ZA200903040B - Urea and sulfamide derivatives as tafia inhibitors - Google Patents

Urea and sulfamide derivatives as tafia inhibitors

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Publication number
ZA200903040B
ZA200903040B ZA2009/03040A ZA200903040A ZA200903040B ZA 200903040 B ZA200903040 B ZA 200903040B ZA 2009/03040 A ZA2009/03040 A ZA 2009/03040A ZA 200903040 A ZA200903040 A ZA 200903040A ZA 200903040 B ZA200903040 B ZA 200903040B
Authority
ZA
South Africa
Prior art keywords
urea
tafia inhibitors
sulfamide derivatives
sulfamide
derivatives
Prior art date
Application number
ZA2009/03040A
Other languages
English (en)
Inventor
Christopher Kallus
Mark Broenstrup
Werngard Czechtizky
Andreas Evers
Markus Follmann
Nis Halland
Herman Schreuder
Original Assignee
Sanofi Aventis
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of ZA200903040B publication Critical patent/ZA200903040B/en

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    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
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    • A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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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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    • C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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
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    • C—CHEMISTRY; METALLURGY
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    • 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
    • C07D317/58—Radicals substituted by nitrogen atoms
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    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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ZA2009/03040A 2006-12-06 2009-05-04 Urea and sulfamide derivatives as tafia inhibitors ZA200903040B (en)

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PCT/EP2007/010101 WO2008067909A2 (de) 2006-12-06 2007-11-22 Harnstoff- und sulfamidderivate als inhibitoren von tafia

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MX2010012793A (es) 2008-06-06 2010-12-14 Sanofi Aventis Derivados de urea macrociclicos y de sulfamida como inhibidores de tafia.
CA2727925A1 (en) 2008-06-23 2009-12-30 Astrazeneca Ab New heterocyclic carboxamides for use as thrombin inhibitors
US8354444B2 (en) 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
AU2009310841A1 (en) * 2008-10-29 2010-05-06 Taisho Pharmaceutical Co., Ltd. Compounds having TAFIa inhibitory activity
RU2015156612A (ru) * 2013-06-10 2017-07-17 Санофи Макроциклические производные мочевины в качестве ингибиторов tafia, их получение и их применение в качестве фармацевтических средств
CN104529859B (zh) * 2015-01-13 2016-08-17 佛山市赛维斯医药科技有限公司 含苯胺和二烯氟代金刚烷结构的化合物、其制备方法和用途
RU2687254C1 (ru) * 2018-10-03 2019-05-08 Федеральное государственное бюджетное учреждение науки Новосибирский институт органической химии им. Н.Н. Ворожцова Сибирского отделения Российской академии наук (НИОХ СО РАН) N-гетероциклические производные борниламина в качестве ингибиторов ортопоксвирусов

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AU749132B2 (en) * 1997-08-28 2002-06-20 Biovitrum Ab Inhibitors of protein tyrosine phosphatase
US6482921B1 (en) * 1999-01-28 2002-11-19 Essential Therapeutics, Inc. Uridyl peptide antibiotic (UPA) derivatives, their synthesis and use
AU3631500A (en) * 1999-03-19 2000-10-09 Du Pont Pharmaceuticals Company N-adamant-1-yl-n'-(4-chlorobenzothiazol-2-yl) urea useful in the treatment of inflammation and as an anticancer radiosensitizing agent
US6359129B1 (en) * 2000-08-15 2002-03-19 University Of Kansas Amino acid-derived, 7-membered cyclic sulfamides and methods of synthesizing the same
PT1311488E (pt) * 2000-08-17 2009-12-30 Pfizer Ltd Imidazóis substituídos utilizados como inibidores de tafia
DE102004020186A1 (de) * 2004-04-22 2005-11-17 Aventis Pharma Deutschland Gmbh Heterocyclylessigsäuren als Inhibitoren von TAFla
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MX2009005516A (es) 2009-06-04
CA2671861A1 (en) 2008-06-12
KR20090087044A (ko) 2009-08-14
TW200838498A (en) 2008-10-01
PL2104497T3 (pl) 2015-07-31
SI2104497T1 (sl) 2015-06-30
CL2007003494A1 (es) 2008-06-13
DK2104497T3 (en) 2015-05-26
RU2009125534A (ru) 2011-01-20
HRP20150514T1 (hr) 2015-09-11
NO20092246L (no) 2009-07-01
PE20081349A1 (es) 2008-10-24
EP2104497A2 (de) 2009-09-30
BRPI0720241A2 (pt) 2013-12-31
ES2537093T3 (es) 2015-06-02
WO2008067909A3 (de) 2009-04-09
PT2104497E (pt) 2015-06-09
CA2671861C (en) 2015-12-29
EP2104497B1 (de) 2015-02-25
CO6180422A2 (es) 2010-07-19
AR064119A1 (es) 2009-03-11
AU2007327959A1 (en) 2008-06-12
TWI399203B (zh) 2013-06-21
MA30968B1 (fr) 2009-12-01
AU2007327959B2 (en) 2013-08-01
JP5396279B2 (ja) 2014-01-22
HK1137928A1 (en) 2010-08-13
JP2010511641A (ja) 2010-04-15
CN101553219B (zh) 2013-04-24
CN101553219A (zh) 2009-10-07
US20100035930A1 (en) 2010-02-11
NZ577312A (en) 2012-02-24
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WO2008067909A2 (de) 2008-06-12
US8389764B2 (en) 2013-03-05

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