KR900018049A - 중추신경계 활성을 갖는 아릴- 및 헤테로아릴 피페라지닐 카복스아미드 - Google Patents
중추신경계 활성을 갖는 아릴- 및 헤테로아릴 피페라지닐 카복스아미드 Download PDFInfo
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Abstract
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Description
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Claims (34)
- 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
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- 상기식에서, R1은 1-아마만틸, 3-메틸-1-아다만틸, 3-노르아다만틸, 비치환되거나 저급 알킬, 저급 알콕시 및 할로중에서 선택된 치환체에 의해 치환된 2-인돌릴, 3-인돌리, 2-벤조푸라닐 또는 3-벤조푸라닐이고;R2는 비치환되거나 저급 알킬, 저급 알콕시, 트리플루오로메틸 및 할로중에서 선택된 치환체에 의해 치환된 페닐, 벤질, 피리디닐, 피리미디닐 또는 피라지닐이고;R3는 수소 또는 탄소수 1 내지 3의 저급 알킬이고;n은 0또는 1의 정수이고;m은 2 내지 5의 정수이다.
- 제1항에 있어서, R1은 1-아마만틸, 3-메틸-1-아다만틸, 2-인돌릴, 2-벤조푸라닐;R2가 비치환되거나 메톡시 클로로중에서 선택된치환체에 의해 치환된 페닐, 또는 피리디닐 또는 2-피리미디닐이고;R3는 수소이고:n은 0 또는 1의 정수이고;m은 2 또는 3의 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(2-메톡시페닐)-1-피페라지닐]프로필]트리사이틀로[3,3,1,13,7]]데칸-1-카복스아미트인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-피리미딜)-1-피페라지닐]에틸]트리사이틀로[3,3,1,13,7]데칸-1-카복스아미트인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-메톡시페닐)-1-피페라지닐]에틸]트리사이틀로[3,3,1,13,7]]데칸-1-카복스아미트인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(3-클로로페닐)-1-피페라지닐]에틸]트리사이틀로[3,3,1,13,7]]데칸-1-카복스아미트인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-피라미딜)-1-피페라지닐]에틸]벤조푸란-3-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(2-피라미딜)-1-피페라지닐]프로필]벤조푸란-3-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(2-피라미딜)-1-피페라지닐]프로필]-(1H)인돌-3-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(3-클로로페닐)-1-피페라지닐]프로필]트리사이틀로[3,3,1,13,7]]데칸-1-카복스아미트인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-피리미딜)-1-피페라지닐]에틸]-3-메틸트리사이틀로[3,3,1,13,7]]데칸-1-아세트산 카복스 아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(2-피리미딜)-1-피페라지닐]프로필]트리사이틀로[3,3,1,13,7]]데칸-1-카복스아미트인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(3-클로로페닐)-1-피페라지닐]에틸]-3-메틸트리사이틀로[3,3,1,13,7]]데칸-1-아세트산 카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-메톡시페닐)-1-피페라지닐]에틸]-3-메틸트리사이틀로[3,3,1,13,7]]데칸-1-아세트산 카복스 아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-피리미딜)-1-피페라지닐]에틸]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(2-메톡시페닐)-1-피페라지닐]에틸]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(3-클로로페닐)-1-피페라지닐]에틸]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[2-[4-(3-(트리플루오로메틸)페닐)]-1-피페라지닐]에틸]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(2-피리미딜)-1-피페라지닐]프로필]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(2-메톡시페닐)-1-피페라지닐]프로필]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- 제2항에 있어서, N-[3-[4-(3-클로로페닐)-1-피페라지닐]프로필]헥사하이드로-2,5-메타노펜탈렌-3a(1H)-카복스아미드인 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염.
- a) 일반식(Ⅲ)의 화합물을, 일반식(Ⅱa)로 표시되는 그룹 R5를 함유하는 아실화제로 아실화시켜 일반식(Ⅰ)의 화합물을 수득하거나; b) 일반식(Ⅳ)의사이클릭 아민 또는 이의 염을 일반식(Ⅴa)의 화합물과 반응시켜 일반식(Ⅴ)로 표시되는 치환된 알킬그룹을 도입하여 알킬화시키거나; c) 일반식(Ⅳ)의 사이클릭 아민 또는 이의 염을 일반식(Ⅵ)의 알제히드를 사용하여 환원적 알킬화 시키거나; d) 일반식(Ⅰ)의 화합물을 산을 가하여 그의 산부가염으로 전환시키거나, 일반식(Ⅰ)의 화합물의 산 부가염을 중화시켜 일반식(Ⅰ)의 화합물을 생성시키는 단계중 어느 한 단계를 포함한 특징으로 하여, 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염을 제조하는 방법.
-
- 상기식에서, R1은 1-아마만틸, 3-메틸-1-아다만틸, 3-노르아다만틸, 비치환되거나 또는 탄소수 1 내지 6의 저급알킬, 탄소수 1 내지 6의 저급 알콕시 및 할로로 이루어진 그룹으로부터 선택된 치환체에 의해 치환된 2-인돌릴, 3-인돌리, 2-벤조푸라닐 또는 3-벤조푸라닐이고; R2는 비치환되거나 또는 탄소수 1 내지 6의 저급 알킬, 탄소수 1 내지 6의 저급 알콕시, 트리플루오로메틸 및 할로로이루어진 그룹으로부터 선택된 치환체에 의해 치환된 페닐, 벤질, 피리디닐, 피리미디닐 또는 피라지닐이고; R3는 수소 또는 탄소수 1 내지 3의 저급 알킬이고; R4는 일반식(Ⅴ)의 그룹이고; Y는 클로로 또는 브로모, 또는 아릴-또는 알킬-설포닐옥시와 같은이탈그룹이고; n은 0또는 1의 정수이고; m은 2 내지 5의 정수이다.
- 일반식(Ⅱ)의 카르복실산 할라이드를 일반식(Ⅲ)의 아미노알킬 피페라진과 반응시킴을 특징으로 하여, 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염을 제조하는 방법.
-
-
- 상기식에서, R1은 1-아마만틸, 3-메틸-1-아다만틸, 3-노르아다만틸, 비치환되거나 또는 탄소수 1 내지 6의 저급알킬, 탄소수 1 내지 6의 저급 알콕시 및 할로로 이루어진 그룹으로부터 선택된 치환체에 의해 치환된 2-인돌릴, 3-인돌리, 2-벤조푸라닐 또는 3-벤조푸라닐이고; R2는 비치환되거나 또는 탄소수 1 내지 6의 저급 알킬, 탄소수 1 내지 6의 저급 알콕시, 트리플루오로메틸 및 할로로이루어진 그룹으로부터 선택된 치환체에 의해 치환된 페닐, 벤질, 피리디닐, 피리미디닐 또는 피라지닐이고; R3는 수소 또는 탄소수 1 내지 3의 저급 알킬이고; n은 0또는 1의 정수이고; m은 2 내지 5의 정수이고;m은 2 내지 5의 정수고; X는 할라이드이다.
- 제1항에서 청구된 일반식(Ⅰ)의 피페라진 유효량을 불안증 또는 우울증 환자에게 투여함을 특징으로 하여 불안증 또는 우울증을 치료하는 방법.
- 제1항에서 청구된 일반식(Ⅰ)의 피페라진 유효량을 정신병 또는 불안증 환자에게 투여함을 특징으로 하는 정신병 또는 불안증을 치료하는 방법.
- 제1항에서 청구된 일반식(Ⅰ)의 화합물 또는 약제학적으로 허용되는 이의 염, 및 약제학적으로 허용되는 담체를 함유함을 특징으로 하는 약제학적 조성물.
- ※ 참고사항 : 최초출원내용에 의하여 공개하는 것임.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19789088A | 1988-05-24 | 1988-05-24 | |
US197,890 | 1988-05-24 | ||
US197890 | 1988-05-24 | ||
US29746089A | 1989-01-13 | 1989-01-13 | |
US297,460 | 1989-01-13 | ||
US297460 | 1989-01-13 |
Publications (2)
Publication Number | Publication Date |
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KR900018049A true KR900018049A (ko) | 1990-12-20 |
KR0128345B1 KR0128345B1 (ko) | 1998-04-03 |
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KR1019890006857A KR0128345B1 (ko) | 1988-05-24 | 1989-05-23 | 중추 신경계 활성을 갖는 아릴-및 헤테로아릴 피페라지닐 카복스아미드, 이의 제조방법 및 이를 함유하는 약제학적 조성물 |
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EP (1) | EP0343961B1 (ko) |
JP (1) | JP2711284B2 (ko) |
KR (1) | KR0128345B1 (ko) |
AT (1) | ATE132862T1 (ko) |
AU (1) | AU628341B2 (ko) |
CA (1) | CA1340113C (ko) |
DE (1) | DE68925385T2 (ko) |
DK (1) | DK168665B1 (ko) |
ES (1) | ES2081302T3 (ko) |
FI (1) | FI94130C (ko) |
GB (1) | GB2218988B (ko) |
GR (1) | GR3019217T3 (ko) |
HU (1) | HU205923B (ko) |
IE (1) | IE64151B1 (ko) |
IL (1) | IL90279A (ko) |
NZ (1) | NZ229225A (ko) |
PT (1) | PT90633B (ko) |
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US5143923B1 (en) * | 1991-04-29 | 1993-11-02 | Hoechst-Roussel Pharmaceuticals Incorporated | Benzoisothiazole-and benzisoxazole-3-carboxamides |
JP3136206B2 (ja) * | 1991-10-22 | 2001-02-19 | 中外製薬株式会社 | ベンゾジオキサン誘導体 |
GB9200293D0 (en) * | 1992-01-08 | 1992-02-26 | Wyeth John & Brother Ltd | Piperazine derivatives |
US5474994A (en) * | 1992-05-26 | 1995-12-12 | Recordati S.A., Chemical And Pharmaceutical Company | Bicyclic heterocyclic derivatives having α1 -adrenergic and 5HT1A |
IT1254469B (it) * | 1992-02-25 | 1995-09-25 | Recordati Chem Pharm | Derivati benzopiranici e benzotiopiranici |
US5605896A (en) * | 1992-02-25 | 1997-02-25 | Recordati S.A., Chemical And Pharmaceutical Company | Bicyclic heterocyclic derivatives having α1 adrenergic and 5HT1A activities |
ES2046107B1 (es) * | 1992-03-05 | 1994-08-01 | Espanola Prod Quimicos | Procedimiento de preparacion de nuevos derivados de la difenilmetilpiperacina. |
SE9201138D0 (sv) * | 1992-04-09 | 1992-04-09 | Astra Ab | Novel phthalimidoalkylpiperazines |
IT1258315B (it) * | 1992-04-10 | 1996-02-22 | Recordati Chem Pharm | Derivati del flavone |
DE69426771T2 (de) * | 1993-06-25 | 2001-06-13 | Pola Chemical Industries, Inc. | Dopaminreinkorporationshemmer zur behandlung des parkinsonschen syndroms |
US5395835A (en) * | 1994-03-24 | 1995-03-07 | Warner-Lambert Company | Naphthalamides as central nervous system agents |
US5574028A (en) * | 1994-10-31 | 1996-11-12 | Eli Lilly And Company | Method for treating anxiety |
US5889006A (en) * | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
US5519025A (en) * | 1995-04-10 | 1996-05-21 | American Home Products Corporation | 4-indolylpiperazinyl derivatives |
US5486518A (en) * | 1995-04-10 | 1996-01-23 | American Home Products Corporation | 4-indolylpiperazinyl derivatives |
IL126411A0 (en) * | 1996-04-05 | 1999-05-09 | Sod Conseils Rech Applic | Alpha1-Adrenergic receptor antagonists |
US5860391A (en) * | 1996-08-06 | 1999-01-19 | First Brands Corporation | Absorbents containing activated carbons |
US6339087B1 (en) | 1997-08-18 | 2002-01-15 | Syntex (U.S.A.) Llc | Cyclic amine derivatives-CCR-3 receptor antagonists |
IL125658A0 (en) | 1997-08-18 | 1999-04-11 | Hoffmann La Roche | Ccr-3 receptor antagonists |
AUPP891299A0 (en) * | 1999-02-26 | 1999-03-25 | Fujisawa Pharmaceutical Co., Ltd. | New 6-membered cyclic compounds |
US6664293B2 (en) | 1999-02-26 | 2003-12-16 | Fujiwawa Pharmaceutical Co., Ltd. | Amide compounds for the potentiation of cholinergic activity |
US6306859B1 (en) | 1999-03-02 | 2001-10-23 | American Home Products Corporation | N-substituted imide derivatives with serotonergic activity |
AU3711500A (en) * | 1999-03-02 | 2000-09-21 | American Home Products Corporation | N-substituted imide derivatives with serotonergic activity |
AU1468001A (en) | 1999-11-12 | 2001-06-06 | Wyeth | Branched adamantyl and noradamantyl aryl- and aralkylpiperazines with serotonin 5-HT1a activity |
US6831084B1 (en) | 1999-11-12 | 2004-12-14 | Wyeth | Branched adamantyl and noradamantyl aryl- and aralkylpiperazines with serotonin 5-HT1A activity |
EP1509213A2 (en) * | 2002-05-23 | 2005-03-02 | Abbott Laboratories | Acetamides and benzamides that are useful in treating sexual dysfunction |
DE10232020A1 (de) | 2002-07-04 | 2004-02-26 | Friedrich-Alexander-Universität Erlangen-Nürnberg | Neurorezeptoraktive Heteroarencarboxamide |
MXPA05000033A (es) * | 2002-07-04 | 2005-04-08 | Sanol Arznei Schwarz Gmbh | Utilizacion de carboxamida de heteroareno como ligandos de dopamina-d3 para el tratamiento de enfermedades de cns. |
DE102004054634A1 (de) * | 2004-11-12 | 2006-05-18 | Schwarz Pharma Ag | Azaindolcarboxamide |
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US3646047A (en) * | 1970-02-02 | 1972-02-29 | American Cyanamid Co | Certain benzo(b)thiophene-2-carboxamide derivatives |
US3734915A (en) * | 1970-02-02 | 1973-05-22 | American Cyanamid Co | N-(-(4-phenyl-1-piperazinyl)alkyl)benzo(b)thiophene or benzofuran-2-carboxamides |
US4001223A (en) * | 1975-01-13 | 1977-01-04 | Idemitsu Kosan Co., Ltd. | Adamantane-piperazine derivatives |
DE3304019A1 (de) * | 1983-02-07 | 1984-08-09 | Kali-Chemie Pharma Gmbh, 3000 Hannover | 3-acyloxy-1-phenyl-2-aminocarbonylindol-verbindungen sowie verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
AU577802B2 (en) * | 1983-10-17 | 1988-10-06 | Duphar International Research B.V. | Blood-pressure lowering piperazine derivatives |
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1989
- 1989-05-12 IL IL9027989A patent/IL90279A/en not_active IP Right Cessation
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- 1989-05-22 AU AU35025/89A patent/AU628341B2/en not_active Ceased
- 1989-05-22 NZ NZ229225A patent/NZ229225A/en unknown
- 1989-05-23 KR KR1019890006857A patent/KR0128345B1/ko not_active IP Right Cessation
- 1989-05-23 JP JP1129975A patent/JP2711284B2/ja not_active Expired - Lifetime
- 1989-05-23 DK DK249989A patent/DK168665B1/da not_active IP Right Cessation
- 1989-05-23 IE IE166289A patent/IE64151B1/en not_active IP Right Cessation
- 1989-05-23 PT PT90633A patent/PT90633B/pt active IP Right Grant
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- 1989-05-24 AT AT89305255T patent/ATE132862T1/de not_active IP Right Cessation
- 1989-05-24 DE DE68925385T patent/DE68925385T2/de not_active Expired - Lifetime
- 1989-05-24 EP EP89305255A patent/EP0343961B1/en not_active Expired - Lifetime
- 1989-05-24 ES ES89305255T patent/ES2081302T3/es not_active Expired - Lifetime
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1996
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Also Published As
Publication number | Publication date |
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DK168665B1 (da) | 1994-05-16 |
HUT53095A (en) | 1990-09-28 |
JP2711284B2 (ja) | 1998-02-10 |
KR0128345B1 (ko) | 1998-04-03 |
ATE132862T1 (de) | 1996-01-15 |
DE68925385D1 (de) | 1996-02-22 |
EP0343961B1 (en) | 1996-01-10 |
EP0343961A2 (en) | 1989-11-29 |
NZ229225A (en) | 1990-12-21 |
CA1340113C (en) | 1998-11-03 |
PT90633A (pt) | 1989-11-30 |
FI892424A0 (fi) | 1989-05-19 |
GB2218988B (en) | 1991-12-18 |
IE891662L (en) | 1989-11-24 |
FI892424A (fi) | 1989-11-25 |
ES2081302T3 (es) | 1996-03-01 |
FI94130C (fi) | 1995-07-25 |
AU3502589A (en) | 1989-11-30 |
IE64151B1 (en) | 1995-07-12 |
IL90279A (en) | 1995-03-30 |
GB8911912D0 (en) | 1989-07-12 |
DE68925385T2 (de) | 1996-05-15 |
DK249989A (da) | 1989-11-25 |
PT90633B (pt) | 1994-11-30 |
IL90279A0 (en) | 1989-12-15 |
HU205923B (en) | 1992-07-28 |
FI94130B (fi) | 1995-04-13 |
EP0343961A3 (en) | 1991-01-16 |
JPH0215059A (ja) | 1990-01-18 |
AU628341B2 (en) | 1992-09-17 |
DK249989D0 (da) | 1989-05-23 |
GB2218988A (en) | 1989-11-29 |
GR3019217T3 (en) | 1996-06-30 |
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