NO329995B1 - Karboksylsyreforbindelse, anvendelse derav, og farmasoytisk preparat omfattende en slik forbindelse - Google Patents
Karboksylsyreforbindelse, anvendelse derav, og farmasoytisk preparat omfattende en slik forbindelse Download PDFInfo
- Publication number
- NO329995B1 NO329995B1 NO20034669A NO20034669A NO329995B1 NO 329995 B1 NO329995 B1 NO 329995B1 NO 20034669 A NO20034669 A NO 20034669A NO 20034669 A NO20034669 A NO 20034669A NO 329995 B1 NO329995 B1 NO 329995B1
- Authority
- NO
- Norway
- Prior art keywords
- phenyl
- acid
- isopropoxypropanoic acid
- isopropoxypropanoic
- methyl
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 121
- -1 Carboxylic acid compound Chemical class 0.000 title claims description 46
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 238000002360 preparation method Methods 0.000 claims description 36
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 27
- 150000003839 salts Chemical class 0.000 claims description 27
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 22
- 230000000694 effects Effects 0.000 claims description 15
- 235000019260 propionic acid Nutrition 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 11
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- KVMLDUFYRBHZLA-JXFKEZNVSA-N (2s)-3-[3-[(2s)-3-(2,4-dichlorophenoxy)-2-hydroxypropoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OC[C@H](O)COC=2C(=CC(Cl)=CC=2)Cl)=C1 KVMLDUFYRBHZLA-JXFKEZNVSA-N 0.000 claims description 5
- FGDSWQUNQRAFGM-UHFFFAOYSA-N 2-ethoxy-3-[3-[2-[[4-(trifluoromethyl)phenyl]carbamoyloxy]ethyl]phenyl]propanoic acid Chemical compound CCOC(C(O)=O)CC1=CC=CC(CCOC(=O)NC=2C=CC(=CC=2)C(F)(F)F)=C1 FGDSWQUNQRAFGM-UHFFFAOYSA-N 0.000 claims description 5
- YRAMODFTOQIPAB-UHFFFAOYSA-N 3-[3-[3-(4-chloro-2-cyanophenoxy)-2-hydroxypropoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)OC(C(O)=O)CC1=CC=CC(OCC(O)COC=2C(=CC(Cl)=CC=2)C#N)=C1 YRAMODFTOQIPAB-UHFFFAOYSA-N 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- KVMLDUFYRBHZLA-UZLBHIALSA-N (2s)-3-[3-[(2r)-3-(2,4-dichlorophenoxy)-2-hydroxypropoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OC[C@@H](O)COC=2C(=CC(Cl)=CC=2)Cl)=C1 KVMLDUFYRBHZLA-UZLBHIALSA-N 0.000 claims description 4
- KSCQWJTZMRLVFD-KNQAVFIVSA-N (2s)-3-[3-[(2r)-3-(2,4-dimethylphenoxy)-2-hydroxypropoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OC[C@@H](O)COC=2C(=CC(C)=CC=2)C)=C1 KSCQWJTZMRLVFD-KNQAVFIVSA-N 0.000 claims description 4
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- CJVSMEAANCYXJX-FQEVSTJZSA-N (2s)-3-[3-[3-(2,4-dichlorophenyl)prop-2-ynoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OCC#CC=2C(=CC(Cl)=CC=2)Cl)=C1 CJVSMEAANCYXJX-FQEVSTJZSA-N 0.000 claims description 4
- HFGYDSHPQNYQLA-FQEVSTJZSA-N (2s)-3-[3-[3-(4-chlorophenyl)prop-2-ynoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OCC#CC=2C=CC(Cl)=CC=2)=C1 HFGYDSHPQNYQLA-FQEVSTJZSA-N 0.000 claims description 4
- OTSMBBLUPFHIJA-FQEVSTJZSA-N (2s)-3-[3-[[2-(4-chlorophenyl)ethoxycarbonylamino]methyl]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(CNC(=O)OCCC=2C=CC(Cl)=CC=2)=C1 OTSMBBLUPFHIJA-FQEVSTJZSA-N 0.000 claims description 4
- CJVSMEAANCYXJX-UHFFFAOYSA-N 3-[3-[3-(2,4-dichlorophenyl)prop-2-ynoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)OC(C(O)=O)CC1=CC=CC(OCC#CC=2C(=CC(Cl)=CC=2)Cl)=C1 CJVSMEAANCYXJX-UHFFFAOYSA-N 0.000 claims description 4
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- JVAGOHKEHAIJRC-IBGZPJMESA-N (2s)-2-propan-2-yloxy-3-[3-[[[3-(trifluoromethoxy)phenyl]methoxycarbonylamino]methyl]phenyl]propanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(CNC(=O)OCC=2C=C(OC(F)(F)F)C=CC=2)=C1 JVAGOHKEHAIJRC-IBGZPJMESA-N 0.000 claims description 3
- AQPYWJWCKLHHPI-IBGZPJMESA-N (2s)-2-propan-2-yloxy-3-[3-[[[4-(trifluoromethyl)phenyl]methoxycarbonylamino]methyl]phenyl]propanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(CNC(=O)OCC=2C=CC(=CC=2)C(F)(F)F)=C1 AQPYWJWCKLHHPI-IBGZPJMESA-N 0.000 claims description 3
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- AIUIRBZEKABETF-UGKGYDQZSA-N (2s)-3-[3-[(2s)-3-(2,4-dimethylphenoxy)-2-fluoropropoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OC[C@H](F)COC=2C(=CC(C)=CC=2)C)=C1 AIUIRBZEKABETF-UGKGYDQZSA-N 0.000 claims description 3
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- QICKBMIIFBKLBR-RXVVDRJESA-N (2s)-3-[3-[(2s)-3-(4-chloro-2-cyanophenoxy)-2-fluoropropoxy]phenyl]-2-propan-2-yloxypropanoic acid Chemical compound CC(C)O[C@H](C(O)=O)CC1=CC=CC(OC[C@H](F)COC=2C(=CC(Cl)=CC=2)C#N)=C1 QICKBMIIFBKLBR-RXVVDRJESA-N 0.000 claims description 3
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Classifications
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- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/54—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- General Health & Medical Sciences (AREA)
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001123346 | 2001-04-20 | ||
JP2002036274 | 2002-02-14 | ||
PCT/JP2002/003866 WO2002100812A1 (fr) | 2001-04-20 | 2002-04-18 | Dérivé de l'acide carboxylique et son sel |
Publications (3)
Publication Number | Publication Date |
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NO20034669D0 NO20034669D0 (no) | 2003-10-17 |
NO20034669L NO20034669L (no) | 2003-12-17 |
NO329995B1 true NO329995B1 (no) | 2011-02-07 |
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NO20034669A NO329995B1 (no) | 2001-04-20 | 2003-10-17 | Karboksylsyreforbindelse, anvendelse derav, og farmasoytisk preparat omfattende en slik forbindelse |
Country Status (19)
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US (1) | US7544835B2 (ko) |
EP (1) | EP1380562A4 (ko) |
JP (1) | JP4131698B2 (ko) |
KR (1) | KR100888001B1 (ko) |
CN (1) | CN100522944C (ko) |
AU (1) | AU2002251481B2 (ko) |
BR (1) | BR0209027A (ko) |
CA (1) | CA2442319C (ko) |
CZ (1) | CZ20032727A3 (ko) |
HU (1) | HUP0303810A3 (ko) |
IL (1) | IL157731A0 (ko) |
MX (1) | MXPA03009565A (ko) |
NO (1) | NO329995B1 (ko) |
NZ (2) | NZ528655A (ko) |
PL (1) | PL206767B1 (ko) |
RU (1) | RU2316537C2 (ko) |
SG (1) | SG161743A1 (ko) |
TW (1) | TWI311133B (ko) |
WO (1) | WO2002100812A1 (ko) |
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CN101679298B (zh) * | 2007-04-05 | 2013-10-23 | 第一三共株式会社 | 稠合二环杂芳基衍生物 |
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- 2002-04-18 NZ NZ528655A patent/NZ528655A/en unknown
- 2002-04-18 PL PL367196A patent/PL206767B1/pl not_active IP Right Cessation
- 2002-04-18 BR BR0209027-9A patent/BR0209027A/pt not_active Application Discontinuation
- 2002-04-18 US US10/472,543 patent/US7544835B2/en not_active Expired - Fee Related
- 2002-04-18 KR KR1020037013180A patent/KR100888001B1/ko not_active IP Right Cessation
- 2002-04-18 AU AU2002251481A patent/AU2002251481B2/en not_active Ceased
- 2002-04-18 MX MXPA03009565A patent/MXPA03009565A/es active IP Right Grant
- 2002-04-18 JP JP2003503583A patent/JP4131698B2/ja not_active Expired - Fee Related
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- 2002-04-18 EP EP02720489A patent/EP1380562A4/en not_active Withdrawn
- 2002-04-18 CN CNB028084985A patent/CN100522944C/zh not_active Expired - Fee Related
- 2002-04-18 SG SG200608047-7A patent/SG161743A1/en unknown
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- 2002-04-18 NZ NZ539708A patent/NZ539708A/en unknown
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- 2002-04-18 HU HU0303810A patent/HUP0303810A3/hu unknown
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IL157731A0 (en) | 2004-03-28 |
CN100522944C (zh) | 2009-08-05 |
RU2003133744A (ru) | 2005-04-20 |
NZ528655A (en) | 2005-12-23 |
JPWO2002100812A1 (ja) | 2004-09-24 |
CZ20032727A3 (cs) | 2004-01-14 |
MXPA03009565A (es) | 2004-02-12 |
WO2002100812A1 (fr) | 2002-12-19 |
US7544835B2 (en) | 2009-06-09 |
RU2316537C2 (ru) | 2008-02-10 |
TWI311133B (en) | 2009-06-21 |
KR100888001B1 (ko) | 2009-03-09 |
PL206767B1 (pl) | 2010-09-30 |
CN1503774A (zh) | 2004-06-09 |
HUP0303810A2 (hu) | 2004-03-01 |
US20040102634A1 (en) | 2004-05-27 |
NO20034669L (no) | 2003-12-17 |
HUP0303810A3 (en) | 2009-10-28 |
AU2002251481B2 (en) | 2007-08-09 |
EP1380562A4 (en) | 2006-03-08 |
JP4131698B2 (ja) | 2008-08-13 |
NZ539708A (en) | 2005-09-30 |
SG161743A1 (en) | 2010-06-29 |
CA2442319A1 (en) | 2002-12-19 |
BR0209027A (pt) | 2005-05-24 |
PL367196A1 (en) | 2005-02-21 |
KR20030093302A (ko) | 2003-12-06 |
CA2442319C (en) | 2011-02-08 |
EP1380562A1 (en) | 2004-01-14 |
NO20034669D0 (no) | 2003-10-17 |
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