BRPI0618381A2 - processo para a preparação do hemi-sal de cálcio do ácido (3r, 5r) -7-[2-(4-fluorofenil) -5-isopropil-3-fenil-4-[(4-hidroximetilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico - Google Patents
processo para a preparação do hemi-sal de cálcio do ácido (3r, 5r) -7-[2-(4-fluorofenil) -5-isopropil-3-fenil-4-[(4-hidroximetilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico Download PDFInfo
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- BRPI0618381A2 BRPI0618381A2 BRPI0618381-6A BRPI0618381A BRPI0618381A2 BR PI0618381 A2 BRPI0618381 A2 BR PI0618381A2 BR PI0618381 A BRPI0618381 A BR PI0618381A BR PI0618381 A2 BRPI0618381 A2 BR PI0618381A2
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- BR
- Brazil
- Prior art keywords
- carbonyl
- isopropyl
- phenyl
- preparation
- fluorophenyl
- Prior art date
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- 238000000034 method Methods 0.000 title abstract 3
- 239000002253 acid Substances 0.000 title abstract 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 title 1
- -1 4-hydroxymethylphenylamino Chemical group 0.000 title 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 title 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid group Chemical group C(CCCCCC)(=O)O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 title 1
- PMFRPLBQEYHUMG-VSGBNLITSA-N (3r,5r)-7-[2-(4-fluorophenyl)-4-[[4-(hydroxymethyl)phenyl]carbamoyl]-3-phenyl-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoic acid Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=C(CO)C=C1 PMFRPLBQEYHUMG-VSGBNLITSA-N 0.000 abstract 1
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- C07—ORGANIC CHEMISTRY
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- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
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Abstract
PROCESSO PARA A PREPARAçãO DO HEMI-SAL DE CáLCIO DO áCIDO (3R, 5R) -7- [2- (4-FLUOROFENIL) -5-ISOPROPIL-3-FENIL-4- [(4- HIDROXIMETILFENILAMINO) CARBONIL] -PIRROL-1-IL] -3, 5-DIIDROXI HEPTANóICO. A presente invenção refere-se a processos para a preparação do hemi-sal de cálcio do ácido (3R,5R)-7-[2-(4- fluorofenil) -5-isopropil-3-fenil-4- [ (4-hidroximetilfenil amino) carbonil] -pirrol-l-il] -3, 5-diidroxiheptanóico.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN2967DE2005 | 2005-11-08 | ||
| IN2964DE2005 | 2005-11-08 | ||
| IN3033DE2005 | 2005-11-14 | ||
| PCT/IB2006/003153 WO2007054790A1 (en) | 2005-11-08 | 2006-11-08 | Process for preparation of (3r, 5r)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-[(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid hemi calcium salt |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0618381A2 true BRPI0618381A2 (pt) | 2011-08-30 |
Family
ID=37719151
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0618379-4A BRPI0618379A2 (pt) | 2005-11-08 | 2006-11-07 | processo para preparação do hemi-sal de cálcio do ácido (3r,5r) -7-[2-(4-fluorofenil)-5-isopropil-3-fenil-4-[(4-hidroxime tilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico |
| BRPI0618381-6A BRPI0618381A2 (pt) | 2005-11-08 | 2006-11-08 | processo para a preparação do hemi-sal de cálcio do ácido (3r, 5r) -7-[2-(4-fluorofenil) -5-isopropil-3-fenil-4-[(4-hidroximetilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico |
| BRPI0618380-8A BRPI0618380A2 (pt) | 2005-11-08 | 2006-11-08 | combinação farmacêutica e seu uso |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0618379-4A BRPI0618379A2 (pt) | 2005-11-08 | 2006-11-07 | processo para preparação do hemi-sal de cálcio do ácido (3r,5r) -7-[2-(4-fluorofenil)-5-isopropil-3-fenil-4-[(4-hidroxime tilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0618380-8A BRPI0618380A2 (pt) | 2005-11-08 | 2006-11-08 | combinação farmacêutica e seu uso |
Country Status (13)
| Country | Link |
|---|---|
| US (5) | US8026377B2 (pt) |
| EP (3) | EP1948599A1 (pt) |
| JP (3) | JP2009514851A (pt) |
| KR (3) | KR101329112B1 (pt) |
| CN (1) | CN102526029A (pt) |
| AU (3) | AU2006313430B2 (pt) |
| BR (3) | BRPI0618379A2 (pt) |
| CA (3) | CA2627599A1 (pt) |
| IL (1) | IL191203A0 (pt) |
| MY (1) | MY147450A (pt) |
| NZ (1) | NZ567738A (pt) |
| SG (1) | SG166829A1 (pt) |
| WO (3) | WO2007054896A1 (pt) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG141430A1 (en) * | 2003-05-30 | 2008-04-28 | Ranbaxy Lab Ltd | Substituted pyrrole derivatives and their use as hmg-co inhibitors |
| BRPI0618379A2 (pt) | 2005-11-08 | 2011-08-30 | Ranbaxy Lab Ltd | processo para preparação do hemi-sal de cálcio do ácido (3r,5r) -7-[2-(4-fluorofenil)-5-isopropil-3-fenil-4-[(4-hidroxime tilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico |
| AU2007205838A1 (en) | 2006-01-19 | 2007-07-26 | Mary Kay, Inc. | Compositions comprising kakadu plum extract or acai berry extract |
| PT2359826E (pt) | 2006-07-05 | 2014-01-20 | Takeda Gmbh | Combinação de um inibidor da hmg-coa redutase rosuvastatina e um inibidor da fosfodiesterase 4, tais como roflumilaste, óxido de n-roflumilaste, para o tratamento de doenças pulmonares inflamatórias |
| JP5366803B2 (ja) | 2007-05-24 | 2013-12-11 | 田辺三菱製薬株式会社 | 脳梗塞治療剤 |
| WO2010066593A1 (en) * | 2008-12-08 | 2010-06-17 | F. Hoffmann-La Roche Ag | Combined drug administration |
| MX2012002424A (es) | 2009-08-28 | 2012-06-27 | Mary Kay Inc | Formulaciones para el cuidado de la piel. |
| EP2322163A1 (en) * | 2009-11-03 | 2011-05-18 | Pharnext | New therapeutics approaches for treating alzheimer disease |
| WO2011153247A1 (en) * | 2010-06-01 | 2011-12-08 | Furiex Pharmaceuticals, Inc. | Combination therapies |
| US20120245188A1 (en) * | 2010-11-15 | 2012-09-27 | Translational Genomics Research Institute | Methods of treating memory loss and enhancing memory performance |
| MX370538B (es) | 2013-03-27 | 2019-12-17 | Hoffmann La Roche | Marcadores genéticos para la predicción de respuesta a la terápia. |
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