AR012674A1 - Acidos sulfonilaminocarboxilicos, procedimiento para su preparacion, compuestos intermediarios para su exclusivo uso en dichos procedimientos medicamentos, procedimiento para la preparacion de medicamentos, uso de dichos compuestos para la preparacion de medicamentos. - Google Patents
Acidos sulfonilaminocarboxilicos, procedimiento para su preparacion, compuestos intermediarios para su exclusivo uso en dichos procedimientos medicamentos, procedimiento para la preparacion de medicamentos, uso de dichos compuestos para la preparacion de medicamentos.Info
- Publication number
- AR012674A1 AR012674A1 ARP980102139A ARP980102139A AR012674A1 AR 012674 A1 AR012674 A1 AR 012674A1 AR P980102139 A ARP980102139 A AR P980102139A AR P980102139 A ARP980102139 A AR P980102139A AR 012674 A1 AR012674 A1 AR 012674A1
- Authority
- AR
- Argentina
- Prior art keywords
- preparation
- phenyl
- drugs
- procedure
- ring
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 238000000034 method Methods 0.000 title 3
- 239000003814 drug Substances 0.000 title 2
- 229940079593 drug Drugs 0.000 title 2
- 239000002253 acid Substances 0.000 title 1
- 150000007513 acids Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000006528 (C2-C6) alkyl group Chemical group 0.000 abstract 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- XOCUXOWLYLLJLV-UHFFFAOYSA-N [O].[S] Chemical group [O].[S] XOCUXOWLYLLJLV-UHFFFAOYSA-N 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- WZHRJGWXUCLILI-UHFFFAOYSA-N sulfonylcarbamic acid Chemical class OC(=O)N=S(=O)=O WZHRJGWXUCLILI-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/42—Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
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- A61P17/00—Drugs for dermatological disorders
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- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
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- A—HUMAN NECESSITIES
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- 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
- C07C311/19—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 carboxyl groups
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- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
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- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
- C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
- C07C311/44—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C317/48—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
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- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/57—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
- C07C323/58—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
- C07C323/59—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton with acylated amino groups bound to the carbon skeleton
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- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/10—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 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
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- C07D209/04—Indoles; Hydrogenated indoles
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
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- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
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- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Hydrogenated Pyridines (AREA)
- Indole Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Acidos sulfonilaminocarboxilicos caracterizados porque comprenden la formula I y/o a una forma estereoisomera del compuesto de la formula I y/o auna sal fisiologicamente compatible del compuesto de la formula I, representando ene lla R2 y R3 en comun un anillo con un grupo carboxilo situadoen un extremo de la formula parcial II, en la que r representa el numero entero cero, 1, 2 o 3 y/o uno de los átomos de carbono que hay en el anillo estáreemplazado por -O-, -S- o -(R7)N-, en que R7 representa 1) un átomo de hidrogeno, 2) alquilo (C1-6), 3) fenilo, en que el fenilo está sin sustituir osustituido como se describe en 2.1 hasta 2.14, o 4) bencilo, en que el bencilo está sin sustituir o sustituido como sedescribe en 2.1 hasta 2.14, o 5)R2N-C(=NH)- teniendo R2 el significado mencionado más arriba, y/o los átomos de carbono que hay en el anillo de la formula parcial II están sustituidos una vezo multiples veces con alquilo (C1-6), fenilo, fenil-(CH2)m- o HO-, representando 1) un átomo de hidrogeno, 2) alquilo (C1-6)-, 3) HO-C(O)-alquilo(C21-6)- 4) fenil-(CH2)n-, en que el fenil está sin sustituir o sustituido una vez o dos veces como se describe en 2.1 hasta 2.14, o con -NH-C(O)-alquilo(C1-3 ) yn representa el numero entero cero, 1 o 2, o representantdo 5) picolilo, o 6) formando R4 y R5, en comun con el grupo amino situado en elanillo, un anillo de 4 a 7 eslabones, en el que eventualmente uno de los átomos de carbono está reemplazado por -O-, -S- o -NH- o dos átomos de C contiguos delanillo de 4 a 7 eslabones son parte de un radical bencilo, A a) un enlace covalente, b) -O-, c) -CH=CH- o d) -C:::C-, B a) -(CH2)m-, en que m tiene elsignificado antes mencionado, b) -O- (CH2)p, en que p significa un numero entero de 1 a 5, o c) -CH=CH- y X -CH=CH-, un átomo de oxígeno de azufre,
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19719621A DE19719621A1 (de) | 1997-05-09 | 1997-05-09 | Sulfonylaminocarbonsäuren |
Publications (1)
Publication Number | Publication Date |
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AR012674A1 true AR012674A1 (es) | 2000-11-08 |
Family
ID=7829102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP980102139A AR012674A1 (es) | 1997-05-09 | 1998-05-07 | Acidos sulfonilaminocarboxilicos, procedimiento para su preparacion, compuestos intermediarios para su exclusivo uso en dichos procedimientos medicamentos, procedimiento para la preparacion de medicamentos, uso de dichos compuestos para la preparacion de medicamentos. |
Country Status (20)
Country | Link |
---|---|
US (2) | US6451824B1 (es) |
EP (1) | EP0877018B1 (es) |
JP (1) | JP4177483B2 (es) |
KR (1) | KR100572494B1 (es) |
CN (1) | CN1280267C (es) |
AR (1) | AR012674A1 (es) |
AT (1) | ATE238984T1 (es) |
AU (1) | AU732723B2 (es) |
BR (1) | BR9801606B1 (es) |
CA (1) | CA2237099C (es) |
CZ (1) | CZ295527B6 (es) |
DE (2) | DE19719621A1 (es) |
DK (1) | DK0877018T3 (es) |
ES (1) | ES2195220T3 (es) |
HU (1) | HU224959B1 (es) |
ID (1) | ID20807A (es) |
PL (1) | PL191876B1 (es) |
PT (1) | PT877018E (es) |
RU (1) | RU2193027C2 (es) |
TR (1) | TR199800815A3 (es) |
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AU2001245863A1 (en) * | 2000-03-21 | 2001-10-03 | The Procter & Gamble Company | Heterocyclic side chain containing metalloprotease inhibitors |
PL365444A1 (en) * | 2000-03-21 | 2005-01-10 | The Procter & Gamble Company | Heterocyclic side chain containing, n-substituted metalloprotease inhibitors |
AU2001245862A1 (en) | 2000-03-21 | 2001-10-03 | The Procter & Gamble Company | Difluorobutyric acid metalloprotease inhibitors |
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PA8591801A1 (es) | 2002-12-31 | 2004-07-26 | Pfizer Prod Inc | Inhibidores benzamidicos del receptor p2x7. |
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KR20070115583A (ko) * | 2004-06-29 | 2007-12-06 | 화이자 프로덕츠 인코포레이티드 | 루이스 산의 존재하에 트리아진의 4-위치에서 치환되지않은5-[4-(2-하이드록시-에틸)-3,5-다이옥소-4,5-다이하이드로-3h-[1,2,4]트리아진-2-일]-벤즈아마이드 유도체와옥시란과의 반응에 의해 p2x7 억제 활성을 갖는 상기유도체의 제조방법 |
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-
1997
- 1997-05-09 DE DE19719621A patent/DE19719621A1/de not_active Withdrawn
-
1998
- 1998-05-02 AT AT98108038T patent/ATE238984T1/de active
- 1998-05-02 DK DK98108038T patent/DK0877018T3/da active
- 1998-05-02 EP EP98108038A patent/EP0877018B1/de not_active Expired - Lifetime
- 1998-05-02 PT PT98108038T patent/PT877018E/pt unknown
- 1998-05-02 DE DE59808121T patent/DE59808121D1/de not_active Expired - Lifetime
- 1998-05-02 ES ES98108038T patent/ES2195220T3/es not_active Expired - Lifetime
- 1998-05-07 ID IDP980667A patent/ID20807A/id unknown
- 1998-05-07 TR TR1998/00815A patent/TR199800815A3/tr unknown
- 1998-05-07 CZ CZ19981438A patent/CZ295527B6/cs not_active IP Right Cessation
- 1998-05-07 CA CA2237099A patent/CA2237099C/en not_active Expired - Fee Related
- 1998-05-07 AR ARP980102139A patent/AR012674A1/es active IP Right Grant
- 1998-05-08 KR KR1019980016385A patent/KR100572494B1/ko not_active IP Right Cessation
- 1998-05-08 JP JP16270698A patent/JP4177483B2/ja not_active Expired - Fee Related
- 1998-05-08 PL PL326216A patent/PL191876B1/pl not_active IP Right Cessation
- 1998-05-08 RU RU98108979/04A patent/RU2193027C2/ru not_active IP Right Cessation
- 1998-05-08 CN CNB981152651A patent/CN1280267C/zh not_active Expired - Fee Related
- 1998-05-08 BR BRPI9801606-7A patent/BR9801606B1/pt not_active IP Right Cessation
- 1998-05-08 AU AU64823/98A patent/AU732723B2/en not_active Ceased
- 1998-05-08 US US09/074,693 patent/US6451824B1/en not_active Expired - Lifetime
- 1998-05-08 HU HU9801044A patent/HU224959B1/hu not_active IP Right Cessation
-
2002
- 2002-06-13 US US10/170,870 patent/US7160903B2/en not_active Expired - Fee Related
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