JP2010513283A - 新規なオキサジアゾール化合物 - Google Patents
新規なオキサジアゾール化合物 Download PDFInfo
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- JP2010513283A JP2010513283A JP2009541394A JP2009541394A JP2010513283A JP 2010513283 A JP2010513283 A JP 2010513283A JP 2009541394 A JP2009541394 A JP 2009541394A JP 2009541394 A JP2009541394 A JP 2009541394A JP 2010513283 A JP2010513283 A JP 2010513283A
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- Prior art keywords
- optionally substituted
- alkyl
- phenyl
- chloro
- mmol
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- 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.)
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- 0 CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2c(CCN(CCC(O)=*)C3)c3ccc2)n1 Chemical compound CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2c(CCN(CCC(O)=*)C3)c3ccc2)n1 0.000 description 5
- MUCYUTNGHUVNLM-UHFFFAOYSA-N CC(C)Oc(c(Cl)c1)ccc1/C(/N)=N/O Chemical compound CC(C)Oc(c(Cl)c1)ccc1/C(/N)=N/O MUCYUTNGHUVNLM-UHFFFAOYSA-N 0.000 description 3
- UGBOYLVBMYDIDP-UHFFFAOYSA-N CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2cccc3c2CCN(CCC(OC(C)(C)C)=O)C3)n1 Chemical compound CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2cccc3c2CCN(CCC(OC(C)(C)C)=O)C3)n1 UGBOYLVBMYDIDP-UHFFFAOYSA-N 0.000 description 2
- CANQTOTXYUNIJU-UHFFFAOYSA-N CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2c(CCN(CC(OC(C)(C)C)=O)C3)c3ccc2)n1 Chemical compound CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2c(CCN(CC(OC(C)(C)C)=O)C3)c3ccc2)n1 CANQTOTXYUNIJU-UHFFFAOYSA-N 0.000 description 1
- XNOLMPZHHVRDRN-UHFFFAOYSA-N CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2c(CCNC3)c3ccc2)n1 Chemical compound CC(C)Oc(c(Cl)c1)ccc1-c1n[o]c(-c2c(CCNC3)c3ccc2)n1 XNOLMPZHHVRDRN-UHFFFAOYSA-N 0.000 description 1
- ABDVPVCTURYQMH-UHFFFAOYSA-N CC(C)Oc(ccc(-c1n[o]c(-c(cc2)ccc2C#N)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c(cc2)ccc2C#N)n1)c1)c1Cl ABDVPVCTURYQMH-UHFFFAOYSA-N 0.000 description 1
- TZRCDTHYFNSSEU-UHFFFAOYSA-N CC(C)Oc(ccc(-c1n[o]c(-c(cc2)ccc2OCC2OC(C)(C)OC2)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c(cc2)ccc2OCC2OC(C)(C)OC2)n1)c1)c1Cl TZRCDTHYFNSSEU-UHFFFAOYSA-N 0.000 description 1
- XYANPFVOBWRHGX-WDZFZDKYSA-N CC(C)Oc(ccc(-c1n[o]c(-c2ccc(/C=C\C(OC)=O)cc2)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c2ccc(/C=C\C(OC)=O)cc2)n1)c1)c1Cl XYANPFVOBWRHGX-WDZFZDKYSA-N 0.000 description 1
- XSRWOPOIGSBMGY-UHFFFAOYSA-N CC(C)Oc(ccc(-c1n[o]c(-c2ccc(C(C)(C)N)cc2)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c2ccc(C(C)(C)N)cc2)n1)c1)c1Cl XSRWOPOIGSBMGY-UHFFFAOYSA-N 0.000 description 1
- RBVKZGDWTYHGSB-UHFFFAOYSA-N CC(C)Oc(ccc(-c1n[o]c(-c2ccc(C(C)(C)NCCC(OC)=O)cc2)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c2ccc(C(C)(C)NCCC(OC)=O)cc2)n1)c1)c1Cl RBVKZGDWTYHGSB-UHFFFAOYSA-N 0.000 description 1
- CUMRVSSSJPQNPU-UHFFFAOYSA-N CC(C)Oc(ccc(-c1n[o]c(-c2ccc(C3(CC3)C#N)cc2)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c2ccc(C3(CC3)C#N)cc2)n1)c1)c1Cl CUMRVSSSJPQNPU-UHFFFAOYSA-N 0.000 description 1
- PPVSBMMMLQOZTI-UHFFFAOYSA-N CC(C)Oc(ccc(-c1n[o]c(-c2ccc(CN(C3)CC3C(O)=O)cc2)n1)c1)c1Cl Chemical compound CC(C)Oc(ccc(-c1n[o]c(-c2ccc(CN(C3)CC3C(O)=O)cc2)n1)c1)c1Cl PPVSBMMMLQOZTI-UHFFFAOYSA-N 0.000 description 1
- MZCXQBGZUCYGEH-UHFFFAOYSA-N CC(C)Oc(ccc(/C(/N)=N/OC(c1c(CCNC2)c2ccc1)=C)c1)c1Cl Chemical compound CC(C)Oc(ccc(/C(/N)=N/OC(c1c(CCNC2)c2ccc1)=C)c1)c1Cl MZCXQBGZUCYGEH-UHFFFAOYSA-N 0.000 description 1
- FBNZJDYBWJYLRY-UHFFFAOYSA-N COC(C1)=NCCN1C(OCc1ccccc1)=O Chemical compound COC(C1)=NCCN1C(OCc1ccccc1)=O FBNZJDYBWJYLRY-UHFFFAOYSA-N 0.000 description 1
- CKSLEPZWEOJBLM-UHFFFAOYSA-N Cc1c(C(O)=O)[n](ccnc2)c2n1 Chemical compound Cc1c(C(O)=O)[n](ccnc2)c2n1 CKSLEPZWEOJBLM-UHFFFAOYSA-N 0.000 description 1
- PHSAWENOVYZOLS-UHFFFAOYSA-N N#CC1(CC1)c(cc1)ccc1C(O)=O Chemical compound N#CC1(CC1)c(cc1)ccc1C(O)=O PHSAWENOVYZOLS-UHFFFAOYSA-N 0.000 description 1
- BAHFPJFBMJTOPU-UHFFFAOYSA-N O=C(N(CCN1)CC1=O)OCc1ccccc1 Chemical compound O=C(N(CCN1)CC1=O)OCc1ccccc1 BAHFPJFBMJTOPU-UHFFFAOYSA-N 0.000 description 1
- RDSNBKRWKBMPOP-UHFFFAOYSA-N OC(C(CC1)CC1=O)=O Chemical compound OC(C(CC1)CC1=O)=O RDSNBKRWKBMPOP-UHFFFAOYSA-N 0.000 description 1
- GFZWHAAOIVMHOI-UHFFFAOYSA-N OC(C1CNC1)=O Chemical compound OC(C1CNC1)=O GFZWHAAOIVMHOI-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
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| US87525106P | 2006-12-15 | 2006-12-15 | |
| PCT/US2007/025602 WO2008076356A1 (en) | 2006-12-15 | 2007-12-14 | Novel oxadiazole compounds |
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- 2007-12-14 EP EP07867755A patent/EP2109364A4/en not_active Withdrawn
- 2007-12-14 NZ NZ577111A patent/NZ577111A/en not_active IP Right Cessation
- 2007-12-14 MX MX2009006304A patent/MX2009006304A/es not_active Application Discontinuation
- 2007-12-14 RU RU2009127095/04A patent/RU2009127095A/ru not_active Application Discontinuation
- 2007-12-14 AU AU2007334436A patent/AU2007334436A1/en not_active Abandoned
- 2007-12-14 CA CA002672616A patent/CA2672616A1/en not_active Abandoned
- 2007-12-14 JP JP2009541394A patent/JP2010513283A/ja not_active Withdrawn
- 2007-12-14 KR KR1020097014830A patent/KR20090095648A/ko not_active Withdrawn
- 2007-12-14 US US12/002,196 patent/US7834039B2/en active Active
- 2007-12-14 CN CNA2007800463459A patent/CN101562977A/zh active Pending
- 2007-12-14 BR BRPI0720043-9A patent/BRPI0720043A2/pt not_active IP Right Cessation
- 2007-12-14 WO PCT/US2007/025602 patent/WO2008076356A1/en not_active Ceased
- 2007-12-17 TW TW096148339A patent/TW200840567A/zh unknown
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2009
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| JP2011524880A (ja) * | 2008-06-20 | 2011-09-08 | グラクソ グループ リミテッド | 化合物 |
| JP2012515788A (ja) * | 2009-01-23 | 2012-07-12 | ブリストル−マイヤーズ スクイブ カンパニー | 自己免疫疾患および炎症性疾患の処置における、s1pアゴニストとしての置換オキサジアゾール誘導体 |
| JP2012515787A (ja) * | 2009-01-23 | 2012-07-12 | ブリストル−マイヤーズ スクイブ カンパニー | 自己免疫疾患および炎症性疾患の処置におけるs1pアゴニストとしての置換オキサジアゾール誘導体 |
| JP2013525478A (ja) * | 2010-05-03 | 2013-06-20 | エスケー バイオファーマスティカルズ カンパニー リミテッド | 神経細胞のアポトーシス又は神経変性を阻害するための医薬組成物 |
| JP2013531070A (ja) * | 2010-07-20 | 2013-08-01 | ブリストル−マイヤーズ スクイブ カンパニー | 置換3−フェニル−1,2,4−オキサジアゾール化合物 |
| JP2013537913A (ja) * | 2010-09-24 | 2013-10-07 | ブリストル−マイヤーズ スクイブ カンパニー | 置換オキサジアゾール化合物およびそれらのs1p1アゴニストとしての使用 |
| JP2015527349A (ja) * | 2012-08-09 | 2015-09-17 | セルジーン コーポレイション | 免疫関連及び炎症性疾患の治療 |
| JP2023518967A (ja) * | 2020-03-27 | 2023-05-09 | レセプトス・リミテッド・ライアビリティ・カンパニー | スフィンゴシン1ホスフェート受容体モジュレーター |
| JP7752629B2 (ja) | 2020-03-27 | 2025-10-10 | レセプトス・リミテッド・ライアビリティ・カンパニー | スフィンゴシン1ホスフェート受容体モジュレーター |
| JP2025525896A (ja) * | 2022-08-01 | 2025-08-07 | コリア・インスティテュート・オブ・サイエンス・アンド・テクノロジー | 新規なヘテロシクリル-フェニル-メチルアミン誘導体、その製造方法及びその多発性硬化症予防、改善、又は治療用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2109364A4 (en) | 2010-04-14 |
| EP2109364A1 (en) | 2009-10-21 |
| SG177221A1 (en) | 2012-01-30 |
| TW200840567A (en) | 2008-10-16 |
| US7834039B2 (en) | 2010-11-16 |
| CA2672616A1 (en) | 2008-06-26 |
| NZ577111A (en) | 2012-05-25 |
| WO2008076356A1 (en) | 2008-06-26 |
| ZA200903693B (en) | 2010-03-31 |
| BRPI0720043A2 (pt) | 2014-01-07 |
| CN101562977A (zh) | 2009-10-21 |
| MX2009006304A (es) | 2009-06-23 |
| AU2007334436A1 (en) | 2008-06-26 |
| US20080280876A1 (en) | 2008-11-13 |
| RU2009127095A (ru) | 2011-01-20 |
| KR20090095648A (ko) | 2009-09-09 |
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