JP2009536618A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2009536618A5 JP2009536618A5 JP2009506701A JP2009506701A JP2009536618A5 JP 2009536618 A5 JP2009536618 A5 JP 2009536618A5 JP 2009506701 A JP2009506701 A JP 2009506701A JP 2009506701 A JP2009506701 A JP 2009506701A JP 2009536618 A5 JP2009536618 A5 JP 2009536618A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- cyclopropyl
- produce
- compound
- following
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- -1 1-methoxycarbonyl-1-methyl-ethyl Chemical group 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- 150000001345 alkine derivatives Chemical class 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 150000001879 copper Chemical class 0.000 claims 2
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 150000003852 triazoles Chemical class 0.000 claims 2
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims 1
- HJKLEAOXCZIMPI-UHFFFAOYSA-N 2,2-diethoxyethanamine Chemical compound CCOC(CN)OCC HJKLEAOXCZIMPI-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- LDDHMKANNXWUAK-UHFFFAOYSA-N 3-iodo-4-methylbenzoic acid Chemical compound CC1=CC=C(C(O)=O)C=C1I LDDHMKANNXWUAK-UHFFFAOYSA-N 0.000 claims 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims 1
- 230000001476 alcoholic effect Effects 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 229940125890 compound Ia Drugs 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical group [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000012336 iodinating agent Substances 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical group CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 claims 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74501006P | 2006-04-18 | 2006-04-18 | |
| PCT/US2007/066684 WO2007121390A1 (en) | 2006-04-18 | 2007-04-16 | Process for making cytokine inhibiting compounds containing 4- and 5- imidazolyl rings and the intermediates thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009536618A JP2009536618A (ja) | 2009-10-15 |
| JP2009536618A5 true JP2009536618A5 (enExample) | 2010-06-03 |
Family
ID=38327037
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009506701A Pending JP2009536618A (ja) | 2006-04-18 | 2007-04-16 | 4−及び5−イミダゾリル環を含むサイトカイン阻害化合物の製造方法及びその中間体 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US7858804B2 (enExample) |
| EP (1) | EP2010522A1 (enExample) |
| JP (1) | JP2009536618A (enExample) |
| CA (1) | CA2647266A1 (enExample) |
| WO (1) | WO2007121390A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0712795A2 (pt) | 2006-07-07 | 2012-09-04 | Boehringer Ingelheim Int | derivados de heteroarila substituìdos com fenila e uso dos mesmos como agentes antitumorais |
| PE20090837A1 (es) * | 2007-07-02 | 2009-07-24 | Boehringer Ingelheim Int | Nuevos compuestos quimicos |
| TW201014860A (en) | 2008-09-08 | 2010-04-16 | Boehringer Ingelheim Int | New chemical compounds |
| EA201100564A1 (ru) | 2008-09-29 | 2011-12-30 | Бёрингер Ингельхайм Интернациональ Гмбх | Антипролиферативные соединения |
| US8569316B2 (en) | 2009-02-17 | 2013-10-29 | Boehringer Ingelheim International Gmbh | Pyrimido [5,4-D] pyrimidine derivatives for the inhibition of tyrosine kinases |
| JP5871896B2 (ja) | 2010-03-26 | 2016-03-01 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | B−rafキナーゼインヒビター |
| WO2011117382A1 (en) | 2010-03-26 | 2011-09-29 | Boehringer Ingelheim International Gmbh | Pyridyltriazoles |
| US8710055B2 (en) | 2010-12-21 | 2014-04-29 | Boehringer Ingelheim International Gmbh | Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| US8889684B2 (en) | 2011-02-02 | 2014-11-18 | Boehringer Ingelheim International Gmbh | Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| EP2701511A4 (en) * | 2011-04-29 | 2015-06-10 | Univ Akron | ANTIQUE AND ANTIMICROBIAL AGENTS WITH AZOLIUM AND PURINIUM SALT |
| WO2013064231A1 (en) | 2011-10-31 | 2013-05-10 | Phenex Pharmaceuticals Ag | SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3) |
| PT2963037T (pt) | 2013-02-27 | 2019-04-23 | Mochida Pharm Co Ltd | Novo derivado de pirazole |
| CN109553591B (zh) * | 2019-01-15 | 2020-12-15 | 山东安信制药有限公司 | 一种富马酸喹硫平中间体的制备方法 |
| WO2022188792A1 (zh) * | 2021-03-12 | 2022-09-15 | 四川科伦博泰生物医药股份有限公司 | 具有蛋白激酶抑制活性的杂环化合物、包含其的药物组合物及其制备方法和用途 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI1725544T1 (sl) * | 2004-03-09 | 2009-10-31 | Boehringer Ingelheim Pharma | 3-(4-heterociklil-1,2,3-triazol-1-il)-N-aril-benzamidi kot inhibitorji proizvodnje citokinov za zdravljenje kroničnih vnetnih bolezni |
-
2007
- 2007-04-16 JP JP2009506701A patent/JP2009536618A/ja active Pending
- 2007-04-16 CA CA002647266A patent/CA2647266A1/en not_active Abandoned
- 2007-04-16 EP EP07760693A patent/EP2010522A1/en not_active Withdrawn
- 2007-04-16 US US12/295,636 patent/US7858804B2/en active Active
- 2007-04-16 WO PCT/US2007/066684 patent/WO2007121390A1/en not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2009536618A5 (enExample) | ||
| JP2011515408A5 (enExample) | ||
| JP2009533369A5 (enExample) | ||
| JP2009543861A5 (enExample) | ||
| JP2018529687A5 (enExample) | ||
| WO2016026380A1 (zh) | 艾德拉尼的制备方法 | |
| MX2007015609A (es) | Proceso para la sintesis de compuestos organicos. | |
| TW200811082A (en) | Process for the preparation of cinacalcet base | |
| JP2014522385A5 (enExample) | ||
| JP2018065832A (ja) | ベンズイミダゾール誘導体の製造方法 | |
| JP5503670B2 (ja) | シナカルセト塩酸塩の製造方法 | |
| JP2019508387A5 (enExample) | ||
| TWI345467B (en) | 4-imidazolines as taar's ligands | |
| JP2008545786A5 (enExample) | ||
| JP2005538088A5 (enExample) | ||
| JP2013531058A5 (enExample) | ||
| JP2009062360A (ja) | シナカルセットの製造方法 | |
| CN108689895A (zh) | 一种硫代酰胺衍生物及其制备方法 | |
| CN104136409B (zh) | 用于制备取代的苯丙酮的方法 | |
| JP2008545782A5 (enExample) | ||
| CN103130810A (zh) | 一种吡唑并[1,5-c]喹唑啉类化合物的合成方法 | |
| CN1662488A (zh) | 制备芳基肼和取代的吲哚的方法 | |
| CN101056853A (zh) | 异吲哚衍生物的制备方法 | |
| CN102863341B (zh) | 一种(1r,2s)-2-芳基环丙胺衍生物的化学合成方法 | |
| JP2012526870A5 (enExample) |