PT846111E - Sintese de compostos opticamente puros uteis como inibidores da garft e seus intermediarios - Google Patents
Sintese de compostos opticamente puros uteis como inibidores da garft e seus intermediariosInfo
- Publication number
- PT846111E PT846111E PT96919095T PT96919095T PT846111E PT 846111 E PT846111 E PT 846111E PT 96919095 T PT96919095 T PT 96919095T PT 96919095 T PT96919095 T PT 96919095T PT 846111 E PT846111 E PT 846111E
- Authority
- PT
- Portugal
- Prior art keywords
- compounds
- optically pure
- uteis
- intermediaries
- synthesis
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring
- C07D333/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D333/70—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
-
- 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/472,233 US5831100A (en) | 1995-06-07 | 1995-06-07 | Syntheses of optically pure compounds useful as GARFT inhibitors and their intermediates |
Publications (1)
Publication Number | Publication Date |
---|---|
PT846111E true PT846111E (pt) | 2004-01-30 |
Family
ID=23874680
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PT96919095T PT846111E (pt) | 1995-06-07 | 1996-06-07 | Sintese de compostos opticamente puros uteis como inibidores da garft e seus intermediarios |
Country Status (11)
Country | Link |
---|---|
US (2) | US5831100A (pt) |
EP (1) | EP0846111B1 (pt) |
JP (1) | JPH11507054A (pt) |
AT (1) | ATE248158T1 (pt) |
AU (1) | AU6152796A (pt) |
CA (1) | CA2224211A1 (pt) |
DE (1) | DE69629703T2 (pt) |
DK (1) | DK0846111T3 (pt) |
ES (1) | ES2206580T3 (pt) |
PT (1) | PT846111E (pt) |
WO (1) | WO1996040674A1 (pt) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5831100A (en) * | 1995-06-07 | 1998-11-03 | Agouron Pharmaceuticals, Inc. | Syntheses of optically pure compounds useful as GARFT inhibitors and their intermediates |
WO2004113337A1 (en) * | 2003-06-25 | 2004-12-29 | Pfizer Inc. | Convergent synthesis of a garft inhibitor containing a methyl substitute thiophene core and a tetrahydropyrido`2,3-d! pyrimidine ring system and intermediates therefor |
WO2004113328A1 (en) * | 2003-06-25 | 2004-12-29 | Pfizer Inc. | Convergent asymmetric synthesis route to produce a key intermediate towards the synthesis of a garft inhibitor |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4123550A (en) * | 1977-10-31 | 1978-10-31 | Syntex (U.S.A.) Inc. | Bicyclo[3.1.0]hexylethylaminocarbonyl-substituted heteroaryl cardiovascular agents |
DE3222914A1 (de) * | 1982-06-18 | 1983-12-22 | Beiersdorf Ag, 2000 Hamburg | Substituierte 5-phenylthio-6-amino-pyrimidinone, verfahren zu ihrer herstellung und ihre verwendung sowie diese verbindungen enthaltende zubereitungen |
US4927828A (en) * | 1985-03-08 | 1990-05-22 | The Trustees Of Princeton University | Diastereoisomeric tetrahydropyrido-(2,3,d) pyrimidine derivatives |
ZA861235B (en) * | 1985-03-08 | 1986-10-29 | Univ Princeton | Pyrido(2,3-d)pyrimidine derivatives |
US4684653A (en) * | 1985-03-08 | 1987-08-04 | The Trustees Of Princeton University | Pyrido(2,3-d)pyrimidine derivatives |
US5026851A (en) * | 1985-03-08 | 1991-06-25 | The Trustees Of Princeton University | Pyrido[2,3-]pyrimidine derivatives |
US4831037A (en) * | 1987-04-20 | 1989-05-16 | The Trustees Of Princeton University | 4 (3H)-oxo-5,6,7,8-tetrahydropyrido-(2,3-d)pyrimidine derivatives |
GB8625019D0 (en) * | 1986-10-18 | 1986-11-19 | Wellcome Found | Compounds |
US4988813A (en) * | 1986-10-20 | 1991-01-29 | The Trustees Of Princeton University | Process for the preparation of fused pyridine compounds |
FR2608155B1 (fr) * | 1986-12-12 | 1990-09-14 | Scient Tech Batimen Centre | Nouveaux alcools furanniques, utilisation de ceux-ci comme polyols dans la formation de polyurethannes, polyurethannes ainsi obtenus et leur procede de preparation |
US4895946A (en) * | 1987-10-26 | 1990-01-23 | The Trustees Of Princeton University | Process for the preparation of fused pyridine compounds |
US4871743A (en) * | 1988-01-19 | 1989-10-03 | The Trustees Of Princeton University | L-glutamic acid derivatives |
US4889859A (en) * | 1988-02-05 | 1989-12-26 | The Trustees Of Princeton University | Pyrido[2,3-d]pyrimidine derivatives |
JPH029869A (ja) * | 1988-04-15 | 1990-01-12 | Wellcome Found Ltd:The | 新規化合物 |
US4882333A (en) * | 1988-05-25 | 1989-11-21 | The Trustess Of Princeton University | N-(5,6,7,8-tetrahydropyrido[2,3-d]pyrimidin-6-yl-alkanoyl)-glutamic acid derivatives |
US4882334A (en) * | 1988-05-25 | 1989-11-21 | The Trustees Of Princeton University | N-(5,6,7,8-tetrahydropyrido]2,3-d]pyrimidin-6-ylethl-thineyl-and furylcarbonyl)-glutamic acid derivatives |
US4871746A (en) * | 1988-05-31 | 1989-10-03 | The Trustees Of Princeton University | N-[N-(tetrahydropyrido[2,3-D]pyrimidinylmethyl)-aminomethylbenzoyl]glutamic acid derivatives as neoplastic growth inhibitors |
US4883799A (en) * | 1988-06-29 | 1989-11-28 | The Trustees Of Princeton University | N-(4-(1-hydroxy-3-(5,6,7,8-tetrahydropyrido(2,3,-d)-pyrimidin-6-yl)prop-2-yl)benzoyl)glutamic acid derivatives |
GB8823041D0 (en) * | 1988-09-30 | 1988-11-09 | Lilly Sa | Organic compounds & their use as pharmaceuticals |
DE3901074A1 (de) * | 1989-01-16 | 1990-07-19 | Basf Ag | Thiophen-2-carbonsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
US4921836A (en) * | 1989-05-17 | 1990-05-01 | Burroughs Wellcome Co. | Substituted glutamic acids |
US4971973A (en) * | 1989-05-17 | 1990-11-20 | Burroughs Wellcome Co. | Glutamic acid derivatives |
US4920125A (en) * | 1989-08-29 | 1990-04-24 | The Trustees Of Princeton University | L-glutamic acid derivatives |
US5179123A (en) * | 1989-12-18 | 1993-01-12 | G. D. Searle & Co. | LTB4 synthesis inhibitors |
EP0438261A3 (en) * | 1990-01-16 | 1992-02-26 | Takeda Chemical Industries, Ltd. | Condensed heterocyclic glutamic acid derivatives, their production and use |
US5013738A (en) * | 1990-04-18 | 1991-05-07 | The Trustees Of Princeton University | L-glutamic acid derivatives |
ZA917355B (en) * | 1990-09-17 | 1992-08-26 | Agouron Pharma | Antiproliferative substituted naphthalene compounds |
US5217974A (en) * | 1991-03-29 | 1993-06-08 | Eli Lilly And Company | Method for treating gar-transformylase tumors in mammals and reducing mammalian toxicity |
US5223503A (en) * | 1991-04-29 | 1993-06-29 | Eli Lilly And Company | 6-substituted pyrido[2,3-d]pyrimidines as antineoplastic agents |
US5969136A (en) * | 1992-10-15 | 1999-10-19 | Eli Lilly And Company | Cyclization for preparing antifolate compounds |
JPH08504765A (ja) * | 1992-12-16 | 1996-05-21 | アグロン・ファーマシュウティカルズ・インコーポレーテッド | 抗増殖性の置換5−チアピリミジノンおよび5−セレノピリミジノン化合物 |
ATE201877T1 (de) * | 1993-01-29 | 2001-06-15 | Agouron Pharma | Kondensierte heterocyclische glutaminsäurederivate als antiproliferative mittel |
US5594139A (en) * | 1993-01-29 | 1997-01-14 | Agouron Pharmaceuticals, Inc. | Processes for preparing antiproliferative garft-inhibiting compounds |
ATE242253T1 (de) * | 1994-07-28 | 2003-06-15 | Agouron Pharma | Verbindungen die als antiproliferierende mittel und garft inhibitoren verwendbar sind |
US5608082A (en) * | 1994-07-28 | 1997-03-04 | Agouron Pharmaceuticals, Inc. | Compounds useful as antiproliferative agents and GARFT inhibitors |
US5831100A (en) * | 1995-06-07 | 1998-11-03 | Agouron Pharmaceuticals, Inc. | Syntheses of optically pure compounds useful as GARFT inhibitors and their intermediates |
-
1995
- 1995-06-07 US US08/472,233 patent/US5831100A/en not_active Expired - Fee Related
-
1996
- 1996-06-07 AU AU61527/96A patent/AU6152796A/en not_active Abandoned
- 1996-06-07 DE DE69629703T patent/DE69629703T2/de not_active Expired - Fee Related
- 1996-06-07 EP EP96919095A patent/EP0846111B1/en not_active Expired - Lifetime
- 1996-06-07 PT PT96919095T patent/PT846111E/pt unknown
- 1996-06-07 WO PCT/US1996/008953 patent/WO1996040674A1/en active IP Right Grant
- 1996-06-07 JP JP9501396A patent/JPH11507054A/ja not_active Withdrawn
- 1996-06-07 CA CA002224211A patent/CA2224211A1/en not_active Abandoned
- 1996-06-07 AT AT96919095T patent/ATE248158T1/de not_active IP Right Cessation
- 1996-06-07 DK DK96919095T patent/DK0846111T3/da active
- 1996-06-07 ES ES96919095T patent/ES2206580T3/es not_active Expired - Lifetime
-
1998
- 1998-07-02 US US09/109,056 patent/US5981748A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0846111B1 (en) | 2003-08-27 |
US5831100A (en) | 1998-11-03 |
DK0846111T3 (da) | 2003-12-22 |
EP0846111A1 (en) | 1998-06-10 |
US5981748A (en) | 1999-11-09 |
ES2206580T3 (es) | 2004-05-16 |
JPH11507054A (ja) | 1999-06-22 |
DE69629703D1 (de) | 2003-10-02 |
ATE248158T1 (de) | 2003-09-15 |
DE69629703T2 (de) | 2004-03-11 |
CA2224211A1 (en) | 1996-12-19 |
WO1996040674A1 (en) | 1996-12-19 |
AU6152796A (en) | 1996-12-30 |
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