KR890701542A - 페닐카르복시산 유도체 및 그 염 - Google Patents
페닐카르복시산 유도체 및 그 염Info
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- KR890701542A KR890701542A KR1019890701126A KR890701126A KR890701542A KR 890701542 A KR890701542 A KR 890701542A KR 1019890701126 A KR1019890701126 A KR 1019890701126A KR 890701126 A KR890701126 A KR 890701126A KR 890701542 A KR890701542 A KR 890701542A
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- group
- phenyl
- halogen atom
- salt
- alkylene
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- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
- C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
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- C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
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- C07C217/86—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical containing six-membered aromatic rings
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (24)
- 일반식[상기식에서, R1및R2는 각각 수소원자, 할로겐원자, C1-C6알킬기, 할로겐원자를 갖는 C1-C6알킬기, C1-C6알카노일기, C3-C8의 시클로알킬기, 니트로기, 아미노기, -O-D-R5(여기서, D는 C1-C6알킬렌기, R5는 수소원자, 아미노기, 모르폴리노기, 카르복시기, 프탈이미도기, 페닐기 또는를 나타냄), 페닐고리상에 치환기로서 할로겐원자 또는 C1-C6알킬기를 선택적으로 갖 페녹시기, 페닐고리상에 치환기로서 C1-C4알킬렌디옥시기를 선택적으로 갖는 페닐 C1-C6알킬아미노기, 또는 카르복시기를 갖는 C2-C6알케닐기를 나타내거나, 또는 양작용기기 인접 탄소원자에 결합한 C1-C4알킬렌 디옥시기를 나타낸다. R3은 수소원자, -E-R5(여기서, E는 C1-C6알킬렌기를, R6은 수소원자, 카르복시기, 시아노기, 수산기, 페닐 C1-C6알콕시기, 할로겐원자를 갖는 페닐기, 또는 할로겐원자를 갖는 페닐 카르바모일기를 나타냄), -CO-G-R7(여기서, G는 C1-C6알킬렌기를, R7은 수소원자, 카르복시기 또는 할로겐원자를 갖는 페닐카르바 모일기를 나타냄), 페닐고리상에 치환기로서 C1-C4-알킬렌디옥시기, 할로겐원자 또는 C1-C6알킬기를 선택적으로 갖는 벤조일기, C2-C6알케닐기, 카르바모일기, 페닐기, 또는 할로겐원자를 갖는 페닐기를 나타낸다. R4는 수소원자 또는 C1-C6알킬기를 나타낸다. A는 C1-C6알킬렌기, CC4-C8시클로 알킬기가 축합한 C2-C6알킬렌기, 또는 C2-C6알케닐렌기를 나타낸다. B는 C1-C6알킬렌기 또는C2-C6알케닐렌기를 나타낸다. 1은 0또는 1을 나타낸다]로 표시되는 페닐카르복시산 유도체 및 그 염.
- 제 1 항에 있어서, A가 C1-C6알킬렌기인 페닐카르복시산 유도체 및 그 염.
- 제 1 항에 있어서, A가 C3-C8시클로 알킬고리가 축합한 C2-C6알킬렌기 또는 C2-C6알케닐렌기인 페닐카르복시산 유도체 및 그 염.
- 제 2 항에 있어서, R3이 수소원자 또는 -E-R5(여기서 E는 C1-C6알킬렌기, R6은 수소원자임)인 페닐카르복시산 유도체 및 그 염.
- 제 2 항에 있어서, R3이 -E-R6(여기서, E는 C1-C6알킬렌기, R6은 카르복시기, 시아노기, 수산기, 페닐 C1-C6알콕시기, 할로겐원자를 갖는 페닐기, 또는 할로겐원자를 갖는 페닐카르바모일기를 나타냄), -CO-G-R7(여기서 G는 C1-C6알킬렌기를, R7은 수소원자, 카르복시기, 또는 할로겐원자를 갖는 페닐카르바 모일기를 나타냄), 페닐고리상에 치환기로써, C1-C4알킬렌디옥시기, 할로겐원자 또는 C1-C6알킬기를 선택적으로 갖는 벤조일기, 카르바모일기, 페닐기, 또는 할로겐원자를 갖는 페닐기인 페닐카르복시산 유도체 및 그 염.
- 제 4 항에 있어서, R1이 수소원자, R2가 수소원자, 할로겐원자, C1-C6알킬기, 할로겐원자를 갖는 C1-C6알킬기, C1-C6알카노일기, C3-C8시클로 알킬기, 니트로기, 아미노기, -C-D-R5(여기서, D는 C1-C6알킬렌기, R5는 수소원자, 아미노기, 모르폴리노기, 카르복시기, 프탈이미도기, 페닐기 또는를 나타냄), 페닐고리상에 치환기로서 할로겐원자 또는 C1-C6알킬기를 선택적으로 갖는페녹시기, 페닐고리상에 치환기로서 C1-C4알킬렌디옥시기를 선택적으로 갖는 페닐 C1-C6알킬아미노기, 또는 카르복시기를 갖는 C2-C6알케닐기를 나타내는 페닐 카르복시산 유도체 및 그 염.
- 제 4 항에 있어서, R1및 R2가 각각 할로겐원자, C1-C4알킬기, 할로겐원자를 갖는C1-C6알킬기, C1-C6알카노일기, C3-C8시클로알킬기, 니트로기, 아미노기, -O-D-R5(여기서, D는 C1-C6알킬렌기를, R5은 수소원자, 아미노기, 모르폴리노기, 카르복시기, 프탈이미도기, 페닐기, 또는기를 나타냄), 페닐고리상에 치환기로서 할로겐원자 또는 C1-C6알킬기를 선택적으로 갖는 페녹시기, 페닐고리상에 치환기로서 C1-C4알킬렌 디옥시기를 선택적으로 갖는 페닐 C1-C6알킬아미노기 또는 카르복시기를 갖는 C2-C6알케닐기를 나타내거나, 또는 양 작용기가 인접 탄소원자에 결합한 C1-C4알킬렌 디옥시기를 나타내는 페닐카르복시산 유도체 및 그 염.
- 제 6 항에 있어서, 1이 0인 페닐카르복시산 유도체 및 그 염.
- 제 8 항에 있어서, R2가 할로겐원자 또는 C1-C6알킬기인 페닐카르복시산 유도체 및 그 염.
- 제 8 항에 있어서, R2가 할로겐원자를 갖는 C1-C6알킬기, C1-C6알카노일기, C3-C6시클로알킬기,니트로기, 아미노기, -O-D- R5(여기서, D는 C1-C6알킬렌기를 R5는 수소원자, 아미노기, 모르폴리노기,카르복시기 프탈이미노기, 페닐기 또는기를 나타냄), 페닐고리상에 치환기로서 할로겐원자 또는 C1-C6알킬기를 선택적으로 갖는 페녹시기, 페놀고리상에 치환기로서 C1-C4알킬렌디옥시기를 선택적으로 갖는 페닐 C1-C6알킬아미노기, 떠는 카르복시기를 갖는 C2-C6알케닐기를 나타내는 페닐카르복시산 유도체 및 그 염.
- 제 9 항에 있어서, R4가 수소원자인 페닐카르복시산 유도체 및 그 염.
- 제 9 항에 있어서, R4가 C1-C6알킬기인 페닐카르복시산 유도체 및 그 염.
- 제 11 항에 있어서, R3이 수소원자인 페닐카르복시산 유도체 및 그 염.
- 제 11 항에 있어서, R3이 -E-R6(여기서, E는 C1-C6알킬렌기를, R6은 수소원자를 나타냄)인 페닐카르복시산 유도체 및 그 염.
- 제 13 항에 있어서, R2이 할로겐원자인 페닐카르복시산 및 그 염.
- 제 13 항에 있어서, R2이 C1-C6알킬기인 페닐카르복시산 및 그 염.
- 제 6 항에 있어서, I 이 1이고, B가 C1-C6알케닐렌기인 페닐카르복시산 및 그 염.
- 제 17 항에 있어서, R2가 할로겐원자 또는 C1-C6알킬기인 페닐카르복시산 및 그 염.
- 제 6 항에 있어서, 1이 1이고, B가 C1-C6알케닐렌기인 페닐카르복시산 및 그 염.
- 제 19항에 있어서, R2가 할로겐원자 또는 C1-C6알킬기인 페닐카르복시산 및 그 염.
- 제 1 항에 있어서, 다음 화합물.4-[3-[N-(4-클로로페닐)아미노]프로폭시]벤조산.4-[3-[N-(4-클로로페닐)아미노]부톡시]벤조산.4-[3-[N-(4-클로로페닐)아미노]프로폭시]벤조산 염산염.4-[3-[N-(4-클로로페닐)아미노]프로폭시]-α-메틸신남산.4-[3-[N-(4-클로로페닐)-N-메틸아미노]프로폭시]벤조산.4-[3-[N-(4-클로로페닐)-N-이소프로필아미노]프로폭시]벤조산 및 4-[3-[N-(4-클로로페닐)아미노]-2-메틸프로폭시]벤조산으로부터 선택된 페닐카르복시산 유도체 및 그 염.
- 제 1 항에 있어서, 다음 공정,a) 일반식(상기식에서, A, B, R4및 1은 특허청구의 범위 제 1 항에 기재한 바와 같으며, X는 할로겐원자, 치환기를 선택적으로 갖는 C1-C6알칸술포닐옥시기, 또는 치환기를 선택적으로 갖는 아릴술포닐 옥시기를 나타냄)로 표시되는 화합물을 염기성 화합물의 존재하에, 일반식(상기식에서, R1, R2및 R3은 특허청구의 범위 제 1 항에 기재한 바와 같음)로 표시되는 화합물과 반응시켜, b) 일반식(상기식에서, B, R4및 1 은 특허청구의 범위 제 1 항에 기재한 바와 같으며, A1은 주사슬의 탄소수가 1개 적은점을 제외하고는 특허청구의 범위 제 1항에 정의한 A와 같음)로 표시되는 화합물을, 일반식(상기식에서, R1및 R2는 특허청구의 범위 제 1 항에 기재한 바와 같음)로 표시되는 화합물과 반응시켜, 일반식,(상기식에서, R1, R2, B, R4및 I은 특허청구의 범위 제1항에 정의한 바와 같으며, A1는 앞서 기술한 바와 같음)로 표시되는 화합물 얻고,C) 일반식(상기식에서, R1, R2, A,B 및 1은 특허청구의 범위 제 1 항에 기재한 바와 같으며, R4a는 C1-C6알킬기를 나타냄)으로 표시되는 화합물을 얻고, 일반식 R3aOH[상기식에서, R3a는 -CO-G-R7기(여기서 G 및 R7은 특허청구의 범위 제 1 항에 정의한 바와 같음), 또는 페닐고리상에 치환기로서 C1-C4알킬렌디옥시기, 할로겐원자 또는 C1-C6알킬기를 갖는 벤조일기를 나타냄]로 표시되는 카르복시기가 활성화된 화합물 또는 그 카르복시기가 활성화된 화합물을 반응시켜,일반식(상기식에서, R1, R2, A, B 및 1은 특허청구의 범위 제 1 항에 정의한 바와 같으며, R3a및R4a는 앞서 기술한 바와 같음)로 표시되는 화합물을 얻고,d) 일반식(1b)의 화합물에, 일반식R3b-X[상기식에서, X는 앞서 기술한 바와 같으며, R3a-E-R6(여기서, E 및 R6은 특허청구의 범위 제 1 항에 기재한 바와 같음) C2-C6알케닐기 또는 할로겐원자를 갖는 페닐기를 나타냄]로 표시되는 화합물을 반응시켜,일반식(상기식에서, R1, R2, A, B 및 1은 특허청구의 범위 제 1 항에 정의한 바와 같으며, 및 R4a는 앞서 기술한 바와 같음)로 표시되는 화합물을 얻고,e) 일반식(상기식에서, R1, R2, R3및 A는 특허청구의 범위 제 1 항에 정의한 바와 같고, X는 앞서 기술한 바와 같음)로 표시되는 화합물을, 일반식(상기식에서, B,R4및 1은 특허청구의 범위 제 1 항에 정의한 바와 같음)으로 표시되는 화합물과 반응시키고, 또는f)일반식(1e)의 화합물을 탈 에스테르화 반응하여, 일반식(상기식에서, R1, R2, R3, A, B 및 1은 특허청구의 범위 제 1 항에 정의한 바와 같음)으로 표시되는 화합물로 유도하는, 것으로된 페닐카르복시산 유도체 및 그 염의 제조방법.
- 제 1 항에 기재한 화합물 또는 그 염을 유효성분으로 함유하는 혈증지질저하용 조성물.
- 제 1 항에 기재한 화합물 또는 그 염의 유효량을 환자에게 투여하는 고 지질혈증의 치료방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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JP???62-264744? | 1987-10-20 | ||
JP62-264744 | 1987-10-20 | ||
JP26474487 | 1987-10-20 | ||
JP63-45339 | 1988-02-26 | ||
JP???63-45339? | 1988-02-26 | ||
JP4533988 | 1988-02-26 | ||
PCT/JP1988/001065 WO1989003819A1 (en) | 1987-10-20 | 1988-10-20 | Phenylcarboxylic acid derivatives |
Publications (2)
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KR890701542A true KR890701542A (ko) | 1989-12-20 |
KR970006890B1 KR970006890B1 (ko) | 1997-04-30 |
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KR1019890701126A KR970006890B1 (ko) | 1987-10-20 | 1988-10-20 | 페닐카르복시산 유도체 및 그 염 |
Country Status (5)
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US (1) | US4999378A (ko) |
EP (1) | EP0394440B1 (ko) |
KR (1) | KR970006890B1 (ko) |
DE (1) | DE3889545T2 (ko) |
WO (1) | WO1989003819A1 (ko) |
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US5504105A (en) * | 1990-03-23 | 1996-04-02 | Chinoin Pharmaceutical And Chemical Works Co. Ltd. | Pharmaceutical compositions containing ipriflavone, process for the preparation thereof and relative therapeutic use |
DE4114733A1 (de) * | 1991-05-06 | 1992-11-12 | Huels Chemische Werke Ag | Verfahren zur herstellung von substituierten malonesteraniliden und malonsaeure-monoaniliden |
GB9207855D0 (en) * | 1992-04-09 | 1992-05-27 | Ici Plc | Therapeutic amines |
KR0146931B1 (ko) * | 1992-04-30 | 1998-08-17 | 고바야시 유끼오 | 옥사졸리딘 유도체 및 그의 약학적으로 허용가능한 염 |
US5731436A (en) * | 1994-08-31 | 1998-03-24 | Eli Lilly And Company | Process for preparing benzoic acid derivative intermediates and benzothiophene pharmaceutical agents |
US5741926A (en) * | 1997-02-12 | 1998-04-21 | Shaman Pharmaceuticals, Inc. | Aniline derivatives having antihyperglycemic activity |
TWI311133B (en) | 2001-04-20 | 2009-06-21 | Eisai R&D Man Co Ltd | Carboxylic acid derivativeand the salt thereof |
EP1452521A4 (en) | 2001-08-17 | 2007-03-14 | Eisai R&D Man Co Ltd | CYCLIC COMPOUND AND AGONIST OF PPAR RECEPTOR |
JP2005521721A (ja) | 2002-03-27 | 2005-07-21 | スミスクライン・ビーチャム・コーポレイション | 酸およびエステル化合物ならびにその使用方法 |
AU2003226094A1 (en) | 2002-03-27 | 2003-10-13 | Smithkline Beecham Corporation | Compounds and methods |
US7247748B2 (en) | 2002-03-27 | 2007-07-24 | Smithkline Corporation | Amide compounds and methods of using the same |
EP1490047B1 (en) | 2002-03-27 | 2009-12-30 | SmithKline Beecham Corporation | Certain pharmaceutically useful substituted aminoalkyl heterocycles |
JP2005533007A (ja) * | 2002-03-27 | 2005-11-04 | スミスクライン・ビーチャム・コーポレイション | Lxr調節因子を用いる治療方法 |
EP1517882A1 (en) * | 2002-06-19 | 2005-03-30 | Eli Lilly And Company | Amide linker peroxisome proliferator activated receptor modulators |
EP1611088B1 (en) * | 2003-04-07 | 2009-06-17 | Pharmacyclics, Inc. | Hydroxamates as therapeutic agents |
RU2446796C2 (ru) | 2006-12-26 | 2012-04-10 | Фармасайкликс, Инк. | Способ использования ингибиторов гистондеацетилазы и мониторинга биомаркеров в комбинированной терапии |
CA2677000A1 (en) | 2007-01-30 | 2008-08-07 | Pharmacyclics, Inc. | Methods for determining cancer resistance to histone deacetylase inhibitors |
US20100274022A1 (en) * | 2007-04-26 | 2010-10-28 | Pharmafrontier Co., Ltd. | G protein-coupled receptor inhibitor and pharmaceutical product |
US8318781B2 (en) | 2007-04-26 | 2012-11-27 | Japan Science And Technology Agency | G-protein-conjugated receptor agonist |
US8603521B2 (en) | 2009-04-17 | 2013-12-10 | Pharmacyclics, Inc. | Formulations of histone deacetylase inhibitor and uses thereof |
MX365393B (es) | 2011-09-13 | 2019-05-31 | Pharmacyclics Llc | Formulaciones de inhibidor de histona deacetilasa en combinación con bendamustina y usos de las mismas. |
TWI649081B (zh) | 2013-08-02 | 2019-02-01 | 製藥公司 | 治療固態腫瘤之方法 |
CN105541648B (zh) * | 2015-12-11 | 2018-03-06 | 苏州大学 | 一种超临界co2用蒽醌型活性分散染料前驱体的合成方法 |
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US2642432A (en) * | 1951-09-05 | 1953-06-16 | Sterling Drug Inc | Lower alkyl 4-substituted-2-(tertiary-aminoalkoxy) benzoates and their preparation |
US3738999A (en) * | 1970-05-28 | 1973-06-12 | Squibb & Sons Inc | 2,3,4,5-tetrahydro-2-phenyl-1,4-benzothiazepine, hydrochloride |
US3857873A (en) * | 1974-02-11 | 1974-12-31 | Warner Lambert Co | 3-hydroxy-5-(3-(substituted-amino)-2-hydroxypropoxy)-benzyl alcohols |
US4144351A (en) * | 1974-12-20 | 1979-03-13 | Klinge Pharma Gmbh & Co. | Substituted propanol-(2) derivatives and their preparation and use as hypolipemic drugs |
US4350822A (en) * | 1975-03-12 | 1982-09-21 | American Cyanamid Company | Antilipidemicpara-[aryl(alkyl or alkenyl)amino]benzoic acid derivatives |
US4094991A (en) * | 1975-06-17 | 1978-06-13 | Nippon Shinyaku Co., Ltd. | Substituted n-(carboxymethyl)-3-aminopropan-2-ol derivatives |
US4260816A (en) * | 1975-12-09 | 1981-04-07 | American Cyanamid Company | Naphthyloxyalkylaminobenzoic acids, salts and esters thereof |
GB1551416A (en) * | 1976-08-27 | 1979-08-30 | Beecham Group Ltd | Long chain dioxy hypolipidaemics |
DE3718765A1 (de) * | 1986-06-11 | 1987-12-17 | Nippon Shinyaku Co Ltd | Benzoesaeurederivate |
-
1988
- 1988-10-20 EP EP88909127A patent/EP0394440B1/en not_active Expired - Lifetime
- 1988-10-20 KR KR1019890701126A patent/KR970006890B1/ko not_active IP Right Cessation
- 1988-10-20 WO PCT/JP1988/001065 patent/WO1989003819A1/ja active IP Right Grant
- 1988-10-20 DE DE3889545T patent/DE3889545T2/de not_active Expired - Fee Related
-
1989
- 1989-06-20 US US07/372,336 patent/US4999378A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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EP0394440B1 (en) | 1994-05-11 |
EP0394440A1 (en) | 1990-10-31 |
US4999378A (en) | 1991-03-12 |
EP0394440A4 (en) | 1990-12-27 |
WO1989003819A1 (en) | 1989-05-05 |
DE3889545D1 (en) | 1994-06-16 |
KR970006890B1 (ko) | 1997-04-30 |
DE3889545T2 (de) | 1994-10-13 |
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