WO2012085935A3 - Diamide piperidine compounds as inhibitors of renin - Google Patents
Diamide piperidine compounds as inhibitors of renin Download PDFInfo
- Publication number
- WO2012085935A3 WO2012085935A3 PCT/IN2011/000870 IN2011000870W WO2012085935A3 WO 2012085935 A3 WO2012085935 A3 WO 2012085935A3 IN 2011000870 W IN2011000870 W IN 2011000870W WO 2012085935 A3 WO2012085935 A3 WO 2012085935A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inhibitors
- diamide
- renin
- piperidine compounds
- synthesis
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
The present invention relates to novel renin inhibitors of general formula (1), novel intermediates involved in their synthesis, their pharmaceutically acceptable salts and pharmaceutical compositions containing them. The present invention also relates to a process of preparing compounds of general formula (1), their tautomeric forms, their pharmaceutically acceptable salts, pharmaceutical compositions containing them, and novel intermediates involved in their synthesis.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN3487/MUM/2010 | 2010-12-22 | ||
IN3487MU2010 | 2010-12-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2012085935A2 WO2012085935A2 (en) | 2012-06-28 |
WO2012085935A3 true WO2012085935A3 (en) | 2013-09-26 |
Family
ID=46314551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2011/000870 WO2012085935A2 (en) | 2010-12-22 | 2011-12-19 | Compounds as inhibitors of renin |
Country Status (2)
Country | Link |
---|---|
AR (1) | AR084546A1 (en) |
WO (1) | WO2012085935A2 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008058387A1 (en) * | 2006-11-17 | 2008-05-22 | Merck Frosst Canada Ltd. | Renin inhibitors |
WO2008141462A1 (en) * | 2007-05-24 | 2008-11-27 | Merck Frosst Canada Ltd. | Novel case of renin inhibitors |
WO2010122580A2 (en) * | 2009-04-24 | 2010-10-28 | Cadila Healthcare Limited | Novel compounds as inhibitors of renin |
-
2011
- 2011-12-19 WO PCT/IN2011/000870 patent/WO2012085935A2/en active Application Filing
- 2011-12-22 AR ARP110104889A patent/AR084546A1/en not_active Application Discontinuation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008058387A1 (en) * | 2006-11-17 | 2008-05-22 | Merck Frosst Canada Ltd. | Renin inhibitors |
WO2008141462A1 (en) * | 2007-05-24 | 2008-11-27 | Merck Frosst Canada Ltd. | Novel case of renin inhibitors |
WO2010122580A2 (en) * | 2009-04-24 | 2010-10-28 | Cadila Healthcare Limited | Novel compounds as inhibitors of renin |
Non-Patent Citations (2)
Title |
---|
GREENE, T.W.; WUTS, P.G.M.: "Protective Groups in organic synthesis - 3rd Edition", part N-Benzylamine (R2N-Bn) 1999, JOHN WILEY AND SONS, ISBN: 0-471-16019-9, pages: 579 - 580, XP002699619 * |
GREENE, T.W.; WUTS, P.G.M.: "Protective groups in organic synthesis - 3rd Edition", part t-Butyl (BOC) Carbamate 1999, JOHN WILEY AND SONS, ISBN: 0-471-16019-9, pages: 518 - 522, XP002698650 * |
Also Published As
Publication number | Publication date |
---|---|
WO2012085935A2 (en) | 2012-06-28 |
AR084546A1 (en) | 2013-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2010105179A3 (en) | Inhibitors of beta-secretase | |
MX342212B (en) | Substituted aminobutyric derivatives as neprilysin inhibitors. | |
MY165087A (en) | Neprilysin inhibitors | |
WO2011015522A3 (en) | Process for the manufacture of pharmaceutically active compounds | |
MX347841B (en) | Process for preparing tetrazole-substituted anthranilamide derivatives and novel crystal polymorph of these derivatives. | |
MY170935A (en) | Neprilysin inhibitors | |
WO2012015681A3 (en) | Drug-ligand conjugates, synthesis thereof, and intermediates thereto | |
MX354476B (en) | Neprilysin inhibitors. | |
PH12015500211B1 (en) | 4-methyl-2,3,5,9,9b-pentaaza-cyclopenta[a]naphthalenes | |
MX2013005833A (en) | Novel fused pyridine compounds as casein kinase inhibitors. | |
JO3577B1 (en) | Pharmaceutical formulations comprising 1-(beta-d-glucopyranosyl)-2-thienylmethylbenzene derivatives as inhibitors of sglt | |
MX2011007978A (en) | Novel method for the synthesis of ivabradine and the pharmaceutically acceptable acid addition salts thereof. | |
MY150280A (en) | Process of preparing derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid | |
MY161749A (en) | Compound, certain novel forms thereof, pharmaceutical compositions thereof and methods for preparation and use | |
MX2010003213A (en) | Novel method for the synthesis of ivabradine and the addition salts thereof with a pharmaceutically acceptable acid. | |
MX2010009876A (en) | New process for the preparation of cyclohexanecarboxylic acid derivatives via the corresponding cyclohexanecarboxamide derivative. | |
WO2011047055A3 (en) | Novel mek inhibitors, useful in the treatment of diseases | |
WO2008059513A3 (en) | Compounds suitable as modulators of hdl | |
MX2010003184A (en) | Novel method for the synthesis of ivabradine and the addition salts thereof with a pharmaceutically acceptable acid. | |
WO2010122580A3 (en) | Piperidine derivatives as inhibitors of renin | |
WO2012015687A3 (en) | Drug-ligand conjugates, synthesis thereof, and intermediates thereto | |
WO2010146595A3 (en) | Novel polymorphs of flibanserin hydrochloride | |
MX2010006218A (en) | Organic compounds. | |
WO2012085935A3 (en) | Diamide piperidine compounds as inhibitors of renin | |
WO2009053999A3 (en) | Sulfoximine derivatives as factor xa inhibitors |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
DPE2 | Request for preliminary examination filed before expiration of 19th month from priority date (pct application filed from 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11851443 Country of ref document: EP Kind code of ref document: A2 |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 11851443 Country of ref document: EP Kind code of ref document: A2 |