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公开(公告)号:US6103936A
公开(公告)日:2000-08-15
申请号:US819619
申请日:1997-03-17
申请人: Jerry Leroy Adams , Peter William Sheldrake , Timothy Francis Gallagher , Ravishanker Garigipati , Paul Elliot Bender , Jeffrey Charles Boehm , Joseph Sisko , Zhi-Qiang Peng , John C. Lee
发明人: Jerry Leroy Adams , Peter William Sheldrake , Timothy Francis Gallagher , Ravishanker Garigipati , Paul Elliot Bender , Jeffrey Charles Boehm , Joseph Sisko , Zhi-Qiang Peng , John C. Lee
IPC分类号: A61K8/19 , A61K8/00 , A61K8/20 , A61K8/23 , A61K31/00 , A61K31/165 , A61K31/4168 , A61K31/4178 , A61K31/44 , A61K31/4409 , A61K31/4427 , A61K31/4439 , A61K31/445 , A61K31/4545 , A61K31/47 , A61K31/505 , A61K31/506 , A61K31/535 , A61K31/5377 , A61P1/00 , A61P1/04 , A61P3/00 , A61P3/06 , A61P3/10 , A61P7/00 , A61P7/02 , A61P9/00 , A61P9/10 , A61P11/00 , A61P11/06 , A61P17/00 , A61P17/06 , A61P19/00 , A61P19/02 , A61P19/06 , A61P19/08 , A61P19/10 , A61P21/00 , A61P25/04 , A61P25/28 , A61P29/00 , A61P31/04 , A61P31/06 , A61P31/12 , A61P31/16 , A61P31/18 , A61P35/00 , A61P37/00 , A61P39/00 , A61P43/00 , A61Q1/00 , A61Q1/12 , A61Q19/00 , C07B61/00 , C07C20060101 , C07C231/12 , C07C231/14 , C07C233/05 , C07C233/36 , C07C311/30 , C07C315/00 , C07C315/02 , C07C317/28 , C07C317/32 , C07C317/40 , C07C319/14 , C07C319/20 , C07C323/25 , C07C323/29 , C07C323/31 , C07C323/41 , C07C323/45 , C07D213/00 , C07D213/53 , C07D213/61 , C07D215/12 , C07D233/54 , C07D239/02 , C07D239/38 , C07D239/42 , C07D295/04 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/14 , C07D409/00 , C07D409/14 , C07D413/00 , C07D413/04 , C07D413/14
CPC分类号: C07D401/04 , C07C315/00 , C07D239/38 , C07D401/14 , C07D403/04 , C07D405/14 , Y10S514/866 , Y10S514/903
摘要: The present invention is to a novel process for the preparation of a compound of the formula: ##STR1## wherein p is 0, or 2;Ar is an optionally substituted phenyl or naphtyl; andinter alia R4 is an optionally susbtituted phenyl, naphth-1-yl, naphth-2-yl, or a heteroaryl ring;which process comprises reacting together an aldehyde of the formula:R.sub.4 --CHO;wherein R.sub.4 is as defined above;a compound of the formula:ArS(O)pH;wherein Ar, and p are as defined above;with formamide, an acid catalyst, and optionally a dehydrating agent.
摘要翻译: 本发明涉及制备下式化合物的新方法:其中p为0或2; Ar是任选取代的苯基或萘基; 尤其是R4是任选被取代的苯基,萘-1-基,萘-2-基或杂芳基环; 该方法包括使下式的醛反应:R4-CHO;其中R4如上定义; 下式的化合物:ArS(O)pH;其中Ar和p如上所定义; 与甲酰胺,酸催化剂和任选的脱水剂。
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公开(公告)号:US5969184A
公开(公告)日:1999-10-19
申请号:US854223
申请日:1997-05-09
申请人: Jerry Leroy Adams , Peter William Sheldrake , Timothy Francis Gallagher , Ravi Shanker Garigipati , Paul Elliot Bender , Jeffrey Charles Boehm , Joseph Sisko , Zhi-Qiang Peng , John C. Lee
发明人: Jerry Leroy Adams , Peter William Sheldrake , Timothy Francis Gallagher , Ravi Shanker Garigipati , Paul Elliot Bender , Jeffrey Charles Boehm , Joseph Sisko , Zhi-Qiang Peng , John C. Lee
IPC分类号: A61K8/19 , A61K8/00 , A61K8/20 , A61K8/23 , A61K31/4168 , A61K31/4178 , A61K31/44 , A61K31/4409 , A61K31/4427 , A61K31/4439 , A61K31/445 , A61K31/4545 , A61K31/47 , A61K31/505 , A61K31/506 , A61K31/535 , A61K31/5377 , A61P1/00 , A61P1/04 , A61P3/00 , A61P3/10 , A61P9/10 , A61P11/00 , A61P11/06 , A61P17/06 , A61P19/00 , A61P19/02 , A61P19/08 , A61P21/00 , A61P25/28 , A61P29/00 , A61P31/04 , A61P31/12 , A61P31/18 , A61P37/00 , A61P39/00 , A61P43/00 , A61Q1/00 , A61Q1/12 , A61Q19/00 , C07B61/00 , C07C231/12 , C07C315/00 , C07C315/02 , C07C317/28 , C07C317/40 , C07C319/14 , C07C319/20 , C07C323/29 , C07C323/41 , C07C323/45 , C07D213/53 , C07D213/61 , C07D215/12 , C07D239/38 , C07D239/42 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/14 , C07D413/14 , C07C233/13
CPC分类号: C07D401/04 , C07C315/00 , C07D401/14 , C07D403/04 , C07D405/14
摘要: The present invention is directed to the novel intermediate compounds of the formula: ##STR1## wherein, interalia, R.sub.4 is a substituted phenyl or an optionally substituted napthyl derivative.
摘要翻译: 本发明涉及下式的新型中间体化合物:其中,杂芳基,R4是取代的苯基或任意取代的萘基衍生物。
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公开(公告)号:US6150557A
公开(公告)日:2000-11-21
申请号:US185059
申请日:1998-11-03
申请人: Jerry Leroy Adams , Peter William Sheldrake , Timothy Francis Gallagher , Ravi Shanker Garigipati , Paul Elliot Bender , Jeffrey Charles Boehm , Joseph Sisko , Zhi-Qiang Peng , John C. Lee
发明人: Jerry Leroy Adams , Peter William Sheldrake , Timothy Francis Gallagher , Ravi Shanker Garigipati , Paul Elliot Bender , Jeffrey Charles Boehm , Joseph Sisko , Zhi-Qiang Peng , John C. Lee
IPC分类号: A61K8/19 , A61K8/00 , A61K8/20 , A61K8/23 , A61K31/4168 , A61K31/4178 , A61K31/44 , A61K31/4409 , A61K31/4427 , A61K31/4439 , A61K31/445 , A61K31/4545 , A61K31/47 , A61K31/505 , A61K31/506 , A61K31/535 , A61K31/5377 , A61P1/00 , A61P1/04 , A61P3/00 , A61P3/10 , A61P9/10 , A61P11/00 , A61P11/06 , A61P17/06 , A61P19/00 , A61P19/02 , A61P19/08 , A61P21/00 , A61P25/28 , A61P29/00 , A61P31/04 , A61P31/12 , A61P31/18 , A61P37/00 , A61P39/00 , A61P43/00 , A61Q1/00 , A61Q1/12 , A61Q19/00 , C07B61/00 , C07C231/12 , C07C315/00 , C07C315/02 , C07C317/28 , C07C317/40 , C07C319/14 , C07C319/20 , C07C323/29 , C07C323/41 , C07C323/45 , C07D213/53 , C07D213/61 , C07D215/12 , C07D239/38 , C07D239/42 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/14 , C07D413/14
CPC分类号: C07D401/04 , C07C315/00 , C07D401/14 , C07D403/04 , C07D405/14
摘要: Novel 1, 4, 5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 新的1,4,5-取代的咪唑化合物和用作治疗作为细胞因子抑制剂的组合物。
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公开(公告)号:US5869660A
公开(公告)日:1999-02-09
申请号:US12946
申请日:1998-01-23
申请人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Zhi Qiang Peng , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
发明人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Zhi Qiang Peng , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
IPC分类号: C07D401/12 , C07D401/14 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14 , C07D413/14
CPC分类号: C07D401/14 , C07D401/12 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14
摘要: Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 新型1,4,5-取代的咪唑化合物和用作治疗作为细胞因子抑制剂的组合物。
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公开(公告)号:US5739143A
公开(公告)日:1998-04-14
申请号:US764003
申请日:1996-12-11
申请人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Zhi Qiang Peng , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
发明人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Zhi Qiang Peng , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
IPC分类号: C07D401/12 , C07D401/14 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14 , A61K31/505
CPC分类号: C07D401/14 , C07D401/12 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14
摘要: Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 新型1,4,5-取代的咪唑化合物和用作治疗作为细胞因子抑制剂的组合物。
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公开(公告)号:US5658903A
公开(公告)日:1997-08-19
申请号:US659102
申请日:1996-06-03
申请人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Zhi-Qiang Peng , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
发明人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Zhi-Qiang Peng , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
IPC分类号: C07D401/04 , A61K31/00 , A61K31/4427 , A61K31/4433 , A61K31/445 , A61K31/4465 , A61K31/4523 , A61K31/4545 , A61K31/505 , A61K31/506 , A61K31/535 , A61K31/5355 , A61P9/00 , A61P11/00 , A61P17/00 , A61P19/00 , A61P25/00 , A61P29/00 , A61P31/00 , A61P31/12 , A61P43/00 , C07D401/12 , C07D401/14 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14 , C07D413/14
CPC分类号: C07D401/14 , C07D401/12 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14
摘要: Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 新型1,4,5-取代的咪唑化合物和用作治疗作为细胞因子抑制剂的组合物。
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7.Process for making pyridyl and pyrimidine substituted imidazole compounds 失效
标题翻译: 制备吡啶基和嘧啶取代的咪唑化合物的方法公开(公告)号:US06218537B1
公开(公告)日:2001-04-17
申请号:US08973594
申请日:1998-05-13
申请人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
发明人: Jerry Leroy Adams , Timothy Francis Gallagher , Joseph Sisko , Irennegbe Kelly Osifo , Jeffrey Charles Boehm
IPC分类号: C07D40104
CPC分类号: C07D401/14 , C07D401/12 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14
摘要: 1,4,5,-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 1,4,5'-取代咪唑化合物和用作治疗作为细胞因子抑制剂的组合物
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公开(公告)号:US06288062B1
公开(公告)日:2001-09-11
申请号:US09467164
申请日:1999-12-20
IPC分类号: A61K3535
CPC分类号: C07D413/04
摘要: This invention relates to the novel oxazole compounds of Formula (I) and novel pharmaceutical compositions comprising a compound of Formula (I) and a pharmaceutically acceptable diluent or carrier. This invention also relates to a method of inhibiting cytokines and the treatment of cytokine mediated diseases, in mammals, thereby by administration of an effective amount of a compound according to Formula (I).
摘要翻译: 本发明涉及式(I)的新型恶唑化合物和包含式(I)化合物和药学上可接受的稀释剂或载体的新型药物组合物。 本发明还涉及在哺乳动物中抑制细胞因子和细胞因子介导的疾病的治疗方法,从而通过施用有效量的根据式(I)的化合物。
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公开(公告)号:US06369068B1
公开(公告)日:2002-04-09
申请号:US09319859
申请日:1999-06-11
IPC分类号: C07D40114
CPC分类号: C07D401/14 , C07D401/12 , C07D403/04 , C07D405/12 , C07D405/14 , C07D409/14
摘要: Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 新型1,4,5-取代的咪唑化合物和用作治疗作为细胞因子抑制剂的组合物。
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10.Compounds of heteroaryl substituted imidazole, their pharmaceutical compositions and uses 失效
标题翻译: 杂芳基取代的咪唑化合物,其药物组合物和用途公开(公告)号:US06730683B2
公开(公告)日:2004-05-04
申请号:US09919251
申请日:2002-06-10
IPC分类号: A61K31535
CPC分类号: C07D401/14 , C07D403/04 , C07D403/14
摘要: Novel 1,4,5-substituted imidazole compounds and compositions for use in therapy as cytokine inhibitors.
摘要翻译: 新型1,4,5-取代的咪唑化合物和用作治疗作为细胞因子抑制剂的组合物。
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