SG11201604502SA - Synthesis of trans-8-chloro-5-methyl-1 -[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crytalline forms thereof - Google Patents
Synthesis of trans-8-chloro-5-methyl-1 -[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crytalline forms thereofInfo
- Publication number
- SG11201604502SA SG11201604502SA SG11201604502SA SG11201604502SA SG11201604502SA SG 11201604502S A SG11201604502S A SG 11201604502SA SG 11201604502S A SG11201604502S A SG 11201604502SA SG 11201604502S A SG11201604502S A SG 11201604502SA SG 11201604502S A SG11201604502S A SG 11201604502SA
- Authority
- SG
- Singapore
- Prior art keywords
- tetraaza
- azulene
- yloxy
- pyridin
- benzo
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13195864 | 2013-12-05 | ||
PCT/EP2014/076041 WO2015082370A1 (en) | 2013-12-05 | 2014-12-01 | Synthesis of trans-8-chloro-5-methyl-1 -[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crytalline forms thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201604502SA true SG11201604502SA (en) | 2016-07-28 |
Family
ID=49726573
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201604502SA SG11201604502SA (en) | 2013-12-05 | 2014-12-01 | Synthesis of trans-8-chloro-5-methyl-1 -[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crytalline forms thereof |
Country Status (20)
Country | Link |
---|---|
US (3) | US10246460B2 (en) |
EP (1) | EP3077396B1 (en) |
JP (1) | JP6454707B2 (en) |
KR (3) | KR102384630B1 (en) |
CN (1) | CN105793263B (en) |
AR (1) | AR098592A1 (en) |
AU (2) | AU2014359409A1 (en) |
CA (2) | CA2931016C (en) |
ES (1) | ES2875411T3 (en) |
HK (1) | HK1223918A1 (en) |
HR (1) | HRP20210966T1 (en) |
IL (2) | IL245450A0 (en) |
MX (1) | MX2016006558A (en) |
MY (1) | MY175464A (en) |
NZ (1) | NZ720340A (en) |
PL (1) | PL3077396T3 (en) |
SG (1) | SG11201604502SA (en) |
SI (1) | SI3077396T1 (en) |
WO (1) | WO2015082370A1 (en) |
ZA (1) | ZA201603304B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2931016C (en) * | 2013-12-05 | 2022-11-01 | F. Hoffmann-La Roche Ag | Synthesis of trans-8-chloro-5-methyl-1-[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crystalline forms thereof |
WO2017191117A1 (en) | 2016-05-03 | 2017-11-09 | Bayer Pharma Aktiengesellschaft | V1a receptor antagonists for use in the treatment of renal diseases |
KR20200097702A (en) * | 2017-12-08 | 2020-08-19 | 에프. 호프만-라 로슈 아게 | Pharmaceutical formulation |
WO2020139670A1 (en) | 2018-12-27 | 2020-07-02 | Teva Pharmaceuticals International Gmbh | Solid state forms of balovaptan |
WO2023059110A1 (en) | 2021-10-06 | 2023-04-13 | 주식회사 엘지에너지솔루션 | Battery module |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1197242A (en) * | 1983-03-02 | 1985-11-26 | Jean A. Gauthier | Pyrimido¬1,2-a|pyrrolo¬2,1-c|¬1, 4|benzodiazepine-3-carboxylic acid derivatives |
ES2277237T3 (en) * | 2003-02-19 | 2007-07-01 | Pfizer Inc. | USEFUL TRIAZOL COMPOUNDS IN THERAPY. |
GB0303852D0 (en) | 2003-02-19 | 2003-03-26 | Pfizer Ltd | Triazole compounds useful in therapy |
GB0400700D0 (en) * | 2004-01-13 | 2004-02-18 | Pfizer Ltd | Compounds useful in therapy |
WO2006021882A1 (en) | 2004-08-25 | 2006-03-02 | Pfizer Limited | Triazolobenzodiazepines and their use as vasopressin antagonists |
US7601715B2 (en) * | 2005-06-22 | 2009-10-13 | Bristol-Myers Squibb Company | Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein |
MX2011005119A (en) * | 2008-11-18 | 2011-05-30 | Hoffmann La Roche | Alkylcyclohexylethers of dihydrotetraazabenzoazulenes. |
NZ592076A (en) * | 2008-11-28 | 2012-06-29 | Hoffmann La Roche | Arylcyclohexylethers of dihydrotetraazabenzoazulenes for use as vasopressin via receptor antagonists |
US8492376B2 (en) | 2010-04-21 | 2013-07-23 | Hoffmann-La Roche Inc. | Heteroaryl-cyclohexyl-tetraazabenzo[e]azulenes |
PE20160203A1 (en) | 2013-08-19 | 2016-04-20 | Hoffmann La Roche | VIA ANTAGONISTS TO TREAT PHASE CHANGE SLEEP DISORDERS |
CA2931016C (en) * | 2013-12-05 | 2022-11-01 | F. Hoffmann-La Roche Ag | Synthesis of trans-8-chloro-5-methyl-1-[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crystalline forms thereof |
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2014
- 2014-12-01 CA CA2931016A patent/CA2931016C/en active Active
- 2014-12-01 EP EP14805290.5A patent/EP3077396B1/en active Active
- 2014-12-01 MY MYPI2016000870A patent/MY175464A/en unknown
- 2014-12-01 JP JP2016536746A patent/JP6454707B2/en active Active
- 2014-12-01 NZ NZ720340A patent/NZ720340A/en unknown
- 2014-12-01 CA CA3142754A patent/CA3142754C/en active Active
- 2014-12-01 MX MX2016006558A patent/MX2016006558A/en active IP Right Grant
- 2014-12-01 PL PL14805290T patent/PL3077396T3/en unknown
- 2014-12-01 KR KR1020217034765A patent/KR102384630B1/en active IP Right Grant
- 2014-12-01 WO PCT/EP2014/076041 patent/WO2015082370A1/en active Application Filing
- 2014-12-01 CN CN201480065960.4A patent/CN105793263B/en active Active
- 2014-12-01 SG SG11201604502SA patent/SG11201604502SA/en unknown
- 2014-12-01 SI SI201431838T patent/SI3077396T1/en unknown
- 2014-12-01 AU AU2014359409A patent/AU2014359409A1/en not_active Abandoned
- 2014-12-01 ES ES14805290T patent/ES2875411T3/en active Active
- 2014-12-01 KR KR1020217034768A patent/KR102384629B1/en active IP Right Grant
- 2014-12-01 KR KR1020167017925A patent/KR102384608B1/en active IP Right Grant
- 2014-12-03 AR ARP140104488A patent/AR098592A1/en unknown
-
2016
- 2016-05-03 IL IL245450A patent/IL245450A0/en unknown
- 2016-05-16 ZA ZA2016/03304A patent/ZA201603304B/en unknown
- 2016-06-03 US US15/172,542 patent/US10246460B2/en active Active
- 2016-10-19 HK HK16112048.9A patent/HK1223918A1/en unknown
-
2019
- 2019-02-18 IL IL264891A patent/IL264891B/en active IP Right Grant
- 2019-02-20 AU AU2019201183A patent/AU2019201183B2/en active Active
- 2019-03-04 US US16/291,887 patent/US11040977B2/en active Active
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2021
- 2021-06-03 US US17/337,547 patent/US20210284648A1/en active Pending
- 2021-06-17 HR HRP20210966TT patent/HRP20210966T1/en unknown
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