 1.30-1.12 (m, 3H), 0.95 (d, 3H), 0.87 (d, 3H).
2o c) Chloromethyl3-(N-CBz-L-valyloxy)-2-methyl-propionate.
To a solution of 3-(N-CBz-L-valyloxy)-2-methyl-propionic acid (3.10 g, 9.2 mmol) in dioxane (100 mL), was added dropwise a 40% aqueous solution of tetrabutylammonium hydroxide (5.97 g). After stirring for 5 min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (6.70 mL, 92 mmol) was added and the solution was stirred for 6h at room temperature.
The solution was concentrated under reduced pressure and the residue was shaken with hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and 3o the filtered through anhydrous sodium sulfate and evaporated to dryness.
The residue was column chromatographed (silica gel, 0.5-2% MeOH in CHZC12), to give 1.90 g of chloromethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate.
d) Iodomethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate.
To a solution of chloromethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate (1.84 g, 4.77 mmol) in acetonitrile (50 mL), was added sodium iodide (2.86 g, 19.0 mmol).
The solution was stirred for 3.5 h at 60 °C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CHZC12 and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1% MeOH in CHZCIz), to give 1.78 g of iodomethyl (N-CBz-L-valyloxy)-2-methyl-propionate.
'H-NMR (CDCl3): 7.35 (s, SH), 5.90 (s, 2H), 5.25 (d, 1H), 5.10 (s, 2H), 4.36-4.18 (m, 3H), 2.94-2.73 (m, 1H), 2.26-2.08 {m, 1H), 1.28-1.18 (m, 3H), 0.96 (d, 3H), 0.87 (d, 3H).
IS
Example A-I-33 Iodometh~(N-CBz-L-t-butyl~lvcvloxy,)-2 2-dimeth~rlnropionate O O~~
CBzHN
O O
a) 4-Methoxybenzyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-2o dimethylpropionate.
To a mixture of DCC (4.95 g, 24 mmol), DMAP (293 mg, 2.4 mmol) and N-CBz-L-t-butylglycine (6.37 g, 24 mmol) in CHzCl2 (100 mL) at 0 °C, was added dropwise a solution of 4-methoxybenzyl 2,2-dimethyl-3-hydroxypropionate (2.86 g, I2 mmol) in CHzCl2 (50 mL). After lh at 0 °C, the temperature of the reaction mixture was 25 allowed to assume room temperature and then the mixture was stirred for 48h at room temperature. The mixture was filtered through a glass filter and the solvent was removed under reduced pressure. The crude product was column chromatographed (silica gel, 1-2% MeOH in CHZC12), to give 5.60 g 4-methoxybenzyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
b) 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionic acid To a solution of 4-methoxybenzyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate (5.60 g, 11.5 mmol) in CHzCl2 (90 mL) at room temperature, was added trifluoroacetic acid (10 mL). After lh at room temperature, the reaction mixture was concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 3--~S% MeOH in CHZC12), to give 2.70 g of 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionic acid.
'H-NMR (CDCl3): 11.2 (br s, 1H), 7.34 (s, SH), 5.44 (d, 1H), 5.11 (s, 2H), 4.25-4.03 to (m, 3H), 1.32-1.22 (m, 6H), 0.97 (s, 9H).
c) Chloromethyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
To a solution of 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionic acid (2.70 g, 7.38 mmol) in dioxane (100 mL), was added dropwise a 40% aqueous solution of 15 tetrabutylammonium hydroxide (4.79 g). After stirnng for S min, the solution was evaporated to dryness through co-evaporation with dioxane and toluene. The residue was dissolved in dichloromethane (100 mL) and then chloroiodomethane (5.37 mL, 73.8 mmol) was added and the solution was stirred for 6h at room temperature.
The solution was concentrated under reduced pressure and the residue was shaken with 2o hexane / ethyl acetate (1:1 v/v, 200 mL). The yellow crystalline solid was filtered off and the filtrate was washed with aqueous solution of sodium thiosulfate (0.1 M) and the filtered through anhydrous sodium sulfate and evaporated to dryness. The residue was column chromatographed (silica gel, 0.5-1% MeOH in CH2C12), to give 2.44 g of chloromethyl 3-(N-CBz-L-t-butylglycyloxy}-2,2-dimethylpropionate.
d) Iodomethyl3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
To a solution of chloromethyl 3-(N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate (2.44 g, 5.90 mmol) in acetonitrile (SO mL), was added sodium iodide (3.54 g, 23.6 mmol). The solution was stirred for 3.S h at 60 °C. The resulting suspension was 3o filtered and the filtrate was evaporated. The residue was dissolved in CHZCIz and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2S04) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 1 % MeOH in CHzCIz), to give 2.61 g of iodomethyl (N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionate.
'H-NMR (CDCI,): 7.32 (s, SH), 5.89-5.82 (m, 2H), 5.40 (d, 1H), 5.07 (s, 2H), 4.17 (d, 1H), 4.11 (s, 2H), 1.22-1.19 (m, 6H), 0.95 (s, 9H).
Example A-I-34 N benzyloxycarbonvl-traps-4-(N be loxycarbonvl-L-valyloxy~ L~roline iodometh, 1 ester.
O ~CBz O
O
to CBzNH O'/I
(a) N benzyloxycarbonyl-traps-4-hydroxy-L-proline p-methoxybenzyl ester.
Cesium carbonate ( 1.23 g, 3.78 mmol) was added to a stirred solution of N
benzyloxycarbonyl-traps-4-hydroxy-L-proline (2.00 g, 7.54 mmol) in 20 mL dry 15 DMF. After 15 min, p-methoxybenzyl chloride ( 1.25 mL, 9.21 mmol) was added and the mixture was stirred for 17 h. The solvent was evaporated under vacuum, and the residue was partitioned between EtOAc (100 mL) and water (50 mL).The organic phase was washed with water (2 x 25 mL), dried over anhydrous Na2S04, and concentrated. Flash column chromatography (silica gel, 2/1 EtOAc - petroleum ether) 2o gave 2.69 g (92%) of the p-methoxybenzyl ester.
(b) N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-proline p-methoxybenzyl ester.
A mixture of N benzyloxycarbonyl-traps-4-hydroxy-L-proline p-methoxybenzyl 25 ester (2.54 g, 6.59 mmol), N benzyloxycarbonyl-L-valine (1.82 g, 7.24 mmol), 4-dimethylaminopyridine (90 mg, 0.7 mmol), and dicyclohexylcarbodiimide (1.64 g, 7.95 mmol) in 26 mL dry CHZCIz was stirred overnight. The slurry was filtered, and the filtrate was concentrated under vacuum to give an oil that was subjected to flash column chromatography (silica gel, 3/1 and~then 2/1 petroleum ether - EtOAc) to 3o yield 3.70 g ( 91 %) of the title compound.
(c) N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-proline chloromethyl ester.
The p-methoxybenzyl group was removed by stirnng a solution of the compound (2.47 g, 4.0 mmol) from step (b) and 8 mL CF,COOH in 40 mL CHZCl2 for 30 min.
The reaction mixture was concentrated under vacuum, coevaporating several times with more CHzCl1 and toluene. A second sample (1.14 g, 1.84 mmol) was treated similarly. The crude products obtained from both samples were combined and subjected to flash column chromatography (silica gel, 15% methanol in CHzCh to to give 2.58 g of cream-colored solids containing N benzyloxycarbonyl-traps-4-(N
benzyloxycarbonyl-L-valyloxy)-1.-proline (TLC 15/85 MeOH/CHZCIz Rf = 0.25).
This material ( 1.14 g) was dissolved in 10 mL dioxane. Tetrabutylammonium hydroxide ( 1.15 mL of a 40 wt % solution in H20, 1.76 mmol) was added, the mixture was evaporated to dryness, and the residue was coevaporated several times 15 with toluene and, lastly, CHzCl2. The resulting. Q salt was stirred with chloroiodomethane (1.30 mL, 17.8 mmol) in dry CHZCIz (20 mL) for 20 h. The solvent was removed under vacuum, 25 mL of 2/1 petroleum ether - EtOAc was added, and the precipitates which formed were filtered. Concentration of the filtrate, followed by flash column chromatography (silica gel, 4/1 and then 2/1 petroleum 2o ether - EtOAc) gave the chloromethyl ester (580 mg) as white solids.
(d) N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-proline iodomethyl ester.
The chloromethyl ester (533 mg, 0.974 mmol) from step (c) and NaI (594 mg, 3.96 25 mmol) were refluxed in dry MeCN (10 mL) at 75 °C for 4 h. After removal of solvent under vacuum, the mixture was partitioned between 20 mL EtOAc and 10 mL water.
The organic phase was washed with S% NazSz03 and then brine, dried over anhydrous NazS04, and concentrated. Flash column chromatography (silica gel, petroleum ether - EtOAc) gave the iodomethyl ester (526 mg, 84%) as white solids.
'H NMR (2S0 MHz, CDC1,) 8 0.86 and 0.94 (2d, 3H each, J= 6.8 Hz), 2.13 (m, 2H), 2.31 (m, 1H), 3.65-3.80 (m, 2H), 4.24 (m, 1H), 4.43 (m, 1H), 5.03-5.19 (m, 4H), 5.30 (br s, 1H), 5.54 (br d, 1H), 5.70 and 5.83-5.97 (s and ABq, 2H total), 7.30-7.32 (m, 1 OH).
Prodru~~s of the invention 4-amino-1-hydroxvbutvlidene-1 1-bisphosphonic acid tri(2 meth 1 valvloxvmethyl~propionvloxvmeth 11 ester.
to a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, tri(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyl-oxymethyl) ester and 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyloxymethyl) ester.
15 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid is prepared by the methodology in Kieczykowski et al, J Org Chem 1995, 60, 8310-8312, and the 4-amino group CBz protected as shown in US 5 227 506. To a solution thereof (195 mg, 0.51 mmole) in dry N,N-dimethylformamide (2 m1), was added diisopropylethyl-amine (0.27 ml, 1.53 mmole), followed by an injection of a solution of iodomethyl 2-2o methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionate (626 mg, 1.27 mmole) in N,N-dimethylformamide (2 mI). After stirnng under argon for 2,5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (10 ml). Crystals were f Itered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate. The organic phase was filtered 25 through anhydrous sodium sulfate and evaporated. The title compounds were isolated by silica gel column chromatography (0-4, 7-8, 20-30% ethanol in dichloromethane).
Triester (70 mg). Rf ( 10%MeOH/ CHC13) 0.45. 'H-NMR (CDC13): 7.30 (m, 20H), 5.85-5.43 (m, 9H), 5.08 (m, 8H), 4.36-3.95 (m, 9H), 3.10 (m, 2H), 2.15-1.75 (m, 30 7H), 1.19 (s, 18H), 0.86 (m, 18H).3'P-NMR (CDC13+1%CD30D) (H3P04 reference):
8 23.8 (d), 11.8(d);
Diester (185 mg), R~(10%MeOH/ CHC13) 0.10 (at the center of oval spot from baseline). 'H-NMR (CDC13+1 %CD30D): 7.31 (m, 15H), 5.79-5.63 (m, 4H), 5.08 (m, 6H), 4.35-4.10 (m, 6H), 3.10 (m, 2H), 2.18-1.70 (m, 6H), 1.19 (m, 12H), 0.87 (m, 12H). 3'P-NMR (CDC13+1%CD,OD)(H3P04 reference): 8 16.6 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, tri(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester.
A solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid tri(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyloxymethyl) to Ester (203 mg, 0.136 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (8.7 ml) was hydrogenated over a Pd-black catalyst (93 mg) at 40 psi of hydrogen for 16 h. The suspension was filtered through Celite on a fine pore sized glassinter and washed with methanol/ethyl acetate (2:1 ). The filtrate was evaporated to dryness in vacuo and the title compound as the tetra acetate was obtained as a white solid after a 1 s few co-evaporations with dioxane and hexane.
3'P-NMR (CDC13+5%CD,OD)(H3P04 reference): 8 23.1 (m), 11:1 (m).
Example A-2 20 4Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid dil2 methyl 2 (L
val loxYmethyl~ronionvloxvmethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionyloxymethyl) ester (130 25 mg, 0.112 mmol) was hydrogenated over Pd-black (48 mg) by the method of Example A-1 b), to give the title compound as the triacetate as a white solid (90 mg).
3'P-NMR (CDC13+5%CD30D)(H3P04 reference}: 8 16.2 (br, s).
3o Example A-3 4-Amino-1-hydroxvbutylidene-1 1-bisphOSphonic acid di(2 methyl 2 ~~L va~loxyl propionyloxymethyll ester WO 99/51613 PCT'/SE99/00528 a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxy) propionyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (306 mg, 0.80 mmole) was esterified by the method described in Example A-1-a. After silica gel column chromatography (2-4, 6-12, 15-20% ethanol in dichloromethane), the pure fractions containing the title compound were pooled together and evaporated.
The residue was then dissolved in ethyl acetate and the solution extracted twice with 1o aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. (116 mg of title compound). Rf. (20%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDC13+1%CD,OD): 7.28 (m, 15H), 5.60 (m, 4H), 5.05 (m, 6H), 4.13 (m, 15 2H), 3.09 (m, 2H), 2.19-1.72 (m, 6H), 1.49 (m, 12H), 0.89 (m, 12H). "P-NMR
(CDCl3+1 %CD30D)(H3P04 reference): 8 15.3 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester.
20 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-2-(N-benzyloxycarbonyl-L-valyloxy) propionyloxymethyl) ester (116 mg, 0.107 mmol) was hydrogenated over Pd-black (46 mg) by the method of Example A-1-b, to give the title compound as the triacetate as a white solid (71 mg).
25 3'P-NMR (CDC13+S%CD,OD)(H3P04 reference): 8 14.9 (s).
Example A-4 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosnhonic acid di (2-~L valyloxy~ 3 methyl ~S)~+~utyr5rloxymethXl) ester.
a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-l,l-bisphosphonic acid, di (2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (383 mg, 1 mmole) was esterified by the method described in Example A-3-a to yield 184 mg of title compound. Rf (20%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDCl3+ 1 %CD30D): 7.27 (m, 15H), 5.62 (m, 4H), 5.15-4.72 (m, 8H), 4.32 (m, 2H), 3.08 (m, 2H), 2.16-1.73 (m, 6H), 0.88 (rn, 24H). "P-NMR
(CDCI,+1%CD30D)(H3P04 reference): 8 15.5 (s).
io b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di (2-(L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di (2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyryloxymethyl) ester (184 mg, 0.166 mmol) was hydrogenated over Pd-black (71 mg) by the method of Example A-i5 1-b, to give the title compound as the triacetate as a white solid (95 mg).
3'P-NMR (CDC13+5%CD30D)(H3P04 reference): b 14.6 (s).
Example A-5 20 4-amino-1-hvdroxvbutvlidene-1 1-bisph~ osnhonic acid mono 2 methyl 2 (L
val~ymethyl) nropionyloxymethyl~ ester.
a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, tribenzyl mono (2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) 25 propionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-I-hydroxybutylidene-1,1-bisphosphonic acid (1.54 g, 4 mmole) in dry N,N-dimethylformamide (24 ml), heated at 50 °C, was added diisopropylethylamine (2.78 ml, 16 mmole), followed by dropwise addition of benzylbromide ( 1.9 ml, 16 mmole). After stirring under argon for 4 h, the solution 3o was concentrated on rotavapor and treated with ethyl acetate (20 ml).
Crystals were filtered off and the filtrate was extracted with brine. The organic phase was filtered through anhydrous sodium sulfate and evaporated. The 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, tribenzylester was isolated by silica geI
column chromatography (2-4, 7-10, 15-20% ethanol in dichloromethane). The pure fractions containing the pure triester were pooled together and evaporated.
The residue was then dissolved in ethyl acetate and the solution extracted three times with 2M aqueous solution of citric acid. Triester (990 mg); Rf (20%MeOH/ CHC13) 0.15 (at the center of oval spot from baseline);
3'P-NMR (CDC13) (H3P04 reference): 8 20.4(d), 13.3 (d); 'H-NMR (CDCI3): 7.35-7.10 (m, 20H), 5.20-4.91 (m, 8H), 4.60 (br, 1H), 3.00 (m, 2H), 2.12-1.75 (m, 4H).
1o b) Dried tribenzyl ester (395 mg) was dissolved in dry N,N-dimethylformamide (3 ml), followed by addition of diisopropylethylamine (99 ml) and a solution of iodornethyl 2-methyl-2-(N-benzyloxycarbonyl-L-valyloxymethyl) propionate (737 mg) in N,N-dimethylformamide (1 ml). After stirring under argon for 4 h at 30 °C, the solution was concentrated to dryness on rotavapor and treated with ethyl acetate (10 ml). Crystals were filtered off and the filtrate was extracted with brine brine containing a small amount of sodium thiosulfate. The organic phase was filtered through anhydrous sodium sulfate and evaporated. The title compound (84 mg) was isolated by silica gel column chromatography (1, 2, 3% ethanol in dichloromethane). Rf (2%MeOH/ CHCI3) 0.60;
3'P-NMR (CDC13) (H3P04 reference): 8 16.4(m). 'H-NMR (CDC13): 7.28 (m, 25H), 5.22 (d, 1H), 5.62-5.53 (m, 3H), 5.07, 5.04 (2xs, lOH), 4.93 (br, 1H), 4.27 (d,d, 1H), 4.1 S (d,d, 2H), 3.11 (m, 2H), 2.13-1.77 (m, SH), 1.17 (s, 6H), 0.92 (d, 3H), 0.83 (d, 3H).
c) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid, mono (2-methyl-2-(L -valyloxymethyl) propionyloxyrnethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid tribenzyl mono (2-methyl-2-(N-benzyloxycarbonyl-L-valyloxyrnethyl) propionyloxymethyl) 3o ester (84 mg, 0.083 mmol) was hydrogenated over Pd-black (60 mg) by the method of Example A-1-b, to give the title compound as a white solid (35 mg).
3'P-NMR (CDC13+5%CD30D)(H3P04 reference): 8 14.5 (m).
Example A-6 4-amino-1-hvdroxvbutvlidene-1 1-bis~hosphonic acid di l2-l-L valyloxy) 2 phenyl DL-acetyloxvmethyll ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (192 mg, 0.5 mmole) was esterified with the corresponding iodomethyl ester by the method described in Example A-3-a to yield 72 mg of the title compound as the tri-N-CBz protected form, ready for deprotection. Rf (20%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDCl3+ 1 %CD30D): 7.44-7.10 (m, 25H), 5.94 (m, 2H), 5.59 (m, 2H), 5.18-4.85 (m, 6H), 4.36 (m, 2H), 3.00 (m, 2H), 2.12-1.63 (m, 6H), 0.95 (m, 12H).
3'P-NMR (CDC13+1%CD,OD)(H3P04 reference): 8 15.5 (s).
Example A-7 4-amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di 111 3 di valvloxy)prop,Yl 2 ox carbonyloxy methvll ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (141 mg, 0.37 mmole) was esterified from the corresponding iodomethyl ester by the method described in Example A-1-a to yield 90 mg of title compound as the tri CBz protected form, ready for deprotection. Rf (10%MeOH/CHC13) 0.20 (at the center of oval spot from baseline). (153 mg of mixture of the diester and triester).
'H-NMR (CDC13+ 1 %CD30D) of title compound: 7.29 (m, 25H), 5.65 (m, 4H), 5.14-4.85 (m, 12H), 4.45-4.05 (m, 12H), 3.11 (rn, 2H), 2.14-1.76 (m, 8H), 0.87 (m, 24H).
3'P-NMR (CDCl3+1 %CD,OD)(H3PO4 reference): 8 16.7 (s).
Example A-8 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di l2-L-valyloxYl DL
propionyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (158 mg, 0.41 mmole) was esterified from the corresponding iodomethyl ester by the method described in Example A-3-a to yield 110 mg of the title compound as the tri N-Boc protected from, ready for deprotection. Rf (20%MeOH/CHCl3) 0.15 (at the center of oval spot from baseline).
'H-NMR (CDCI,+1%CD30D): 7.29 (m, 15H), 5.65 (m, 4H), 5.15-4.95 (m, 8H), 4.33 (m, 2H), 3.09 (m, 2H), 2.22-1.74 (m, 6H), 1.52 (m, 6H), 0.92 (m, 12H). 3'P-NMR
(CDC13+1 %CD30D)(H,P04 reference): 8 16.8 (s).
Example A-9 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di l5 ~L valYloxv) 2 2 dimethvlvalervloxXlneth Il ester a) 4-Benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(S-(N-CBz-L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (575 mg, 1.50 mmol) in DMF (10 mL), was added diisopropylamine (0.78 mL, 4.5 mmol), followed by an injection of a solution of give iodomethyl 5-(N-CBz-L-valyloxy)-2,2-dimethylvalerate (1.95 g, 3.75 mmol) in DMF (5 mL). After stirnng under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mI,). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate.
The organic phase was filtered through anhydrous sodium sulfate and evaporated.
After silica gel column (silica gel, 4-X20% MeOH in CHZCl2), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl 3o acetate phase was evaporated, to give 171 mg of 4-benzyloxy carbonylamino-1 hydroxybutylidene-1,1-bisphosphonic acid di-(5-(N-CBz-L-valyloxy)-2,2 dimethylvaleryloxymethyl) ester.
'H-NMR (CDC13): 7.30 (br s, 15H), 5.85-5.25 (m, 4H), 5.20-4.95 (m, 6H), 4.30-3.95 (m, 6H), 3.18-3.00 (m, 2H), 2.20-1.75 (m, 6H), 1.7-1.4 (m, 8H), 1.3-1.0 (s, 12H), 1.0-0.8 (m, 12H).
s "P-NMR (CDC13)(H,PO4 reference): 16.0 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester.
to A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(5-(N-CBz-L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester (171 mg, 0.147 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst (30 mg) at 40 psi of hydrogen for 6 h.
The suspension was filtered through celite and the filtrate was evaporated to dryness 15 under reduced pressure, to give 95 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(5-(L-valyloxy)-2,2-dimethylvaleryloxymethyl) ester was obtained as a white solid.
'H-NMR (CDCI,): 5.75-5.30 (m, 4H), 5.20-4.95 (m, 6H), 4.20-3.80 (m, 6H), 3.00-20 2.80 (m, 2H), 2.20-1.40 (m, 14H), 1.3-1.0 (m, 12H), 1.0-0.8 (m, 12H).
3'P-NMR (CDC13+CD3pD)(H,P04 reference): 8 17.3 (br s) Example A-10 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di-((2 (L valylo~) 25 ethox carbonvloxv) methyl) ester a) 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(N-CBz-L-valyloxy)-ethoxycarbonyloxy) methyl) ester To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 3o acid (550 mg, 1.44 mmol) in DMF (10 mL), was added diisopropylamine (0.75 mL, 4.32 mmol), followed by an injection of a solution of 2-(N-CBz-L-valyloxy)-ethyl iodomethyl carbonate (1.40 g, 3.60 mmol) in DMF (5 mL). After stirnng under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mL). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate. The organic phase was filtered through anhydrous sodium sulfate and evaporated. After silica gel column (silica gel, 4-X20% MeOH in CHZC12), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 160 mg of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(N-CBz-L-valyloxy}-ethoxycarbonyloxy) methyl) ester.
'H-NMR (CDC13): 7.29 (br s, 15H), 5.90-5.30 (m, 4H), S.1 S-4.90 (m, 6H), 4.50-4.00 (m, 10H), 3.18-3.00 (m, 2H), 2.20-1.50 (m, 6H), 1.05-0.80 (m, 12H).
"P-NMR (CDCl3)(H,P04 reference): 16.5 (s}.
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester.
A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(N-CBz-L-valyloxy)-ethoxycarbonyloxy) methyl) ester (160 mg, 0.147 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was 2o hydrogenated over a Pd-black catalyst (30 mg) at 40 psi of hydrogen for 7 h. The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 100 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-((2-(L-valyloxy)-ethoxycarbonyloxy) methyl) ester was obtained as a white solid.
'H-NMR (CDC13): 5.80-5.40 (m, 4H), 4.70-4.05 (m, l OH), 4.4-4.2 (m, 4H), 3.00-2.80 (m, 2H), 2.20-1.50 (m, 6H), 1.05-0.80 (m, 12H).
3'P-NMR (CDC13+CD30D)(H3P04 reference): b 17.5 (br s).
3o Example A-11 4-Amino-1-hvdroxvbutvliden-1 1-bisphosphonic acid bis j2 2 dimethvl 3 (D
valvloxyl-~ropion~vmethyl~! ester WO 99/51613 PCT/SE99/O(lSZ8 a) 4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid bis [2,2-dimethyl-3-(N-CBZ-D-valyloxy)-propionyloxymethylJ ester To a solution of 4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid (382 mg, 1 mmole) and diisopropylethyl (0.43 ml, 2.5 mmole) in DMF (3 ml) at -40° C was added 2,2-dimethyl-3-(N-CBz-D-valyloxy)-propionic acid iodomethyl ester (1.23 g, 2.5 mmole) in DMF (4 ml). The reaction was kept at 0° C
for 2.5 hr and then at 4° C for 18 hr. The reaction mixture was evaporated in vacuo and ethyl acetate (20 ml) was added. The precipitate was filtered off and the organic phase was to washed with sodium bicarbonate aqueous solution and dried. The product was isolated with silica gel column chromatography. 125 mg.
'H-NMR (CDCI3): 7.31 (m, 15 H) 5.71 (m, 4 H) 5.58 (d, 2 H) 5.12 (s, 4H) 5.05 (s, 2H) 4.30 (dd, 2H) 4.12 (m, 4 H) 3.18 (m, 2H) 2.05 (m, 6 H) 0.92 (dd, I2 H).
3'P-NMR (CDC13): 15.1 b) 4-Amino-1-hydroxybutyliden-1,1-bisphosphonic acid bis [2,2-dimethyl-3-(D-valyloxy)-propionyloxymethyl] ester.
4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid bis [2,2-dimethyl-3-(N-CBZ-D-valyloxy)-propionyloxymethyl) ester (130 mg) was dissolved in a mixed solvent of EtOAc/MeOH/AcOH (6 ml/3 ml/1.5 ml). To the solution was added palladium black (60 mg). The reaction was kept under hydrogen atmosphere (40 psi) until sampling showed the complete deprotection of the benzyloxycarbonyl groups. The reaction mixture was filtered, and then dried and coevaporated with 2s toluene and methanol, giving the titled product. 102 mg.
3'P-NMR ( CDC13 + CD30D ) : 14.1 Example A-12 4-Amino-I-h~droxybutvliden-1 1-bisnhosnhonic acid bis j4 (N CBz L valvloxv) butanoyloxvmethyl]! ester a) 4-Benzyloxycarbonylamino-1-hydroxybutyliden-I,1-bisphos~t~ni~~tcitt'tiiS
[4-(N-CBz-L-valyloxy)-butanoyloxymethyl] ester.
4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid (573 mg, 1.5 mmole) was dissolved in dioxane (10 ml). To the solution was added tetrabutylammonium hydroxide (40 %, 2.43 ml, 3.75 mmole). The solution was evaporated and coevaporated with DMF several times. The residue was dissolved in DMF (5 ml). To the solution was added 4-(N-CBz-L-valyloxy) butyric acid iodomethyl ester ( 1.79 g, 3.75 mmole) in DMF (S ml) portionwise in one hour.
The reaction was kept at room temperature for 3 hr and then evaporated in vacuo.
Later, 1 o ethyl acetate (20 ml) was added. The precipitate was filtered off and the organic phase was washed with sodium bicarbonate aqueous solution and dried. The product was isolated with silica gel column chromatography. 135 mg.
'H-NMR (CDC13):7.25 (m, 15 H) 5.60 (m, 6 H ) 5.05 (m, 8H) 4.30-3.90 (m, 6 H) 3.10 (m, 2 H) 2.50-1.80 (m, 14 H) 0.85 (m, I2 H).
3'P-NMR (CDC13): 13.7.
b) 4-amino-1-hydroxybutyliden-I,I-bisphosphonic acid bis 4-(L-valyloxy)-butanoyloxymethyl] ester.
4-Benzyloxycarbonylamino-I-hydroxybutyliden-I,1-bisphosphonic acid bis [4-(N-CBz-L-valyloxy)-butanoyloxymethyl] ester (100 mg) was dissolved in a mixed solvent of EtOAc/MeOH/AcOH (6 ml/3 ml/1.5 ml). To the solution was added palladium black (80 mg). The reaction was kept under hydrogen atmosphere (40 psi) until sampling showed the complete deprotection of the benzyloxycarbonyl groups.
The reaction mixture was filtered, and then dried and coevaporated with toluene and methanol, giving the titled product. 70 mg.
3'P-NMR (CD,OD): 17.7 3o Example A-13 4-amino-1-hydroxybutvliden-1 1-bisphosphonic acid di (3 (L valyloxy) benzovlox~methyl) ester WO 99/51613 PC"f/SE99/00528 a) 4-B enzyloxycarbonylamino- I -hydroxybutyliden-1,1-bisphonic acid, di-(3-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-biphosphonic acid (0.59g, I.5 mmole) and diisopropylethyl-amine (0.64g, S mmole) in N,N-dimethylformamide (40 ml) was added dropwise a solution of iodomethyl-3-(N-benzyloxycarbonyl-L-valyloxy)-benzoate (2.2g, 4.3 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (50 1o ml) was added and the mixture was filtered after 2 hours. The organic phase was washed twice with 5% sodium hydrogencarbonate solution and dried with sodium sulfate. The product was isolated by silica gel column chromatography.
Yield: 0.23g = 15%
'H-NMR (CDCI3 + 5% CD30D) 0.89 (m, 12H) 1.58-2.28 (m, 6H) 2.92 (m, 2H) 4.26 (m, 2H) 5.00 (m, 6H) 5.46-6.02 (m, 4H) 6.78- 7.86 (8m, 23H) 3'P-NMR (CDCl3 + 5% CD30D) 16.5 (s) b) 4-amino-1-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-(L-2o valyloxy) benzoyloxymethyl) ester.
Deprotection of the CBz groups of 4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphonic acid, di-(3-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester using mild conditions as specified in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 1981 ) yields the title compound.
Example A-14 4-Amino-1-hvdroxvbutvliden-1 1-bisnhosnhonic acid di l3 fL valvloxvl ~ropionyloxymethyl] ester 3o a) 4-Benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-( N-benzyloxycarbonyl-L-valyloxy)-propionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutyliden-I,I-bisphosphonic acid (0.88g, 2,5 mmole) and diisopropylethyl-amine (0.78g, 6 mmole) in N,N-dimethylformamide {40 ml) was added dropwise a solution of iodomethyI-3-(N-benzyloxycarbonyl-L-valyloxy)-propionate (2.3g, 4.95 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature under argon and evaporated under reduced pressure. Ethyl acetate (50 ml) was added and the mixture was filtered after 2 hours. The organic phase was washed twice with S% sodium hydrogencarbonate solution and dried with sodium sulfate. The product was isolated by silica gel column chromatography.Yield: 0.19g = 8%
'H-NMR {CDC13 + 5% CD30D) 0.89 (m, 12H) 1.62-2.16 (m, 6H) 2.60 (m, 4H) 3.08 (m, 2H) 4.12 (m, 2H) 4.30 (m, 4H) 5.02 (m, 6H) 5.42-5.64 (m, 4H) 7.24 (m, 15H) to "P-NMR (CDC13 + 5% CD30D) 16,9 (s) b) 4-Amino-I-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-(L-valyloxy)-propionyloxymethyl) ester.
Deprotection ofthe CBz groups of4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid, di-(3-(N-benzyloxycarbonyl-L-valyloxy)-propionyloxyrnethyl) ester using mild conditions as specified in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 1981 ) yields the title compound.
2o Example A-15 4-amino-1-hydroxvbutvlidene-1 1-bisnhosnhonic acid di (4 lL va~lox~
benzoyloxvmethvll ester a) 4-B enzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 2s acid, di-(4-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (14I mg, 0.37 mmole) was esterified from the con esponding iodomethyl ester by the method described in Example A-3-a) to yield 55 mg of title compound. Rf (20%MeOH/CHCI,) 0.15 (at the center of oval spot from baseline).
'H-NMR (CDC13+ I %CD30D): 7.82 (m, 4H), 7.29 (m, I 5H), 6.97 (m, 4H), 5.85 (m, 4H), 5.11 (m, 6H), 4.46 (m, 2H), 3.10 (m, 2H), 2.30-1.77 (m, 6H), 1.52 (m, 6H), 0.99 (m, 12H).
3'P-NMR (CDCI,+1%CD30D)(H3P04 reference): 8 15.6(s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di-(4-(L-valyloxy) benzoyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid, di-(4-(N-benzyloxycarbonyl-L-valyloxy) benzoyloxymethyl) ester is CBz deprotected using mild conditions as prescribed in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 1981 ) to yield the title compound.
to Example A-16 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di !3 !3 4 di !L va~loxv) phenyl) propionvlox~nethyl~ ester a) 4-benzyloxycarbonylamino-1-hydroxybutylidene- l , l -bisphosphonic 15 acid, di-(3-(3,4-di(N-benzyloxycarbonyl-L-valyloxy) phenyl) propionyloxy-methyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (143 mg, 0.37 mmole) was esterified from the corresponding iodoemthyl ester by the method described in Example A-3-a) to yield 169 mg of the title compound. Rr 20 (20%MeOH/CHCI3) 0.15 (at the center of oval spot from baseline).
'H-NMR (CDCI3+ 1%CD30D): 7.40-6.85 (m, 31H), 5.62 (m, 4H), 5.02 (m, lOH), 4.43 (m, 4H), 3.10 (m, 2H), 2.84 (m, 4H), 2.61 (m, 4H), 2.35-1.73 (m, 8H), 1.52 (m, 6H), 0.99 (m, 24H). "P-NMR (CDCl3+1 %CD30D)(H3P04 reference): 8 14.3 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di-(3-(3,4-di-(L-valyloxy) phenyl) propionyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutyIidene-1,1-bisphosphonic acid, di-{3-(3,4-di(N-benzyloxycarbonyl-L-valyloxy) phenyl) propionyloxy- methyl) ester 3o is CBz deprotected using mild conditions as prescribed in Greene, "Protecting Groups in Organic Synthesis, (John Wiley & Sons, New York, 198I) to yield the title compound.
Example A-17 4-Amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid tril3 lL valvloxyl 2 2 dimethvlpropoxycarbonvloxymethyl,fester a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid tri(3-(N benzyloxycarbonyl-L-valyloxy)-2,2-dimethylpropoxycarbonyl oxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (174 mg, 0.45 mmol) in dry DMF (1 mL) were added diisopropylethylamine (240 p,L, 1.38 mmol), followed by 3-(N benzyloxycarbonyl-L-valyloxy)-2,2-1o dimethylpropyl iodomethyl carbonate (592 mg, 1.14 mmol). After stirring for 5 h at ambient temperature, under nitrogen, the reaction mixture was concentrated on a rotavapor, treated with ethyl acetate (15 mL), and filtered. The organic solution was washed with 5% NazS203, followed by brine. Drying over anhydrous NazS04 and concentration gave a yellow oil that was subjected to column chromatography (silica, 15 2/1 petroleum ether - ethyl acetate, 2.5 - 20% methanol in CHZCIz) to give fine, white solids (147 mg) enriched in the triester. The solids were dissolved in ethyl acetate, washed twice with 5% aqueous EDTA-disodium salt, dried over anhydrous NazSO,, and evaporated to dryness under vacuum.
Rf (10% methanol in CHzCl2) 0.30; ' H NMR (250 MHz, CDCl3 + 1 % CD30D) 8 20 0.85-0.95 (m, 36 H), 1.70-2.20 (m, 7H), 3.10 (br s, 2H), 3.85-3.95 (br, 12 H), 4.25 (m, 3H), 5.05 (s, 8H), 5.52-6.0 (m, lOH), 7.30 (s, 20H); 3'P NMR (101 MHz, + 1% CD30D) 8 13.6 and 24.6 (2d, .I= 47 Hz). The diester was a minor component:
"p NMR 8 18.6 (s).
b) Removal of benzyloxycarbonyl protecting groups.
25 The triester (110 mg} from step (a) was hydrogenated at 40 psi over Pd black (14 mg) in 4.2 mL solvent (2/1/1 ethyl acetate - methanol - acetic acid) for 18.5 h.
The suspension was filtered through a small column of celite and washed with ethyl acetate - methanol. The filtrate was evaporated to dryness under vacuum to give white solids (97 mg). Because proton NMR showed incomplete deprotection, the material was resubmitted for hydrogenation (14 mg Pd, 10 mL solvent) overnight to give the deprotected triester (as the acetate salt, 79 mg) as shown by the disappearance of peaks for the benzyloxy group at 8 5.05 and 7.30.
"P NMR ( 1 O 1 MHz, CDC13) 8 12.5 and 24Ø
Example A-18 4-Amino-1-hvdroxvbutvlidene-1 1-bisnhosnhonic acid di j2-methyl 1 ~ valvloxvl 2-propoxycarbonYloxymethyll ester a) 4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid to di(1-(N benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propoxycarbonyloxymethyl) ester.
4-Benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (460 mg, 1.2 mmol) was esterified by the method described in Example A-17 a) with 1-(N
benzyloxycarbonyl-L-valyloxy)-2-methyl-2-propyl iodomethyl carbonate (1.54 g, 3.0 15 mmol) for 2h. After column chromatography (silica, 4-20% methanol in CHZC12), the pure fractions containing the title compound were pooled together and concentrated.
The residue was dissolved in ethyl acetate, washed twice with 5% aqueous EDTA-disodium salt, and then, water, dried over NazS04, and evaporated to dryness under vacuum to give the diester as off white solids (92 mg).
20 "P NMR (101 MHz, CDC13 + 1% CD30D) 8 19.5 (s);'H NMR (250 MHz, CDCl3 +
1% CD30D) 8 0.76-1.41 (m, 24H), 1.74 (br s, 4H), 2.05 (m, 2H), 3.02 (br s, CHIN), 3.90-4.30 (m, CHZOC=O and CHa valine), 4.93-5.01 (m, 6H), 5.30-5.90 (m, OCH~O
and NHC=O), 7.22 (s, 15H).
(b ) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid, di(2-methyl-1-25 (L-valyloxy)-2-propoxycarbonyloxymethyl) ester.
The benzyloxycarbonyl-protected diester (86 mg) from step (a) was hydrogenated by the method described in Example A-17 b) to give the title compound (as the acetate salt) as a white powder (72 mg).
3'P NMR (101 MHz, CDC13) b 19.2 (s).
Example A-19 4-amino-1-hydroxybutylidene-1 1-bisphosphonic acid di (2 methyl 2 (L
isoleuc~ox~!nneth~l)propion~loxvmethvll ester.
a) 4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di (2-methyl-2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl)propionyl-oxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (824mg, 2.1 mmole) and diisopropylethylamine (0.8g, 6.3 mmole) in dry N,N-dimethylformamide (15 ml) was added dropwise a solution of iodomethyl 2-methyl-is 2-(N-benzyloxycarbonyl-L-isoleucyloxymethyl) propionate (3.1g, 5.21 mmole) in N,N-dimethylformamide (6 ml). The mixture was stirred 2 hours at room temperature and evaporated under reduced pressure. Ethyl acetate (70 ml) was added and after 1 hour the crystals were filtered. The organic phase was washed two times with saturated sodium hydrogencarbonate solution, dried with sodium sulfate and 2o evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol.Yield: 0.36g 'H-NMR (CDCl3) 0.86(m, 12H) 1.20 (m, 16H) 1.60-2.20 (m, 6H) 3.10 (m, 2H) 3.80-4.40 (m, 6H) 5.08 (m, 6H) 5.45 (m, 4H) 7.29 (m, 15H) 25 "P-NMR (CDCl3 +S~~o CD30D) 14.2 (s) b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di (2-methyl-2-(isoleucyloxymethyl)propionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 3o acid di (2-methyl-2-(N-benzyloxycarbonylamino-L-isoleucyloxymethyl)propionyl-oxymethyl) ester (0.195g, 0.171 mmole) in ethyl acetate (10 ml), methanol (10 ml) and acetic acid (S ml) was added palladium black (100mg). The mixture was hydrogenated overnight at 45 psi. The catalyst was filtered and washed with ethyl acetate, methanol and acetic acid. The solution was evaporated under reduced pressure and the product was dried in vacuo to yield the title compound as the triacetate salt. Yield: 150mg.
"P-NMR (CDC13 +S% CD30D) 18.1 (s) Example A-20 4-amino-1-hydroxybutvlidene-1 1-bisphosnhonic acid di (4 fL valyloxyl ~yclohexano Ioxmethyl) ester a) 4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di (4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoyloxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-biphosphonic acid (0.706g, 1.8 mmole) and diisopropylethylamine (07g, 5.4 mmole) in N,N-dimethylformamide (15 m1) was added dropwise a solution of iodomethyl 4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoate (2.35g, 4.5 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature 2o under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (60 ml) was added and the solid was filtered after 2 hours. The organic phase was washed twice with saturated sodium hydrogencarbonate and brine. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The products were isolated by silica gel column chromatography with dichloromethane/
methanol. After silica gel column chromatography the fractions were dissolved in ethyl acetate and washed three times with 5% aqueous EDTA-disodium salt solution, dried with sodium sulfate, evaporated under reduced pressure and dried in vacuo to yield 298mg 'H-NMR (CDC13) 0.84 (m, 12H) 1.35-2.35 (m, 24H) 3.10 (m, 2H) 4.08 (m, 2H) 5.02 (m, 8H) 5.55 (m, 4H) 7.24 (m, 15H) 3'P-NMR (CDCI3 + S% CD30D) 15.2 (s) -WO 99/S1b13 PCT/SE99/00528 b) 4-amino-I-hydroxybutylidene-1,1-bisphosphonic acid di (4-(L-valyloxy)-cyclohexanoyloxymethyl) ester.
4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di (4-(N-benzyloxycarbonyl-L-valyloxy)-cyclohexanoyloxymethyl) ester is de-CBz protected using conventional conditions as exemplified above to yield the title compound.
Example A-21 4-amino-I-hydroxvbutvlidene-1 1-bisphosnhonic acid tri l4 (L valvloxy,~
to cvclohexano loxvmethvll ester The appropriate fraction of Example A-20, step a) was dissolved in ethyl acetate and washed three times with 5% aqueous EDTA-disodium salt solution, dried with sodium sulfate, evaporated under reduced pressure and dried in vacuo to yield 15 mg which is deprotected using conventional conditions as exemplified above to yiled the title compound.
'H-NMR (protected form) (CDCl3) 0.86 (m, 18H) I.3-2.5 (m, 34H) 3.10 (m, 2H) 4.22 (m, 3H) 4.55-5.10 (m, 11H) 5.50 (m, 6H) 7.28 (m, 20H) 20 "P-NMR (CDCI, + 5% CD30D) 20.8 (d) 10.0 (d) Example A-22 4amino-1-hvdroxvbutvlidene-1 1-bisph_ osnhonic acid di 11V (2 L val ~~loxv 1 1 dimethvl-ethyl)aminocarbonvloxvmethvllester.
a) 4-N-benzyloxycarbonylamino- I -hydroxybutylidene-1,1-bisphosphonic acid di [N-(2-L-valyloxy-1,1-dimethyl-ethyl)aminocarbonyloxymethyl]ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidenel,l-biphosphonic aid (O.lg, 0. mmole) and diisopropylethylamine (0.31g, 2.4 mmole) in N,N-3o dimethylformamide (5 ml) was added dropwise a solution of 2-(N-( iodomethoxy-carbonyl)-amino)-2-methyl-1-(N-benzyloxycarbonyl-L-valyloxy)-propane in N,N-dimethylformamide (2.5 ml). The mixture was stirred 2 hours at room temperature under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (40 ml) was added and the solid was filtered after 2 hours. The organic phase was washed twice with saturated sodium hydrogencarbonate and brine. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol acetic acid. After silica gel column chromatography the fractions were dissolved in ethyl acetate and washed three times with 5% aqueous EDTA-disodium salt solution, dried with sodium sulfate, evaporated under reduced pressure and dried in vacuo.
Yield: 165mg.
'H-NMR (CDC13) 0.80 (m, 12H) 1.20 (m, 12H) 1.88 (m, 6H) 3.00 (m, 2H) 3.64 (m, 4H) 4.20 (m, 2H) 5.00 (m, 6H) 5.50 (m, 4H) 7.26 (m, 15H) "P-NMR (CDCl3 + 5% CD30D) 14.8 (s) b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di [N-(2-L-valyloxy-1,1-dimethyl-ethyl)aminocarbonyloxymethyl] ester.
A solution of 4-N-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-bisphosphonic acid di[N-(2-L-valyloxy-1,1-dimethyl-ethyl)aminocarbonyloxymethyl] ester (0.16g 0.14mmole) in ethyl acetate (Sml), methanol (10 ml) and acetic acid (5 ml) was hydrogenated with palladium black O.lg) at room temperature and 45 psi overnight .
2o The catalyst was filtered and washed with ethyl acetate and methanol. The solution was evaporated under reduced pressure and the product was dried in vacuo to yield the triacetate salt. Yield: 100mg 3'P-NMR (CDCl3 + 5% CD30D) 14.7 (s) Example A-23 4-amino-1-h~droxvbutylidene-1 1-bisphOSDhonic acid di 1 (2 L valylox~th ly-) 6 oxo-1.6-dihvd. ro-nyridine-3-carbonyloxymeth~) ester 3o a) 4-Benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester.
To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (565 mg, 1.44 mmol) in DMF (10 mL), was added diisopropylamine (0.75 mL, 4.32 mmol), followed by an injection of a solution of give 1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid iodomethyl ester (2.00 g, 3.60 mmol) in DMF (5 mL). After stirring under argon for 1.5 h at room temperature, the solution was concentrated and treated with ethyl acetate (100 mL).
Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate. The organic phase was filtered through anhydrous sodium sulfate and evaporated. After silica gel column (silica gel, 4-a20%
MeOH in 1o CHZCIZ), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 205 mg of benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester.
'H-NMR (CDCI3): 8.35-7.95 (m, 2H), 7.85-7.50 (m,2H), 7.26 (br s, 15H), 6.60-6.20 (m,2H), 5.90-5.35 (m, 4H), 5. i 5-4.80 (m, 6H), 4.50-4.00 (m, l OH), 3.18-3.00 (m, 2H), 2.45-1.55 (m, 6H), 1.00-0.80 (m, 12H).
3'P-NMR (CDCI,)(H3P0, reference): 16.8 (s).
b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester.
A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-l,l-bisphosphonic 2s acid di-(1-(2-N-CBz-L-valyloxyethyl)-6-oxo-1,6-dihydro-pyridine-3-carbonyloxymethyl) ester ( 180 mg, 0. i 45 mmol) in methanol / ethyl acetate /
acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst (30 mg) at 40 psi of hydrogen for 10 h. The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 85 mg of 4-amino-1-3o hydroxybutylidene-1,1-bisphosphonic acid di-(1-(2-L-valyloxyethyl)-6-oxo-1,6 dihydro-pyridine-3-carbonyloxymethyl) ester was obtained as a white solid.
'H-NMR (CDC13): 8.65-8.20 (m, 2H), 7.95-7.65 (m, 2H), 6.65-6.30 (m, 2H), 5.90-5.35 (m, 4H), 4.70-4.00 (m, lOH), 3.18-3.00 (m, 2H), 2.45-1.55 (m, 6H), 1.00-0.80 (m, 12H).
3'P-NMR (CDC13)(H3P04 reference): 13.9 (s).
Example A 24 4-Amino-1-hydroxvbutvlidene-1 1-bisnhosphonic acid di (fl 3 di (valvloxvlnronvl 2-oxycarbonvloxy methyl) ester to a) 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di ((1,3-di-(N-benzyloxycarbonyl)valyloxy)propyl-2-oxycarbonyloxy methyl) ester.
4-benzyloxycarbonylamino-1-hydroxybutylidene-l,l-bisphosphonic acid (141 mg, 0.37 mmole) was esterified by the method described in Example A-1 a using the 1 s corresponding iodomethyl ester to give 90 mg of the title compound.
Rf (10%MeOH/CHC13) 0.20 (at the center of oval spot from baseline).
'H-NMR (CDC13+ 1 %CD30D): 7.29 (m, 25H), 5.65 (m, 4H), 5.14-4.85 (m, 12H), 4.45-4.05 (m, 12H), 3.11 (m, 2H), 2.14-1.76 (m, 8H), 0.87 (m, 24H). "P-NMR
20 (CDC13+1 %CD30D)(H,P04 reference): 8 16.7 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid di ((1,3-di-(valyloxy)propyl-2-oxycarbonyloxy methyl) ester.
A solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic 25 acid di ((1,3-di-(N-benzyloxycarbonyl)valyloxy)propyl-2-oxycarbonyloxy methyl) ester (162 mg, 0.1 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (6 ml) was hydrogenated over a Pd-black catalyst (70 mg) at 40 psi of hydrogen for 16 h.
The suspension was filtered through Celite on a fine pore sized glass sinter and washed with methanol/ethyl acetate (2:1). The filtrate was evaporated to dryness in 3o vacuo and the title compound was obtained as the pentacetate, a white solid after a few co-evaporations with dioxane and hexane.
3'P-NMR (CDCl3+ 5%CD30D)(H3P04 reference): b 13.5 (br).
Example A 25 4-Amino-1-hvdroxvbutyliden-1 1-bisnhosphonic acid di~2 lL valvloxymethyl) 2 ethyl butvrovloxymethyl) ester a) 4-N-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di-(2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl )-butyroyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutyliden-1,1-biphosphonic acid (0.777g, 2.0 mmole) and diisopropylethylamine (0.78g, 6.0 mmole) in N,N-to dimethylformamide (15 ml) was added dropwise a solution of iodomethyl 2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyrate (2.6g, 5 mmole) in N,N-dimethylformamide (5 ml). The mixture was stirred 2 hours at room temperature under argon. The mixture was evaporated under reduced pressure. Ethyl acetate (60 ml) was added and the solid was filtered after 2 hours. The organic phase was washed 1 s twice with saturated sodium hydrogencarbonate and brine. The organic phase was dried with sodium sulfate and evaporated under reduced pressure. The products were isolated by silica gel column chromatography with dichloromethane/methanol.
After silica gel column chromatography the~pure fractions were dissolved in ethyl acetate and washed three times with S% aqueous EDTA-disodium salt solution, dried with 2o sodium sulfate, evaporated under reduced pressure and dried in vacuo.Yield:
320mg 'H-NMR (CDC13) 0.84 (m, 24H) 1.5-2.2 (m, 14H) 3.10 (m, 2H) 4.20 (m, 2H) 5.0 (m, 6H) 5.50 (m, 4H) 7.26 (m, 15H) 3'P-NMR (CDC13 + 5% CD30D) 14.5 (s) 2s b) 4-amino-1-hydroxybutyliden-1,1-bisphosphonic acid di-(2-(L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester.
A solution of4-benzyloxycarbonylamino-1-butylidene-1,1-bisphosphonic acid di-(2-(N-benzyloxycarbonyl-L-valyloxymethyl)-2-ethyl butyroyloxymethyl) ester (0.195g, 0.167 mmole) in methanol (15 ml), ethyl acetate (5 ml) and acetic acid (10 3o ml) was hydrogenated with palladium black (120mg) at room temperature overnight with 45 psi. The catalyst was filtered and washed with ethyl acetate, methanol and acetic acid. The solution was evaporated under reduced pressure and solidified with ether. The product was filtered and dried in vacuo to yield the tri acetate salt.
Yield: 0.125g. "P-NMR (CDC13 + 5% CD30D) 14.9 (s) Example A 26 4-Amino-1-hvdroxybutvlidene-1 1-bisphosphonic acid bis l3 fL valvloxvl 2 methvl-propionvloxymethvl) ester a) 4-Benzyloxy carbonylamino-I-hydroxybutylidene-I,1-bisphosphonic acid bis (3-(N-CBz-L-valyloxy)-2-methyl-propionyloxymethyl) ester.
to To a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (580 mg, 1.48 mmol) in DMF (10 mL), was added diisopropylamine (0.773 mL, 4.44 mmol), followed by an injection of a solution of iodomethyl 3-(N-CBz-L-valyloxy)-2-methyl-propionate ( 1.77 g, 3.70 mmol) in DMF (5 mL). After stirring under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mL). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate.
The organic phase was filtered through anhydrous sodium sulfate and evaporated.
After silica gel column (silica gel, 4-X20% MeOH in CHZCIz), the pure fractions containing the title compound were combined and evaporated. The residue was then 2o dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 189 mg of 4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(N-CBz-L-valyloxy)-2-methyl-propionyloxymethyl) ester.
'H-NMR (CDC13+1 %CD30D): 7.32 (br s, I SH), 5.85-5.30 (m, 4H), 5.18-4.93 (m, 6H), 4.30-3.95 (m, 6H), 3.22-3.00 (m, 2H), 2.93-2.70 (m, 2H), 2.20-1.65 (m, 6H), 1.35-1.05 (m, 6H), 1.00-0.75 (m, 12H).
3'P-NMR (CDCl3)(H3P04 reference): 15.1 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester.
A solution of4-benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(N-CBz-L-valyloxy)-2-methyl-propionyloxymethyl) ester (189 mg, 0.175 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst (35 mg) at 50 psi of hydrogen for 7h.
The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 110 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-(L-valyloxy)-2-methyl-propionyloxymethyl) ester as the acetate salt, a white solid.
3'P-NMR (CDCI,+CD30D)(H3P04 reference): & 14.7 (br s) Example A 27 4-Amino-1-hvdroxvbutvlidene-1 1-bisnhosphonic acid bis l3 (L t butvlQlvcvloxv) 2 2-dimethvlnronionvloxvmethvl) ester a) 4-Benzyloxy carbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-( N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester.
To a solution of 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (588 mg, 1.50 mmol) in DMF (10 mL), was added diisopropylamine (0.783 mL, 4.50 mmol), followed by an injection of a solution of iodomethyl 3-(N-CBz-L-t-1o butylglycyloxy)-2,2-dimethylpropionate (1.90 g, 3.75 mmol) in DMF (5 mL).
After stirring under argon for 1.5 h at room temperature, the solution was concentrated on rotavapor and treated with ethyl acetate (100 mL). Crystals were filtered off and the filtrate was extracted with brine containing a small amount of sodium thiosulfate.
The organic phase was filtered through anhydrous sodium sulfate and evaporated.
After silica gel column (silica gel, 520% MeOH in CHZCIz), the pure fractions containing the title compound were combined and evaporated. The residue was then dissolved in ethyl acetate and the solution extracted twice with aqueous saturated sodium bicarbonate and then twice with 5% aqueous EDTA-disodium salt. The ethyl acetate phase was evaporated, to give 158 mg of 4-benzyloxy carbonylamino-1-2o hydroxybutylidene-1,1-bisphosphonic acid bis (3-( N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester.
'H-NMR (CDCl3+1 %CD30D): 7.26 (br s, 1 SH), 5.85-5.40 (rn, 4H), S.15-4.88 (m, 6H), 4.20-3.95 (m, 6H), 3.20-3.00 (m, 2H), 2.10-1.65 (m, 4H), 1.22-1.05 (m, 12H), 1.00-0.75 (m, 18H).
3'P-NMR (CDCI3)(H3P04 reference): 15.1 (s).
b) 4-Amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-( L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester.
3o A solution of 4-benzyloxy carbonylamino-1-hydroxybutylidene-l,l-bisphosphonic acid bis (3-( N-CBz-L-t-butylglycyloxy)-2,2-dimethylpropionyIoxymethyl) ester (158 mg, 0.139 mmol) in methanol / ethyl acetate / acetic acid (2:1:1 v/v/v) (20 mL) was hydrogenated over a Pd-black catalyst {40 mg) at 50 psi of hydrogen for 16h.
The suspension was filtered through celite and the filtrate was evaporated to dryness under reduced pressure, to give 100 mg of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid bis (3-( L-t-butylglycyloxy)-2,2-dimethylpropionyloxymethyl) ester as a white solid.
3'P-NMR (CDCl3+CD3pD)(H3P04 reference): 8 14.6 (br s) Example A 28 4-amino-1-hvdroxvbutvlidene-1 1-bisphosphonic acid di~trans 4 (L valvloxvl L
1 o prolyoxvmeth~] ester a) 4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid di[N benzyloxycarbonyl-traps-4-(N benzyloxycarbonyl-L-valyloxy)-L-prolyoxymethyl] ester.
15 Diisopropylethylamine (195 p,L, 1.12 mmol) was added to a solution of4-benzyloxycarbonylamino-1-hydroxybutylidene-1,1-bisphosphonic acid (144 mg, 0.38 mmol) in 1 mL dry DMF, followed by the dropwise addition of a solution of the iodomethyl ester (520 mg, 0.814 mmol) from step (d) in 3 mL DMF. After stirring at ambient temperature for 5.5 h, the reaction mixture was concentrated on a rotavapor, 2o treated with EtOAc (20 mL), and filtered. The precipitates were washed with 10 mL
more EtOAc. The organic solution was washed with 10 mL saturated aqueous NaHC03 containing a small amount of NazS203, followed by reextraction of the aqueous phase with 10 mL EtOAc. The organic phases were combined, washed with mL brine, dried over anhydrous NazS04, and concentrated. Flash column 25 chromatography (silica gel, 5 - 25 % MeOH in CHZClZ (20 mL) yielded a fraction that gave light yellow solids (59 mg) enriched in the diester. The solids were dissolved in 25 mL EtOAc, washed with 5% aqueous EDTA-disodium salt (2 x 2 mL), dried over anhydrous Na2S04, and evaporated to dryness under vacuum.
30 'H NMR (250 MHz, CDCI, + 1% CD30D) 8 0.81-0.97 (m, 12H), 1.60-2.50 (br, l OH), 3.09 (br s, 2H), 3.55-3.77 (m, 4H), 4.20 (br s, 2H), 4.43 (m, 2H), 4.80-5.40 (m, 12H), 5.64 (br, 4H), 7.28-7.35 (m, 25H);
3'P NMR (101 MHz, CDC13 + 1% CD30D) 8 18.3.
b) 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid di[traps-4-(N
benzyloxycarbonyl-L-valyloxy)-L-prolyoxymethyl] ester.
The product of step a) is deCBz protected by gentle conditions as described in Greene supra to yield the title compound.
Biological Example 1 The bioavailability of prodrugs of the invention built on the bis-phosphonate alendronate was assayed in rats. The prodrugs of the invention were orally administered at a dose corresponding to 0.1 mmol/kg to triplicate rats in a propylene glycol vehicle. The mother compound was also administered IV at 1/10 of that does for the calculation of absolute oral bioavailability.
Urine was collected over 24 hours in a metabolic cage and analysed as shown in to Kline et al J Chromat. 534 (1990) 139-149, but modified as follows: 1 ml of urine is mixed with 50 p,l or 1.25 M calcium chloride and 100 p.l of 1 M sodium hydroxide.
After centrifugation, the urine was aspirated off and the pellet redissolved in 0.8 ml 0.2 M acetic acid, 0.4 ml of 0.01 M EDTA and 0.4 ml of 0.2 m sodium acetate. 1 ml of water was added and the solution loaded onto a preconditioned DEA
cartridge.
i5 The cartridge was washed with 1 ml of water and alendronate eluted with 1 ml of 1M
carbonate buffer, pH 10.4. A part of the eluent, 150 ~l was mixed with 5 p,l of 0.05 M potassium cyanide and 5 p,l of NDA solution (1 mg/ml) in methanol. 50 p,l was injected into the chromatograph.
2o Absolute bioavailability is determined as the ratio between the AUC for the mother compound administered N against the AUC for the prodrug administered orally.
Results are presented in table 1 below:
Table 1 compound absolute bioavailability (%) alendronate 2.2 Example A-2 42 Example A-11 34 Example A-3 25 Example A-S 14 Example A-4 12 Example A-18 10 Example A-10 Example A-19 g Example A-24 11 Example A-22 g Example A-23 10 Example A-12 g The compounds of the invention exhibit substantially enhanced oral bioavailability relative to the alendronate. The pivaloyloxymethyl alendronate ester presented as the preferred prodrug in US 5 227 506 provided no better bioavailability than the mother compound in this assay (results not shown).
Although the invention has been illustrated by reference to a number of examples 1 o built on the phosphorous-containing drug alendronate and employing various linkers and amino acids, it will be appreciated that the invention is not so limited to these values but extends throughout the spirit and scope of the accompanying claims.
Claims (48)
1 pharmaceutical compound with the formula:
Drug-P(=O)-O-Linker (-R2')k-R2 where Drug-P(=O)-O- is the residue of a drug comprising a phosphonate, phosphinate or phosphoryl function, R1 and R2' (if present) are independently the acyl residue of an aliphatic amino acid;
Linker is an at least difunctional moiety comprising a first function ester-bonded to the phosphonate, phosphinate or phosphoryl function spaced from a second function ester-bonded to R2; and k is 1 or zero.
Drug-P(=O)-O-Linker (-R2')k-R2 where Drug-P(=O)-O- is the residue of a drug comprising a phosphonate, phosphinate or phosphoryl function, R1 and R2' (if present) are independently the acyl residue of an aliphatic amino acid;
Linker is an at least difunctional moiety comprising a first function ester-bonded to the phosphonate, phosphinate or phosphoryl function spaced from a second function ester-bonded to R2; and k is 1 or zero.
2 A compound according to claim 1, wherein Drug-P(=O)-O- is derived from the group consisting of phosfestrol, (E)-(.alpha.,.beta.-diethyl-4,4'-stilbenylen)bis(dihydrogenphosphate), nucleoside analogue phosphonates, nucleotide analogue mono-, di or triphosphates, phosphonoformic acid, phosphonoacetic acid, bis phosphonate bone metabolism agents, fosinoprilate, .beta.-phosphonocarboxylic acid farnesyl protein transferase inhbitors, .alpha.-phosphonosulfonate squalene synthase inhibitors, phosphonomethylamine neutral endopeptidase (24.11) inhibitors.
3 A compound according to claim 1, wherein the structure of the formula -linker(-R2')k-R2 has one of the formulae:
where R2 is the aryl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-C6cycloalkyl, C1-C3alkyl-C1-C6cycloalkyl, phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4 or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
where R2 is the aryl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-C6cycloalkyl, C1-C3alkyl-C1-C6cycloalkyl, phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4 or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
4 A compound according to claim 3, wherein R4R and R4R' are hydrogen.
5 A compound according to claim 3, with the structure:
6. A compound according to claim 5, wherein R4L and R4L' are respectively: methyl, methyl;
7. A compound according to claim 5, wherein R4L and R4L' are respectively methyl, hydrogen; or ethyl, ethyl.
8 A compound according to claim 3, wherein ql and qr are respectively 1,0;
2,0;
3,0; or 4,0;
2,0;
3,0; or 4,0;
9 A compound according to claim 8, wherein ql and qr are respectively 1,0.
10 A compound according to claim 3, wherein ql and qr are respectively 1,1;
2,1;
3,1;
4,1; or 2,2.
2,1;
3,1;
4,1; or 2,2.
11 A compound according to claim 3 wherein -ring- is phenyl, furyl, pyridyl, cyclobutyl cyclopentyl or cyclohexyl.
12 A compound according to claim 3, wherein the optional substituent to -ring- comprises a structure of the formula: R2-()ql-.
13 A compound according to claim 3, wherein R2 is derived from valyl.
14. A compound according to claim 13, wherein R2 is derived from L-valine.
15 A compound according to claim 3, wherein T is a bond.
16 A compound according to claim 3, wherein T is -NH-.
17 A compound according to claim 3, wherein T is -O-.
18 A compound according to claim 2, wherein the bis-phosphonate is derived from a compound of the formula:
where X is H, halo, hydroxy; and Y is a) C1-10 alkyl, optionally substituted with heterocycle, -NR a R b, where R a and R b are independently hydrogen, C1-6 alkyl or join together to form a 5 to 7 membered ring, optionally containing a further hetero atom, OH, halo, -S(C1-6 alkyl), phenyl, -C1-7 cycloalkyl, (optionally substituted with -NR a R b or OH);
b) C3-7 cycloalkyl, optionally substituted with -NR a R b, OH, halo, -S(C1-6 alkyl), phenyl, morpholino or pyridyl;
c) halo;
d) piperidinyl;
e) pyrrolidinyl;
f) -S(C1-6 alkyl), optionally substitued with -NR a R b, OH, halo or phenyl;
g) -S-phenyl, optionally substituted with halo, nitro, C1-6 alkyl, C1-6 alkoxy, trifluormethyl, -CONR a R b or -COOH.
where X is H, halo, hydroxy; and Y is a) C1-10 alkyl, optionally substituted with heterocycle, -NR a R b, where R a and R b are independently hydrogen, C1-6 alkyl or join together to form a 5 to 7 membered ring, optionally containing a further hetero atom, OH, halo, -S(C1-6 alkyl), phenyl, -C1-7 cycloalkyl, (optionally substituted with -NR a R b or OH);
b) C3-7 cycloalkyl, optionally substituted with -NR a R b, OH, halo, -S(C1-6 alkyl), phenyl, morpholino or pyridyl;
c) halo;
d) piperidinyl;
e) pyrrolidinyl;
f) -S(C1-6 alkyl), optionally substitued with -NR a R b, OH, halo or phenyl;
g) -S-phenyl, optionally substituted with halo, nitro, C1-6 alkyl, C1-6 alkoxy, trifluormethyl, -CONR a R b or -COOH.
19 A compound according to claim 18 wherein the bisphosphonate has the formula A-1.
wherein YY and XX have the following values:
NH2(CH2)3- OH (alendronate) NH2(CH2)2- OH (pamidronate) cycloheptylamino- H (cimadronate) chloro- chloro (clodronate) pyrrolidin-1-ylCH2CH2- OH (EB 1053) CH3- OH (etidronate) methylpentylaminoCH2CH2- OH (ibandronate) dimethylaminoCH2CH2- OH (olpadronate) pyridin-3-ylCH2- OH (risedronate) (4-chlorophenyl)-thio- H (tiludronate) imidazo-(1,2-a)pyridin-3-ylCH2- OH (YH 529) 1H-imidazol-1ylCH2- OH (zoledronate);
at least one of Ra1-Ra4 is a structure of the formula -linker (-R2')k -R2 and the remainder are H.
wherein YY and XX have the following values:
NH2(CH2)3- OH (alendronate) NH2(CH2)2- OH (pamidronate) cycloheptylamino- H (cimadronate) chloro- chloro (clodronate) pyrrolidin-1-ylCH2CH2- OH (EB 1053) CH3- OH (etidronate) methylpentylaminoCH2CH2- OH (ibandronate) dimethylaminoCH2CH2- OH (olpadronate) pyridin-3-ylCH2- OH (risedronate) (4-chlorophenyl)-thio- H (tiludronate) imidazo-(1,2-a)pyridin-3-ylCH2- OH (YH 529) 1H-imidazol-1ylCH2- OH (zoledronate);
at least one of Ra1-Ra4 is a structure of the formula -linker (-R2')k -R2 and the remainder are H.
20 A compound according to claim 19, wherein at least one of Ra1-Ra4 is a structure of the formula where R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
-ring- is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and the remainder of Ra1-Ra4 are hydrogen or conventional pharmaceutically acceptable esters.
-ring- is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and the remainder of Ra1-Ra4 are hydrogen or conventional pharmaceutically acceptable esters.
21 A compound according to claim 20, wherein Ra1 and Ra2 are each a structure IIa or IIb as defined in claim 20 and Ra3 and Ra4 are H.
22 A compound according to claim 19, derived from alendronate, zoledronate or risedronate.
23 A compound according to claim 22, selected from:
alendronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester alendronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester alendronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester alendronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester risedronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester risedronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester risedronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester risedronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester zoledronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester zoledronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester,
alendronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester alendronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester alendronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester alendronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, alendronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester risedronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester, risedronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester risedronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester risedronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester risedronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester zoledronate mono-(2-methyl-2-(D-valyloxymethyl) propionyloxymethyl) ester zoledronate di-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(L-valyloxy) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester, zoledronate mono-(2-methyl-2-(D-valyloxy) propionyloxymethyl) ester,
24 A compound according to claim 19, selected from:
alendronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof.
alendronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, risedronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, zoledronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, pamidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, cimadronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, clodronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-3-(1-pyrrolidinyl)-propylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, etidronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, ibandronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, olpadronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, tiludronate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, [1-hydroxy-2imidazo-(1,2-a)pyridin-3-ylethylidine]-bis-phosphonate di-(2-methyl-2-(L-valyloxymethyl) propionyloxymethyl) ester, and pharmaceutically acceptable salts thereof.
25 A compound according to claim 2 with the formula:
where R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
Rf1 is H or a further -linker-(R2')k-R2 structure as defined in claim 3, and Rf2 is H, a conventional pharmaceutically acceptable ester or a further -linker-(R2')k-R2 structure as defined in claim 3, and pharmaceutically acceptable salts thereof.
where R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
Rf1 is H or a further -linker-(R2')k-R2 structure as defined in claim 3, and Rf2 is H, a conventional pharmaceutically acceptable ester or a further -linker-(R2')k-R2 structure as defined in claim 3, and pharmaceutically acceptable salts thereof.
26 A compound according to claim 25, wherein Rf1 is H
27 A compound according to claim 25, wherein Rf1 is the same - linker (-R2')k-R2 structure as depicted in claim 25.
28 A compound according to claim 25, wherein Rf1 is H, methyl or ethyl.
29 A compound according to claim 2 of the formula:
wherein nuc is a cyclic or acyclic nucleoside analogue phosphonate;
Rn10 is H or a further -linker(R2')k-R2 structure as defined in claim 3;
R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl q1 is 0-3, qr is 0-3, T is a bond, -NR4 or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and pharmaceutically acceptable salts thereof.
wherein nuc is a cyclic or acyclic nucleoside analogue phosphonate;
Rn10 is H or a further -linker(R2')k-R2 structure as defined in claim 3;
R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl q1 is 0-3, qr is 0-3, T is a bond, -NR4 or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle;
and pharmaceutically acceptable salts thereof.
30 A compound according to claim 29, wherein Rn10 is identical to the linker-(R2')k-R2 structure in the depicted formula.
31 A compound according to claim 29, wherein Rn10 is H.
32 A compound according to claim 29, wherein the nucleoside analogue is derived from adefovir, cidefovir, PMPA (9(2-phosphonylmethoxypropyl)adenine), HPMPA (9(3-hydroxy-2-phosphonylmethoxypropyl)adenine), HPMPG (9(3-hydroxy-2-phosphonylmethoxypropyl)adenine or HPMPDAP
(9(3-hydroxy-2-phosphonylmethoxypropyl)adenine.
(9(3-hydroxy-2-phosphonylmethoxypropyl)adenine.
33 A compound according to claim 2 of the formula PF3:
where R2 is the acyl residue of an aliphatic amino acid, Rf2 is H, a pharmaceutically acceptable ester or a further linker(R2')-R2 structure as defined in claim 3, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle, and pharmaceutically acceptable salts thereof.
where R2 is the acyl residue of an aliphatic amino acid, Rf2 is H, a pharmaceutically acceptable ester or a further linker(R2')-R2 structure as defined in claim 3, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle, and pharmaceutically acceptable salts thereof.
34 A compound according to claim 33, wherein Rf2 is H, methyl or ethyl.
35 A compound according to claim 2 wherein the neutral endopeptidase inhibitor has the structure:
where Rf1 is H or a further structure as depicted in claim 3 Rf2 is H or a pharmaceutically acceptable ester, R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle, and pharmaceutically acceptable salts thereof.
where Rf1 is H or a further structure as depicted in claim 3 Rf2 is H or a pharmaceutically acceptable ester, R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C,C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, q1 is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle, and pharmaceutically acceptable salts thereof.
36 A compound according to claim 35, wherein Rf1 is H.
37 A compound according to claim 35, wherein Rf1 is the same -Linker (-R2')k R2 structure as depicted in claim 35.
38 A compound according to claim 35, wherein Rf2 is hydrogen, methyl or ethyl.
39 A compound according to claim 2, wherein the .alpha.-phosphonosulphonate has the formula PF5:
where Rf1 is H or a further -linker(R2')k-R2 structure as depicted in claim 3, Rf2 is H or a pharmaceutically acceptable ester, Rf3 is a polyunsaturated, branched C6-22 alkyl, R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H or C1-3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR4 or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle, and pharmaceutically acceptable salts thereof.
where Rf1 is H or a further -linker(R2')k-R2 structure as depicted in claim 3, Rf2 is H or a pharmaceutically acceptable ester, Rf3 is a polyunsaturated, branched C6-22 alkyl, R2 is the acyl residue of an aliphatic amino acid, R4L and R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H or C1-3 alkyl ql is 0-3, qr is 0-3, T is a bond, -NR4 or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle, and pharmaceutically acceptable salts thereof.
40 A compound according to claim 39, wherein the polyunsaturated alkyl Rf3 has the formula:
wherein the asterisk denotes the point of attachment.
wherein the asterisk denotes the point of attachment.
41 A compound according to claim 39, wherein Rf1 is H.
42 A compound according to claim 39, wherein Rf1 is the same -Linker (-R2')k R2 structure as depicted in claim 39.
43 A compound according to claim 39, wherein Rf2 is H, methyl or ethyl.
44 A compound according to claim 2 wherein the .beta.-phosphonocarboxylic acid has the formula PF4:
Rf1 is H or a further -linker (-R2')k R2 structure as depicted in claim 3, Rf2 is H or a pharmaceutically acceptable ester , Rf3 is a polyunsaturated, branched C6-22 alkyl, R2 is the acyl residue of an aliphatic amino acid, R4Land R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
Rf1 is H or a further -linker (-R2')k R2 structure as depicted in claim 3, Rf2 is H or a pharmaceutically acceptable ester , Rf3 is a polyunsaturated, branched C6-22 alkyl, R2 is the acyl residue of an aliphatic amino acid, R4Land R4L' are independently H, C1-3 alkyl, C3-6cycloalkyl, C1-3alkyl-C1C6cycloalkyl phenyl or benzyl, R4R and R4R' are independently H, C1-3 alkyl or phenyl, ql is 0-3, qr is 0-3, T is a bond, -NR4- or -O-R4 is H or C1-3alkyl;
ring is an optionally substituted aromatic or non-aromatic, hetero-or carbocycle.
45 A compound according to claim 44, wherein the polyunsaturated alkyl Rf3 has the formula:
wherein the asterisk denotes the point of attachment.
wherein the asterisk denotes the point of attachment.
46 A compound according to claim 44, wherein Rf1 is H.
47 A compound according to claim 44, wherein Rf1 is a further -Linker(R2')k-R2 structure:
48 A compound according to claim 44, wherein Rf2 is H, methyl or ethyl.
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9801216-4 | 1998-04-03 | ||
| SE9801216A SE9801216D0 (en) | 1998-04-03 | 1998-04-03 | Pharmaceuticals |
| ZA98/7267 | 1998-08-13 | ||
| ZA987267A ZA987267B (en) | 1997-08-15 | 1998-08-13 | Nucleosides |
| SEPCT/SE98/01467 | 1998-08-14 | ||
| PCT/SE1998/001467 WO1999009031A1 (en) | 1997-08-15 | 1998-08-14 | Nucleosides analogues, such as antivirals including inhibitors of retroviral reverse transcriptase and the dna polymerase of hepatitis b virus (hbv) |
| US09/249,317 | 1999-02-12 | ||
| US09/249,317 US6458772B1 (en) | 1909-10-07 | 1999-02-12 | Prodrugs |
| SEPCT/SE99/00194 | 1999-02-15 | ||
| PCT/SE1999/000194 WO1999041275A1 (en) | 1998-02-13 | 1999-02-15 | Prodrugs |
| PCT/SE1999/000528 WO1999051613A1 (en) | 1998-04-03 | 1999-03-30 | Prodrugs of phosphorous-containing pharmaceuticals |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2325523A1 true CA2325523A1 (en) | 1999-10-14 |
Family
ID=20410882
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002325523A Abandoned CA2325523A1 (en) | 1998-04-03 | 1999-03-30 | Prodrugs of phosphorous-containing pharmaceuticals |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1121366A1 (en) |
| JP (1) | JP2002510698A (en) |
| AU (1) | AU750407B2 (en) |
| CA (1) | CA2325523A1 (en) |
| SE (1) | SE9801216D0 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3353145B1 (en) * | 2015-09-23 | 2022-09-28 | XWPharma Ltd. | Prodrugs of gamma-hydroxybutyric acid, compositions and uses thereof |
-
1998
- 1998-04-03 SE SE9801216A patent/SE9801216D0/en unknown
-
1999
- 1999-03-30 EP EP99921327A patent/EP1121366A1/en not_active Withdrawn
- 1999-03-30 JP JP2000542334A patent/JP2002510698A/en active Pending
- 1999-03-30 CA CA002325523A patent/CA2325523A1/en not_active Abandoned
- 1999-03-30 AU AU38567/99A patent/AU750407B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002510698A (en) | 2002-04-09 |
| EP1121366A1 (en) | 2001-08-08 |
| SE9801216D0 (en) | 1998-04-03 |
| AU750407B2 (en) | 2002-07-18 |
| AU3856799A (en) | 1999-10-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO1999051613A1 (en) | Prodrugs of phosphorous-containing pharmaceuticals | |
| US6458772B1 (en) | Prodrugs | |
| US6638919B2 (en) | Antiviral purine derivatives | |
| US6455513B1 (en) | Chemical compounds | |
| FI87790B (en) | PROCEDURE FOR THE FRAMSTATION OF THE EPIPODOFYLLOTOXINGLUKOSID-4'-PHOSPHATIVES MED ANTITUMOER EFFEKT | |
| ES2221887T3 (en) | PROCEDURE FOR MANUFACTURING GEMINAL BIOPHOSPHONATES. | |
| EA019559B1 (en) | Antiviral compounds, in particular that inhibitis hiv, pharmaceutical composition based thereon and method for inhibiting using same | |
| EA018098B1 (en) | Phosphinate compounds (embodiments) | |
| US5227506A (en) | Acyloxymethyl esters of bisphosphonic acids as bone resorption inhibitors | |
| KR20020093824A (en) | Phosphonate nucleotide compound | |
| WO1996026729A1 (en) | Phosphono substituted tetrazole derivatives as ece inhibitors | |
| EP0988304B1 (en) | Nucleosides analogues, such as antivirals including inhibitors of retroviral reverse transcriptase and the dna polymerase of hepatitis b virus (hbv) | |
| JPH05500949A (en) | Gem-diphosphonic acid, its production method, and pharmaceutical compositions containing the same | |
| AU705248B2 (en) | Water-soluble derivatives of epipodophyllotoxin, process for their preparation, their use as medicinal product and their intended use in anticancer treatments | |
| AU750407B2 (en) | Prodrugs of phosphorous-containing pharmaceuticals | |
| US7214794B2 (en) | Ceramide analogs, process for their preparation and their use as antitumor agents | |
| US20020128301A1 (en) | Non-nucleoside reverse transcriptase inhibitors | |
| IE921083A1 (en) | Substituted 2',3'-dideoxy-5-trifluoromethyluridines,¹processes for their preparation and their use in medicaments | |
| JP3148139B2 (en) | Phosphonate nucleotide compounds | |
| JP3619275B2 (en) | Ascorbic acid phosphoramide derivative and method for producing the same | |
| AU775578B2 (en) | Nucleosides analgoues, such as antivirals including inhibitors of retroviral reverse transcriptase and the DNA polymerase of hepatitis B virus (HBV) | |
| CN117624239A (en) | Cytidine derivatives and process for preparing same | |
| EP1150956A1 (en) | Non-nucleoside reverse transcriptase inhibitors | |
| CZ20011145A3 (en) | Antiviral purine derivatives and their use |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Dead |