WO2008132154A1 - Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives - Google Patents
Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives Download PDFInfo
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- WO2008132154A1 WO2008132154A1 PCT/EP2008/055042 EP2008055042W WO2008132154A1 WO 2008132154 A1 WO2008132154 A1 WO 2008132154A1 EP 2008055042 W EP2008055042 W EP 2008055042W WO 2008132154 A1 WO2008132154 A1 WO 2008132154A1
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- Prior art keywords
- formula
- compound
- amino
- hydroxy
- isobutyl
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- 0 CC(C)CNCC(C(Cc1ccccc1)N*)O Chemical compound CC(C)CNCC(C(Cc1ccccc1)N*)O 0.000 description 4
- GXFDZVGLTFTUMM-BJKOFHAPSA-N CC(C)CN(C[C@H]([C@H](CCc1ccccc1)NC(OC(C)(C)C)=O)O)S(c(cc1)ccc1N)(=O)=O Chemical compound CC(C)CN(C[C@H]([C@H](CCc1ccccc1)NC(OC(C)(C)C)=O)O)S(c(cc1)ccc1N)(=O)=O GXFDZVGLTFTUMM-BJKOFHAPSA-N 0.000 description 1
- LTUKXZAZCBEJBX-XTEPFMGCSA-N CC(C)Cc1cc(S(N(CC(C)C)C[C@H]([C@H](CCc2ccccc2)NC(OC(C)(C)C)=O)O)(=O)=O)ccc1[N+]([O-])=O Chemical compound CC(C)Cc1cc(S(N(CC(C)C)C[C@H]([C@H](CCc2ccccc2)NC(OC(C)(C)C)=O)O)(=O)=O)ccc1[N+]([O-])=O LTUKXZAZCBEJBX-XTEPFMGCSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/38—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reaction of ammonia or amines with sulfonic acids, or with esters, anhydrides, or halides thereof
Definitions
- the present invention relates to methods for the preparation of N-isobutyl-
- N-isoButyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives and especially 3N-protected derivatives such as the tert-butyloxycarbonyl derivative are important intermediates in the synthesis of retroviral protease inhibitors such as those described in WO 99/65870, WO 99/67254, WO 99/67417, WO00/47551, WO 00/76961, WO 05/063770 and EP 0 715 618. Said publications are herein incorporated by reference.
- protease inhibitor which has been approved in the USA for human clinical use for the treatment of retroviral infections and having the above structural moiety is the compound having the USAN approved name darunavir with the chemical name [(lS,2R)-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)- amino]-2-hydroxy-l-(phenylmethyl)propyl]- carbamic acid (3R,3aS,6aR) hexahydrofuro[2,3-b]furan-3-yl ester and the structure of formula (A):
- N(3)-Protected derivatives ofN-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)- p-nitrobenzenesulfonylamide derivatives of formula I below may be prepared by the reaction of a compound of formula (II) with a p-nitrophenylsulfonyl halide of formula (III) as shown in the reaction scheme below: in which PG represents a protecting group and X represents a halogen atom.
- a major disadvantage of this procedure is that the desired product of formula (I), especially when PG is a tertbutyloxycarbonyl group, has only a low solubility in most organic solvents. To enable a washing step to be performed the product must remain in solution. The choice of solvents is therefore determined by a) its suitability for use in the reaction and b) its need to be non-miscible with water, otherwise extraction cannot be performed.
- solvents it is necessary to use large volumes of solvent to ensure solubilisation of the product, which is disadvantageous for both economic and environmental reasons.
- PG is a protecting group and X is a halogen atom.
- the protecting group PG is advantageously an alkyl-, aryl- or arylalkyl-oxycarbonyl group, a Ci_4 alkyl group being preferred, especially the tert-butyloxycarbonyl group.
- the halogen atom X is preferably a chlorine atom.
- the secondary or tertiary alcohol is preferably a Ci_5 alkanol for example a C3_salkanol such as 2-butanol, 2,2-dimethyl-l-propanol (neopentyl alcohol) or 2-methyl-2-butanol (tert-amyl alcohol) but especially a propanol, isopropanol being especially preferred.
- tert-butanol can be advantageously used.
- the reaction is generally performed in the presence of an acid scavenger such as a tertiary amine base, triethylamine being especially preferred.
- an acid scavenger such as a tertiary amine base, triethylamine being especially preferred.
- suitable bases include N-methylmorpholine and diisopropylethylamine (Hunig's base), and also inorganic bases for example a phosphate base such as disodium hydrogen phosphate.
- the reaction is generally performed at an elevated temperature for example 40 to 80°C especially 50 to 7O 0 C.
- the desired product of formula (I) crystallises from solution, enabling it to be readily separated from the reaction mixture.
- Water is generally added subsequently to the reaction mixture to form a suspension with the organic reaction solvent to remove water-soluble reaction by-products or impurities such as acid addition salts formed by reaction of the acid scavenger and the halide compound of formula (III).
- the crystallised product can then be filtered off from the organic/water suspension and optionally purified for example by washing with a water/iso-propanol mixture.
- alkyl alone or in combination with any other term refers, except where otherwise specified, to straight-chain or branched- chain saturated aliphatic hydrocarbon radicals or, in the event that at least three carbon atoms are present, cyclic saturated aliphatic hydrocarbon radicals, containing 1 to 10 carbon atoms, preferably 1 to 8 carbon atoms, more preferably 1 to 6 carbon atoms or even more preferably 1 to 4 carbon atoms.
- radicals include but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, iso-pentyl, n-hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like.
- aryl alone or in combination with any other term, refers to a carbocyclic aromatic moiety and includes monocyclic, bicyclic and other polycyclic radicals.
- aryl radicals include but are not limited to phenyl and naphthyl radicals.
- halogen refers to a fluorine, chlorine, bromine or iodine atom.
- the present invention also includes the stereoisomeric forms of the compounds employed in the process according to the invention including starting materials and compounds subsequently prepared from compounds which are themselves prepared in accordance with the present invention.
- stereoisomeric forms as used herein defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of the present invention may possess. Unless otherwise mentioned or indicated, the chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound. Except where specified, all stereoisomeric forms of the compounds employed in the present invention both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.
- stereoisomeric forms of the compounds mentioned herein i.e. where a particular stereoisomeric form is specified, are defined as isomers substantially free of other enantiomeric or diastereomeric forms of the same basic molecular structure of said compounds or intermediates.
- the term 'stereoisomerically pure' concerns compounds or intermediates having a stereoisomeric excess of at least 80% (i. e. minimum 90% of one isomer and maximum 10% of the other possible isomers) up to a stereoisomeric excess of 100% (i.e.
- Pure stereoisomeric forms of the compounds mentioned herein may be obtained by the application of art-known procedures. For instance, enantiomers may be separated from each other by the selective crystallization of their diastereomeric salts with optically active acids. Alternatively, enantiomers may be separated by chromatographic techniques using chiral stationary phases. Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereoselectively. Preferably, if a specific stereoisomer is desired, said compound will be synthesized by stereoselective methods of preparation. These methods will advantageously employ enantiomerically pure starting materials.
- the compounds of formula (II) can be prepared in conventional manner for example by methods described in the literature for example that described in WO 05/063770 including the synthesis described below.
- the compound of formula (IV) is a compound of formula (IV") as shown below wherein PG is a tert-butyloxycarbonyl or "Boc” group.
- Compounds of formula (IV), (IV) and (IV") are commercially available and may be prepared in several ways available in the literature, for example as described in WO95/06030 (Searle & Co.), as described by Kaneka Corporation in EP0754669 EP1029856 and EP1067125, and as disclosed by Ajinomoto KK in EP1081133 and EP1215209.
- the isobutyl amination of the compound of formula (IV) may be accomplished in several ways available in the literature, for example as described in WO95/06030, which is incorporated herein by reference.
- the compound of formula (IV") is reacted with isobutylamine to yield the compound of formula (H").
- the amination agent isobutylamine
- the amination process is performed in the presence of one or more solvents other than isobutylamine.
- said solvents are used in the work-up of compounds of formulae (II), (IF) and (H").
- the amination reaction is carried out in the presence of about 15 equivalents of isobutylamine, using toluene as solvent, and heating to reflux at about 79°C.
- the compounds of formula (I) and in particular the compounds of formulae (F) and (I") above are useful in the preparation of medicaments.
- the compounds of formula (I) including the compounds of formulae (F) and (I") are used as precursors in the preparation of anti- viral drugs, in particular anti-HIV drugs, more in particular HIV protease inhibitors.
- the compound of formula (I) and all intermediates leading to the formation of said compounds are of particular interest in preparing HIV protease inhibitors as disclosed in WO 99/65870, WO 99/67254, WO 99/67417, WO-00/47551, WO 00/76961, WO 05/063770 and EP 0 715 618.
- HIV protease inhibitor [(lS,2R)-3-[[(4-aminophenyl)sulfonyl]- (2-methylpropyl)amino] -2-hydroxy- 1 -(phenyl-methyl)propyl] -carbamic acid (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl ester, namely darunavir referred to above .
- the present invention also relates to the HIV protease inhibitor darunavir whenever obtained using a compound of formula (I), particularly a compound of formula (F) or (F '), prepared according to the present invention in the chemical synthesis of said HIV protease inhibitors.
- a compound of formula (I) particularly a compound of formula (F) or (F ')
- Such chemical synthesis is disclosed in the literature, for instance in the above patent and literature references.
- the compounds of formulae (I) above can be used, after formation of an activated derivative, to synthesise the protease inhibitor darunavir of formula (A) above, as described for example in WO2005/063770, the contents of which are incorporated herein by reference.
- Reducing agents suitable for reduction of the nitro moiety are metallic reducing reagents such as borane complexes, diborane, sodium borohydride, lithium borohydride, sodium borohydride-LiCl, aluminum lithium hydride, or diisobutyl- aluminium hydride; metals such as iron, zinc, tin and the like; and transition metals such as palladium-carbon, platinum oxide, Raney-nickel, rhodium, ruthenium and the like. When catalytic reduction is applied, ammonium formate, sodium dihydrogen- phosphate, hydrazine may be used as the hydrogen source.
- metallic reducing reagents such as borane complexes, diborane, sodium borohydride, lithium borohydride, sodium borohydride-LiCl, aluminum lithium hydride, or diisobutyl- aluminium hydride
- metals such as iron, zinc, tin and the like
- transition metals such as palla
- Removal of the amino-protecting-group can be achieved using conditions which will not affect the remaining portion of the molecule. These methods are well known in the art and include acid hydrolysis, hydrogeno lysis and the like, thus using commonly known acids in suitable solvents.
- the compound of formula (VI) is then coupled with a hexahydrofuro [2,3-b] furan- 3-yl derivative to obtain darunavir of formula (A).
- the hexahydrofuro [2,3-b] furan- 3-yl derivative is advantageously an activated derivative of hexahydrofuro [2,3-b] furan-3-ol of formula (VII):
- the compound of formula (VII) above can be prepared in conventional manner for example as described in WO 03/022853, US 2004/0162340, WO 2004/033462, US 6867321, WO-2005/095410 and also Ghosh et al, J. Org Chem. 2004, 69,
- the compound of formula (VII) is suitably activated with a coupling agent to generate a hexahydrofuro [2,3-b] furan-3-yl derivative which is then carbamoylated with the compound of formula (VI) to obtain the protease inhibitor darunavir.
- Examples of coupling agents used in carbamoylation reactions are carbonates such as bis-(4-nitrophenyl)carbonate, disuccinimidyl carbonate (DSC), carbonyl diimidazole (CDI).
- Other coupling agents include chloroformates, such as p-nitrophenylchloro- formate, phosgenes such as phosgene and triphosgene.
- Reaction of the (3R,3aS,6aR)-hexahydrofuro [2,3-b] furan-3-yl derivative with the compound of formula (VI) will be performed in the presence of suitable solvents, such as tetrahydrofuran, dimethylformamide, acetonitrile, dioxane, dichloromethane or chloroform, and optionally with bases, such as triethylamine although further cominations from the solvents and bases hereinabove disclosed are also embodied.
- suitable solvents such as tetrahydrofuran, dimethylformamide, acetonitrile, dioxane, dichloromethane or chloroform
- bases such as triethylamine although further cominations from the solvents and bases hereinabove disclosed are also embodied.
- solvents preferred solvents are aprotic solvents such as tetrahydrofuran, acetonitrile, dimethylformamide, ethyl acetate, and the
- the above carbamoylation reaction is suitably carried out at a temperature between -70 0 C and 40 0 C, preferably between -10 0 C and 20 0 C.
- darunavir namely [(I S,2R)-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)amino]- 2-hydroxy- 1 -(phenylmethyl)propyl]-carbamic acid (3R,3aS,6aR)-hexahydrofuro- [2,3-b]furan-3-yl ester of formula (A), whenever synthesised using an intermediate of formula (I), including an intermediate of formula (F), prepared in accordance with the present invention.
- Example is illustrative of the present invention.
- the Example is presented to exemplify the invention and are not to be construed as limiting the scope of the invention.
Abstract
Description
Claims
Priority Applications (14)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT08749718T ATE498606T1 (en) | 2007-04-27 | 2008-04-25 | PRODUCTION PROCESS FOR N-ISOBUTYL-N-(2-HYDROXY-3-AMINO-4-PHENYLBUTYL)- - NITROBENZENESULFONYLAMIDE DERIVATIVES |
DE602008005012T DE602008005012D1 (en) | 2007-04-27 | 2008-04-25 | PREPARATION FOR N-ISOBUTYL-N- (2-HYDROXY-RIVATE |
CA002682616A CA2682616A1 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
PL08749718T PL2152667T3 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
EP08749718A EP2152667B1 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
US12/597,088 US8076513B2 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
DK08749718.6T DK2152667T3 (en) | 2007-04-27 | 2008-04-25 | Methods for Preparation of N-Isobutyl-n- (2-hydroxy-3-amine-4-phenylbutyl) -p-nitrobenzenesulfonylamide derivatives |
JP2010504703A JP2010525029A (en) | 2007-04-27 | 2008-04-25 | Process for producing N-isobutyl-N- (2-hydroxy-3-amino-4-phenylbutyl) -P-nitrobenzenesulfonylamide derivative |
AU2008244306A AU2008244306A1 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
SI200830232T SI2152667T1 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
MX2009011574A MX2009011574A (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4- phenylbutyl)-p-nitrobenzenesulfonylamide derivatives. |
BRPI0810609-6A2A BRPI0810609A2 (en) | 2007-04-27 | 2008-04-25 | METHODS FOR PREPARING N-ISOBUTIL-N- (2-HYDROXY-A-AMINO-4-PHENYLBUTIL) -P-NITROBE NZENOSULFONILAMIDE DERIVATIVES |
IL200811A IL200811A0 (en) | 2007-04-27 | 2009-09-08 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
HR20110290T HRP20110290T1 (en) | 2007-04-27 | 2011-04-19 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07107177 | 2007-04-27 | ||
EP07107177.3 | 2007-04-27 |
Publications (1)
Publication Number | Publication Date |
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WO2008132154A1 true WO2008132154A1 (en) | 2008-11-06 |
Family
ID=38924830
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2008/055042 WO2008132154A1 (en) | 2007-04-27 | 2008-04-25 | Methods for the preparation of n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide derivatives |
Country Status (20)
Country | Link |
---|---|
US (1) | US8076513B2 (en) |
EP (1) | EP2152667B1 (en) |
JP (1) | JP2010525029A (en) |
CN (1) | CN101668734A (en) |
AT (1) | ATE498606T1 (en) |
AU (1) | AU2008244306A1 (en) |
BR (1) | BRPI0810609A2 (en) |
CA (1) | CA2682616A1 (en) |
CY (1) | CY1111457T1 (en) |
DE (1) | DE602008005012D1 (en) |
DK (1) | DK2152667T3 (en) |
ES (1) | ES2360654T3 (en) |
HR (1) | HRP20110290T1 (en) |
IL (1) | IL200811A0 (en) |
MX (1) | MX2009011574A (en) |
PL (1) | PL2152667T3 (en) |
PT (1) | PT2152667E (en) |
RU (1) | RU2009143867A (en) |
SI (1) | SI2152667T1 (en) |
WO (1) | WO2008132154A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011158259A1 (en) * | 2010-06-18 | 2011-12-22 | Matrix Laboratories Ltd | Novel process for the preparation of (3s)-tetrahydrofuran-3-yl (is, 2r)-3-[[(4-aminophenyl) sulfonyl] (isobutyl) amino]-1-benzyl-2-(phosphonooxy) propylcarbamate and its pharmaceutically acceptable salts thereof |
US8829208B2 (en) | 2010-01-28 | 2014-09-09 | Mapi Pharma Ltd. | Process for the preparation of darunavir and darunavir intermediates |
US8921415B2 (en) | 2009-01-29 | 2014-12-30 | Mapi Pharma Ltd. | Polymorphs of darunavir |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2607279T3 (en) | 2010-11-23 | 2017-03-29 | Mylan Laboratories, Limited | Procedure for the preparation of (3R, 3aS, 6aR) -hexahydrofuro [2,3-b] furan-3-ol |
CN105315178B (en) * | 2014-07-09 | 2018-07-06 | 浙江九洲药业股份有限公司 | Prezista related substances and preparation method thereof |
CN117142989A (en) * | 2020-12-30 | 2023-12-01 | 上海飞腾医药科技有限公司 | Growth method of anti-HIV drug intermediate crystal A and crystal obtained by same |
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WO2001046120A1 (en) * | 1999-12-23 | 2001-06-28 | Aerojet Fine Chemicals Llc | Improved preparation of 2s,3s-n-isobutyl-n-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide hydrochloride and other derivatives of 2-hydroxy-1,3-diamines |
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2008
- 2008-04-25 EP EP08749718A patent/EP2152667B1/en not_active Not-in-force
- 2008-04-25 JP JP2010504703A patent/JP2010525029A/en active Pending
- 2008-04-25 AU AU2008244306A patent/AU2008244306A1/en not_active Abandoned
- 2008-04-25 SI SI200830232T patent/SI2152667T1/en unknown
- 2008-04-25 MX MX2009011574A patent/MX2009011574A/en active IP Right Grant
- 2008-04-25 US US12/597,088 patent/US8076513B2/en not_active Expired - Fee Related
- 2008-04-25 DE DE602008005012T patent/DE602008005012D1/en active Active
- 2008-04-25 RU RU2009143867/04A patent/RU2009143867A/en not_active Application Discontinuation
- 2008-04-25 DK DK08749718.6T patent/DK2152667T3/en active
- 2008-04-25 PT PT08749718T patent/PT2152667E/en unknown
- 2008-04-25 ES ES08749718T patent/ES2360654T3/en active Active
- 2008-04-25 CN CN200880013559A patent/CN101668734A/en active Pending
- 2008-04-25 CA CA002682616A patent/CA2682616A1/en not_active Abandoned
- 2008-04-25 WO PCT/EP2008/055042 patent/WO2008132154A1/en active Application Filing
- 2008-04-25 BR BRPI0810609-6A2A patent/BRPI0810609A2/en not_active IP Right Cessation
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8921415B2 (en) | 2009-01-29 | 2014-12-30 | Mapi Pharma Ltd. | Polymorphs of darunavir |
US9453024B2 (en) | 2009-01-29 | 2016-09-27 | Mapi Pharma Ltd. | Polymorphs of darunavir |
US8829208B2 (en) | 2010-01-28 | 2014-09-09 | Mapi Pharma Ltd. | Process for the preparation of darunavir and darunavir intermediates |
WO2011158259A1 (en) * | 2010-06-18 | 2011-12-22 | Matrix Laboratories Ltd | Novel process for the preparation of (3s)-tetrahydrofuran-3-yl (is, 2r)-3-[[(4-aminophenyl) sulfonyl] (isobutyl) amino]-1-benzyl-2-(phosphonooxy) propylcarbamate and its pharmaceutically acceptable salts thereof |
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DE602008005012D1 (en) | 2011-03-31 |
US20100121094A1 (en) | 2010-05-13 |
ATE498606T1 (en) | 2011-03-15 |
SI2152667T1 (en) | 2011-06-30 |
AU2008244306A1 (en) | 2008-11-06 |
EP2152667A1 (en) | 2010-02-17 |
CY1111457T1 (en) | 2015-08-05 |
DK2152667T3 (en) | 2011-05-16 |
BRPI0810609A2 (en) | 2014-10-21 |
ES2360654T3 (en) | 2011-06-08 |
HRP20110290T1 (en) | 2011-05-31 |
JP2010525029A (en) | 2010-07-22 |
RU2009143867A (en) | 2011-06-10 |
MX2009011574A (en) | 2009-11-09 |
EP2152667B1 (en) | 2011-02-16 |
CN101668734A (en) | 2010-03-10 |
US8076513B2 (en) | 2011-12-13 |
PT2152667E (en) | 2011-04-06 |
PL2152667T3 (en) | 2011-06-30 |
IL200811A0 (en) | 2010-05-17 |
CA2682616A1 (en) | 2008-11-06 |
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