NZ550534A - Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, and preparation and uses thereof - Google Patents
Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, and preparation and uses thereofInfo
- Publication number
- NZ550534A NZ550534A NZ550534A NZ55053405A NZ550534A NZ 550534 A NZ550534 A NZ 550534A NZ 550534 A NZ550534 A NZ 550534A NZ 55053405 A NZ55053405 A NZ 55053405A NZ 550534 A NZ550534 A NZ 550534A
- Authority
- NZ
- New Zealand
- Prior art keywords
- oct
- indazole
- azabicyclo
- carboxamide
- carbon atoms
- Prior art date
Links
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- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 235000010378 sodium ascorbate Nutrition 0.000 description 1
- 229960005055 sodium ascorbate Drugs 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 229940048181 sodium sulfide nonahydrate Drugs 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- WMDLZMCDBSJMTM-UHFFFAOYSA-M sodium;sulfanide;nonahydrate Chemical compound O.O.O.O.O.O.O.O.O.[Na+].[SH-] WMDLZMCDBSJMTM-UHFFFAOYSA-M 0.000 description 1
- 230000001148 spastic effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 208000003755 striatonigral degeneration Diseases 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
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- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229940032330 sulfuric acid Drugs 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000005062 synaptic transmission Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 150000003899 tartaric acid esters Chemical class 0.000 description 1
- GTNJYSHYBCIFTF-UHFFFAOYSA-N tert-butyl 5-bromo-1h-indazole-3-carboxylate Chemical compound C1=C(Br)C=C2C(C(=O)OC(C)(C)C)=NNC2=C1 GTNJYSHYBCIFTF-UHFFFAOYSA-N 0.000 description 1
- VSLFHIMHDHPVST-UHFFFAOYSA-N tert-butyl 6-bromo-1h-indazole-3-carboxylate Chemical compound BrC1=CC=C2C(C(=O)OC(C)(C)C)=NNC2=C1 VSLFHIMHDHPVST-UHFFFAOYSA-N 0.000 description 1
- ACNRTYKOPZDRCO-UHFFFAOYSA-N tert-butyl n-(2-oxoethyl)carbamate Chemical compound CC(C)(C)OC(=O)NCC=O ACNRTYKOPZDRCO-UHFFFAOYSA-N 0.000 description 1
- 238000011285 therapeutic regimen Methods 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- QNMBSXGYAQZCTN-UHFFFAOYSA-N thiophen-3-ylboronic acid Chemical compound OB(O)C=1C=CSC=1 QNMBSXGYAQZCTN-UHFFFAOYSA-N 0.000 description 1
- 230000001732 thrombotic effect Effects 0.000 description 1
- GZNAASVAJNXPPW-UHFFFAOYSA-M tin(4+) chloride dihydrate Chemical compound O.O.[Cl-].[Sn+4] GZNAASVAJNXPPW-UHFFFAOYSA-M 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- FWPIDFUJEMBDLS-UHFFFAOYSA-L tin(II) chloride dihydrate Substances O.O.Cl[Sn]Cl FWPIDFUJEMBDLS-UHFFFAOYSA-L 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- SEDZOYHHAIAQIW-UHFFFAOYSA-N trimethylsilyl azide Chemical compound C[Si](C)(C)N=[N+]=[N-] SEDZOYHHAIAQIW-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical class CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 210000001186 vagus nerve Anatomy 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
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Classifications
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Landscapes
- Health & Medical Sciences (AREA)
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Applications Claiming Priority (3)
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|---|---|---|---|
| US55595104P | 2004-03-25 | 2004-03-25 | |
| US61603304P | 2004-10-06 | 2004-10-06 | |
| PCT/US2005/010120 WO2005092890A2 (en) | 2004-03-25 | 2005-03-25 | Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, and preparation and uses thereof |
Publications (1)
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|---|---|
| NZ550534A true NZ550534A (en) | 2009-07-31 |
Family
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Family Applications (1)
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| NZ550534A NZ550534A (en) | 2004-03-25 | 2005-03-25 | Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, and preparation and uses thereof |
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| JP (2) | JP4995075B2 (https=) |
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| CN (1) | CN103724343A (https=) |
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| BR (1) | BRPI0508771A (https=) |
| CA (1) | CA2560741C (https=) |
| CR (2) | CR8711A (https=) |
| EC (1) | ECSP066951A (https=) |
| IL (2) | IL178188A (https=) |
| MA (1) | MA28972B1 (https=) |
| MX (1) | MXPA06010852A (https=) |
| NO (1) | NO20064826L (https=) |
| NZ (1) | NZ550534A (https=) |
| RU (1) | RU2417225C2 (https=) |
| SG (1) | SG165199A1 (https=) |
| WO (1) | WO2005092890A2 (https=) |
Families Citing this family (82)
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| DE10164139A1 (de) | 2001-12-27 | 2003-07-10 | Bayer Ag | 2-Heteroarylcarbonsäureamide |
| SE0202598D0 (sv) * | 2002-09-02 | 2002-09-02 | Astrazeneca Ab | Alpha-7 Nicotinic receptor agonists and statins in combination |
| CA2567977A1 (en) * | 2004-04-22 | 2006-01-05 | Memory Pharmaceutical Corporation | Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof |
| CA2591817A1 (en) * | 2004-12-22 | 2006-06-29 | Memory Pharmaceuticals Corporation | Nicotinic alpha-7 receptor ligands and preparation and uses thereof |
| BRPI0619672A2 (pt) * | 2005-11-09 | 2011-10-11 | Memory Pharm Corp | composto, composição farmacêutica, e, uso de um composto |
| CA2654098A1 (en) | 2006-06-13 | 2007-12-21 | Merck Frosst Canada Ltd. | Azacyclopentane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| CL2008000836A1 (es) | 2007-03-26 | 2008-11-07 | Actelion Pharmaceuticals Ltd | Compuestos derivados de tiazolidina, antagonistas del receptor de orexina; composicion farmaceutica que los comprende; y su uso en el tratamiento de neurosis emocional, depresion grave, trastornos psicoticos, alzheimer, parkinson, dolor, entre otras. |
| ES2371514T3 (es) | 2007-07-03 | 2012-01-04 | Actelion Pharmaceuticals Ltd. | Compuestos de 3-aza-biciclo[3.3.0]octano. |
| EP2183246A2 (en) | 2007-07-27 | 2010-05-12 | Actelion Pharmaceuticals Ltd. | 2-aza-bicyclo-[3.3.0]-octane derivatives |
| NZ585298A (en) * | 2007-11-16 | 2012-08-31 | Rigel Pharmaceuticals Inc | Carboxamide, sulfonamide and amine compounds for metabolic disorders |
| MX2010009462A (es) * | 2008-02-29 | 2010-09-24 | Pfizer | Derivados de indazol. |
| WO2009106980A2 (en) * | 2008-02-29 | 2009-09-03 | Pfizer Inc. | Indazole derivatives |
| KR101098335B1 (ko) * | 2008-07-18 | 2011-12-26 | 성균관대학교산학협력단 | 신코나 기재 이작용성 유기 촉매 및 이를 이용한 메소-고리산무수물의 비대칭 고리 열림 반응을 통한 키랄성헤미에스터의 제조방법 |
| ES2407647T3 (es) | 2008-10-13 | 2013-06-13 | F. Hoffmann-La Roche Ag | Método libre de diazonio para obtener un intermediario indazol en la síntesis de amidas de ácido bicíclico 5-(trifluorometoxi)-1H-3-indazol carboxílico |
| LT2889033T (lt) | 2008-11-19 | 2018-07-10 | Forum Pharmaceuticals Inc. | Šizofrenijos negatyvių simptomų gydymas (r)-7-chlor-n-(chinuklidin-3-il)benzo[b]tiofen-2-karboksamidu ir jo farmaciniu požiūriu priimtinomis druskomis |
| CN105037355B (zh) | 2009-08-10 | 2017-06-06 | 萨穆梅德有限公司 | Wnt信号传导途径的吲唑抑制剂及其治疗用途 |
| JO3250B1 (ar) | 2009-09-22 | 2018-09-16 | Novartis Ag | إستعمال منشطات مستقبل نيكوتينيك أسيتيل كولين ألفا 7 |
| US9095596B2 (en) | 2009-10-15 | 2015-08-04 | Southern Research Institute | Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such |
| LT3001903T (lt) | 2009-12-21 | 2018-01-10 | Samumed, Llc | 1h-pirazolo[3,4-b]piridinai ir jų terapinis panaudojimas |
| US20110172428A1 (en) | 2010-01-12 | 2011-07-14 | Shan-Ming Kuang | Methods for the preparation of indazole-3-carboxylic acid and n-(s)-1-azabicyclo[2.2.2]oct-3-yl-1h-indazole-3-carboxamide hydrochloride salt |
| MX2012013197A (es) | 2010-05-12 | 2013-04-03 | Abbvie Inc | Inhibidores de indazol de cinasa. |
| PE20170923A1 (es) * | 2010-05-17 | 2017-07-12 | Forum Pharmaceuticals Inc | Una forma cristalina de clorhidrato de (r)-7-cloro-n-(quinuclidin-3-il)benzo[b]tiofeno-2-carboxamida monohidratado |
| US8242276B2 (en) | 2010-06-30 | 2012-08-14 | Hoffmann-La Roche Inc. | Methods for the preparation of N-(S)-1-azabicyclo[2.2.2]oct-3-yl-1H-indazole-3-carboxamide hydrochloride salt |
| BR112013001939A2 (pt) | 2010-07-26 | 2017-07-11 | Envivo Pharmaceuticals Inc | tratamento de distúrbios cognitivos com determinados agonistas receptores de ácido alfa-7-nicotínico em combinação com inibidres de acetilcolinesterase |
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-
2005
- 2005-03-25 EP EP05745169A patent/EP1735306A2/en not_active Withdrawn
- 2005-03-25 CN CN201310692588.7A patent/CN103724343A/zh active Pending
- 2005-03-25 CA CA2560741A patent/CA2560741C/en not_active Expired - Fee Related
- 2005-03-25 BR BRPI0508771-6A patent/BRPI0508771A/pt not_active IP Right Cessation
- 2005-03-25 MX MXPA06010852A patent/MXPA06010852A/es active IP Right Grant
- 2005-03-25 NZ NZ550534A patent/NZ550534A/en not_active IP Right Cessation
- 2005-03-25 EP EP10013706A patent/EP2336128A1/en not_active Withdrawn
- 2005-03-25 JP JP2007505233A patent/JP4995075B2/ja not_active Expired - Fee Related
- 2005-03-25 AU AU2005227324A patent/AU2005227324A1/en not_active Abandoned
- 2005-03-25 KR KR1020067022085A patent/KR101176670B1/ko not_active Expired - Fee Related
- 2005-03-25 WO PCT/US2005/010120 patent/WO2005092890A2/en not_active Ceased
- 2005-03-25 SG SG200902028-0A patent/SG165199A1/en unknown
- 2005-03-25 RU RU2006137472/04A patent/RU2417225C2/ru not_active IP Right Cessation
- 2005-03-25 US US11/089,533 patent/US20050234095A1/en not_active Abandoned
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2006
- 2006-09-19 IL IL178188A patent/IL178188A/en not_active IP Right Cessation
- 2006-10-20 MA MA29406A patent/MA28972B1/fr unknown
- 2006-10-24 EC EC2006006951A patent/ECSP066951A/es unknown
- 2006-10-24 NO NO20064826A patent/NO20064826L/no not_active Application Discontinuation
- 2006-10-25 CR CR8711A patent/CR8711A/es unknown
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2009
- 2009-12-04 US US12/631,435 patent/US8263619B2/en not_active Expired - Fee Related
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2011
- 2011-06-21 US US13/165,370 patent/US8486937B2/en not_active Expired - Fee Related
- 2011-08-04 JP JP2011171124A patent/JP2011252002A/ja active Pending
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2012
- 2012-01-09 CR CR20120010A patent/CR20120010A/es unknown
- 2012-03-18 IL IL218692A patent/IL218692A0/en unknown
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- 2013-03-15 US US13/838,088 patent/US8691841B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005092890A3 (en) | 2006-02-02 |
| IL218692A0 (en) | 2012-05-31 |
| CR8711A (es) | 2007-08-28 |
| EP2336128A1 (en) | 2011-06-22 |
| AU2005227324A1 (en) | 2005-10-06 |
| CA2560741A1 (en) | 2005-10-06 |
| IL178188A0 (en) | 2006-12-31 |
| RU2417225C2 (ru) | 2011-04-27 |
| NO20064826L (no) | 2006-12-20 |
| IL178188A (en) | 2012-10-31 |
| BRPI0508771A (pt) | 2007-08-14 |
| US20050234095A1 (en) | 2005-10-20 |
| US8263619B2 (en) | 2012-09-11 |
| JP2011252002A (ja) | 2011-12-15 |
| JP2007530590A (ja) | 2007-11-01 |
| US20130217683A1 (en) | 2013-08-22 |
| ECSP066951A (es) | 2006-12-20 |
| US20100105677A1 (en) | 2010-04-29 |
| KR20070015406A (ko) | 2007-02-02 |
| JP4995075B2 (ja) | 2012-08-08 |
| EP1735306A2 (en) | 2006-12-27 |
| MXPA06010852A (es) | 2007-01-16 |
| CA2560741C (en) | 2013-08-06 |
| MA28972B1 (fr) | 2007-11-01 |
| CN103724343A (zh) | 2014-04-16 |
| US20110319407A1 (en) | 2011-12-29 |
| US8486937B2 (en) | 2013-07-16 |
| WO2005092890A2 (en) | 2005-10-06 |
| SG165199A1 (en) | 2010-10-28 |
| KR101176670B1 (ko) | 2012-08-23 |
| US8691841B2 (en) | 2014-04-08 |
| RU2006137472A (ru) | 2008-04-27 |
| CR20120010A (es) | 2012-02-13 |
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