RU92004429A - DERIVATIVES 2- (1-PIPERASINIL) -4-PHENYL-CYCLO-ALKANOPYRIDINE - Google Patents
DERIVATIVES 2- (1-PIPERASINIL) -4-PHENYL-CYCLO-ALKANOPYRIDINEInfo
- Publication number
- RU92004429A RU92004429A RU92004429/04A RU92004429A RU92004429A RU 92004429 A RU92004429 A RU 92004429A RU 92004429/04 A RU92004429/04 A RU 92004429/04A RU 92004429 A RU92004429 A RU 92004429A RU 92004429 A RU92004429 A RU 92004429A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- phenyl
- hydrogen atom
- piperasinil
- alkanopyridine
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000003435 aroyl group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Claims (1)
ЫЫЫ (I)
в которой n =3,4,5,6 или 7; R1 - атом водорода , С1 - С1 0 алкил, С2 - С6 алкенил, С2 - С6 алкинил, С3 - С8 циклоалкил, С3 - С6 циклоалкил - (С1 - С4) алкил, гидрокси - (С2 - С6) алкил, С1 - С3 алкокси - (С2 - С6) алкил, ацилокси - (С2 - С6) алкил, незамещенный или замещенный ароил - (С1 - С6) алкил, незамещенный или замещенный арил, гетероарил, или ацил; R2 и R3 одинаковые или различные, каждый представляет атом водорода, атом галогена, С1 - С6 алкил, С1 - С6 алкокси, трифторметил, или гидрокси; R4, R5 и R6 одинаковые или различные, каждый представляет атом водорода, С1 - С6 алкил, или фенил, или два из R4, R5 и R6 соединяются с образованием одинарной связи или C1 - C3 алкилена; R7 и R8 одинаковые или различные, каждый представляет атом водорода или С1 - С3 алкил; m =2 или 3, и их кислотно-аддитивные соли.The proposed compounds of formula (I):
YYY (I)
in which n = 3,4,5,6 or 7; R 1 is a hydrogen atom, C 1 - C 1 0 alkyl, C 2 - C 6 alkenyl, C 2 - C 6 alkynyl, C 3 - C 8 cycloalkyl, C 3 - C 6 cycloalkyl - (C 1 - C 4 ) alkyl , hydroxy - (C 2 - C 6 ) alkyl, C 1 - C 3 alkoxy - (C 2 - C 6 ) alkyl, acyloxy - (C 2 - C 6 ) alkyl, unsubstituted or substituted aroyl - (C 1 - C 6 a) alkyl, unsubstituted or substituted aryl, heteroaryl, or acyl; R 2 and R 3 are the same or different, each represents a hydrogen atom, a halogen atom, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, trifluoromethyl, or hydroxy; R 4 , R 5 and R 6 are the same or different, each represents a hydrogen atom, C 1 - C 6 alkyl, or phenyl, or two of R 4 , R 5 and R 6 combine to form a single bond or C 1 - C 3 alkylene ; R 7 and R 8 are the same or different, each represents a hydrogen atom or C 1 - C 3 alkyl; m = 2 or 3, and their acid addition salts.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5254489 | 1989-03-03 | ||
JP52544/1989 | 1989-03-03 | ||
JP52544/89 | 1989-03-03 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU4743292 Division |
Publications (2)
Publication Number | Publication Date |
---|---|
RU92004429A true RU92004429A (en) | 1995-08-20 |
RU2075478C1 RU2075478C1 (en) | 1997-03-20 |
Family
ID=12917732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU92004429/04A RU2075478C1 (en) | 1989-03-03 | 1992-11-12 | 2-(4-ethyl-1-piperazinyl)-4-(4-fluorophenyl)-5,6,7,8,9,10-hex- -ahydrocycloocta[b]pyridine or its acid-additive salt |
Country Status (15)
Country | Link |
---|---|
US (1) | US5021421A (en) |
EP (1) | EP0385237B1 (en) |
KR (1) | KR0149649B1 (en) |
AT (1) | ATE107922T1 (en) |
AU (1) | AU623981B2 (en) |
CA (1) | CA2011346C (en) |
DD (1) | DD292909A5 (en) |
DE (1) | DE69010232T2 (en) |
DK (1) | DK0385237T3 (en) |
ES (1) | ES2058630T3 (en) |
FI (1) | FI94413C (en) |
HK (1) | HK1005872A1 (en) |
HU (1) | HU204810B (en) |
NO (1) | NO177095C (en) |
RU (1) | RU2075478C1 (en) |
Families Citing this family (49)
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US5041443A (en) * | 1989-02-21 | 1991-08-20 | Dainippon Pharmaceutical Co., Ltd. | Medicament for treating cerebral insufficiency diseases, novel 2-(1-piperazinyl)-4-phenylcycloalkanopyrimidine derivatives, and process for the production thereof |
ATE199318T1 (en) * | 1993-06-25 | 2001-03-15 | Pola Chem Ind Inc | DOPAMINE INCORPORATION INHIBITORS FOR THE TREATMENT OF PARKINSON'S SYNDROME |
CA2144669A1 (en) | 1994-03-29 | 1995-09-30 | Kozo Akasaka | Biphenyl derivatives |
US6458789B1 (en) | 1999-09-29 | 2002-10-01 | Lion Bioscience Ag | 2-aminopyridine derivatives and combinatorial libraries thereof |
MXPA04007612A (en) * | 2002-02-05 | 2004-11-10 | Novo Nordisk As | Novel aryl- and heteroarylpiperazines. |
AU2006228378A1 (en) | 2005-03-31 | 2006-10-05 | Pfizer Products Inc. | Cyclopentapyridine and tetrahydroquinoline derivatives |
BRPI0613564A2 (en) | 2005-07-04 | 2011-01-18 | Novo Nordisk As | compounds, their uses in the preparation of pharmaceutical compositions and pharmaceutical compositions comprising the same |
CA2653062A1 (en) | 2006-05-23 | 2007-11-29 | Transtech Pharma, Inc. | 6- (4-cyclopropylpiperazin-1-yl) -2 ' -methyl- [3, 4 ' ] -bipyridine and its use as a medicament |
AU2007267197B2 (en) | 2006-05-29 | 2011-12-01 | High Point Pharmaceuticals, Llc | 3- (1, 3-Benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine H3 receptor antagonist |
AU2007255724B2 (en) * | 2006-06-09 | 2012-05-10 | Dainippon Sumitomo Pharma Co., Ltd. | Novel tape preparation |
US20090192143A1 (en) * | 2006-07-14 | 2009-07-30 | Cox Christopher D | Substituted diazepan orexin receptor antagonists |
EP2083811B1 (en) | 2006-11-22 | 2016-10-26 | Clinical Research Associates, LLC | Methods of treating down's syndrome, fragile x syndrome and autism |
EP2014656A3 (en) | 2007-06-11 | 2011-08-24 | High Point Pharmaceuticals, LLC | New heteocyclic h3 antagonists |
CN101530412A (en) * | 2008-03-10 | 2009-09-16 | 北京德众万全医药科技有限公司 | Pharmaceutical composition of blonanserin and preparation method thereof |
CN101531634B (en) * | 2008-03-10 | 2013-09-18 | 北京德众万全医药科技有限公司 | High-purity blonanserin and preparation method thereof |
CN101747273B (en) * | 2008-12-02 | 2012-03-07 | 浙江华海药业股份有限公司 | Preparing method of blonanserin intermediate |
CN101747272B (en) * | 2008-12-02 | 2012-11-28 | 浙江华海药业股份有限公司 | Crystal form B of blonanserin and preparing method thereof |
CN101766626B (en) * | 2008-12-30 | 2012-03-07 | 丽珠医药集团股份有限公司 | Blonanserin-contained oral preparation for treating schizophrenia |
ES2740424T3 (en) | 2009-03-13 | 2020-02-05 | Agios Pharmaceuticals Inc | Methods and compositions for disorders related to cell proliferation |
AU2010266386C1 (en) | 2009-06-29 | 2017-03-09 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
CN101619039B (en) * | 2009-06-30 | 2011-04-13 | 严洁 | 2-(4-ethyl-1-piperazinyl)-4-(4-fluorophenyl)-5,6,7,8,9,10-hexahydro-cycloocta[b]pyridine (blonanserin, Blonanserin) and composition thereof |
EP2525790B1 (en) | 2009-10-21 | 2020-05-27 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
ES2594402T3 (en) | 2009-10-21 | 2016-12-20 | Agios Pharmaceuticals, Inc. | Methods and compositions for disorders related to cell proliferation |
WO2012020301A2 (en) | 2010-08-10 | 2012-02-16 | Lupin Limited | Oral controlled release pharmaceutical compositions of blonanserin |
CN102372673B (en) * | 2010-08-27 | 2014-04-09 | 天津市医药集团技术发展有限公司 | Blonanserin crystallization and preparation method thereof |
CN102093289B (en) * | 2010-10-29 | 2012-12-19 | 常州华生制药有限公司 | New preparation method of Blonanserin intermediate |
CN102030707A (en) * | 2010-11-12 | 2011-04-27 | 深圳万和制药有限公司 | Method for preparing Blonanserin intermediate |
CA2834602C (en) | 2011-05-03 | 2020-10-06 | Agios Pharmaceuticals, Inc. | Pyruvate kinase activators for use in therapy |
CN102827170A (en) * | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | Active treatment compositions and use method thereof |
CN102827073A (en) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | Therapeutically active compositions and application methods thereof |
EP2800743B1 (en) | 2012-01-06 | 2018-04-04 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
CA2888360A1 (en) | 2012-10-15 | 2014-04-24 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
WO2015003360A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
WO2015006591A1 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | 2,4- or 4,6-diaminopyrimidine compounds as idh2 mutants inhibitors for the treatment of cancer |
WO2015003355A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
CN112159391A (en) | 2014-03-14 | 2021-01-01 | 阿吉奥斯制药公司 | Pharmaceutical compositions of therapeutically active compounds |
CN104311487B (en) * | 2014-09-22 | 2016-08-24 | 江苏正大丰海制药有限公司 | A kind of blonanserin crystal formation and preparation method thereof |
SI3307271T1 (en) | 2015-06-11 | 2023-11-30 | Agios Pharmaceuticals, Inc. | Methods of using pyruvate kinase activators |
IL258684B2 (en) | 2015-10-15 | 2023-04-01 | Agios Pharmaceuticals Inc | Combination therapy comprising isocitrate dehydrogenase 1 (idh1) inhibitor for use in treating acute myelogenous leukemia (aml) characterized by the presence of a mutant allele of idh1 |
MX2018004586A (en) | 2015-10-15 | 2018-08-16 | Agios Pharmaceuticals Inc | Combination therapy for treating malignancies. |
KR20190028109A (en) | 2017-09-08 | 2019-03-18 | 연성정밀화학(주) | Sustained Release Formulation Comprising Blonanserin |
CN110575438A (en) * | 2018-06-07 | 2019-12-17 | 湖南省湘中制药有限公司 | preparation and application of blonanserin solid dispersion |
US10980788B2 (en) | 2018-06-08 | 2021-04-20 | Agios Pharmaceuticals, Inc. | Therapy for treating malignancies |
CA3132953A1 (en) | 2019-03-13 | 2020-09-17 | Otsuka Pharmaceutical Co., Ltd. | Method for introducing deuterated lower alkyl into amine moiety of compound containing secondary amine |
CN113698346A (en) * | 2020-05-22 | 2021-11-26 | 湖南省湘中制药有限公司 | Preparation method of impurity B in blonanserin process |
CN113698347A (en) * | 2020-05-22 | 2021-11-26 | 湖南省湘中制药有限公司 | Preparation method of impurity F in blonanserin process |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS54128588A (en) * | 1978-03-29 | 1979-10-05 | Dainippon Pharmaceut Co Ltd | Antidepressive drugs consisting mainly of 2-(1-piperazinyl)- 4-phenylquinoline |
DE3124673A1 (en) * | 1981-06-24 | 1983-01-13 | Bayer Ag, 5090 Leverkusen | SUBSITUATED 2-AMINO-PYRIDINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, THEIR USE IN MEDICINAL PRODUCTS AND THE PRODUCTION THEREOF |
FR2602771B1 (en) * | 1986-08-12 | 1988-11-04 | Rhone Poulenc Sante | NOVEL BENZYL-4 PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
-
1990
- 1990-02-20 ES ES90103244T patent/ES2058630T3/en not_active Expired - Lifetime
- 1990-02-20 US US07/481,183 patent/US5021421A/en not_active Expired - Lifetime
- 1990-02-20 DK DK90103244.1T patent/DK0385237T3/en active
- 1990-02-20 DE DE69010232T patent/DE69010232T2/en not_active Expired - Lifetime
- 1990-02-20 EP EP90103244A patent/EP0385237B1/en not_active Expired - Lifetime
- 1990-02-20 AT AT90103244T patent/ATE107922T1/en not_active IP Right Cessation
- 1990-03-01 FI FI901030A patent/FI94413C/en active IP Right Grant
- 1990-03-01 NO NO900991A patent/NO177095C/en not_active IP Right Cessation
- 1990-03-01 AU AU50604/90A patent/AU623981B2/en not_active Expired
- 1990-03-01 DD DD90338287A patent/DD292909A5/en unknown
- 1990-03-02 HU HU901275A patent/HU204810B/en unknown
- 1990-03-02 CA CA002011346A patent/CA2011346C/en not_active Expired - Lifetime
- 1990-03-03 KR KR1019900002874A patent/KR0149649B1/en not_active IP Right Cessation
-
1992
- 1992-11-12 RU RU92004429/04A patent/RU2075478C1/en active
-
1998
- 1998-06-05 HK HK98105004A patent/HK1005872A1/en not_active IP Right Cessation
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