CA2662000C - Thiophene pyrazolopyrimidine compounds - Google Patents
Thiophene pyrazolopyrimidine compounds Download PDFInfo
- Publication number
- CA2662000C CA2662000C CA2662000A CA2662000A CA2662000C CA 2662000 C CA2662000 C CA 2662000C CA 2662000 A CA2662000 A CA 2662000A CA 2662000 A CA2662000 A CA 2662000A CA 2662000 C CA2662000 C CA 2662000C
- Authority
- CA
- Canada
- Prior art keywords
- mmol
- reaction
- hexane
- add
- thiophene
- 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.)
- Expired - Fee Related
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- UIVVICIYVFEGIH-UHFFFAOYSA-N 1h-pyrazolo[4,3-d]pyrimidine;thiophene Chemical class C=1C=CSC=1.N1=CN=C2C=NNC2=C1 UIVVICIYVFEGIH-UHFFFAOYSA-N 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 90
- 238000011282 treatment Methods 0.000 claims abstract description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 6
- 150000003839 salts Chemical class 0.000 claims description 35
- -1 nitro, methoxy, methoxymethyl Chemical group 0.000 claims description 16
- 239000003814 drug Substances 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
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- 208000011117 substance-related disease Diseases 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
- 208000020401 Depressive disease Diseases 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 241
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- 238000006243 chemical reaction Methods 0.000 description 91
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 51
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- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 22
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
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- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 10
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- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 8
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- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 8
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- 125000000623 heterocyclic group Chemical group 0.000 description 8
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- 229930192474 thiophene Natural products 0.000 description 7
- CRVNUZXQVCHLQW-UHFFFAOYSA-N 3-(5-bromo-3-chlorothiophen-2-yl)-2,5-dimethyl-7-pentan-3-ylpyrazolo[1,5-a]pyrimidine Chemical compound CC1=NN2C(C(CC)CC)=CC(C)=NC2=C1C=1SC(Br)=CC=1Cl CRVNUZXQVCHLQW-UHFFFAOYSA-N 0.000 description 6
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- USVZFSNDGFNNJT-UHFFFAOYSA-N cyclopenta-1,4-dien-1-yl(diphenyl)phosphane (2,3-dichlorocyclopenta-1,4-dien-1-yl)-diphenylphosphane iron(2+) Chemical compound [Fe++].c1cc[c-](c1)P(c1ccccc1)c1ccccc1.Clc1c(cc[c-]1Cl)P(c1ccccc1)c1ccccc1 USVZFSNDGFNNJT-UHFFFAOYSA-N 0.000 description 6
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
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- QOEYTZPVSXRHCY-UHFFFAOYSA-M zinc;3-methyl-2h-thiophen-2-ide;bromide Chemical compound Br[Zn+].CC=1C=CS[C-]=1 QOEYTZPVSXRHCY-UHFFFAOYSA-M 0.000 description 1
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Classifications
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- 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
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
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- Pulmonology (AREA)
- Pregnancy & Childbirth (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82627306P | 2006-09-20 | 2006-09-20 | |
| US60/826,273 | 2006-09-20 | ||
| PCT/US2007/078352 WO2008036541A1 (en) | 2006-09-20 | 2007-09-13 | Thiophene pyrazolopyrimidine compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2662000A1 CA2662000A1 (en) | 2008-03-27 |
| CA2662000C true CA2662000C (en) | 2013-01-08 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2662000A Expired - Fee Related CA2662000C (en) | 2006-09-20 | 2007-09-13 | Thiophene pyrazolopyrimidine compounds |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8110580B2 (OSRAM) |
| EP (1) | EP2076515B1 (OSRAM) |
| JP (1) | JP5184536B2 (OSRAM) |
| KR (1) | KR101088196B1 (OSRAM) |
| CN (1) | CN101516886B (OSRAM) |
| AU (1) | AU2007297481B2 (OSRAM) |
| BR (1) | BRPI0717070A2 (OSRAM) |
| CA (1) | CA2662000C (OSRAM) |
| EA (1) | EA016056B1 (OSRAM) |
| ES (1) | ES2428543T3 (OSRAM) |
| MX (1) | MX2009003098A (OSRAM) |
| WO (1) | WO2008036541A1 (OSRAM) |
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| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP2250160B1 (en) | 2008-01-25 | 2015-11-11 | Millennium Pharmaceuticals, Inc. | Thiophenes and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors |
| WO2010090716A1 (en) | 2009-01-30 | 2010-08-12 | Millennium Pharmaceuticals, Inc. | Heteroaryls and their use as pi3k inhibitors |
| US8796314B2 (en) | 2009-01-30 | 2014-08-05 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| US9062038B2 (en) | 2010-08-11 | 2015-06-23 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| UY33554A (es) | 2010-08-11 | 2012-02-29 | Millennium Pharm Inc | Heteroarilos y usos de los mismos |
| WO2012021615A1 (en) | 2010-08-11 | 2012-02-16 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| BR112013009166A2 (pt) | 2010-10-13 | 2016-07-26 | Millennium Pharm Inc | heteroarilas e uso das mesmas. |
| US8946432B2 (en) | 2011-07-05 | 2015-02-03 | Lupin Limited | Biaryl derivatives as nAChR modulators |
| EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| CN106102740A (zh) | 2014-01-21 | 2016-11-09 | 纽罗克里生物科学有限公司 | 治疗先天性肾上腺增生的crf1受体拮抗剂 |
| JP6364967B2 (ja) * | 2014-05-30 | 2018-08-01 | 東ソー株式会社 | ジチエノベンゾジチオフェンの製造方法 |
| EP3238676B1 (en) | 2016-04-29 | 2019-01-02 | The Procter and Gamble Company | Absorbent core with profiled distribution of absorbent material |
| WO2019036503A1 (en) | 2017-08-14 | 2019-02-21 | Spruce Biosciences, Inc. | CORTICOTROPIN RELEASE FACTOR RECEPTOR ANTAGONISTS |
| CA3064445A1 (en) * | 2017-08-14 | 2019-02-21 | Spruce Biosciences, Inc. | Corticotropin releasing factor receptor antagonists |
| EP3984523B1 (en) | 2018-12-07 | 2025-09-03 | Neurocrine Biosciences, Inc. | Crf1 receptor antagonist, pharmaceutical formulations and solid forms thereof for the treatment of congenital adrenal hyperplasia |
| WO2021062246A1 (en) | 2019-09-27 | 2021-04-01 | Neurocrine Biosciences, Inc. | Crf receptor antagonists and methods of use |
| AR120649A1 (es) * | 2019-12-04 | 2022-03-09 | Neurocrine Biosciences Inc | Antagonistas del receptor de crf y métodos de uso |
| EP4175572A4 (en) | 2020-08-12 | 2024-03-27 | Spruce Biosciences, Inc. | Methods and compositions for treating polycystic ovary syndrome |
| US11708372B2 (en) | 2021-11-19 | 2023-07-25 | Spruce Biosciences, Inc. | Crystalline composition of tildacerfont and methods of use and preparation thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2128544T3 (es) | 1992-12-17 | 1999-05-16 | Pfizer | Pirrolopirimidinas como antagonistas del crf. |
| PL191271B1 (pl) * | 1996-02-07 | 2006-04-28 | Neurocrine Biosciences Inc | Pochodna pirazolopirymidyny i jej zastosowanie oraz kompozycja farmaceutyczna |
| ES2294800T3 (es) | 1996-07-24 | 2008-04-01 | Bristol-Myers Squibb Pharma Company | Azolo triazinas y pirimidinas. |
| BR9711970A (pt) | 1996-08-28 | 1999-08-24 | Pfizer | Derivados 6,5-substitu¡do-heterobic¡clicos |
| ATE347553T1 (de) | 1999-09-30 | 2006-12-15 | Neurogen Corp | Amino-substituierte pyrazolo 1,5-aö-1,5- pyrimidine und pyrazolo 1,5-aö-1,3,5-triazine |
| RU2394035C2 (ru) * | 2003-12-22 | 2010-07-10 | Эс Би ФАРМКО ПУЭРТО РИКО ИНК. | Антагонисты crf-рецепторов и способы, относящиеся к ним |
| DK1869049T3 (da) * | 2005-03-21 | 2009-05-18 | Lilly Co Eli | Imidazopyridazinforbindelser |
-
2007
- 2007-09-13 ES ES07814842T patent/ES2428543T3/es active Active
- 2007-09-13 CN CN2007800349472A patent/CN101516886B/zh not_active Expired - Fee Related
- 2007-09-13 WO PCT/US2007/078352 patent/WO2008036541A1/en not_active Ceased
- 2007-09-13 EA EA200970302A patent/EA016056B1/ru not_active IP Right Cessation
- 2007-09-13 US US12/438,953 patent/US8110580B2/en active Active
- 2007-09-13 MX MX2009003098A patent/MX2009003098A/es active IP Right Grant
- 2007-09-13 KR KR1020097005694A patent/KR101088196B1/ko not_active Expired - Fee Related
- 2007-09-13 JP JP2009529307A patent/JP5184536B2/ja not_active Expired - Fee Related
- 2007-09-13 BR BRPI0717070-0A2A patent/BRPI0717070A2/pt not_active IP Right Cessation
- 2007-09-13 CA CA2662000A patent/CA2662000C/en not_active Expired - Fee Related
- 2007-09-13 EP EP07814842.6A patent/EP2076515B1/en not_active Not-in-force
- 2007-09-13 AU AU2007297481A patent/AU2007297481B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008036541A1 (en) | 2008-03-27 |
| MX2009003098A (es) | 2009-04-01 |
| BRPI0717070A2 (pt) | 2013-09-24 |
| EA016056B1 (ru) | 2012-01-30 |
| JP5184536B2 (ja) | 2013-04-17 |
| KR20090053921A (ko) | 2009-05-28 |
| EP2076515B1 (en) | 2013-07-17 |
| CN101516886A (zh) | 2009-08-26 |
| JP2010504343A (ja) | 2010-02-12 |
| AU2007297481A1 (en) | 2008-03-27 |
| EP2076515A1 (en) | 2009-07-08 |
| AU2007297481B2 (en) | 2012-03-08 |
| KR101088196B1 (ko) | 2011-11-30 |
| US20100022560A1 (en) | 2010-01-28 |
| EA200970302A1 (ru) | 2009-10-30 |
| ES2428543T3 (es) | 2013-11-08 |
| CN101516886B (zh) | 2012-02-29 |
| US8110580B2 (en) | 2012-02-07 |
| CA2662000A1 (en) | 2008-03-27 |
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