JP2008530106A5 - - Google Patents
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- Publication number
- JP2008530106A5 JP2008530106A5 JP2007555215A JP2007555215A JP2008530106A5 JP 2008530106 A5 JP2008530106 A5 JP 2008530106A5 JP 2007555215 A JP2007555215 A JP 2007555215A JP 2007555215 A JP2007555215 A JP 2007555215A JP 2008530106 A5 JP2008530106 A5 JP 2008530106A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- optionally substituted
- alkyl
- substituted
- aryl
- 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
- 125000004432 carbon atom Chemical group C* 0.000 claims 100
- 125000005842 heteroatom Chemical group 0.000 claims 30
- 239000004098 Tetracycline Substances 0.000 claims 26
- 150000003839 salts Chemical class 0.000 claims 26
- 125000000217 alkyl group Chemical group 0.000 claims 22
- -1 furanyl compound Chemical class 0.000 claims 20
- 229910052736 halogen Inorganic materials 0.000 claims 20
- 150000002367 halogens Chemical class 0.000 claims 20
- 229910052739 hydrogen Inorganic materials 0.000 claims 20
- 239000001257 hydrogen Substances 0.000 claims 20
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 20
- 238000000034 method Methods 0.000 claims 20
- 125000000547 substituted alkyl group Chemical group 0.000 claims 20
- 229960002180 tetracycline Drugs 0.000 claims 20
- 235000019364 tetracycline Nutrition 0.000 claims 19
- 150000003522 tetracyclines Chemical class 0.000 claims 19
- 229930101283 tetracycline Natural products 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 16
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 16
- 125000004426 substituted alkynyl group Chemical group 0.000 claims 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims 11
- 125000003118 aryl group Chemical group 0.000 claims 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims 11
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 150000001602 bicycloalkyls Chemical group 0.000 claims 10
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 10
- 229910052760 oxygen Inorganic materials 0.000 claims 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 10
- 229910052717 sulfur Inorganic materials 0.000 claims 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 10
- 229920002554 vinyl polymer Polymers 0.000 claims 10
- 125000003107 substituted aryl group Chemical group 0.000 claims 9
- 125000000304 alkynyl group Chemical group 0.000 claims 6
- 239000000010 aprotic solvent Substances 0.000 claims 6
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 claims 6
- GUVUOGQBMYCBQP-UHFFFAOYSA-N dmpu Chemical compound CN1CCCN(C)C1=O GUVUOGQBMYCBQP-UHFFFAOYSA-N 0.000 claims 6
- 229940040944 tetracyclines Drugs 0.000 claims 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000001246 bromo group Chemical group Br* 0.000 claims 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims 4
- 229910021595 Copper(I) iodide Inorganic materials 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 claims 3
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 208000035143 Bacterial infection Diseases 0.000 claims 1
- YPWZRSAWHVBHKT-HJYUBDRYSA-N C([C@H]1C2)C3=C(N(C)C)C=C(NC(=O)CN(O)C(C)(C)C)C(O)=C3C(=O)C1=C(O)[C@@]1(O)[C@@H]2[C@H](N(C)C)C(O)=C(C(N)=O)C1=O Chemical compound C([C@H]1C2)C3=C(N(C)C)C=C(NC(=O)CN(O)C(C)(C)C)C(O)=C3C(=O)C1=C(O)[C@@]1(O)[C@@H]2[C@H](N(C)C)C(O)=C(C(N)=O)C1=O YPWZRSAWHVBHKT-HJYUBDRYSA-N 0.000 claims 1
- LEKRFUONRYATJQ-HJYUBDRYSA-N C([C@H]1C2)C3=C(N(C)C)C=C(NC(=O)CNOC(C)(C)C)C(O)=C3C(=O)C1=C(O)[C@@]1(O)[C@@H]2[C@H](N(C)C)C(O)=C(C(N)=O)C1=O Chemical compound C([C@H]1C2)C3=C(N(C)C)C=C(NC(=O)CNOC(C)(C)C)C(O)=C3C(=O)C1=C(O)[C@@]1(O)[C@@H]2[C@H](N(C)C)C(O)=C(C(N)=O)C1=O LEKRFUONRYATJQ-HJYUBDRYSA-N 0.000 claims 1
- BWFPJHYJGVQIAK-IRBJOYOSSA-N C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(C=1SC=CC=1)C=C2NC(=O)CN1CCCCO1 Chemical compound C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(C=1SC=CC=1)C=C2NC(=O)CN1CCCCO1 BWFPJHYJGVQIAK-IRBJOYOSSA-N 0.000 claims 1
- RXXSNMINZIRUMC-ISIOAQNYSA-N C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(I)C=C2NC(=O)CN1CCCCO1 Chemical compound C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(I)C=C2NC(=O)CN1CCCCO1 RXXSNMINZIRUMC-ISIOAQNYSA-N 0.000 claims 1
- GBIOERKSNVSFTF-IRBJOYOSSA-N C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(N(C)C)C=C2NC(=O)CN(O)C1CCCCC1 Chemical compound C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(N(C)C)C=C2NC(=O)CN(O)C1CCCCC1 GBIOERKSNVSFTF-IRBJOYOSSA-N 0.000 claims 1
- AOKMMNCWNFRPTP-XAGJCVETSA-N C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(N(C)C)C=C2NC(=O)CN(O)CC1=CC=CC=C1 Chemical compound C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(N(C)C)C=C2NC(=O)CN(O)CC1=CC=CC=C1 AOKMMNCWNFRPTP-XAGJCVETSA-N 0.000 claims 1
- UTMNATNBZYCWRV-WOTXACPJSA-N C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(N(C)C)C=C2NC(=O)CN1CCCCO1 Chemical compound C([C@H]1C[C@H]2[C@@H](C(=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C1C(=O)C1=C2O)O)N(C)C)C1=C(N(C)C)C=C2NC(=O)CN1CCCCO1 UTMNATNBZYCWRV-WOTXACPJSA-N 0.000 claims 1
- TZOYOTIAAROPSL-ISIOAQNYSA-N CN(C)[C@@H]([C@@H]1C2)C(O)=C(C(N)=O)C(=O)[C@@]1(O)C(O)=C1[C@H]2CC2=C(N(C)C)C=C(NC(=O)CN(C)OC)C(O)=C2C1=O Chemical compound CN(C)[C@@H]([C@@H]1C2)C(O)=C(C(N)=O)C(=O)[C@@]1(O)C(O)=C1[C@H]2CC2=C(N(C)C)C=C(NC(=O)CN(C)OC)C(O)=C2C1=O TZOYOTIAAROPSL-ISIOAQNYSA-N 0.000 claims 1
- YSPKKPBDIDKKCZ-QFBSOPCBSA-N CN(C)[C@@H]([C@@H]1C2)C(O)=C(C(N)=O)C(=O)[C@@]1(O)C(O)=C1[C@H]2CC2=C(N(C)C)C=C(NC(=O)CN(O)C(C)C)C(O)=C2C1=O Chemical compound CN(C)[C@@H]([C@@H]1C2)C(O)=C(C(N)=O)C(=O)[C@@]1(O)C(O)=C1[C@H]2CC2=C(N(C)C)C=C(NC(=O)CN(O)C(C)C)C(O)=C2C1=O YSPKKPBDIDKKCZ-QFBSOPCBSA-N 0.000 claims 1
- XJXCOWXBDNRXCB-NXHKEXIGSA-N CN(C)[C@@H]([C@@H]1C2)C(O)=C(C(N)=O)C(=O)[C@@]1(O)C(O)=C1[C@H]2CC2=C(N(C)C)C=C(NC(=O)CNOC)C(O)=C2C1=O Chemical compound CN(C)[C@@H]([C@@H]1C2)C(O)=C(C(N)=O)C(=O)[C@@]1(O)C(O)=C1[C@H]2CC2=C(N(C)C)C=C(NC(=O)CNOC)C(O)=C2C1=O XJXCOWXBDNRXCB-NXHKEXIGSA-N 0.000 claims 1
- 208000022362 bacterial infectious disease Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 0 Cc(c(*)c1NC(CBr)=*)c(CC(CC([C@](*)C(O)=C(C(N)=O)C2=O)[C@@]22O)C(C3=O)=C2O)c3c1O Chemical compound Cc(c(*)c1NC(CBr)=*)c(CC(CC([C@](*)C(O)=C(C(N)=O)C2=O)[C@@]22O)C(C3=O)=C2O)c3c1O 0.000 description 6
- MYUWXCFJYLQEHX-UHFFFAOYSA-N CC1CNOCC1 Chemical compound CC1CNOCC1 MYUWXCFJYLQEHX-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65326905P | 2005-02-15 | 2005-02-15 | |
| PCT/US2006/004562 WO2006088720A2 (en) | 2005-02-15 | 2006-02-09 | 9-substituted tetracyclines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008530106A JP2008530106A (ja) | 2008-08-07 |
| JP2008530106A5 true JP2008530106A5 (enExample) | 2009-02-05 |
Family
ID=36676182
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007555215A Pending JP2008530106A (ja) | 2005-02-15 | 2006-02-09 | ９−置換テトラサイクリン |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7812008B2 (enExample) |
| EP (1) | EP1848686A2 (enExample) |
| JP (1) | JP2008530106A (enExample) |
| CN (1) | CN101119964A (enExample) |
| AR (1) | AR053131A1 (enExample) |
| AU (1) | AU2006214543A1 (enExample) |
| BR (1) | BRPI0607353A2 (enExample) |
| CA (1) | CA2597870A1 (enExample) |
| GT (1) | GT200600063A (enExample) |
| MX (1) | MX2007009863A (enExample) |
| TW (1) | TW200640469A (enExample) |
| WO (1) | WO2006088720A2 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2649221A1 (en) * | 2006-04-17 | 2007-10-25 | Evgeny Tsiperman | Isolation of tetracycline derivatives |
| US8198470B2 (en) * | 2006-04-24 | 2012-06-12 | Teva Pharmaceutical Industries Ltd. | Crystalline form II of tigecycline and processes for preparation thereof |
| DE202007019460U1 (de) * | 2006-04-24 | 2012-10-24 | Teva Pharmaceutical Industries Ltd. | Kristalline Tigecyclin-Formen |
| WO2008066935A2 (en) * | 2006-11-29 | 2008-06-05 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of tigecycline and processes for preparation thereof |
| WO2008066908A1 (en) * | 2006-11-30 | 2008-06-05 | Teva Pharmaceutical Industries Ltd. | Processes for preparation of 9-haloacetamidominocyclines |
| EP2114865A1 (en) * | 2007-03-01 | 2009-11-11 | Teva Pharmaceutical Industries Ltd. | Processes for purification of tigecycline |
| US7939513B2 (en) | 2007-09-07 | 2011-05-10 | Dr. Reddy's Laboratories Limited | Tetracycline derivatives as antibacterial agents |
| ES2655911T3 (es) * | 2008-08-08 | 2018-02-22 | Tetraphase Pharmaceuticals, Inc. | Compuestos de tetraciclina sustituidos con C7-fluoro |
| ES2627772T3 (es) | 2009-05-08 | 2017-07-31 | Tetraphase Pharmaceuticals, Inc. | Compuestos de tetraciclina |
| JP5944825B2 (ja) * | 2009-08-28 | 2016-07-05 | テトラフェース ファーマシューティカルズ，インコーポレイテッド | テトラサイクリン化合物 |
| CN101955443B (zh) * | 2010-09-30 | 2012-05-23 | 浙江大学 | 一种替加环素中间体及其盐的制备方法 |
| WO2013013504A1 (zh) * | 2011-07-26 | 2013-01-31 | 山东亨利医药科技有限责任公司 | 替加环素衍生物 |
| BR112015004523B1 (pt) | 2012-08-31 | 2020-08-04 | Tetraphase Pharmaceuticals, Inc | Compostos de tetraciclina, composições farmacêuticas e seus usos |
| CN107759503A (zh) * | 2016-08-16 | 2018-03-06 | 四川科伦博泰生物医药股份有限公司 | 一种四环素衍生物及其用途 |
| ES2978198T3 (es) | 2016-10-19 | 2024-09-06 | Tetraphase Pharmaceuticals Inc | Formas cristalinas de eravaciclina |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2482055A (en) | 1948-02-11 | 1949-09-13 | American Cyanamid Co | Aureomycin and preparation of same |
| US3007965A (en) | 1959-02-13 | 1961-11-07 | American Cyanamid Co | New tetracyclines produced by streptomyces aureofaciens |
| US3043875A (en) | 1959-10-22 | 1962-07-10 | Pfizer & Co C | Halogenated tetracycline derivatives and processes for their preparation |
| FR1430859A (enExample) | 1960-05-23 | 1966-05-25 | ||
| US3338963A (en) | 1960-10-28 | 1967-08-29 | American Cyanamid Co | Tetracycline compounds |
| US3148212A (en) | 1961-12-22 | 1964-09-08 | American Cyanamid Co | Reductive alkylation process |
| US3360557A (en) | 1963-05-10 | 1967-12-26 | American Cyanamid Co | 9-hydroxytetracyclines and a process of preparing same |
| USRE26253E (en) | 1963-05-17 | 1967-08-15 | And z-alkylamino-g-deoxytetracycline | |
| US3341585A (en) | 1966-05-06 | 1967-09-12 | American Cyanamid Co | Substituted 7-and/or 9-amino-6-deoxytetracyclines |
| US3360561A (en) | 1967-06-19 | 1967-12-26 | American Cyanamid Co | Nitration of tetracyclines |
| US3518306A (en) | 1968-02-19 | 1970-06-30 | American Cyanamid Co | 7- and/or 9-(n-nitrosoalkylamino)-6-demethyl-6-deoxytetracyclines |
| US4806529A (en) | 1982-11-18 | 1989-02-21 | Trustees Of Tufts College, Tufts University | Tetracycline activity enhancement |
| US5494903A (en) | 1991-10-04 | 1996-02-27 | American Cyanamid Company | 7-substituted-9-substituted amino-6-demethyl-6-deoxytetracyclines |
| US5328902A (en) * | 1992-08-13 | 1994-07-12 | American Cyanamid Co. | 7-(substituted)-9-[(substituted glycyl)amido]-6-demethyl-6-deoxytetracyclines |
| US5420272A (en) * | 1992-08-13 | 1995-05-30 | American Cyanamid Company | 7-(substituted)-8-(substituted)-9-](substituted glycyl)amido]-6-demethyl-6-deoxytetracyclines |
| US5442059A (en) * | 1992-08-13 | 1995-08-15 | American Cyanamid Company | 9-[(substituted glycyl)amido)]-6-demethyl-6-deoxytetracyclines |
| US5834450A (en) * | 1994-02-17 | 1998-11-10 | Pfizer Inc. | 9- (substituted amino) -alpha-6-deoxy-5-oxy tetracycline derivatives, their preparation and their use as antibiotics |
| DE60144375D1 (de) * | 2000-07-07 | 2011-05-19 | Trustees Of Tufts College Medford | 7-, 8- und 9-substitutierte tetracyclinverbindungen |
| EP2298732A1 (en) * | 2001-03-13 | 2011-03-23 | Paratek Pharmaceuticals, Inc. | 7,9-Substituted tetracycline compounds |
| WO2004064728A2 (en) * | 2003-01-16 | 2004-08-05 | Paratek Pharmaceuticals, Inc. | Use of specific tetracycline compounds in therapy |
-
2006
- 2006-02-09 MX MX2007009863A patent/MX2007009863A/es active IP Right Grant
- 2006-02-09 JP JP2007555215A patent/JP2008530106A/ja active Pending
- 2006-02-09 CA CA002597870A patent/CA2597870A1/en not_active Abandoned
- 2006-02-09 CN CNA2006800049045A patent/CN101119964A/zh active Pending
- 2006-02-09 AU AU2006214543A patent/AU2006214543A1/en not_active Abandoned
- 2006-02-09 BR BRPI0607353-0A patent/BRPI0607353A2/pt not_active IP Right Cessation
- 2006-02-09 EP EP06720553A patent/EP1848686A2/en not_active Withdrawn
- 2006-02-09 WO PCT/US2006/004562 patent/WO2006088720A2/en not_active Ceased
- 2006-02-14 GT GT200600063A patent/GT200600063A/es unknown
- 2006-02-14 TW TW095104895A patent/TW200640469A/zh unknown
- 2006-02-14 AR ARP060100514A patent/AR053131A1/es not_active Application Discontinuation
- 2006-02-14 US US11/354,306 patent/US7812008B2/en not_active Expired - Fee Related