FI120342B - Menetelmä retrovirusproteaasi-inhibiittoreina käyttökelpoisten N-(alkanoyyliamino-2-hydroksipropyyli)-sulfonamidien valmistamiseksi - Google Patents
Menetelmä retrovirusproteaasi-inhibiittoreina käyttökelpoisten N-(alkanoyyliamino-2-hydroksipropyyli)-sulfonamidien valmistamiseksi Download PDFInfo
- Publication number
- FI120342B FI120342B FI950841A FI950841A FI120342B FI 120342 B FI120342 B FI 120342B FI 950841 A FI950841 A FI 950841A FI 950841 A FI950841 A FI 950841A FI 120342 B FI120342 B FI 120342B
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- Finland
- Prior art keywords
- amino
- formula
- phenylmethyl
- compound
- propyl
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 47
- 238000002360 preparation method Methods 0.000 title claims description 43
- 230000008569 process Effects 0.000 title claims description 22
- 239000000137 peptide hydrolase inhibitor Substances 0.000 title abstract description 7
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 title abstract description 6
- 229940124530 sulfonamide Drugs 0.000 title description 10
- 150000003456 sulfonamides Chemical class 0.000 title description 9
- 241001430294 unidentified retrovirus Species 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 92
- -1 methoxyphenyl Chemical group 0.000 claims description 54
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 33
- 239000002253 acid Substances 0.000 claims description 27
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 26
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 20
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 18
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 8
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- LDECUSDQMXVUMP-UHFFFAOYSA-N benzyl 3-[6-[[2-(butylamino)-1-[3-methoxycarbonyl-4-(2-methoxy-2-oxoethoxy)phenyl]-2-oxoethyl]-hexylamino]-6-oxohexyl]-4-methyl-2-oxo-6-(4-phenylphenyl)-1,6-dihydropyrimidine-5-carboxylate Chemical compound O=C1NC(C=2C=CC(=CC=2)C=2C=CC=CC=2)C(C(=O)OCC=2C=CC=CC=2)=C(C)N1CCCCCC(=O)N(CCCCCC)C(C(=O)NCCCC)C1=CC=C(OCC(=O)OC)C(C(=O)OC)=C1 LDECUSDQMXVUMP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
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- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
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- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
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Classifications
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
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- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4409—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid
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- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/05—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/18—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93549092A | 1992-08-25 | 1992-08-25 | |
US93549092 | 1992-08-25 | ||
US9307815 | 1993-08-24 | ||
PCT/US1993/007815 WO1994004491A1 (en) | 1992-08-25 | 1993-08-24 | N-(alkanoylamino-2-hydroxypropyl)-sulfonamides useful as retroviral protease inhibitors |
Publications (3)
Publication Number | Publication Date |
---|---|
FI950841A0 FI950841A0 (fi) | 1995-02-23 |
FI950841A FI950841A (fi) | 1995-02-23 |
FI120342B true FI120342B (fi) | 2009-09-30 |
Family
ID=25467232
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI950841A FI120342B (fi) | 1992-08-25 | 1995-02-23 | Menetelmä retrovirusproteaasi-inhibiittoreina käyttökelpoisten N-(alkanoyyliamino-2-hydroksipropyyli)-sulfonamidien valmistamiseksi |
Country Status (15)
Country | Link |
---|---|
US (2) | US5463104A (de) |
EP (1) | EP0656886B1 (de) |
JP (1) | JP4091653B2 (de) |
KR (1) | KR100296461B1 (de) |
AT (1) | ATE154800T1 (de) |
AU (1) | AU674702B2 (de) |
CA (1) | CA2142998C (de) |
DE (1) | DE69311810T2 (de) |
DK (1) | DK0656886T3 (de) |
ES (1) | ES2103488T3 (de) |
FI (1) | FI120342B (de) |
GR (1) | GR3024181T3 (de) |
NO (1) | NO302883B1 (de) |
RU (1) | RU2130016C1 (de) |
WO (1) | WO1994004491A1 (de) |
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US7141609B2 (en) | 1992-08-25 | 2006-11-28 | G.D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
US6022994A (en) * | 1992-08-25 | 2000-02-08 | G. D. Searle &. Co. | Succinoylamino hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
KR100336699B1 (ko) | 1992-08-25 | 2002-05-13 | 윌리암스 로저 에이 | 레트로바이러스 프로테아제 저해제로서 유용한히드록시에틸아미노 술폰아미드 |
US5723490A (en) * | 1992-09-08 | 1998-03-03 | Vertex Pharmaceuticals Incorporated | THF-containing sulfonamide inhibitors of aspartyl protease |
IS2334B (is) | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl próteasi hemjari af nýjum flokki súlfonamíða |
US5783701A (en) | 1992-09-08 | 1998-07-21 | Vertex Pharmaceuticals, Incorporated | Sulfonamide inhibitors of aspartyl protease |
EP0749421B1 (de) * | 1994-03-07 | 1999-09-15 | Vertex Pharmaceuticals Incorporated | Sulfonamidderivate als aspartylprotease-inhibitoren |
US5527829A (en) * | 1994-05-23 | 1996-06-18 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
CA2210889C (en) | 1995-01-20 | 2007-08-28 | G.D. Searle & Co. | Bis-sulfonamide hydroxyethylamino retroviral protease inhibitors |
US5691372A (en) * | 1995-04-19 | 1997-11-25 | Vertex Pharmaceuticals Incorporated | Oxygenated-Heterocycle containing sulfonamide inhibitors of aspartyl protease |
US6004957A (en) * | 1995-06-07 | 1999-12-21 | Vertex Pharmaceuticals, Incorporated | Sulfonamide inhibitors of aspartyl protease |
DE69608121T2 (de) | 1995-11-16 | 2000-09-28 | G.D. Searle & Co., Chicago | N-geschützte/n-substituierte beta-aminohydroxysulfonate |
US5962725A (en) | 1996-09-05 | 1999-10-05 | Agouron Pharmaceuticals, Inc. | Intermediate compounds useful for making HIV protease inhibitors such as nelfinavir |
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US5705647A (en) * | 1996-09-05 | 1998-01-06 | Agouron Pharmaceuticals, Inc. | Intermediates for making HIV-protease inhibitors |
DE19703713A1 (de) * | 1997-01-23 | 1998-07-30 | Hans Prof Dr Schick | Verfahren für die Herstellung von Oxetan-2-onen und Zwischenprodukte |
US6001851A (en) * | 1997-03-13 | 1999-12-14 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
US6590106B2 (en) | 1997-05-09 | 2003-07-08 | Pharm-Eco Laboratories, Inc. | Amino acid derivatives and methods of making the same |
US6479669B2 (en) | 1997-05-09 | 2002-11-12 | Pharm-Eco Laboratories, Inc. | Amino acid derivatives and methods of making the same |
US6084107A (en) * | 1997-09-05 | 2000-07-04 | Agouron Pharmaceuticals, Inc. | Intermediates for making HIV-protease inhibitors |
US6436989B1 (en) | 1997-12-24 | 2002-08-20 | Vertex Pharmaceuticals, Incorporated | Prodrugs of aspartyl protease inhibitors |
WO1999065870A2 (en) | 1998-06-19 | 1999-12-23 | Vertex Pharmaceuticals Incorporated | Sulfonamide inhibitors of aspartyl protease |
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US6506786B2 (en) | 2001-02-13 | 2003-01-14 | Pharmacor Inc. | HIV protease inhibitors based on amino acid derivatives |
AU2002310818B2 (en) * | 2001-05-11 | 2007-12-13 | Tibotec Pharmaceuticals Ltd. | Broadspectrum 2-amino-benzoxazole sulfonamide HIV protease inhibitors |
CA2473461C (en) * | 2002-01-11 | 2011-11-01 | Sankyo Company, Limited | Amino alcohol derivative or phosphonic acid derivative and medicinal composition containing these |
BRPI0507944A (pt) | 2004-02-24 | 2007-07-24 | Sankyo Co | composição farmacêutica |
US7388008B2 (en) * | 2004-08-02 | 2008-06-17 | Ambrilia Biopharma Inc. | Lysine based compounds |
JP2008533017A (ja) * | 2005-03-11 | 2008-08-21 | スミスクライン ビーチャム コーポレーション | Hivプロテアーゼ阻害薬 |
US20060287316A1 (en) * | 2005-04-27 | 2006-12-21 | Ambrilia Biopharma Inc. | Method for improving pharmacokinetics of protease inhibitors and protease inhibitor precursors |
US8227450B2 (en) * | 2005-11-30 | 2012-07-24 | Ambrilia Biopharma Inc. | Lysine-based prodrugs of aspartyl protease inhibitors and processes for their preparation |
US8410300B2 (en) * | 2006-09-21 | 2013-04-02 | Taimed Biologics, Inc. | Protease inhibitors |
DE102015001289A1 (de) | 2015-01-29 | 2016-08-04 | Wolfgang Winkelmann | Pharmazeutische Zusammensetzungen und Pflanzenschutzmittel enthaltend mit Sauerstoff angereicherte Pflanzenöle oder Fettsäuren |
UY36649A (es) * | 2015-04-23 | 2016-11-30 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Inhibidores de la replicación del virus de la inmunodeficiencia humana |
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-
1993
- 1993-08-24 AT AT93920213T patent/ATE154800T1/de active
- 1993-08-24 JP JP50653194A patent/JP4091653B2/ja not_active Expired - Lifetime
- 1993-08-24 ES ES93920213T patent/ES2103488T3/es not_active Expired - Lifetime
- 1993-08-24 DK DK93920213.1T patent/DK0656886T3/da active
- 1993-08-24 US US08/110,912 patent/US5463104A/en not_active Expired - Lifetime
- 1993-08-24 KR KR1019950700730A patent/KR100296461B1/ko not_active IP Right Cessation
- 1993-08-24 EP EP93920213A patent/EP0656886B1/de not_active Expired - Lifetime
- 1993-08-24 CA CA002142998A patent/CA2142998C/en not_active Expired - Lifetime
- 1993-08-24 WO PCT/US1993/007815 patent/WO1994004491A1/en active IP Right Grant
- 1993-08-24 DE DE69311810T patent/DE69311810T2/de not_active Expired - Lifetime
- 1993-08-25 AU AU50819/93A patent/AU674702B2/en not_active Expired
- 1993-08-25 RU RU95106823A patent/RU2130016C1/ru active
-
1995
- 1995-02-22 NO NO950670A patent/NO302883B1/no not_active IP Right Cessation
- 1995-02-23 FI FI950841A patent/FI120342B/fi not_active IP Right Cessation
- 1995-10-10 US US08/541,350 patent/US5714605A/en not_active Expired - Lifetime
-
1997
- 1997-07-22 GR GR970401826T patent/GR3024181T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
CA2142998C (en) | 2008-01-29 |
DE69311810T2 (de) | 1997-11-27 |
JP4091653B2 (ja) | 2008-05-28 |
WO1994004491A1 (en) | 1994-03-03 |
EP0656886A1 (de) | 1995-06-14 |
RU2130016C1 (ru) | 1999-05-10 |
KR100296461B1 (ko) | 2001-11-14 |
NO950670D0 (no) | 1995-02-22 |
EP0656886B1 (de) | 1997-06-25 |
DE69311810D1 (de) | 1997-07-31 |
KR950702959A (ko) | 1995-08-23 |
NO950670L (no) | 1995-02-22 |
AU674702B2 (en) | 1997-01-09 |
US5463104A (en) | 1995-10-31 |
US5714605A (en) | 1998-02-03 |
RU95106823A (ru) | 1996-11-20 |
FI950841A0 (fi) | 1995-02-23 |
ATE154800T1 (de) | 1997-07-15 |
JPH08500824A (ja) | 1996-01-30 |
CA2142998A1 (en) | 1994-03-03 |
NO302883B1 (no) | 1998-05-04 |
FI950841A (fi) | 1995-02-23 |
GR3024181T3 (en) | 1997-10-31 |
AU5081993A (en) | 1994-03-15 |
ES2103488T3 (es) | 1997-09-16 |
DK0656886T3 (da) | 1998-02-02 |
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